Correction
16 Nov 2016: Carella M, Agell G, Cárdenas P, Uriz MJ (2016) Correction: Phylogenetic Reassessment of Antarctic Tetillidae (Demospongiae, Tetractinellida) Reveals New Genera and Genetic Similarity among Morphologically Distinct Species. PLOS ONE 11(11): e0167011. https://doi.org/10.1371/journal.pone.0167011 View correction
Figures
Abstract
Species of Tetillidae are distributed worldwide. However, some genera are unresolved and only a few genera and species of this family have been described from the Antarctic. The incorporation of 25 new COI and 18S sequences of Antarctic Tetillidae to those used recently for assessing the genera phylogeny, has allowed us to improve the resolution of some poorly resolved nodes and to confirm the monophyly of previously identified clades. Classical genera such as Craniella recovered their traditional diagnosis by moving the Antarctic Tetilla from Craniella, where they were placed in the previous family phylogeny, to Antarctotetilla gen. nov. The morphological re-examination of specimens used in the previous phylogeny and their comparison to the type material revealed misidentifications. The proposed monotypic new genus Levantinella had uncertain phylogenetic relationships depending on the gene partition used. Two more clades would require the inclusion of additional species to be formally established as new genera. The parsimony tree based on morphological characters and the secondary structure of the 18S (V4 region) almost completely matched the COI M1-M6 and the COI+18S concatenated phylogenies. Morphological synapomorphies have been identified for the genera proposed. New 15 28S (D3-D5) and 11 COI I3-M11 partitions were exclusively sequenced for the Antarctic species subset. Remarkably, species within the Antarctic genera Cinachyra (C. barbata and C. antarctica) and Antarctotetilla (A. leptoderma, A. grandis, and A. sagitta), which are clearly distinguishable morphologically, were not genetically differentiated with any of the markers assayed. Thus, as it has been reported for other Antarctic sponges, both the mitochondrial and nuclear partitions used did not differentiate species that were well characterized morphologically. Antarctic Tetillidae offers a rare example of genetically cryptic (with the traditional markers used for sponges), morphologically distinct species.
Citation: Carella M, Agell G, Cárdenas P, Uriz MJ (2016) Phylogenetic Reassessment of Antarctic Tetillidae (Demospongiae, Tetractinellida) Reveals New Genera and Genetic Similarity among Morphologically Distinct Species. PLoS ONE 11(8): e0160718. https://doi.org/10.1371/journal.pone.0160718
Editor: Bernd Schierwater, Tierarztliche Hochschule Hannover, GERMANY
Received: April 27, 2016; Accepted: July 22, 2016; Published: August 24, 2016
Copyright: © 2016 Carella et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files, except sequences, which are available from the NCBI database. Accession numbers: KT124318 KT124341 KT124328 KT124362 KT124319 KT124343 KT124329 KT124365 KT124324 KT124344 KT124330 KT124363 KT124325 KT124346 KT124331 KT124364 KT124314 KT124356 KT124336 KT124313 KT124355 KT124361 KT124317 KT124367 KT124351 KT124358 KT124323 KT124347 KT124354 KT124353 KT124335 KT124368 KT124321 KT124340 KT124366 KT124322 KT124348 KT124359 KT124349 KT124360 KT124345 KT124326 KT124339 KT124316 KT124315 KT124327 KT124350 KT124334 KT124312 KT124352 KT124342 KT124333 KT124320 KT124332 KT124369 KT124371 KT124337 KT124370
Funding: This work was supported by MarSymBiomics project, Spanish Ministry of Economy & Competitiveness, grant ref. CTM2013-43286-P, MJU; Benthic Ecology Consolidate Award, Generalitat of Catalonian ref. 214-SGR-120, MJU; BluePharm Train FP7 People-INT no: 607786 to MJU; and Bluegenics KBBE-2012-6, EU’s Seventh Framework Programme (FP7) GA No. 311848, PC. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Sponges dominate some benthic communities in the Antarctic, in terms of both biomass [1], [2] and diversity [3]. The Antarctic clockwise circumpolar current [4] and the low water temperatures contribute to the biogeographic isolation of the Antarctic continental shelf, which partly explains the high degree of sponge endemism in the area [5], [6], [7]. Taxonomic affinities between Antarctic sponges and those of the Magellanic region (South America) and the Falkland Islands have also been reported [8], [5], [9] but the studies are still incomplete and subject to debate [10], [7]. Most of the currently known Antarctic sponge species were discovered during the oceanographic campaigns of the twentieth century [11], [12], [13], [14], [8], [15], [16], [17], [18], [19], [20], [21], [22], [23]. However, recent findings of many new species [24], [7], [25], [26], [27], [28], [29], [30], [31], [32] suggest that the sponge biodiversity of this area has not been fully explored yet and that more species remain to be discovered.
While collecting sponges during the Antarctic Polarstern ANT-XXVII/3 expedition in 2011, we realized the difficulty to identify the fairly common, well known, large conspicuous species belonging to the family Tetillidae Sollas, 1886. The World Porifera Database [33] currently lists only four valid Tetillidae species from the Antarctic—Cinachyra barbata (Sollas, 1886), Cinachyra antarctica (Carter, 1872), Tetilla leptoderma (Sollas, 1886) and Craniella sagitta (Lendenfeld, 1907). Furthermore, intra-specific variations of the mitochondrial cytochrome c oxidase subunit 1 (COI), from Antarctic and New Zealand Tetillidae, also suggest that the diversity of this group is underestimated [34]. We also noticed that there is no consensus in the literature regarding the allocation of some Antarctic species to the genus Craniella or Tetilla [35], [36], [34].
The family Tetillidae (Demospongiae, Tetractinellida, Spirophorina) contains 156 species distributed worldwide [33]. Many of them inhabit sedimentary bottoms to which they anchor by means of long spicule bundles, which represent a suitable substrate for many other hard-bottom invertebrates [37]. Their representatives are characterized by a globular habit, a radiate skeleton composed chiefly of the following spicules: megascleres are protriaenes, oxeas, and sometimes ortho/anatriaenes or calthrops, which often protrude the ectosomal layer outward; microscleres are characteristic sigmaspires and occasionally raphides [36]. To this day, the Tetillidae have no clear morphological synapomorphy, as triaenes are shared with all Tetractinellida, and sigmaspires are found in most Spirophorina families. The Tetillidae appears monophyletic with COI [38], but polyphyletic in 18S and 28S (C1-D2) phylogenies [39], [40], [38].
Using the COI of 14 Tetillidae species, Szitenberg et al. [41] suggested that most Tetillidae genera were not monophyletic. Later, Szitenberg et al. [34], using this time a set of three molecular markers (COI, 28S and 18S) on 28 Tetillidae species belonging to eight genera, obtained five main clades (with COI and 28S): (i) Acanthotetilla (ii) Cinachyrella, Paratetilla, and Amphitethya, (iii) Cinachyrella levantinensis, (iv) tropical-temperate Tetilla, and (v) Craniella, Cinachyra, and Fangophilina. Results were similar with 18S, except that Acanthotetilla sequences were lacking from the NCBI genbank. One of the main issues raised by this study concerned the Craniella/Cinachyra/Fangophilina clade, which included all the Antarctic species. Results suggested the polyphyly of the genus Craniella distributed in three clades: (i) Craniella cf. leptoderma (Antarctic, New Zealand), (ii) Craniella sagitta (Antarctic, New Zealand) and (iii) a Craniella clade with boreo-arctic Atlantic species mixed with New Zealand/Australian species. Based on this polyphyly, Szitenberg et al. [34] propose to reallocate the Antarctic Tetilla, Fangophilina, and Cinachyra to the genus Craniella, despite the absence of morphological support for such a proposal.
The goal of the current study was to investigate the relationships between the Antarctic and tropical/temperate Tetillidae to revise the taxonomy and phylogeny of the family and to assess the purported endemism of its Antarctic genera. We improved the sampling of previous phylogenies by incorporating additional Antarctic and Sub-Antarctic specimens from geographically distant localities. We used four gene partitions (mitochondrial and nuclear) to conduct molecular phylogenetic analyses. The morphology of new specimens, type species, and some specimens previously sequenced [34] was examined. Finally, we also performed a maximum parsimony phylogenetic analysis based on morphological characters and the secondary structure of the V4 region of the 18S rDNA.
Our findings confirm the monophyly of the Antarctic genera and allow us to erect two new Tetillidae genera: Antarctotetilla gen. nov., restricted to Antarctic and sub-Antarctic waters, and Levantinella gen. nov. so far limited to eastern Mediterranean. This study also resurrects a sub-Antarctic species and reveals four potential new species. The genetic homogeneity of the markers used among morphologically distinct Antarctic Tetillidae species, contrasts with the habitual finding of genetically distinct, morphologically cryptic species. A restricted geographical distribution of some Tetillidae genera has become evident.
