Chapter 25
Marine Protected Areas and Key Biodiversity Areas of the
Alboran Sea and adjacent areas
Ángel Mateo-Ramírez, Pablo Marina, Diego Moreno, Andrés Alcántara, Ricardo
Aguilar, José Carlos Báez, Patricia Bárcenas, Jorge Baro, José Antonio CaballeroHerrera, Juan Antonio Camiñas, Mohammed Malouli, Ana de la Torriente, Teresa
García, José Enrique García Raso, Serge Gofas, Emilio González-García, Juan
Antonio González García, Elena Moya-Urbano, Antonio-Román Muñóz, Luis
Sánchez-Tocino, Carmen Salas, José Templado, José Manuel Tierno de Figueroa,
Javier Urra, Juan-Tomás Vázquez, José Luis Rueda
Ángel Mateo-Ramírez, Pablo Marina, José Carlos Báez, Patricia Bárcenas, Jorge Baro,
Teresa García, Emilio González-García, Javier Urra, Juan-Tomás Vázquez, José Luis
Rueda
Instituto Español de Oceanografía, Centro Oceanográfico de Málaga, Fuengirola, Spain
e-mail: angel.mateo@ieo.es; pablo.marina@ieo.es; josecarlos.baez@ieo.es;
patricia.barcenas@ieo.es; jorgebaro@ieo.es; teresa.garcia@ieo.es;
emilio.gonzalez@ieo.es; javier.urra@ieo.es; juantomas.vazquez@ieo.es;
jose.rueda@ieo.es
Andrés F. Alcántara
UICN Centro de Cooperación del Mediterráneo, Parque Tecnológico de Andalucía.
Campanillas, Málaga, Spain
e-mail: andres.alcantara@iucn.org
Ricardo Aguilar
Oceana. Gran Via, 59-9, Madrid, Spain
e-mail: raguilar@oceana.org
José Antonio Caballero-Herrera, Elena Moya-Urbano, J. Enrique García Raso, Serge,
Gofas, Antonio-Román Muñóz, Carmen Salas
Universidad de Málaga, Departamento de Biología Animal, Málaga, Spain
e-mail:caballero.jant@gmail.com;emoyaurbano@gmail.com;garciaraso@uma.es;
sgofas@uma.es; roman@uma.es; casanova@uma.es
Juan Antonio Camiñas
Asociación Herpetológica Española, Madrid, Spain
e-mail: caminas.fao@gmail.com
Mohammed Malouli Idrissi
INRH, Centre Régional de Tanger, Tanger, Morocco
e-mail: malouli@inrh.ma; idrissi.malouli@gmail.com
Ana de la Torriente
Instituto Español de Oceanografía, Centro Oceanográfico de Santander, Santander,
Spain
e-mail: ana.torriente@ieo.es
Juan Antonio González García, Luis Sánchez-Tocino, José Manuel Tierno de Figueroa
Universidad de Granada, Facultad de Ciencias, Departamento de Zoología, Granada,
Spain
e-mail: jagg@ugr.es; lstocino@ugr.es; jmtdef@ugr.es
Diego Moreno
Agencia de Medio Ambiente y Agua/Consejería de Agricultura, Ganadería, Pesca y
Desarrollo Sostenible/Junta de Andalucía, Spain
e-mail: diego.moreno@juntadeandalucia.es
José Templado
Museo Nacional de Ciencias Naturales (CSIC), Madrid, Spain
e-mail: templado@mncn.csic.es
Corresponding autor, e-mail: angel.mateo@ieo.es
Abstract
Marine Protected Areas (MPAs) and Key Biodiversity Areas (KBAs) are important
tools for preserving species, habitats and ecological-geological-oceanographical
processes. Nowadays, more than 10% of the Alboran Sea is under some protected figure
or is on its way to be protected. This chapter presents the current state of the MPAs and
KBAs of the Alboran Sea. Most of the habitats included in the Annex I of the Habitats
Directive or the Barcelona Convention are represented in MPAs-KBAs of the Alboran
Sea. More than 290 threatened species are also occurring in these MPAs-KBAs, but
some of them have experienced a strong decline even within them (e.g. Zostera marina,
Pinna nobilis, etc.). Although important progress in the protection of the Alboran Sea
has been made in the last decades, there is still much to be done for effective
conservation of the habitats and species. The main efforts may focus on improving (1)
knowledge of the habitats and species, (2) the surveillance and mitigation against
current impacts, (3) the coordination between local, national and international agencies
and (4) the measures for improving habitats and threatened species populations, among
others. A deep change in the socio-economic model is then needed for preserving the
Alboran Sea natural heritage, promoting then a sustainable use of its resources.
Keywords: Biodiversity, conservation, birds, marine mammals, invertebrates, benthic
communities, habitats, impacts.
1. Introduction and historical background of marine and coastal
conservation in the Alboran Sea
Biodiversity conservation probably represents one of the biggest challenges for humans
in the 21st century, especially considering the continuing human impacts on most of the
ecosystems at different scales (Rands et al. 2010). Effective conservation of biodiversity
is essential for human survival and as well as for maintenance of ecosystem processes
and services. Despite some conservation successes (especially at local scales) and
increases of the public and government interest in living sustainably, habitats and
species are still declining at an unprecedented rate (Ichii et al. 2019). Moreover, this rate
is expected to rise in the future due to human population growth, depletion and
inefficient management of natural resources and unsustainable practices affecting on
ecosystems, among other causes (Ichii et al. 2019). Marine species and habitats are
experiencing a similar decline than terrestrial ones; however knowledge for the marine
environment is more limited and marine conservation has always lagged behind
terrestrial conservation in most coastal countries (Maxwell et al. 2015). At the end of
the 20th century, the concept of protecting certain marine areas was widely accepted
and since then this idea has been consolidated with hundreds of Marine Protected Areas
(MPAs) established around the world. As their numbers have grown rapidly, so has
their diversity and complexity, MPAs vary dramatically in concept, size, design,
purpose, focus, name, and effectiveness (Norse 1993). This same process recognized in
other seas and countries has followed a similar trend in the Alboran Sea. In this way,
MPAs have been defined by IUCN as “any area of intertidal or subtidal terrain, together
with its overlying water and associated flora, fauna, historical and cultural features,
which has been reserved by law or other effective means to protect part or all of the
enclosed environment” (Kelleher et al. 1999). MPAs represent a traditional way for
preserving species, habitats and ecological-geological-oceanographical processes and
currently are an important central axis of marine conservation efforts (Kelleher et al.
1999; Kuempel et al. 2019). The benefits of establishing well-designed and enforced
fully protected MPAs are well-documented (Giakoumi et al. 2018). Scientific evidence
indicates that MPAs can produce ecological, economic and social benefits under
appropriate design and management conditions (Ban et al. 2012; 2017).
According to the IUCN (2016), Key Biodiversity Areas (KBAs) are sites that contribute
significantly to the global persistence of biodiversity. The identification of a site as a
KBA simply implies that the site should be managed in ways that ensure the persistence
of the biodiversity elements for which it was considered important. Nevertheless, some
KBAs may sometimes not have in itself any character of protection. In this sense,
several KBAs can also overlap wholly or partly with existing MPAs, including sites
designated under international, national and local levels. Thereby, it is expected that
some MPAs overlap with KBAs, however this is not always the case, because MPAs
are sometimes established locally by different criteria, and opportunities. IUCN (2016)
established global standard criteria for the identification of KBAs worldwide. The main
criteria are based on the presence of threatened species/habitats for which site-scale
conservation is appropriate, including the importance of such site in the biology,
ecology and preservation of these species and habitats (Butchart et al. 2012, IUCN
2016). Other criteria are that the KBA can host a significant number of endemic/rare
species, and/or has a high pristine status. Therefore, MPAs and KBAs designation are
useful steps for conservation of global biodiversity, for identification of key sites for
elements of biodiversity and for provision of resources to decision-makers that are
essential for guiding decisions on the conservation and sustainable management of a
particular region.
1.1. International agreements for marine and coastal conservation of the Alboran Sea
MPAs and KBAs have been identified as potentially multifunctional areas which could
provide ecosystem and socio-economic services useful for conservation management in
the Alboran Sea (Robles 2010; UICN 2012a). These MPAs and KBAs (without
IMMAS) cover ca. 7% of the world's ocean (UNEP-WCMC IUCN 2017), whereas in
the Alboran Sea these areas represent ca. 10%. The political scenario of the Alboran Sea
region is characterized by a clear division between the north and south sectors, and
national interests predominate both north and south in terms of the maritime map, with a
resulting mosaic of jurisdictions that facilitates neither bilateral nor multilateral
agreements (Talamo and Riera 2019). The north-south asymmetry of the Alboran Sea
can also be seen in the existence of two distinct and greatly differing socio-economic
and cultural models. The north has high or very high human development indicators,
whereas the south has average human development indicators.
International agreements have been helpful in the designation of some of the MPAs and
KBAs of the Alboran Sea. Some of the most widely known KBAs focussing on
vertebrates are the Important Bird and Biodiversity Areas (IBAs) adopted by Birdlife
International and the Birds Directive (2009/147/EC) (only in countries of the European
Union) and Important Marine Mammal Areas (IMMAs) adopted by IUCN (IUCN
2016). The Biosphere Reserves (e.g. Cabo de Gata-Níjar, Intercontinental of the
Mediterranean) recognized by the UNESCO Man and Biosphere Program are areas
made up of terrestrial, marine and coastal ecosystems. The objectives of this UNESCO
program are to promote solutions to reconcile the conservation of biodiversity with its
sustainable use, economic development, research and education. Global Geoparks, also
recognized by the UNESCO (e.g. Cabo de Gata-Níjar) are single, unified geographical
areas where sites and landscapes of international geological significance are managed
with a holistic concept of protection, education and sustainable development. Their
bottom-up approach of combining conservation with sustainable development while
involving local communities is becoming increasingly popular. The Ramsar Convention
aims to the conservation and wise use of all wetlands through local and national actions
and international cooperation, as a contribution towards achieving sustainable
development throughout the world. In the Alboran Sea, this convention has recognized
three Ramsar Sites in Spain (Cabo de Gata-Níjar, Punta Entinas-Sabinar, Albufera de
Adra) and another three in Morocco (Cape Trois Fourches, Sebkha Bou Areg, Mouth of
River Moulouya). Another figure is the Specially Protected Areas of Mediterranean
Importance (SPAMI) that are areas declared under the Protocol on Specially Protected
Areas and Biological Diversity in the Mediterranean (SPA/BD Protocol) under the
Convention for the protection of the marine environment and from the Mediterranean
coastal region (also known as Barcelona Convention 1995). These SPAMIs guarantee
the survival of the biological values and resources of the Mediterranean Sea, since they
contain typical ecosystems of the Mediterranean area or habitats of endangered species,
which have a special scientific, aesthetic or cultural interest. It is also important to
highlight the Ecologically or Biologically Significant Marine Areas (EBSAs)
recognized by the Convention on Biological Biodiversity (CBD). In 2009, the ninth
meeting of the CBD-COP9 adopted different scientific criteria for identifying
ecologically or biologically significant marine areas in need of protection in open-ocean
waters and deep-sea habitats (Malcolm et al. 2014). The Regional Workshop of the
Mediterranean region agreed on the description of 17 areas meeting EBSA criteria,
among them the Strait of Gibraltar, Alboran Sea and connected Spanish, Moroccan and
Algerian areas. In 2014, despite the positive results of this workshop, the COP 12 of
CBD governments have not reached an agreement in the same direction, therefore, to
date, it appears not feasible the creation of an EBSA area in the Alboran Sea. Talamo
and Riera (2019) aimed to renew and underline the importance and value added of
creating an EBSA to support more and better cooperation in the policies of conservation
and sustainable development of the Mediterranean Sea. A recent concept is the Peace
Park which is defined as ‘transboundary protected areas that are formally dedicated to
the protection and maintenance of biological diversity and of natural and associated
cultural resources, and to the promotion of peace and cooperation’ (Sandwith et al.
2001). In 2010, during the CIESM workshop in Siracusa (Italy), eight Peace Parks were
proposed for the Mediterranean Sea, being the Near Atlantic Marine Peace Park (IberoMoroccan Gulf, Straits of Gibraltar and the Alboran Sea) the first one of them (Aguilar
et al. 2010). An integrated governance framework as set out in process may offer
appropriate horizontal tools to help policy makers and economic and environmental
actors to join up their policies, interlink their activities and optimize the use of marine
and coastal space in an environmentally sustainable manner.
Another international tool for preservation on marine life has been through the
Convention on International Trade in Endangered Species of Wild Fauna and Flora
(CITES). Its aim is to ensure that international trade in specimens of wild animals and
plants does not threat their survival. Roughly 5800 species of animals and 30000
species of plants are protected by CITES against over-exploitation through international
trade, and some of them are present in the Alboran Sea (e.g. black corals, red coral).
These species are listed in the three CITES Appendices according to how threatened
they are regarding international trade.
1.2. Marine and coastal conservation in the Spanish sector of the Alboran Sea
The Spanish legislative framework regulating the figure of MPA, focused on
maintaining the sustainability of the marine environment and biological diversity, is
referred to the Law on Natural Heritage and Biodiversity (Law 42/2007, of December
13) that identifies the MPA concept for the first time and contemplates the creation of a
network of MPAs. This law thus incorporated into the Spanish legal system the
possibility of creating MPAs and also established different protection figures: Natural
and National Parks (Parques Naturales, Parques Nacionales), Natural Reserves
(Reservas Naturales), MPAs, Natural Monuments (Monumentos Naturales) and
Protected Landscapes (Paisajes Protegidos) (Fig. 1) (Mateo-Ramírez et al. 2020a),
depending on the assets and values to be protected as well as the management objectives
to be met. Later on, the Marine Environment Protection Act (March 12, 2010; BOCG
121/000059) addressed new aspects of marine environment protection and management,
with three key elements: (1) marine strategies as a planning instrument, (2) the creation
of a network of MPAs and (3) the incorporation of environmental criteria in the uses of
the marine environment. Previously the Law 1/2002, of April 4, regulated the
management, promotion and control of marine fishing, shell fishing and marine
aquaculture (BOE106 / 2002 of May 3, 2002, p. 16189; BOJA45 / 2002 of April 04,
2002). Legislation at the autonomous level of Andalusia has also created different
regulations for the protection of marine natural areas and their resources. In 1989 (Law
2/1989 of July 18, BOJA 60 of July 27) the inventory of the Protected Natural Areas of
Andalusia was approved. Currently, more than 30 years later, the Network of Protected
Natural Areas of Andalusia (Red de Espacios Naturales Protegidos de Andalucía,
RENPA) is composed of 249 protected areas, with ca. twenty of them marine. This
network includes, among others, the following national and regional protection figures
(only those with marine spaces are mentioned): Natural Park (Parque Natural), Natural
Area (Paraje Natural) and Natural Monument (Monumento Natural) (Fig.1). In the
context of the Alboran Sea, it should be noted that the Cabo de Gata-Níjar Natural Park
(maritime-terrestrial), declared in 1988, is considered the first MPA sensu stricto (in
this case mixed), declared in the Spanish state (Ortiz García 2002).
Spain is an EU member and, therefore, has to fulfil with community policies regarding
environment. Considering that other protection figures have been developed at
European level, under the framework of the Natura 2000 Network, such as Site of
Community Importance (SCI) (previous step without management plan) and Special
Areas of Conservation (SAC) (once a SCI has approved a management plan) (Council
Directive 92/43/EEC of May 1992 - Habitats Directive) and Special Protection Areas
for Birds (SPA) (Council Directive 79/409/EEC of April 1979 - Birds Directive actually Directive 2009/147/EEC). It is interesting to clarify that, currently, some MPAs
of the Andalusian coast included in the Natura 2000 Network are managed by the
Spanish Government and others by the Andalusian Government (Fig. 1). The Habitat
Directive (HD) on the conservation of natural habitats and of wild fauna and flora aims
to promote the maintenance of biodiversity, taking account of economic, social, cultural
and regional requirements. It forms the cornerstone of Europe's nature conservation
policy, together with the Birds Directive (BD), and establishes the wide EU Natura
2000 ecological network of protected areas, safeguarded against potentially damaging
developments. Over 1.000 animal and plant species, as well as 200 habitat types, listed
in the HB annexes are protected in various ways. The BD is one of the oldest piece of
EU legislation for environmental conservation and one of its cornerstones. Amended in
2009, it became the Directive 2009/147/EC and it places great emphasis on the
protection of habitats for endangered and migratory birds. It establishes a network of
Special Protection Areas (SPAs) including all the most suitable territories for these
species. Since 1994, all SPAs are included in the Natura 2000 ecological network, set
up under the HD. The ca. 500 wild bird species naturally occurring in the European
Union are protected in various ways under the annexes of the BD.
Another tool for the conservation of wild flora and fauna in Spain is provided by the
National Catalogue of Threatened Species (Catálogo Nacional de Especies
Amenazadas), regulated by the Royal Decree 439/1990, under the List of Wild Species
under Special Protection Regime (Listado de Especies Silvestres en Régimen de
Protección Especial, LESRPE). Both the Catalogue and the List have been later on
updated in 2011, 2012, 2015, 2016 and 2019. In that list, the species are categorized
according to their degree of threat for their persistence and in accordance to some
specific measures for the recovery of their populations. Likewise, and following a
similar approach, the Andalusian Catalogue of Endangered Species (Catálogo Andaluz
de Especies Amenazadas) has been elaborated under the framework of the Andalusian
List of Wild Species under Special Protection Regime (Listado Andaluz de Especies
Silvestres en Régimen de Protección Especial, LAESPE) (Decree 104/1994, of May
10). Both the List and Catalogue were also updated in 2003 and 2012.
1.3. Marine and coastal conservation in the Moroccan sector of the Alboran Sea
In Morocco, several institutions are involved in the conservation and management of its
marine biodiversity, including various coordination, management, monitoring and
control institutions. The Moroccan Fourth National Report on Biodiversity (2009)
contains the Moroccan strategy for the conservation and sustainable use of its
biodiversity. Morocco has made great strides in creating an institutional and legislative
framework for the conservation and management of biodiversity. One of the first steps
was done with the legal regulation on maritime fishing of November 23, 1973 and its
revisions, which aimed to guarantee the sustainable management of fishery resources. In
this law, it is important to highlight the laws on Maritime Fisheries Code and on the
preservation of marine ecosystems and of the coastline. The Law no. 11/2003
represented another step towards conservation, focussing on the enhancement of the
environment in which "Specially Protected Areas" are defined as those "terrestrial or
marine spaces with a particular natural and cultural value within which measures must
be taken for the protection and environmental management”. A new law on protected
areas was adopted in July 2010 and it defines the roles and responsibilities of the
different administrations and the possibility of delegating the management of these
spaces. Regarding the law, the figures of protected spaces are grouped into the
categories of National Park (Parc National), Natural Park (Parc Naturel), Biological
Reserve (Réserve Biologique), Natural Reserve (Réserve Naturelle) and Natural Site
(Site Naturel) (Fig. 1) (Mateo-Ramírez et al. 2020a).
Regarding conservation sites, Morocco has developed an initiative to identify sensitive
areas in relation to their ecological functions, such as feeding, breeding and/or breeding
sites for the main demersal species, and their richness in biodiversity, including fauna
and flora species that sometimes unique at the regional level. These areas, under the
responsibility of the Water and Forest Administration, are declared as Sites of
Biological and Ecological Interest (Site d'intérêt Biologique et Écologique, SIBE, Fig.
1) of priority 1, 2 or 3, according to the following definition: Priority 1 SIBE: areas that
must be declared under some protection status (such as the Nature Reserve) for a period
of 5 years; Priority 2 SIBE: areas that must receive a protection status for 10 years;
Priority 3 SIBE: areas where any human activity is excluded and must enjoy a
protection status for a period of 10 years.
1.4. Marine and coastal conservation in the Algerian sector of the Alboran Sea
In Algeria, the legislation on marine and coastal areas has adopted during the last
decades regional and international legal instruments to which the country is signatory
(Boubekri and Djebar 2016). The development of protected areas through the National
Framework of Land Management (Schéma National d’Aménagement du Territoire)
constitutes the cornerstone of in situ conservation of biological diversity in Algeria. As
part of its environmental strategy, an important effort is being carried out aimed at the
knowledge and protection of coastal marine areas of relevance to biodiversity, as well as
complementary actions for the development of a management plan in a series of
preselected areas (e.g. Habibas islands). According to this strategy, measures related to
the protection and conservation of the coastal heritage will be applied in the future.
Changes in national legislation to adapt the country to the international legal
background include a Law on Land Use (2001), relative to the organization and
sustainable development of the territory, together with Coastal Law No. 02-02 (2002),
followed by enactment of Costal Area Management Programs in 2003 and creation of
the CNL (National Commission for the Littoral) in 2004 to coordinate the management
of Marine Nature Reserves in Algeria. According to Boubekri and Djebar, (2016) the
interest in the establishment of MPAs in Algeria started in the 1980’s. At that time,
there was a lack of legislative structures for their designation, and only one location
(Banc des Kabyles) was declared a Marine Reserve as part of Taza National Park. Later
on 2002, Law No. 02-02 on the protection and valorisation of the coast, encouraged the
creation of a second MPA, which was subsequently established at Habibas Islands in
2003 under Decree No. 03.147. The purpose of that law is the elaboration and
application of a specific national policy for the management and protection of the coast.
The law 11-02 of February 2011 defined the functions and responsibilities of the
different administrations and the possibility of delegating the management of protected
areas. According to this law, the following categories were established: National Park
(Parc National), Natural Park (Parc Naturel), Integral Nature Reserve (Réserve
Naturelle Intégrale), Nature Reserve (Réserve Naturelle), among others (Fig. 1) (MateoRamírez et al. 2020a). For this, the law institutes a National Commission of Protected
Areas that will be in charge of evaluating the proposal and categorization of each
proposed area. The management of each proclaimed area falls also on the institution that
prepares the proposal.
2. Important Marine Mammals Areas and other cetacean critical areas
within the Alboran Sea
The IUCN expert group for Marine Mammals has identified a set of KBAs known as
Important Marine Mammals Areas (IMMAs), which are defined as “discrete portions of
habitat, important to marine mammal species, that have the potential to be delineated
and managed for conservation” (Corrigan et al. 2014, Hoyt 2015). Currently, the
IMMAs have no status and their proposal as protected areas have to make by the coastal
countries that have the authority to implement. Some IMMAs described in different
basins (IMMA group 2020) overlap, and the Alboran Sea represents an example
regarding this, since the entire basin and its adjacent areas (e.g. Strait of Gibraltar) host
four different IMMAs (Figure 2) known as: Alboran Corridor IMMA, Alboran Deep
IMMA, Alboran Sea IMMA and Strait of Gibraltar and Gulf of Cádiz IMMA. Thus,
within the Alboran Sea, IMMA areas cover a large proportion of the Alboran Sea,
overlapping. Table 1 shows the area covered by each IMMA, and the main marine
mammals for which each IMMA has been delineated. For more details on the biology of
those cetaceans, and of the main threats within the Alboran Sea, please consult Báez et
al. (Chapter 21, of this volume).
A recent study based on opportunistic sightings assessed the suitability of IMMAs for
cetacean conservation in the Western Mediterranean Sea. In this same study, Báez et al.
(2019) demonstrated the higher abundance of cetaceans in IMMAs of the Alboran Sea
compared to those in other Mediterranean IMMAs.
3. Important Bird and Biodiversity Areas
The Important Bird and Biodiversity Areas (IBAs) are sites of international importance
for bird conservation on land and sea, which have world-wide recognition as practical
conservation and management tools (Donald et al. 2018).The concept of IBA has been
applied during the last decades and a big effort has been made to agree on a robust and
simple criterion to be applied consistently worldwide. The selection of these important
areas has been completed through the use of quantitative ornithological data and
considering up-to-date knowledge of the sizes and trends of bird populations. In this
way, it is ensured that all selected IBAs are of high interest for bird conservation at the
international levelling terms of the presence and abundance of species that occur there
seasonally or all year round (Heath et al. 2000).
At present 1873 out of 13599 existing worldwide IBAs are exclusively marine IBAs
(www.birdlife.org/datazone/site, accessed 3rd April 2020). Spain and Portugal were
pioneers in the design of marine IBAs in the open sea, where these important areas for
birds typically coincide with areas of interest for other organisms, such as cetaceans or
marine turtless (Arcos et al. 2009). The Alboran Sea hosts 9 marine IBAs, which cover
an area of 718766 km2 and include representatives of “areas of high-intensity use at
sea”, “seaward extensions of breeding colonies”, and “migration hotspots”.
Furthermore, there are 6 IBAs in the Alboran Sea occupying inshore (coastal) waters
(see Table 2).
The Strait of Gibraltar, in the Western limit of the Alboran Sea, is the only connection
between the Atlantic Ocean and the Mediterranean Sea and represents a clear example
of a bottleneck for seabirds, with migrants being constrained from both sides into a
narrow front of only 14.4 km at the nearest point between the European and African
coasts. It concentrates the majority of seabird populations entering and leaving the
Mediterranean Sea, being especially remarkable the cases of three Mediterranean
endemic species, the Balearic and Scopoli’s Shearwaters and the Audouin’s Gull, as
well as the Mediterranean Gull and the Northern Gannet, among many others. Tarifa
Island is a strategically located point from where populations of some species can be
estimated through coast-based counts (Arroyo et al, 2016). From this point to the East,
the Alboran Sea as a whole could consider a migration corridor, with certain areas of
special interest where seabirds occur in high numbers for foraging purposes, as the bays
of Málaga and Almería, and several locations that host important breeding colonies of
species listed in Annex I of EC Birds Directive, as the Audouin’s Gull or the Scopoli’s
Shearwater (see Table 2).
Seabirds are one of the most threatened groups of birds at global level, mostly due to
human activities at sea and on land, especially in their colonies (Croxall et al. 2012). As
the identification and designation of IBAs do not guarantee full legal protection,
conservation initiatives should be implemented to ensure the protection of the most
interesting enclaves and areas, including the open sea. The regular monitoring of the
IBAs, together with the identification and assessment of the main threats affecting the
species all year-round, would be important tools to guide and design effective
conservation and management initiatives. This is particularly important because most of
the seabirds inhabiting the Alboran Sea are highly mobile species (González-Solís et al.
2007, Bécares et al. 2016, Pérez-Roda et al. 2017).
4. SPAMIs and other overlapping-connected Marine Protected Areas
The Specially Protected Areas of Mediterranean Importance (SPAMIs) are marine and
coastal sites for conserving “the components of biological diversity in the
Mediterranean, ecosystems specific to the Mediterranean area or the habitats of
endangered species, which are of special interest at the scientific, aesthetic, cultural or
educational levels”. These SPAMIs were created under the Protocol concerning
Specially Protected Areas and Biological Diversity in the Mediterranean (SPA/BD
Protocol) and the contracting parties to the Barcelona Convention (BC). The SPA/BD
Protocol was adopted in 1995 and called for the creation of SPAMIs, however entered
into force in 1999. Nowadays there are 35 SPAMIs in the Mediterranean Sea, with 6 of
them located in the Alboran Sea and its adjacent areas (http://www.rac-spa.org/spami);
New SPAMIs could be included in the future as this is an ongoing process. The
SPAMIs have to follow the criteria listed in the Annex I of the SPA/BD Protocol: a)
uniqueness, b) natural representativeness, c) diversity, d) naturalness, e) presence of
habitats that are critical to become endangered or threatened or to harbour endemic
species and f) cultural representativeness. In addition, they have to follow the procedure
and the stages to be included as SPAMI in the List. SPAMIs are one of the most
important networks of MPAs recognised by all Mediterranean country signatories to the
BC. Each SPAMI needs a management plan and all the parties of the SPA/BD protocol
are committed to respect the protection and conservation measures defined in the
proposal for inclusion.
The main SPAMIs located in the Alboran Sea are presented from west to east direction
and from north to south order. In some cases these SPAMIs also overlap with other
figures of protection, which has also been indicated and explained.
4.1. Maro-Cerro Gordo Cliffs SPAMI and collateral figures of protection (Spain)
The Maro-Cerro Gordo cliffs (Acantilados de Maro-Cerro Gordo) are located on the
northern part of the Alboran Sea, between Nerja (Málaga) and Almuñécar (Granada). It
includes a narrow strip of 12 km along the coast, from Maro beach to Cerro Gordo cliff,
which contains a series of small beaches, coves and cliffs (Fig. 3). The total extension
of this maritime - terrestrial site is 19.13 km2, of which 3.84 km2 are terrestrial and
15.29 km2 are marine (one nautical mile from the coastline) with a depth range from the
coast to ca. 70 m in front of Cerro Gordo cliff. In these cliffs the outcrop of various
units of the Alpujárride Complex occurs where the age of the rocks and their degree of
metamorphism increases generally towards the east, consisting of Middle-Upper
Triassic carbonates or marbles, together with mica-schists and quartzites of low
metamorphic grade and Lower-Middle Triassic age, graphite schist of middle to high
metamorphic grade and locally migmatitic gneiss both of Palaeozoic age.
This MPA was firstly declared as Natural Area (Paraje Natural) by the Andalusian
Government (Junta de Andalucía) in July 1988 and it represents one of the few MPAs
within the RENPA that is also a SPAMI. In October 2002, this MPA was classified as
Special Protection Area (SPA, ES6170002) according to the Birds Directive (BD), but
due to its relevance in the Mediterranean basin, it was also declared as SPAMI in 2003.
Later on, the SPAMI was also confirmed as a Site of Community Importance (SCI)
(Acantilados de Maro-Cerro Gordo, ES6170002) in July 2006 and designated as a
Special Area of Conservation (SAC) in January 2015, in compliance with the Habitats
Directive (HD).
The confluence of Atlantic and the Mediterranean waters, the occurrence of upwellings,
the presence of soft (with variable grain sizes) and rocky bottoms, cliffs and underwater
seawalls and submerged caves makes this a privileged location where several types of
marine habitats and a high biodiversity has been described (Rueda and Marina 2009).
Around 16 types of natural habitats included in Annex I of the HD are present, four of
which are strictly marine: Sandbanks which are slightly covered by sea water all the
time (Habitat 1110), Reefs (1170), Submerged or partially submerged sea caves (8330)
and the priority habitat Posidonia beds (1120) (Mateo-Ramírez et al. 2020b). The most
representative structure for the habitat 8830 is the Cerro Gordo cave, which has ca.
100m length and that present a diverse fauna assemblages that changes towards the end
of the cave. (https://litoraldegranada.ugr.es/).
Moreover, some vertebrates included in Annex II of the HD have also been detected
such as the Striped Dolphin (Stenella coeruleoalba) (Fig. 3), or the Loggerhead Turtle
(Caretta caretta) as well as birds species such as Mediterranean Gull (Ichthyaetus
melanocephalus), the Audouin's Gull (Ichthyaetus audouinii), the Sandwich Tern
(Thalasseus sandvicensis) (Fig. 3) and the Osprey (Pandion haliaetus) during migration
and winter, the Cory’s and Scopoli’s Shearwaters (Calonectris borealis and C.
diomedea, respectively) during migration and summer, and the Peregrine Falcon (Falco
peregrinus) breeding in coastal cliffs, all included in Annex I of the Birds Directive
(2009/147/EC) (Mateo-Ramírez et al. 2020c).
A wide variety of fish species occur in this MPA, such as the Sunfish (Mola mola), the
Ornate Wrasse (Thalassoma pavo), the African Striped Grunt (Parapristipoma
octolineatum), the Pearly Razor Fish (Xyrichthys novacula) or Opeatogenys gracilis, a
small cryptic fish that inhabits the seagrass meadows (Rueda and Marina 2009). In the
rocky reefs it is still possible to spot some Dusky Grouper (Epinephelus marginatus)
and shoals of the Grey Triggerfish (Balistes capriscus), being the only member of the
balistidae family in the Mediterranean Sea. The invertebrates in this MPA are also of
importance, with some of them included in different conventions, the HD or the Listado
de Especies Silvestres en Régimen de Protección Especial (LESRPE) from the Spanish
Government, such as the Hatpin Urchin (Centrostephanus longispinus), the Star Coral
(Astroides calycularis), the Knobbed Triton (Charonia lampas) as well as the vermetid
Dendropoma lebeche (previously known as Dendropoma petraeum, Templado et al.
2016) classified as “Vulnerable” (Vulnerable) or the endangered Ribbed Mediterranean
Limpet Patella ferruginea as "En Peligro de Extinción" (In Extinction Risk) in the
Catálogo Español de Especies Amenazadas (CEEA), the scarce and beautiful Brown
Cowry (Luria lurida), (Endangered species in the BC) and the Noble Pen Shell (or Fan
Mussel) (Pinna nobilis) (included in the Annex IV of the HD and in Annex II of the
SPA/BD Protocol) (Fig. 3). The Noble Pen Shell has practically disappeared since 2016
due to the cryptogenic parasite Haplosporidium pinnae that caused an extensive mass
mortality of this large and endemic bivalve in the Mediterranean Sea (Catanese 2018;
Templado et al. Chapter 10 in this book). In the underwater caves and hard bottoms,
different gorgonians (the Pink Sea Fan Eunicella verrucosa, the Violescent Sea-whip
Paramuricea clavata, Leptogorgia sarmentosa), some of them listed as Vulnerable in
the Libro Rojo de los Invertebrados de Andalucía occur. Biological communities of
some seagrass beds of this MPA (e.g. Zostera marina, Posidonia oceanica) have been
studied and displayed a high diversity of fauna, but unfortunately they have experienced
a strong decline in the last years (Rueda et al. Chapter 09 of this volume).
