Skip to main content

The Families of Decapod Shrimps

  • Chapter
  • First Online:
Shrimps

Part of the book series: Fish & Fisheries Series ((FIFI,volume 42))

Abstract

The taxonomy and classification of the ~4400 decapod shrimps are constantly evolving as new research clarifies their nomenclature and relationships. Synopses of all shrimp families reveal the biological diversity and lifestyles of the Dendrobranchiata (penaeoids and sergestoids), Procarididea, Caridea, and Stenopodidea. The seven families of Dendrobranchiata have a similar overall morphology and coloration compared to other major taxa. However, the structure of their genitalia is much more complex than that of other shrimp groups. Most species are found in pelagic and benthic habitats of continental shelves and slopes in subtropical and tropical latitudes. In contrast, the 38 families of carideans inhabit marine habitats of all depths and latitudes, as well as many subtropical and tropical freshwater environments. This ecological diversity is reflected in their considerable variation in body shape, appendage structure, and coloration. The Stenopodidea consists of two strictly marine families, one primarily occupying shallow tropical waters and another mostly symbiotic primarily with deep-sea glass sponges and other invertebrates. The other family, the Macromaxillocarididae, is monotypic in anchialine cave waters. The taxonomic status of one pelagic shrimp (Amphionides reynaudii) is still somewhat uncertain although it may be the larval form of a pandalid caridean. The anchialine achelate Procarididea is considered a sister taxon of the Caridea.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Abele LG (1970) Semi-terrestrial shrimp (Merguia rhizophorae). Nature 226:661–662

    Article  CAS  PubMed  Google Scholar 

  • Abele LG (1972) A review of the genus Ambidexter (Crustacea: Decapoda: Processidae) in Panama. Bull Mar Sci 22:365–380

    Google Scholar 

  • Abele LG, Felgenhauer BE (1985) Observations on the ecology and feeding behavior of the anchialine shrimp Procaris ascensionis. J Crustac Biol 5:15–24

    Article  Google Scholar 

  • Aguzzi JB, Company JB, Abelló P, García JA (2006) Daily activity patterns of the mud shrimp Solenocera membranacea (Decapoda: Penaeoidea: Solenoceridae) in the western Mediterranean: a comparison by depth and season. Bull Mar Sci 79:353–364

    Google Scholar 

  • Aguzzi J, Company JB, García JA (2008) The circadian behavioural regulation of the shrimp, Processa canaliculata Leach, 1815 (Decapoda, Processidae) in relation to depth, ontogeny, and the reproductive cycle. Crustaceana 81:1301–1316

    Article  Google Scholar 

  • Ahamed F, Cardoso IA, Ahmed ZF, Hossain Y, Ohtomi J (2017) An overview of the genus Plesionika Bate, 1888 (Decapoda, Caridea, Pandalidae) in Asian waters. Zootaxa 4221:575–593

    Article  Google Scholar 

  • Ahyong ST (2003) Gnathophyllum taylori, a new species of caridean shrimp from south-eastern Australia (Crustacea: Decapoda: Gnathophyllidae). Mem Mus Vic 60:237–242

    Article  Google Scholar 

  • Alvarez F, Villalobos JL, Iliffe TM (2004) A new species of Agostocaris (Caridea: Agostocarididae) from Acklins Island, Bahamas. Proc Biol Soc Wash 117:382–390

    Google Scholar 

  • Alvarez F, Iliffe TM, Villalobos JL (2006) Macromaxillocarididae, a new family of stenopodidean shrimp from an anchialine cave in the Bahamas, with the description of Macromaxillocaris bahamaensis, n. gen., n. sp. J Crustac Biol 26:366–378

    Article  Google Scholar 

  • Alves D, Barros-Alves S, Almeida A (2021) Sex change and reproductive investment of the protandric shrimp Merguia rhizophorae (Rathbun, 1900) (Decapoda, Merguiidae). J Nat Hist 55:2673–2690

    Article  Google Scholar 

  • Anderson WW, Lindner MJ (1971) Contributions to the biology of the royal red shrimp, Hymenopenaeus robustus, Smith. Fish Bull 69:313–336

    Google Scholar 

  • Anderson SL, Clark WH, Chang ES (1985) Multiple spawning and molt synchrony in a free spawning shrimp (Sicyonia ingentis: Penaeoidea). Biol Bull 168:377–394

    Article  Google Scholar 

  • Anker A (2003) Alpheid shrimps from the mangroves and mudflats of Singapore. Part 1. Genera Salmoneus, Athanas and Potamalpheops, with the description of two new species (Crustacea: Decapoda: Caridea). Raffles Bull Zool 51:283–314

    Google Scholar 

  • Anker A (2011) Three new species of the alpheid shrimp genus Salmoneus Holthuis, 1955 (Crustacea, Decapoda) from the tropical western Pacific. Zootaxa 2839:67–84

    Article  Google Scholar 

  • Anker A (2012) The shrimp family Pseudochelidae De Grave & Moosa, 2004 (Crustacea, Decapoda, Caridea) in Brazil, with the description of a new species. Zootaxa 3544:79–87

    Article  Google Scholar 

  • Anker A, Baeza JA (2012) Morphological and molecular phylogeny of hooded shrimps, genera Betaeus and Betaeopsis (Decapoda, Caridea, Alpheidae): testing the Center of Origin biogeographic model and evolution of life habits. Mol Phylogenet Evol 64:401–415

    Article  PubMed  Google Scholar 

  • Anker A, Ahyong ST, Noël PY, Palmer AR (2006) Morphological phylogeny of alpheid shrimps: parallel preadaptation and the origin of a key morphological innovation, the snapping claw. Evolution 60:2507–2528

    Article  PubMed  Google Scholar 

  • Anker A, Hurt C, Knowlton N (2007) Revision of the Alpheus nuttingi (Schmitt) species complex (Crustacea: Decapoda: Alpheidae), with description of a new species from the tropical eastern Pacific. Zootaxa 1577:41–60

    Article  Google Scholar 

  • Arana P, Ahumada M (2006) Camarón navaja (Campylonotus semistriatus), crustáceo de aguas profundas frente a la costa central de Chile (Crustacea, Decapoda, Campylonotidae). Investigaciones Marinas Valparaíso 34:3–14

    Google Scholar 

  • Ayón-Parente M, Salgado-Barragán J (2013) A new species of the caridean shrimp genus Ogyrides Stebbing, 1914, (Decapoda: Ogyrididae) from the eastern tropical Pacific. Zootaxa 3683:589–594

    Article  PubMed  Google Scholar 

  • Baeza JA (2009) Protandric simultaneous hermaphroditism is a conserved trait in Lysmata (Caridea: Lysmatidae): implications for the evolution of hermaphroditism in the genus. Smithson Contrib Mar Sci 38:95–110

    Google Scholar 

  • Baeza JA (2010) Observations on the sexual system and the natural history of the semi-terrestrial shrimp Merguia rhizophorae (Rathbun, 1900). Invertebr Biol 129:266–276

    Article  Google Scholar 

  • Baeza JA (2013) Multi-locus molecular phylogeny of brokenback shrimps (genus Lysmata and allies): a test of the ‘Tomlinson-Ghiselin’ hypothesis explaining the evolution of simultaneous hermaphroditism. Mol Phylogenet Evol 69:46–62

    Article  PubMed  Google Scholar 

  • Baeza JA, Piantoni C (2010) Sexual system, sex ratio and group living in the shrimp Thor amboinensis (De Man): relevance to resource-monopolization and sex-allocation theories. Biol Bull 219:151–165

    Article  CAS  PubMed  Google Scholar 

  • Baeza JA, Bauer RT, Okuno J, Thiel M (2014) Molecular phylogeny of hinge-beak shrimps (Decapoda: Caridea: Rhynchocinetes and Cinetorhynchus) and allies: a formal test of familiar and generic monophyly using a multilocus phylogeny. Zool J Linnean Soc 172:426–450

    Article  Google Scholar 

  • Bailey-Brock JH, Brock RE (1993) Feeding, reproduction, and sense organs of the Hawaiian anchialine shrimp Halocaridina rubra (Atyidae). Pac Sci 47:338–355

    Google Scholar 

  • Ballard RD, Grassle JF (1979) Return to oases of the deep. Natl Geogr Mag 156:689–703

    Google Scholar 

  • Barnard KH (1950) Descriptive catalogue of South African decapod Crustacea (crabs and shrimps). Ann South Afr Mus 38:1–837

    Google Scholar 

  • Bauer RT (1975) Grooming behaviour and morphology of the caridean shrimp Pandalus danae Stimpson (Decapoda: Natantia: Pandalidae). Zool J Linnean Soc 56:45–71

    Article  Google Scholar 

  • Bauer RT (1979) Antifouling adaptations of marine shrimp (Decapoda: Caridea): gill cleaning mechanisms and grooming of brooded embryos. Zool J Linnean Soc 65:281–303

    Article  Google Scholar 

  • Bauer RT (1981) Color patterns of the shrimps Heptacarpus pictus and H. paludicola. Mar Biol 46:141–152

    Article  Google Scholar 

  • Bauer RT (1982) Polymorphism of colour pattern in the caridean shrimps Heptacarpus pictus and H. paludicola. Mar Behav Physiol 8:249–265

    Article  Google Scholar 

  • Bauer RT (1984) Morphological trends in the genus Heptacarpus (Decapoda, Caridea) and their phylogenetic significance. J Crustac Biol 4:201–225

    Article  Google Scholar 

  • Bauer RT (1985a) Penaeoid shrimp fauna from tropical seagrass meadows: species composition, diurnal and seasonal variation in abundance. Proc Biol Soc Wash 98:177–190

    Google Scholar 

  • Bauer RT (1985b) Diel and seasonal variation in species composition and abundance of the caridean shrimps (Crustacea, Decapoda) from seagrass meadows in northern Puerto Rico. Bull Mar Sci 36:150–162

    Google Scholar 

  • Bauer RT (1986) Sex change and life history pattern in the shrimp Thor manningi (Decopoda: Caridea): a novel case of partial protandric hermaphroditism. Biol Bull 170:11–31

    Article  Google Scholar 

  • Bauer RT (1989) Functional morphology, adaptive value, and phylogenetic significance of grooming in Decapod Crustacea. In: Felgenhauer B, Watling L (eds) Functional morphology of grooming and feeding appendages. Balkema Press, Boca Raton, FL, pp 49–73

    Google Scholar 

  • Bauer RT (1992a) Repetitive copulation and variable success of insemination in the marine shrimp Sicyonia dorsalis (Decapoda, Penaeoidea). J Crustac Biol 12:153–160

    Article  Google Scholar 

  • Bauer RT (1992b) Testing generalizations about latitudinal variation in reproductive and recruitment patterns with caridean and sicyoniid shrimps. J Invertebr Reprod Dev 22:193–202

    Article  Google Scholar 

  • Bauer RT (1994) Usage of the terms thelycum and spermatheca in the reproductive morphology of the Decapoda, with special reference to the Penaeoidea. J Crustac Biol 14:715–721

    Article  Google Scholar 

  • Bauer RT (1996a) Role of the petasma and appendices masculinae during copulation and insemination in the penaeoid shrimp, Sicyonia dorsalis (Crustacea: Decapoda: Dendrobranchiata). Invertebr Reprod Dev 29:173–184

    Article  Google Scholar 

  • Bauer RT (1996b) A test of hypotheses on male mating systems and female molting in decapod shrimp, using Sicyonia dorsalis (Decapoda: Penaeoidea). J Crustac Res 16:429–437

    Article  Google Scholar 

  • Bauer RT (2000) Simultaneous hermaphroditism in caridean shrimps: a unique and puzzling sexual system in the Decapoda. J Crustac Biol 20(2):116–128

    Article  Google Scholar 

  • Bauer RT (2004) Remarkable shrimps: adaptations and natural history of the Carideans. University of Oklahoma Press, Norman

    Google Scholar 

  • Bauer RT (2011) Amphidromy and migrations of freshwater shrimps. I. Costs, benefits, evolutionary origins, and an unusual case of amphidromy. In: Asakura A (ed) New frontiers in crustacean biology. Proceedings of the TCS Summer Meeting, Tokyo, 20–24 September 2009. Brill, Leiden, The Netherlands, pp 145–156

    Chapter  Google Scholar 

  • Bauer RT (2013) Amphidromy in shrimps: a life history pattern between rivers the sea. Lat Am J Aquat Res 41:633–650

    Article  Google Scholar 

  • Bauer RT (2020) Shrimp fisheries. In: Thiel M, Lovrich G (eds) The natural history of the crustacea: Volume 8. Fisheries and aquaculture. Oxford University Press, Oxford, pp 91–116

    Chapter  Google Scholar 

  • Bauer RT, Conner SL (2011) Gonochoric sexual system in the caridean shrimps Processa riveroi and P. bermudensis (Decapoda: Processidae) inhabiting a tropical seagrass meadow. J Mar Biol Assoc U K 92:521–529

    Article  Google Scholar 

  • Bauer RT, Holt GJ (1998) Simultaneous hermaphroditism in the marine shrimp Lysmata wurdemanni (Caridea: Hippolytidae): an undescribed sexual system in the decapod Crustacea. Mar Biol 132:223–235