Material and Methods
The collection of sponge samples was conducted in strict accordance with Spanish and European regulations under the rules of the Spanish National Research Council with the approval of the Directorate of Research of the Spanish Government. The study was found exempt from ethics approval by the ethics commission of the University of Barcelona since, according to article 3.1 of the European Union directive (2010/63/UE) from the 22/9/2010, no approval is needed for sponge sacrification, as they are the most primitive Animals and lack any nervous system Moreover, the collected sponges are not listed in CITES."
Sampled sponges
The majority of the samples were collected in Antarctic and sub-Antarctic regions during the Polarstern ANT-XXVII/3 expedition from Punta Arenas, Chile (February 8, 2011) to Cape Town, South Africa (18 April 2011) with Agassiz (AGT) and bottom trawl (BT) gears. During this expedition, Tetillidae were collected in South Georgia, South Orkneys Islands, and Newmayer in the Antarctic continent. A Remote Operated Vehicle (ROV) was deployed during the Polarstern cruise to gather samples between 300 and 450 meters and to photograph underwater living specimens. Given the large size (up to 30 cm in diameter) of most Antarctic Tetillidae, once the individuals were photographed, a fragment ca. 3 cm3 in size was preserved in absolute ethanol, which was changed three times before packing at -20°C for transportation and storage at the CEAB (Centre d’Estudis Avançats de Blanes, Spain). Other Tetillidae from this study were collected during the Collaborative East Antarctic Marine Census (CEAMARC) Dec. 2007- Jan. 2008 in Adélie Land, Antarctica [42], [43]. The CEAMARC specimens were dredged between 170 and 1700 m; the complete specimens were bulk-fixed with ethanol (80%) in 60L metallic drums. A few samples also came from a fishery-independent biomass survey “POissons de KERguelen” (POKER II) conducted in 2010 on the Kerguelen Plateau. The complete specimens were collected using a Grande Ouverture Verticale (GOV) trawl, frozen on board and bulk-fixed in ethanol 80% at the Muséum National d’Histoire Naturelle (MNHN), Paris, France. Specimens from these two expeditions are housed at the MNHN and stored in the ‘Zoothèque’ at a constant 18°C temperature. Three additional samples were collected between Lavoisier and the Antarctic Peninsula between 847 and 960 m (R/V LM Gould, 2010) and were obtained from Bill Baker (University of South Florida). The samples used in this study, voucher numbers, Genbank accession numbers, and collecting localities are provided in Table 1.
Additional specimens of particular interest to obtain a more comprehensible sampling for our taxonomic study and to verify previous identifications were obtained on loan from several institutions: paratype of Fangophilina submersa Schmidt, 1880 (MSZ.PO160, Musée Zoologique de Strasbourg, France); paratype of Craniella quirimure Peixinho, Cosme, Hajdu, 2005 (MNRJ 8417, Museu nacional/UFRG, Brazil); paratype of Tetilla radiata Selenka, 1879 (MNRJ 576, Museu nacional/UFRG, Brazil); Tetilla muricyi Fernandez, Peixinho, Pinheiro, Menegola, 2011 (UFBA 2569, Museu de História Natural da Bahia, Brazil); Craniella sp. (QMG 316342, and QMG 316372, Queensland Museum, Brisbane, Australia); nine individuals of Cinachyrella levantinensis Vacelet, Bitar, Carteron, Zibrowius, Pérez, 2007 from Lebanon (06/07/2003-1 and 31/07/2003-2, Station Marine d’Endoume, Marseille) and seven specimens collected across the shore of Ma’agan Michael, Israel (courtesy of Jean Vacelet); Craniella sagitta Lendenfeld, 1907 (syn. Tethya sagitta) (NIWA 28491 and NIWA 28929 National Institute of Water & Atmospheric Research, New Zealand); a small piece of the syntype of Tethya sagitta Lendenfeld, 1907 (ZMB Por 3504, Museum für Naturkunde Leibniz, Germany); Fangophilina sp. (NIWA 28601 National Institute of Water & Atmospheric Research, New Zealand). Moreover, several specimens from Szitenberg et al. [34] were re-examined from photographs or specimens (see Results).
Selected outgroups for the phylogenetic analyses, which mainly aimed at establishing relationships among genera, belonged to the Astrophorina (families Geodiidae and Theneidae) since previous molecular phylogenies of Demospongiae based on mitochondrial [44], [38] and nuclear [45], [46] genes placed Astrophorina either as a sister clade of the Tetillidae (COI), or sister to some Tetillidae (18S, 28S).
DNA extraction, amplification and sequencing
Genomic DNA was extracted according to the manufacturer’s protocol for the DNeasy Blood & Tissue kit (Qiagen). Two mitochondrial markers were sequenced, both from COI: the M1-M6 partition, using primers LCO1490 and HCO2198 [47] and the I3-M11 partition, using primers PorCOI2 fwd. and PorCOI2 rev. [48]. Two nuclear markers were also sequenced: 18S, using primers 1F and 1795R, [49] and the D3-D5 partition of 28S, using primers Por28S-830F and Por28S-1520R [50]. Different amplification protocols were performed for each marker: COI M1-M6 partition (94°C, 2 min [94°C, 1 min, 43°C, 1 min, 72°C, 1 min] x 35–40 cycles, 72°C, 5 min); COI I3-M11 partition (95°C, 3 min, [94°C, 30 s, 57°C, 45 s, 72°C, 90 s] x 35–40 cycles, 72°C, 10 min); 18S (94°C, 5 min, [94°C, 1 min, 50–55°C, 1 min, 72°C, 1 min] x35-40 cycles, 72°C, 5 min); 28S D3-D5 partition (94°C, 5 min [94°C,30 s, 53°C, 30 s, 72°C,30 s] x 30 cycles, 72°C, 5 min). COI M1-M6 partition amplifications were performed in a 50 μL volume reaction, containing 37,6 μL H₂0, 5 μL buffer KCL (BIORON), 2μL BSA, 2μL dNTP (Sigma), 1 μL primers forward/reverse, 0,4 μL Taq (BIORON) and 1μL of genomic DNA. Amplifications of the COI I3-M11 partition were performed in a 50 μL volume reaction, containing 34,45 μL H₂0, 5 μL buffer (INVITROGEN), 0,75 μL MgCl (INVITROGEN), 2,4 μL DMSO (dimethyl sulfoxide), 2 μL BSA, 2 dNTP (Sigma), 1 μL primers forward/reverse, 0,4 Taq (INVITROGEN) and 1 μL of genomic DNA. Amplifications of 18S rRNA were performed in a 50 μL volume reaction, containing 36,85 μL H₂0, 5 μL buffer (INVITROGEN), 0,75 μL MgCl (INVITROGEN), 1,2 μL DMSO (dimethyl sulfoxide), 1 μL BSA, 1,5 μL dNTP (Sigma), 1 μL primers forward/reverse, 0,7 μL Taq (INVITROGEN) and 1 μL of genomic DNA. On the other hand, partition D3-D5 of 28S rRNA amplifications were performed in a 50 μL volume reaction, containing 36,85 μL H₂0, 5 μL buffer (INVITROGEN), 0,75 μL MgCl (INVITROGEN), 2μL BSA, 2 μL dNTP (Sigma), 1 μL primers forward/reverse, 0,4 μL Taq (INVITROGEN) and 1 μL of genomic DNA. Purified PCR products were sequenced in both directions using Applied Biosystems 3730xl DNA analyzers (Macrogen, South Korea).
Sequence alignment and phylogenetic reconstructions
Once the poriferan origin of the obtained sequences was verified using BLAST (http://blast.ncbi.nlm.nih.gov/Blast.cgi), sequences were aligned using Clustal W v.1.81 [51]. In cases where the forward and reverse reads do not match, we used BioEdit v.7.2.5 [52] and kept either the best quality of the two reads or introduced an IUPAC ambiguity code into the consensus sequence.
JModelTest 0.1.1 [53] was used to determine the best-fitting evolutionary model for each dataset. The model GTR+I+G was used for the mitochondrial and nuclear genes under the Akaike information criterium. Phylogenetic trees were constructed under Bayesian Inference (BI) and Maximum Likelihood (ML) criteria. BI analyses were performed with MrBayes 3.2.1 [54]. Four Markov Chains were run with one million generations sampled every 1000 generations. The chains converged significantly and the average standard deviation of split frequencies was less than 0.01 at the end of the run. Early tree generations were discarded by default (25%) until the probabilities reached a stable plateau (burn-in) and the remaining trees were used to generate a 50% majority-rule consensus tree. ML analyses were executed with PhyMLv3.0 program [55], [56]. We assessed the robustness of the tree clades in PhyML by a nonparametric bootstrap resampling with 1000 replicates.
Incongruence Length Difference (ILD) test (PAUP 4.0b10) was run [57] to verify sequence homogeneity or incongruence between the 18S and COI markers. The ILD test indicated no significant conflict (p = 0.93) between the two markers so a concatenated 18S-COI dataset was constructed with the species for which we had sequences for both markers.