Agriculture and fisheries (mainly, artisanal purse seining, gillnetting, and longlining)
have historically sustained human settlements around the MPA, but the increasing
tourism and recreational activity offered by its natural environment has nowadays taken
on enormous importance. Nevertheless, this represents one of the main impacts on this
MPA, especially during summer when tourist affluence increases. Unauthorized
activities such as free camping, transit and anchoring of motor boats, recreational
fishing or scuba diving, as well as urban solid waste and untreated sewage from nearby
villages (e.g. Nerja) are the main threats. In the same way, agriculture greenhouses have
proliferated in recent years in the western part of the MPA (e.g. Maro village),
generating a high visual impact and a large amount of solid (plastic) and liquid
(pesticides, fertilizers, etc.) waste, which can negatively affect the long-term stability of
habitats that are sensitive to coastal water quality such as seagrass beds. This together
with some illegal bottom trawling was postulated among the potential drivers that led
Zostera marina beds to their local extinction (Rueda et al. 2009).
4.2. Alboran Island SPAMI and collateral figures of protection (Spain)
The Alboran Island is a small and flat island, 642 m long and 265 m wide, located in the
centre of the Alboran Sea from which it received its name. It belongs administratively to
the Almería province, distant ca. 85 km and is situated ca. 55 km away from Morocco.
The island is of volcanic origin and represents the top of the Alboran Ridge, an
elongated submarine seamount that is one of the main structural highs of the Alboran
Basin. This island is flat (not exceeding 15 m in height) with an irregular morphology,
as well as the surrounding insular platform, due to the abrasive marine erosion. It
corresponds to an outcrop of volcanic breccias and tuff of the calcoalkaline series that
varies from pyroxene andesites to basalt-andesites, of Upper Tortonian age (IGME
1983; Aparicio et al. 1991). This outcrop is abraded by several levels of quaternary
marine terraces with detrital limestone deposits, which provide a characteristic tabular
relief to the island, and covered by a deposit of Holocene eolic sands (IGME 1983).
The island is located on a linear NE-SW elongated platform that is ca. 45 km long and
10 km wide, and is disconnected from the nearest continental areas (Bárcenas et al.
2004). The platform is located in the NE sector of the Alboran Ridge, an elevation of ca.
200 km in length which controls the physiography of the southern part of the Alboran
Sea. This structure is made up of a series of tight anticlinal-syncline folds generated
since the Upper Tortonian to the present and are located over a main thrust (Vázquez et
al. 2015a) according to the convergence of the Nubian plate towards the northwest
(Vázquez et al. Chapter 5 of this volume). This elevation is dotted with volcanic
outcrops, highlighting the trapezoidal building that corresponds to the basal Alboran
island edifice (Vázquez et al. 2004).
The insular platform is connected to a high slope flank that extends down to 10002000m (Vázquez et al. 2015a). The morphology and sediments spatial distribution
indicates the existence of two different hydrodynamic areas on the Alboran Ridge
(Bárcenas et al. 2018): a) The northern area with energetic hydrodynamics and a
predominance of erosive processes together with the presence of kelp beds (Fig.4),
which have been found in very specific areas of the Mediterranean subjected to Atlantic
influence (Templado et al. 2006) and b) the southern area with less energetic
hydrodynamics conditions, mostly harbouring muddy sediments, but with a high biotic
productivity associated with upwelling currents, as occurs off the Málagacoast. These
could be responsible of the formation of rhodoliths and higher concentration of biogenic
gravel and carbonates.
The first two protection figures of the area surrounding the island, a Marine Reserve
(4.29 km2) and a Fishing Reserve (ca. 490 km2), were declared in 1997 by the Spanish
Ministry of Agriculture, Fisheries and Food (MAPA). The fisheries regulations in the
Marine Reserve were revised in 2018, with a ban of bottom trawling between 0 and 100
m and below 1000 m. In 2001, the Alboran Island, with its underwater platform, was
declared SPAMI, according to the BC. In 2003, the Andalusian Government declared
the island and its platform (ca. 264.56 km2) a Natural Area (Paraje Natural) and the
management plan for this and the associated SPAMI was approved in 2005. In 2003, the
terrestrial part (ca. 0.8 km2) was also declared a SPA (SPA ES0000336). In 2006, a SCI
(SCI ES6110015), coincident with the marine part of the Natural Area (ca. 263 km2)
was approved for the Alboran Island platform. In 2014, just after the Life+
INDEMARES project, a new SCI proposal was adopted and named as Espacio Marino
de Alboran (Marine Space of Alboran) (ESZZ16005), which expanded the extension of
the previous SCI (an additional 108.9 km2). The objectives of the Life+ INDEMARES
project were to characterize and identify the main habitats and biocoenoses of this
offshore area, to evaluate their conservation status and possible threats, and to propose
management measures in order to include this site in the Natura 2000 Network. The
Life+ INDEMARES studies covered an area of 2753.46 km2, which corresponded to the
platform surrounding the island of Alboran down to 200 metres depth. Finally a new
SPA (ES0000505) named Espacio Marino de la Isla de Alboran (Marine space of the
Island of Alboran) (ca. 661 km2) was declared in 2014. Albeit the Andalusian
Government declared in 2015 a SAC (ES6110015) for the Alboran Island (BOJA
2015/153) with associated Management Measures (BOJA 2015/193), alleging an
ecological continuity between the terrestrial and the marine adjacent area, the Superior
Court of Justice of Andalusia cancelled both orders in 2017 (Order of December 18th,
2017 in BOJA 244/2017). The main reason for that was that the ecological continuity
between the land and the adjacent marine area could not be credited. Therefore, the
competence for declaring and managing both SCIs (ES6110015 and ESZZ16005)
corresponds nowadays to the Spanish Government. This judgment does not affect the
Natural Area and its Management Plan which remains in force under competence of the
Andalusian Government.
The terrestrial part of the MPA is the home of interesting endemic plants such as
Diplotaxis siettiana and Senecio alboranicus (Mota et al. 2006), as well as of few
invertebrates (Paracuellos et al. 2006). Nowadays, the colony of the Audouin’s Gull of
the Alboran Island is the main one for the Alboran Sea, and it has suffered an increase
of its population up to 800 breeding pairs reported in 2019 (Paracuellos and Nevado
1995, 2003, 2010; SEO CEUTA 2019). Several cetaceans display important populations
in the waters around the island (Fig. 4), such as the Cuvier’s Beaked Whale (Ziphius
cavirostris) (Annex IV of the HD among other conservation lists) (Mateo-Ramírez et al.
2020c) and the Risso’s Dolphin (Grampus griseus) (Annex V of the HD among others)
(Mateo-Ramírez et al. 2020c) (Cañadas et al. 2005; Junta de Andalucía, 2011).
The Alboran Sea has been considered a hot spot of marine biodiversity within the
Mediterranean Sea (Rueda et al Chapter 9; Templado et al. Chapter 10 of this volume);
hosting most of the Andalusian threatened marine species (Barea-Azcón et al. 2008).
The marine biodiversity of the Alboran platform is very rich. The macroalgae, with 220
known species, are very abundant in the sublittoral zone, including extraordinary forests
of the kelp Laminaria ochroleuca that surrounds the Alboran Island between 30 and 60
m depth (Fig. 4). Nevertheless, seagrass meadows which otherwise characterize most of
the coastal protected areas of the Alboran Sea are completely absent around the Island
(Moreno 2006). Thirteen benthic communities have been identified in the sublittoral
bottoms of the Alboran Island and its platform during the INDEMARES+Life project
(Gofas et al. 2014). From these, the rhodolith beds (related to Habitat 1110 of the HD),
which extend from 20 to 100 m depth should be highlighted (Mateo-Ramírez et al.
2020b). More than 300 species of invertebrates have been identified in this habitat;
some of them shared with coralligenous and with coarse bioclastic bottoms. Two
different communities are found on circalittoral rocky bottoms (Habitat 1170 of the HD)
surrounding the Alboran platform. A shallower occurring one (coralligenous), between
30 and 100 m depth, is very heterogeneous and rich in species. In this habitat the most
conspicuous are the gorgonians (Pink Sea Fan, Violescent Sea-whip or L. sarmentosa).
Some colonies of the Red Coral (Corallium rubrum) (Annex V of the HD between other
conservation lists) (Mateo-Ramírez et al. 2020c) can be present from 50 to 150 m depth,
under overhangs of the rock. Some species of echinoderms, such as the sea urchins
Sphaerechinus granularis, Gracilechinus acutus and the Hatpin Urchin (Annex IV of
HD between others) (Mateo-Ramírez et al. 2020c) as well as the ophiuroid Astrospartus
mediterraneus are frequent, the latter usually attached on the gorgonians. On deeper
rocky bottoms, from 100 to 200 m depth, there are different species of gorgonians, such
as Viminella flagellum, Acanthogorgia hirsuta, Eunicella filiformis and Callogorgia
verticillata. The latter is characteristic of the bathyal, but it reaches the edge of the
platform in the Alboran Island. Some deep rocky bottoms harbour the so-called
“Sponge Gardens” with some interesting species, such as Phakellia robusta, P.
ventilabrum, and the “lollipop” sponge Crella pyrula or the Atlantic Asconema
setubalense among others. One of the most extended habitats is the coarse bioclastic
bottoms that are present mostly below 100 m and at the edge of the platform (Gofas et
al. 2014), replacing the rhodolith beds. This is one of the most species-rich communities
of the Alboran platform, with 415 species of invertebrates identified during the
INDEMARES project (Gofas et al. 2014). The sea pens are particularly conspicuous
and include the species Veretillum cynomorium, Pennatula rubra and Virgularia
mirabilis. Other species present in this habitat are the sea cucumber Parastichopus
regalis, the sea stars Anseropoda placenta, Chaetaster longipes, Marginaster
capreensis and the small sea urchin Genocidaris maculata. The bioclastic bottoms are
rich in crustaceans, with Galathea intermedia, Inachus dorsettensis and Munida
speciosa as dominant species.
Among the studied marine fauna (Templado et al. 1986; Templado and Luque 1986;
García Raso 1989; Templado et al. 1993; Templado et al. 2006), one of the best known
groups is the molluscs (Salas and Luque 1986; Peñas et al. 2006) with more than 650
species listed for the Alboran Island, including some endemic species. The Ribbed
Mediterranean Limpet, catalogued as “In Extinction Risk in the (CEEA) has in this
MPA one of its best populations, with ca. 950 individuals (Paracuellos et al. 2003;
Moreno and Arroyo 2008; Arroyo et al. 2011; Junta de Andalucía 2014, 2018) (Fig. 4).
The sponges and cnidarians are also noteworthy, with more than 198 species (Gofas et
al. 2014; Sitjà and Maldonado 2014), and 76 species (of which 36 are anthozoans)
respectively (César Megina and Pablo López, pers. com.). Among the cnidarians, in
addition to the great diversity of gorgonians, important elements are the Star Coral
(Vulnerable in CEEA) (Fig. 4), the Red Coral, which was exploited for many years
(Templado et al. 2006; Moreno 2008) or the rare and giant Whip Gorgonian (Ellisella
paraplexauroides) (LESRPE) (Mateo-Ramírez et al. 2020c), a unique Mediterranean
relic from the Mauritanian-Senegalese Pleistocene interglacial expansion (Maldonado et
al. 2013). Altogether, about 1500 species have been reported around the Alboran island
(an exhaustive catalogue can be found in Templado et al. 2006), making the Marine
Space of Alboran a biodiversity hot spot for the Alboran Sea and, therefore, the
Mediterranean Sea (Barea-Azcón et al. 2008, Gofas et al. 2014).
In the Marine Reserve, outside the Integral Reserve, professional fishing is only
permitted with the gears and equipment traditionally used such as bottom longline,
trolling, fishing rods with live bait and purse seine for small pelagics, as well as
recreational trolling. Bottom trawling is only allowed in the Fishing Reserve, and it
represents the most important fisheries targeting deep water species such as the Blue
and Red Shrimp (Aristeus antennatus). The number of authorized bottom trawling boats
is currently 51 being the main base port Almería. One of the main threats of this MPA is
the contamination derived from maritime traffic and possible oil spills. Although the
emerged part of the island is guarded by a service of military forces, the MPA is very
large and the limits are far from the coast, so illegal fishing is also a threat.
Competences shared by regional and national governments should not affect the good
management and conservation goals of the MPA.
4.3. Natural Park of Cabo de Gata-Níjar SPAMI and Parque Natural del Cabo de
Gata-Níjar (Spain)
The Cabo de Gata (Gata Cape) and its surroundings (mountains, salt pans and seabeds)
are located in the Almería province (south-eastern Spain) and they were declared as
Natural Park (Parque Natural), with the name “Cabo de Gata-Níjar” by the Andalusian
Government in 1987 (published in January 1988). It included more than 50 km of
coastline and 120 km2 of marine area, constituting the first maritime-terrestrial protected
area of Andalusia and of the northern Alboran Sea. The marine area spans one nautical
mile from the coast along the 50 km of coastline, with maximum depths of ca. 90 m and
six zones of maximum protection: Cabo de Gata, Los Genoveses, Punta de la Loma
Pelada, Punta de la Polacra, Punta Javana and Mesa Roldán. The first Management Plan
was published in 1994 (with an extension of the terrestrial part to the current 375 km2)
and it was later on updated in 2008. This Natural Park is provided with management
and scientific team, offices and equipment, and it has been a pioneer in many
conservation activities of its rich natural heritage. For example, it has the only artificial
conservation reef in Andalusia, installed between 1993 and 1994 to protect the integral
reserve in front of Cabo de Gata (Guirado et al. 1997). In 1989, the salt pans area
(Salinas) was included in the Ramsar Convention, and together with the adjacent
mountains were classified IBA (ES216), and the entire MPA was then proposed SPA in
1992. In 1995, it was declared a Marine Reserve (only the external waters) by the
Spanish Ministry of Agriculture, Fisheries and Food, and Biosphere Reserve by the
UNESCO in 1997. In 2001 it was catalogued as a Geopark, entering in the European
Geoparks Network in 2006 and in the UNESCO Global Geoparks Network in 2015.
Moreover, it was declared SPAMI in 2001, following the BC. At the same time, this
MPA was designated SCI (Cabo de Gata-Níjar, ES0000046) in 2001, which was further
ratified in 2006 and 2009, and finally designated SAC (ES0000046) in 2012. Regarding
that, this MPA is one of the most recognized coastal areas in Spain and it contains a
significant number of protection figures.
This MPA nowadays spans over ca. 500 km2, including the Gata Cape (Cabo de Gata)
that is a first-order geographical accident (Fig. 5). The promontory “Charidemo”, as
named by the ancients, is where the volcanic mountains of Cabo de Gata end and it is
characterized by an extensive outcrop of volcanic rocks mainly from the Calco alkaline
series. They are constituted by a dominance of andesites and dacites Miocene in age
(between 14 and 7.5 Ma) (Fernández Soler 1996). On the volcanic structures, especially
at the North-eastern zone, there are important Messiniense reef limestone deposits
(Villalobos 2003) from a period in which the Mediterranean Sea was warmer than
today. The volcanic complex of Cabo de Gata is the largest in the SE of the Iberian
Peninsula and is characterized by its diversity (Villalobos 2003).
In addition to the mountain and the succession of cliffs, the native vegetation includes
numerous endemic species (Mota et al. 1997, 2011). This MPA has also extensive
sandy beaches in the Bay of Almería, with dune areas and large shrub vegetation
dominated by species of African origin such as Ziziphus lotus (Tirado 2009). Middle
Pleistocene fossil beaches, with Strombus shells, also occur in specific areas (e.g. mouth
of the seasonal river of the Amoladeras) (IGME 1983). The salt pans located close to
Gata Cape, on an old natural coastal lagoon that was transformed by humans, are still of
importance for the salt industry. They house a high biodiversity of birds, including the
Black-winged Stilt (Himantopus himantopus), Pied Avocet (Recurvirostra avosetta),
Kentish Plover (Charadrius alexandrinus) and the Greater Flamingo Phoenicopterus
roseus, all included in Annex I of the BD.
A wide variety of habitats occurs in this MPA, with sedimentary bottoms (Habitat 1110
of the HD), hard bottoms (1170), seagrass meadows, mostly of P. oceanica (1120) and
some marine caves (8330) (Fig. 5), among others. Regarding fauna, several cetaceans
included in directives (Annex II - V of HD) and catalogues inhabit the waters of this
MPA (e.g. the Fin Whale Balaenoptera physalus, the Common Dolphin Delphinus
delphis, Orca Orcinus orca). Some threatened invertebrates are the vermetid D. lebeche
(Vulnerable), Ribbed Mediterranean Limpet (Endangered), the Star Coral (Vulnerable)
(Fig. 5), Knobbed Triton (Vulnerable) and the Noble Pen Shell (Critically endangered)
(Moreno and Barrajón Domenech 2008a; Moreno and De la Rosa 2008) (MateoRamírez et al. 2020c). The latter, as already mentioned in Templado et al. (Chapter 11
of this volume), suffered a mass mortality event in 2016 (Vázquez-Luis et al. 2017) and
no live specimens have been currently detected here and in the northern Alboran Sea
(Junta de Andalucía 2018).
Regarding seagrass meadows, the most extensive ones are those of P. oceanica (Fig. 5),
especially in the northern zone, with some meadows on hard bottoms in the southern
zone (García Raso et al. 1992). Cymodocea nodosa meadows are also well represented
in the MPA and there are specific sites with presence of Zostera noltei (Luque and
Templado 2004). In the mesolittoral rock, Ribbed Mediterranean Limpet is nowadays
scarce but it was probably more abundant in the past as witnessed by the archaeological
sites in the mountains (Moreno 1992; Moreno and Arroyo 2008, Arroyo et al. 2011).
One of the most characteristic formations of this MPA is the vermetid reefs of D.
lebeche which are the most important ones in the northern Alboran Sea (García Raso et
al. 1992; Moreno 2008; Junta de Andalucía 2017, 2018). In shallow rocky bottoms there
is great diversity of photophilous algae, including different species of Cystoseira (e.g.
C. mediterranea, C. tamariscifolia, etc.) as well as Padina pavonica, Halopteris
scoparia and Acetabularia acetabulum (Ballesteros and Catalán 1984). Some
zooxanthellate scleractinians, such as the Pillow Coral (Cladocora caespitosa) (Moreno
et al. 2008a; Junta de Andalucía 2018) and Oculina patagonica (Zibrowius and Ramos
1983; Moreno 2010; Junta de Andalucía 2018) as well as the Rough Pen Shell (Pinna
rudis) (Moreno and Barrajón Domenech 2008b) also inhabit these shallow rocky
bottoms. In the sciaphilous rock walls, there is a wide diversity of macroalgae
(Peyssonnelia spp., Flabellia petiolata, Codium bursa, Cystoseira zosteroides and
Dictyopteris polypodioides), bryozoans (e.g. Myriapora truncata) and tunicates (e.g.
Clavelina dellavallei), among other invertebrates (García Raso et al. 1992; Ballesteros
and Pinedo, 2004). Important precoralligenous habitats also occur in shallow areas
(down to 6 m depth) with the presence of Star Coral colonies (García Raso et al. 1992),
a species that has its main Spanish populations in the Alboran Sea westwards of Gata
Cape (Moreno et al. 2008b) and the Purple Sea Star (Ophidiaster ophidianus) (Moreno
and Pérez Ruzafa 2008). Interesting rhodolith beds occur in the MPA (Luque and
Templado 2004), but coralligenous communities are not well developed and are
characterized by some hardy gorgonians and small kelp such as Phyllariopsis
purpurascens, which is just occasional in some years (Moreno et al. 2005). There is a
good knowledge on the marine flora and fauna of this MPA, at least regarding mega and
macrofauna, and it can be considered a biodiversity hot spot for the Mediterranean Sea
(Barea-Azcón et al. 2008). García Raso et al. (1992) listed more than 1400 species, later
on updated and increased by Luque et al. (1999) and Moreno (2003). In summary, ca.
265 species of macroalgae (168 red algal species), more than 50 sponges, 60 cnidarians,
5 ctenophores, ca. 175 polychaete annelids, ca. 375 molluscs, 120 crustaceans, 17
lophophorians, 32 echinoderms, 46 tunicates, more than 150 fish, two marine turtles, ca.
30 sea birds (Guirado et al. 1997) and at least 8 cetaceans have been recorded so far in
this MPA. Unfortunately, the monk seal Monachus monachus has not been detected
since the mid-twentieth century when it was considered very rare. Nevertheless, it
certainly lived in the area because several places were named in relation to the monk
seals (e.g. Arrecife de las sirenas-Sirens reef, Torre y Colina de los Lobos - hill and
tower of the Wolves).
The ichthyofauna of the artificial reefs installed in the integral reserve has been
monitored for more than 20 years in summer and winter. An increase of 72 fish species
has been detected, as well as an evolution of the typical soft bottom fish assemblages
(dominating Pagellus acarne and Mullus surmuletus) to more stable and typical hard
bottom fish assemblages with large predators (e.g. Dusky Grouper and Goldblotch
Grouper E. costae), and some pelagic species (e.g. Seriola dumerili) that benefit from
the reef environment (Moreno et al. 2006). Several fishing nets hooked on the reefs
were removed during monitoring, confirming the effectiveness of this passive method
against bottom trawling (Junta de Andalucía, 2015) (Fig. 5). Similar monitoring was
carried out for shallow rocky bottoms inside and outside the maximum protection areas
for testing the “reserve effect” in coordination with other MPAs of South-eastern Spain
(Moreno 1995; García-Charton et al. 2004). In all these MPAs, the Dusky Grouper was
more abundant within maximum protection areas than outside them, and smaller
serranids than this grouper (e.g. Goldblotch Grouper, Serranus cabrilla, Serranus
scriba) were more abundant in Cabo de Gata-Níjar than in other MPAs (García Charton
et al. 2004).
The Andalusian Administration has also done big efforts for increasing the knowledge
and conservation of seagrass meadows of this MPA, with projects for mapping P.
oceanica meadows of the coasts along Almería (the largest meadows in the Andalusian
coasts) in 1995-1996 by the Universidad Autónoma of Madrid (Luque et al. 2004).
Recently, further mapping was carried out with the EU Life+ Posidonia Andalucía
project between 2011 and 2016 (Mendoza et al. 2014; Arroyo et al. 2015). The project
also carried out numerous divulgation actions and promoted the definitive establishment
of a monitoring network for P. oceanica (POSIMED) with 5 fixed sampling stations (3
of them for demographic studies) in this MPA (Junta de Andalucía 2017, 2018).
Recently, the Life Blue Natura project, is studying the CO2 stock of P. oceanica
meadows, with one station in Agua Amarga. Here, a corer of more than one metre was
retrieved in the deep meadows (-18 m) and resulted in ages of more than 3000 years BP
(Mateo et al. 2018).
The socio-economic importance of this MPA is mainly related to the appreciation of its
natural values by tourism, sport and recreational activities (e.g. sun bathing beaches,
swimming, scuba diving). In addition to the natural and landscape values, the MPA
contains interesting and diverse historical (Roman salting factories, watchtowers and
castles, etc.) and cultural heritages (cottages, waterwheels, abandoned mines, etc.), as
well as numerous artisanal activities, such as traditional crops, fisheries and salt
extraction in the salt pans (Villalobos et al. 2004). Regarding fisheries there is a fleet of
30 artisanal vessels and 15 purse-seine boats. The main artisanal gears used are gillnets
targeting European Hake (Merluccius merluccius), Cuttlefish (Sepia officinalis), mullets
(Mullus sp.) or Spiny Lobster (Palinurus elephas), “moruna” that is similar to a small
“almadraba” targeting small tunas such as Greater Amberjack (Seriola dumerili),
Atlantic Bonito (Sarda sarda) or Little Tunny (Euthynnus alletteratus) and pots
targeting Common Octopus (Octopus vulgaris) and Soldier Striped Shrimps (Plesionika
edwardsii). Recreational fishing from the coast or using a boat is subjected to different
restrictions. The authorized recreational modalities from the boat are “chambel” or
“volantín” to be used outside the limit of the P. oceanica meadows, and surface
trolling, being subject to a series of restrictions (e.g. number of gears per fisherman,
catch limits) and some species are prohibited with this modality such as Dusky and
Goldblotch groupers, Shi Drum (Umbrina cirrosa), Meagres (Sciaena umbra /
Argyrosomus regius), all types of commercial crustaceans and molluscs except the
Common Squid (Loligo vulgaris). Bottom trawling and spearfishing are not allowed in
the entire MPA.
The semi-arid climate of Almería, one of the most arid ones in Europe (200 mm of
annual rainfall) (Guirado et al. 1994), probably has not allowed important human
settlements. In adition to the oceanographic conditions, this may have favoured the
transparency of the seawater and the good status of its seabeds. Among the notable
threats, it is possible to highlight the maritime traffic that passes very close to the Gata
Cape, the increasing tourism, the arrival of invasive alien species (Caulerpa cylindracea
in 2012; Junta de Andalucía 2012) and poaching. A greater coordination between
national, regional and local administrations is desirable for improving the management
of this MPA.
4.4. Sea bottoms of the Levante of Almería SPAMI and Terreros and Negra Islands
Natural Monument (Spain)
This MPA is located between Almería and Murcia provinces (adjacent area to the northeastern Alboran Sea). It was proposed as SIC in 1997 and approved in 2006 with the
name “Fondos Marinos del Levante Almeriense” (Sea bottoms of the Levante of
Almería) (ES6110010) with an area of 63.13 km2. In 2001, it was also approved as
SPAMI, but the limits were modified several times between 2009 and 2015, partly
towards the coastline, until reaching 106.92 km2. In 2016, it was declared SAC
(ES6110010), spanning 45 km from Carboneras village to the border with the Murcia
province, and a depth range from the coastline to ca. 200 m. A small extension of its
southern limit (0.5 km2) was proposed by the Life+ Posidonia Andalucía Project in
order to include the C. nodosa meadow located outside the MPA (Aranda and Otero
2014). Within this MPA, there is also one Natural Monument of biotic character called
“Terreros Island and Isla Negra” (Fig. 6), which was declared in 2001 by Andalusian
Government. This Natural Monument only protects the emerging part of these two
volcanic islets that harbour interesting sea bird colonies. The Natural Monument
declaration includes basic management criteria and a list of unsupported activities
(Castro et al. 2003). Previous to the declaration of this area as SPA (ES0000507)
“Espacio marino de los Islotes Litorales de Murcia y Almería” (123.35 km2) in 2014,
the Islands Negra and Terreros (ca. 0.17 km2, Almería) was included inside the IBA
(ES170), which are formed by these and the islet Las Palomas (Murcia). The islet of
Terreros harbours one the few breeding colonies in the Mediterranean Sea of the
Atlantic Cory’s Shearwater (Calonectris borealis), with 30-35 breeding pairs, and both
islets host breeding colonies of European Storm-Petrels (Hydrobates pelagicus); a
minimum of 100 breeding pairs in the islet of Las Palomas, and a lower but unknown
population in Terreros (Arcos et al. 2009; Reyes-González and González-Solis 2016)
(Fig. 6).
Seven marine habitats are represented in the MPA, including P. oceanica beds (Habitat
1120 of the HD), caves (8330), sandbanks (1110) or reefs (1170), among others (Fig. 6)
(Mateo-Ramírez et al. 2020b). Two clearly differentiated zones can be distinguished. In
the northern zone (Almanzora River towards Murcia province), the seabed has extensive
and vigorous seagrass meadows (Luque and Templado 2004), especially of P. oceanica
(Moreno et al. 2004a; Arroyo et al. 2015) (Fig. 6). Further south, the stretch until
reaching Villaricos runs parallel to the Almagrera mountains range that is composed of
shales and other minerals, and where there was a large mining activity of lead and silver
(Navarro et al. 1997). From the south of the Almanzora River to Carboneras, the seabed
is predominantly sedimentary with different sediment types, including areas of fine
sand, others of gravel and also of mud, as in the canyon in front of Garrucha where they
exceed 200 m depth. In this southern area C. nodosa meadows are well represented
(Moreno and Guirado 2003; Moreno et al. 2004b; Arroyo et al. 2015).
From 1995 to 2016 a high number of studies were carried out in this MPA, from P.
oceanica mapping and demographic studies to faunistic inventories (e.g. Luque et al.
2004; Life+ Posidonia Andalucía Project 2011-2016). Thanks to the Life+ Posidonia
Andalucía Project, six stations of P. oceanica were monitored within the POSIMED
Network and eleven ecological buoys were installed along scuba diving areas and
around the island of Terreros to avoid anchoring on the meadows (Mendoza et al.
2014).
The protected species of this MPA are similar to those of Cabo de Gata-Níjar MPA.
Nevertheless, the best population of the Noble Pen Shell for the whole Andalusian coast
lived on P. oceanica meadows of this MPA, and it was monitored annually by the
Marine Environment Management program of the Andalusian Administration until its
mass mortality in 2016 (Moreno and Barrajón Domenech 2008a; Junta de Andalucía
2015; Vázquez-Luis et al. 2017). In the northern area between San Juan de los Terreros
and Villaricos there are reefs of the vermetid D. lebeche (Vulnerable), which are
monitored annually (Junta de Andalucía 2018). There are also several rocky areas (from
ca 5-30 m depth) that are very visited by sports divers, such as El Calón, Loza del Payo
and El Cerro. The Hatpin Urchin (Annex IV of HD) also showed in these heterogeneous
rocky bottoms their densest known population for the Andalusian coasts (Junta de
Andalucía 2014) (Mateo-Ramírez et al. 2020c). Other species inhabiting these rocky
bottoms are the sciaphilic algae Halimeda tuna and D. polypodioides, together with the
bryozoan Ross Coral (Pentapora fascialis) (Fig. 6). In these submerged rocky
elevations there are some cracks and caves. The most important cave is known as La
Catedral whose roofs and walls are upholstered with sponges such as Oscarella
lobularis and Chondrosia reniformis, corals such as Madracis pharensis and
Leptopsammia pruvoti and the Smooth Starfish (Hacelia attenuata) catalogued as
Vulnerable (Mateo-Ramírez et al. 2020c).
The main threats of this MPA are the increase in tourism, maritime traffic (very intense
near Garrucha), illegal trawling, pollution, invasive alien species and the absence of
regulations for underwater fishing. Several housing developments have been built
mainly on the coast of Vera, Garrucha and Mojácar, but also in San Juan de Los
Terreros. In spite of the coastal population increase and the associated sewage, the main
contamination threat is the discharge of the chemical plant Deretil northwards of
Villaricos. This discharge occurs on the shore and has affected the seabed, mainly the P.
oceanica meadows down to ca. 10 m depth, leaving large areas of “dead matte”
(Moreno et al. 1999, 2001; Arroyo et al. 2015). In 2008, the invasive algae C.
cylindracea (previously known as C. racemosa) was detected near the island of Terreros
at 17 m depth, representing the first record for the Andalusian coasts (Moreno 2010). In
a short time it extended extensively and covered ca. 1.2 km2 in 2009, and nowadays it is
mainly affecting rhodolith beds (15-30 m depth) (Junta de Andalucía 2014). Other
invasive species are also abundant in the area, such as the crab Percnon gibbesi (since
2006) and the seaweed Lophocladia lallemandii (in Cocedores since 2012) (Junta de
Andalucía 2014). The scleractinian O. patagonica, of an invasive nature, is very
abundant locally in the southern area of this MPA, mainly in port areas (Junta de
Andalucía 2018) but also in shallow rocky bottoms (0-3 m) (Serrano et al. 2012).
4.5. Al-Hoceima National Park SPAMI and collateral figures (Morocco)
The Al-Hoceima National Park (Parc National d’Al-Hoceima) was declared in 2004 by
the High Commission for Water & Forests. It is the main MPA and the only National
Park in the Mediterranean part of Morocco. Due to its significant biodiversity,
comparable to that of the main hot spots of the Mediterranean Sea, it was also declared
as a SPAMI in 2009. This MPA is located in northern Morocco, close to the city of Al
Hoceima, and covers an area of 480 km2, with a terrestrial part limited to the west by
Mestassa valley and to the east by the Rhis River. The maritime area extends ca 200
km2 over approximately 40 km of coastline and a depth range from the coastline to ca.
200 m. This MPA includes a Marine Natural Resources Management Area, a Strict
Nature Reserve and a Natural Sanctuary.
The coastline is dominated by steep cliffs (more than 60 m high) of the limestone ridge
(Khouakhi et al. 2013) that have significant gravitational instabilities at the top, and at
times are spaced by small coves and sandy bays as well as some islets (Fig.7). Due to
the erosion caused by the intense wave action, there are caves and shallow underwater
openings that can exceed 60 m in length. The beaches are relatively rare and not very
extensive, and they mostly occur in protected areas of bays such as the beaches of
Cebadilla or Tala Youssef, or can form isthmus such as those of Cala-Iris and Badès.
The rest of the coast is mainly conformed of pebble and gravel beaches with some
coarse sand. The sublittoral domain is characterized by hard bottoms, made of blocks of
fallen rocks, and also by soft bottoms, mostly with medium and fine sands, and with
fairly gentle slopes. These singular geological features provide a wide environmental
variety of great geological and biological value, where several types of marine habitats
are present harbouring a high biodiversity (Mateo-Ramírez et al. 2020b).