    Article  Google Scholar 

  • Bauer RT, Lin JM (1993) Spermatophores and plug substance of the marine shrimp Trachypenaeus similis (Crustacea: Decapoda: Penaeidae): formation in the male reproductive tract and disposition in the inseminated female. Biol Bull 185:174–185

    Article  CAS  PubMed  Google Scholar 

  • Bauer RT, Newman WA (2004) Protandric simultaneous hermaphroditism in the marine shrimp Lysmata californica (Caridea: Hippolytidae). J Crustac Biol 24:131–139

    Article  Google Scholar 

  • Bauer RT, Thiel M (2011) First description of a pure-search mating system and protandry in the shrimp Rhynchocinetes uritai (Decapoda: Caridea). J Crustac Biol 31:286–295

    Article  Google Scholar 

  • Bauer RT, VanHoy R (1996) Variation in sexual systems (protandry, gonochorism) and reproductive biology among three species of the shrimp genus Thor (Decopoda: Caridea). Bull Mar Sci 59:53–73

    Google Scholar 

  • Bauer RT, Okuno J, Thiel M (2014) Inferences on mating and sexual systems of two Pacific Cinetorhynchus shrimps (Decapoda, Rhynchocinetidae) based on sexual dimorphism in body size and cheliped weaponry. Zookeys 457:187–209

    Article  Google Scholar 

  • Bergström B (2000) The biology of Pandalus. Adv Mar Biol 38:1–245

    Google Scholar 

  • Berkeley AA (1930) The post-embryonic development of the common pandalids of British Columbia. In: Contributions to Canadian Biology New Series, vol 6. University of Toronto Press, Toronto, pp 79–163

    Google Scholar 

  • Bochini GL, Cunha AM, Terossi M, Almeida AO (2020) A new genus and species from Brazil of the resurrected family Macromaxillocarididae Alvarez, Iliffe & Villalobos, 2006 and a worldwide list of Stenopodidea (Decapoda). J Crustac Biol 40:704–714

    Article  Google Scholar 

  • Boddeke R, Bosschieter JR, Goudswaard PC (1991) Sex change, mating, and sperm transfer in Crangon crangon (L.). In: Bauer RT, Martin JW (eds) Crustacean sexual biology. Columbia University Press, New York, pp 164–182

    Chapter  Google Scholar 

  • Boltana S, Thiel M (2001) Associations between two species of snapping shrimp, Alpheus inca and Alpheopsis chilensis (Decapoda: Caridea: Alpheidae). J Mar Biol Assoc U K 81:633–638

    Article  Google Scholar 

  • Boone L (1927) Crustacea from tropical east American seas. Scientific results of the first oceanographic expedition of the “Pawnee,” 1925. In: Bulletin Bingham oceanographic collection, vol 1. Yale University, New Haven, CT, pp 1–147

    Google Scholar 

  • Boothe BB, Heard RW (1987) Discias vernbergi, new species, a caridean shrimp (Crustacea: Decapoda: Bresiliidae) from the northwestern Atlantic. Proc Biol Soc Wash 100:506–514

    Google Scholar 

  • Bowles DE, Aziz K, Knight CL (2000) Macrobrachium (Decapoda: Caridea: Palaemonidae) in the contiguous United States a review of the species and assessment of threats to their survival. J Crustac Biol 20:158–171

    Article  Google Scholar 

  • Bracken HD, Toon A, Felder DL, Martin JW, Finley M, Rasmussen J, Palero F, Crandall KA (2009) The Decapod tree of life: compiling the data and moving toward a consensus of Decapod evolution. Arthropod Syst Phylogeny 67:99–116

    Google Scholar 

  • Braga AA, Lopez Greco LS, Santos DC, Fransozo A (2009) Morphological evidence for protandric simultaneous hermaphroditism in the caridean Exhippolysmata oplophoroides. J Crustac Biol 29:34–41

    Article  Google Scholar 

  • Bruce AJ (1966) Bathypalaemonella humilis sp. nov., a new species of shrimp from the South China Sea (Decapoda, Campylonotidae). Crustaceana 11:277–287

    Article  Google Scholar 

  • Bruce AJ (1972) Pycnocaris chagoae gen. nov., sp. nov., a new shrimp from the Chagos Archipelago (Decapoda Natantia, Gnathophyllidae). Crustaceana 23:50–64

    Article  Google Scholar 

  • Bruce AJ (1973) Gnathophylloides robustus sp. nov., a new commensal gnathophyllid shrimp from western Australia, with the designation of a new genus Levicaris (Decapoda, Caridea). Crustaceana 24:17–32

    Article  Google Scholar 

  • Bruce AJ (1975) Coral reef shrimps and their colour patterns. Endeavour 34:23–27

    Article  Google Scholar 

  • Bruce AJ (1976) Shrimps and prawns of coral reefs, with special reference to commensalism. In: Jones O, Endean R (eds) Biology and geology of coral reefs, Biology 2, vol III. New York, Academic Press, pp 38–94

    Google Scholar 

  • Bruce AJ (1983a) Miropandalus hardingi, new genus, new species, a bizarre commensal pandalid shrimp from the Marshall Islands. J Crustac Biol 3:482–490

    Article  Google Scholar 

  • Bruce AJ (1983b) Epipontonia anceps n. sp., a sponge-associated pontoniine shrimp from Heron Island, Queensland. (Crustacea: Decapoda: Palaemonidae). Rec Aust Mus 35:19–28

    Article  Google Scholar 

  • Bruce AJ (1986a) Two new species of Bathypalaemonella Balss (Crustacea, Decapoda, Campylonotidae) from the Australian Northwest Shelf. Zool Scr 15:251–264

    Article  Google Scholar 

  • Bruce AJ (1986b) Observations on the family Gnathophyllidae Dana, 1852 (Crustacea: Decapoda). J Crustac Biol 6:463–470

    Article  Google Scholar 

  • Bruce AJ (1986c) Redescriptions of five Hong Kong carideans first described by William Stimpson, 1860. In: Morton B (ed) Proceedings of the second international marine biological workshop: the marine flora and fauna of Hong Kong and Southern China. Hong Kong University Press, Hong Kong, pp 569–610

    Google Scholar 

  • Bruce AJ (1991) The ‘African’ shrimp genus Potamalpheops in Australia, with the description of P. hanleyi, new species (Decapoda: Alpheidae). J Crustac Biol 11:629–638

    Article  Google Scholar 

  • Bruce AJ (1993) The occurrence of the semi-terrestrial shrimps Merguia oligodon (De Man 1888) and M. rhizophorae (Rathbun 1900) (Crustacea Decapoda Hippolytidae) in Africa. Trop Zool 6:179–187

    Article  Google Scholar 

  • Burkenroad MD (1934) The Penaeidea of Louisiana with a discussion of their world relationships. Bull Am Mus Nat Hist 68:61–143

    Google Scholar 

  • Burkenroad MD (1936) The Aristaeinae, Solenocerinae and pelagic Penaeinae of the Bingham Oceanographic collection. Bull Bingham Oceanogr Collect 5:1–151

    Google Scholar 

  • Burkenroad MD (1983) Natural classification of Dendrobranchiata, with a key to recent genera. In: Schram FR (ed) Crustacean phylogeny. Crustacean issues, vol 1. A.A. Balkema, Rotterdam, pp 279–290

    Google Scholar 

  • Burukovsky RN (1988) New representatives of the family Bresiliidae (Crustacea, Decapoda) from the north-east Atlantic [in Russian]. Zoologicheskii Zhurnal 67:456–460

    Google Scholar 

  • Burukovsky RN (2012) Deep sea shrimps of the family Nematocarcinidae. Prospekt Nauki Publishing House, Saint Petersburg, Russia, pp 1–288

    Google Scholar 

  • Burukovsky RN, Falkenhaug T (2015) Feeding of the pelagic shrimp Acanthephyra pelagica (Risso, 1816) (Crustacea: Decapoda: Oplophoridae) in the northern Mid-Atlantic Ridge area in 1984 and 2004. [In Russian with English summary]. Arthropoda Selecta 24:303–316

    Article  Google Scholar 

  • Burukovsky RN (2017) Distribution, reproduction, and feeding of West African shrimp Plesionika carinata Holthuis, 1951 (Decapoda, Pandalidae). Oceanology 57:668–674

    Article  CAS  Google Scholar 

  • Butler TH (1964) Growth, reproduction, and distribution of pandalid shrimps in British Columbia. J Fish Res Board Can 21:1403–1452

    Article  Google Scholar 

  • Butler TH (1980) Shrimps of the Pacific coast of Canada. Can Bull Fish Aquat Sci 202:1–80

    Google Scholar 

  • Cai Y, Ng PKL, Shokita S, Satake K (2006) On the species of Japanese atyid shrimps (Decapoda: Caridea) described by William Stimpson (1860). J Crustac Biol 26:392–419

    Article  Google Scholar 

  • Calado R (2008) Marine ornamental shrimp: biology, aquaculture and conservation. Wiley and Blackwell, Oxford

    Google Scholar 

  • Calado R, Chevaldonne P, dos Santos A (2004) A new species of the deep-sea genus Bresilia (Crustacea: Decapoda: Bresiliidae) discovered from a shallow-water cave in Madeira. J Mar Biol Assoc UK 84:191–199

    Article  Google Scholar 

  • Calman WT (1909) On a blind prawn from the Sea of Galilee (Typhlocaris galilea g. et sp. n.). Transactions of the Linnean Society London, Zoology 11:93–97

    Article  Google Scholar 

  • Campos JC, Moreira C, Freitas F, van der Veer HW (2012) Short review of the eco-geography of Crangon. J Crustac Biol 32:159–169

    Article  Google Scholar 

  • Cardoso IA, Fransen CHJM (2012) A new species of the deepwater shrimp genus Leontocaris (Hippolytidae: Caridea) from the South Mid-Atlantic Ridge. J Mar Biol Assoc U K 92:1083–1088

    Article  Google Scholar 

  • Cartes JE (1993) Feeding habits of pasiphaeid shrimps close to the bottom on the western Mediterranean slope. Mar Biol 117:459–468

    Article  Google Scholar 

  • Cartes JE (1995) Diets of, and trophic resources exploited by, bathyal penaeoidean shrimps from the Western Mediterranean. Mar Freshw Res 46:889–896

    Article  Google Scholar 

  • Cartes JE, Papiol V, Guijarro B (2008) The feeding and diet of the deep-sea shrimp Aristeus antennatus off the Balearic Islands (Western Mediterranean): influence of environmental factors and relationship with the biological cycle. Prog Oceanogr 79:37–54

    Article  Google Scholar 

  • Carvalho-Batista A, Castilho AL, Fransozo A, Costa RC (2012) Diel comparison of the catch and size of the shrimp Artemesia longinaris (Dendrobranchiata, Penaeidae) in the Ubatuba region, northern coast of the state of São Paulo. Crustaceana 85:1179–1191

    Article  Google Scholar 

  • Castilho AL, Costa RC, Fransozo A, Negreiros-Fransozo ML (2008) Reproduction and recruitment of the South American red shrimp, Pleoticus muelleri (Crustacea: Solenoceridae), from the southeastern coast of Brazil. Mar Biol Res 4:361–368

    Article  Google Scholar 

  • Chace FA (1939) Reports on the scientific results of the first Atlantis Expedition to the West Indies, under the joint auspices of the University of Havana and Harvard University preliminary descriptions of one new genus and seventeen new species of decapod and stomatopod Crustacea. Memorias de la Sociedad Cubana de Historia Natural 13:31–54

    Google Scholar 

  • Chace FA (1940) Plankton of the Bermuda Oceanographic Expedition. IX. The bathypelagic caridean Crustacea. Zool N Y 25:117–209

    Google Scholar 

  • Chace FA (1951) The number of species of decapod and stomatopod Crustacea. J Wash Acad Sci 41:370–372

    Google Scholar 

  • Chace FA (1975) Cave shrimps (Decapoda: Caridea) from the Dominican Republic. Proc Biol Soc Wash 88:29–44

    Google Scholar 

  • Chace FA (1976) Shrimps of the pasiphaeid genus Leptochela with descriptions of three new species (Crustacea: Decapoda: Caridea). Smithsonian Contributions to Zoology No. 222, p 51

    Google Scholar 

  • Chace FA (1983) The caridean shrimps (Crustacea: Decapoda) of the Albatross Philippine Expedition, 1907-1910, Part 1: Family Stylodactylidae. Smithsonian Contributions to Zoology No. 381, p 21

    Google Scholar 

  • Chace FA (1984) The caridean shrimps (Crustacea: Decapoda) of the Albatross Philippine Expedition, 1907-1910, Part 2: Families Glyphocrangonidae and Crangonidae. Smithsonian Contributions to Zoology No. 397, p 63

    Google Scholar 

  • Chace FA (1985) The caridean shrimps (Crustacea: Decapoda) of the Albatross Philippine Expedition, 1907-1910, Part 3: Families Thalassocarididae and Pandalidae. Smithsonian Contributions to Zoology, No. 411, p 143