18S rRNA secondary structure and morphological analysis
RNAfold web server (http://rna.tbi.univie.ac.at/cgi-bin/RNAfold.cgi) [58], [59] was used to determine the predicted secondary structure of the 18S V4 variable region for all species following Voigt et al. [60]. We used the default setting for all parameters except for the folding temperature. As the specimens came from different localities, we fixed the folding temperatures according to that of the specimen locality. However, the specimens belonging to Geodia spp., which were used as outgroups, lived in locations with contrasting temperatures. Only in this case, we used the default setting of 37°C [61]. The program automatically chooses the secondary structures with the lowest free energy (dG in kcal/mol) [60]. Following Gazave et al. [62], we encoded the different parts of the predicted secondary structures as elements and treated them as binary characters (presence/absence) in the morphological matrix. As the V4 of 18S secondary structure motifs were conserved across genera, according to the species sequenced, we assumed that the few species for which the 18S sequence was not available, shared the secondary structure motifs of the genus. The morphological/secondary structure matrix, consisting of 26 morphological characters and 13 18S secondary structure motifs, is made available in S1 File. A phylogenetic-tree was built with the morphological matrix under the maximum parsimony (MP) criterion using PAUP 4.0b10 [57] using a heuristic search and the branch swapping method with the tree bisection and reconnection (TBR) algorithm and ACCTRAN character-state optimization.
Results
Mitochondrial COI
The COI (M1-M6 partition) dataset comprised 70 sequences (16 new) of 537 nucleotides (nt.) (158 nt. variable, of which 148 nt. were parsimony informative). Phylogenetic trees from ML and BI analyses retrieved congruent topologies, although some clades were differently supported (Fig 1). The Antarctic/New Zealand Tetillidae clustered in a well-supported group (93/1), which split in three well-defined clades henceforth called clades 1, 2 and 3.
Species names are followed by their accession numbers (sequences downloaded from Genbank) or the specimen reference. Individuals sequenced in this study are in bold. Only supporting values higher than 70% (ML bootstrap, between parentheses on the left) or 0.75 (BI posterior probability) are represented on the tree nodes.
Clade 1 (80/0.95, ML bootstrap supporting values /BI posterior probability) contained all the species of Cinachyra sequenced plus an unidentified species named Tetillidae ANT 27211.
Clade 2 (88/0.95) clustered individuals of Tetilla grandis, T. sagitta, and T. leptoderma, including those individuals called Craniella leptoderma in previous phylogenies. The position of three Craniella sagitta sequences (NIWA 25206, 28491, and 28929) was unresolved. These specimens were placed clearly apart from our Tetilla sagitta specimens from Antarctica, which morphologically conformed to the type species. Those three sequences belonged to two haplotypes with a difference of 8 nt.: NIWA 28491 and NIWA 25206 specimens from New Zealand versus NIWA 28929 from Antarctica.
Clade 3 (-/0.91) included the sequences of Fangophilina sp. (NIWA 28601, NIWA 28586, and NIWA 28617) and Craniella sp. (QMG 316342 and 316372), and was retrieved only in BI analyses.
Clade 4 (81/1) was a sister group of Antarctic sponges and included non-Antarctic/New Zealand species of Craniella.
Clade 5 (100/1) contained the non-Antarctic Tetilla (i.e. from tropical seas).
Clade 6 (98/1) included sequences of Cinachyrella levantinensis from the eastern Mediterranean, and was clearly apart from the rest of the Cinachyrella species.
Clade 7 (84/0.99) consisted of Cinachyrella species from tropical and subtropical waters and was divided in two well-supported sub-clades (posterior probability 0.80 and 0.84): the first included C. australiensis, C. kuekenthali, Amphitethya cf. microsigma, and C. apion, while the second included C. alloclada, Cinachyrella sp., C. schulzei, and Paratetilla bacca. The latter two species clustered together (100/1).
Clade 8 (100/1), included two species of Acanthotetilla, and appeared as the sister group of the remaining Tetillidae.
Almost no intra-species variation was found for the M1-M6 partition for the Antarctic genera, with the notable exception of two individuals: Cinachyra barbata (JX177864), which differed in 3 nt. from the other Cinachyra sequences, and Craniella cf. leptoderma (JX177865), which differed in 2 nt. from the other Tetilla/Craniella sequences (Fig 1).
We obtained 11 new sequences of the COI I3-M11 partition, 614 nt. long (11 nt. variable and parsimony informative). This partition (Fig 2), although it has been considered more variable than the M1-M6 partition [63], failed to reveal any difference among the Antarctic species of Cinachyra or Tetilla/Craniella.
Bootstrapping and posterior probability (ML and BI, respectively) values are represented on the node of the only resulting clade. Individuals sequenced in the current study are indicated in bold.
Nuclear 18S rRNA and 28rDNA
The full-length 18S dataset comprised 48 sequences (19 new) of 1483 nt. (83 nt. variable, of which 60 nt. were parsimony informative). ML and BI analyses gave congruent topologies (Fig 3). These trees recovered the same clades as the COI tree, except for the absence of clade 8, since no sequences of Acanthotetilla were available for this marker, and clade 2. Like in the COI analyses, 18S failed to discriminate among species of the Antarctic Tetilla (including species named Craniella in previous phylogenies) or Cinachyra. As in the COI phylogeny, the Antarctic/New Zealand Tetillidae clustered in a clade (75/0.94) comprising Cinachyra spp., Tetilla spp, Craniella sagitta (NIWA 25206), Fangophilina spp., and Craniella sp. (QMG 316342 and 316372) representatives.
Species names are followed by the accession numbers (sequences downloaded from Genbank) or the specimen reference. Individuals sequenced in this study are in bold). Only supporting values higher than 70% (ML bootstrap, between parentheses on the left) or 0.75 (BI posterior probability) are represented on the tree nodes.
Clade 1 (-/0.99) contained the species that split in clades 1 and 2 in COI phylogeny. The specimen Tetillidae ANT27211 groups this time with Tetilla spp. and not with Cinachyra spp., as in the COI phylogeny.
Clade 3 (-/0.76) comprises Fangophilina sp. plus Craniella sp. (QMG 316342 and 316372) and Craniella sagitta (NIWA 25206) as in the COI phylogeny but without statistical support.
Clade 4 (97/1) included the same Craniella species as in the COI phylogeny plus C. neocaledoniae, a species absent from the COI sampling.
Clade 5 (100/1) encompassed non-antarctic Tetilla (i.e. from tropical seas).
Clade 6 (95/0.97) was formed exclusively by C. levantinensis sequences. This clade was sister to clade 7 whereas it was sister to clade 1–5 in the COI tree.
Clade 7 (95/0.78), as in the COI tree, clustered all Cinachyrella species plus Paratetilla bacca.
The 28S rRNA gene (D3-D5 partition) comprised 15 new sequences of 650 nt. (11 nt. variables, of which 10 nt. were parsimony informative). Phylogenetic trees were consistent in ML and BI analyses (Fig 4). Species within any of these two genera (Cinachyra and Tetilla/Craniella) were not discriminated.
Species names are followed by the accession numbers (sequences downloaded from Genbank) or the specimen reference. Individuals sequenced in this study are in bold. Only supporting values higher than 70% (ML bootstrap, between parentheses on the left) or 0.75 (BI posterior probability) are represented on the tree nodes.
Concatenated COI and 18S rRNA
The dataset for the concatenated mitochondrial and nuclear partitions (COI M1-M6 partition and 18S) comprised 39 sequences of 2019 nt. The resulting phylogenetic trees were consistent in ML and BI analyses (Fig 5) and were for the most part similar to the COI tree (i.e. clades 1, 3, 4, 5, and 7), except for clade 6, which was shared only with the 18S tree (Fig 3). On the other hand, contrarily to 18S phylogeny, clade 2 was well supported (87/0.92). Clade 3 was similar to both COI and 18S phylogenies. The supporting values of the clades slightly varied in some cases with respect to those of the previous phylogenies.
Species names are followed by the accession numbers (sequences downloaded from Genebank) or the specimen reference. Individuals sequenced in this study are in bold. Only supporting values higher than 70% (ML bootstrap, between parentheses on the left) or 0.75 (BI posterior probability) are represented on the tree nodes.
Morphological identifications and re-examination of specimens
To understand our phylogenetic results, which were fairly congruent with both nuclear and mitochondrial genes, we examined the morphology of our specimens, several holotypes and also some specimens previously sequenced by Szitenberg et al. [34]. The resulting decisions from our examinations are detailed below and summarized in Table 1 and S2 File.
Clade 1 comprised individuals that belonged to the Cinachyra genus. Most of these individuals were morphologically similar except for the specimen of C. barbata (NIWA 28877), and that of Cinachyra antarctica (QMG 311149). The former differed from the other C. barbata in 3 nt, and pictures of the specimen (courtesy of M. Kelly) show porocalices spread on the sponge body instead of being concentrated on the lateral zone: we decided to name it Cinachyra cf. barbata until the specimen could be studied. Underwater pictures (courtesy of J. Hooper) of Cinachyra antarctica (QMG 311149) show a hairy surface covered with sediments with high palisades of spicules just around the openings: we tentatively renamed it as Cinachyra sp.