The geomorphology of the coast, with inaccessible steep cliffs, and the high fish
richness and productivity constitute favourable conditions for some individuals of the
Mediterranean monk seal (Tunesi et al. 2003), which is included as Critically
Endangered in the IUCN Red List (Mateo-Ramírez et al. 2020c). It is also possible to
spot some cetaceans of conservation interest (i.e. included in Annex IV of the HD) such
as the Common Dolphin, the Stripped Dolphin and the Bottle-nosed Dolphin. It is also
an important area for the Loggerhead Turtle (Caretta caretta) and more rarely for the
Leatherback Turtle (Dermochelys coriacea) or the Green Turtle (Chelonia mydas)
(UICN 2012b) (Mateo-Ramírez et al. 2020c).
This SPAMI shows a high diversity of seabirds, favoured by the presence of rocky
cliffs, caves and islets. It is remarkable the presence of the only breeding nucleus of
Ospreys in Morocco, with a population of 20-25 adult birds and, at least, 6 breeding
pairs (Monti et al. 2013). The Mediterranean population of Osprey shows an
unfavourable conservation status and currently holds less than 100 breeding pairs. In
Al-Hoceima National Park a strong decrease in population size has occurred during the
last decades, from 14-16 pairs in the 1980s to only 6 in 2012-2013 (Berthon and
Berthon 1984; Hodgkins and Beaubrun 1990; Monti et al. 2013), being still exposed to
local extinction risk. Other species of interest in the area are the Audouin's Gull, the
Scopoli’s Shearwater, the Mediterranean subspecies of the European Shag
(Phalacrocorax aristotelis desmarestii) (Fig. 8), the Lesser Crested Tern (Thalasseus
bengalensis) during its migration, and the Sandwich Tern during winter.
The marine habitats of this MPA were recently explored in the framework of the
MedMPAnet Project by Espinosa et al. (2015). Ten different habitats were detected,
including some key conservation habitats such as seagrass meadows, dark and semi
dark cave communities, rhodolith beds and coralligenous assemblages. Some of these
habitats are similar to those included in Annex I of the HD: Sandbanks which are
slightly covered by sea water all the time (Habitat 1110), Reefs (1170), Vegetated sea
cliffs of the Mediterranean coasts with endemic Limonium spp. (1240), with Limonium
asparagoides (endemic to Morocco and Algeria), and Submerged or partially
submerged sea caves (8330) (Mateo-Ramírez et al. 2020b). The marine vegetation
displays a high diversity with more than 300 species reported, including kelps (S.
polyschides, L. ochroleuca, P. purpurascens, P. brevipes) (UNEP-MAP-RAC/SPA.
2014; Moussa et al. 2018). On the coastal rocks some red algae, such as Lithophyllum
incrustans, build a formation called "Lithophyllum sidewalk" together with other
species of corallinaceae like Mesophyllum lichenoides (Moussa et al. 2018). In high
hydrodynamic deep areas, some free calcareous red algae form rhodolith beds which
shelter a great variety of fauna and flora. The C. nodosa meadows, included in the
Annex I of the Bern Convention and in the Annex II of the BC, are also abundant in this
MPA.
The marine fauna is very diverse and includes most of the Mediterranean species of
conservation importance. For example, the Ribbed Mediterranean Limpet displays
populations in Cala Iris that are important for conservation (Bazairi et al. 2004) (Fig. 7).
There are also formations of the vermetid D. lebeche (Fig. 7) and the coralligenous
communities are well developed with coral such as the Star and Red Corals as well as
gorgonians as Eunicella cavalonii, the White Sea Fan (Eunicella singularis) and the
Violescent Sea-whip (UICN 2012a; MedPAN and SPA/RAC, 2019). The ichthyological
diversity is high, with more than 100 species, some of them of commercial interest such
as the Common Dentex (Dentex dentex), Redbanded Seabream (Pagrus auriga) as well
as several species of groupers including the Dusky Grouper (UICN 2012a) (MateoRamírez et al. 2020c).
Al-Hoceima National Park has a great potential for tourism activities and the human
development has slowed down in a large part of its coastal area, due to ecological and
environmental constrains. Tourism represents an impact on the environment and on the
local people culture, who may be threatened by uncontrolled housing developments,
including massive tourist developments. An ethical debate is currently taking into
account the need for preserving the natural and cultural resources of this MPA or,
conversely, for promoting the economic development of the local population. Fishing
can be considered as one of the main economic activities, with two main ports (AlHoceima port and Cala-Iris port) and seven artisanal fishing sites (Torrès, Badès,
Taoussert, Tikket, Boussekour, Inouaren and Adouz). The fishing fleet is mainly
composed of trawlers, sardine boats, longliners and boats, and the fishery resources
exploited are demersal species, such as the Red Mullet (Mullus barbatus barbatus),
small and large pelagics such as European Pilchard (Sardina pilchardus) and Swordfish
(Xiphias gladius) and small tuna, such as the Atlantic Bonito (Sarda sarda). After a
socio-economic analysis of the sustainability of the fishing activity carried out in 2011,
fishermen of this MPA have proposed management measures (e.g. a zonation of the
marine area close to the coast) in order to reduce illegal fishing activities.
4.6. Habibas Islands SPAMI and collateral figures (Algeria)
In 2005, several sites (Banc des Kabyles, Habibas Islands, Rachgoun Island and Cap de
Garde) were listed as potential MPAs in Algeria (UNEP 2005). Only two of them were
designated as SPAMIs, Banc des Kabyles and Habibas Islands (Les îles Habibas) being
the later the one located in the Alboran Sea. Habibas Islands consist of two rocky
islands lying 12 km west of the Algerian coastline just below the headland known as
“Les Andalouses” (which itself lies 45 km west of Oran). The larger island is called
“Gharbia” and reaches 103 m in height. The smaller and more easterly island is called
“Charguia” and reaches no more than 25 m in height. They were firstly declared a
Marine Nature Reserve in 2003 and SPAMI at the Seventh Meeting of National Focal
Points for SPAs of 2005, covering ca. 26 km2 and a depth range between the coastline
and 485m depth. Habibas Islands represent the first MPA, and also the first SPAMI,
established in Algeria.
Habibas Islands are of volcanic origin and they belong to the Sahel d’Oran volcanic
complex that has been characterized by rocks of andesitic to rhyolitic composition of
the Calcoalkaline series and Tortonian age (Bellon et al. 1984).
This MPA was also internationally recognised as IBA in 2001. Under the tutelage of the
Commissariat National du Littoral (CNL), this MPA has benefited since its creation
from a number of activities implemented in the framework of international
collaborations and is currently co-managed by the CNL in collaboration with the local
NGO “Barbarous”. The management plan for the Habibas Islands was finalised in 2013
as part of the “Development support of the CNL” project by the Conservatoire du
Littoral. Its implementation was deferred to 2015 with 5 year management objectives
focused on conservation and development (MedPan Web page visited the 06022020)
http://medpan.org/seven-new-medpan-small-projects-on-track-in-the mediterranean/.
Different and interesting bird species use this MPA as a breeding location, including the
Audouin’s and Yellow-legged Gulls, Scopoli’s Shearwater, the Mediterranean
subspecies of the European Shag, Osprey and Eleonora’s Falcon (Falco eleonorae)
(Fig. 8) (Mateo-Ramírez et al. 2020c). The habitat Halonitrophilic thickets (PeganoSalsoletea) (similar to the Habitat 1430 of the HD) is well represented in the Habibas
Island with important population of plants such as Salsola longifolia or Withania
frutescens.
The sublittoral part of this MPA hosts a high diversity of habitats and species. One of
the most abundant habitats are the rocky bottoms (similar to Habitat 1170 - Reefs of the
HD) in which several species included in various conventions and annexes thrive, such
as the Ribbed Mediterranean Limpet with populations exhibiting high densities, a wellstructured size distribution and high reproductive output in mesolittoral bottoms
(Espinosa et al. 2014). Other protected species are the macroalgae Cystoseira spp. (C.
zosteroides and C. amentacea), some cnidarians such as the Star Coral in the
infralittoral, echinoderms such as the Purple Sea Star, molluscs such as the Knobbed
Triton or the Noble Pen Shell (probably extinct at present) and large fishes such as the
Dusky Grouper at larger depths (Bache et al. 2007) (Mateo-Ramírez et al. 2020c).
Coralligenous communities are the most abundant at the circalittoral zone, with species
of interest for conservation, such as the gorgonians Violescent Sea-whip, the White Sea
Fan or Leptogorgia sarmentosa. The second habitat in order of importance is similar to
the Sandbanks which are slightly covered by sea water all the time of the HD (Habitat
1110), and displays different kinds of bottoms, such as rhodolith beds or detritic
bottoms with sea pens and soft bottom octocorals (Paralcyonium spinulosum, V.
cynomorium) (Bachet et al. 2007). It is remarkable the absence of P. oceanica, which is
however present on the continent towards the west until Melilla (Bachet et al. 2007).
One of the socio-economic benefits of the MPA is recreational diving, which may also
represent a threat, because of the potential impact on vulnerable and slow growing
habitats such as the gorgonian aggregations. Nevertheless, the main threats of this MPA
are related to fisheries and mainly to underwater fishing. Bachet et al. (2007) presented
some evidence of this, the observations of school of commercial fish species with small
size as well as their elusive behaviour. This is confirmed by old photos and testimonies
of fishing carried out several decades ago, which indicate a great abundance of fish
(grouper in particular) and large crustaceans. The increasing presence of invasive
species such as the macroalgae Asparagopsis armata, Asparagopsis taxiformis and
Codium fragile or the scleractinian O. patagonica represents other threats to these
islands (Bachet et al. 2007).
5. Other Marine Protected Areas and Key Biodiversity Areas from the
northern Alboran Sea and adjacent areas
Different MPAs and KBAs located in the northern Alboran Sea and adjacent areas are
presented from west to east direction, including remarks on their location, protection
figure status, natural heritage, socio-economic importance and main threats.
5.1. Parque Natural del Estrecho & SAC (Spain)
Situated in the north-western limit of the Alboran Sea the “Parque Natural del Estrecho”
SAC (Strait Natural Park) (ES0000337) was proposed as Nature Park (Parque Natural)
by the Andalusian Government and as SCI in 2003. Finally it was declared SCI in July
2006 and SAC in September 2012. The Intercontinental Biosphere Reserve of the
Mediterranean, declared in 2006, includes a marine strip of this Natural Park. It is
located on the northern part of the Strait of Gibraltar between Getares Cove (westwards
of Algeciras Bay) and Gracia Cape (westwards of Bolonia Bay), with a discontinuity in
front of Tarifa harbour. It covers an area of ca. 192 km2 of which 96 km2 are located in
the marine environment, and a depth range from the coastline to ca. 300 m. The Strait of
Gibraltar is characterized on both banks by the Flysch Complex, which are usually
made up of alternating marls and/or shales, gray limestones and micaceous sandstones,
deposited in turbidite systems, their age varies from the upper Cretaceous to the lower
Miocene (Didon et al. 1973; Balanya et al. 2007). This stratigraphical pattern is
reflected in the geomorphology of both terrestrial and marine areas, where the sandstone
layers are much better marked in the relief. The MPA is characterized by large areas of
rocky outcrops increasing towards Algeciras where the slope is steepest and sandy
sediments arranged as large bottom forms generated by the wave and current action
(Maldonado et al. 2003).
The main marine-related habitats included in Annex I of HD are Coastal lagoons
(Habitat 1150), Reefs (1170) and Sandbanks which are slightly covered by sea water all
the time (1110) (Mateo-Ramírez et al. 2020b). Nevertheless, the SAC contains a total of
25 coastal and terrestrial habitats included in the HD, with some of them interconnected
with the marine system. This MPA also has an important natural heritage and a high
biodiversity, with more than 1900 species of plants and animals, including endemic
species and new species that have been recently described. Some large species are
included in Annex II of the HD such as the Loggerhead Turtle (Caretta caretta), the
Leatherback (Dermochelys coriacea), the Bottle-nosed Dolphin (Tursiops truncatus)
(Fig. 9) and the Common Porpoise (Phocaena phocaena), with some of them frequently
detected in the MPA because of its strategic position between two continents (Africa
and Europe) and two basins (Atlantic Ocean and Mediterranean Sea). Other common
cetaceans of this MPA are the Long-finned Pilot Whale (Globicephala melas) (Fig. 9),
the Common Dolphin (Delphinus delphis), the Striped Dolphin (Stenella coeruleoalba),
together with larger species such as the Sperm Whale (Physeter macrocephalus) and the
Orca (Orcinus orca). The occurrence of Orca populations in this MPA is apparently
related to the migration of one of their main prey, Bluefin Tuna (Thunnus thynnus),
towards the Mediterranean Sea (Esteban et al. 2016). Moreover, a good variety of
seabird species occurs in this MPA such as the Scopoli’s and Cory's Shearwaters
(Calonectris diomedea and C. borealis), Northern Gannet (Morus bassanus), Sandwich
Tern (Stenella sandvicensis), the Great Skua (Stercorarius skua), the Balearic
Shearwater (Puffinus mauretanicus) and the European Storm Petrel (Hydrobates
pelagicus) (Mateo-Ramírez et al. 2020c). In the mainland, it is also possible to spot
migratory species, especially soaring birds, that include this MPA along their migratory
routes towards Africa such as the White Stork (Ciconia ciconia), the Black Kite (Milvus
migrans), the European Honey Buzzard (Pernis apivorus), the Booted Eagle
(Hieraaetus pennatus), and the Short-toed Eagle (Circaetus gallicus), among others.
Other important birds occurring in the terrestrial part of this MPA are the Spanish
imperial eagles (Aquila adalberti), the Egyptian Vultures (Neophron percnopterus), and
the Bald Ibis (Geronticus eremita), a critically endangered bird species that disappeared
from Europe during the 16th century, but has been introduced in specific Spanish
locations of the Strait of Gibraltar at the beginning of the 21st century.
In the intertidal and shallow infralittoral rocks, some protected species display
important populations such as the Ribbed Mediterranean Limpet (Patella ferruginea)
and the Saffian Limpet (Cymbula safiana; more frequent in the eastern part of the
MPA), the vermetid Dendropoma lebeche (more frequent in the western part) as well as
some endemism of the Strait of Gibraltar such as the nassarid Nassarius tingitanus and
the cerithiid Cassiella abylensis (Gofas 1998; Barea-Azcón et al. 2008; Ruiz-Giráldez et
al. 2011) (Mateo-Ramírez et al. 2020c). In some infralittoral hard bottoms (e.g. Tarifa
Island), extensive seaweed meadows occur, including those with large kelps exposed to
strong bottom currents (e.g. Saccorhiza polyschides, Laminaria ochroleuca and
Phyllariopsis spp.) (Fig. 9), however recent observations have indicated a strong decline
of these meadows. In the infralittoral hard bottoms, the presence of the Knobbed Triton
(Charonia lampas) and the Star Coral (Astroides calycularis) on the rocky bottoms,
represent indicators of a good environmental quality. Seagrass beds conformed by
Cymodocea nodosa occur in specific areas with soft bottoms of this MPA (e.g. Tarifa),
but the mediterranean Posidonia oceanica does not occur in this and other parts of the
northern Strait of Gibraltar.
The socio-economic importance of the MPA is mainly related to tourism activities (e.g.
bird watching, whale watching, cultural sites - i.e. the ancient Roman city of Baelo
Claudia), sports (e.g. windsurf, kite surf, scuba-diving) and artisanal fisheries. The main
fishing modalities are small gears and purse seine, from the inshore fleets of Tarifa and
Algeciras. There is a specific fishery for the Blackspot Seabream (Pagellus bogaraveo)
being the most caught species in the area, mainly by the Tarifa fleet among the Spanish
one. Other commercial species caught are: Horse Mackerel (Trachurus spp), Blackbelly
Rosefish (Helicolenus dactylopterus), Dusky Grouper (Epinephelus marginatus),
Bluefin Tuna (Thunnus thynnus), and Black Sea Bream (Brama brama). There is also
an important seafood fishing activity, carried out mainly in the intertidal area, and
therefore on foot. In addition sport fishing from boats and from the coast is very
widespread in the area.
The main threats include marine pollution and eutrophication, maritime traffic, electric
lines and wind turbines deployment (bird collisions), development of human
infrastructures (mainly beach bars, pathways, port expansion). Some invasive species
such as the brown algae Rugulopteryx okamurae have recently colonized massively the
rocky bottoms down to 35 m depth and have displaced other photophilic seaweeds
(García-Gómez et al. 2020). This seaweed was detected in 2015 for the first time in
Ceuta, south of the Strait of Gibraltar, probably from ballast waters of a ship from Asian
origin (Rosas Guerrero et al. 2018; Baeza 2019). Since then it has shown a surprising
establishment and dispersion that has almost completely displaced the local biota,
producing also important negative effects on the local fishermen. Later on, this brown
algae has expanded massively on subtidal illuminated marine hard-bottoms within the
strait of Gibraltar and the adjacent Alboran Sea in the past two years, producing big
impacts and economic losses to the fishermen from the area as well as serious impacts
on the benthic communities previously established, accumulation of hundreds of tons of
seaweed in nearby beaches and wrack zones and hooks on fishing nets (Junta de
Andalucía 2018; García-Gómez et al. 2020). García-Gomez et al. (2020) described a
possible linkage with global warming. On December 20, 2019, the Sub-Directorate
General for Biodiversity and Natural Environment received the proposal for cataloguing
R. okamurae as an invasive species, which includes the risk analysis prepared by the
University of Málaga. Another invasive species has been recently detected, Caulerpa
cylindracea, which probably arrived through maritime traffic between Ceuta and Tarifa
(Pellón et al. 2017). Although the invasion is incipient, the species should be considered
successfully established, because of its wide spread in this MPA (Pellón et al. 2017).
5.2. Paraje Natural de Marismas del Río Palmones and SAC - Fondos Marinos
Marismas del Río Palmones SAC (Spain)
The Paraje Natural (Natural Area) Marismas del Río Palmones (Palmones River Salt
marshes) was firstly declared a Natural Area (Paraje Natural) by the Andalusian
Government in 1989. Later on it was proposed as SCI in January 2001, declared as SCI
in July 2006 and SAC (ES6120006) in November 2013. It is located on the salt marshes
area of Palmones River within Algeciras Bay (northern Strait of Gibraltar) (Fig. 10),
and it covers an area of 1 km2 of fluvial, estuarine and terrestrial habitats, with a depth
range from the coastline down to ca. 4 m. This SAC is connected with another SAC
known as Fondos Marinos Marismas del Río Palmones (Marine bottoms of Palmones
River Salt marshes) (ES6120033), which was proposed as SCI in May 2007, declared
SCI in December 2008 and SAC in August 2015. This last SAC is connected to the
previous one, and covers an area of 1 km2 of marine habitats with a depth range from
the coastline to ca. 30 m. The mouth of the Palmones River is characterized by a salt
marsh area consisting of two levels, high and low, bounded to the north-western by a
system of coalescent alluvial fans, to the east by a system of fossil dunes and to the
south by another system of active dunes and the littoral barrier itself (IGME 2012a). In
the marine part, outcrops of the Flysch Complex to the east of the Guadarranque river
mouth stand out. The main marine-related habitats included in Annex I of the HD are
Estuaries (Habitat 1130), Mudflats and sandflats not covered by seawater at low tide
(1140) and Sandbanks which are slightly covered by sea water all the time (1110)
(Mateo-Ramírez et al. 2020b). Nevertheless, the first MPA also contains a wide variety
of terrestrial habitats that are interconnected with the salt marshes.
These 2 MPAs were proposed because of the presence of more than 40 bird species, as
well as 2 mammals (Eurasian Otter Lutra lutra and the Bottle-Nosed Dolphin) (Fig. 10)
and 1 reptile (the Loggerhead Turtle) included in Annex II of the HD, among other
species. Due to its strategic geographic position it is an important area for migratory
species, mostly shorebirds and herons, but also raptors and passerines. During winter it
is frequently visited by species such as the White Stork, the Osprey (Fig. 10) and ducks,
among other species (Mateo-Ramírez et al. 2020c).
These MPAs represent one of the few coastal wetlands that still retain the characteristics
of the original salt marshes and estuarine areas and the ecological values associated with
these natural habitats (Habitats 1130, 1140, 1320, 1410, 1420 of the HD). The
Marismas del Río Palmones has a strategic location for migratory birds that cross the
Strait of Gibraltar, as a resting, feeding and even reproductive area. Different marine
species also take advantage of the ecological characteristics of this space to develop
basic functions of its life cycle, such as spawning and feeding. In the intertidal zone it is
possible to spot meadows of the small seagrass Zostera noltei (Fig. 10), which displays
a very limited distribution in the Mediterranean Sea and experienced a strong regression
in the last decades. The dune habitat plays an important role in the stabilization of the
wetland, housing flora of interest at regional level such as the Cat's Ear (Hypochaeris
salzmanniana), which occurs in the nesting habitat of the Kentish Plover (Charadrius
alexandrinus). The strictly marine SAC (Fondos Marinos Marismas del Río Palmones)
plays an important role as a connecting element between the fluvial-estuarine and
marine environments, for physical and biological continuity and ecological processes.
The ecological connectivity of the fluvial-estuarine-marine system provided by the 2
MPAs is of importance for conservation of different fish species that frequent the
marshes and/or the river, either as a refuge, breeding and nursery.
The socio-economic importance is related to tourism activities (e.g. bird watching),
sport (e.g. windsurf, kite surf, recreational fishing) and artisanal fisheries mainly
targeting some fish species (e.g. Anguilla anguilla, Sparus aurata) as well as estuarine
bivalves such as the Cockle (Cerastoderma edule) and other clams (Ruditapes
decussatus, Ruditapes philippinarum, Venerupis aureus). The main threats include
marine pollution because the proximity of an industrial area and eutrophication, electric
lines (bird collisions) and invasive species such as the brown seaweed R. okamurae
(Junta de Andalucía 2018).
5.3. Estrecho Oriental SAC (Spain)
The Estrecho Oriental SAC (eastern Strait of Gibraltar) (ES6120032) was originally
proposed SCI in May 2007, approved SCI in February 2009 and designated SAC in
December 2012. The SAC is located in the north-eastern part of the Strait of Gibraltar,
bordering the Gibraltar rock and La Línea de la Concepción (Cádiz), covering an area of
236 km2 and a depth range between the coastline to ca. 880 m. The main
geomorphological features of this SAC include two submarine canyons (Algeciras and
La Línea) characterized by their proximity to the coastline. The Algeciras submarine
canyon has a complex geomorphology with three sectors (headwall, middle course and
distal sectors) where the different dominant sedimentary processes reflect a recent
sedimentary dynamics along the system (Vázquez et al. 2017). The erosive processes
dominate in the middle and distal sector (especially in the incisive gullies and crescentshaped bed forms) indicating sediment reworking caused probably by the interaction of
the Mediterranean water mass. La Línea turbidite system comprises four architectural
elements (canyon, channel, overbank and lobe deposits) that have developed from the
continental shelf (15 m depth) towards the basin (835 m depth) (Palomino et al. 2019).
Another interesting geomorphological structure present in this area is a pockmark field
detected in the deepest part of the SAC (Vázquez et al. 2015b).
The abundance and richness of species is largely influenced by the strong currents and
upwellings that are characteristic of the Strait of Gibraltar. This SAC was originally
proposed because of the presence of four types of natural habitats included in Annex I
of the HD: Sandbanks which are slightly covered by sea water all the time (Habitat
1110), Reefs (1170) (Fig. 11), Submarine structures made by leaking gases (1180) and
Submerged or partially submerged sea caves (8330). Moreover, three species included
in Annex II of the HD such as the Bottle-nosed Dolphin, Common Porpoise and the
Loggerhead Turtle were also included in the original proposal because they are
generally found in this SAC. A total of 14 species of birds were also included in the
original proposal, including the Audouin´s Gull (Ichthyaetus audouinii), the Balearic
Shearwater (Puffinus mauretanicus) and the Scopoli`s Shearwater (Calonectris
diomedea). This area has also been indicated as important for other cetaceans such as
the Common Dolphin, the Stripped Dolphin, the Long-finned Pilot Whale and the
Sperm Whale as well as for some invertebrates such as the Star Coral and the Knobbed
Triton, classified as “Vulnerables” in the Catálogo Español de Especies Amenazadas
(CEEA) and Catálogo Andaluz de Especies Amenazadas (CAEA) or the Hatpin Urchin
(Centrostephanus longispinus) included in the Listado de Especies Silvestres en
Régimen de Protección Especial (LESRPE) (Fig. 11) (Mateo-Ramírez et al. 2020c). The
location and extension of habitats and associated biota of this SAC has not been detailed
studied so far, but there is some knowledge on the populations of cetaceans
(Notarbartolo Di Sciara et al. 2016). A recent study by Vázquez et al. (2015) listed
different habitat types and associated communities of La Línea submarine canyon,
including sea-pen and cerianthiid communities, gorgonians aggregations and cold-water
coral banks (mainly of the White Coral Madrepora oculata, the Yellow Tree Coral
Dendrophyllia cornigera and Coenocyathus) (Fig. 11).
The socio-economic importance of this SAC is mainly related to fisheries, aquaculture
and tourism. Regarding fisheries, the artisanal fleet of mechanized dredging that targets
bivalves (e.g. Acanthocardia tuberculata, Chamelea gallina) is of importance in the
infralittoral bottoms, together with the artisanal fleet using trammel nets, purse seine
and longlines. One of the most valuable species fished in the area (with its eastern limit
in front of Gibraltar) is the Backspot Sea-bream which is caught by a locally designed
hook line known as “voracera”. In circalittoral and bathyal zones, bottom trawling is the
most common fisheries type and is performed by trawlers coming from harbours located
close by (e.g. Algeciras, Estepona). Aquaculture practices have experienced a decline in
the last decades, but mussel culture still occurs close to the La Atunara harbour. An
increasing socio-economic activity in the area since the 80s is whale-watching, mainly
for spotting different species of dolphins and small cetaceans.
The main threats of this SAC include the intense marine traffic across the Strait of
Gibraltar (mainly for cetaceans and marine turtless), the bunkering (fuel delivery to
anchored ships), marine pollution and eutrophication, coastal infrastructures and
material deposition for beach regeneration, deployment of submarine cables and pipes,
bottom trawling and other types of fisheries that may be in contact with the seabed (e.g.
bottom-set longline). Recently, the area has also been colonized by some invasive
macroalgae, being the brown seaweed R. okamurae the one that is causing the greatest
impact on the habitats and socio-economic activities of the area (e.g. artisanal fisheries)
(Junta de Andalucía 2018).
5.4. Southern Waters of Gibraltar SAC (United Kingdom)
The Southern Waters of Gibraltar was approved as SCI in July 2006; however a
protection regime has been in existence since 1991 through the Nature Protection Act.
Following its approval as SCI, the Government of Gibraltar declared the Southern
Waters of Gibraltar as a dual SAC (UKGIB0002) and SPA in March 2011. The MPA is
located around the southernmost tip of Gibraltar, covering an area of 55 km2 and a depth
range from the coastline to ca. 800 m. This MPA overlaps with the Estrecho Oriental
SAC proposed by the Spanish Government and the questions of sovereignty and
jurisdiction over the waters around Gibraltar are still in debate between United
Kingdom and Spain (Fig. 9). Moreover, the withdrawal of United Kingdom from the
European Union (known as Brexit) in February 2020 may change the administrative
status of this MPA because SACs are based on EU derived legislation to member states.
Regarding its natural heritage, similar habitats and species occur in this MPA in
comparison to the one of Estrecho Oriental SAC. This MPA was proposed because of
the presence of two types of natural habitats included in Annex I of the HD: Reefs
(Habitat 1170) and Submerged or partially submerged sea caves (Habitat 8330).
Moreover, species included in Annex II such as the Bottlenose Dolphin (Fig. 9), the
Loggerhead Turtle and 36 bird species were also included in the original proposal
Mateo-Ramírez et al. 2020c). The MPA is also located in an important migration route
for sea birds and several species stopover and feed during their migratory journeys, such
as the Scopoli’s Shearwater. Other species use the area during winter in variable
numbers depending on weather conditions (e.g. high numbers of Northern Gannets
feeding during storms). The Rock hosts several resident breeding pairs of European
Shags (Phalacrocorax aristotelis desmarestii) (Fig. 8). Seasonal abundance due to
migratory movements between the Mediterranean and the Atlantic, results in a
multitude of pelagic and predatory fishes along with cetaceans including the Common
and the Stripped dolphins which breed in the Bay of Algeciras (Ruiz et al. 2018). The
rocky shores display important populations of the endangered Ribbed Mediterranean
Limpet (Espinosa et al. 2005) (Mateo-Ramírez et al. 2020c).
The socio-economic importance of the Southern Waters of Gibraltar is related to
tourism activities (two beaches namely Camp Bay and Little Bay), sport and
recreational angling along with scuba diving and fisheries that are regulated through the
Marine Protection Regulations of 2012 which build on the legislative provisions of the
Nature Protection Act 1991. The main threats are somehow similar to those of the
Estrecho Oriental SAC and include marine traffic, bunkering, marine pollution and
eutrophication, coastal infrastructures and material deposition for beach regeneration
and increasing the coastal area and invasive species such as the brown seaweed R.
okamurae (Junta de Andalucía 2018).
5.5. Estuario del río Guadiaro SAC and Fondos Marinos Estuario del Río Guadiaro
SAC (Spain)
The Estuario del río Guadiaro (Guadiaro River Estuary) was firstly designated Paraje
Natural (Natural Area) in 1989. Posteriorly was proposed SCI (ES6120003) in
December 1997, declared SCI in July 2006 and as SAC in November 2013. It is located
on the western part of the Guadiaro River, between the Málaga and Cádiz provinces
(northern Alboran Sea). It covers an area of less than 1 km2 of estuarine and terrestrial
habitats, and a depth range from the coastline to ca. 4 m. It is connected with another
SAC known as Fondos Marinos Estuario del Río Guadiaro (Marine bottoms of
Guadiaro River Estuary) (ES6120034), which was proposed SCI in May 2007, declared
SCI in December 2008 and SAC in August 2015. This last SAC covers an area of 1 km2
of marine habitats with a depth range between the coastlines to ca. 20 m. The Guadiaro
River estuary is framed by hillside deposits from nearby reliefs located both to the
south-west and north-east where sandstone and shales formations of the Flysch
Complex predominate, Lower Miocene in age (IGME 2012b). The most resistant layers
of these units also outcrop on the outer continental shelf, near the Guadiaro submarine
canyon, although the inner continental shelf is dominated by the deltaic deposits related
to the Guadiaro river mouth.
The main estuarine-marine-related habitats represented in this 2 SACs are Estuaries
(Habitat 1130 of the Annex I of the HD) and Sandbanks which are slightly covered by
sea water all the time (1110). Nevertheless, the first SAC also contains a couple of
terrestrial-riparian habitats that are interconnected with the estuarine system. The former
SAC contains lush riparian vegetation associated with the Guadiaro River, which
constitutes the habitat of some migratory birds. Despite the small size of this wetland,
its strategic location on the north-eastern side of the Strait of Gibraltar favours the
presence of birds such as the Purple Heron (Ardea purpurea), the Purple Gallinule
(Porphyrio porphyrio) or the Common Little Bittern (Ixobrychus minutus). Other
species are directly linked to the aquatic environment such as the Southern Straightmouth Nase (Pseudochondrostoma willkommii an endemic river fish of the southwestern Iberian peninsula), Great Sea Lamprey (Petomyzon marinus) (included in
Annex II of the HD) and the Eurasian Otter (Mateo-Ramírez et al. 2020c). The marine
SAC represents an important area for the ecological connectivity function the Guadiaro
River, being part of a fluvio-tidal system. The two SACs stand out as one of the few
estuaries on the northern Alboran Sea, harbouring an ecosystem with an important
ecological function, as a refuge, breeding and feeding area for various birds,
invertebrates and fishes highlighting among them the Great Sea Lamprey.
The socio-economic importance of the two SACs is related to tourism activities (e.g.
bird watching), sport (e.g. windsurf, kite surf, recreational fishing) and artisanal
fisheries.The main threats include marine pollution and eutrophication, electric lines
(bird collisions), development of human infrastructures (mainly pathways), illegal arid
extraction and debris deposition, invasive terrestrial plant species (e.g. Arundo donax,
Cortaderia selloana) as well as the brown algae R. okamurae (Junta de Andalucía
2018).
5.6. Fondos marinos de la bahía de Estepona SAC (Spain)
The Fondos marinos de la bahía de Estepona SAC (Estepona Bay marine bottoms)
(ES6170036) (Fig. 12) was designed SCI in December 2000 with an extension of 5.5
km2 but it increased to ca. 6 km2 when it was declared SAC in August 2016. This SAC
is located in front of Estepona between the harbour of Estepona and Punta de la Plata,
separated ca. 150 m from the coastline and with a depth range from 1 to ca. 50 m. The
Estepona Bay geology is dominated by the outcrop of the Estepona Flysch units dated
from, Lower Miocene (IGME 1978a), and the submerged part by the development of
sandy deposits associated with the littoral wedge.