    Google Scholar 

  • Chace FA (1986) The caridean shrimps (Crustacea: Decapoda) of the Albatross Philippine Expedition, 1907-1910, Part 4: Families Oplophoridae and Nematocarcinidae. Smithsonian Contributions to Zoology, No. 432, p 82

    Google Scholar 

  • Chace FA (1992) On the classification of the Caridea (Decapoda). Crustaceana 63:70–80

    Article  Google Scholar 

  • Chace FA (1997) The caridean shrimps (Crustacea: Decapoda) of the Albatross Philippine Expedition, 1907–1910, Part 7: Families Atyidae, Eugonatonotidae, Rhynchocinetidae, Bathypalaemonellidae, Processidae, and Hippolytidae. Smithsonian Contributions to Zoology 587:1–106

    Google Scholar 

  • Chace FA, Brown DE (1978) A new polychelate shrimp from the Great Barrier Reef of Australia and its bearing on the family Bresiliidae (Crustacea: Decapoda: Caridea). Proc Biol Soc Wash 91:756–766

    Google Scholar 

  • Chace FA, Bruce AJ (1993) The Caridean Shrimps (Crustacea: Decapoda) of the Albatross Philippine Expedition, 1907-1910, Part 6: Superfamily Palaemonoidea. Smithsonian Contributions to Zoology, No. 543, p 152

    Google Scholar 

  • Chace FA, Fuller SLH (1971) A new shrimp of the genus Gnathophyllum (Decapoda, Caridea) from Puerto Rico. Proc Biol Soc Wash 83:493–504

    Google Scholar 

  • Chace FA, Hobbs HH (1969) The freshwater and terrestrial decapod crustaceans of the West Indies with special reference to Dominica. U S Natl Mus Bull 292:1–258

    Article  Google Scholar 

  • Chace FA, Holthuis LB (1978) Psalidopus: the scissor-foot shrimps (Crustacea: Decapoda: Caridea). Smithsonian Contributions to Zoology No. 277, p 22

    Google Scholar 

  • Chace FA, Manning RB (1972) Two new caridean shrimps, one representing a new family, from marine pools on Ascension Island (Crustacea: Decapoda: Natantia). Smithsonian Contributions to Zoology No. 131, p 18

    Google Scholar 

  • Chan T-Y, Yu H-P (1988) An uncommon deep-sea shrimp Eugonatonotus crassus (A. Milne Edwards, 1881) (Crustacea: Decapoda: Eugonatonotidae) from Taiwan. Bull Inst Zool Acad Sin 27:259–263

    Google Scholar 

  • Chan T-Y, Yu H-P (1991) Eugonatonotus chacei sp. nov., second species of the genus (Crustacea, Decapoda, Eugonatonotidae), Bulletin du Muséum national d’Histoire naturelle (4) section A, Zoologie. Biologie et Écologie animales 13:143–152

    Google Scholar 

  • Chan BKK, Lin I-C, Shin T-W, Chan TY (2008) Bioluminescent emissions of the deep-water pandalid shrimp, Heterocarpus sibogae De Man, 1917 (Decapoda, Caridea, Pandalidae) under laboratory conditions. Crustaceana 81:341–350

    Article  Google Scholar 

  • Chan T-Y, Lei HC, Li CP, Chu KH (2010) Phylogenetic analysis using rDNA reveals polyphyly of Oplophoridae (Decapoda: Caridea). Invertebr Syst 24:172–181

    Article  Google Scholar 

  • Chan TY, Kumar AB, Yang CH (2017) Photophore counts in the deep-sea commercial shrimp Aristeus alcocki Ramadan, 1938 (Crustacea: Decapoda: Aristeidae), with a revised key to the Indo-West Pacific species of the genus. Zootaxa 4329:392–400

    Article  PubMed  Google Scholar 

  • Chartosia N, Tzomos T, Kitso M-S, Karani I, Tselepides A, Koukouras A (2005) Diet comparison of the bathyal shrimps, Aristeus antennatus (Risso, 1816) and Aristaeomorpha foliacea (Risso, 1827) (Decapoda, Aristeidae) in the eastern Mediterranean. Crustaceana 78:273–284

    Article  Google Scholar 

  • Chávez-Solís EM, Mejía-Ortíz LM, Simões N (2018) Predatory behavior of the cave shrimp Creaseria morleyi (Creaser, 1936) (Caridea: Palaemonidae), the blind hunter of the Yucatán cenotes, Mexico. J Crustac Biol 38:1–7

    Article  Google Scholar 

  • Chen C-L, Goy JW, Bracken-Grissom HD, Felder DL, Tsang LM, Chan T-Y (2016) Phylogeny of Stenopodidea (Crustacea: Decapoda) shrimps inferred from nuclear and mitochondrial genes reveals non-monophyly of the families Spongicolidae and Stenopididae and most of their composite genera. Invertebr Syst 30:479–490

    Article  Google Scholar 

  • Chiba S (2007) A review of ecological and evolutionary studies on hermaphroditic decapod crustaceans. Plankton Benthos Res 2:107–119

    Article  Google Scholar 

  • Chockley BR, St. Mary CM (2003) Effect of body size on growth, survivorship and reproduction in the banded coral shrimp Stenopus hispidus. J Crustac Biol 23:836–848

    Article  Google Scholar 

  • Chockley BR, St. Mary CM, Osenberg CW (2008) Population sinks in the Upper Florida Keys: the importance of demographic variation in population dynamics of the marine shrimp Stenopus hispidus. Mar Ecol Prog Ser 360:135–145

    Article  Google Scholar 

  • Chow S, Okazaki M, Takeda M, Kubota T (2000) A rare abyssal shrimp, Galatheocaris abyssalis, found in the stomach of a lancetfish. Crustaceana 73:243–246

    Google Scholar 

  • Chow LH, De Grave S, Tsang LM (2020) The family Anchistioididae Borradaile, 1915 (Decapoda: Caridea) is a synonym of Palaemonidae Rafinesque, 1815 based on molecular and morphological evidence. J Crustac Biol 40:277–287

    Article  Google Scholar 

  • Christodoulou M, Anastasiadou C (2017) Sexual dimorphism in the shrimp genus Atyaephyra (Caridea: Atyidae): the case study of Atyaephyra thyamisensis. J Crustac Biol 37:588–601

    Article  Google Scholar 

  • Christodoulou M, Antoniou A, Magoulas A, Koukouras A (2012) Revision of the freshwater genus Atyaephyra (Crustacea, Decapoda, Atyidae) based on morphological and molecular data. Zookeys 229:53–110

    Article  Google Scholar 

  • Christoffersen ML (1986) Phylogenetic relationships between Oplophoridae, Atyidae, Pasiphaeidae, Alvinocarididae Fam. N., Bresiliidae, Psalidopodidae and Disciadidae (Crustacea Caridea Atyoidea). Bol Zool 10:273–281

    Article  Google Scholar 

  • Christofferson ML (1990) A new superfamily classification of the Caridea (Crustacea: Pleocyemata) based on phylogenetic pattern. Zeitschrift für Zoologische Systematik und Evolutionsforschung 28:94–106

    Article  Google Scholar 

  • Clark WH, Griffin FJ (1988) The morphology and physiology of the acrosome reaction in the sperm of the decapod, Sicyonia ingentis. Dev Growth Differ 30:451–462

    Article  Google Scholar 

  • Cleva R (1990) Crustacea Decapoda: Les genres et les espèces indo-ouest pacifiques de Stylodactylidae. In: Crosnier A (ed) Résultats des Campagnes Musorstom, vol 6. Mémoires du Muséum national d’Histoire naturelle, Paris, pp 71–136

    Google Scholar 

  • Cleva R (2001) Les Bathypalaemonellidae de Saint Laurent, 1985 (Crustacea, Decapoda, Caridea) avec description d’une espèce nouvelle et définition d’un genre nouveau. Zoosystema 23:757–782

    Google Scholar 

  • Cleva R (2004) Stylodactylidae and Bathypalaemonellidae from Taiwan (Crustacea: Decapoda: Caridea). Raffles Bull Zool 52:497–511

    Google Scholar 

  • Corliss JB, Ballard RD (1977) Oases of life in the cold abyss. Natl Geogr Mag 152:441–453

    Google Scholar 

  • Correa C, Thiel M (2003a) Mating systems in caridean shrimp (Decapoda: Caridea) and their evolutionary consequences for sexual dimorphism and reproductive biology. Rev Chil Hist Nat 76:187–203

    Article  Google Scholar 

  • Correa C, Thiel M (2003b) Population structure and operational sex ratio in the rock shrimp Rhynchocinetes typus (Decapoda: Caridea). J Crustac Biol 23:849–861

    Article  Google Scholar 

  • Correa C, Baeza JA, Dupré E, Hinojosa IA, Thiel M (2000) Mating behavior and fertilization success of three ontogenetic stages of male rock shrimp Rhynchocinetes typus (Decapoda: Caridea). J Crustac Biol 20:628–641

    Article  Google Scholar 

  • Correa C, Baeza JA, Hinojosa IA, Thiel M (2003) Male dominance hierarchy and mating tactics in the rock shrimp Rhynchocinetes typus (Decapoda: Caridea). J Crustac Biol 23:33–45

    Article  Google Scholar 

  • Covich AP (2006) Dispersal-limited biodiversity of tropical insular streams. Pol J Ecol 54:523–547

    Google Scholar 

  • Covich AP (2009) Freshwater ecology. In: Gillespie RG, Clague DA (eds) Encyclopedia of islands. University of California Press, Berkeley, pp 343–347

    Google Scholar 

  • Covich AP, McDowell WH (1996) The stream community. In: Reagan DP, Waide RB (eds) The food web of a tropical rain forest. University of Chicago Press, Chicago, pp 433–459

    Google Scholar 

  • Covich AP, Palmer MA, Crowl TA (1999) Role of benthic invertebrate species in freshwater ecosystems. Bioscience 49:119–127

    Article  Google Scholar 

  • Cowles DL (1994) Swimming dynamics of the mesopelagic vertically migrating penaeid shrimp Sergestes similis: modes and speed of swimming. J Crustac Biol 14:247–257

    Article  Google Scholar 

  • Criales MM (1997) Microprosthema granatense new species, from the southern Caribbean, with a key to shrimps of the genus Microprosthema from the western Atlantic and a new record of Odontozona liberate (Decapoda: Stenopodidea). J Crustac Biol 17:538–545

    Article  Google Scholar 

  • Crosnier A (1978) Crustacés Décapodes pénéides Aristeidae (Benthesicyminae, Aristeinae, Solenocerinae). Faune de Madagascar 46:1–197

    Google Scholar 

  • Crosnier A, Forest J (1973) Les crevettes profondes de l’Atlantique oriental tropical. Faune Tropicale (Cahiers de l’Office de la Recherche Scientifique et Technique Outre Mer), No. 19, p 409

    Google Scholar 

  • Cross WF, Covich AP, Crowl TA, Benstead JP, Ramirez A (2008) Secondary production, longevity, and consumption rates of freshwater shrimps in two tropical streams with contrasting geomorphology and food web structure. Freshw Biol 53:2504–2519

    Article  Google Scholar 

  • Crowl TA, Welsh V, Heartsill-Scalley T, Covich AP (2006) Effects of different types of conditioning on rates of leaf-litter shredding by Xiphocaris elongata, a neotropical freshwater shrimp. J N Am Benthol Soc 25:198–208

    Article  Google Scholar 

  • D’Onghia G, Maiorano P, Matarrese A, Tursi A (1998) Distribution, biology, and population dynamics of Aristaeomorpha foliacea (Risso, 1827) (Decapoda, Natantia, Aristeidae) in the northwestern Ionian Sea (Mediterranean Sea). Crustaceana 71:518–544

    Article  Google Scholar 

  • d’Udekem d’Acoz C (1996) The genus Hippolyte Leach, 1814 (Crustacea: Decapoda: Caridea: Hippolytidae) in the East Atlantic Ocean and the Mediterranean Sea, with a checklist of all species in the genus. Zoologische Verhandelingen, Leiden 303:1–133. https://repository.naturalis.nl/pub/317714

    Google Scholar 

  • d’Udekem d’Acoz C, Degrave S (2018) A new genus and species of large-bodied caridean shrimp from the Crozet Islands Southern Ocean (Crustacea Decapoda Lipkiidae) with a checklist of Antarctic and sub-Antarctic shrimps. Zootaxa 4392(2):201. https://doi.org/10.11646/zootaxa.4392.2.1

    Article  Google Scholar 

  • Dall W (2001) Australian species of Aristeidae and Benthesicymidae (Penaeoidea: Decapoda). Mem Queensl Mus 46:409–441

    Google Scholar 

  • Dall W (2007) Recent molecular research on Penaeus sensu lato. J Crustac Biol 27:380–382

    Article  Google Scholar 

  • Dall W, Hill BC, Rothlisberg PC, Sharples DJ (1990) The biology of the Penaeidae. Adv Mar Biol 27:1–489

    Google Scholar 

  • Dana TF, Newman WA, Fager EW (1973) Acanthaster aggregations: interpreted as primarily responses to natural phenomena. Pac Sci 26:355–372