Clade 2 included Tetilla/Craniella specimens from Antarctica/New Zealand. These specimens belonged to three species (leptoderma, sagitta and grandis) that had been formally placed either in the genus Tetilla or the genus Craniella by previous authors. However, these species did not have the characteristic conspicuous double-layered cortex of Craniella [36]. Instead, they all had a loose arrangement of cortical oxeas perpendicular to the surface, which we will henceforth call ‘pseudocortex’ (Figs 6F and 6H and 7B and 7D). Therefore these species cannot belong to Tetilla either, which lacks a cortical specialization. Moreover, all these species have pores clustered in small, depressed areas and their oscula, single or multiple, are usually larger than in typical Craniella. Finally, they never harbored direct developing embryos as observed in both typical Craniella and some Tetilla. All these characteristics prompted us to erect a new genus for these three species: Antarctotetilla gen. nov. (see definition below). We will henceforth call these species Antarctotetilla leptoderma, Antarctotetilla sagitta and Antarctotetilla grandis. The latter had been synonymized with A. leptoderma [14], [22] but it is clearly different from A. leptoderma as it has several small oscula and a spherical body while A. leptoderma is slightly elongate/ovoid body with a sole large oscule on top. Therefore we propose to officially resurrect this species so far only recorded from the Antarctic and Sub-Antarctic.
A) Cinachyra barbata from Newmayer (Antarctica) arrows point to the porocalices. B) Transversal section of C. barbata: arrows point to the cortex and one porocalyx. C) Underwater picture of Cinachyra antarctica from McMurdo, (Antarctica). D) Transversal section of C. antarctica: arrows point to the collagenous cortex. E) Antarctotetilla leptoderma from South Georgia: arrows point to the unique osculum on top. F) Transversal section of A. leptoderma: arrows point to the dense ectosomal layer (pseudocortex). G) Antarctotetilla grandis from Newmayer, Antarctica: arrows point to the multiple oscula. H) Transversal section of A. grandis: arrows point to the slightly marked ectosomal layer. All the pictures are by the authors.
A) Tetillidae ANT 27211 from Newmayer, Antarctica: arrows point to the hair-like hispidation pattern formed by bundles of fusiform oxeas, protriaenes and sometimes anatriaenes. B) Transversal section of Tetillidae ANT 27211: arrows point to the ectosomal layer. C) Antarctotetilla sagitta from Adélie Land: arrows point to the oscula; inset: detail of the even surface around the oscula. D) Transversal section of A. sagitta: arrows point to the ectosomal layer. E) Surface of A. sagitta: arrows point to the pores clustered in sieve-like areas; inset: T. sagitta pores in sieves by Kirkpatrick (1908). F) Craniella sagitta NIWA 28491 from New Zealand. G) cf. Fangophilina sp. NIWA 28601 from New Zealand: arrows point to the osculum. H) Lectotype of Fangophilina submersa MZSPO 160 from Northern Gulf of Mexico: arrow points to the porocalyx. All the pictures are by the authors except figures G, which were courtesy of Sadie Mills.
Five out of the eight specimens of Craniella cf. leptoderma from Szitenberg et al. [34] were confirmed morphologically to be A. leptoderma. Pictures of NIWA 28910 and NIWA 36097 showed that these specimens had a smooth surface and multiple small oscula, which matched the morphology of Antarctotetilla grandis. Finally, underwater pictures of QMG 315031 showed that the specimen had at least two oscula, which differs from the large single oscule on top, constantly present in A. leptoderma. QMG 315031 was therefore tentatively re-identified as Antarctotetilla cf. sagitta.
The three specimens of Craniella sagitta (NIWA 28491, NIWA 25206, and NIWA 28929 (Table 1) were examined (see pictures of NIWA 28491 in Fig 7F) and compared with the syntype of Tethya sagitta (ZMB Por 3504). These three specimens possessed a pseudocortex but lacked the main diagnostic characters of the species, such as pores grouped in sieve-like areas and oscula on the top of smooth flattened zones (Fig 7C and 7E) [16]. Thus, they cannot be identified with A. sagitta but we are unsure to which species or even genera they should belong. We could distinguish two morphotypes that corresponded to two haplotypes (differing in 8 nt.), which suggests that they represent two different species, here named Tetillidae sp. 1 and 2. Interestingly, these specimens were originally identified as two different species based on external morphology (S2 File).
Clade 3 included two misidentified genera: Craniella sp. (QMG 316342 and QMG 316372) and Fangophilina sp. (NIWA 28601, NIWA 28586, and NIWA 28617). The individuals called Craniella sp. from the Norfolk Ridge (Fig 8A), had porocalices and a spiculous cortex, similar to that of Cinachyra. They are therefore tentatively identified as Cinachyra sp. As for Fangophilina sp., its morphology was different from the species type of Fangophilina, F. submersa (Fig 7H). However, the small size of these specimens (ca. 1cm in diameter) prevented us to verify whether the only visible orifice was a true porocalyx or an oscule and thus they have been provisionally named cf. Fangophilina sp.
A) Craniella sp. QMG 316342 from Australia: arrows point to the porocalices. B) Craniella cf. cranium ZMBN 85240 from Norway. C) Transversal section of Craniella cf. cranium ZMBN 85240: arrow points to the double-layered cortex. D) Holotype of Tetilla euplocamos MZSPO 206 from Brazil. E) Paratype of Tetilla muricyi UFBA 2569 from Brazil. F) Transversal section of the paratype of T. muricyi UFBA 2569. G) Levantinella levantinensis from Lebanon. H) Transversal section of L. levantinensis: arrows point to the dense ectosomal region formed by sediment accumulation. All the pictures are by the authors except figures A, and D, which were courtesy of John Hooper, and Marie Meister, respectively.
Clade 4 included Craniella species from the Boreo-Arctic Atlantic and the Norfolk ridge. We confirm that they possessed the typical double-layered cortex of Craniella (Fig 9D), and were thus considered true Craniella. Craniella cranium Müller, 1776 (ZMBN 85239) and Craniella sp. (ZMBN 85240) from Korsfjord-Norway [64] were reexamined. ZMBN 85239 was re-identified as Craniella aff. zetlandica since it only differed from C. zetlandica Carter, 1872 in the presence of sigmaspires. ZMBN 85240 was re-identified as Craniella cf. cranium because it closely resembled Craniella pilosa Montagu, 1818, a synonym of C. cranium (Fig 8B and 8C). However, we keep the ‘cf.’ for now, until a world-wide revision of C. cranium can be made, this species having a long and complicated taxonomic history.
A) Antarctotetilla leptoderma from Adélie Land, Antarctica, MNHN IP-2009-544a. B) A. leptoderma, close-up of C. C) Antarctotetilla sagitta from Adélie Land, Antarctica, MNHN IP-2009-31. D) Craniella aff. zetlandica from Korsfjord, Norway, ZMBN 85239. E) Levantinella levantinensis from Israel, PC 705. F) Cinachyrella alloclada from Bocas del Toro, Panama, ZMBN 81788. G) Cinachyra barbata from Adélie Land, Antarctica, MNHN IP-2009-387. H) Cinachyra antarctica from Adélie Land, Antarctica, MNHN IP-2009-328.
Clade 5 contained Tetilla species, which are characterized by the absence of a true cortical structure. Re-examination of a picture of the type species, T. euplocamus (Fig 8D), and the types of T. muricyi Fernandez, Peixinho, Pinheiro, and Menegola, 2011 (Fig 8E and 8F) and T. radiata Selenka, 1879, under the stereomicroscope seems to confirm previous studies of Tetilla radiata Santos and Hajdu, 2003 (Figs 5 and 6), and T. muricy Fernandez et al. 2011 (Fig 4C and 4D), which showed the absence of a cortical specialization in these Tetilla. However, a loose layer of para-tangential large oxeas below the surface may be present in some cases, as it has been reported for T. rodriguezi Fernandez et al. 2011 (Fig 6C).
Clade 6 only contained Cinachyrella levantinesis. We re-examined nine specimens of C. levantinensis trying to understand why they did not group with any of the other Cinachyrella species in the molecular trees. C. levantinensis lacks cortex as Cinachyrella (Figs 8H and 9E). Its surface is mostly covered with a dense layer of sand, which was retained by the protruding spicules (Fig 8G) as in some Cinachyrella (Fig 9F). However, while Cinachyrella species have typical large porocalices, C. levantinensis has numerous small rounded depressions, difficult to assign to porocalices with certainty. As stated by Vacelet et al. [65], these depressions were not visible in specimens heavily covered by sand. These depressions are sometimes concentrated in sand free lateral areas, whereas usually porocalices are evenly distributed in typical Cinachyrella. All these characteristics prompted us to officially create Levantinella gen. nov. (see definition below) to welcome this species.