This SAC was initially designated due to the presence of Posidonia oceanica beds
(Habitat 1120 of the HD), which are associated with shallow rocky bottoms, at depths
not exceeding 4 m. These are distributed in two zones which occupy an area of 0.023
km2 and a linear coverage of less than 30%. Other habitats such as Reefs (1170) and
Submerged or partially submerged sea caves (8330) were detected once the SAC was
declared. Reefs are represented by photophilic biocoenoses of the upper infralittoral
rock in calm mode (1.5- 4m depth) and by circalittoral hard bottoms with coralligenous
communities and some kelp. The most characteristic macroalgae varies with depth,
including Sargassum vulgare, Cystoseira usneoides, L. ochroleuca, P. purpurascens,
Mesophyllum alternans, Lithophyllum stictaeforme, Lithophyllum incrustans or
Peyssonnelia rubra, among others. Regarding fauna, it is interesting to highlight the
presence of species included in the Annex II and III of the HD such as the molluscs
Saffiana Limpet and Knobbed Triton, the Broad Lobster (Scyllarus arctus), the Red
Sea-squirt (Halocynthia papillosa), the bryozoan Ross Coral (Pentapora fascialis) or
the fishes Seahorse (Hippocampus hippocampus) or Dusky Grouper. Other species
occurring in this MPA are included in conservation or threatened lists (e.g. CAEA,
Libro Rojo de los de Invertebrados de Andalucía) such as sponges (Spongia sp.) or
gorgonians (Pink Sea Fan, E. labiata, Leptogorgia sarmentosa). Special relevance has
the caves habitats because of the fragility and vulnerability their associated species,
including invertebrates from Annex II of the HD such as the Hatpin Urchin or the Star
Coral (Mateo-Ramírez et al. 2020c).
Tourism is one important socio-economic activity with a large number of hotels, beach
bars, nautical channels and boathouses located nearby. The marina of Estepona has a
large number of moorings (more than 400). Other economic activities are scuba-diving,
nautical activities as well as recreational fisheries. The fishing port of Estepona has and
important fishing activity, with a fleet of 75 boats, representing the second in
importance in the Málagaprovince. The majority of these boats are dedicated to small-
scale gear (60 boats) as well as bottom trawling (7) and purse seining (6). The main
target species are the European Sardine (Sardina pilchardus), Anchovy (Engraulis
encrasicolus), Atlantic Bonito (Sarda sarda) and European Hake (Merluccius
merluccius) as well as the Common Octopus (Octopus vulgaris). Regarding seafood
fisheries, the target species in the SAC include bivalves such as the Banded Venus
(Polititapes rhomboides), the Warty Venus (Venus verrucosa), Striped Venus Clam
(Chamelea gallina), Wedge Clam (Donax trunculus), Smooth Clam (Callista chione)
and Rough Cockle (Acanthocardia tuberculata) and the St. James' shell (Pecten
maximus); gastropods such as the Trunk Murex (Hexaplex trunculus) and the Purple
Dye Murex (Bolinus brandaris); the Sea Anemone Anemonia sulcata and echinoderms
such as the Stony Sea Urchin (Paracentrotus lividus) and the Black Sea Urchin
(Arbacia lixula).
The main threats are related with tourism, housing developments and maritime
constructions that can cause burial and/or physical alteration of the seabed,
modifications of environmental characteristics (increase in turbidity, modification of
stream dynamics, erosion and sedimentation processes), marine pollution and
eutrophication. In relation with scuba-diving, some impacts can be caused by the
damage produced by physical contact, accumulation of bubbles, sediment resuspension,
and collection of protected species or detachment of colonies of Star Coral from the
substrate. Regarding fisheries, the main impacts are mechanical abrasion of the seabed,
marine pollution and illegal collection of protected species. Different invasive species
have also been detected in the SAC such as A. taxiformis, C. cylindracea and the brown
seaweed R. okamurae (Junta de Andalucía 2018).
5.7. El Saladillo-Punta de Baños SAC (Spain)
The Saladillo-Punta de Baños SAC (Saladillo-Baños Point) (ES6170037) (Fig. 12) was
proposed SCI in May 2007, designated SCI in February and designated SAC in August
2016. This SAC is located on the continental shelf, between Marbella and Estepona,
covering an area of ca. 32 km2 and a depth range between the coastline and ca. 50 m. It
also includes the rocky known as “Placer de las Bóvedas” that rises from 60 m depth to
23 m depth located 5.6 km from the coast and situated close to the head of a submarine
canyon. The coast is controlled by a series of coalescing alluvial fans from the nearby
reliefs generated in different phases (IGME 1978b), with the seabed close to the coast
characterized by hardened bottoms of various characteristics and rocky outcrops.
This SAC was firstly proposed by the presence of P.oceanica beds (Habitat 1120 of the
HD) (Mateo-Ramírez et al. 2020b). The small P. oceanica patches develop on rocky
outcrops between 3.5 - 6m depth covering an estimated area of ca. 0.01 km2 (Fig. 12).
Nevertheless, rocky reefs (Habitat 1170) were also included in this SAC after the
inclusion of Placer de las Bóvedas inside the SAC. The rocky bottoms are represented
by Cystoseira spp beds on rock and detritic bottoms as well as by pre-coralligenous and
coralligenous communities in the area of Placer de las Bóvedas, occupying 3.03 km2
(Fig. 12). The presence of rhodophytes such as L. stictaeforme and Peyssonnelia spp is
highlighted, (Fig. 12) as well as species included in the Annex II of Berna and
Barcelona convention such as the Star coral, the Knobbed Triton or the Hatpin Urchin.
Other species included in conventions and threatened species lists, are the gorgonians L.
sarmentosa, Eunicella gazella, E. labiata, the Pink Sea Fan and the Violescent Seawhip, the Orange Tree Coral, the echinoderms A. mediterraneus and the Smooth
Starfish (Hacelia attenuata), the bryozoan Ross Coral, the decapod crustaceans Spider
Crab (Maja squinado) and the Spiny Lobster (Palinurus elephas) and fishes as the
Dusky grouper (Mateo-Ramírez et al. 2020c). Another interesting habitat occurring in
the SAC is the rhodolith beds, which are especially abundant between 25-35m around
Placer de las Bóvedas. These rhodolith beds are one of the very few occurring along the
coasts of Málagaand are conformed by the coralligenous algae Phymatolithon
calcareum and Lithothamnion valens.
The socio-economic importance of this SAC is mainly related to tourism, fisheries and
aquatic activities such as scuba diving, sport fishing and recreational boats, all of them
of importance in the area around Placer de las Bóvedas. Regarding tourism there is a
high coastal development and urban services in the SAC and adjacent areas, including
beach bars, hammocks, nautical channels and boathouses. The fishing fleet operating in
this SAC is the same than in the Fondos marinos de la bahía de Estepona SAC. The
main threats are punctual mechanical seabed abrasion (anchoring, artisanal fishery),
bottom trawling in prohibited bottoms, marine pollution (Guadalmansa EDAR waste
water treatment plant, long lines, plastic debris and litter), accidental capture of
protected species, seabed alterations (increase in turbidity and sedimentation) due to
beach restoration. At present, in addition to the occurrence of the algae C. cylindracea
and A. taxiformis, the new recently arrived brown algae R. okamurae is increasing its
populations (Junta de Andalucía 2018). This species has spread eastwards from the
Strait of Gibraltar, producing impacts on fisheries and tourism because of the enormous
quantity of seaweed wastes.
5.8. Calahonda SAC (Spain)
The coastline between Punta de Calaburras and Calahonda in the Málaga province was
proposed SCI (Fig. 13) in January 2001, approved SCI in July 2006 and designated
SAC in August 2015 (Calahonda, ES6170030). The SAC is located in the western part
of Málaga province along ca. 10 km of coastline between Fuengirola and Marbella, and
covering an area of 14 km2 and a depth range from the coastline to ca. 30 m. The coastal
geomorphology and lithology display natural rocky outcrops in very few locations along
the coast of Málaga province, being the area of Calahonda one of them. This area is
characterized by rocky outcrops, abrasion surfaces and sandy deposits on the
infralittoral wedge (Fig. 13). The main characteristics of this coastal sector are an active
dune belt located to the west of the Cabopino harbour (also known as Artola harbour)
and an alluvial fan system between the eolic system and the Palaeozoic rock outcrops
that constitute the reliefs located to the north (IGME 1978c).
In the north-western sector of the Alboran basin, there are upwellings of cold deep and
nutrient-rich waters due to hydrological and oceanographic features that promote an
abundant phytoplankton production (García Raso et al. 2010). This high productivity
and nutrient availability, together with the diversity of soft and hard bottoms, promote a
great diversity of species which have leaded the Calahonda SAC to be recognized a
biodiversity hotspot for the European waters (García Raso et al. 2010).
This MPA was proposed because of the presence of three types of habitats included in
Annex I of the HD: Sandbanks which are slightly covered by sea water all the time
(Habitat 1110), Posidonia beds (1120) and Reefs (1170) (Figure 13) (Mateo-Ramírez et
al. 2020b). Moreover, two species included in Annex II of the HD such as the Bottlenosed Dolphin and the Loggerhead Turtle, and three species included in the Annex IV
of the HD such as the Hatpin Urchin, the Ribbed Mediterranean Limpet and the Noble
Pen shell (Pinna nobilis) were also included in the original proposal (Figure 13). The
offshore area bordering Calahonda is of importance for other cetaceans such as the
Common Dolphin, the Stripped Dolphin and the Long-finned Pilot Whale, all of them
included in Annex IV of the HD. In addition, Fin Whales (Balaenoptera physalus) and
occasionally Orca, Pilot whales and Common Minke Whales (Balaenoptera
acutorostrata) (also included in the Annex IV) spotted close to the SAC (MateoRamírez et al. 2020c).
Other species with different protection status occur in the SAC, with the presence of
emblematic species with a key role in the ecosystem, and therefore representing good
ecosystem health indicators. This group of species includes the seagrass C. nodosa,
included in the Annex I (strictly protected flora species) of the Bern Convention and in
the Annex II (endangered or threatened species) of the BC; as well as two sponges (e.g.
Common Antlers Sponge Axinella polypoides), nine molluscs (e.g. Knobbed Triton,
Zoned Mitre Episcomitra zonata), five crustaceans (e.g. Spiny Lobster) and two
echinoderms (e.g. Purple Sea Star) (Mateo-Ramírez et al. 2020c), all of them included
in the Annex II and III of the BC, and some of them classified as “Vulnerable” or “in
Risk of Extinction” in the CEEA and CAEA (Mateo-Ramírez et al. 2020c). The location
and extension of some habitats and their associated biota of this SAC have been studied
in detail by García Raso et al. (2010), with detailed works focused on dominant faunal
groups such as molluscs (Urra et al. 2011, 2013a, 2013b, 2017) and decapod
crustaceans (García Muñoz et al. 2008; Mateo-Ramírez et al. 2012, 2016, 2018),
including the description of some new species for the science as Pagurus
pseudosculptimanus. (García Muñóz et al. 2014). A large proportion of tropical West
African species is found in the SAC, with some of them reaching here their
distributional limit towards the Mediterranean Sea, such as the bivalves Ungulina
cuneata and Modiolus lulat (Figure 13). The rocky outcrop located at the western sector
of the SAC (locally known as “Laja del Almirante”) harbours an interesting
coralligenous community, which is considerably shallower than in other Mediterranean
areas due to the high turbidity levels. This coralligenous community is conformed,
besides mobile groups (e.g. molluscs and decapods) by colonial organisms such as the
gorgonians White Sea Fan, Pink Sea Fan, E. labiata, and L. sarmentosa as well as the
bryozoans Ross Coral and Myriapora truncata (Figure 13), which are supported by the
almost permanent highly nutrient upwellings occurring in the area. The presence of
these bioconstructing species promotes a higher complexity that enhance the number of
niches that can be potentially occupied by a large number of species, as found in
Calahonda for decapod crustaceans (García Muñóz et al. 2008) and molluscs (Urra et al.
2012).
The socio-economic importance of this SAC is mainly related to fisheries, both
professional and recreational, and tourism. Regarding fisheries, small-scale gear fleets
operating in the area include those using mechanical dredges targeting the Wedge Clam,
the Striped Venus Clam, the Smooth Clam and the Rough Cockle, with the former three
species being the most important ones in the regional market. Other artisanal fleets
include those using minor gears, purse seine and traps. Main professional fishing
harbours are located close by in Fuengirola and Marbella, whereas recreational ones are
located in Cabopino (Marbella) and Fuengirola. The tourism sector is essential for the
economy of the area. The strategic location within the Costa del Sol attracts many
tourists because of its warm and sunny weather all year round, beaches and restaurants,
with many small lodging establishments and hotels that offer overnight accommodation
along the coastline of the SAC.
The main threats include the use of fishing gears that may cause seabed abrasion,
especially when impacting the seagrass meadows, non-professional shell fishing such as
the collection of intertidal sea anemones, holothurians, urchins and limpets, pollution by
marine outfalls discharging local or industrial wastewaters and uncontrolled dumping,
the alteration of the coastline by coastal infrastructures and material deposition for
beach regeneration, the extraction of aggregates from marine deposits and the presence
of invasive species. The presence of the new invasive species R. okamurae should be
highlighted, which was detected at a depth of 20 m in the Laja del Almirante in 2018
(Junta de Andalucía 2018).
5.9. Paraje Natural Desembocadura del río Guadalhorce (Spain)
The Paraje Natural Desembocadura del río Guadalhorce (Mouth of the River
Guadalhorce Natural Area) is a coastal wetland included in the Inventory of Wetlands
of Andalucía (code 617024) (Fig. 10) and listed as IBA by SEO/BirdLife (ES224). This
site was proposed as Natural Area in July 1989, but before that the council of Málaga
city declared it as a protected area in 1982 and prohibited housing developments. This
MPA is located westwards of Málaga, covering an area of ca. 0.7 km2. The original
marsh at the mouth of the river was reduced by the construction of the Guadalhorce dam
(1914-1921). Later on, although it was an agricultural area, the extraction of aggregates
began in the 70s, forming the current lagoons which brought the water to the surface.
Since then, it was protected after several discussions and agreements with the previous
land owners. Nowadays, it is delimited by two channels of the Guadalhorce River, plus
a third auxiliary one, forming an alluvial delta composed of detritic carbonated
materials in witch there are five small artificial lagoons of brackish and of fresh waters
covering the gaps from the extraction of aggregates. The Guadalhorce river mouth is
characterized by the development of a deltaic deposit inside an estuary that has
progressively filled. The fluvial deposits and the littoral wedge are separated by a dune
belt. In the submerged area, the fluvial flows and sediment loads form a submarine
deltaic deposit off the Guadalhorce River, representing the main geomorphological
feature. These deposits are generally composed of muddy sediments (Medialdea et al.
2014). Other submarine morphologies such as undulations field and creeping areas
developed on the submarine deltaic deposit, infralittoral wedge, scarp or abrasion
surface areas occur off the coast of this MPA (Fernández-Salas et al. 2015). In adjacent
areas to the deltaic system the sedimentary cover is composed by fine and coarse sands.
The predominant littoral drift to the south-west produces a dynamic of active bars
oblique to the coastline.
In the wetland area, different habitats included in the Annex I of the HD are present
such as Coastal lagoons (Habitat 1150) or Mediterranean and thermo-Atlantic
halonitrophilic thickets (Sarcocornetea fruticosi) (1420) (Mateo-Ramírez et al. 2020b).
The salt marsh and riparian vegetation is diverse, including Sarcocornia perennis,
Scirpus maritimus, Juncus maritimus Othanthus maritimus, Medicago marina, Ruppia
maritima and Tamarix canariensis, among others.
This MPA was designed because of its high ornithological diversity and its value as a
stopover area for migratory birds. A large number of species included in the BD and
lists of protections and conventions (Mateo-Ramírez et al. 2020c) use this MPA.
Although it is located within the urban footprint of Málaga city, and despite its small
size, it is unique for its extremely high diversity of birds, remarkable in the context of
the Iberian Peninsula. The diversity and number of individuals seen rise dramatically
during spring and autumn migrations, and also during winter, when numerous ducks (as
Northern Shovelers Anas clypeata, Common Pochards Aythya ferina and Green-winged
Teals Anas carolinensis), grebes (Little Grebe Tachybaptus ruficollis and Eared Grebe
Podiceps
nigricollis),
egrets,
herons,
Greater
Flamingos,
Great
Cormorants
(Phalacrocorax carbo), gulls (e.g. Mediterranean, Black-headed, Lesser Black-backed
and Slender-billed Gulls), sandpipers, plovers, raptors (mostly Ospreys, Booted Eagles
Hieraaetus pennatus and Marsh Harriers Circus aeruginosus) (Mateo-Ramírez et al.
2020c), and a variety of passerines can be observed. It is particularly noteworthy the
presence of three Critically Endangered Species along the year, the Ferruginous Duck
(Aythya nyroca), the Marbled Teal (Marmaronetta angustirostris), and the Whiteheaded Duck (Oxyura leucocephala), which breeds in the lagoons. Along the coastal
fringe it is possible to watch a variety of seabirds, such as the Scopoli’s and Balearic
Shearwaters, terns and gulls, during migration, and Northern Gannets and scoters during
winter (Mateo-Ramírez et al. 2020c). The beach hosts a breeding population of Kentish
Plovers. Other protected or endangered vertebrate species occurring on this MPA are
the Eurasian Otter (Fig. 10) and the Mediterranean turtle Mauremys leprosa, among
others (Mateo-Ramírez et al. 2020c).
The main socio-economic values are tourism and environmental education in a
protected area located close to Málaga, the largest city in the Alboran Sea. The tourism
and guided tours oriented to environmental education can enjoy a natural beach, trails
and observatories for exploring the high diversity of birds, with up to 80 different
species spotted within the same day, and 304 different species observed in the area. On
the other hand, the protected area contains historical heritages, such as the Phoenician
city of Cerro del Villar (S. IX B.C).
The main threat of this natural area is the pressure of Málaga city over this MPA (e.g.
Málaga waster water treatment plant, etc.). Other important threats are the introduction
of invasive species such as the Florida Turtle (Trachemys scripta elegans), which
compete with some native species (e.g. M. leprosa) or the Monk Parakeet (Myiopsitta
monachus). Another important factor is related to the high affluence of people to the
beach during spring and summer months, that do not respect the delimited breeding
zone in the MPA.
5.10. Acantilados y fondos marinos de la Punta de la Mona SAC (Spain)
The Acantilados y fondos marinos de la Punta de la Mona SAC (Cliffs and Marine
bottoms of Punta de la Mona) (ES6140016) were proposed SIC in December 2003,
approved in July 2006 and appointed SAC in August 2015. This SAC occupies an area
of ca. 1.2 km2 is located in the coast of Almuñécar (Granada), limiting to the east with
the Peñón de las Caballas and to the west with the northern part of Las Terrazas
development. It comprises small strips of coastal cliffs and a coastal strip, with a depth
range from the coastline to ca. 60 m depth. Similar geological characteristics as the ones
described in the Maro-Cerro Gordo Cliffs occur in this MPA (section 4.1 of this
chapter).
Regarding habitats, its election as SCI was due to the presence of rocky bottoms (Reefs,
Habitat 1170 of the HD), which in some areas reach 49 m depth, and harbour
precoralligenous and coralligenous communities with a great richness of benthic species
(Mateo-Ramírez et al. 2020b). Another habitat type is represented by submerged and
semi-submerged caves (8330). Some threatened species, such as the Ribbed
Mediterranean Limpet, the Star Coral, the Hatpin Urchin and the Common Antlers
Sponge, inhabit these areas (Fig. 14). Populations of other species included in the Libro
Rojo de los Invertebrados Andalucía, such as the gorgonian Violescent Sea-whip and
the scleractinian Orange Tree Coral, are also present in this SAC (Fig. 14) MateoRamírez et al. 2020c).
Snorkelling and scuba diving, apart from other touristic activities, are the main socioeconomic activities, with several diving centres offering diving tours and with a large
number of divers using Marina del Este beach as the point of origin for their dives.
Small-scale gear fishing, with two boats that use the trammel nets, longlines and pots,
targeting cephalopods and rockfish, operate in the SAC. Since 1980, this area has been
subjected to a continuous series of anthropogenic disturbances. The main one was the
construction of the artificial beach of Marina del Este, in the inlet of Los Berengueles,
and the recreational harbour of Marina del Este in the Roca de las Caballas, destroying
areas with a high environmental value. These two constructions resulted on a massive
housing development that still continues with the construction of new urbanizations.
These cliffs hosted the last breeding pair of Ospreys in mainland Spain, which
disappeared in 1982 due to the urban development pressures. Although Osprey has been
recently reintroduced in western Andalusia, it can be observed only during migration.
The increase of tourism led to an increase in wastewater discharges, boat anchoring, the
number of sport fishers, illegal fishing and shellfish, etc (Fig. 14). Fishing, both
artisanal and sport, has led to the disappearance of large serranids (e.g. large Dusky
Grouper) and other large fishes, and it has had a great impact on benthic communities.
The ropes of pots and longlines, the trammel nets, and fishing lines and hooks tear or
split sponges and colonies of corals, gorgonians and bryozoans. The designation of this
SAC should be supported by an effective management plan regulating all the activities
that are causing current impacts.
5.11. Acantilados y Fondos Marinos Tesorillo-Salobreña SAC (Spain)
The Acantilados y Fondos Marinos Tesorillo-Salobreña SAC (Coastal cliffs and marine
bottoms of Tesorillo-Salobreña) (ES6140013) were proposed as SCI in January 2001,
approved in July 2006 and appointed as SAC in August 2015. This SAC occupies an
area of ca. 10 km2 and is located in the coasts of Almuñécar and Salobreña (Granada),
limiting eastwards with El Pozuelo beach and westwards with Caleta de Salobreña. It
comprises coastal cliffs reaching up to 15 m height from the sea and a marine strip with
a depth range from the coastline to ca. 70 m depth. The cliffs located west of Salobreña
correspond to graphite schists with quartzites and quartz-mica-schists with a medium to
high metamorphic degree, although the town of Salobreña is located on an outcrop of
marbles, all of them are of Palaeozoic age belonging to units of the Alpujarride
complex. To the west of Salobreña, the submerged marine area is characterized by
muddy and sandy sediments on the infralittoral wedge; while to the east correspond to
the deltaic plain and the submarine prodeltaic area of the Guadalfeo deltaic system.
Its election as SCI was due to the presence of Zostera marina meadows (Habitat 1110
of the HD), which unfortunately disappeared in 2009, and to the marine bird diversity
with protected species such as Sanderlings (Calidris alba), the Little Egret (Egretta
garzetta) or the Balearic Shearwater, as well as cetacean species as the Common or
Bottle-nosed Dolphins among others (Mateo-Ramírez et al. 2020c). The reef habitat
(Habitat 1170 from HD) is well represented in this SAC, with threatened species such
the Ribbed Mediterranean Limpet, the Star Coral and numerous colonies of the
gorgonian L. sarmentosa can be also highlighted (Fig. 15) (Mateo-Ramírez et al.
2020c). Since 2016, the presence of an incipient C. nodosa meadow has been observed
in the bottoms previously occupied by Z. marina (Fig. 15).
Tourism is the main socio-economic activity, especially in Almuñécar, where beaches
for swimming are more accessible by car. Recreational and artisanal fishing are both
used in this area, being some of the target species Common Pandora (Pagellus
erythrinus), Sea-bream (Pagellus spp.), Forkbeard (Phycis phycis), the Cuttlefish (Sepia
officinalis), Striped Venus Clam and the Rough Cockle, among others.
There is also an installation of aquaculture cages in the north-eastern part that is
currently obsolete. The illegal capture of invertebrates is one of the main threats, both
the furtive shell fishing of molluscs and crustaceans, which occurs especially during the
summer months, as well as the catch of the Sea Anemone. The great demand of this
anemone in other Andalusian provinces has practically resulted in its disappearance in
this area. In recent years, the illegal catch of holothurians for the Chinese market must
be also mentioned (Fig. 15). The different types of fishing, without specific restricting
rules, have resulted in a decrease of fish populations. Particularly important is the
pressure on the large serranids as the Dusky and Goldblotch Groupers. Poachers catch
juveniles of these species that they sell to bars and restaurants. Although less frequently,
some trawlers do not respect the limits of depth and/or distance, approaching a few
meters from the coast. On some occasions the remains and debris of works carried out
on the National 340 road and in housing developments are dumped on the cliffs,
covering the vegetation and sometimes reaching the mesolittoral rocks.
5.12. Acantilados y Fondos Marinos de Calahonda-Castell de Ferro SAC (Spain)
The cliffs and marine bottoms located between the rocky coastlines of Gualchos and
Motril were proposed as the Acantilados y fondos marinos de Calahonda-Castell de
Ferro SIC (Cliffs and marine bottoms of Calahonda-Castell de Ferro) (ES6140014) in
December 2003, approved SCI in July 2006 and designated SAC in August 2015. The
SAC is located in the central part of the Granada coast and covers an area of ca. 9 km2
with a depth range between the coastline and ca. 65 m. The coastal strip within the SAC
is mainly configured by high cliffs and rocky formations with submerged and semisubmerged caves promoted by karst processes (Fig. 16). The cliffs are conformed by
phyllites and quartzites, Lower to Middle Triassic age, and limestones or marbles of
Middle to Upper Triassic age; however an unit of graphite schists with quartzites of
medium metamorphic grade and Palaeozoic age emerges to the east of Cape Sacratif
and Castell de Ferro (IGME 1981). There is only one pebble beach within the SAC
known as “Rijana beach” with ca. 250 m length and located in a sheltered area. The
Llanos de Carchuna has been characterized as a Holocene delta fan system. Massive
rocky outcrops occur on the shelf, as well as unconsolidated sediments covering from
very fine sand to medium-coarse sand on the infralittoral wedge and continental shelf.
Off Castell de Ferro, the Gualchos River has generated small prodeltaic deposits both to
the west and east (Bárcenas et al. 2018).
The Atlantic anticyclone gyre promotes an upwelling of cold deep and nutrient-rich
waters along the coasts of Málaga and Granada, which is enhanced by the westerly
winds that usually blow in this area (Cebrián and Ballesteros 2004). This makes the area
within the SAC to be subjected to a high productivity and nutrient availability, as
detected in other MPAs located close. Furthermore, bottom currents and upwellings
may favour the connectivity among deep and shallow soft bottoms, promoting the
existence of bathyal species in circalittoral bottoms within the SAC (Marina et al.
2015).
This SAC was proposed because of the presence of nine types of natural habitats
included in Annex I of the HD, of which five belong to the marine realm including
Sandbanks which are slightly covered by sea water all the time (Habitat 1110),
Posidonia beds (1120), Large shallow inlets and bays (1160), Reefs (1170) and
Submerged or partially submerged sea caves (8330) (Fig. 16) (Mateo-Ramírez et al.
2020b). Moreover, two species included in Annex II of the HD such as the Bottle-nosed
Dolphin and the Loggerhead Turtle, and at least five species included in the Annex IV
such as the Ribbed Mediterranean Limpet, the Date Mussel (Lithophaga lithophaga),
the Leatherback Marine turtles, the Common and Striped dolphins were also included in
the original proposal (Mateo-Ramírez et al. 2020c). During migration it is easy to detect
Audouin’s Gulls and Balearic Shearwaters, while during the breeding period the most
common seabird is the Yellow-legged Gull (Larus michahellis) (Fig. 16). The eastern
area bordering Calahonda-Castell de Ferro is also of importance for the endemic
Mediterranean seagrass P. oceanica (included in the Annex I of the Bern Convention
and in the Annex II of the BC), which presents extensive meadows down to ca. 10 m
depth (Junta de Andalucía 2018). These beds provide a high ecological value, being the
refuge and recruitment area for numerous species of commercial interest (Urra et al.
2015).
In addition, several species with different protection status have been found in the area,
such as the Knobbed Triton, the Noble Pen Shell (probably extinct since 2017) (Fig.
16), the Mediterranean reef-building vermetid gastropod (D. lebeche), the Star Coral
and the Orange Puffball Sponge (Tethya aurantium) (Mateo-Ramírez et al. 2020c), all
of them included in the Annex II of the BC, and some of them classified as
“Vulnerable” in the CEEA and CAEA (Mateo-Ramírez et al. 2020c).
Sublittoral soft bottom assemblages within the SAC were detailed studied by Marina et
al. (2015) in relation to sediment and water column variables. These authors
documented the presence of some rare and poorly known invertebrates that are scarce in
other areas of the Mediterranean Sea, such as the hippolytid decapod Bythocaris
cosmetops and the tropical hermit crab Pagurus mbizi (García Raso et al. 2011, 2014)
(Figure 16). Some bathyal molluscs (e.g. Poromya granulata, Alvania testae) display
populations at shallower depths in the circalittoral zone of this MPA (Marina et al.
2015). The geographic location of the SAC, which represents a transitional and
settlement zone for Atlantic species, the heterogeneity of soft bottoms and the
occurrence of upwellings may favour the high biodiversity found in the studied soft
bottoms.
The socio-economic importance of this SAC is mainly related to fisheries, both
professional and recreational, aquaculture, agriculture and tourism. The activity of the
artisanal fleet in the SAC is scarce, the remoteness of the closest port, located in Motril,
influences this low activity. The main small gear used are gillnets for mullets (Mullus
sp.), S. officinalis and sparids as Diplodus sargus, Pagellus erythrinus, Pagellus acarne,
etc. and pots (called “Alcatrúz” in the area) to catch Common Octopus. Recreational
fishing from coasts and boats is usual in this SAC using surf-casting, trolling and
jigging and targeting sparids, with the White Seabream (D. sargus) standing out.
Aquaculture is an activity that is beginning to have some relevance on the coast of
Motril, with one fishing farm located off Carchuna for the production of European
Seabass (Dicentrarchus labrax) and Gilthead Seabream (Sparus aurata). The tourism
sector is also very important in the area. The SAC stands out for its beautiful cliffs,
which attract many visitors looking for activities related to scuba-diving, which is a
deeply rooted activity in the seabeds of Calahonda-Castell de Ferro. The main threats
include the use of fishing gears that may be in contact with the seabed, especially
considering the seagrass meadows located close by; trampling over intertidal and upper
infralittoral areas and illegal extraction of invertebrates such as the rock-boring Date
Mussel, whose harvesting causes significant environmental damage; diving activities,
which are very intense in summer and can affect populations of some species but also
the overall community structure through physical injury or the removal of certain
species. One of the most endangered invertebrates of the Mediterranean, the Ribbed
Mediterranean Limpet, presents a population within the SAC and it is affected by
recollection for human consumption, as bait for fishing, coastal developments, habitat
modification and contamination.
5.13. Sur de Almería - Seco de los Olivos SCI (Spain)
The Sur de Almería- Seco de los Olivos SCI (Southern Almería - Seco de los Olivos)
(ESZZ16003), was designated SCI in December 2014 and incorporated in the Natura
2000 Network in November 2015. This SCI will become a SAC after the development
of its corresponding management plan, including integrated measures to ensure the
conservation of the habitats and species for which it was created.
The SCI is located in front of the Almería province, covering an area of ca. 2830 km2
and a depth range from the coastline to ca. 1000 m depth. From the coast to the bathyal
zone there is a great diversity of bottoms types, both rocky outcrops and sedimentary
ones with different lithologies such as sands on the infralittoral of the continental shelf
and muds on the continental slope, providing a wide diversity of habitats and marine
organisms. Over the continental shelf a series of geomorphological features such as
submarine escarpments, abrasion surfaces, sand wave fields and submarine fluvial
deposit associated with the Adra River occur. Other geomorphological structures occur
on the continental slope at greater depths such as submarine canyons (e.g. one section of
the Almería canyon) and underwater elevations such as the promontory of Cabo de Gata
and some banks such as Avenzoar - El Sabinar complex, Pollux and Chella, the latter
also known as the Seco de los Olivos Seamount. This seamount is a volcanic outcrop
included in the peri-Alboran Neogene volcanism. It is constituted by a central edifice,
partially eroded, and covered by a sedimentary shelf wedge around it that generates a
small isolated platform, and two NW-SE directed ridges located to the NE and SW
respectively of the main edifice.
This SCI was proposed because of the presence of two habitats included in Annex I of
the HD: Posidonia oceanica beds (Habitat 1120) and Reefs (1170); and two species of
Annex II of the HD such as the Loggerhead Turtle and the Bottle-nosed Dolphin.
Moreover, this SCI is also of importance for other occasional cetaceans, including the
Cuvier's Beaked Whale, the Long-finned Pilot Whale and the Common Minke Whale,
as well as for different birds including the Balearic Shearwater and the Audouin’s Gull
(Mateo-Ramírez et al. 2020c).
More than 600 species including fish and invertebrates have been listed so far in this
SCI (de la Torriente et al. 2014). Many of these invertebrates are of importance because
they appear in high densities and form three-dimensional structures that are home to
other species, which settle, feed and take shelter in those habitats. In the coastal area,
different seagrasses (mainly P. oceanica and C. nodosa) form extensive meadows
(Habitats 1120 and 1110 of the HD). Rhodolith beds and coralligenous bottoms (Habitat
1170 of the HD) also appear in the coastal area, but mainly over the summit of some
seafloor elevations, such as over the central “guyot” of the Seco de los Olivos Seamount
(Mateo-Ramírez et al. 2020b). Further away a variety of habitats distributed in a patchy
mosaic (some of them related to Habitat 1170) occur on Avenzoar Bank and the Seco de
los Olivos seamount, including cold-water coral reefs (White Stony Coral
Desmophyllum pertusum and White Coral), bamboo corals (Isidella elongata) and black
corals (Leiopathes glaberrima, Antipathes dichotoma, Antipathella subpinnata)
aggregations, glass sponges (Asconema setubalense, Sympagella delauzei) and
demosponges (Phakellia spp., Pachastrella monilifera, Thenea muricata) aggregations,
giant oyster banks (Neopycnodonte zibrowii), large gorgonian gardens containing more
than a dozen species (Pink Sea Fan, Violescent Sea-whip, Swiftia dubia, Callogorgia
verticillata, Viminella flagellum, Acanthogorgia hirsuta, Dendrobrachia bonsai, among
others), soft corals (Alcyonium palmatum, Paralcyonium spinulosum, Nidalia studeri)
and Red Coral (Corallium rubrum) banks (Fig. 17) (Mateo-Ramírez et al. 2020c). A
good representation of sedimentary habitats with habitat-forming species occurs in the
SCI including, sea pen communities (Funiculina quadrangularis, Kophobelemnon spp.,
Pennatula rubra, Pennatula phosphorea, Pteroeides griseum, Virgularia mirabilis) and
bamboo coral aggregations (Fig. 17).