    Google Scholar 

  • Dardeau MR (1984) Synalpheus shrimps (Crustacea: Decapoda: Alpheidae). I. The Gambarelloides group, with a description of a new species. Mem Hourglass Cruises 7:1–125

    Google Scholar 

  • Dardeau MR, Heard RW (1983) Crangonid shrimps (Crustacea: Caridea), with a description of a new species of Pontocaris. Mem Hourglass Cruises 6:39

    Google Scholar 

  • De Busserolles FJ, Gauthier O, Gélinas Y, Fabri MC, Sarradin PM, Desbruyères D (2009) Are spatial variations in the diets of hydrothermal fauna linked to local environmental conditions? Deep Sea Res II 56:1649–1664

    Article  Google Scholar 

  • De Grave S (2007) A new species of Euryrhynchus Miers, with a discussion of the systematic position of the Euryrhynchidae Holthuis (Crustacea, Decapoda). Zool Anz 246:193–203

    Article  Google Scholar 

  • De Grave S, Ashelby CW (2013) A re-appraisal of the systematic status of selected genera in Palaemoninae (Crustacea: Decapoda: Palaemonidae). Zootaxa 3734:331–344

    Article  PubMed  Google Scholar 

  • De Grave S, Fransen CHJM (2011) Carideorum catalogus: the recent species of the dendrobranchiate, stenopodidean, procarididean and caridean shrimps, vol 85. Zoologische Mededellingen, Leiden, pp 195–589

    Google Scholar 

  • De Grave S, Moosa MK (2004) A new species of the enigmatic shrimp genus Pseudocheles (Decapoda: Bresiliidae) from Sulawesi (Indonesia), with the designation of a new family Pseudochelidae. Crust Res 33:1–9

    Article  Google Scholar 

  • De Grave S, Livingston D, Speight MR (2006) Diel variation in sea grass dwelling shrimp: when to sample at night? J Mar Biol Assoc 86:1421–1422

    Article  Google Scholar 

  • De Grave S, Cai Y, Anker A (2008) Global diversity of shrimps (Crustacea: Decapoda: Caridea) in freshwater. Hydrobiologia 595:287–293

    Article  Google Scholar 

  • De Grave S, Chu KH, Chan T-Y (2010) On the systematic position of Galatheacaris abyssalis (Decapoda: Galatheacaridoidea). J Crustac Biol 30:521–527

    Article  Google Scholar 

  • De Grave S, Li CP, Tsang LM, Chu KH, Chan T-Y (2014) Unweaving hippolytoid systematics (Crustacea, Decapoda, Hippolytidae): resurrection of several families. Zool Scr 43:496–507

    Article  Google Scholar 

  • De Grave S, Fransen CHJM, Page TJ (2015a) Let’s be pals again: major systematic changes in Palaemonidae (Crustacea: Decapoda). PeerJ 3:e1167. https://doi.org/10.7717/peerj.1167

    Article  PubMed  PubMed Central  Google Scholar 

  • De Grave S, Chan T-Y, Chu KH, Yang CH, Landeira JM (2015b) Phylogenetics reveals the crustacean order Amphionidacea to be larval shrimps (Decapoda: Caridea). Sci Rep 5:17464. https://doi.org/10.1038/srep17464

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • De Grave S, Arjun CP, Raghavan R (2018a) The discovery of Euryrhynchidae (Crustacea: Decapoda) in India, with the description of a new genus and species. Zootaxa 4462:367–378

    Article  PubMed  Google Scholar 

  • De Grave S, Piscart C, Kayo RPT, Anker A (2018b) A new groundwater-dwelling species of Euryrhynchina from Cameroon (Malacostraca, Decapoda, Euryrhynchidae). Zootaxa 4254:120–126

    Article  Google Scholar 

  • Demestre M (1995) Moult activity-related spawning success in the Mediterranean deep-water shrimp Aristeus antennatus (Decapoda: Dendrobranchiata). Mar Ecol Prog Ser 127:57–64

    Article  Google Scholar 

  • Dietz RS, Holden JC (1972) The breakup of Pangaea. In: Wilson JT (ed) Scientific American, Continents Adrift. W.H. Freeman and Company, San Francisco, pp 102–113

    Google Scholar 

  • Dineshbabu AP, Manissery JK (2009) Food and feeding of the ridgeback shrimp, Solenocera choprai Nataraj, along Karnataka coast. Indian Journal of Fisheries 56:21–26

    Google Scholar 

  • Duffy JE (1996) Eusociality in a coral-reef shrimp. Nature 381:512–514

    Article  CAS  Google Scholar 

  • Duffy JE, Macdonald KS (2010) Kin structure, ecology and the evolution of social organization in shrimp: a comparative analysis. Proc R Soc Lond B 277:1–13

    Google Scholar 

  • Dumont CP, Urriagoa JD, Abarca A, Gaymer CF, Thiel M (2009) The native rock shrimp Rhynchocinetes typus as a biological control of fouling in suspended scallop cultures. Aquaculture 292:74–79

    Article  Google Scholar 

  • Felgenhauer BE, Abele LG (1983) Phylogenetic relationships among shrimp-like decapods. In: Schram FR (ed) Crustacean phylogeny. A.A. Balkema, Rotterdam, pp 291–311

    Google Scholar 

  • Felgenhauer BE, Abele LG, Kim W (1988) Reproductive morphology of the anchialine shrimp Procaris ascensionis. J Crustac Biol 8:333–349

    Article  Google Scholar 

  • Fiedler GC (1998) Functional, simultaneous hermaphroditism in female-phase Lysmata amboinensis (Decapoda: Caridea: Hippolytidae). Pac Sci 52:161–169

    Google Scholar 

  • FIGIS (Fisheries Global Information System) (2021) Global Capture Production 1950-2019. FI Institutional Websites. FAO Fisheries and Aquaculture Department, Rome, Italy. http://www.fao.org/fishery/statistics/global-capture-production/query/en

  • Flegel TW (2007) The right to refuse revision in the genus Penaeus. Aquaculture 264:2–8

    Article  Google Scholar 

  • Foxton P (1969) The morphology of the antennal flagellum of certain of the Penaeidea (Decapoda, Natantia). Crustaceana 16:33–43

    Article  Google Scholar 

  • Foxton P, Herring PJ (1970) Recent records of Physetocaris microphthalma Chace with notes on the male and description of the early larvae (Decapoda, Caridea). Crustaceana 18:93–104

    Article  Google Scholar 

  • Fransen CHJM (2010) Order Amphionidacea Williamson. 1973. In: Schram FR, von Vaupel Klein JC (eds) Treatise on zoology-anatomy, taxonomy, biology. The Crustacea, vol 9A. Brill, Leiden, pp 83–95

    Google Scholar 

  • Fransen CHJM, De Grave S (2009) Evolution and radiation of the shrimp-like Decapoda. In: Martin JW, Crandall KA, Felder DF (eds) Decapod phylogenetics. Crustacean issues 18. CRC Press, Boca Raton, FL, pp 245–260

    Chapter  Google Scholar 

  • Fransozo V, Costa RC, Bertini G, Cobos VJ (2005) Population biology of the spine shrimp Exhippolysmata oplophoroides in a subtropical region, São Paulo Brazil. Revista Brazileira de Zoologia 22:1078–1084

    Article  Google Scholar 

  • Fryer G (1977) Studies of the functional morphology and ecology of the atyid prawns of Dominica. Philos Trans R Soc Lond B Biol Sci 277:57–129

    Article  CAS  PubMed  Google Scholar 

  • Fujino T, Takeda M (1977) Levicaris mammillata (Edmondsn), a gnathophyllid shrimp associated with slate-pencil sea urchin, Heterocentrotus mammillatus (Linnaeus), from the Ogasawara and Ryukyu Islands. Bull Natl Mus Sci Ser A (Zool) 3:131–140

    Google Scholar 

  • Fuss CM (1964) Observations on burrowing behavior of the pink shrimp, Penaeus duorarum Burkenroad. Bull Mar Sci Gulf Caribb 14:62–73

    Google Scholar 

  • Gebruk AV, Pimenov NV, Savichev AS (1993) Feeding specialization of bresiliid shrimps in the TAG site hydrothermal community. Mar Ecol Prog Ser 98:247–253

    Article  Google Scholar 

  • Gherardi F, Calloni C (1993) Protandrous hermaphroditism in the tropical shrimp Athanas indicus (Decapoda: Caridea), a symbiont of sea urchins. J Crustac Biol 13:675–689

    Article  Google Scholar 

  • Gillikin DP, De Grave S, Tack JF (2001) The occurrence of the semi-terrestrial shrimp Merguia oligodon (De Man, 1888) in Neosarmatium smithi H. Milne Edwards, 1853 burrows in Kenyan mangroves. Crustaceana 74:505–508

    Article  Google Scholar 

  • Goy JW (2010) Infraorder Stenopodidea Claus, 1872. In: Schram FR, von Vaupel Klein JC, Forest J, Charmantier-Daures M (eds) Treatise on zoology – Anatomy, taxonomy, biology. The Crustacea, Decapoda. Vol 9. Part A: Eucarida: Euphausiacea, Amphionidacea, and Decapoda (partim). Koninklijke Brill NV, Leiden, pp 215–265

    Chapter  Google Scholar 

  • Gregati RA, Fransozo VL, Lopez-Greco LS, Negreiros-Fransozo ML (2010) Reproductive cycle and ovarian development of the marine ornamental shrimp Stenopus hispidus in captivity. Aquaculture 206:185–190

    Article  Google Scholar 

  • Gregati RA, Fransozo V, López-Greco LS, Negreiros-Fransozo ML, Bauer RT (2014) Functional morphology of the reproductive system and sperm transfer in Stenopus hispidus (Crustacea: Decapoda: Stenopodidea) and their relation to mating system. Invertebr Biol 133:381–393

    Article  Google Scholar 

  • Gros P (1979) Biologie de Processa nouveli Holthuisi, Al-Adhub et Williamson (Crustacea, Decapoda) dans le secteur nord du Golfe de Gascogne. Annals de l’Institut Océanographique Paris 55:49–70

    Google Scholar 

  • Guo ZL, Wang XQ, Zhang JP (2005) On the genus Exopalaemon (Decapoda, Caridea, Palaemonidae) in Guangdong Province, southern China. Crustaceana 78:839–850

    Article  Google Scholar 

  • Guy-Haim T, Simon-Blecher N, Frumkin A, Naaman I, Achituv Y (2018) Multiple transgressions and slow evolution shape the phylogeographic pattern of the blind cave-dwelling shrimp Typhlocaris. PeerJ 6:e26616v1. https://doi.org/10.7287/peerj.preprints.26616v1

    Article  Google Scholar 

  • Hacker SD, Madin LP (1991) Why habitat architecture and color are important to shrimps living in pelagic Sargassum: use of camouflage and plant-part mimicry. Mar Ecol Prog Ser 70:143–155

    Article  Google Scholar 

  • Haefner PA (1979) Comparative review of the biology of North Atlantic shrimps (Crangon), with emphasis on C. septemspinosa. Bull Biol Soc Wash 3:1–40

    Google Scholar 

  • Haley C, von der Meden C, Atkinson L, Reed C (2017) Habitat associations and distribution of the hyperbenthic shrimp, Nauticaris marionis, around the sub-Antarctic Prince Edward Islands. Deep Sea Res I 127:41–48

    Article  Google Scholar 

  • Hart JFL (1964) Shrimps of the genus Betaeus on the Pacific coast of North America with description of three new species. Proc U S Natl Mus 115:431–466

    Article  Google Scholar 

  • Hart CW, Manning RB (1986) Two new shrimps (Procarididae and Agostocarididae, new family) from marine caves of the western North Atlantic. J Crustac Biol 6:408–416

    Article  Google Scholar 

  • Hart CW, Manning RB, Iliffe TM (1985) The fauna of Atlantic marine caves: evidence of dispersal by sea floor spreading while maintaining ties to deep waters. Proc Biol Soc Wash 98:288–292

    Google Scholar 

  • Hay WP, Shore CA (1918) The decapod crustaceans of Beaufort, NC, and the surrounding region. Bull U S Bur Fish 35:369–476

    Google Scholar 

  • Hayashi K-I (1975) The Indo-West Pacific Processidae (Crustacea, Decapoda, Caridea). J Shimonoseki Univ Fish 24:47–145

    Google Scholar 

  • Hayashi K-I, Miyake S (1968) Notes on the family Stylodactylidae with the description of a new genus Neostylodactylus. J Fac Agric Kyushu Univ 14(4):583–611

    Article  Google Scholar 

  • Hayashi K-I, Miyake S (1970) Bathyhippolyte yaldwyni n. gen., n. sp., a deepsea hippolytid (Decapoda, Natantia) from New Zealand. R Soc N Z Biol Sci 12:41–47

    Google Scholar 

  • Hedgpeth JW (1949) The North American species of Macrobrachium. Tex J Sci 1:28–38

    Google Scholar 

  • Hedgpeth JW (1968) The atyid shrimps of the genus Syncaris in California. Internationale Revue der gesamten Hydrobiologie und Hydrographie 53:511–524