Clade 7 contained only specimens of Cinachyrella. Some individuals of dubious identification were revised (S2 File). Amphitethya cf. microsigma (SAM-S1189) from Szitenberg et al. [34] showed an external morphology and spicules corresponding to the original description of A. microsigma Lendenfeld, 1907. Furthermore the individual SAM-S1189 was collected in southern Australia, not far from the type locality of A. microsigma. We therefore confirmed the species identification. Using the online SpongeMaps (http://www.spongemaps.org), we also examined underwater pictures of Cinachyrella schulzei Keller, 1891 (QMG 320143, QMG 320636) from Szitenberg et al. [41, 34]. These specimens are reddish pink (QMG 320636) to pale pink (QMG 320143), and completely devoid of sand, in contrast to the typical yellowish-grey color of C. schulzei, which is often covered with sand [66]. These specimens may instead be conspecific with Cinachyrella tenuiviolacea Pulitzer-Finali, 1982, which has a typical pink color and is fairly common in Australian shallow waters and were here provisionally referred to as C. cf. tenuiviolacea.
Maximum parsimony phylogeny on phenotypic characters
The MP analysis included 33 OTUs, one for each species, 26 morphological characters, and 13 motifs of the V4 18S secondary structure (S3 File), which were treated as binary elements (S1 File). The astrophorin Geodia cydonium and Geodia neptuni were used as outgroups. The MP analysis retrieved 6 most parsimonious trees of 48 steps (CI = 0.684; RI = 0.887). Character states are shown at the nodes of the phylogram corresponding to tree number 1 (Fig 10). Clade support resulting from the majority-rule consensus tree is also shown on the phylogram (Fig 10).
A) Phylogram of one of the most parsimonious trees on morphological characters plus the several zones identified for the V4 region of 18S secondary structure–SSRs–(numbered and encircled). Characters that represent either synapomorphies or apomorphies are depicted in the tree. The supporting bootstrap values of clades resulting from the Majority-rule consensus tree are also indicated. B) legends to character drawings on the tree.
The Tetillidae appeared divided in two strongly supported clades (100% bootstrap value), here called clade A and B. Clade A was characterized by pores grouped in several ways and was formed by two well supported sub-clades: A1 embraced two groups with the same V4 secondary structure, A1a formed by Acanthotetilla, with acanthoxeas, small porocalices, and a cortical region made of a palisade of acanthoxeas. The clade A1b was formed by the genus Cinachyrella and Levantinella gen. nov. The latter species is characterized by absence of a well-formed cortex, small, little conspicuous porocalice-like structures, and a dense incorporation of sand to its surface. The genus Cinachyrella included Paratetilla bacca despite the presence of triaenes in the former, and was characterized by the absence of a defined cortex and the presence of true hemispherical large porocalices. No morphological characters could differentiate the two subgroups of Cinachyrella found in the molecular phylogenies (i.e. the C. australiensis/C. apion group versus the C. alloclada/C. cf. tenuiviolacea group).
A2 corresponded to the Antarctic clade, characterized by sharing the same V4 secondary structure. A2a included the Cinachyra genus, with cortex and flask-shaped porocalices as synapomorphies, and two Cinachyra sp. (QMG 316342 and QMG 316372), which also have cortex and porocalices but show a slightly different secondary structure. Clade A2b, with pseudocortex as a synapomorphy (Fig 9A, 9B and 9C), was subdivided in 2 groups: A2ba and A2bb. A2ba included Antarctotetilla gen. nov. with pores clustered in shallow small depressions as a synapomorphy, and Tetillidae sp.3 (ANT 27211, Figs 7A and 9B) totally covered by long hair-like spicules, without porocalices, and with pores clustered in shallow small depressions. A2bb comprised Tetillidae sp. 1 and sp. 2 individuals (NIWA 28491, 25206 and 28929).
Clade B included species that had spread pores as a synapomorphy and was also formed by two well-supported sub-clades:
B1 included two groups. Group B1a was formed by species of Craniella with a two-layered cortex made of collagen plus spicules, and a hispid-conulose surface, and a specific V4 secondary structure. Group B1b included cf. Fangophilina sp, with a particular V4 secondary structure region and a hispid surface (Fig 7G).
B2 was divided in two groups: B2a formed by the genus Tetilla (tropical species) with a particular V4 secondary structure and B2b containing Amphitethya microsigma.
Species of the genera Cinachyra and Antarctotetilla gen. nov. were clearly differentiated, despite the fact that they shared the same V4 secondary structure: Cinachyra antarctica has a collagen cortex as an autopomorphy (Figs 6C and 6D and 9H) while C. barbata and the two Cinachyra sp. (QMG 316342 and QMG 316372) have a spicule-collagenous cortex (Figs 6A and 6B and 9G).
All molecular analyses suggested that the latter species was related to cf. Fangophilina sp. and not to Cinachyra. Within Antarctotetilla gen. nov., A. leptoderma and A. sagitta have a corrugate surface (Figs 6E and 7C), but while the former has a single large apical osculum, A. sagitta shows several small oscules (Fig 7C). On the other hand, A. grandis shows an even surface, spread small oscula, and pores clustered in small depressions (Fig 6G), while A. sagitta is characterized by their pores in sieves covering sub-ectosomal spaces (Fig 7C and 7E).
Formal diagnoses of the currently proposed genera
Family Tetillidae
Tetilla Schmidt, 1868
Type species: Tetilla euplocamos Schmidt, 1868.
Diagnosis: Tetillidae without porocalices, without cortical specialization, without auxiliary megascleres [36].
Cinachyrella Wilson, 1925
Type species: Tetilla hirsuta Dendy, 1889.
Diagnosis: Tetillidae usually with hemispherical porocalices (except in some stalked species), without spiculous cortical specialization; modified from [36].
Remarks: Amphithetya and Paratetilla are within the Cinachyrella clade in our pylogenies. The several well-supported subgroups within the Cinachyrella clade might correspond to sub-generes. However, a more in deep study of Cinachyrella by including additional species would be necessary to formally propose those subgeneres.
Levantinella gen. nov.
Type species: Levantinella levantinensis (Vacelet et al., 2007) by monotypy.
Diagnosis: Tetillidae with small porocalices formed by rounded shallow depressions, without cortex, without auxiliary megascleres.
Craniella Schmidt, 1870
Type species: Craniella tethyoides Schmidt, 1870.
Diagnosis: Globular sponges without porocalices and with a distinct, two-layered cortex (visible to the naked eye). The outer cortex layer often with sub-dermal cavities and the inner layer made of collagen and a tight arrangement of cortical oxeas. Presence of direct-developing embryos within the sponge tissue; modified from [36].
Cinachyra Sollas, 1886
Type species: Cinachyra barbata Sollas, 1886.
Diagnosis: Tetillidae with a collagenous cortex, sometimes reinforced by auxiliary oxeas, with flask-shaped porocalices; modified from [36].
Remarks: Most described Cinachyra have been transferred to Cinachyrella (see World Porifera Dadabase)
Antarctotetilla gen. nov.
Synonymy: Tetilla sensu Sollas, 1886 (part.), Craniella sensu Kirkpatrick, 1908 (part.).
Type species: Tetilla leptoderma Sollas, 1886 by designation.
Diagnosis: Tetillidae with single or multiple oscule(s) on top, pores clustered in shallow depressions (no porocalices) and a pseudocortex (very slight cortical differentiation) made of perpendicular oxeas, loosely arranged.
Remarks: Our molecular and morphological results suggest that that three species should be assigned to this genus: A. leptoderma, A. sagitta, and A. grandis. These species are only known (up to now) from the Antarctic, New Zealand, Kerguelen Islands and the Magellanic region. Moreover, Craniella coactifera Lendenfeld, 1907 shows strong similarities with A. grandis and is likely a synonym of this species. We reallocate C. coactifera to Antarctotetilla gen. nov. and keep this species valid until its type can be compared with the type of A. grandis.
Discussion
Molecular markers
The molecular markers used in this study were informative enough to resolve the relationships of Tetillidae genera but did not resolve Antarctic species. Phylogenetic trees inferred with the COI M1-M6 partition (also known as the barcoding Folmer fragment) gave a better resolution of the genera, in part because of the higher number of individuals sequenced for this marker and those already available in Genbank. However, although the COI M1-M6 partition differentiated all the species of temperate and tropical genera of Tetillidae included in this study it failed to separate species within the Antarctic genera Cinachyra and Antarctotetilla gen. nov., despite clear morphological differences. Although uncommon, strictly identical COI M1-M6 sequences for different sponge species have previously been found in other demosponge groups [67], [68], [69], [70] and also in Antarctic hexactinellid sponges: only two COI haplotypes were found among the Antarctic Rosella species [71], which had been recognized by Barthel and Tendal [72].