The conservation of the cited habitats as well as many of their associated species
depends on the development of appropriate management measures for the SCI.
Considering just Seco de los Olivos Seamount, 45 species have been identified as
protected and included in national and/or international conservation lists, including
chordates (11 species), cnidarians (16 species), sponges (8 species), molluscs (5
species), crustaceans (2 species), echinoderms (1 species), tunicates (1 species) and
bryozoans (1 species) (Mateo-Ramírez et al. 2020c).
The socio-economic importance of this SCI is mainly related to fisheries and tourism. In
the area, fishermen use a great diversity of fishing techniques to catch different
resources: purse-seine fishing for Atlantic Mackerel (Scomber scomber), European
Sardine, Atlantic Horse Mackerel (Trachurus trachurus) and Round Sardinella
(Sardinella aurita); bottom trawling for Atlantic Horse Mackerel, European Hake
(Merluccius merluccius) and Blue and Red Shrimp (Aristeus antennatus); bottom longline fishing for Blackspot Seabream; gillnet fishing for Scorpion Fish (Scorpaena spp.),
mullets (Mullus spp.) and Cuttlefish; and fishing with traps or pots for Soldier Striped
Shrimps. Moreover, recreational fishing has increased in the area, especially in specific
seafloor elevations with steep rocky bottoms where species as the Dogtooth Grouper
(Epinephelus caninus) occurs. Additionally, the area is highly frequented by tourists,
including sport boat navigation and scuba diving in the coastal areas of Almería and
more recently, activities associated with whale watching. The main threats facing the
biodiversity of this SCI include some types of fishing such as bottom trawling, which
generate incidental bycatch of sharks and cetaceans and the abrasion of the seabed and
their benthic habitats; and marine traffic responsible for pollution caused by both the
ship’s bilge water releases and by plastics and waste disposal (Fig. 17).
5.14. Fondos Marinos de Punta Entinas-Sabinar SAC (Spain)
The Fondos Marinos de Punta Entinas-Sabinar SAC (Marine bottoms of Punta EntinasSabinar) (ES6110009) is located in the submerged platform in front of the Punta
Entinas-Sabinar SAC (ES0000048), in the west of the Almería province (Fig. 18). This
area was proposed SCI in 1997, approved in 2006 with ca. 20 km2 and declared SAC in
2016 with an area of ca. 40 km2.
The seabed of the SAC constitutes the submerged continuation of the great plain located
at the foot of the Gádor mountains range between the housing developments of
Roquetas de Mar and Almerimar (El Ejido harbour) characterized by sandstones and
silts of Messinian - Lower Pliocene age. All this coast is low and is part of the Punta
Entinas-Sabinar SAC and contains some coastal lagoons, wet areas and old salt marshes
that are no longer used (Pérez Hurtado de Mendoza 2004), as well as a strip of
Holocene dunes with Phoenicean Junipers Juniperus phoenicea subsp. turbinata and
Mastic Trees Pistacia lentiscus (López-Martos et al. 2010).
The SAC occurs on the infralittoral wedge and is mainly characterized by fine sands,
small areas with gravels and rhodolith beds together with some flattened rocks
associated with rocky outcrops, on which P. oceanica also develops (Moreno and
Guirado 2003; Moreno et al. 2004a; Arroyo et al. 2015) (Fig. 18). The main habitats of
this SAC are the seagrass meadows of P. oceanica (Habitat 1120 of the HD); the
Sandbanks which are slightly covered by sea water all the time (1110) in which C.
nodosa frequently forms meadows (Moreno et al. 2004b) and the Reefs (1170), in some
areas of flattened rocks with macroalgae meadows of the Cystoseira spp. between 10
and 20 m depth (Fig. 18). The cartography of seagrass meadows was firstly carried out
using scuba-diving in 1995-1996 (Luque et al. 2004) and later on updated with side scan
sonar during the Life+ Posidonia Andalucía Project (2011-2016) (Mendoza et al. 2014;
Arroyo et al. 2015). In 2008, OCEANA conducted a restoration experience of C.
nodosa meadows by collecting seeds in front of Punta Elena (next to the Cerrillos
tower) and planting them in Roquetas de Mar and Punta Elena (García et al. 2009).
In this SAC, a P. oceanica sampling station with demographic grids has been monitored
every year within the POSIMED Network under the framework of the Life+ Posidonia
Andalucía Project (Junta de Andalucía 2017, 2018). During this project, censuses of
fish, macroalgae, epiphytes and macro invertebrates were carried out for studying the
biodiversity of those meadows (Junta de Andalucía 2012, 2013).
Some threatened invertebrate species such as the Hatpin Urchin and the Knobbed Triton
(Vulnerable) occur in this SAC (Junta de Andalucía 2018) (Mateo-Ramírez et al.
2020c). The Noble Pen Shell was scarce in the seagrass meadows, and no individuals
could be detected in 2016 after a massive mortality event that has affected 100% of the
population of the northern Alboran Sea (Junta de Andalucía 2017; Vázquez-Luis 2017).
The entire west coastline of the Almería province, except just the narrow strip of the
adjacent SAC, is very urbanized and intensively used for agriculture appearing from
satellites covered by plastic greenhouses (campo de Dalías-El Ejido and Roquetas de
Mar). Therefore, this SAC could be affected by spills from nearby urban and
agricultural areas, as well as waste of all kinds, mainly of plastics. This coast is very
open and receives storms coming from the east as well as from the west, so it could
receive potential contamination from maritime traffic accidents such as oil spills. In
addition, overfishing, including recreational fisheries, can affect the ichthyofauna that is
already very scarce in the SAC.
5.15. Arrecife barrera de Posidonia Natural Monument and Arrecifes de Roquetas de
Mar SAC (Spain)
The area known as “Los Bajos de Roquetas”, located between Roquetas de Mar and
Aguadulce in the western part of the bay of Almería, has a low and sandy coast and
predominantly soft bottoms on which extensive seagrass meadows develop on the
infralittoral wedge. One of the most notable formations is the barrier reef of P. oceanica
(Fig. 19), which is next to the wetland area called Ribera de la Algaida and the
Turaniana site, where there was a small Roman port (Cara Barrionuevo 1994). This
remarkable reef of P. oceanica is the largest and most complete in the northern Alboran
Sea. It was declared in 2001 as a Natural Monument (Monumento Natural) of biotic
character, with the name of Arrecife barrera de Posidonia (Barrier Reef of Posidonia)
and covering an area of ca. 1.1 km2 (Guirado et al. 2002; Castro et al. 2003). The
declaration of this Natural Monument was done by the Andalusian Government and
included basic management criteria and a list of unsupported activities, such as
anchoring and trawling, among others. This MPA is 2 km long and 550 m wide (50m
stretch along the beach) and a depth range between the coastline to ca. 10-12 m.
Subsequently, this MPA was approved as SCI in 2006 with the name Arrecifes de
Roquetas de Mar (Roquetas de Mar Reefs) (ES6110019), occupying an area of ca. 2
km2, and finally designated SAC in 2016.
The main value of this SAC is P. oceanica meadows (Habitat 1120 of the HD) that
conforms an extraordinary barrier reef, where seagrasses reach the surface. The
structure of the Posidonia reef is similar to that of tropical hermatypic (or reef-building)
corals that conform a separate coastline ridge where waves break and an inland lagoon
with muddy sediments colonized by other marine angiosperms such as C. nodosa and Z.
noltei (Habitat 1110 of the HD) (Moreno 2003; Luque and Templado 2004; Arroyo et
al. 2015) (Fig. 19). It should be highlighted that the four species of native marine
angiosperms of European waters (P. oceanica, C. nodosa, Z. noltei and Z. marina)
occurred in the SAC at the end of the 20th century, before the acute regression of Z.
marina in the northern Alboran Sea during 2006-2007 (Moreno and Guirado 2003). The
cartography of these seagrass meadows was firstly carried out using scuba-diving in
1995-1996 (Luque et al. 2004), and later on updated with side scan sonar during the
Life+ Posidonia Andalucía Project (2011-2016) (Mendoza et al. 2014; Arroyo et al.
2015). Demographic grids and biodiversity census were carried out in this SAC from
2011 to 2018 during the latter project (Junta de Andalucía 2012, 2013, 2017, 2018).
In the P. oceanica meadows, the concretions of the coralline algae Mesophyllum
alternans algae are frequent, which are home to a rich and diverse fauna with abundant
polychaetes, crustaceans and small molluscs (Salas and Hergueta 1986; Hergueta and
Salas 1987). The macrofauna of the seagrass meadows is known from different studies
(Ballesteros et al. 1986), including the results of cartography campaigns (Luque and
Templado 2004). It is important to note that the waves bring a large amount of debris
from the nearby P. oceanica (leaves, rhizomes) to the shore that accumulate on the
beach and support an interesting detritivorous fauna adapted to this habitat, with
different species of amphipods, isopods and polychaetes, among others (Luque and
Templado 2004).
Different species of echinoderms, mainly of the genus Holothuria, and the sea urchin
Paracentrotus lividus (Annex II of the BC) (Fig. 19) (Mateo-Ramírez et al. 2020c), are
very abundant in the SAC, which could contribute to seagrass degradation because that
sea urchin feed on P. oceanica (Junta de Andalucía 2012, 2013). The endangered Noble
Pen Shell was scarce in these meadows, but it no longer lives there because of the
aforementioned massive mortality event in 2016 (Junta de Andalucía 2017; VázquezLuis 2017).
The main socio-economic activities are related with tourism, scuba-diving (prohibited
inside the Natural Monument) and fisheries. In the fishing port of Roquetas de Mar the
main gears used are small-gear fishing, e.g. trammel (10 boats). Nevertheless, other
boats use other gears such as long-line (4), shellfish dredges and purse-seine fishing (3).
The main target species of those fisheries are Common Octopus and Cuttlefish. In
addition the port of Roquetas has 183 moorings for recreational boats, with some of
them fishing in the MPA. Different human pressures, such as mass tourism and urban
discharges as well as marks of dredges and illegal trawlers have been mentioned for this
MPA (Arroyo et al. 2015). The latter affected the Posidonia meadows outside 12-14 m
depth at the end of the 20th century which caused meadow degradation with a large area
of “dead matte”. In addition, the green algae C. cylindracea was detected for the first
time at a depth of 14 m on “dead matte” in 2014, which may represent a very suitable
bottom for the development of this exotic invader (Junta de Andalucía 2014).
5.16. Isla de San Andrés Natural Monument and SAC (Spain)
The island of Carboneras (also known as Isla de San Andrés) is located at the
northeastern limit of the Alboran Sea, in front of Carboneras (Almería) (Fig. 20). It was
declared a Natural Monument of mixed nature (geological and biotic), with the name of
“Isla de San Andrés”, in 2003 by the Andalusian Government (Castro et al. 2003). The
protected area covered ca. 0.7 km2 and included both the emerged part of the island and
the infralittoral bottoms around it. In 2006, the area was approved as SCI with the name
Islote de San Andrés (San Andrés islet) (ES6110020), covering a larger area (0.35 km2)
and including both the island and one small islet located close to the beach. In 2015, it
was declared SAC, covering the same area of 0.35 km2. The 180 m long island is quite
flattened and reaches a height of only 14 m above sea level, but in the submerged part
reaches 40-50 m depth relatively close to the shore. The island is constituted of volcanic
materials, mainly dacites and andesites from the Calcoalkaline series of the Neogene
volcanic peri-Alboran Sea domain. These materials are covered by Quaternary age
alluvial deposits made up of conglomerates with a great diversity of boulders. The
seabeds are rocky corresponding to the volcanic materials and are characterized by the
presence of cornices, cracks and caves.
The main biological values are found in the submerged part where a very steep rocky
substrate dominates, with walls and passages, which harbour extraordinary dives for
dive centres. In the mesolittoral, there are some formations of the vermetid D. lebeche.
In addition there are excellent P. oceanica meadows (Habitat 1120 of the HD), partly on
rock, as well as sand bottoms with C. nodosa meadows (1110). In those P. oceanica
meadows, there was an annual monitoring station of the endangered Noble Pen Shell
until its massive mortality and extinction in 2016 (Junta de Andalucía 2016; VázquezLuis et al. 2017).
In 2008, the Sustainable Management Program of the Marine Environment of the
Andalusian Government carried out the bionomic mapping of this SAC and its adjacent
areas, covering 0.75 km2 in total, of which 0.08 km2 corresponded to P. oceanica
meadows (Junta de Andalucía 2008). There are also an interesting coralligenous
bottoms (Habitat 1170 of the HD) with gorgonians, mainly L. sarmentosa (included
Libro Rojo de los Invertebrados de Andalucía) as well as caves and rocky passageways
with solitary corals such as Leptopsammia pruvoti (Figure 20) (Mateo-Ramírez et al.
2020c).
In this MPA, a P. oceanica sampling station with demographic grids has been
monitored every year within the POSIMED Network under the framework the Life+
Posidonia Andalucía Project (Junta de Andalucía 2017, 2018). Within the same project,
demographic grids and biodiversity census were carried out in this SAC from 2011 to
2018 (Junta de Andalucía 2012, 2013, 2017, 2018). This MPA displayed the highest
species richness for fish (21 species) and macro invertebrates (19 species) after
comparisons with other sampling stations of the northern Alboran Sea (from Almería,
Granada and Málaga) (Junta of Andalusia 2012, 2013) (Mateo-Ramírez et al. 2020c).
The socio-economic importance is related to fisheries and tourism. The port of
Carboneras has the highest influence within the MPA, being the main fishing gear
surface longline and small-gear fishing. Tourism activities are related with the
recreational fishing and scuba diving / snorkelling. The main threat to this MPA is the
increase of diving activities because 4 dive centres from Carboneras perform dives
continuously in fragile environments such as small caves. During the Life+ Posidonia
Project, the Junta de Andalucía installed 4 ecological buoys around the island to avoid
anchoring in the seagrass meadows (Mendoza et al. 2014). In addition, this MPA is
located in the area of influence of two underwater emissaries of urban activity located in
front of Playa del Lacón.
6. Other Marine Protected Areas and Key Biodiversity Areas from the
southern Alboran Sea and adjacent areas
Different MPAs and KBAs located in the southern Alboran Sea and adjacent areas are
presented from west to east direction, with remarks on their location, figure status,
natural heritage, socio-economic importance and main threats.
6.1. Jbel Moussa Nature Reserve, Site d'Intérêt Biologique et Ecologique (SIBE) and
Réserve de Chasse Permanente (RCP)
Jbel Moussa was designated a Biological and Ecological Interest Site (Site d'Intérêt
Biologique et Ecologique) with priority 1 because of its interest and uniqueness. It is
also part of the Intercontinental Biosphere Reserve of the Mediterranean, declared by
UNESCO in 2006, which covers various protected natural areas in Andalusia and
Morocco. Moreover, it has also been recognized as an Important Bird and Biodiversity
Area (IBA) and in 2014 was proposed as Nature Reserve. This MPA occupy a total area
of 48 km2 from which ca. 11 km2 are marine with depths range from coastal lines to
more than 400 m depth.
This is the northernmost protected natural area of Morocco and its boundaries include
the rural communes of Taghremt and Ksar Majaz, as well as the village of Belyounech.
This karstic limestone massif, rising more than 800 m above sea level, is constituted by
units from the internal Rif domains, represented by the Séptides, Gomárides and the
Dorsal units, where Jbel Moussa himself is made up of the latter, and also by the
domain of the Flysch Complex, formed the Tariquides and Mauritanides units.
Limestones and dolomites of the Upper Triassic-Lower Liasic dominate in the area. The
coastal section is characterised by capes, steep cliffs, coastal abrasion platforms, small
beaches and two rocky islets, one of them consisting of limestones (known as Perejil)
and the other forms by sandstones (known as El Guardian).
The maritime area of this MPA is represented by several habitats that are similar to the
ones listed in Annex I of the HD can be identified in the area such as Reefs (Habitat
1170), Sandbanks which are slightly covered by sea water all the time (1110), Mudflats
and sandflats not covered by seawater at low tide (1140) or Submerged or semisubmerged marine caves (8330). Vegetated bottoms are predominantly located at the
northern area of the MPA, with rocky outcrops dominated by stratified algal
communities that are organized from green to brown and red algae following a depth
gradient down to ca. 25 m (Kazzaz 1989). Seagrass meadows are also found on soft
bottoms of the MPA (1110 and 1140), mainly composed of Zostera noltei and
Cymodocea nodosa (Mateo-Ramírez et al. 2020b). Furthermore, the islet of Perejil
(island of Leila in Moroccan) is located 200 m off the coast, and it represents a refuge
for many species due to its isolation and the difficulty of access. This islet harbours
interesting underwater seawalls, caves and coral formations.
Regarding birds, this MPA represents an important migration hot spot for the pass of
migrating seabirds between the Atlantic Ocean and the Mediterranean Sea, with a large
number of species of seagulls (Ichthyaetus spp.) with a nesting colony of Caspian Gull
(I. cachinnans), in Perejil islet, different terns (Sterna spp.), shearwaters, including the
highly
threatened
Balearic
Shearwater
(Puffinus
mauretanicus),
cormorants
(Phalacrocorax spp.), small plovers (Charadrius spp.) and knots (Calidris spp.) that can
be observed in the area and around (Mateo-Ramírez et al. 2020c).
Marine mammals are commonly observed, as they cross the Strait of Gibraltar in their
migratory routes. Common species include the Bottle-nosed Dolphin (Tursiops
truncatus), the Common Dolphin (Delphinus delphis), the Striped Dolphin (Stenella
coeruleoalba), the Common Porpoise (Phocaena phocaena), the Orca (Orcinus orca),
the Long-finned Pilot Wale (Globicephala melas), the Sperm Whale (Physeter
macrocephalus) and the Fin Whale (Balaenoptera physalus) (Mateo-Ramírez et al.
2020c). Other threatened and/or endangered species include marine turtles (e.g.
Loggerhead Caretta caretta, Leatherback Dermochelys coriacea), fishes such as the
Bluefin Tuna (Thunnus thynnus), the Dusky Grouper (Epinephelus marginatus)
including sharks such as the Sweet William (Mustelus mustelus), Common
Hammerhead Shark (Sphyrna zygaena), among others (Mateo-Ramírez et al. 2020c).
The seawater quality provides the optimal conditions for threatened/endangered and
vulnerable invertebrate species such as the Red Coral (Corallium rubrum) and the
crustaceans Slipper Lobster (Scillarides latus) or Spider Crab (Maja squinado) (MateoRamírez et al. 2020c).
The main socio-economic activities are tourism and fishing. The surrounding cities and
towns have an important urban and tourist-residential component. The whole area has
an important potential for outdoor activities such as hiking, trekking, ornithological or
scientific tourism, environmental education, diving and sport fishing, apart from the
traditional sun and beach tourism (VVAA 2013). The presence of large numbers of
whales fed a highly lucrative Whaling industry at both sides of the Strait, and the
remains of the old whaling stations can be found at Belyounech (Morocco) and
Algeciras (Spain). A permanent and locally important artisanal fishing activity, with
trammel nets, purse seine from coast, longlines and jigging can be found in this MPA,
targeting species such as the European Sardine (Sardina pilchardus), European Sea
Bass (Dicentrarchus labrax), European Conger (Conger conger), Axillary Seabream
(Pagellus acarne), Common Octopus (Octopus vulgaris), Mediterranean Mussel
(Mytilus galloprovincialis) or the Pink Spiny Lobster (Palinurus mauritanicus) (VVAA
2013).
The main threats of the area are trawling and overfishing, as well as a potential largescale industrial and maritime trade development. In addition, the lack of regulation of
some traditional activities, such as fisheries, lack of adequate infrastructures for fishing,
poor waste and wastewater management, together with low sensitivity to waste
dumping and its visual impact, poaching, and lack of a Management Plan for the MPA
are also important weakness (VVAA 2013). Further studies and analyses on the
different uses of the area and their possible impacts on biological communities and
ecosystems are needed.
6.2. Zona marítimo-terrestre del Monte Hacho (SAC (Spain)
The Zona marítimo-terrestre del Monte Hacho SAC (Maritime-terrestrial zone of Monte
Hacho) (ES6310002) was proposed SCI in April 1999 and declared SAC in July 2012.
This SAC occupies ca. 9 km2 of which 96% are of marine character, with a depth range
from the coastline down to 200 m depth. The coastline of Monte Hacho presents an
irregular and rugged relief where cliffs are the predominant structures with lesser extent
areas of medium-thick material deposits, with similar characteristics for the sublittoral
areas. The Monte Hacho massif is constituted by metabasites and amphibolites with
local outcrops of peridotites and leucogranite that corresponds to the mafic formations
present in the Septide Complex (IGME 2013).
In this SAC some habitats included in Annex I of the HD are Reefs (Habitat 1170),
followed by Submerged or semi-submerged marine caves (8330) and Vegetated sea
cliffs of the Atlantic and Baltic Coasts (1230) (Mateo-Ramírez et al. 2020b). Associated
with the reefs a wide diversity of communities has been detected, including different
gastropods included in conservation lists (e.g. the Ribbed Mediterranean Limpet Patella
ferruginea, the vermetid Dendropoma lebeche) as well as coralline algae (Lithophyllum
byssoides) at the intertidal level, photophilous macroalgae beds (Cystoseira spp.) as
well as pre- and coralligenous communities with the Filigreed Coral-worm (Filograna
implexa) or the Star Coral (Astroides calycularis) in the shallow infralittoral level and
some gorgonians and Red Coral aggregations with the Whip Gorgonian (Ellisella
paraplexauroides, Annex II from BC), Phyllangia mouchezii (Barea-Azcón et al. 2008)
or the endangered Red Coral at larger depths (Mateo-Ramírez et al. 2020c). Sand and
detritic bottoms are also abundant at the circalittoral level with high abundances of
pennatulaceans dominated by Veretillum cynomorium.
This SAC is an important area for migratory seabirds, especially for the Cory's
Shearwater (Calonectris diomedea), because every autumn more than half a million of
individuals leave the Alboran Sea and pass very close to the coast. Other species are the
Audouin's Gull (Ichthyaetus audouinii), recently established as a breeding species in
Ceuta, and the Sandwich Tern (Thalasseus sandvicensis) during winter and migration.
The cliffs and abrupt walls are used by cliff nesting species such as the Peregrine Falcon
(Falco peregrines), the Kestrel (Falco tinnunculus), the Crag Martin (Ptyonoprogne
rupestris) and Blue Rock Thrush (Monticola solitarius) for nesting and wintering
(Mateo-Ramírez et al. 2020c).
Regarding socio-economic activities, some of them are recreational marine fishing, in
its different modalities, from the shore or using boats and snorkel equipment. Scuba
diving is an activity that has been on the rise in recent years with several Dive centres
operating from Ceuta. There are also two beaches (Santa Catalina and El Desnarigado)
with a low affluence. In contrast, the main threats are related to the presence of the
invasive macroalgae Rugulopteryx okamurae which was detected in Ceuta during 2015
and which has suffered a huge expansion in the last years (Rosas-Guerrero et al. 2018),
competing over other invasive species such as Asparagopsis armata and Caulerpa
cylindracea (MTERD 2020) and affecting both photophilic/sciaphilic algae to pre- and
coralligenous habitats. Other threats are the presence of a submarine emissary in the
northern area of the SAC, development of transport systems (roads), construction of
residential or recreational areas, modifications of the coastline, reductions of fish
populations and physical damage of marine habitats by fisheries and recreational
activities such as scuba diving.
6.3. Lagune de Smir SIBE and collateral figures of protection (Morocco)
The Smir lagoon is one of the coastal wetlands with the highest natural value for the
Mediterranean Moroccan coasts. In 1995, it was declared a SIBE by the High
Commission for Water & Forests for combating desertification. In 2006, this wetland
was included in the Intercontinental Mediterranean Biosphere Reserve AndalusiaMorocco (Reserva Intercontinental de la Biosfera de Andalucía-Marruecos), of the
UNESCO MaB programme, and as a Ramsar site in 2019.
The Smir lagoon is located on the coastal plain of the Smir River north of the city of
M'diq. It is flanked to the north by the Jebel Zem-Zem mountain range, to the south by
the Koudiet-Taifo mountain range, and to the west by limestone and dolomitic ridges.
The MPA has an extension of 2.46 km2 occupied by a permanent lagoon and some
marshes, located in the lowest area of the valley. This lagoon has a maximum depth of
2.5 m and it is mainly fed by the sea because it is connected by a permanent channel
that passes under a bridge on the national road that leads to the Port of Kabila. This
ecosystem, which functioned before as a lake, has been transformed into a coastal
lagoon. The lake had an area of about 2 km2, but its functioning was affected by the
construction of a water dam on the Smir River and the construction of a port at its
mouth, which have modified the hydrological system and induced a progressive
salinization of the waters. This increase in salinity has affected the composition,
structure and functioning of the biological communities, benefiting halophytic plant
communities and the intrusion of marine species with the total disappearance of
freshwater species.
This SIBE is represented by coastal and halophytic vegetation habitats, similar to the
ones listed by the European HD such as Estuaries (Habitat 1130) and Salicornia and
other annuals colonizing mud and sand (1310), as well as by Sandbanks which are
slightly covered by sea water all the time (1110) (Dakki et al. 2005) (Mateo-Ramírez et
al. 2020b). Different habitats conformed by aquatic angiosperms occur in the lagoon. At
the mouth of the Smir River, where a confluence of fresh and sea water occurs,
vegetated habitats dominated by Potamogeton pectinatus and Z. noltei occur. Whereas,
the southern sector near the channel is dominated by R. maritima and C. nodosa.
Finally, the communities closer to the sea are dominated by macroalgae (Benhissoune et
al. 2005).
The Smir lagoon is a stopover area for the birds that cross the Strait of Gibraltar and the
high variety of biotopes and the heterogeneity of its plant formations promotes a high
ornithological richness. Most of the birds are similar to the ones listed on the Annexes
of the European BD with migratory species such as shorebirds, herons, the Glossy Ibis
(Plegadis falcinellus), raptors as the Osprey (Pandion haliaetus) or the Marsh Harrier
(Circus aeruginosus), and passerines (Mateo-Ramírez et al. 2020c). Other birds are
subject of special conservation measures, such as the Pied Avocet (Recurvirostra
avosetta),
the Purple
Heron
(Ardea
purpurea) or the
Black-headed
Gull
(Chroicocephalus ridibundus). Furthermore, every year thousands of birds winter in this
lagoon, mainly anatidae such as the Northern Pintail (Anas acuta), the Northern
Shoveler (Anas clypeata) or the Common Pochard Tufted Duck (Aythya ferina). It is
remarkable the presence and reproduction of the Red-knobbed Coot (Fulica cristata)
(Castro et al. 2006) (Mateo-Ramírez et al. 2020c).
In the Smir lagoon, an important diversity of other vertebrates occurs, with similar
fishes as included in Annexes of the HD like the Greater Pipefish (Syngnathus acus),
the Seahorse (Hippocampus hippocampus) together with gobies or mammals such as the
Eurasian Otter (Lutra lutra) (https://rsis.ramsar.org/ris/2380 ). The benthic macrophytes
of this lagoon host a diverse community of benthic invertebrates with amphipods,
isopods, polychaetes, bivalves and gastropods as dominant groups (Chaouti and Bayed
2005).
Tourism is the most important socio-economic activity for the city of M'diq and the
surrounding urban areas. Agro-pastoral activities are also a source of income, mainly
from cereal crops and the production of local cattle. Currently, the MPA is under high
urban pressure, related to population growth throughout the coastal area. Tourism
pressure and summer residences are causing the expansion of the city of M'diq, which
threatens the lagoon to the south and east. Despite being a SIBE and a Biosphere
Reserve, no agency has intervened to stop the advance of the developments that are
proliferating around the lagoon, which may seriously affect its vegetation. The
destruction of the habitat and the discharge of wastewater into the lagoon are seriously
affecting the life cycle of the birds. Birds are also greatly affected by human pressure,
mainly from illegal hunting.
6.4. Koudiet Taifour SIBE and Réserve de Chasse Permanente (Morocco)
Koudiet Taifour was declared as SIBE in 1995 by the High Commission for Water &
Forests and combating desertification, and it was included in the third level of priority
for conservation. The reason it was listed as SIBE was the presence of species and
habitats of conservation interest for the Mediterranean, ecological, biological and
aesthetic integrity of the site involved, as well as the socio-economic importance of the
area (fishing, recreational and tourism activities). Additionally, Koudiet Taifour was
designated a Permanent Hunting Reserve (Réserve de Chasse Permanente, RCP) in
2012.
The RCP occupies an area ca. 11 km2, whereas the MPA covers an area of 5.32 km2 but
only 0.65 km2 correspond to marine area which goes down to 30m depth form the costal
line. It is bounded to the north by Cabo Negro and the city of M'diq, and to the south by
the Martin River that runs between Matril and Tetouan. Koudiet Taifour is a highly
urbanized area with ports and tourist accommodations, which has led to the loss of its
character and its high-quality landscape.
In this MPA different types of habitats have been listed, with some of them representing
similarities with the ones listed in Annex I of the HD. In the terrestrial part, dunes with
Pinus pinea (similar to Habitat 2270 of HD) are present. Strictly marine habitat are
Sandbanks which are slightly covered by sea water all the time (1110) with seagrass
meadows conformed by C. nodosa. The second main habitat is Reef (1170) (MateoRamírez et al. 2020b), with mesolittoral communities and associated species such as the
Saffian Limpet (Cymbula safiana), the Ribbed Mediterranean Limpet (and vermetid
reefs of D. lebeche, and with coralligenous communities formed by red algae L.
byssoides, the Star Coral and other molluscs species such as the Rough Pen Shell (Pinna
rudis) on infralittoral bottoms (MedMPAnet 2012). All these species are included in the
Annex I (strictly protected species) of the Bern Convention and/ or in the Annex II
(endangered or threatened species) of the BC (Mateo-Ramírez et al. 2020c).
Although, the fishing activity in the area is carried out on a small scale by artisanal
fishing boats docked in the port of M'diq, the tourism is the main socio-economic
activity in this coast (Jiménez and Almonacid 2008). In spite of being a SIBE, the coast
of Koudiet Taifour has suffered a landscape and functional transformation in the last
decades, caused essentially by the boom in the construction of urbanizations for
tourism. This expansive strategy of tourism infrastructure, which has had a great impact
on the environment, threatens to continue in the future due to its high economic
importance.
6.5. Côte Rhomara SIBE and RCP (Morocco)
Côte Rhomara was proposed as SIBE under the framework of the Protected Areas
Master Plan of Morocco of 1996 (AEFCS 1996) because of its aesthetic value, scientific
and educational interest. Its declaration as SIBE was done because of certain artisanal
fishing practices in this sector of the Mediterranean Moroccan coasts but also in relation
to the landscape quality and the heritage value of this area. Additionally, Côte Rhomara
was designed as a RCP in 2012.
The RCP has an area of 68 km2, whereas the SIBE occupies an area about ca. 42 km2
and reaches a maximum depth of 8 m. This MPA is on the province of Chefchaouen,
and is located between Oued Ouringa and the locality of Kaâ Sras. It is a trimmed and
relatively inhospitable coast formed by a succession of small sandy beaches and rocky
capes isolating a few islets at their base.
The best represented habitat of the MPA is similar to reefs (Habitat 1170) of the Annex
I of the HD. A total of ten species of conservation interest appear occasionally on cliffs
of this MPA such as Audouin’s Gull, the Osprey and the European Shag
(Phalacrocorax aristotelis desmarestii). Some species of the mesolittoral and
infralittoral rocks are the macroalgae L. byssoides and Peyssonnelia squamaria,
together with the Star Coral and Ribbed Mediterranean Limpet (Mateo-Ramírez et al.
2020c). In specific infralittoral rocky bottoms there are macroalgae communities with
Cystoseira compressa, Cystoseira humilis, Sargassum vulgare and Saccorhiza
polyschides (UNEP-MAP RAC/SPA, 2009). In some sublittoral bottoms the Giant Tun
(Tonna galea) can be relatively common unlike other parts of the Mediterranean Sea.
The main socio-economic activity of Côte Rhomara is the artisanal fishing,
complemented with the growing tourism and its derived recreational activities. The
main threat is the illegal fishing mainly that of bottom trawling that usually takes place
near the coast of the regions Amtar, Chmaâla, Stihat and Targha. Nevertheless, there are
other illegal types of fisheries in the area as the collection of Common Octopus in the
area from Iâraben, and suspected dynamite fishing in the localities of Takamount / Sidi
Ftouh. Another important threat is related to the development of the road network in the
region (Mediterranean bypass), construction of residential or recreational areas and
touristic coastal developments, that modifies the coastal line and increases the
discharges of wastewater and litter.