    Article  Google Scholar 

  • Heegaard P (1967) On the behaviour, sex-ratio and growth of Solenocera membranacea (Risso) (Decapoda, Penaeidae). Crustaceana 13:227–237

    Article  Google Scholar 

  • Hendrickx ME (2002) A new deep water species of Odontozona Holthuis (Decapoda, Stenopodidae) from the southern Gulf Of California, Mexico. Crustaceana 75:405–412

    Article  Google Scholar 

  • Hendrickx ME (2012) Distribution and abundance of the pelagic processid, Processa pippinae Wicksten & Méndez, 1985 (Decapoda, Caridea, Processidae), collected during the Talud XIV cruise in the Gulf Of California, Mexico, and description of a new genus. Crustaceana 85:463–472

    Article  Google Scholar 

  • Hendrickx ME (2014) First record of the caridean shrimp genus Bresilia Calman, 1896 (Crustacea: Decapoda: Bresiliidae) from the East Pacific and description of a new species. Zootaxa 3878:185–195

    Article  PubMed  Google Scholar 

  • Herring PJ (1981) The comparative morphology of hepatic photophores in decapod Crustacea. J Mar Biol Assoc U K 61:723–737

    Article  Google Scholar 

  • Herring PJ, Barnes AT (1976) Light stimulated bioluminescence of Thalassocaris crinita (Crustacea: Caridea). Crustaceana 31:107–109

    Article  Google Scholar 

  • Herring PJ, Roe HSJ (1988) The photoecology of pelagic oceanic decapods. Symp Zool Soc Lond 59:263–290

    Google Scholar 

  • Hobbs HH, Hart CW (1982) The shrimp genus Atya (Decapoda: Atyidae). Smithsonian Contributions to Zoology, No. 364, p 143

    Google Scholar 

  • Holthuis LB (1947) The Decapoda of the Siboga Expedition, part IX. The Hippolytidae and Rhynchocinetidae collected by the Siboga and Snellius Expeditions with remarks on other species. Siboga Expeditie 39a8:100

    Google Scholar 

  • Holthuis LB (1952a) A general revision of the Palaemonidae (Crustacea Decapoda Natantia) of the Americas. II. The subfamily Palaemoninae. Allan Hancock Foundation Publications, Occasional Papers 12:1–396

    Google Scholar 

  • Holthuis LB (1952b) The Decapoda of the Siboga Expedition. Part XI The Palaemonidae collected by the Siboga and Snellius Expeditions with remarks on other species II Subfamily Pontoniinae. Siboga Expéditie 39(A10):1–253

    Google Scholar 

  • Holthuis LB (1971) The Atlantic shrimps of the deep-sea genus Glyphocrangon. A. Milne Edwards, 1881. Bull Mar Sci 21:267–373

    Google Scholar 

  • Holthuis LB (1973) Caridean shrimps found in land-locked pools at four Indo-West Pacific localities (Sinai Peninsula, Funafuti Atoll, Maui and Hawaii islands), with the description of one new genus and four new species. Zoologische Verhandelingen 128:1–48

    Google Scholar 

  • Holthuis LB (1980) FAO species catalogue. Vol. 1. Shrimps and prawns of the world. An annotated catalogue of species of interest to fisheries. FAO Fisheries Synopsis 125, vol 1, p 261

    Google Scholar 

  • Holthuis LB (1993) The recent genera of the Caridean and Stenopodidean Shrimps (Crustacea, Decapoda): with an Appendix on the Order Amphionidacea. Nationaal Natuurhistorisch Museum, Leiden

    Google Scholar 

  • Hopkins TL, Flock ME, Gartner JV, Torres JJ (1994) Structure and trophic ecology of a low latitude midwater decapod and mysid assemblage. Mar Prog Ecol Ser 109:143–156

    Article  Google Scholar 

  • Horká I, De Grave S, Ďuriš Z (2014) A new species of shrimp of the genus Anachlorocurtis Hayashi, 1975 from the Red Sea, with range extension of A. commensalis Hayashi, 1975 (Crustacea, Decapoda, Pandalidae). ZooKeys 407:9–28

    Article  Google Scholar 

  • Hufnagl M, Temming A, Pohlmann T (2014) The missing link: tidal-influenced activity a likely candidate to close the migration triangle in brown shrimp Crangon crangon (Crustacea, Decapoda). Fish Oceanogr 23:242–257

    Article  Google Scholar 

  • Jensen GC (2011) Feeding behavior of the horned shrimp, Paracrangon echinata (Caridea: Crangonidae). J Crustac Biol 31:246–248

    Article  Google Scholar 

  • Jensen GC (2014) Crabs and Shrimps of the Pacific Coast. A guide to shallow-water Decapods from Southeastern Alaska to the Mexican Border. Mola Marine, Bremerton, Washington

    Google Scholar 

  • Jobe CF, Brooks WR (2009) Habitat selection and host location by symbiotic shrimps associated with Sargassum communities: the role of chemical and visual cues. Symbiosis 49:77–85

    Article  Google Scholar 

  • Johnson VR (1969) Behavior associated with pair formation in banded shrimp Stenopus hispidus (Olivier). Pac Sci 23:40–50

    Google Scholar 

  • Johnson VR (1977) Individual recognition in the banded shrimp Stenopus hispidus (Olivier). Anim Behav 25:418–428

    Article  Google Scholar 

  • Juarrero de Varona A (1993) Nueva especie del género Xiphocaris (Crustacea: Atyidae) de Cuba. Poeyana 440:1–12

    Google Scholar 

  • Judkins D, Kensley B (2008) New genera in the family Sergestidae (Crustacea: Decapoda: Penaeidea). Proc Biol Soc Wash 121:72–84

    Article  Google Scholar 

  • Kagwade PV (1982) The hermaphrodite prawn Hippolysmata ensirostris Kemp. Indian J Fish 28:189–194

    Google Scholar 

  • Kapiris K, Thessalou-Legaki M (2009) Comparative reproduction aspects of the deep-water shrimps Aristaeomorpha foliacea and Aristeus antennatus (Decapoda, Aristeidae) in the Greek Ionian Sea (Eastern Mediterranean). Int J Zool 2009:979512. https://doi.org/10.1155/2009/979512

    Article  Google Scholar 

  • Karplus I (1987) The association between gobiid fishes and burrowing alpheid shrimps. Oceanogr Mar Biol Annu Rev 25:507–562

    Google Scholar 

  • Karuppasamy PK, Menon NG, Nair KKC, Achuthankutty CT (2006) Distribution and abundance of pelagic shrimps from the deep scattering layer of the eastern Arabian Sea. J Shellfish Res 25:1013–1019

    Article  Google Scholar 

  • Katneni VK, Mudagandur SL, Jangam AK, Paran BC, Selvaraj A, Krishnan K, Kaikkolante N, Prabhudas SK, Gopalapillai G, Koyadan VK (2021) Phylogenetic relations and mitogenome-wide similarity metrics reveal monophyly of Penaeus sensu lato. Ecol Evol. https://doi.org/10.1002/ece3.7148

  • Kayal M, Vercelloni J, Lison de Loma T, Bosserelle P, Chancerelle Y, Geoffroy S, Stievenart C, Michonneau F, Penin L, Planes S, Adjeroud M (2012) Predator crown-of-thorns starfish (Acanthaster planci) outbreak, mass mortality of corals, and cascading effects on reef fish and benthic communities. PLoS One 7(10):e47363. https://doi.org/10.1371/journal.pone.0047363

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kensley B (1983) New records of bresiliid shrimp from Australia, South Africa, Caribbean, and Gulf of Mexico (Decapoda: Natantia: Caridea). Smithson Contrib Zool 394:1–31

    Article  Google Scholar 

  • Kensley B (1988) New species and records of cave shrimps from the Yucatan peninsula (Decapoda: Agostocarididae and Hippolytidae). J Crustac Biol 8:688–699

    Article  Google Scholar 

  • Kensley B, Walker U (1982) Palaemonid shrimps from the Amazon Basin, Brazil (Crustacea: Decapoda: Natantia). Smithson Contrib Zool 362:28

    Google Scholar 

  • Kensley B, Williams D (1986) New shrimps (families Procarididae and Atyidae) from a submerged lava tube on Hawaii. J Crustac Biol 6:417–437

    Article  Google Scholar 

  • Kikkert DA, Crowl TA, Covich AP (2009) Upstream migration of amphidromous shrimp in the Luquillo Experimental Forest, Puerto Rico: temporal patterns and environmental cues. J N Am Benthol Soc 28:233–246

    Article  Google Scholar 

  • Kim JN, Komai T (2002) Sclerocrangon gasuyebi Yokoya synonymized with Sclerocrangon salebrosa (Owen) (Decapoda, Caridea, Crangonidae). Crustaceana 74:1335–1347

    Article  Google Scholar 

  • Kitsos MS, Tzomos T, Anagnostopoulou L, Koukouras A (2008) Diet composition of the pandalid shrimp, Plesionika narval (Fabricius, 1787) (Decapoda, Pandalidae) in the Aegean sea. Crustaceana 81:23–33

    Article  Google Scholar 

  • Knowlton N (1980) Sexual selection and dimorphism in two demes of a symbiotic, pair-bonding snapping shrimp. Evolution 34:161–173

    Article  PubMed  Google Scholar 

  • Komai T (1994) Deep-Sea shrimps of the genus Pandalopsis (Decapoda: Caridea: Pandalidae) from the Pacific coast of eastern Hokkaido, Japan, with the description of two new species. J Crustac Biol 14:538–555

    Article  Google Scholar 

  • Komai T (1999) A revision of the genus Pandalus (Crustacea: Decapoda: Caridea: Pandalidae). J Nat Hist 33:1265–1372

    Article  Google Scholar 

  • Komai T (2004) Deep-sea shrimps of the genus Glyphocrangon A. Milne-Edwards (Crustacea, Decapoda, Caridea, Glyphocrangonidae) from off southeastern coast of Brazil collected during the Revizee Program. Arquivos do Museu Nacional (Rio de Janeiro) 62:31–44

    Google Scholar 

  • Komai T (2005) Current status of taxonomy of the family Glyphocrangonidae (Crustacea: Decapoda: Caridea). Taxa 19:8–19

    Google Scholar 

  • Komai T, Ivanov BG (2008) Identities of three taxa of the hippolytid shrimp genus Heptacarpus (Crustacea: Decapoda: Caridea), with description of a new species from East Asian waters. Zootaxa 1684:1–34

    Article  Google Scholar 

  • Komai T, Kohtsuka H (2017) A new deep-sea species of the caridean genus Bresilia Calman, 1896 (Crustacea: Decapoda: Bresiliidae) from Sagami Bay, central Japan. Zootaxa 4299:405–414

    Article  Google Scholar 

  • Komai T, Lin CW, Chan TY (2012) Bathypelagic Shrimp of the genus Pasiphaea (Decapoda: Caridea: Pasiphaeidae) from waters around Taiwan, with descriptions of four new species. J Crustac Biol 32:295–325

    Article  Google Scholar 

  • Komai T, de Grave S, Saito T (2016) Two new species of the stenopodidean shrimp genus Spongiocaris Bruce & Baba, 1973 (Crustacea: Decapoda: Spongicolidae) from the Indo-West Pacific. Zootaxa 4111:421–447

    Article  PubMed  Google Scholar 

  • Komai T, Chan T-Y, De Grave S (2019) Establishment of a new shrimp family Chlorotocellidae for four genera previously assigned to Pandalidae (Decapoda, Caridea, Pandaloidea). Zoosyst Evol 95:391–402

    Article  Google Scholar 

  • Komai T, Chan T-Y, Chang SC (2021) Redescription of the colorful deep-water shrimp Lebbeus compressus Holthuis, 1947 and description of a closely allied new species from Taiwan (Decapoda: Caridea: Thoridae). J Crustac Biol 41:1–13

    Google Scholar 

  • Kou Q, Li X, Chan T-Y, Chu KH, Gan Z (2013) Molecular phylogeny of the superfamily Palaemonoidea (Crustacea:Decapoda: Caridea) based on mitochondrial and nuclear DNA reveals discrepancies with the current classification. Invertebr Syst 27:502–514

    Article  Google Scholar 

  • Kuris AM, Ra’anan Z, Sagi A, Cohen D (1987) Morphotypic differentiaton of male Malaysian giant prawns, Macrobrachium rosenbergii. J Crustac Biol 7:219–237

    Article  Google Scholar 

  • Kutschera V, Maas A, Waloszek D, C, Haug and J, T. Haug. (2012) Re-study of larval stages of Amphionides reynaudii (Malacostraca: Eucarida) with modern imaging techniques. J Crustac Biol 32:916–930

    Article  Google Scholar 

  • Lakin RC, Jinks RN, Battelle BA, Herzog ED, Kass L, Renninger GH, Chamberlain SC (1997) Retinal anatomy of Chorocaris chacei, a deep-sea hydrothermal vent shrimp from the Mid-Atlantic Ridge. J Comp Neurol 385:503–514