Similarly, the 18S, 28S (D3–D5) and COI I3-M11 partitions did not succeed in discriminating all Antarctic species. This was to be expected from the slow evolving 18S or even from the faster evolving 28S (D3-D5), which has rather been used for inter-species relationships. However, this was rather surprising for the COI I3-M11 partition, which is considered more variable than the Folmer partition [63], and has been used in population genetics and phylogeography studies of demosponges [73], [48], [74].
This may be an indication of contrasting evolutionary rates between sponge groups [75], [69]. Thus, our results suggest either a particularly slow genetic evolutionary rate of the markers 28S (D3-D5) and COI or a recent radiation with phenotypic characters evolving faster than the genes studied. Further studies on other Demospongiae families and/or more variable markers are required to shed light on the evolutionary processes that affect Antarctic sponges, which are poorly studied so far.
Phylogeny and taxonomic actions
Insufficient knowledge on the morphological characters of Antarctic/New Zealand Tetillidae along with misidentifications biased the interpretation of previous phylogenetic studies [34]. The re-examination of some of these specimens as well as holotypes (S2 File) proved essential to understand previous puzzling results such as the polyphyly of Craniella [34]. Overall, our results improve and clarify the Tetillidae phylogeny. All COI and 18S trees, as well as the COI+18S trees were mostly congruent, except for the positions of Tetillidae sp.3 (ANT 27211), Tetillidae sp.1 (“Craniella sagitta” NIWA 28929), Tetillidae sp.2 (“Craniella sagitta” NIWA 25206 and 28491) and Levantinella levantinensis.
The MP trees allowed us to identify phenotypic synapomorphies for the proposed genera. The MP phylogeny on phenotypic characters, plus the motifs of the 18S secondary structure (V4 region), differed from the molecular phylogenies only in the position of the two Cinachyra sp. (QMG 316342 and QMG 316372, previously wrongly identified as Craniella sp.): they form a strongly supported clade with cf. Fangophilina sp. (NIWA 28601, 28586, 28617) in molecular trees, whereas they group with Cinachyra in the MP tree (because of their porocalices and spiculous cortex).
According to Szitenberg et al. [34], the presence of cortex or/and porocalices, which have been traditionally used to differentiate Tetilllidae genera [35], [36], do not represent synapomorphies according to our molecular analyses. Instead, the types of cortex (with spicules, without spicules, with one or two layers) and/or of porocalices (e.g. deep flask-shaped, hemispherical porocalices, and small, shallow cavities) are the derived characters shared within each genus.
In the current study, we see the Tetillidae basically divided in seven well-supported clades, instead of the five recovered in Szitenberg et al. [34]. Most of these clades correspond to genera: Antarctotetilla gen. nov., Cinachyra, Acanthotetilla, Tetilla, Cinachyrella, Craniella, and Levantinella gen. nov.
The new genus Antarctotetilla contains exclusively those Tetillidae without cortex, without porocalices, and with grouped ostia. The presence of a pseudocortex (not visible with the naked eye) instead of a clearly conspicuous cortex in those species may explain why they have been assigned to the genus Tetilla by previous authors [76], [77], [19], [22]. However, the type species of Tetilla (T. euplocamos Schmidt, 1868) and other tropical representatives that we have examined (e.g. T. radiata, T. muricyi), do not have any kind of obvious cortical specialization.
After moving the traditional Antarctic “Tetilla” (Craniella in Szitenberg et al. [34]) to Antarctotetilla gen. nov., the genus Tetilla recovers its classical diagnosis [35] by including those Tetillidae without cortex and without porocalices. Similarly, by moving the two misidentified Craniella sp. (QMG 316342 and QMG 316372) to Cinachyra sp., Craniella senso stricto [35], [36] was recovered as a monophyletic genus, with a characteristic two-layered cortex as synapomorphy.
Szitenberg et al. [34] proposed the inclusion of Fangophilina and Cinachyra within the genus Craniella, as either junior synonyms or sub-genera. However, this proposal was based on a series of misidentifications: QMG 316342 and QMG 316372 had been wrongly identified as Craniella sp. (now Cinachyra sp.), NIWA 28929, NIWA 28491 and NIWA 25206 had been wrongly identified as Craniella sagitta (here renamed Tetillidae sp. 1 and sp. 2). Conversely four confirmed A. sagitta specimens (ANT IP 31, IP 351, IP 359 and A. cf. sagitta QMG 315031) joined the Antarctotetilla gen. nov. clade in both molecular and morphological phylogenies.
We missed true Fangophilina species in our molecular analyses, since, as stated above, the three cf. Fangophilina sp. did not completely match the diagnostic morphological characters of the genus. The type species F. submersa was reported to have two opposite porocalyces: one with an inhalant function and the other exhalant [78], [36]. The revision of the type material showed that only the cavity containing the ostia is a true porocalyx since the other one corresponded to a deep cloacal osculum. Morphological and genetic investigations on further individuals of F. submersa, which is known just by a single specimen, are necessary to resolve the phylogenetic position and morphological variation of this genus, which has been considered dubious [36].
Our phylogenetic trees retrieved the type species of Amphitethya (A. microsigma) and Paratetilla (P. bacca) within the large Cinachyrella clade, as in previous phylogenies [34]. The position of Paratetilla within Cinachyrella is also recovered in the morphological tree as species of both genera have similar external morphology. Although the type species of Cinachyrella, C. hirsuta Dendy, 1889, is not included in our sampling, we are confident that it would group in the large Cinachyrella clade, based on its morphology [36]. We would therefore have enough arguments to synonymize Amphitethya Lendenfeld, 1907 and Cinachyrella Wilson, 1925 with Paratetilla Dendy, 1905, the oldest genus name. However, reallocating the so far described 40 species of Cinachyrella [33] to Paratetilla without previous reexamination would not be the most conservative option since it would hide the morphological difference we currently recognize (calthrop-like triaenes) to identify Paratetilla. Instead, we prefer to wait for further molecular phylogeny studies on this group to take taxonomic action. Since Cinachyrella species are distributed in several clades, we believe a future revision of this group with a wider sampling might indicate where to place C. hirsuta.
The presence of Amphitethya within the Cinachyrella clade of our molecular trees was unexpected, due to its stalked morphology and the absence of porocalices, which, conversely, placed A. microsigma as a sister species of Tetilla in the morphological tree. However, we note that the characteristic amphitriaenes of Amphitethya have also been occasionally observed in Paratetilla species: P. aruensis [79], and P. merguiensis [80].
In our 18S phylogeny, a few sequences from Redmond et al. [39] had suspicious phylogenetic affinities: Acanthotetilla cf. seychellensis (KC902033), and Cinachyra sp. (KC902124) clustered with Cinachyrella while Craniella sp. (KC902265) clustered with Tetilla. We suspect these are misidentifications but we could not re-examine the corresponding specimens.
Szitenberg et al. (S3 File) [34] suggested erecting Levantinella gen. nov. for the species C. levantinensis, which substantially diverged from the rest of the Cinachyrella species in their study. However, no formal definition was proposed thus making Levantinella a nomen nudum. We agree with these authors in that this species belongs to a new genus and we formally propose to make Levantinella gen. nov. available with C. levantinensis as type species by monotypy. The phylogenetic affinities of Levantinella, however, differed depending on the gene partition used: it appeared as a sister group of the Tetilla/Craniella/Fangophilina/Antarctotetilla/Cinachyra clade with COI while it was a sister group to the other Cinachyrella with 18S.
The family Tetillidae appeared paraphyletic or polyphyletic in previous 18S phylogenies [39], [38] and 28S phylogenies [81]: the Craniella/Cinachyra/Antarctotetilla gen. nov. clade was sister to the Astrophorina. However, these results may be due to a sampling bias, a possibility further suggested by a wide COI phylogeny that recovers a monophyletic Tetillidae [38]. A more thorough worldwide study of representatives of this family is needed to further test its monophyly.
Geographical distribution of Tetillidae genera
The geographical location of the studied Tetillidae suggests a temperature related distribution of some genera (Fig 11). Cinachyrella shows a tropical–subtropical distribution, while Craniella species mainly inhabit temperate-cold seas. The genera Cinachyra and Antarctotetilla appear confined to the Antarctic and Sub-Antarctic regions, contributing to the reported Antarctic sponge endemism [82], [5], which underlines the importance of the Polar Front in isolating the Southern Ocean fauna. Other Cinachyra species, which have been reported out of the Antarctic, may have been incorrectly attributed to this genus. For example, Cinachyra helena Rodriguez and Muricy, 2007 from Brazil does not belong to Cinachyra since its purported porocalyx rather looks like a cloacal oscula with macro-orifices inside the depression [83]. Moreover, its two-layered cortex [83] suggests that it is a Craniella. We therefore propose to reallocate this species to the genus Craniella. Other described Cinachyra have been moved to Cinachyrella posteriorly (see WPD). Current representatives of the genus Tetilla are mainly living in arctic-temperate-warm seas.