6.6. Cirque d'El-Jebha SIBE and RCP (Morocco)
The Cirque d'El-Jebha was proposed as SIBE for its aesthetic value, scientific and
educational interest and is currently part of the Intercontinental Mediterranean
Biosphere Reserve Andalusia-Morocco. This SIBE occupies an area of 0.85 km2 and
reaches down to 27 m depth. In 2012, Cirque d'El-Jebha was also designated as a RCP
with an area of ca. 3.6 km2.
This MPA is located east of the city of Jebha, just after the fishing port, in the province
of Chefchaouen, that is located in the Rif Central (Morocco). The Cirque d’El-Jebha is a
horseshoe depression developed over a folded and trusted sequence of Jurassic
limestones and Aquitanian turbidites (Vitale et al. 2015). The Cirque d’El-Jebha is a
remarkable geomorphological structure, with an amphitheatre form limited by high
cliffs and connected to the sea northwards. It is a very small rib, formed of a succession
of small sandy beaches, coves and rocky capes isolating a few islets at their base. A
series of ravines cut the relief into very narrow valleys perpendicular to the coast.
In this MPA a high diversity of species has been detected, with 20 of them included in
different conventions of protection (Mateo-Ramírez et al. 2020c). In their cliffs
threatened birds nest such as the Audouin's Gull and the Osprey. The predominant
habitat in this MPA is similar to the Reefs (Habitat 1170) of the HD. In steep cliffs and
slopes and ledges exposed to waves and strong hydrodynamics, the mesolittoral
community is conformed by cirripeds (Barnacle Pollicipes pollicipes), the red algae L.
byssoides and other protected species such as the Ribbed Mediterranean Limpet and
Saffian Limpet (Mateo-Ramírez et al. 2020c). In the subtidal zone other threatened
species are the Star Coral, and some macroalgae such as Cystoseira zosteroides,
Cystoseira amentacea and Cystoseira elegans. In the central part of the horseshoe
depression, the seabed is composed of large blocks that host a very interesting
biodiversity, including macroalgae such as Dictyopteris polypodioides, S. polyschides
and S. vulgare, sponges like Ircinia sp., the Dusky Grouper, the Knobbed Triton as well
as an important diversity of coralligenous communities with different corals and
gorgonians such as the Red Coral, the Orange Tree Coral, the Violescent Sea-whip
(Paramuricea clavata), the White Sea Fan (Eunicella singularis) and Leptogorgia sp.
(UNEP-MAP RAC/SPA, 2009). Some of those aforementioned species are included in
the Annex II of the BC. Small cetaceans such as the Common Dolphin have also been
frequently observed in the area (Mateo-Ramírez et al. 2020c).
The Cirque d’El-Jebha has a high socio-economic importance for the town of Jebha.
The proximity to the town and the port facilitates the artisanal fishing that exploits a
wide variety of fishes (more than thirty species). Some of the target species are the very
valued Dusky Grouper, Cuttlefish (Sepia officinalis), Common Octopus, Spider Crab
and the Spiny Lobsters (Palinurus elephas). The main threats are the increase of
housing developments, as well as the urban discharges from the port and town that
constitutes a source of significant contamination to the adjacent ecosystems. Other
threats are the lack of wastewater and garbage treatment plants, the release of litter such
as bottles, tires, ghost nets, etc. as well as the overfishing and illegal fishing, in
particular of species included in conservation lists such as groupers and the Red Coral.
6.7. Cap des Trois Fourches SIBE and collateral protection figures (Morocco)
The Cap des Trois Fourches (Cape of Three Forks) was declared SIBE in 1996 and
Ramsar Site in 2005 (CAR/ASP - PNUE/PAM 2012). Later, the terrestrial part was
designated as RCP in 2012, with an area of 24 km2. Finally, in 2014 a Réserve Naturelle
was proposed, that included most of the terrestrial area of the RCP, and a maritime area
of 68.2 km2 ranging from coastal line to more than 230 m.
This MPA is located at the Trois Fourches peninsula, in the Moroccan commune of
Beni Chiker (province of Nador) and north of Melilla (Fig. 21). This MPA is
characterized by a cliff coast, containing small coves. In this area, the outcrop of two
geological units occurs, separated by an extensional fault of NE-SW trend, towards the
south of the fault micaschists with orthogneises, quarzities and marbles of Tarjât unit
and lower greenschist shales and quarzites of the Taïdant unit, and to the north of the
fault, calcano-alkaline series volcanoclastic rocks and detritic sediments of Tortonian
age (Azdimousa et al. 2019). One aspect to consider is the different physionomy of the
eastern and western coasts of the Cap des Trois Fourches. Due to the geological nature,
the eastern coast is much steeper, with deep bottoms just few metres from the coast, but
the western coast is smoother. This could also be related to the different hydrodynamics
with stronger easterly winds compared to westerly ones.
Terrestrial ecosystems, without large human populations and minimal touristic
influence, are rich and varied, with several habitats that are similar to those included in
the Annex I of the HD. Some of the terrestrial habitats are Thermomediterranean and
pre-esthetic scrubland (Habitat 5330), the most coastal Cliffs with vegetation on the
Mediterranean coast with endemic Limonium spp. (1240) and Halonitrophile scrubs
(Pegano-Salsoletea) (1430) (Mateo-Ramírez et al. 2020b).
The marine life of this MPA is influenced by the nutrient-rich waters and the
biogeographic confluence of Atlantic species that are not common eastwards and of
Mediterranean species that are not common westwards (González García 1994). This is
clearly reflected in the algal communities, with the presence of the typical Atlantic algae
Fucus spiralis, Cystoseira gibraltarica or Gelidium sesquipedale and of the typical
mediterranean Rissoella verruculosa, Cystoseira crinita and the seagrass P. oceanica.
The first marine expedition in the Alboran Sea was carried out in 1910 by Odon de
Buen, including the area of Cap des Trois Fourches to the Muluya river mouth
(Camiñas 2018). The main marine habitats are Reefs (similar to Habitat 1170 of the
HD), Submerged and semi-submerged caves (similar to Habitat 8330 of the HD) and
Sandbanks which are slightly covered by sea water all the time (similar to Habitat 1110
of the HD) containing C. nodosa meadows (Mateo-Ramírez et al. 2020b).
In the mesolittoral reefs, well-preserved populations of the vermetid D. lebeche
(Vulnerable) have been detected as well as of the limpet Ribbed Mediterranean Limpet
(Critically Endangered), the latter with more than 20000 individuals (González García
et al. 2006). In sublittoral rocky bottoms, protected or regulated commercial species
occur such as the Common Antlers Sponge (Axinella polypoides), the cnidarians Star
Coral, Pink Sea Fan, Violescent Sea-whip, Whip Gorgonian Orange Tree Coral, Yellow
Tree Coral (Dendrophyllia cornigera), Mediterranean Pillow Coral (Cladocora
caespitosa), Eunicella verrucosa, Eunicella gazella, Savalia savaglia, Leptogorgia
lusitanica; the molluscs Knobbed Triton, Rough Pen Shell, Zoned Mitre (Episcomitra
zonata), Pear Cowry (Zonaria pyrum), Date Shell (Lithophaga lithophaga), Wandering
Triton (Ranella olearium), Brown Cowry (Luria lurida); the crustaceans Spider Crab,
Spiny Lobster, Slipper Lobster, European Lobster (Hommarus gammarus); the
echinoderms Hatpin Urchin (Centrostephanus longispinus), Purple Sea Star
(Ophidiaster ophidianus), Smooth Starfish (Hacelia attenuata); and the large fishes
Dusky Grouper, Brown Meagre (Sciaena umbra) and Moray Eel (Muraena Helena),
among others (Yus et al. 2013) (Mateo-Ramírez et al. 2020c).
Another interesting habitat of the MPA is the Kelp beds that are located in the most
reophilic areas, specifically between “Los Farallones” and the tip of the “Farola” as well
as in the vicinity of the “Tío Pinar” slab. The main kelp species are S. polyschides and
Phyllariopsis brevipes that form extensive and dense meadows between 8 and 30 m
depth with fronds up to 2 m high (González and Conde 1993). In the submerged and
semi-submerged caves a rich fauna of invertebrates has been detected, especially in
those of “Los Farallones” canal, the “Tío Pinar” slab, the tip of the “La Farola”, the
“Puntilla” and “Cabo Viejo” (CAR/ASP - PNUE/PAM 2012).
In this MPA, some large pelagic species of marine vertebrates that are passing or
stranding are common. Among fishes, the most singular ones are sharks (Isurus
oxyrrhynchus, Prionace glauca), Bluefin Tuna and Swordfish (Xiphias gladius). There
are some records of the Leatherback and Loggerhead Turtles and of cetaceans such as
the Common Dolphin, the Stripped Dolphin, Bottle-nosed Dolphin, Long-finned Pilot
Whale, Risso's Dolphin (Grampus griseus), Sperm Whale and the Fin Whale (MateoRamírez et al. 2020c). Special mention deserves the Monk Seal (Monachus monachus),
"Critically Endangered", of which, in the beaches of the volcanic caves of the tip of Cap
des Trois Fourches, resting specimens can be sporadically seen (Fig. 21) (MateoRamírez et al. 2020c).
The main socio-economic activity in the MPA is artisanal fisheries. There are 70 boats
from the village of Kahf Dounia, Tibouda and Ouled Lahsen that operate in the area. All
of these use artisanal fishing gears and the target species are the Common Octopus,
groupers, Axillary Seabream (Pagellus acarne), Albacore (Thunnus alalunga) and the
Red Mullet (Mullus surmuletus). Another complementary and important activity is
tourism. All year round, the fisherman rent their houses to tourists during weekends and
in summer (CAR/ASP – PNUE/PAM 2012).
Human influence on the coast is still scarce, because the abrupt terrain of the MPA has
not allowed important human developments that could threat the landscape.
Nevertheless, three negative human activities should be mentioned such as the use of
explosives for fishing that were carried out by the coastal population of “Cala Viñas” in
the area of the “Farallones” during decades, which has reduced populations and sizes of
large fish, especially groupers; the punctual bottom trawling and longline fishing carried
out at short distance from the coast; and scheduled trips of one or several days of small
vessels carrying underwater fishing experts that decisively influenced the decline of
populations, especially of the Dusky Grouper, the Atlantic Wreckfish (Polyprion
americanus) and the Goldblotch Grouper (Epinephelus costae). Nevertheless, this is
something that seems already in decline, perhaps due to the decrease in the availability
and size of large fish in the MPA.
6.8. Zona marítimo terrestre de los acantilados de Aguadú SAC (Spain)
The Zona marítimo terrestre de los acantilados de Aguadú SAC (Maritime-terrestrial
zone of the Aguadú cliffs) (ES6320001) (Fig. 22) was designed as SCI in March 2006
and as SAC in September 2013, with a final area of ca. 0.55 km2 (0.44 marine and 0.11
terrestrial). It is located in the northern part of the Melilla city, with an altitude of 120 m
“Quemadero” ravine and a depth range between the coastline and ca. 30 m depth. On
the land side, in addition to the aforementioned ravine, the cliffs of Aguadú occur from
the seawater desalination plant to the border with Morocco, about 700 m of coastline.
On the cliffs Messinian formations outcrops, from base to top, there is a succession of
conglomerates, calcarenites, limestones of algae and breccia, and sands and silts, and
finally covered by caliches and carbonate crusts of Holocene age.
Several habitats listed in Annex I of the HD can be identified in the SAC, with two of
them being of marine character such as Reefs (Habitat 1170) and Submerged or semisubmerged marine caves (8330), and three terrestrial ones: Thermomediterranean and
pre-steppics scrub (5330), Cliffs with Mediterranean coastal vegetation with endemic
Limonium spp. (1240) and Halonitrophile scrub (Pegano-Salsoletea) (1430). In those
terrestrial habitats, interesting vascular flora occurs such as the Thuja Articulata
(Tetraclinis articulata) and Helianthemum caput-felis (protected in the HD) and the
North African endemism Bupleurum balansae. In these areas, the Audouin's Gull
displays a nesting population of several hundreds of specimens since 2015 (González
García and Enrique Mirón 2018a) (Fig. 22) (Mateo-Ramírez et al. 2020b).
Regarding marine life, there are two protected molluscs associated with mesolittoral
reefs with strong hydrodynamics (Habitat 1170 of the HD): the Ribbed Mediterranean
Limpet (Critically Endangered UICN list), which forms dense populations of ca. 3000
adult specimens and a high number of immature specimens (González García et al.
2013, 2015; González García and Enrique Mirón 2019) and the vermetid (D. lebeche)
(Vulnerable) conforming small groups of individuals or forming small continuous
aggregates (González García et al. 2014). (Fig. 22) Other vulnerable protected species
of the SAC are the Barnacle and the Saffian Limpet (Fig. 22). In addition, some
protected species of rocky-mixed bottoms, vertical walls, hollows or small caves at
depths larger than 10 m (Habitat 8330 of the HD) are found in the SAC such as the Star
Coral, the Knobbed Triton, the Rough Pen shell, the gorgonians Pink Sea Fan and E.
gazella, the starfishes Purple Sea Star and Smooth Starfish, and the solitary Red Seasquirt (Halocynthia papillosa) (González García and Enrique Mirón 2018b) (MateoRamírez et al. 2020c).
This MPA has no human activities due to the prohibition and the restricted access and it
has only been explored by the Spanish army for the last 15 years. The main threat
comes from the desalination plant located in Punta de Rostrogordo that occupies 8000
m2 at the foot of the cliffs located adjacent to the SAC. This desalination plant
discharges the brine in the same area ("Overflow on a cliff", as defined in the CEDEX
technical report for the Ministry of the Environment, Rural and Marine Affairs in 2011)
(Fig. 22), as well as through an underwater outfall of 1 m in diameter at a depth of 9 m.
Other substances are also discharged such as biocides, anticoagulants, flocculants,
antifoulants, detergents, pH adjusters, etc. Currently, the project to expand the plant,
already approved, with the further destruction of the habitat that this will imply,
reinforces the threat. In 2005 and 2006, the works of the desalination plant (dredging,
blasting and concreting, installation of pipes and a water tower, construction of a coastal
breakwater, destruction of the cliff, etc.) and of a coastal road with anti-immigration
purposes, caused a strong landscape and ecological impact, but, paradoxically, in the
medium term and due to the total isolation of the human presence, the recovery of the
diversity in 15 years has been very high.
6.9. Sebkha Bou Areg SIBE and collateral figures of protection (Morocco)
The Sebkha Bou Areg Réserve Naturelle (Nature Reserve) and RCP, also known as Mar
Chica, is a coastal lagoon located close to Nador and Melilla that reaches 6 m depth,
representing a unique formation within the Alboran Sea (Fig. 21). This lagoon is
bounded to the east by the Gourougou volcanic massif, formed by pyroxene-biotitic
andesites of a calc-alkaline series, to the north by rocky outcrops of Mesozoic and
Neogene sedimentary units, while to the south by the plains of Bou Areg, constituted by
marls and sandstones of Miocene and Pliocene age (Torcal Sainz and López Bermúdez
1997). It is separated from the open sea by a sandy littoral bar of about 24 km in length
that is currently communicated with the sea through two channels or artificial “mouths”
of about 300 m wide. The terrestrial area is a RCP declared in 2012 with 93 km2. In
2014 the marine area was proposed as Nature Reserve, increasing the area up to 169
km2 with 111 km2 of marine area, with a maximum depth of ca 6 m.
In the littoral bar there is vegetation that is typical of coastal sandy beaches conforming
some protected habitats that are similar to those of the Annex I of the HD, such as
Annual vegetation on accumulated marine debris (Habitat 1210), Cliffs with vegetation
of the Mediterranean coasts with Limonium spp. Endemic (1240), Mediterranean and
thermo-Atlantic
halonitrophilic
thickets
(Sarcocornetea
fruticosi)
(1420)
and
Halonitrophilic thickets (Pegano-Salsoletea) (1430) (Mateo-Ramírez et al. 2020b).
Sebkha Bou Areg was also declared as IBA by the BirdLife International Program in
2001 and SIBE and Ramsar Site in 2005. This was mainly due to its importance for
biodiversity and breeding area, with nesting birds such as the Sandwich Tern, Pied
Avocet, Marsh Harrier, Little Tern (Sternula albifrons), the Lesser Crested Tern
(Thalasseus bengalensis) and the Kentish Plover (Charadrius alexandrinus). Other
wintering and migratory species are the Little Ringed Plover (Charadrius dubius),
Black-tailed Godwit (Limosa limosa), Black Tern (Chlidonia sniger), Eurasian Curlew
(Numenius arquata), Greater Flamingo (Phoenicopterus roseus) and Purple Heron
(Ardea purpurea), among others (Fig. 21) (Mateo-Ramírez et al. 2020c).
Muddy sand occupies almost all of the lagoon bottoms, with the exception of the coast
of the volcanic elevation of El Atalayón and the small sandstone formations of some
areas of the littoral bar. Depth and sediment characteristics (e.g. organic matter
concentration) determine the presence of different vegetated habitats such as small
meadows of Z. noltei, meadows of C. nodosa and the macroalgae C. prolifera,
sometimes mixed with those seagrasses (Habitat 1110 of the HD) (Fig. 21). Other
macroalgae species proliferating in shallow areas of the lagoon with high salinity and
clear signs of eutrophication are Ulva rigida, Enteromorpha spp. and Chaetomorpha
linum. In boulders and small vertical barrels of the sleeve of El Atalayón, the vegetated
habitats are conformed by fucoid meadows (C. crinita, C. compresssa and S. vulgare)
and other species such as Gelidium pusillum, Laurencia obtusa, Spyridia filamentosa or
A. acetabulum, among others.
Animal diversity is reduced compared to the open sea, but there are some protected
species that inhabit the lagoon, including the Rough and the Noble Pen shells, the latter
until its decline in 2016 (Fig. 21), as well as the Long-snouted Seahorse (Hippocampus
guttulatus), the Brown Cowry in sparse and only under sandstone cornices, the Captain
Star (Asterina gibbosa) under stones in El Atalayón, the Mediterranean Pillow Coral
and the Orange Puffball Sponge (Tethya aurantium). Other species are the Triplegrooved Shrimp (Penaeus kerathurus), abundant in freshwater outcrops of the internal
part of the lagoon and the Eel (Anguilla anguilla) breeding in cane field ditches with
agricultural discharges. Other marine species, most of them associated with
macrophytes are the Holothurian (Holothuria tubulosa), the Shore Crab (Carcinus
maenas), Pink Cuttlefish (Sepia orbignyana), the Golden Grey Mullet (Chelon aurata),
muricid gastropods (Hexaplex trunculus, Bolinus brandaris), nudibranchs (Aplysia
punctata, Pleurobranchaea meckelii, Berthella stellata), epizoic colonial bryozoans of
C. nodosa (Botryllus schloseri, Botrylloides leachi) and a wide variety of bivalve
molluscs.
Regarding socio-economic activities, the MPA has been a fishing source of Triplegrooved Shrimp, Cuttlefish (S. officinalis, S. orbignyana), Common Octopus, Striped
Seabream (Lithognathus mormyrus) and Sand Smelt (Atherina presbyter). In the 1980s,
the MAROST Company introduced marine farms of various species in El Atalayón,
including the Chequered Venus (Ruditapes decussatus), Kuruma Shrimp (Penaeus
japonicus), Gilthead Seabream (Sparus aurata) and Common Oyster (Ostrea edulis).
Tourism is concentrated on the coast of Nador and Beni-Enzar where the Melilla
population spends their holidays.
The main threats are the increasing tourism pressure as well as the urban associated
discharges and wastes of nutrients and herbicides from irrigated crops of the internal
section between Nador and the southwestern end. There are also some invasive species
such as the opistobranch Bursatella leachi, the American Brine Shrimp (Artemia
franciscana) or the Kuruma Shrimp which has displaced some native shrimp species.
The future of the MPA remains uncertain because of the transformation that has already
begun, which aims to transform the area into an extensive tourist complex. In this way,
the disposal of urban waste has improved; two artificial mouths have been opened to the
sea; important dredging have been done in the bottoms and the so-called “7 Cités de la
Mar Chica” are under construction at the moment, with “marinas”, lagoons and artificial
islets. This may represent an important threat for the persistence of some of the habitats
and species of this MPA.
6.10. Islas Chafarinas National Refuge of Hunting & SAC (Spain)
The Chafarinas Islands are an archipelago that consists of three islands: Congress,
Isabel II and Rey Francisco that located in the southern Alboran Sea, 48 km west of
Melilla city and ca. 3 km in front of Cabo de Agua, and also located 11 km to the northwest of the Moulouya river mouth, very close to the border between Morocco and
Algeria (Fig. 23). The presence of specimens of the Monk Seal (M. monachus) (Fig.
21), a large colony of Scopoli's Shearwater and Audouin's Gull, endemic flora species
and well preserved bottoms communities, motivated its designation as National Refuge
of Hunting (Refugio Nacional de Caza) in April 1982. Later on, these islands were
declared as SPA in 1989. In November 1998 a SCI was proposed, approved in 2006
(ES6300001), and designated as SAC in 2018. Currently, these islands are under the
shared administration of the Spanish Army and the Organismo Autónomo de Parques
Nacionales (OAPN) of the Ministerio para la Transición Ecológica (Spanish Ministry
for the Ecological Transition). These islands have been described as the eroded remains
of a volcanic massif Upper Miocene-Pliocene in age (Barrera and Pineda 2006). These
authors indicated the presence of mainly andesitic units from the calc-alkaline series
(breccia, lava flows, domes and pythons) and basalts from the alkaline series. Covering
these materials, carbonate crusts, hillside and eolic deposits appear, while the seabed is
largely sedimentary due to the deposition of sediments transported by the coastal drift,
predominantly westwards, from the Moulouya River (Barrera and Pineda 2006).
In this MPA, there are habitats included in the Annex I of HD such as P. oceanica
meadows (Habitat 1120) displaying a healthy status, Submerged or semi-submerged
marine caves (8330) and Reefs (1170) with interesting and rich associated benthic
communities (Fig. 23) (Mateo-Ramírez et al. 2020b). The littoral and the sublittoral
bottoms harbour different species included in the Annex II of the BC, such as the
critically endangered Ribbed Mediterranean Limpet, with one of the most important
populations (Guallart and Templado 2016), the Hatpin Urchin, the vermetid gastropod
D. lebeche or the Common Antlers Sponge, among others (Maldonado et al. 2011;
Templado et al. 2016) (Mateo-Ramírez et al. 2020c). The peculiar characteristics of its
waters, with a high degree of turbidity due to its proximity to the Ouad-Moulouya river
mouth, enhance suspended sediment supply. This is probably one of the reasons for the
presence at shallow waters of characteristic species of deeper areas such as the Whip
Gorgonian, that display here the largest known population for the Alboran Sea
(Maldonado et al. 2013) (Fig. 23), the black coral Antipathella subpinnata (SánchezTocino et al. 2014), or the Gold Coral Savalia savaglia (Maldonado et al. 2011) (MateoRamírez et al. 2020c). They are also remarkable the large populations of the Violescent
Sea-whip and the presence of the Orange Tree Coral (Sánchez-Tocino et al. 2019) (Fig.
23) (Mateo-Ramírez et al. 2020c). Furthermore, a high species richness of molluscs has
been highlighted by Oliver et al. (2015) in the bottoms around the islands.
Because the access to the islands is nowadays restricted, the only economic activity in
the area is some small-scale fishing by Moroccan fishermen from “Cabo del Agua” and
also some recreational fishing activity. This has been done both by Moroccan fishermen
and the military detachment over several years, and it has caused significant damage on
sessile benthic invertebrates. Some nets, lines and hooks have especially damaged the
large Whip Gorgonian, with different colonies having fishing lines and pieces of net
material tangled in their branches (Maldonado et al. 2013). On the other hand, the
increase in spear fishing, due to the professionalization of the outstanding troops on the
islands, resulted in a sharp reduction of large fish, especially groupers and sparids.
Likewise, the lack of recycling by the Moroccan population of plastic bottles and litter
favours their accumulation in the P. oceanica meadows. Moreover, some mortality
events of the gorgonians Violescent Sea-whip and White Sea Fan have been detected in
recent years (de la Linde et al. 2018) (Fig. 23) and no living specimens of the Noble Pen
Shell were found in 2019 due to the aforementioned massive decline of 2016. Finally,
the presence of the invasive algae C. cylindracea and R. okamurae was confirmed in
2018 and 2019 (Sánchez-Tocino, personal observation).
The declaration of these islands as SAC and the regulation of fishing activities have
been fundamental for stopping (or at least slowing down) the degradation of their
habitats and associated communities. Nevertheless, in addition to these measures, it is
necessary to intensify the surveillance to prevent the less visible areas of the islands
from being used by Moroccan fishermen that throw their gillnets close to the coastline,
by furtive underwater fishermen and for other types of activities that use the islands as
an anchorage place, leaving the bottoms full of remains of their unsustainable activities
(Fig. 23). At present, the increase in the breeding colony of Yellow-legged Gulls (Larus
michahellis) seems to be affecting the Audouin’s Gull, whose population is significantly
decreasing.
7. Gaps of knowledge and future management ideas
The Alboran Sea is an area of importance regarding historical, social, geopolitical,
strategic and scientific aspects, and it is the engine for different Mediterranean aspects.
Its characteristic oceanography, as well as its strategic location, makes the Alboran Sea
one of the areas with the greatest biodiversity in Europe and with a high amount of
protected/threatened habitats and species, as it has been presented in this chapter. A
natural marine heritage off the coasts of the southern Iberian Peninsula and northern
Morocco and Algeria that should be protected in its entirety due to its uniqueness.
Nevertheless, its management and protection entails a difficulty arising from the need of
designing a strategy of collaboration between different countries, which in this case
belong to different continents and cultures. Therefore, in order to ensure the
conservation of the biodiversity and the sustainable use of the resources of the Alboran
Sea, it is necessary to adopt a coordinated management strategy based on different
approaches including a network of Marine Protected Areas (MPAs), an Integrated
Coastal Zone Management (ICZM), an effective plan for the protection and recovery of
threatened and endangered habitats and species as well as a sustainable use of exploited
resources (IUCN 2010).
7.1. Marine Protected Areas and Key Biodiversity Areas network
For consolidating the Marine Protected Areas and Key Biodiversity Areas (MPAs and
KBAs), a network is needed for increasing the number and extension of MPAs as well
as for implementing effective conservation measures in order to increase the protection
of the Alboran Sea. The network should increase the number of MPAs in all
surrounding countries, moving ahead to equilibrate the protected surface and the
number of MPAs concerning the coastline length of each country. Currently the main
problem to the sustainability of the good condition of the MPAs-KBAs is related to the
needs for improving the human resources in relation to the control and surveillance in
MPAs that is still inadequate regarding the number of officers and vessels for
surveillance. A second gap is related to the lack of coordination and collaboration in
terms of regulations and shared actions among local, regional, national governments and
between countries.
It is remarkable the unbalanced number of protected areas between the northern and
southern sectors of the Alboran Sea, because all MPAs-KBAs (including only IBAS) of
the Alboran Sea accumulate a total area of ca. 5661km2, but ca. 91% belongs to those of
the northern sector. The MPAs-KBAs network of the Alboran Sea is complex because
MPAs-KBAs are very diverse from different points of view, both in terms of their
conception and objectives, and in terms of their scope and responsibility for their
management. It is important to distinguish between MPAs that are effectively protected
and those that are in the process of improving their management (e.g. some KBAs,
SCIs). There are only ca. 15 of the ca. 35 detected MPAs-KBAs (including only IBAS)
that incorporate some protection figure and/or a management plan (Natural Park,
Permanent Hunting Reserve, Natural Monument or Natural Site), which depends on the
country where they are located. There are very few of them with effective protection
measures. In parallel for increasing human and funding resources in the existing MPAKBAs, the inclusion of new MPA or KBA should be accompanied of financial
resources in order to provide surveillance and monitoring systems. Moreover, adequate
infrastructures and services (e.g. waste water treatment plants, delimitation of restricted
areas, etc.) should be provided in those areas where significant human developments
and unsustainable practices are still occurring.
The current conservation and protection measures are not sufficient and it should be
amplified and extended to all MPAs from the northern and southern Alboran Sea, which
is especially needed for the MPAs of the southern sector. Moreover, there is a need for
improving the integration and visibility of the Alboran Sea in the governance processes
of the Mediterranean Sea, particularly those related to the Convention for the Protection
of the Marine Environment and the Mediterranean Coastal Region (Barcelona
Convention).
Furthermore, there are a high number of MPAs-KBAs that have not been explored in
detail regarding habitat mapping, associated biodiversity, status of the populations of
endangered/threatened species, among other aspects. According to IUCN (2012) and the
suggestions made by NGOs (e.g. Oceana) and marine experts, there are other KBAs that
should be incorporated to the current MPAs-KBAs network such as the submarine
canyons of Algeciras, Ceuta and Almería; the seamounts Banc de Xauen, Banc de
Tofiño, Banco de Avempace, Banco de Djibouti Ville, Cabliers Coral Mound Province,
Banco de Catifas or carbonate mounds of Melilla as well as others areas with poor
current information (e.g. submarine canyon of Guadiaro or Almería, mud volcanoes of
the Alboran Sea) or no information (the seamounts of Trois Fourches and Provençaux).
In those areas, protected habitats and species have been reported by previous studies
(Gil et al. 2009; de Mol et al., 2011; Pardo et al. 2011; Aguilar et al. 2013; OCEANA,
2014; Palomino et al. 2015; Corbera et al. 2019). Some of these habitats are reefs
formed by cold-water-corals (harbouring protected species such as Madrepora oculata,
Desmophyllum pertusum, Dendrophyllia ramea, among others), gorgonian and black
coral aggregations (with protected species such as Callogorgia verticillata, Antipathes
dichotoma, Leiopathes glaberrima, among others), sponge aggregations, sea-pen and
bamboo coral communities, as well as protected species of elasmobranches (Oxynotus
centrina, Centrophorus granulosus, Leucoraja circularis, Cetorhinus maximus, and
Squalus acanthias) and molluscs such as Giant Oysters (Neopycnodonte zibrowii). In
order to incorporate those new areas to the current MPA-KBA network, the
relationships between administrations and scientists of each country and at regional
level should be created if necessary, or at least improved. For example, the
communication of the results obtained by the scientists to managers and policy-makers
concerning new results, additional needs and new proposals of protected areas, should
be done in an easier and more didactic way.
7.2. Conservation of habitats and diversity
Regarding cetaceans, it would be essential to implement the recommendations of the
Agreement on the Conservation of Cetaceans of the Black Sea, Mediterranean Sea and
Contiguous Atlantic Area (ACCOBAMS), of which both Spain and Morocco are
members. A management plan for cetaceans in the entire Alboran Sea, which has been
identified by ACCOBAMS and IUCN as an "Area of Conservation Interest", should be
implemented. Experts also recommended the implementation of management plans
already developed for the Bottle-nosed Dolphin and the Common Dolphin. In 2007,
Spain requested that ships crossing the Strait of Gibraltar may not exceed the speed of
13 knots, with precautions during those months when Sperm Whales return to the Strait
of Gibraltar for feeding (UCIN 2007, 2010).
In relation to marine turtless, a “Strategy for the conservation of the Loggerhead Turtle
(Caretta caretta) and other marine turtless in Spain” is under elaboration under the
framework of the Action Plan for the Conservation of Mediterranean Marine turtless
(Barcelona Convention, BC) and for the fulfilment of the commitments established by
other international conventions ratified by Spain such as OSPAR, Bonn and Bern. The
MITECO, through the General Directorate for Sustainability of the Coast and the Sea
(DGCSM) and the regional and autonomous city governments are preparing this
national strategy, drafting the basic technical document within the Working Group of
Marine turtless of the Committee of Wild Flora and Fauna. The Spanish Strategy should
be reviewed by the State Commission for Natural Heritage and Biodiversity. There are
some other national initiatives for the Loggerhead Turtle which includes limiting
accidental catches by fishing gear. Nevertheless, this action plan is not yet being applied
because of the lack of approach between the different parts involucres (UICN 2007,
Robles 2010).
For the Monk Seal, there is a need for reducing significantly human impacts and
affluence in some MPAs and create new MPAs that may harbour the habitats and
resources needed for the establishment of Monk Seal populations, both in the southern
and northern Alboran Sea.
Some habitats are experiencing a current decline (e.g. seagrass beds on soft bottoms,
Sea-pen-bamboo coral communities) (Waycott et al. 2009; Fabri et al. 2014) and there
is a need to achieve their recovery through restocking in specific areas, and effective
conservation of the remaining patches of such habitats. For an effective conservation,
water quality should be improved, illegal bottom fishing should be controlled as much
as possible, boats should be prevented from anchoring on them and coastal erosion
should be mitigated (IUCN Grupo de Coordinación Alborán).
The MPAs-KBAs network of the Alboran Sea, even though, seem to present a good
representation of habitats from the Habitat Directive and Barcelona Convention, such as
Posidonia oceanica beds (Habitat 1120 of the HD), Reefs (Habitat 1170) or Sandbanks
which are slightly covered by sea water all the time (Habitat 1110), there are others such
as Submarine structures made by leaking gases (Habitat 1180) and Caves (8330) that
are still underrepresented. Subtypes of the Habitat 1170 such as Cold-water Coral reefs
or antipatharian aggregations are also not well respresented, The inclusion of new
MPAs-KBAs that may have these habitats (e.g. mud volcanoes of the Alboran Sea or
the Cabliers Coral Mound Province with the biggest CWC reef of the Alboran Sea),
would help to increase the conservation of these habitats in the MPAs-KBAs Alboran
network.