    Article  CAS  PubMed  Google Scholar 

  • Laubenheimer H, Rhyne AL (2008) Experimental confirmation of protandric simultaneous hermaphroditism in a caridean shrimp outside of the genus Lysmata. J Mar Biol Assoc U K 88:301–305

    Article  Google Scholar 

  • Lee WY, Omori M, Peck RW (1992) Growth, reproduction and feeding behavior of the planktonic shrimp, Lucifer faxoni Borradaile, off the Texas coast. J Plankton Res 14:61–69

    Article  Google Scholar 

  • Li X, Mitsuhashi M, Chan T-Y (2008) Deep-sea pontoniines (Decapoda: Palaemonidae) from the Philippine “Panglao 2005” expedition, with descriptions of four new species. J Crustac Biol 28:385–411

    Article  Google Scholar 

  • Li CP, De Grave S, Chan T-Y, Lei HC, Chu KH (2011) Molecular systematics of caridean shrimps based on five nuclear genes: implications for superfamily classification. Zool Anz 250:270–279

    Article  Google Scholar 

  • Liao YS, De Grave TW, Hoa BHY, Ip LM, Tsang TYC, Chua KH (2017) Molecular phylogeny of Pasiphaeidae (Crustacea, Decapoda, Caridea) reveals systematic incongruence of the current classification. Mol Phylogenet Evol 115:171–180

    Article  PubMed  Google Scholar 

  • Liao Y, Ma KY, De Grave S, Komai T, Chan T-Y, Chu KH (2019) Systematic analysis of the caridean superfamily Pandaloidea (Crustacea: Decapoda) based on molecular and morphological evidence. Mol Phylogenet Evol 134:200–210

    Article  CAS  PubMed  Google Scholar 

  • Limbaugh C, Pederson H, Chace FA (1961) Shrimps that clean fishes. Bull Mar Sci 11:237–257

    Google Scholar 

  • Lisowski EA (1983) Distribution, habitat, and behavior of the Kentucky cave shrimp Palaemonias ganteri Hay. J Crustac Biol 3:88–92

    Article  Google Scholar 

  • Lloyd AJ, Yonge CM (1947) The biology of Crangon vulgaris L. in the Bristol Channel and Severn Estuary. J Mar Biol Soc U K 26:626–661

    Article  CAS  Google Scholar 

  • Lunina AA, Kulagin DN, Vereshchaka AL (2019) Oplophoridae (Decapoda: Crustacea): phylogeny, taxonomy, and evolution studied by a combination of morphological and molecular methods. Zool J Linn Soc 186:213–232

    Article  Google Scholar 

  • Lyons PJ (2013) The benefit of obligate versus facultative strategies in a shrimp–goby mutualism. Behav Ecol Sociobiol. https://doi.org/10.1007/s00265-013-1497-6

  • Ma KY, Chan T-Y, Chu KH (2011) Refuting the six-genus classification of Penaeus s.l. (Dendrobranchiata, Penaeidae): a combined analysis of mitochondrial and nuclear genes. Zool Scr 40:498–508

    Article  Google Scholar 

  • Maciá S, Robinson MP (2009) Why be cryptic? Choice of host urchin is not based on camouflage in the caridean shrimp Gnathophylloides mineri. Acta Ethol 12:105–113

    Article  Google Scholar 

  • Magalhães C (1988) The larval development of palaemonid shrimps from the Amazon region reared in the laboratory. II. Extremely abbreviated larval development in Euryrhynchus Miers, 1877 (Decapoda, Euryrhynchinae). Crustaceana 55:39–52

    Article  Google Scholar 

  • Magalhães C, Campos MR, Collins PA, Mantelatto FL (2016) Diversity, distribution and conservation of freshwater crabs and shrimps in South America. In: Kawai T, Cumberlidge N (eds) A global overview of the conservation of freshwater decapod crustaceans. Springer, Cham, pp 303–322. https://doi.org/10.1007/978-3-319-42527-6_10

    Chapter  Google Scholar 

  • Manning RB (1963) The east American species of Gnathophyllum (Decapoda, Caridea), with the description of a new species. Crustaceana 5:47–63

    Article  Google Scholar 

  • Manning RB, Chace FA (1971) Shrimps of the family Processidae from the Northwestern Atlantic Ocean (Crustacea: Decapoda: Caridea). Smithson Contrib Zool 89:41

    Google Scholar 

  • Manning RB, Hart CW (1991) A new species of Processa from Bermuda (Crustacea: Decapoda: Caridea). Proc Biol Soc Wash 104:317–321

    Google Scholar 

  • Marin I (2010) Redescription of the alpheid shrimp Betaeus levifrons Vinogradov, 1950 (Crustacea, Decapoda, Alpheidae) from Peter the Great Bay, Russian coast of the Sea of Japan. Zootaxa 2613:51–60

    Article  Google Scholar 

  • Marin I, Chan T-Y (2011) New records of the caridean shrimp family Thalassocarididae Bate, 1888 (Decapoda, Caridea) from Asia. Crustaceana 84:243–249

    Article  Google Scholar 

  • Marin I, Okuno J, Chan T-Y (2011) On the “Hippolyte commensalis Kemp, 1925” species complex (Decapoda, Caridea, Hippolytidae), with the designation of a new genus and description of two new species from the Indo-West Pacific. Zootaxa 2768:32–54

    Article  Google Scholar 

  • Martin JW (1986) A late embryo of the deep water shrimp Psalidopus barbouri Chace, 1939 (Decapoda, Caridea). Crustaceana 51:299–302

    Article  Google Scholar 

  • Martin JW, Davis GE (2001) An updated classification of the recent Crustacea. Nat Hist Mus Los Ang Contrib Sci 39:124

    Google Scholar 

  • Martin JW, Kutschera V (2014) Amphionidacea. In: Martin JW, Olesen J, Høeg JT (eds) Atlas of crustacean larvae. Johns Hopkins University Press, Baltimore, pp 226–229

    Chapter  Google Scholar 

  • Martin JW, Wicksten MK (2004) Review and redescription of the freshwater atyid shrimp genus Syncaris Holmes, 1900, in California. J Crustac Biol 24:447–462

    Article  Google Scholar 

  • Mascetti P, Fernandez R, Albornoz L, Oyarzún S, Gorny M, Wehrtmann I (1997) Gonopore development and sex change in the Antarctic shrimp Chorismus antarcticus (Caridea: Hippolytidae). Polar Biol 17:384–388

    Article  Google Scholar 

  • Mathews LM (2007) Evidence for high rates of in-pair paternity in the socially monogamous snapping shrimp Alpheus angulosus. Aquat Biol 1:55–62

    Article  Google Scholar 

  • McDowall RM (2007) On amphidromy, a distinct form of diadromy in aquatic organisms. Fish Fish 8:1–13

    Article  Google Scholar 

  • McLaughlin PA, Lemaitre R, Ferrari FD, Felder DL, Bauer RT (2008) A reply to T.W. Flegel. Aquaculture 275:370–373

    Article  Google Scholar 

  • Mejía LM, Zarza E, López M (2008) Barbouria yanezi sp. nov., a new species of cave shrimp (Decapoda, Barbouriidae) from Cozumel island Mexico. Crustaceana 81:663–672

    Article  Google Scholar 

  • Mejía-Ortíz LM, Yañez G, López-Mejía M (2017) Anchialocarididae, a new family of anchialine decapods and a new species of the genus Agostocaris from Cozumel Island, Mexico. Crustaceana 90:381–398

    Article  Google Scholar 

  • Méndez MG (1981) Claves para la identificación y distribución de los langostinos y camarones (Crustacea, Decapoda) del mar y ríos de la costa del Perú. Boletín Instituto del Mar del Perú 5:1–170

    Google Scholar 

  • Menon PG, Williamson DI (1971) Decapod Crustacea from the International Indian Ocean Expedition; the species of Thalassocaris and their larvae. J Zool (Lond) 165:27–51

    Article  Google Scholar 

  • Meyer R, Lochner R, Melzer R (2009) Decapoda – crabs, shrimps & lobsters. In: Häussermann V, Försterra G (eds) Marine Benthic Fauna of Chilean Patagonia. Nature in Focus, Santiago, Chile, pp 623–670

    Google Scholar 

  • Misamore MJ, Browdy CL (1996) Mating behavior in the white shrimps Penaeus setiferus and P. vannamei: a generalized model for mating in Penaeus. J Crustac Biol 16:61–70

    Article  Google Scholar 

  • Moore PG, Rainbow PS, Larson RJ (1993) The mesopelagic Notostomus robustus Smith (Decapoda: Oplophoridae) observed in situ feeding on the medusan Atolla wyvillei Haeckel in the northwest Atlantic, with notes on gut contents and mouthpart morphology. J Crustac Biol 13:690–696

    Article  Google Scholar 

  • Murray KB, Demko AM, Ward BK, Delillo CA, Balazadeh K, Bourque BD, Rhyne AL (2012) The absence of male features and functionality in the monotypic shrimp genus Lysmatella, a simultaneous hermaphrodite. Meeting Abstract, Society for Integrative and Comparative Biology

    Google Scholar 

  • Nakashima Y (1987) Reproductive strategies in a partially protandric shrimp, Athanas kominatoensis (Decapoda: Alpheidae): sex change as the best of a bad situation for subordinates. J Ethol 5:145–159

    Article  Google Scholar 

  • Noël P (1973) Cycle biologique et inversion sexuelle du crustacés Décapode Natantia Processa edulis. Cah Biol Mar 14:217–227

    Google Scholar 

  • Noël P (1976) L’évolution des caractères sexuels chez Processa edulis (Risso) (Décapode, Natantia). Vie et Milieu 26:65–104

    Google Scholar 

  • Noël P, Chassard-Bouchaud C (1994) Chromatophores et pigmentation. In: Forest J (ed) Traité de Zoologie. Tome VII. Crustacés. Fascicule I. Masson, Paris, pp 91–105

    Google Scholar 

  • Nouvel H, Holthuis LB (1957) Les Processidae (Crustacea Decapoda Natantia) des eaux européennes, vol 32. Zoologische Verhandelingen, Leiden, pp 1–53

    Google Scholar 

  • Ohtomi J, Irieda S (1997) Growth of the deep-water mud shrimp Solenocera melanthos De Man, 1907 (Decapoda, Penaeoidea, Solenoceridae) in Kagoshima Bay, Southern Japan. Crustaceana 70:45–58

    Article  Google Scholar 

  • Okuno J (1997a) Crustacea Decapoda: review on the genus Cinetorhynchus Holthuis, 1995 from the Indo-West Pacific (Caridea: Rhynchocinetidae). In: Richer de Forges B (ed) Les Fond Meubles Des Lagons De Nouvelle-Calédonie (Sédimentologie, Benthos). Études et Thèses, vol 3. ORSTOM, Paris, pp 31–58

    Google Scholar 

  • Okuno J (1997b) A new shrimp of the genus Rhynchocinetes from the great Australian Bight (Crustacea: Decapoda: Rhynchocinetidae). Records South Austr Mus 30:13–18

    Google Scholar 

  • Oliveira MV, Costa-Souza AC, Guimarães F, Almeida AO, Baeza JA (2015) Observations on the life history of a rare shrimp, Salmoneus carvachoi (Crustacea: Caridea: Alpheidae), a possible simultaneous hermaphrodite. Mar Biodivers Rec. https://doi.org/10.1017/S1755267215001219

  • Omori M (1974) The biology of pelagic shrimps in the ocean. Adv Mar Biol 12:233–324

    Article  Google Scholar 

  • Omori M (1979) Growth, feeding, and mortality of larval and early postlarval stages of the oceanic shrimp Sergestes similis Hansen. Limnol Oceanogr 24:273–288

    Article  Google Scholar 

  • Onaga T, Fiedler GC, Baeza JA (2012) Protandric simultaneous hermaphroditism in Parahippolyte misticia (Crustacea: Decapoda: Hippolytidae): implications for the evolution of mixed sexual systems in marine shrimps. J Crustac Biol 32:383–394

    Article  Google Scholar 

  • Orsi Relini L, Relini G (1998) Seventeen instars of adult life in female Aristeus antennatus (Crustaeea: Decapoda: Aristeidae). A new interpretation of life span and growth. J Nat Hist 32:1719–1734

    Article  Google Scholar 

  • Orsi Relini L, Tunesi L (1987) The structure of the spermatophore in Aristeus antennatus (Risso, 1816). Investig Pesq 51(1):461–470

    Google Scholar 

  • Ortega A, Queiroga H, González-Gordillo JI (2005) Planktonic stages of Processa macrodactyla (Decapoda: Caridea: Processidae) reared in the laboratory. J Mar Biol Assoc U K 85:1449–1460

    Article  Google Scholar 

  • Ortmann AE (1894) A study of systematic and geographical distribution of the decapod family Atyidae Kingsley. Proc Acad Natl Sci Phila 46:397–416

    Google Scholar 

  • Ory NC, Dudgeon D, Duprey N, Thiel M (2014) Effects of predation on diel activity and habitat use of the coral-reef shrimp Cinetorhynchus hendersoni (Rhynchocinetidae). Coral Reefs 33:639–650