NASA OB.DAAC. http://oceancolor.gsfc.nasa.gov/cgi/l3. Accessed on: 2015/04/29). White points represent exact sampling locations. Cr. = Craniella; Ci. = Cinachyrella; L. = Levantinella; Fango. = Fangophilina; A. = Acanthotetilla; T. = Tetilla; Amp. = Amphitethya; P = Paratetilla; Cin. = Cinachyra; Ant. = Antarctotetilla.
In relation to depth, Cinachyrella is distributed in shallow-waters (<30 m depth) with few exceptions that can be found up to 100 m depth (e.g. Cinachyrella kuekenthali, Amphitethya microsigma) while other genera such as Craniella or Fangophilina are nearly restricted to the deep-sea. Antarctotetilla and Cinachyra are eurybathic inhabiting from 30 to 600 m of depth, but they are particularly abundant between 200 and 300 m of depth where they may dominate in sponge grounds (Fig 12).
Black arrows point to Antarctotetilla grandis. White arrows indicate Cynachyra spp. Red arrow points to Tetillidae sp3.
Sponge molecular phylogenies have greatly contributed to emend the traditional sponge systematics, in particular for demosponges [50], [84]. The sponge phylogenetic tree resolution continuously improves as new genetic markers, and more importantly, additional taxa are included in the datasets. However, a careful morphological identification of the individuals sequenced and included in the molecular phylogenies is required for a precise interpretation of the molecular results. In other words, molecular phylogenies should consistently be associated with thorough morphological studies of the specimens sequenced, as we have tried to do with the Tetillidae species.
Supporting Information
S1 File. Morphological data matrix (including secondary structure shapes of the 18S V4 variable region) used for the maximum parsimony phylogeny.
https://doi.org/10.1371/journal.pone.0160718.s001
(PDF)
S2 File. Original and revised identifications of Tetillidae voucher specimens from previous studies (Cárdenas et al. 2011, Szitenberg et al. 2010, Szitenberg et al. 2013) after morphological re-examination.
Localities, depths, and Genbank accession numbers of the corresponding sequences are also listed. QMG, Queensland Museum, Brisbane, Australia; NIWA, National Institute of Water & Atmospheric Research, New Zealand; SAM, South Australia Museum; ZMBN, Zoological Museum in Bergen, Norway. In bold, specimens re-examined in this study. Specimens with (*) were only seen on pictures.
https://doi.org/10.1371/journal.pone.0160718.s002
(PDF)
S3 File. The different parts of the predicted secondary structures (V4 region of 18S) are encircled and numbered.
https://doi.org/10.1371/journal.pone.0160718.s003
(PDF)
Acknowledgments
This study would not have been possible without the kind invitation to one of us (MJU) to take part of the XXVII Polarstern cruise funded by the Alfred-Wegener-Institut, AWI (Bremenhaven) and led by R. Knust. We thank J.M. Gili (Instituto de Ciencias del Mar de Barcelona, ICM) for making this invitation possible. T. Lundälv guided the ROV, and took sponge samples and pictures. E. Isla, S. Rossi (ICM), A. Wolf, J. Gut, and D. Gerde (AWI) helped in sampling and facilitated on board work. D. Janussen (Senckenberg Research Institute and Nature Museum, Frankfurt am Main, Germany) was in charge of the Agasiz (AGT) and bottom trawl (BT) gears. We also thank the crew and participants of the CAML-CEAMARC cruise funded by Australian Antarctic Division and the French polar institute IPEV and the scientific team of the FV Austral POKER 2 (2010) cruise and in particular the cruise leader, Pr. G. Duhamel (MNHN), for giving us access to the sponge material. The work at sea was supported by the ‘Terres Australes et Antarctiques Françaises’ (TAAF), the ‘Syndicat des Armateurs Réunionnais de Palangriers Congélateurs (SARPC), the ‘Direction des Pêches Maritimes et de l’Aquaculture’ (DPMA) and the ‘Réserve Naturelle’ of TAAF. We also thank Noémie Vasset (Département Milieux et Peuplements Aquatiques, unité BOrEA, MNHN, Paris, France), Eduardo Hajdu and Carla Menegola (Universidade Federal do Rio de Janeiro, Brasil), Michelle Kelly and Sadie Mills (National Institute of Water & Atmospheric Research, NIWA, New Zealand), John Hooper (Queensland Museum, Brisbane, Australia) Marie Meister (Muséum Zoologique de Strasbourg, France), Jean Vacelet (Station Marine d’Endoume, Marseille, France), and Karsten Luter (Humboldt University of Berlin, Germany) for sharing specimens, pictures of specimens and collecting information. We acknowledge the help of Elena Gerasimova (University of Bergen, Norway) for making some of the thick sections used in this study. We also thank Yaniv Aluma (Tel Aviv University, Israel) and T. Lundälv (University of Gothenburg, Sweden) for the pictures provided. Special thanks go to Martin Mann (University of Freiburg, Germany), Miquel Arnedo (University of Barcelona, Spain) and Eve Gazave (Université Paris-Diderot, France) for helping with phylogenetic software. The study has been partially funded by MarSymBiomics project (Spanish FECYT agency grant ref. CTM2013-43286-P), Benthic Ecology Consolidate Award (Generalitat of Catalonian ref. 214-SGR-120), and BluePharm Train FP7 People-INT no: 607786 to MJU. PC received some support from the EU’s Seventh Framework Programme (FP7) under grant agreement No. 311848 (Bluegenics KBBE-2012-6).
Author Contributions
- Conceived and designed the experiments: MJU.
- Performed the experiments: MC GA.
- Analyzed the data: MC GA.
- Contributed reagents/materials/analysis tools: MJU PC.
- Wrote the paper: MJU MC PC GA.
- Sampling: MJU PC. Laboratory work: MC GA. Phylogenetic reconstructions: MC. Data interpretation: MC MJU PC.
References
- 1. Belyaev GM, Ushakov PV. Certain regularities in the quantitative distribution of the bottom fauna in Antarctic waters. Dolk Akad Nauk SSSR Mosk. 1975; 112: 137–140.
- 2. Voss J. Zoogeography and community analysis of macrozoobenthos of the Weddell Sea (Antarctica). Ber Polarforsch. 1988; 45:1–144.
- 3. Clarke A, Johnston NM. Antarctic marine benthic diversity. Oceanogr Mar Biol Ann Rev. 2003; 41: 47–114.
- 4.
Thompson MRA, Crame JA, Thompson J. Geological evolution of Antarctica (Vol.1). Cambridge University Press; 1991.
- 5. Sarà M, Balduzzi A, Barbieri M, Bavestrello G, and Burlando B. Biogeographic traits and checklist of Antarctic demosponges. Polar Biol. 1992; 12: 559–585.
- 6. McClintock JB, Amsler CD, Baker BJ, Van Soest RW. Ecology of Antarctic marine sponges: an overview. Integr Comp Biol. 2005; 45(2): 359–368. pmid:21676781
- 7. Ríos P, Cristobo J. A new species of Biemna (Porifera: Poecilosclerida) from Antarctica: Biemna strongylota. J Mar Biol Ass U.K. 2006; 86: 949–955.
- 8. Burton M. Sponges. Discovery Rep. 1932; 6: 237–392.
- 9. Dayton PK, Morbida BJ, and Bacon F. Polar marine communities. Amer Zool. 1994; 34: 90–99.
- 10. Goodwin C, Jones J, Neely K. and Brickle P. Sponge biodiversity of Beauchêne and the Sea Lion Islands and south-east East Falkland, Falkland Islands, with a description of nine new species. J Mar Biol Ass U.K., First View. 2016; 96(2): 263–290.
- 11. Lendenfeld R. Die Tetraxonia Wissenschaftliche Ergebnisse der Deutschen Tiefsee-Expedition auf der Dampfer 'Valdivia' 1898–1899.1907; 11(1–2): i–iv, 59–374, pls IX-XLVI.
- 12. Schulze FE, and Kirkpatrick R. "Preliminary notice on Hexactinellida of the Gauss-Expedition." Zool Anz. 1910; 35(9–10): 293–302.
- 13. Hentschel E. Monaxone Kieselschwamme und Hornschamme der Deutchen Sudpolar Expedition 1901–1903. Deutschen Sudpolar Exp (zool 7). 1914; 15(1): 37–141.
- 14. Burton M. Porifera II. Antarctic sponges. British Antarctic Terra Nova expedition 1910. Natural History Report. Zoology.1929; 6: 393–458.
- 15. Burton M. Sponges. Fhurther zool. Results Swedish Antarctic expedition 1901–1903. Stockholm.1934; 3(2): 1–58.
- 16. Kirkpatrick R. Porifera II. Tetraxonida. Nat Antarctic Exp. 1908; 4(2): 1–56.
- 17. Koltun VM. Sponges of the Antarctic. I. Tetraxonida and Cornacuspongida. Biological Reports of the Soviet Antarctic Expedition (1955–1958). Issledovania Fauni Morei. 1964; 2: 6–116.