Regarding habitats with good representation, the lack of updated habitat mapping for
the total Alboran Sea still represents a key factor for its effective conservation and
management (Rueda et al. Chapter 9 of this volume). Some projects (e.g. LIFE +
INDEMARES, LIFE+ Posidonia Andalucía, LIFE Blue Natura, etc.), have done
significant efforts for improving habitat mapping in specific areas, but accurate mapping
is generally absent in most MPAs-KBAs, and even for priority habitats such as P.
oceanica beds. This kind of information is essential for a good management and Marine
Spatial Planning that can ensure the effective conservation of the habitats.
Inclusion of new MPAs-KBAs as mentioned in the previous section as well as effective
conservation of the populations in the already designated MPAs-KBAs would also
improve the connectivity between populations of threatened species. The number of
protected species in MPAs of the Alboran Sea is relatively high but it is remarkable that
most of them are for vertebrates, particularly birds and mammals (cetaceans), probably
because invertebrates and macro algae despite its undeniable importance for
ecosystems, have less interest to the general public and always been underrepresented in
official conservation lists. Some invertebrate species such as gorgonians, corals or
sponges are slow-growing organisms with a low reproductive output that are very
threatened. Some of them provide shelter, food provision and nursery habitats to a wide
variety of species, but most of them are still not included in national conservation lists.
Moreover, there is a need for increasing the knowledge on the biology and ecology of
some of these invertebrates as well as on their resilience to human impacts (Templado et
al. Chapter 10 of this volume). Regarding this, it is important to create a hub of research
and knowledge on marine biodiversity between local, regional, national governments as
well as between countries, including new projects based on research, ecosystem
management, transfer of information, education / awareness and on the integration of
the experiences of different sectors that use each MPA and KBA.
7.3. Sustainable exploitation of the resources and main threats
The fishing resources from the Alboran Sea are managed under the framework of two
Regional Fisheries Organisation (RFOs): the General Fisheries Commission for the
Mediterranean (GFCM) and the International Commission for the Conservation of
Atlantic Tunas (ICCAT). The main aim is achieving a sustainable management of the
different exploited resources. All countries surrounding the Alboran Sea are members of
these two RFOs and therefore they are involved in the implementation of joint
regulations and agreements adopted by the parties aiming to the protection of the tuna
and tuna like species (ICCAT) and to the demersal and small pelagic species and
respective fisheries. Unfortunately there is no automatic compliance with all regulatory
measures adopted by the RFOs and, if these measures are translated into national
regulations, the existence of the necessary means, tools and human resources to verify
and control the implementation is still lacking.
Although important progress have been made for the conservation of the Alboran Sea, it
is necessary to improve the role of political and social (e.g. fishermen) sectors towards
the environment and sustainable development.
The status of most of the Mediterranean exploited resources stated that ca. 78% of the
stocks assessed, including stocks of all priority species, were overexploited (FAO
2018). This percentage has slightly decreased since 2014 (88%), which reflects the
different recent management measures that have been made, but underlines the need to
go further. Nevertheless, the last GFCM Report 2019 (FAO 2020) underlined that
ca.11% of the Mediterranean stocks assessed were considered sustainably exploited
while 80% of the stocks were considered to be outside biological safe limits. In
particular, European Hake (Merluccius merluccius) was found to be the most exploited
species in the Mediterranean Sea and current measures (minimum landing size, mesh
size, etc.) were found to have been ineffective for reducing the overexploitation. The
overexploitation of fishery resources is also affecting the biodiversity in relation to
discards as well as to sensitive habitats (e.g. Posidonia meadows, coralligenous
communities, etc). The majority of the fisheries opperating in the MPAs of the Alboran
Sea use small scale-gears, although medium bottom trawl vessels and some purse
seiners and trammel nets are illegally operating on some algae and Posidonia meadows
of these MPAs, impacting these communities and the stability of the ecosystems. Small
scale fisheries are considered the most appropriate methods to be substantial and to
extract fishery resources and management plans of the MPAs have to include the local
fishing communities. The idea is the implementation of strategies of adaptive
management based on the application of: a) regulatory measures and fleet management,
with well-defined objectives and with sufficient and continued funding; b) integrated
coastal zone management and c) an ecosystem approach in relation to the biology and
life cycle of commercial and threatened species and interactions among them, effects of
climate change on stocks and fisheries, relationships between coastal and deep-sea
stocks, define appropriate biological units of management, between others (Robles
2010). For example, in Al Hoceima National Park (Morocco), innovative and effective
strategies have been incorporated such as a funding system for the conversion of some
fishing gears or diversification of fishermen’s income (fishing tourism, whale-watching,
etc), establishment of the Observatory of Al-Hoceima (ODYSSEA) and the adoption
and implementation of the EU Marine Strategy Framework Directive (MSFD), among
others (Nibani 2019).
Summarizing, the fundamental weakness that prevents an improvement of fisheries, is
the lack of the real implementation of the important regulatory measures, together with
a lack of integration in co-management schemes at all levels (national, regional and
especially at a more local level) (UICN 2010).
An interesting way for controlling illegal fishing inside the MPAs, as well as
productivity of some fishes (e.g. groupers) is the use of artificial reefs whose purpose is,
on the one hand, to exercise passive surveillance against illegal fishing and, on the other
hand, to provide shelter and protection for marine fauna. For example some MPAs of
the northern Alboran Sea (e.g. Natural Park of Cabo de Gata-Níjar or Paraje Natural de
Acantilados Maro-Cerro Gordo) deployed artificial reefs and detected promising results
on the fish communities as well as in the number of illegal fishing lines and nets
entangled in these reefs (Junta de Andalucía 2017). The artificial reefs are a very
valuable tool for passive surveillance. In this sense, there is also a need for more
collaboration between organisms in order to have more complete and effective reefs,
and not only for fishing purposes. The installation of artificial reefs around all MPAs of
the Alboran Sea could be a way for supplying the lack of surveillance systems,
especially for those MPAs from Morocco and Algeria coast.
Generally speaking, the tourism system is based on mass tourism and, sometimes, has
limited impact on the local economy. These tourism activities are environmentally
unsustainable because they bring with them economic problems (income fall, over
construction
of
infrastructures,
etc.),
environmental
(loss
of
natural
areas,
decrease/disappearance of species, etc.) and socio-cultural (loss of cultural identity,
increased illegal activities, etc.) (UICN 2010). This kind of tourism should be
reconsidered in the MPAs.
Pollution (e.g. sewage, oil spills, litter) is still one of the most important threats for
some habitats (e.g. vegetated habitats) and species, particularly the derivative from
dangerous substances or outdated chemicals. The number of waste water plants and the
effective treatment of these waste water plants should be improved, as well as
regulations minimize the use of non-degradable plastics. However, the high
concentration of PCBs and DDTs found in the population of Common Dolphin is
another important indicator (UICN 2010). In the southern Alboran Sea, more
wastewater treatment plants are also urgently needed (Colloca et al. 2003).
Invasive species represent a recentmain threat for MPAs-KBAs of the Alboran Sea, and
some of these species are increasing due to the global change and deterioration of the
ecosystems. For example the recently expansion of the exotic invasive algae
Rugulopteryx okamurae, throughout the northern and southern sectors of Alboran Sea,
has generated huge problems by displacing native macroalgae species (with further
effects on the ecosystem), producing important losses to the artisanal fishermen, and
finally affecting the native biota associated to photophilous bottoms. The tourism has
also suffered consequences because hundreds of tons of the alga upset the beaches and
even the underwater system used by the desalination plant in Marbella (Spain) had
troubles due to the massive growth of this brown algae. The main way of introduction
of these invasive species seems to be due to maritime traffic (commercial and
recreational). It is essential to provide the necessary elements for the control of the
introduction and/or reintroduction of invasive alien species by adopting a specific code
of conduct according to the Code of Practices (1995) of the International Council for
Exploration of the Sea, the lines of action (1994) of the International Maritime
Organization on ballast water and fouling, and the Precautionary Approach of FAO
(1996) (UICN 2010).
7.4. Management measures
In 2006, the IUCN decided to start an initiative with the aim of achieving better
conservation and sustainable development in the Alboran Sea. The long term objective
of this analysis was to create the conditions and to construct the basis required for the
establishment of co-ordinated management of the Alboran Sea (Robles 2010). This
initiative had the support of the Málaga Provincial Council, the Agence de
Développement de l'Oriental (Morocco), Instituto Español de Oceanografía (Spain) and
the Institut National de Recherche Halieutique (Morocco). Different meetings have been
made in Spain (Barcelona 2008) and Morocco (Oujda, 2009), as well as projects such as
POCTEFEX-Alboran (Spain, Morocco and Algeria, 2012-2014) or fisheries projects
such as CopeMed I-II (2009-2020). During the POCTEFEX-Alboran project, some
progress was achieved for the establishment of an Alboran conservation and sustainable
development technology platform (Geoportal of Alboran Sea), meetings of artisanal
fishing entities (e.g. in Alhoucemas in 2014), cooperative working groups (biodiversity,
MPA and Integrated Coastal Zone Management), and initial assessment of the Cap des
Trois Fourches, in accordance with the MSFD, among others.
Recently, two projects have promoted the implementation of the ecosystem approach
(EcAp), in coherence with the MSFD and in the context of the BC (EcAp-MED I-II,
2010–2019). The first initiated the EcAp roadmap, especially in relation to the
development of an integrated monitoring and assessment programme for the
Mediterranean. Whereas the second have provided assistance to the Southern
Mediterranean contracting parties to the BC for implementing the EcAp
(https://www.rac-spa.org/ecapmed_ii).
Significant steps with important efforts have been done and much progress has been
made in scientific knowledge about habitats, species, threats, etc. affecting the
ecosystems. Nevertheless, there is still a weak coordination between national and
international agencies that may result in negative effects on the conservation and
management of some MPAs-KBAs, generally due to the complex existing legislation
regarding competences in the marine part (e.g. Alboran Island). For such reason, further
collaboration within local, regional and national governments of the countries around
the Alboran Sea as well as of the different sectors exploiting its different resources (e.g.
fisheries, tourism industry, etc.) is urgently needed in order to switch for an effective
conservation of the Alboran Sea natural heritage.
Acknowledgements
José L. Rueda and other coauthors would like to thank the projects ESMARES
(MITECO and Instituto Español de Oceanografía-IEO funding), LIFE + INDEMARES
(EU contract 07/NAT/E/000732) and LIFE IP INTEMARES, REMALA (Junta de
Andalucía and IEO), VIATAR (IEO), DEMALBORAN (IEO and the European
Maritime and Fisheries Fund) and IRIS-SES (IEO and European Commission). A good
part of the conservation efforts of seagrass meadows in the Alboran Sea is due to the
Government of Andalusia and its Sustainable Management Program for the Marine
Environment, as well as to the Life Projects (Life+Posidonia Andalucía 09/NAT/ES/00534, from 2011 to 2016; and Life Blue Natura –14/CMM/ES/000957,
from 2015 to 2019, and still in progress). Diego Moreno participated in those projects
and also thank all the people who have participated in these projects (Rosa Mendoza in
the direction; Soledad Vivas in the coordination; and Agustín Barrajón Domenech,
Antonio de la Linde, José Miguel Remón, Julio De la Rosa, Manuel Fernández-Casado
and Mari Carmen Arroyo in the underwater work). We also thank to Agustín Barrajón
Domenech its disinterested photographic contribution. Thanks to the IUCN MMPATF
Important Marine Mammal Area (IMMA) for providing in shape files for the Strait of
Gibraltar and Alboran Sea).
References
Aguilar R, Aksissou M, Templado J, Romani M (2010) Scientific rationale for the
proposed CIESM Near Atlantic Marine Peace Park. In CIESM 2011 Marine Peace
Parks in the Mediterranean A CIESM proposal. N 41 in CIESM Workshop
Monographs [F. Briand, ed.], 128 p., Monaco.
Aguilar R, Pastor X, García S, Marín P (2013) Importance of seamount-like feature for
conserving Mediterranean marine habitats and threatened species. OCEANA,
Madrid, Spain.
Aranda Y, Otero M (2014) Estudio de las figuras de protección de áreas marinas
protegidas de Andalucía con fanerógamas marinas y propuestas de mejora para su
gestión. Málaga, España, UICN, 76 pp.
Arcos JM, Becares J, Rodríguez B, Ruiz A (2009) Áreas Importantes para la
Conservación de las Aves Marinas en España. LIFE04NAT/ES/000049, Sociedad
Española de Ornitología (SEO/BirdLife)
Arroyo MC, Moreno D, Barrajón Domenech A et al (2011) Trabajos de seguimiento de
la lapa ferruginosa Patella ferruginea Gmelin, 1791 en Andalucía en el marco de
la Estrategia Nacional de Conservación de la especie. Mediterránea, Serie de
Estudios Biológicos. Época II, Número Especial 9-46.
Arroyo MC, Barrajón Domenech A, Brun FG et al (2015) Praderas de angiospermas
marinas de Andalucía. In Ruiz, JM Guillén JE Ramos Segura A and Otero MM
(Eds) Atlas de las praderas marinas de España. IEO/IEL/UICN, Murcia-AlicanteMálaga 312-397.
Arroyo GM, Mateos-Rodríguez M, Muñoz AR, De La Cruz A, Cuenca D (2016) New
population estimates of a critically endangered species, the Balearic Shearwater
Puffinus mauretanicus, based on coastal migration counts. Bird Conserv Int 26:
87-99.
Aparicio A, Mitjavila JM, Araña V, Villa IM (1991) La edad del volcanismo de las islas
Columbrete Grande y Alborán (Mediterraneo occidental). Bol Geol Min 102 (4):
562-570.
Azdimousa A, Jabaloy-Sánchez A, Münch P et al (2019) Structure and exhumation of
the Cap des Trois Fourches basement rocks (Eastern Rif, Morocco). J Afr Earth
Sci 150: 657-672.
Bachet F, Benhaj S, Bernard F et al (2007) Réserve des îles Habibas. Notes naturalistes.
Petites îles de Méditerranée 2004/2007. Conservatoire de l’espace littoral et des
rivages lacustres 70 pp.
Baeza JV (2019). Espacios marinos protegidos en el área del Estrecho de Gibraltar:
Incidencia
del
Brexit.
Rev
catalana
dret
ambient,
10
(2):
https://doi.org/10.17345/rcda2722
Báez JC, Camiñas JA, Serna Quintero JM et al (2019) Using opportunistic sightings to
assess the suitability of Important Marine Mammal Areas (IMMAs) for cetacean
conservation
in
the
Western
Mediterranean
Sea.
Galemys.
10.7325/Galemys.2019.A9
Balanyá JC, Crespo-Blanc A, Díaz Azpiroz M, Expósito I, Luján M (2007) Structural
trend line pattern and strain partitioning around the Gibraltar Arc accretionary
wedge: insights as to the mode of orogenic arc building. Tectonics 26(2):
doi:10.1029/2005TC001932.
Ballesteros E, Catalán J (1984) Flora y vegetación marina y litoral del cabo de Gata y el
Puerto de Roquetas de Mar (Almería). Primera aproximación. Anales de la
Universidad de Murcia, sec. Ciencias, 42 (1-4):237-276.
Ballesteros M, Barrajón Mínguez A, Luque A et al (1986) Contribución al
conocimiento de los gasterópodos marinos de Almería. Iberus 6(1):39-55.
Ballesteros E, Pinedo S (2004) Los bosques de algas pardas y rojas. In Luque AA,
Templado J. (Coords.) Praderas y bosques marinos de Andalucía. Consejería de
Medio Ambiente, Junta de Andalucía, Sevilla 199-222.
Ban NC, Cinner JE, Adams VM et al (2012) Recasting shortfalls of marine protected
areas as opportunities through adaptive management. Aquat Conserv: Mar Freshw
Ecosyst 22:262–271.
Ban NC, Davies TE, Aguilera SE et al (2017) Social and ecological effectiveness of
large marine protected areas. Glob Environ Change 43:82–91
Bárcenas P, Vázquez JT, Díaz del Río V, Fernández-Salas LM (2004) Geomorfología
del Banco de la Isla de Alborán. Geo-Temas 6(2):209-212.
Bárcenas P, Vázquez JT, Fernández-Salas LM, López-González N, García-Martínez
MC (2018). The influence of the Atlantic Jet and the Mediterranean Waters (MW)
on the Alboran Ridge, Western Mediterranean Sea. In: Atas do IX Simpósio sobre
a Margem Ibérica Atlântica. Departamento de Ciências da Terra da Universidade
de Coimbra (Ed.). Coimbra, Portugal. 295-296
Barea-Azcón JM, Ballesteros-Duperón E, Moreno D (2008) Libro Rojo de los
invertebrados de Andalucía, Vol. 1-4. Consejería de Medio Ambiente, Junta de
Andalucía, Sevilla.
Barrera JL, Pineda A (2006) Islas chafarinas: La geología de un archipiélago deseado
por todos. Tierra y Tecnología 30:13-30.
Bazaïri H, Salvati E, Benhissoune S et al (2004). Considerations on a population of the
endangered marine mollusc Patella ferruginea Gmelin, 1791 (Gastropoda,
Patellidae) in the Cala Iris islet (National Park of Al Hoceima-Morocco, Alboran
sea). Boll Mallacol 40:95-100
Bécares J, Arcos JM, Oro D (2016) Migración y ecología espacial de la gaviota de
Audouin en el Mediterráneo occidental y noroeste africano. Monografía nº1
Programa Migra. SEO/BirdLife. Madrid.
Bellon H, Guardia P, Magne J (1984) Les associations volcaniques du Miocène
Supérieur
de
la
région
oranaise
(Algérie
occidentale).
Conséquences
géodynamiques. Geol. Mediterr 11(3):255-264.
Beger M, Bustamante RH, Charles A et al (2018) Revisiting “Success” and “Failure” of
Marine Protected Areas: A Conservation Scientist Perspective. Front Mar Sci
5:223. doi: 10.3389/fmars.2018.00223
Benhissoune S, Chaouti A, Bayed A (2005) Distribution des macrophytes benthiques
dans la lagune de Smir (nord-ouest du Maroc), In Bayed A, Scapini F (Éditeurs).
Ecosystèmes côtiers sensibles de la Méditerranée: cas du litoral de Smir. Trav Inst
Sci 4:27-32
Berthon D, Berthon S (1984) Compterendu de l’expéditionBalbuzard sur les
côtesméditerranéennes du Maroc. L`Oiseau et RFO 54:201–213
Boubekri I, Djebar AB (2016) Marine protected areas in Algeria: Future marine
protected area of “Taza” (SW Mediterranean), continuing challenges and new
opportunities facing an integrated coastal management. Ocean Coast Manag
130:277-289.
Butchart SHM, Scharlemann JPW, Evans MI, et al (2012) Protecting important sites for
biodiversity contributes to meeting global conservation targets. PLoS One
7:e32529.
Camiñas JA (2018) Ciencia, Oceanografía y Patrimonio. Inicios del Laboratorio,
Acuario y Museo Oceanográfico de Málaga, Cuadernos del Rebalaje Nº41. Edita
ABJ:ISSN (ed. impresa): 2530-6286 / (ed. digital): 2174-9868
Cañadas A, Sagarminaga R, De Stephanis R, Urquiola E, Hammond PS (2005) Habitat
preference modelling as a conservation tool: proposals for marine protected areas
for cetaceans in southern Spanish waters. Aquat Conserv 15: 495-521.
CAR/ASP - PNUE/PAM (2012) Le Cap des Trois Fourches (Mediterranée, Maroc):
caracterisation écologique et orientations de gestion. Par Bazairi H, Limam A,
Benhoussa A, Mellouli M, El Khalidi K, Navarro-Barrancoa C, González AR,
Maestre M, García-Gómez JC, Espinosa F. Ed. RAC/SPA - Projet MedMPAnet,
Tunis: 122 p + Annexes.
Cara Barrionuevo L, Cara Rodríguez J (1994) Roquetas de Mar: Arqueología e historia.
Desde la Prehistoria hasta inicios de la Edad Moderna. Instituto de Estudios
Almerienses, 272 pp
Castro H, Molina F, Díaz F et al (2003) Monumentos Naturales de Andalucía. Junta de
Andalucía, 303 pp.
Castro M, Arroyo G, Bekkali R, Nachite D, Anfuso G (2006) Características
ambientales del entorno de la laguna de Smir. Anfuso G, Nachite D (Coords).
Dep. Legal: CA/206/06. 40pp.
Catanese G, Grau A, Valencia JM et al (2018) Haplosporidium pinnae sp. nov., a
haplosporidan parasite associated with mass mortalities of the fan mussel, Pinna
nobilis, in the Western Mediterranean Sea. J Inverbr Pathol 157:9–24.
Cebrián E, Ballesteros E (2004) Zonation patterns of benthic communities in an
upwelling area from the western Medierranean (La Herradura, Alboran Sea). Sci
Mar 68:69-84.
CEDEX (Centro de Estudios y experimentación de Obras Públicas) (2011) El sistema
de protección del medio marino frente a los vertidos de las plantas desaladoras en
España: análisis y propuesta de mejora (A7-T1I7). Informe técnico para el
Ministerio de Medio Ambiente, Medio Rural y Marino.
Chaouti A, Bayed A (2005) Diversité Taxonomique et structure de la macrofaune
benthique des substrats meubles de la lagune de Smir. In Bayed A, Scapini F
(Éditeurs). Ecosystèmes côtiers sensibles de la Méditerranée: cas du litoral de
Smir. Trav Inst Sci,4: 33-42 pp.
Colloca F, Crespi V, Coppola SR (2003): Evolution of the artisanal fishery in Cilento,
Italy: Case study. FAO, COPEMED.
Contrats MedMPAnet 04/2012, MedMPAnet 06/2012 et MedMPAnet 07/2012.
Corbera G, Lo Iacono C, Gràcia E et al (2019) Ecological characterisation of a
Mediterranean cold-water coral reef: Cabliers Coral Mound Province (Alboran Sea,
western Mediterranean). Prog Oceanogr 175:245-262
Corrigan C, Ardron J, Comeros-Raynal M et al (2014) Developing important marine
mammal area criteria: learning from ecologically or biologically significant areas and
key biodiversity areas IUCN Marine Mammal Protected Areas Task Force/ Whale
and Dolphin Conservation, UK e IUCN Marine Mammal Protected Areas Task
Force. Aquat Conserv 24:166-183
Croxall JP, Butchart SHM, Lascelles B et al (2012) Seabird conservation status, threats
and priority actions: a global assessment. Bird Conserv Int 22:1-34.
Dakki M, Hamman F, Hammada S (2005) Cartographie des habitats naturels d’une zone
humide côtière méditerranéenne: les marais de Smir (région de Tétouan, Maroc).
Bayed A, Scapini F (Éds.) Ecosystèmes sensibles de la Méditerranée: cas du
littoral de Smir. Trav Inst Sci, Rabat, sér. Générale (4) 9-15.
de la Linde Rubio A, Tierno de Figueroa JM, López-Rodríguez MJ, Sánchez-Tocino L
(2018) Mass mortality of Eunicellas ingularis (Anthozoa: Octocorallia) in the
Chafarinas Islands (North Africa, Western Mediterranean Sea). Rev Biol Mar
Oceanogr 53(2): 285–290.
de la Torriente A, Aguilar R, Serrano A et al (2014) Sur de Almería - Seco de los
Olivos. Proyecto LIFE+ INDEMARES. Ed. Fundación Biodiversidad del
Ministerio de Agricultura, Alimentación y Medio Ambiente 102 pp.
de Mol B, Amblas D, Calafat A et al (2011) Cold-Water Coral Colonization of Alborán
Sea Knolls, Western Mediterranean Sea. In: Harris PT, Baker EK (eds.), Seafloor
Geomorphology as Benthic Habitat: GeoHab Atlas of Seafloor Geomorphic
Features and Benthic Habitats. Elsevier, 2012. Amsterdam, 819-829 pp.
Didon J, Durand-Delga M, Kornporbst J (1973) Homologies géologiques entre les deux
rives du Détroit de Gibraltar. Bull Soc Géol Fr 7(15):77-105.
Donald PF, Lincold DC, Ajagbe A et al (2018) Important Bird and Biodiversity Areas
(IBAs): the development and characteristics of a global inventory of key sites for
biodiversity. Bird Conserv Int 29:177-198.
Espinosa F, Fa D, Ocaña T (2005) Estado de la especie amenazada Patella ferruginea
Gmelin, 1791 (Gastropoda: Patellidae) en la bahía de Algeciras y Gibraltar. Iberus
23(2):39-46.
Espinosa F, Rivera-Ingraham G, Maestre M et al (2014). Updated global distribution of
the threatened marine limpet Patella ferruginea (Gastropoda: Patellidae): An
example of biodiversity loss in the Mediterranean. Oryx 48(2):266-275.
Esteban R, Verborgh P, Gauffier P (2016) Chapter Five - Conservation Status of Killer
Whales, Orcinus orca, in the Strait of Gibraltar. Adv Mar Biol 75:141-172.
Fabri MC, Pedel L, Beuck L et al (2014) Megafauna of vulnerable marine ecosystems
in
French
mediterranean
submarine
canyons:
Spatial
distribution
and
anthropogenic impacts, Deep-Sea Res Part II 104:184-207.
FAO (2018) The State of Mediterranean and Black Sea Fisheries. General Fisheries
Commission for the Mediterranean. Rome. 172 pp.
FAO. (2020) Report of the forty-third session of the General Fisheries Commission for
the Mediterranean (GFCM) − Athens, Greece, 4–8 November 2019. GFCM
Report no. 43. Rome. https://doi.org/10.4060/ca8379en
Fernández-Salas LM., Durán R, Mendes I et al (2015) Shelves of the Iberian Peninsula
and the Balearic Islands (I): Morphology and sediment types. Boletín Geológico y
Minero, 126 (2-3): 327-376ISSN: 0366-017
Fernández Soler JM (1996) El volcanismo calco-alcalino en el Parque Natural de Cabo
de Gata-Níjar (Almería). Estudio volcanológico y petrológico. Tesis doctoral,
Monografías del Medio Natural nº 2, Sociedad Almeriense de Historia NaturalConsejería de Medio Ambiente 295 pp.
García S, Aguilar R, de la Torriente A (2009) Restauración de praderas marinas.
Fundación Banco Santander. Manuales de Desarrollo Sostenible 8: 48 pp.
García Muñoz JE, Manjón-Cabeza ME, García Raso JE (2008a) Decapod crustacean
assemblages from littoral bottoms of the Alborán Sea (Spain, west Mediterranean
Sea): spatial and temporal variability. Sci Mar 72(3):437-449.
García Muñoz JE, Cuesta JA, García Raso JE (2001) Taxonomic study of the Pagurus
forbesii "complex" (Crustacea: Decapoda: Paguridae). Description of Pagurus
pseudosculptimanus sp. nov. from Alborán Sea (Southern Spain, Western
Mediterranean Sea). Zootaxa 3753 (1): 25-46.
García Raso JE (1989) Resultados de la segunda campaña del IEO para la exploración
de los fondos de coral rojo en el mar de Alborán. Bol Inst Esp Oceanogr 5(2):2736.
García Raso JE, Luque AA, Templado J et al (1992) Fauna y flora marinas del Parque
Natural de Cabo de Gata-Níjar. Madrid, 288 pp.
García Raso JE, Gofas S, Salas C et al (2010) El mar más rico de Europa: Biodiversidad
del litoral occidental de Málaga entre Calaburras y Calahonda. Consejería de
Medio Ambiente, Junta de Andalucía, Sevilla. 138 pp.
García Raso JE, Marina P, Baro J (2011) Bythocaris cosmetops (Decapoda: Caridea:
Hippolytidae) in the western Mediterranean Sea. Mar Biodivers Rec 4:e52
García Raso JE, Salmerón F, Baro J, Marina P, Abelló P (2014) The tropical African
hermit crab Pagurus mbizi (Crustacea, Decapoda, Paguridae) in the Western
Mediterranean Sea: a new alien species or filling gaps in the knowledge of the
distribution? Mediterr Mar Sci 15(1):172-178.
García-Charton JA, Pérez-Ruzafa A, Sánchez-Jerez P et al (2004) Multi-scale spatial
heterogeneity, habitat structure, and the effect of marine reserves on Western
Mediterranean rocky reef fish assemblages. Mar Biol 144:161-182.
García-Gómez J, Sempere-Valverde J, González AR et al (2020) From exotic to
invasive in record time: The extreme impact of Rugulopteryx okamurae
(Dictyotales, Ochrophyta) in the strait of Gibraltar. Sci Total Environ 704:
135408.
Giakoumi S, Mc Gowan J, Mills Met al (2018) Revisiting “Success” and “Failure” of
Marine Protected Areas: A Conservation Scientist Perspective. Front Mar Sci 5:
10.3389/fmars.2018.00223
Gil J, Canoura J, Palomino D, López N, Sánchez R (2009) Informe Campaña DEEPER
0409. Instituto Español de Oceanografía, 39 pp.
Gofas S (1998) Marine molluscs with a very restricted range in the Strait of Gibraltar.
Divers Distrib 4:255-266.
González García JA (1994) La Flora Marina del litoral próximo a Melilla. Ensayos
Melillenses 2:1-211.
González García JA, Conde Poyales F (1993) Estudio biogeográfico de las fucales y
laminariales atlánticas en el litoral mediterráneo de Marruecos. Acta Bot Malac
18: 39-44.
González García JA, Enrique Mirón C (2018a)
Estudio de hábitats y especies
protegidas de las SAC de Melilla y el litoral. 1er Informe (noviembre) 1er Convenio
UGR-Ciudad Autónoma de Melilla.
González García JA, Enrique Mirón C (2018b) Estudio de hábitats y especies protegidas
de las SAC de Melilla y el litoral. 2º Informe (diciembre) 1er Convenio UGRCiudad Autónoma de Melilla.
González García JA, Enrique Mirón C (2019) Estudio de hábitats y especies protegidas
de las SAC de Melilla y el litoral. 1er Informe (junio) 2º Convenio UGR-Ciudad
Autónoma de Melilla.
González García JA, Paredes Ruiz P, Enrique Mirón C et al (2013). Estudio para la
conservación de las poblaciones de Patella ferruginea en Melilla ante futures
obras de ampliación del puerto. Autoridad Portuaria de Melilla
González García JA, Paredes P, Enrique C, Calzado P, Bueno I (2014) Estado actual de
Patella ferruginea Gmelin, 1791, Dendropoma petraeum Monterosato, 1884 y
Astroides calycularis Pallas, 1776 en la SAC de Aguadú (Melilla). Avances en
Estudios de Biología Marina: Contribuciones del XVIII SIEBM GIJÓN: 87-94.
González García JA, Paredes Ruiz P, Enrique Mirón C, Calzado Liarte P, Bueno del
Campo I (2015) Patella ferruginea. Patrimonio del litoral melillense: biología,
ecología y conservación. Melilla: GEEPP.
González-Solís J, Croxall J, Oro D, Ruiz X (2007) Trans-equatorial migration and
mixing in the wintering areas of a pelagic seabird. Front Ecol Environ 5:297-301
Guallart J, Templado J (2016) Distribución, abundancia y selección del hábitat de
Patella ferruginea (Mollusca, Gastropoda) en las islas Chafarinas (Mediterráneo
suroccidental). Iberus 34(2):127-162.
Guirado J, Mendoza R, Castro H et al (1994) Conservación y manejo en un medio
semiárido Parque Natural «Cabo de Gata-Níjar» (Almería, SE España). Papel
Geogr 20:65-80.
Guirado J, Moreno D, Castro H, López Carrique E (1997) Observaciones de aves
marinas en el litoral del Parque Natural Cabo de Gata-Níjar. Invest Gest 1:91-107.
Guirado J, Moreno D, Castro Nogueira H, Vicioso L, Tamayo F (1997) Gestión de los
recursos marinos en el Mediterráneo Occidental Arrecife Artificial de Cabo de
Gata. In García Rossell L, Navarro Flores A (Eds.) Recursos Naturales y Medio
Ambiente en el Sureste Peninsular. Instituto de Estudios Almerienses, 147-159.
Guirado J, Castro H, Moreno D (2002) Arrecife Barrera de los Bajos, Roquetas de Mar
(Almería): Monumento Natural. Medio Ambiente 40:20-26.
Heath MF, Evans MI, Hoccom DG, Payne AJ, Peet NB (2000) Important Bird Areas in
Europe: priority sites for conservation, 1 Northern Europe, 2 Southern Europe.
Cambridge, UK: BirdLife International.
Hergueta E, Salas C (1987) Estudio de los moluscos asociados a concreciones de
Mesophyllum lichenoides (Ellis) Lemoine del Mar de Alborán. Iberus 7(1):85-97.
Hodgkins M, Beaubrun P (1990) Description et cartes de 52 emplacements de nids de
Balbuzard (Pandion haliaetus) sur lacôte du Parcbiologique des Bokkoyas et
dansd’autreslieux dela Provinced’AlHoceima. Unpublished report. USAID et
Eaux et Forêts Maroc Ed.
Hoyt E (2015) Summary Proceedings of the Third International Conference on Marine
Mammal Protected Areas (ICMMPA 3), Adelaide, Australia, 9-11 Nov. 2014, 85
pp.