    Article  Google Scholar 

  • Osawa Y, Aoki MN, Thiel M, Bauer RT (2015) Analysis of life-history traits in a sex-changing marine shrimp (Decapoda: Caridea: Rhynchocinetidae). Biol Bull 228:125–136

    Article  PubMed  Google Scholar 

  • Pachelle PPG, Tavares M (2018) The freshwater shrimp family Euryrhynchidae (Crustacea: Decapoda: Caridea) revisited, with a taxonomic revision of the genus Euryrhynchus Miers, 1878. Zootaxa 4380:1–110

    Article  PubMed  Google Scholar 

  • Pakhomov EA, Kuun PJ, McQuaid CD (2000) Biology of the bottom-dwelling shrimp Nauticaris marionis Bate, 1888 at the sub-Antarctic Prince Edward Islands. Polar Biol 23:522–530

    Article  Google Scholar 

  • Papiol V, Hendrickx ME (2016) Ecology of Benthesicymus tanneri Faxon, 1893 (Dendrobranchiata: Benthesicymidae) from the Mexican Pacific slope. J Crustac Biol 36:50–60

    Article  Google Scholar 

  • Patton WK, Patton RJ, Barnes A (1985) On the biology of Gnathophylloides mineri, a shrimp inhabiting the sea urchin Tripneustes ventricosus. J Crustac Biol 5:616–626

    Article  Google Scholar 

  • Pearse AS, Humm HJ, Wharton GW (1942) Ecology of sand beaches at Beaufort. N C Ecological Monographs 12:135–190

    Article  CAS  Google Scholar 

  • Pelli DG, Chamberlain SC (1989) The visibility of 350 °C black-body radiation by the shrimp Rimicaris exoculata and man. Nature 337:460–461

    Article  CAS  PubMed  Google Scholar 

  • Penn JW (1984) The behavior and catchability of some commercially exploited penaeids and their relationship to stock and recruitment. In: Gulland JA, Rothschild BJ (eds) Penaeid shrimps: their biology and management. Fishing News Books, Farnham, Surrey, pp 173–186

    Google Scholar 

  • Pérez Farfante I (1975) Spermatophores and thelyca of the American white shrimps, genus Penaeus, subgenus Litopenaeus. Fish Bull 73:463–486

    Google Scholar 

  • Pérez Farfante I (1977) American solenocerid shrimps of the genera Hymenopenaeus, Haliporoides, Pleoticus, Hadropenaeus new genus, and Mesopenaeus new genus. Fish Bull 75:261–346

    Google Scholar 

  • Pérez Farfante I (1980) Revision of the penaeid shrimp genus Penaeopsis (Crustacea: Decapoda). Fish Bull 77:721–773

    Google Scholar 

  • Pérez Farfante I (1985) The rock shrimp genus Sicyonia (Crustacea: Decapoda: Penaeoidea) in the Eastern Atlantic. Fish Bull 83:1–79

    Google Scholar 

  • Pérez FI, Kensley B (1997) Penaeoid and sergestoid shrimps and prawns of the world. Keys and diagnoses for the families and genera. Mémoires du Muséum National d’Histoire Naturelle 175:1–233

    Google Scholar 

  • Pérez Reyes O, Crowl TA, Covich AP (2015) Effects of food supplies and water temperature on growth rates of two species of freshwater tropical shrimps. Freshw Biol. https://doi.org/10.1111/fwb.12584

  • Pillai MC, Griffin FJ, Clark WB Jr (1988) Induced spawning of the decapod crustacean Sicyonia ingentis. Biol Bull 174:181–185

    Article  Google Scholar 

  • Poore GCB (2009) Leontocaris alexander, a new deepwater hippolytid shrimp from Tasmanian seamounts and a phylogeny of the genus (Decapoda, Caridea). Crustaceana 82:951–967

    Article  Google Scholar 

  • Powell CB (1976) Two new freshwater shrimps from West Africa: the first euryrhynchinids (Decapoda Palaemonidae) reported from the Old World. Revue de Zoologie Africaine 90:883–902

    Google Scholar 

  • Powell CB (1977) A revision of the African freshwater shrimp genus Desmocaris Sollaud, with ecological notes and description of a new species (Crustacea, Decapoda, Palaemonidae). Revue Zoologique Africaine 91:649–674

    Google Scholar 

  • Powell CB (1979a) Three alpheid shrimp species of a new genus from West African fresh and brackish waters: taxonomy and ecological zonation (Crustacea Decapoda Natantia). Revue Zoologique Africaine 93:116–150

    Google Scholar 

  • Powell CB (1979b) Suppression of larval development in the African freshwater shrimp Desmocaris trispinosa (Aurivillius) (Decapoda Palaemonidae). Crustaceana 5:185–194

    Google Scholar 

  • Prakash S, Kumar TTA (2013) Feeding behavior of harlequin shrimp Hymenocera picta Dana, 1852 (Hymenoceridae) on sea star Linckia laevigata (Ophidiasteridae). J Threat Taxa 5:4819–4821

    Article  Google Scholar 

  • Prakash S, Babu I, Gopi M, Thangappanpillai T, Kumar A, Balasubramanian T (2011) Discovery of the shrimp Pycnocaris chagoae Bruce, 1972 (Decapoda: Caridea: Gnathophyllidae) in the Lakshadweep Archipelago, India. Zootaxa 2998:66–68

    Article  Google Scholar 

  • Prakash S, Ajithkumar TT, Bauer R, Thiel M, Subramoniam T (2016) Reproductive morphology and mating behavior in the hingebeak shrimp Rhynchocinetes durbanensis Gordon, 1936 (Decapoda: Caridea: Rhynchocinetidae) in India. J Mar Biol Assoc U K 96:1331–1340

    Article  Google Scholar 

  • Pratoomyot J, Choosria S, Muthuwan V, Luangoon N, Charoendee W, Phuangsanthia W, Shinn AP (2018) Sand star, Astropecten indicus Döderlein, 1888, as an alternative live diet for captive harlequin shrimp, Hymenocera picta Dana, 1852. Aquaculture 484:51–36

    Article  Google Scholar 

  • Provenzano AJ (1978) Feeding behavior of the primitive shrimp, Procaris (Decapoda, Procarididae). Crustaceana 35(2):170–176

    Article  Google Scholar 

  • Rainer SF (1992) Diet of prawns from the continental slope of north-western Australia. Bull Mar Sci 50:258–274

    Google Scholar 

  • Rasch JA, Bauer RT (2015) Reproductive pattern and sexual system of the nocturnal seagrass shrimp Ambidexter symmetricus (Decapoda: Caridea: Processidae) in a Florida bay. Mar Freshw Res 67:1141–1152

    Article  Google Scholar 

  • Rasch JA, Bauer RT (2016) The functional morphology and role of the thelycum in insemination, and its relation to the mating system in the seagrass shrimp Ambidexter symmetricus (Decapoda: Processidae). Invertebr Biol 135:163–173

    Article  Google Scholar 

  • Rétaux S, Casane D (2013) Evolution of eye development in the darkness of caves: adaptation, drift, or both? EvoDevo 4:26. https://doi.org/10.1186/2041-9139-4-26

    Article  PubMed  PubMed Central  Google Scholar 

  • Rhyne AL, Lin J (2006) A western Atlantic peppermint shrimp complex: redescription of Lysmata wurdemanni, description of four new species, and remarks on Lysmata rathbunae (Crustacea: Decapoda: Hippolytidae). Bull Mar Sci 79:165–204

    Google Scholar 

  • Rice AL (1981) The abdominal locking mechanism in the deep-sea shrimp genus Glyphocrangon (Decapoda, Glyphocrangonidae). Crustaceana 40:316–319

    Article  Google Scholar 

  • Rieley G, Van Dover CL, Hedrick DB, Eglinton G (1999) Trophic ecology of Rimicaris exoculata: a combined lipid abundance/stable isotope approach. Mar Biol 133:495–499

    Article  Google Scholar 

  • Saito T, Komai T (2008) A review of species of the genera Spongicola de Haan, 1844 and Paraspongicola de Saint Laurent & Cleva, 1981 (Crustacea, Decapoda, Stenopodidea, Spongicolidae). Zoosystema 30:87–147

    Google Scholar 

  • Saito T, Konishi K (1999) Direct development in the sponge-associated deep-sea shrimp Spongicola japonica (Decapoda: Spongicolidae). J Crustac Biol 19:46–52

    Article  Google Scholar 

  • Saito T, Takeda M (2003) Phylogeny of the Spongicolidae (Crustacea: Stenopodidae): evolutionary trend from shallow-water free-living to deep-water sponge-associated habitat. J Mar Biol Assoc U K 83:119–131

    Article  Google Scholar 

  • Saito T, Uchida I, Takeda M (2002) Skeletal growth of the deep-sea hexactinellid sponge Euplectella oweni, and host selection by the symbiotic shrimp Spongicola japonica (Crustacea: Decapoda: Spongicolidae). J Zool 258:521–529

    Article  Google Scholar 

  • Saito T, Tsuchida S, Yamamoto T (2006) Spongicoloides iheyaensis, a new species of dee-sea sponge-associated shrimp from the Iheya Ridge, Ryukyu Islands, southern Japan (Decapoda: Stenopodidea: Spongicolidae). J Crustac Biol 29:224–233

    Article  Google Scholar 

  • Saito T, Okuno J, Chan T-Y (2009) A new species of Stenopus (Crustacea: Decapoda: Stenopodidae) from the Indo-West Pacific, with a redefinition of the genus. Raffles Bull Zool 20:109–120

    Google Scholar 

  • Sardà F, Company JB, Costa C (2005) Morphological approach for relating decapod crustacean cephalothorax shape with distribution in the water column. Mar Biol 147:611–618

    Article  Google Scholar 

  • Scelso MA (1991) Cópula en cautiverio y desove del camarón Artemesia longinarus Bate, 1888 (Decapoda, Penaeidae). Informes Técnicos de Scientia Marina 164:16

    Google Scholar 

  • Schaffmeister BE, Hiddink JG, Wim JW (2006) Habitat use of shrimps in the intertidal and shallow subtidal seagrass beds of the tropical Banc d’Arguin, Mauritania. J Sea Res 55:230–243

    Article  Google Scholar 

  • Segonzac M, de Saint Laurent M, Casanova B (1993) L’énigme du compartement ophique des crevettes Alvinocarididae des sites hydrothermaux de la dorsale médio-Atlantique. Cah Biol Mar 34:535–571

    Google Scholar 

  • Seibt U (1973) Sense of smell and pair-bond in Hymenocera picta. Micronesica 9:231–236

    Google Scholar 

  • Seibt U, Wickler W (1979) The biological significance of the pair-bond in the shrimp Hymenocera picta. Zeitschrift fur Tierpyschologie 50:166–179

    Google Scholar 

  • Shumway SE, Perkins HC, Schick DF, Stickney AP (1985) Synopsis of biological data on the pink shrimp, Pandalus borealis Kröyer, 1838. NOAA Technical Report NMFS 30. FAO Fisheries Synopsis No 144:1–57

    Google Scholar 

  • Smaldon G (1979) British coastal shrimps and prawns. Academic Press, London

    Google Scholar 

  • Sokolov V (2000) Deep-sea shrimps of the genus Bythocaris G.O. Sars in the collections of Russian museums, with the description of a new species (Crustacea: Decapoda: Hippolytidae). Zool Meded 74:403–468

    Google Scholar 

  • Sokolov VI, Spiridonov VA (2006) Development of external sexual characters of deep sea Bythocaris shrimps (Crustacea: Decapoda: Hippolytidae). J Mar Biol Assoc UK 86:349–359

    Article  Google Scholar 

  • Suzuki H (1970) Taxonomic review of four alpheid shrimps belonging to the genus Athanas with reference to their sexual phenomena. Sci Rep Yokohama Natl Univ Sect 2(17):1–37

    Google Scholar 

  • Tavares C, Martin JW (2010) Suborder Dendrobranchiata Bate, 1888. In: Schram FR, von Vaupel Klein JC (eds) Treatise on zoology - Anatomy, taxonomy, biology - The Crustacea Volume 9 Part A. Koninklijke Brill NV, Leiden, pp 99–164

    Chapter  Google Scholar 

  • Taylor J, Poore GCB (1998) A review of the genus Leontocaris (Crustacea: Caridea: Hippolytidae) with descriptions of three species from southeastern Australian seamounts and slope. Mem Mus Vic 57:57–69

    Article  Google Scholar 

  • Thatje S (2003) Campylonotus arntzianus, a new species of the Campylonotidae (Crustacea: Decapoda: Caridea) from the Scotia Sea (Antarctica). Polar Biol 26:242–248

    Article  Google Scholar 

  • Thatje S, Lovrich GA, Anger K (2004) Egg production, hatching rates, and abbreviated larval development of Campylonotus vagans Bate, 1888 (Crustacea: Decapoda: Caridea) in subantarctic waters. J Exp Mar Biol Ecol 301:15–27

    Article  Google Scholar 

  • Thiel M, Chak STC, Dumont CP (2010) Male morphotypes and mating behavior of the dancing shrimp Rhynchocinetes brucei (Decapoda: Caridea). J Crustac Biol 30:580–588

    Article  Google Scholar 

  • Thompson JV (1829) On the luminosity of the ocean, with descriptions of some remarkable species of luminous animals (Pyrosoma pigmaea and Sappharina indicator) and particularly of the four new genera, Noctiluca, Cynthia, Lucifer, and Podopsis, of the Shizopodae. In: Hennessy J (ed) Zoological researches, and illustrations; or, natural history of nondescript or imperfectly known animals, in a series of memoirs, illustrated by numerous figures. Memoir 3. French Church Street Press, Cork, pp 37–66. Plates 5–8

    Google Scholar 

  • Thompson JR (1967) Comments on phylogeny of section Caridea (Decapoda Natantia) and the phylogenetic importance of the Oplophoroidea. In: Proceedings Symposium on Crustacea, Ernakulam, Marine Biological Association India, vol 1. Marine Biological Association of India, Cochin, pp 314–326

    Google Scholar 

  • Toriyama M, Horikawa H (1993) A New Caridean Shrimp, Psalidopus tosaensis, from Tosa Bay, Japan (Decapoda: Caridea, Psalidopodidae). Bull Nansei Natl Fish Res Inst 26:1–8

    Google Scholar 

  • Torti MR, Boschi EE (1973) Nuevos aportos al conociemento de los crustáceos Decápodos Caridea del género Campylonotus Bate 1988. Physis Sección A 32:65–84

    Google Scholar 

  • Toth E, Bauer RT (2007) Gonopore sexing technique allows determination of sex ratios and helper composition in eusocial shrimps. Mar Biol 151:1875–1886

    Article  Google Scholar 

  • Tsurnamal M (1978) The biology and ecology of the blind prawn, Typhlocaris galilea Calman (Decapoda, Caridea). Crustaceana 34:195–213

    Article  Google Scholar 

  • Tsurnamal M (2008) A new species of the stygobiotic blind prawn Typhlocaris Calman, 1909 (Decapoda, Palaemonidae, Typhlocaridinae) from Israel. Crustaceana 81:487–501

    Article  Google Scholar 

  • Tunesi L (1987) La formation du spermatophore chez Aristaeomorpha foliacea (Risso, 1827). Investig Pesq 51(1):471–476

    Google Scholar 

  • Van Dover CL, Fry B, Grassle JF, Humphries S, Rona P (1988) Feeding biology of the shrimp Rimicaris exoculata at hydrothermal vents on the Mid-Atlantic Ridge. Mar Biol 98:209–216

    Article  Google Scholar 

  • Van Dover CL, Szuts EZ, Chamberlain SC, Cann JR (1989) A novel eye in “eyeless” shrimp from hydrothermal vents of the Mid-Atlantic Ridge. Nature 337:458–460

    Article  PubMed  Google Scholar 

  • Vaughan DB, Grutter AS, Costello MJ, Hutson KS (2016) Cleaner fishes and shrimp diversity and a re-evaluation of cleaning symbioses. Fish Fish 2016:1–19. https://doi.org/10.1111/faf.12198

    Article  Google Scholar 

  • Vereshchaka AL (1997) New family and superfamily for a deep-sea caridean shrimp from the Galathea collections. J Crustac Biol 17:361–373

    Article  Google Scholar 

  • Vereshchaka AL (2017) The shrimp superfamily Sergestoidea: a global phylogeny with definition of new families and an assessment of the pathways into principal biotopes. R Soc Open Sci 4:170221. https://doi.org/10.1098/rsos.170221

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Vereshchaka AL, Olesen J, Lunina AA (2014) Global diversity and phylogeny of pelagic shrimps of the former genera Sergestes and Sergia (Crustacea, Dendrobranchiata, Sergestidae), with definition of eight new genera. PLoS One 9:e112057. https://doi.org/10.1371/journal.pone.0112057

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Vereshchaka AL, Kulagin DN, Lunina AA (2015) Phylogeny and new classification of hydrothermal vent and seep shrimps of the family Alvinocarididae (Decapoda). PLoS One 10(7):e0129975. https://doi.org/10.1371/journal.pone.0129975

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Vereshchaka AL, Olesen J, Lunina AA (2016) A phylogeny-based revision of the family Luciferidae De Haan, 1849 (Crustacea: Decapoda). Zool J Linn Soc 178:15–32

    Article  Google Scholar 

  • Vereshchaka AL, Corbari L, Kulagin DN, Lunina AA, Olesen J (2019) A phylogeny-based revision of the shrimp genera (Crustacea: Decapoda: Benthesicymidae). Zool J Linn Soc 189:207–227

    Article  Google Scholar 

  • Vereshchaka AL, Kulagin DN, Lunina AA (2021) Across the benthic and pelagic realms: a species-level phylogeny of Benthesicymidae (Crustacea: Decapoda). Invertebr Syst 35:776–796

    Article  Google Scholar 

  • von Rintelen K, Cai Y (2007) Radiation of endemic species flocks in ancient lakes: systematic revision of the freshwater shrimp Caridina H. Milne Edwards, 1837 (Crustacea: Decapoda: Atyidae) from the ancient lakes of Sulawesi, Indonesia, with the description of eight new species. Raffles Bull Zool 57:343–452

    Google Scholar 

  • von Rintelen K, Page TJ, Cai Y, Roe K, Stelbrink B (2012) Drawn to the dark side: a molecular phylogeny of freshwater shrimps (Crustacea: Decapoda: Caridea: Atyidae) reveals frequent cave invasions and challenges current taxonomic hypotheses. Mol Phylogenet Evol 63:82–96

    Article  Google Scholar 

  • Voss GL (1956) Protective coloration and habitat of the shrimp Tozeuma carolinensis Kingsley (Caridea: Hippolytidae). Bull Mar Sci 6:359–363

    Google Scholar 

  • Walker I (1992) Life history traits of shrimps (Decapoda: Palaemonldae) of Amazonian inland waters and their phylogenetic interpretation. Stud Neotropical Fauna Environ 27:131–143

    Article  Google Scholar 

  • Wang Y, Ma KY, Tsang LM, Wakabayashi K, Chan T-Y, De Grave S, Chu KH (2021) Confirming the systematic position of two enigmatic shrimps, Amphionides and Procarididae (Crustacea: Decapoda). Zool Scr 50:812–823

    Article  Google Scholar 

  • Wasmer RA (1985) Records for Physetocaris microphthalma Chace (Decapoda, Caridea, Physetocarididae). Crustaceana 49:315–321

    Article  Google Scholar 

  • Weese DA, Santos SR (2009) Genetic identification of source populations for an aquarium-traded invertebrate. Anim Conserv 12:13–19

    Article  Google Scholar 

  • Wharton DN, Jinks RN, Herzog ED, Battelle BA, Kass L, Renninger GH, Chamberlain SC (1997) Morphology of the eye of the hydrothermal vent shrimp, Alvinocaris markensis. J Mar Biol Assoc U K 77:1097–1108

    Article  Google Scholar 

  • Wheeler JFG, Brown FA (1936) The periodic swarming of Anchistioides antiguensis (Schmitt) (Crustacea Decapoda) at Bermuda. J Linn Soc Lond Zool 39:413–428

    Article  Google Scholar 

  • Wickler W (1973) Biology of Hymenocera picta Dana. Micronesica 9:225–230

    Google Scholar 

  • Wickler W, Seibt U (1970) Das Verhalten von Hymenocera picta Dana, einer Seesterne fressenden garnele (Decapod, Natantia, Gnathophyllidae). Z Tierpsychol 27:352–368

    Article  Google Scholar 

  • Wickler W, Seibt U (1981) Monogamy in Crustacea and Man. Z Tierpsychol 57:215–234

    Article  Google Scholar 

  • Wicksten MK (1989) Encantada spinoculata, a new genus and species of shrimp from the Galapagos Islands (Caridea: Bresiliidae). J Crustac Biol 9:667–671

    Article  Google Scholar 

  • Wicksten MK (2010) Infraorder Caridea. In: Schram FR, von Vaupel Klein JC (eds) Treatise on zoology–anatomy, taxonomy, biology. The crustacea. Volume 9, Part A. Eucarida: Euphausiacea, Amphionidacea and Decapoda (partim). Koninklijke Brill NV, Leiden, pp 165–206

    Chapter  Google Scholar 

  • Wicksten MK, Heathman T (2015) New host records for Bathypalaemonella serratipalma (Caridea: Bathypalaemonellidae) in the northern Gulf of Mexico. Mar Biodivers Rec 8:1–4

    Article  Google Scholar 

  • Wicksten MK, Martin JW (2004) A new species of caridean shrimp of the family Stylodactylidae from the eastern Pacific Ocean. Proc Biol Soc Wash 117:377–384

    Google Scholar 

  • Wicksten M, De Grave S, France S, Kelley C (2017) Presumed filter-feeding in a deep-sea benthic shrimp (Decapoda, Caridea, Stylodactylidae), with records of the deepest occurrence of carideans. ZooKeys 646:17–23

    Article  Google Scholar 

  • Williams AB (1984) Shrimps, lobsters, and crabs of the Atlantic Coast of the Eastern United States, Maine to Florida. Smithsonian Institution Press, Washington, DC

    Google Scholar 

  • Williams AB, Chace FA (1982) A new caridean shrimp of the family Bresiliidae from thermal vents of the Galapagos Rift. J Crustac Biol 2:136–147

    Article  Google Scholar 

  • Williams AB, Rona PA (1986) Two new caridean shrimps (Bresiliidae) from a hydrothermal vent on the mid-atlantic ridge. J Crustac Biol 6:446–462

    Article  Google Scholar 

  • Williamson DI (1973) Amphionides reynaudii (H. Milne Edwards), representative of a proposed new order of Eucaridan Malacostraca. Crustaceana 25:35–50

    Article  Google Scholar 

  • Williamson DI (1980) Larval development in a species of Ambidexter Manning & Chace (Decapoda, Caridea, Processidae). Crustaceana 39:235–246

    Article  Google Scholar 

  • Williamson K (2002) Charles Bruce Powell 1943-1998. Crustaceana 75:1275–1278

    Article  Google Scholar 

  • Wong JM, Pérez-Moreno JL, Chan T-Y, Frank TM, Bracken-Grissom HD (2015) Phylogenetic and transcriptomic analyses reveal the evolution of bioluminescence and light detection in marine deep-sea shrimps of the family Oplophoridae (Crustacea: Decapoda). Mol Phylogenet Evol 83:278–292

    Article  CAS  PubMed  Google Scholar 

  • Wood LE, De Grave S (2015) Functional morphology of the first pereiopod in crangonoid shrimps (Crustacea, Decapoda, Caridea, Crangonoidea). Zoomorphology 134:469–486

    Article  Google Scholar 

  • Woodmansee RA (1966) Daily vertical migration of Lucifer. Planktonic numbers in relation to solar and tidal cycles. Ecology 47:847–850

    Article  Google Scholar 

  • WoRMS (World Register of Marine Species) (2022). https://www.marinespecies.org. Accessed 08 November 2021

  • Xiao Y, Greenwood JG (1993) The biology of Acetes (Crustacea, Sergestidae). Oceanogr Mar Biol Annu Rev 31:259–444

    Google Scholar 

  • Xuan NV (2000) Redescription of Mimocaris heterocarpoides Nobili, 1903 (Decapoda, Caridea, Hippolytidae) with remarks on its occurrence in Vietnam. Crustaceana 73:857–868

    Article  Google Scholar 

  • Yaldwyn JC (1960) Crustacea Decapoda Natantia from the Chatham Rise: a deep water bottom fauna from New Zealand. New Zealand Department of Scientific And. N Z Dept Sci Ind Res 139:13–53

    Google Scholar 

  • Yeo DCJ, Ng PKL (1996) A new species of freshwater snapping shrimp, Alpheus cyanoteles (Decapoda: Caridea: Alpheidae) from peninsular Malaysia and a redescription of Alpheus paludicola. Raffles Bull Zool 44:37–63

    Google Scholar 

  • Yeo DCJ, Ng PKL (1997) The alpheid shrimp Potamalpheops Powell, 1979, (Crustacea: Decapoda: Caridea: Alpheidae) from Southeast Asia, with description of three new species. J Nat Hist 31:163–190

    Article  Google Scholar 

  • Zbinden M, Berthod C, Montagné N, Machon J, Léger N, Chertemps T, Rabet N, Shillito B, Ravaux J (2017) Comparative study of chemosensory organs of shrimp from hydrothermal vent and coastal environments. Chem Senses 42:319–331

    Article  CAS  PubMed  Google Scholar 

  • Zupo V, Messina P, Carcaterra A, Aflalo ED, Sagi A (2008) Experimental evidence of a sex reversal process in the shrimp Hippolyte inermis. Invertebr Reprod Dev 2:93–100

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

Copyright information

© 2023 The Author(s), under exclusive license to Springer Nature Switzerland AG

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Bauer, R.T. (2023). The Families of Decapod Shrimps. In: Shrimps. Fish & Fisheries Series, vol 42. Springer, Cham. https://doi.org/10.1007/978-3-031-20966-6_3

Download citation

Publish with us

Policies and ethics