Ichii K, Molnár Z, Obura D, Purvis A, Willis K (2019) Status and Trends-Nature In
IPBES Global Assessment on Biodiversity and Ecosystem Services 171 pp
IGME (1978a) Mapa geológico de España (1:50.000), segunda serie (MAGNA); hoja
1072 (Estepona). Memoria y mapa. Instituto Geológico y Minero de España
(IGME), 37 pp+Map.
IGME (1978b) Mapa geológico de España (1:50.000), segunda serie (MAGNA); hoja
1065 (Marbella). Memoria y mapa. Instituto Geológico y Minero de España
(IGME), 65 pp+Map.
IGME (1978c) Mapa geológico de España (1:50.000), segunda serie (MAGNA); hoja
1066 (Coín). Memoria y mapa. Instituto Geológico y Minero de España (IGME),
71 pp+Map.
IGME (1981) Mapa geológico de España (1:50.000), segunda serie (MAGNA); hoja
1056 (Albuñol). Memoria y mapa. Instituto Geológico y Minero de España
(IGME), 39 pp+Map.
IGME (1983) Mapa geológico de España (1:50.000), segunda serie (MAGNA); hojas
1059 (El Cabo de Gata) y 1078 bis (isla de Alborán). Memoria y mapa. Instituto
Geológico y Minero de España (IGME), 41 pp+Map.
IGME (2012a) Mapa geológico de España (1:50.000), segunda serie (MAGNA); hoja
1078 (Algeciras). Memoria y mapa. Instituto Geológico y Minero de España
(IGME), 29 pp+Map.
IGME (2012b) Mapa geológico de España (1:50.000), segunda serie (MAGNA); hoja
1075 (La Línea de la Concepción). Memoria y mapa. Instituto Geológico y
Minero de España (IGME), 30 pp+Map.
IGME (2013) Mapa geológico de España (1:25.000), segunda serie (MAGNA); hoja
1110-III (Ceuta). Memoria y mapa. Instituto Geológico y Minero de España
(IGME), 88 pp+Map.
IUCN (2016). A Global Standard for the Identification of Key Biodiversity Areas,
Version 1.0. First edition. Gland, Switzerland: IUCN
Jiménez EA, Almonacid AG (2008). Koudiat Taifour y la llanura de Tetuán:
oportunidades para su conservación. Taiqui L, Araque Jiménez E, Youbi Idrissi M
(Edit.), Conservación y valorización de KoudiatTaifour, Tétouan, Imprimerie Al
Khalij Al Arabi, 4-38.
Junta de Andalucía (2008) Programa de Gestión Sostenible del Medio Marino. Informe
Regional 20081. Consejería de Medio Ambiente, Sevilla, 72 pp.
Junta de Andalucía (2011) Programa de Gestión Sostenible del Medio Marino. Informe
Regional 2011. Consejería de Medio Ambiente, Sevilla, 153 pp.
Junta de Andalucía (2012) Programa de Gestión Sostenible del Medio Marino. Informe
Regional 2012. Consejería de Agricultura, Pesca y Medio Ambiente, Sevilla, 109
pp.
Junta de Andalucía (2013) Programa de Gestión Sostenible del Medio Marino. Informe
Regional 2013. Consejería de Agricultura, Pesca y Medio Ambiente, Sevilla, 143
pp.
Junta de Andalucía (2014) Programa de Gestión Sostenible del Medio Marino. Informe
final de resultados 2014. Consejería de Medio Ambiente y Ordenación del
Territorio, Sevilla, 153 pp.
Junta de Andalucía (2015) Programa de Gestión Sostenible del Medio Marino. Informe
final de resultados 2015. Consejería de Medio Ambiente y Ordenación del
Territorio, Sevilla, 127 pp.
Junta de Andalucía (2016) Programa de Gestión Sostenible del Medio Marino. Informe
final de resultados 2016. Consejería de Medio Ambiente y Ordenación del
Territorio, Sevilla, 130 pp.
Junta de Andalucía (2017) Programa de Gestión Sostenible del Medio Marino. Informe
final de resultados 2017. Consejería de Medio Ambiente y Ordenación del
Territorio, Sevilla, 168 pp.
Junta de Andalucía (2018) Programa de Gestión Sostenible del Medio Marino. Informe
Regional 2018. Consejería de Agricultura, ganadería, Pesca y Desarrollo
Sostenible, Sevilla, 162 pp.
Kazzaz M (1989) Contribution à l’étude de la flore algale de la région ouest de la
Méditerranée. Ph.D. Thesis. Maroc: University of Mohammed V, Rabat.
Kelleher G (1999) Guidelines for Marine Protected Areas. IUCN, Gland,Switzerland
and Cambridge, UK. xxiv +107pp.
Khouakhi A, Snoussi M, Niazi S, Raji O (2013) Vulnerability assessment of Al
Hoceima bay (Moroccan Mediterranean coast): a coastal management tool to
reduce potential impacts of sea-level rise and storm surges. J Coastal Res 65: 968–
973.
Kuempel CD, Kendal RJ, Watson JEM, Possinghan HP (2019) Quantifying biases in
marine-protected-area placement relative to abatable threats. Conserv Biol
33(6):1350-1359.
López-Martos JM, Frías A, Navarro J, Schwarzer H, Vargas V (2010) Naturaleza
Almeriense: Espacios del Litoral. Guías de Almería, Territorio, Cultura y Arte 8,
Instituto de Estudios Almerienses, Almería, 215 pp.
Luque AA, Templado J, García Raso JE, Moreno D, Guirado D (1999) La reserva
marina del Parque Natural de Cabo de Gata-Níjar quince años de investigación de
su biodiversidad. En 1st International Workshop on Marine Reserves, Murcia. 7576.
Luque AA, Templado J, Moreno D et al (2004) Cartografiado de las formaciones
vegetales marinas. Cartografiado de las praderas de Posidonia oceanica de
Almería. En Luque AA y Templado J (Coords.). Praderas y bosques marinos de
Andalucía. Consejería de Medio Ambiente, Junta de Andalucía, Sevilla, 255-269.
Malcolm RC, Rowden AA,. Schlacher TA et al (2014) Identifying Ecologically or
Biologically Significant Areas (EBSA): A systematic method and its application
to seamounts in the South Pacific Ocean. Ocean Coast Manage 91:65-79.
Maldonado A, Rodero J, Pallarés L et al (2003). Mapa Geológico de la Plataforma
Continental Española y Zonas Adyacentes. Escala 1:200.000, Hojas nº 86-86S87S (Cádiz) y Memoria. Instituto Geológico y Minero de España. Madrid.
Maldonado M, Sánchez-Tocino L, López Acosta M, Sitjà C (2011) Invertebrados claves
del sistema infralitoral y circalitoral rocoso de las Islas Chafarinas: estudio con
vistas a futuras estrategias de conservación. Organismo Autónomo de Parques,
Ministerio de medio Rural y Marino, Madrid, 84pp.
Maldonado M, López-Acosta M, Sánchez-Tocino L, Sitjà C (2013) Therare,
giantgorgonian
Ellisella
paraplexauroides:
conservationconcerns. Mar Ecol Progr Ser 479:127–141.
demographics
and
Marina P, Rueda JL, Urra J et al (2015) Sublittoral soft bottom assemblages within a
Marine Protected Area of the northern Alboran Sea. J Mar Biol Assoc UK
95(5):871-884.
Marine Mammal Habitat (2020) https://www.marinemammalhabitat.org. Acceded
23/06/2020.
Mateo MA, Díaz-Almela E, Piñeiro-Juncal N et al (2018) Carbon stocks and fluxes
associated to Andalusian seagrass meadows. Deliverable C1: Results Report. Life
Blue Natura (LIFE14CCM/ES/000957). Group of Aquatic Macrophyte Ecology
(GAME), CEAB-CSIC, Blanes, 95 pp.
Mateo Ramírez Á, García Raso JE (2012) Temporal changes in the structure of the
crustacean decapod assemblages associated with Cymodocea nodosa meadows
from the Alboran Sea (Western Mediterranean Sea). Mar Ecol-Evol Persp 33:302316.
Mateo-Ramírez Á, Urra J, Marina P, Rueda JL, García Raso JE (2016) Crustacean
decapod assemblages associated with fragmented Posidonia oceanica meadows in
the Alboran Sea (Western Mediterranean Sea): composition, temporal dynamics
and influence of meadow structure. Mar Ecol-Evol Persp 37(2):344-358
Mateo-Ramírez Á, Urra J, Rueda JL, Marina P, Raso JG (2018) Decapod assemblages
associated with shallow macroalgal communities in the northwestern Alboran
Sea: Microhabitat use and temporal variability. J Sea Res 135:84-94.
Mateo-Ramírez Á, Marina P, Moreno D et al (2020a) List and date of establishment of
Marine Protected Areas and Key Biodiversity Areas of the Alboran Sea.
https://doi.org/10.5281/zenodo.3885003
Mateo-Ramírez Á, Marina P, Moreno D et al (2020b) List of the main marine and
coastal habitats detected in Marine Protected Areas and Key Biodiversity Areas of
countries around the Alboran Sea, with annotations on the year on which the
habitat was listed or publications. https://doi.org/10.5281/zenodo.3898180
Mateo-Ramírez Á, Marina P, Moreno D et al (2020c) List of marine species found in
Marine Protected Areas and Key Biodiversity Areas of the Alboran Sea and
included in national and international lists and conventions of threatened species.
Maxwell SM, Hazen EL, Lewison RL et al (2015) Dynamic ocean management:
defining and conceptualizing real-time management of the ocean. Mar Policy 58:
42-50.
Medialdea T, Terrinha P, Somoza L et al (2014) Mapa Geológico de España y Portugal:
Margen continental. Mapa escala 1/1.000.000. Instituto Geológico y Minero de
España. Madrid. Depósito legal: M-35958-2014. NIPO en papel: 7281500515.
Nipo online: 7281500520. ISBN: 978-84-7840-949-5.
MedPAN, SPA/RAC (2019) The 2016 status of Marine Protected Areas in the
Mediterranean. By Meola B. and Webster C. Ed SPA/RAC & MedPAN. Tunis
222 pp.
Mendoza R, Barrajón Domenech A, de la Rosa J et al (2014) Nuestras praderas bajo el
agua: dónde y cuántas. Quercus 3(supplement): 14-19.
Monti F, Nibani H, Dominici JM et al (2013) The vulnerable Osprey breeding
population of the Al Hoceima National Park, Morocco: present status and threats.
Ostrich 84(3):199–204.
Moreno D (1992) Presencia de Patella ferruginea (Gmelin, 1791) en el Cabo de Gata
(Almería, SE España). Cuadernos de Investigación Biológica 17:71.
Moreno D, Aguilera PA, Castro H et al (1999) Valoración del impacto de los vertidos
hídricos industriales en el litoral aproximación metodológica al estudio de la
pradera de Posidonia oceanica (L.) Delile. In Navarro Flores A, Sánchez Garrido
JA, Collado Fernández DM (Eds.). Minería, industria y medio ambiente en la
cuenca mediterránea, 227-236.
Moreno D, Aguilera PA, Castro H (2001) Assessment of the conservation status of
seagrass (Posidonia oceanica) meadows implications for monitoring strategy and
the decision-making process. Biol Conserv 102(3):325-332.
Moreno D (2003) El espectacular patrimonio natural litoral y sumergido de Cabo de
Gata (España). In Moreno D, Frías A (Eds.). Actas de las I Jornadas sobre
Reservas Marinas y I Reunión de la Red Iberoamericana de Reservas Marinas
(RIRM) 25-46.
Moreno D, Luque AA, Templado J (2004a). Las praderas de Posidonia oceanica.
Distribución en Andalucía. In Luque AA, Templado J (Coords.). Praderas y
bosques marinos de Andalucía. Consejería de Medio Ambiente, Junta de
Andalucía, Sevilla 60-63.
Moreno D, Templado J, Sánchez Moyano E, Luque AA (2004b) Las praderas de
Cymodocea nodosa. Distribución en Andalucía. In Luque AA, Templado J
(Coords.). Praderas y bosques marinos de Andalucía. Consejería de Medio
Ambiente, Junta de Andalucía, Sevilla 134-136.
Moreno D, De la Rosa J, Sánchez-Castillo P, Flores-Moya (2005) Una nueva localidad
almeriense de Phyllariopsis purpurascens (C. Agardh) Henry et South. Acta Bot
Malac, 30: 176.
Moreno D, Guirado J, Mendoza R (2006) El arrecife artificial de Cabo de Gata una
década de gestión activa del medio marino. En Ocaña Martín A and Sánchez
Castillo P (Eds.). Conservación de la biodiversidad y explotación sostenible del
medio marino. Centro Mediterráneo de la Universidad de Granada y Sociedad
Granatense de Historia Natural, Granada: 255-293.
Moreno D, de la Linde A, Remón JM et al (2007) Programa de Gestión Sostenible de
Recursos para la Conservación del Medio Marino Andaluz Datos preliminares de
los censos de especies de invertebrados amenazados. In Paracuellos M. (Coord.)
Ambientes Mediterráneos. Funcionamiento, biodiversidad y conservación de los
ecosistemas mediterráneos: actas de las XV jornadas del Aula de Ecología, 2005.
Instituto de Estudios Almerienses, 27-48.
Moreno D (2008) Dendropoma petraeum (Monterosato, 1884). In Barea-Azcón JM,
Ballesteros-Duperón E, Moreno D (Coords.). Libro Rojo de los Invertebrados de
Andalucía. Junta de Andalucía, Sevilla 323-329.
Moreno D, Arroyo MC (2008) Patella ferruginea Gmelin, 1791. In Barea-Azcón JM,
Ballesteros-Duperón E, Moreno D (Coords.). Libro Rojo de los Invertebrados de
Andalucía. Consejería de Medio Ambiente, Junta de Andalucía, Sevilla 308-319.
Moreno D, Barrajón Domenech A (2008a) Pinna nobilis Linnaeus, 1758. In BareaAzcón JM, Ballesteros-Duperón E, Moreno D (Coords.). Libro Rojo de los
Invertebrados de Andalucía. Consejería de Medio Ambiente, Junta de Andalucía,
Sevilla 396-402.
Moreno D, Barrajón Domenech A (2008b) Pinna rudis Linnaeus, 1758. In Barea-Azcón
JM, Ballesteros-Duperón E, Moreno D (Coords.). Libro Rojo de los Invertebrados
de Andalucía. Consejería de Medio Ambiente, Junta de Andalucía, Sevilla 403407.
Moreno D, De la Rosa J (2008) Charonia lampas (Linnaneus, 1758). In Barea-Azcón
JM, Ballesteros-Duperón E, Moreno D (Coords.). Libro Rojo de los Invertebrados
de Andalucía. Consejería de Medio Ambiente, Junta de Andalucía, Sevilla 281287.
Moreno D, Pérez-Ruzafa A (2008) Ophidiaster ophidianus (Lamarck, 1816). In BareaAzcón JM, Ballesteros-Duperón E, Moreno D (Coords.). Libro Rojo de los
Invertebrados de Andalucía. Consejería de Medio Ambiente, Junta de Andalucía,
Sevilla, 281-287.
Moreno D, Barrajón Domenech A, Gordillo I, López-González PJ (2008a) Cladocora
caespitosa (Linnaeus, 1767). In Barea-Azcón JM, Ballesteros-Duperón E, Moreno
D (Coords.). Libro Rojo de los Invertebrados de Andalucía. Consejería de Medio
Ambiente, Junta de Andalucía, Sevilla 256-262
Moreno D, de la Linde A, Arroyo MC, López-González PJ (2008b). Astroides
calycularis (Pallas, 1766). In Barea-Azcón JM, Ballesteros-Duperón E, Moreno
D (Coords.). Libro Rojo de los Invertebrados de Andalucía. Consejería de Medio
Ambiente, Junta de Andalucía, Sevilla 281-287.
Moreno D (2010) Flora y fauna alóctona del medio marino andaluz. In Cobos FJ,
Ortega F (Eds.). Especies exóticas invasoras en Andalucía. Talleres provinciales
2004-2006. Consejería de Medio Ambiente, Junta de Andalucía, Sevilla 214-229.
Mota JF, Cabello J, Cueto M et al (1997) Datos sobre la vegetación del sureste de
Almería (Desierto de Tabernas, Karst en Yesos de Sorbas y Cabo de Gata).
Universidad de Almería, 130 pp.
Mota JF, Merlo ME, Jiménez-Sánchez ML et al (2006) Sobre islas, vagabundos y
fantasmas: la flora terrestre. In Paracuellos M, Nevado JC, Mota JF (Edit.) Entre
África y Europa. Historia Natural de la Isla de Alborán. RENPA, Consejería de
Medio Ambiente (Junta de Andalucía), Sevilla: 101-118.
Mota JF, Cueto Romero M, Mendoza Fernández A et al (2011) Patrimonio vegetal del
Cabo de Gata. In Serra L (Ed.) Jornadas Estatales de estudio y divulgación de la
flora de los Parques Nacionales y Naturales. CAM. Alcoi 199-222.
Moussa H, Hassoun M, Salhi G, Zbakh H, Riadi H (2018) Checklist of seaweeds of AlHoceima National Park of Morocco (Mediterranean Marine Protected Area). Act
Bot Malac 43:91-109.
MTERD (Ministry for Ecological Transition and Demographic Challenge) (2020) EU
non-native organism risk assessment scheme. 54 pp.
Navarro A, Collado Fernández D., Font Cisteró X, Viladevall Solé M (1997)
Geoquímica de las mineralizaciones auríferas de Sierra Almagrera (Almería,
España). In: García Rossell L, Navarro A (Edits.) Recursos Naturales y Medio
Ambiente en el SE Peninsular, IEA, Almería: 321-333.
Nibani H (2019) Innovation for sustainable management of marine resources in
Alhoceima national park. In Rueda F, Camiñas JA, Alcántara A, Martínez de
Victoria E, Bataller J I Foro Mar de Alborán. Encuentro de mares, ciencia y
culturas. ISBN: 978-84-09-09277-2, 240 pp.
Norse EA (1993) Global Marine Biological Diversity. A strategy for Building
Conservation into Decision Making. Center for Marine Conservation, Islands
Press, Washington D.C. (USA), World Conservation Union (IUCN), World
Wildlife Fund, United Nations Environment Programme, World Bank, 383 pp.
Notarbartolo Di Sciara G, Podestà M, Curry Barbara E (2016) Mediterranean Marine
Mammal Ecology and Conservation. Academic Press, 75: 2-428.
OCEANA (2014) Scientific Information to Describe Areas Meeting Scientific Criteria
for Mediterranean EBSAs. OCEANA, Madrid, Spain.
Oliver D, Calvo M, Guallart J, Sánchez-Tocino L, Templado J (2015) Gasterópodos
marinos de las islas Chafarinas (Mediterráneo suroccidental). Iberus 33 (1): 97–
150.
Ortiz García M (2002) La conservación de la biodiversidad marina: Las Areas Marinas
Protegidas. Editorial Comares, Granada. Colección Ecorama 16, 761 pp.
Palomino D, Alonso B, Lo Iacono, Casas D, D’Acremont et al (2015) Seamounts and
Seamount-like Structures of the Alborán Sea. In Würtz M, Rovere M (eds). Atlas
of the Mediterranean Seamounts and Seamount-like Structures. Gland,
Switzerland and Málaga, Spain: IUCN 276 pp.
Palomino D, Alonso B, Ercilla G, Casas D, López-González N et al (2019) Bedforms in
the la Linea Turbidite System (NW Alboran Sea). 34th IAS Meeting of
Sedimentology 10-13/09.
Paracuellos M, Nevado JC (1995) Nidificación de láridos en la provincia de Almería
(SE Ibérico). Doñana, Act Vertebr 22: 102-106.
Paracuellos M, Nevado JC, Moreno D, Giménez A, Alesina JJ (2003) Conservational
status and demographic characteristics of Patella ferruginea Gmelin, 1791
(Mollusca, Gastropoda) on the Alborán Island (Western Mediterranean). Anim
Biodiv Conserv, 26(2) 29-37.
Paracuellos M, Nevado JC, Mota JF (2006) Entre África y Europa. Historia Natural de
la Isla de Alborán. RENPA, Consejería de Medio Ambiente, Junta de Andalucía,
Sevilla 267 pp.
Paracuellos M, Nevado JC (2010) Culling Yellow-legged Gull Larus michahellis
benefits Audouin’s Gull Larus audouinii at a small and remote colony. Bird
Study, 57: 26-30.
Pardo E, Aguilar R, García A, de la Torriente A, Ubero J (2011) Documentación de
arrecifes de corales de agua fría en el Mediterráneo occidental (Mar de Alborán).
Chronica naturae 1: 20-34.
PePellón J, Bermejo R, Chacón M et al (2017) Presence of Caulerpa cylindracea
(Chlorophyta) in the North of Strait of Gibraltar: Effectiveness of CitizenScientist in Detecting Invasion and Record in Atlantic European Coast. J Mar Biol
Oceanogr 6:1.
Peñas A, Rolán E, Luque AA et al (2006) Moluscos marinos de la isla de Alborán.
Iberus, 24 (1): 23-151
Pérez Hurtado de Mendoza A (2004) Salinas de Andalucía. Consejería de Medio
Ambiente, Junta de Andalucía, Sevilla, 301 pp.
Pérez-Roda A, Delord K, Boué A et al (2017) Identifying Important Atlantic Areas for
the conservation of Balearic shearwaters: Spatial overlap with conservation areas.
Deep Sea Rese Part II 141: 285-293.
Rands MR, Adams WM, Bennun L et al (2010) Biodiversity conservation: challenges
beyond 2010. Science. 329 (5997): 1298-1303.
Reyes-González JM, González-Solís J (2016) Pardela cenicienta atlántica - Calonectris
borealis. In Salvador A, Morales MB (Eds.). Enciclopedia Virtual de los
Vertebrados Españoles. Museo Nacional de Ciencias Naturales, Madrid.
http://www.vertebradosibericos.org/
Robles R (2010) Conservación y desarrollo sostenibledel mar de Alborán /
Conservation et développement durable de la mer d’Alboran.
Rosas-Guerrero J, Meco YE, Altamirano M (2018) Could Rugulopteryx okamurae
(Dictyotales, Ochrophyta) have been introduced by ballast waters? Algas 54: 52.
Rueda JL, Gofas S, Urra J, Salas C (2009) A highly diverse molluscan assemblage
associated with eelgrass beds (Zostera marina L.) in Europe: Micro-habitat
preference, feeding guilds and biogeographical distribution. Sci Mar 73 (4): 679700.
Rueda JL, Marina P (2009) “Paraje Natural Acantilados de Maro-Cerro Gordo”. In
Enciclopedia de Andalucía, “Espacios Naturales Protegidos” 6(4): 206-220.
Rueda JL, Gofas S, Aguilar R et al (this volume) Benthic fauna of littoral and deep-sea
habitats of the Alboran Sea: A hotspot of biodiversity. In: JC Baéz, JA Camiñas,
JT Vázquez, M Malouli (eds.) Alboran Sea and Its Marine Resources, Ch. 9,
Springer Nature Switzerland AG.
Ruiz RE, Moreno EM, Haasova L, Ponzone LO, García-Gómez JC (2018). “Presencia
permanente del delfín común en la bahía de Algeciras. Hacia un plan de gestión,
vigilancia y conservación de la especie. Almoraima: revista de estudios
campogibraltareños (49): 185-196.
Ruiz-Giráldez F, Guerra-García JM, Espinosa F et al (2011) Especies protegidas
intermareales del Parque Natural del Estrecho - Intertidal endangered species from
“The Strait Natural Park”. Zool Baetica 22: 19-32.
Salas C, Hergueta E (1986b) La fauna de moluscos de las concreciones calcáreas de
Mesophyllum lichenoides (Ellis) Lemoine. Estudio de la diversidad de un ciclo
anual. Iberus, 6 (1) 57-65.
Salas C, Luque AA (1986a) Contribución al conocimiento de los moluscos marinos de
la Isla de Alborán. Iberus, 6 (1): 29-37.
Sánchez-Tocino L, Tierno de Figueroa M, de la Linde A (2014) Two new records for
the Chafarinas Islands: the black coral Antipathella subpinnata (Anthozoa) and
the invasive crab Percnon gibbesi (Crustacea). Zool Baetica 25: 89-93.
Sánchez-Tocino L, de la Linde Rubio A, López-Rodríguez MJ, Tierno de Figueroa JM
(2019) Conservation status of the Paramuricea clavata (Risso, 1826) (Anthozoa,
Alcyonacea) in the Chafarinas Islands (Mediterranean Sea). Anim Biodivers
Conserv 42(2): 253–256.
Sandwith T, Shine C, Hamilton L, Sheppard D (2001) Transboundary Protected Areas
for Peace and Co-operation. Gland, Switzerland and Cambridge, UK: IUCN.
https://portals.iucn.org/library/efiles/documents/PAG-007.pdf
SEO CEUTA 2019. Jornadas Técnicas sobre Gaviota de Audouin en el Mar de Alborán
celebradas en Melilla. https://www.seoceuta.es/
Serrano E, Coma R, Ribes M (2012) A phase shift from macroalgal to coral dominance
in the Mediterranean. Coral Reefs, 31(4): 1199.
Sitjà C, Maldonado M (2014) New and rare sponges from the deep shelf of the Alboran
Island (Alboran Sea, Western Mediterranean). Zootaxa 3760(2): 141-179
SPA/BD (1995) Protocol Concerning Specially Protected Areas and Biological
Diversity in the Mediterranean.
Talamo D, Riera R (2019) Elements for a future EBSA (Ecologically or Biologically
Significant marine Area) process in the Alborán Sea and connected areas. A case
study for north-south cooperation. Cah Biol Mar 60: 211-222.
Templado J, García-Carrascosa AM, Baratech L et al (1986) Estudio preliminar de la
fauna asociada a los fondos coralíferos del mar de Alborán (SE de España). Bol
Inst Esp Oceanogr 3(4): 93-104.
Templado J, Luque AA (1986) Braquiópodos de los fondos de Corallium rubrum (L.)
próximos a la isla de Alborán (SE de España). Bol Inst Esp Oceanogr 3(4): 111114.
Templado J, Guerra A, Bedoya J et al (1993) Fauna marina circalitoral del sur de la
Península Ibérica. Museo Nacional de Ciencias Naturales, CSIC, Madrid, 135 pp.
Templado J, Calvo M, Moreno D et al (2006) Flora y fauna de la Reserva Marina y
Reserva de Pesca de la Isla de Alborán. Secretaría General de Pesca Marítima,
MAPA, Madrid, 269 pp.
Templado J, Richter A, Calvo M (2016) Reef building Mediterranean vermetid
gastropods: disentangling the Dendropoma petraeum species complex. Mediter
Mar Sci 7(1): 13-31.
Torcal Sainz L, López Barmúdez F (1997) Caracterización mineralógica y microtextural
de la barra que cierra la sebkha Bou-Areg (Marruecos). Cuater Geomorf, 11 (1-2):
19-32.
Tirado R (2009) 5220 Matorrales arborescentes con Ziziphus (*). VV.AA., Bases
ecológicas preliminares para la conservación de los Tipos de Hábitat de Interés
Comunitario en España. Ministerio de Medio Ambiente, y Medio Rural y Marino.
68 pp.
Tunesi L, Mo G, Salvati E et al (2003) Rapport global des travaux de prospection de la
partie marine du Parc National d’Al-Hoceima. Projet Régional pour le
Développement
d´Aires
Protégées
Marineset
Côtières
dans
la
Région
Méditerranéenne (Project MedMPA). CAR/ASP-PAM-PNUE: 1-111.
UICN (2007). Arturo López Ornat, Anna Pons Reynés (Pangea consultores S.L.) en
colaboración con Mika Noguera, Utilización de las categorías de gestión de áreas
protegidas de UICN en la región mediterránea. Consejería de Medio Ambiente de
la Junta de Andalucía, Sevilla, España y UICN, Gland, Suiza y Málaga, España.
211 pp.
UICN (2012a) Propuesta de una red representativa de áreas marinas protegidas en el
mar de Alborán / Versun réseau représentatif d’aires marines protégées dans la
mer d’Alboran. Gland, Suiza y Málaga, España, 124 pp.
UICN (2012b). Atlas du Parc National d’Al Hoceima. Gland, Suisse et Málaga,
Espagne :UICN-Centre de Coopération pour la Méditerranée. 104 pp.
UNEP (2005) Informe de la decimocuarta reunión ordinaria de las Partes Contratantes
en la Convención para la Protección del Medio Marino y la Región Costera del
Mediterráneo y sus Protocolos, 149 pp.
UNEP-MAP-RAC/SPA (2009) Diagnostic de la biodiversité marine du Rif central
(Méditerranée, Maroc) et orientations de gestion. Par Ben Haj S, Bazairi H,
Benhissoune S. Contrat CAR/ASP 47, 48, 49: 100 pp.
UNEP-MAP-RAC/SPA (2014) Ecology and Human Activities in the Alboran Sea. By
IUCN Med. Draft internal report for the purposes of the Mediterranean Regional
Workshop to Facilitate the Description of Ecologically or Biologically Significant
Marine Areas, Málaga, Spain, 7-11 April.
UNEP-WCMC and IUCN (2017) Marine Protected Planet [On-line], [December, 2017].
Cambridge:
UNEP-WCMC
and
IUCN.
Available
online
at:
www.protectedplanet.net
Urra J, Gofas S, Rueda JL, Marina P (2011) Molluscan assemblages in littoral soft
bottoms of the Alboran Sea (Western Mediterranean Sea). Mar Biol Res 7 (1): 2742.
Urra J, Rueda JL, Gofas S, Marina P, Salas C (2012) A species-rich molluscan
assemblage in a coralligenous bottom of the Alboran Sea (south-western
Mediterranean): intra-annual changes and ecological considerations. J Mar Biol
Assoc UK, 92 (4): 665-677.
Urra J, Mateo-Ramírez ÁM, Marina P et al (2013a) Highly diverse molluscan
assemblages of Posidonia oceanica meadows in northwestern Alboran Sea (W
Mediterranean): seasonal dynamics and environmental drivers. Estuar Coast Shelf
Sci 117: 136-147.
Urra J, Rueda JL, Mateo-Ramírez ÁM, et al (2013b) Seasonal variation of molluscan
assemblages in different strata of photophilous algae in the Alboran Sea (western
Mediterranean). J Sea Res 83: 83-93.
Urra J, Marina P, Rueda JL et al (2015) New Marine Protected Areas for the benthic
biodiversity conservation in the Alboran Sea. VIII Simposio MIA15, Málaga 675678.
Urra J, Gofas S, Rueda JL et al (2017) Biodiversity and biogeographical patterns of
molluscan assemblages in vegetated and unvegetated habitats in the northern
Alboran Sea (W Mediterranean Sea). Mar Biodivers 47(1):187-201.
Vázquez JT, Alonso B, Fernández-Puga MC et al (2015a) Seamounts along the Iberian
continental margins. Bol Geol Min 126 (2-3): 483-514.
Vázquez JT, Ercilla G, Alonso B et al (2015b) Submarine Canyons and related features
in the Alboran Sea: continental margins and major isolated reliefs. In: Submarine
Canyon Dynamics in the Mediterranean and Tributary Seas - An integrated
geological, oceanographic and biological perspective. CIESM Research
Workshop 47:183-196.
Vázquez JT, Casas D, Palomino D et al (2017) Geomorphology and evolutive processes
of the Algeciras submarine canyon. In Mudanças em Sistemas Ambientais e sua
Expressão Temporal - Livro de Resumos da IX Reunião do Quaternário Ibérico:
103-104.
Vázquez JT, Ercilla G, Catalán M et al (this volume) A Geological history for the
Alboran Sea region. In: JC Baéz, JA Camiñas, JT Vázquez, M Malouli (eds.)
Alboran Sea and Its Marine Resources, Ch. 5, Springer Nature Switzerland AG.
Vázquez-Luis M, Álvarez E, Barrajón Domenech A et al (2017) S.O.S. Pinna nobilis A
Mass Mortality Event in Western Mediterranean Sea. Front Mar Sci, 4: 220.
Villalobos M (2003) Geología del entorno árido almeriense. Guía didáctica de campo.
Consejería de Medio Ambiente, Acusur, 163 pp.
Villalobos M, Salas R, González Lastra J (2004) Cabo de Gata. Un espacio de leyenda.
ACUSUR, Confederación Hidrográfica del Sur de España, Consejería de Medio
Ambiente-Junta de Andalucía, 318 pp.
Vitalea S, Zaghloul MN, El Ouaragli B, Tramparuloa FD, Ciarcia S (2015) Polyphase
deformation of the Dorsale Calcaire Complex and the Maghrebian Flysch Basin
Units in the Jebha area (Central Rif, Morocco): New insights into the Miocene
tectonic evolution of the Central Rif belt. J Geodyn 90: 14–31.
Waycott M, Duarte CM, Carruthers TJB et al (2009) Accelerating loss of seagrasses
across the globe threatens coastal ecosystems. PNAS 106(30): 12377-2381.
Yus R, González JA, Jerez D et al (2013). La Península de Tres Forcas. In Yus, R, Cabo
JM Historia Natural de la región de Melilla (Guelaya, Alborán y Chafarinas).
Fundación Gaselec, Melilla.
Zibrowius H, Ramos AA (1983) Oculina patagonica, Scléractiniaire exotique en
Méditerranée a nouvelles observations dans le Sudest de l'Espagne. Rapp PV
Reun Comm Int Explor Mer Mediterr 28 (3): 297-301.