- 18. Koltun VM. Porifera. Part I: Antarctic Sponges. B.A.N.Z. Antarct Res Exp 1929–1931. 1976; 9: 147–198.
- 19. Topsent E. Spongiaires. Resultats Voyage SY ‘‘Belgica” 1897–1899 sous le commandement de A. de Gerlache de Gomery. Expédition Antarctique Belge. Zoologie. 1901; 1–54.
- 20. Topsent E. Spongiaires. Expédition Antarctique Française (1903–1905) commandé par le Dr Jean Charcot. Masson et Cie. 1908; 4: 1–37.
- 21.
Topsent E. Spongiares. In: Joubin L Deuxième Expédition Antarctique Française (1908–1910) commandé par le Dr. Jean Charcot. Sciences Physiques: Documents scientifiques (Paris). 1917; 4: 1–88.
- 22. Boury-Esnault N, Van Beveren M. Les Démosponges du plateu continental de Kerguelen-Heard. Comité National Français des Réchérches Antarctiques, CNFRA. 1982; 51: 3–175.
- 23. Vacelet J, Arnaud F. Invertébrés Marins des XIIème et XVème Expéditions Antarctiques Françaises en Terre Adélie. 2. Démosponges. Tethys Supplement. 1972; 4: 9–24.
- 24. Janussen D, Tabachnick KR, Tendal OS. Deep-sea Hexactinellida (Porifera) of the Weddell Sea. Deep-Sea Res Part II. 2004; 51: 1857–1992.
- 25.
Ríos P, Cristobo J. Sponges of the genus Myxilla Schmidt, 1862 collected in Antarctic waters by Spanish Antarctic expeditions. In Custodio MR, Lôbo-Hajdu G, Hajdu E, Muricy G, editors. Porifera Research: Biodiversity, Innovation, and Sustainability; 2007a. pp. 525–546.
- 26. Ríos P, Cristobo JA. New species of Phorbas (Porifera: Poecilosclerida) from the Bellingshausen Sea, Antarctica. J Mar Biol Ass U.K. 2007b; 87: 1485–1490.
- 27. Plotkin AS, Janussen D. New genus and species of Polymastiidae (Demospongiae: Hadromerida) from the Antarctic deep sea. J Mar Biol Ass U.K. 2007; 87(6): 1395–1401.
- 28. Uriz MJ, Gili JM, Orejas C, Perez-Porro AR. Do bipolar distributions exist in marine sponges? Stylocordyla chupachups sp. nv. (Porifera: Hadromerida) from the Weddell Sea (Antarctic), previously reported as S. borealis (Lovén, 1868). Polar Biol. 2011; 34(2): 243–255.
- 29. Göcke C, Janussen D. ANT XXIV/2 (SYSTCO) Hexactinellida (Porifera) and bathymetric traits of Antarctic glass sponges (incorporating ANDEEP-material); including an emendation of the rediscovered genus Lonchiphora. Deep-Sea Res Part II: Topical Studies in Oceanography. 2011; 58(19–29): 2013–2021.
- 30. Göcke C, Janussen D. Hexactinellida of the genus Rossella of ANTXXIV/2 (SYSTCOI) Expedition Antarctic Eastern Weddell Sea. Zootaxa 3692. 2013; 1: 102–122.
- 31. Rapp HT, Janussen D, Tendal S. Calcareous sponges from abyssal and bathyal depths in the Weddell Sea Antarctica. Deep-Sea Res Part II: Topical Studies in Oceanography. 2011; 58(1–2): 58–67.
- 32. Rapp HT, Göcke C, Tendal OS, Janussen D. Two new species of calcareous sponges (Porifera: Calcarea) from the deep Antarctic Eckström shelf and a revised list of species found in Antarctic waters. Zootaxa 3692. 2013; 1: 149–159.
- 33.
Van Soest RWM, Boury-Esnault N, Hooper JNA, Rützler K, de Voogd NJ, et al. World Porifera database. 2016. Available: http://www.marinespecies.org/porifera on 2016-03-18.
- 34. Szitenberg A, Becking LE, Vargas S, Fernandez JCC, Santodomingo N, Wörheide G et al. Phylogeny of Tetillidae (Porifera, Demospongiae, Spirophorida) based on three molecular markers. Mol Phylogenet Evol. 2013; 67(2): 509–519. pmid:23485919
- 35.
Rützler K, Tetillidae (Spirophorida, Porifera): a taxonomic reevaluation. In: Taxonomy of Porifera. Springer Berlin Heidelberg; 1987. pp. 187–203.
- 36.
Van Soest RWM, Rützler K. Family Tetillidae Sollas, 1886. In: Hooper JNA, van Soest RWM, editors. Systema Porifera: A Guide to the Classification of Sponges. Kluwer Academic, Plenum Publishers, New York; 2002. pp. 85–98.
- 37. Gutt J, Böhmer A, Dimmler W. Antarctic sponge spicule mats shape macrobenthic diversity and act as a silicon trap. Marine ecology. Progress series. 2013; 480: 57–71.
- 38. Kelly M, Cárdenas P. An unprecedented new genus and family of Tetractinellida (Porifera, Demospongiae) from New Zealand’s Colville Ridge, with a new type of mitochondrial group I intron. Zool J Linn Soc-Lond. (in press).
- 39. Redmond NE, Morrow CC, Thacker RW, Diaz MC, Boury-Esnault N, Cárdenas P et al. Phylogeny and systematics of Demospongiae in light of new small-subunit ribosomal DNA (18S) sequences. Integr Comp Biol. 2013; ict078.
- 40. Schuster A, Erpenbeck D, Pisera A, Hooper J, Bryce M, Fromon J et al. Deceptive Desmas: Molecular Phylogenetics Suggests a New Classification and Uncovers Convergent Evolution of Lithistid Demosponges. PLoS ONE. 2015; 10(1): e116038. pmid:25565279
- 41. Szitenberg A, Rot C, Ilan M, Huchon D. Diversity of sponge mitochondrial introns revealed by cox 1 sequences of Tetillidae. Evol Biol. 2010; 10: 288.
- 42.
Beaman RJ, O’Brien P. Collaborative East Antarctic Marine Census (CEAMARC): Post-Survey Report, RSV Aurora Australis Voyage 3, December 2007 –January 2008. Geoscience Australia Record; 2009. pp. 5–61.
- 43. Hosie G, Koubbi P, Riddle M, Ozouf-Costaz C, Moteki M, Fukuchi M et al. CEAMARC, the collaborative East Antarctic marine census for the census of Antarctic marine life (IPY# 53): an overview. Polar Sci. 2011; 5(2): 75–87.
- 44. Lavrov DV, Wang X, Kelly M. Reconstructing ordinal relationships in the Demospongiae using mitochondrial genomic data. Mol Phylogenet Evol. 2008; 49: 111–124. pmid:18583159
- 45. Borchiellini C, Chombard C, Manuel M, Alivon E, Vacelet J, Boury-Esnault N. Molecular phylogeny of Demospongiae: implications for classification and scenarios of character evolution. Mol Phylogenet Evol. 2004; 32: 823–837. pmid:15288059
- 46. Nichols SA. An evaluation of support for order-level monophyly and interrelationships within the class Demospongiae using partial data from the large subunit rDNA and cytochrome oxidase subunit I. Mol Phylogenet Evol. 2005; 34: 81–96. pmid:15579383
- 47. Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R. DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biotech. 1994; 3: 294–299.
- 48. Xavier JR, Rachello-Dolmen PG, Parra-Velandia F, Schönberg CHL, Breeuwer JAJ, Van Soest RWM. Molecular evidence of cryptic speciation in the “cosmopolitan” excavating sponge Cliona celata (Porifera, Clionaidae). Mol Phylogenet Evol. 2010; 56(1): 13–20. pmid:20363344
- 49. Medlin LK, Elwood HJ, Stickel S, Sogin ML. The characterization of enzymatically amplified eukaryotic 16S-like rRNA-coding regions. Gene. 1988; 71: 491–499. pmid:3224833
- 50. Morrow CC, Picton BE, Erpenbeck D, Boury-Esnault N, Maggs CA, Allcock AL. Congruence between nuclear and mitochondrial genes in Demospongiae: A new hypothesis for relationships within the G4 clade (Porifera: Demospongiae). Mol Phylogenet Evol. 2012; 62: 174–190. pmid:22001855
- 51. Thompson JD, Higgins DG, and Gibson TJ. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994; 22: 4673–4680. pmid:7984417
- 52. Hall TA. Bioedit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser. 1999; 41: 95–98.
- 53. Posada D. jModelTest: phylogenetic model averaging. Mol Biol Evol.2008; 25: 1253–1256. pmid:18397919
- 54. Ronquist F, Huelsenbeck JP. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003; 19: 1572–1574. pmid:12912839
- 55. Guindon S and Gascuel O. A simple, fast and accurate method to estimate large phylogenies by maximum-likelihood. Syst Biol. 2003; 52: 696–704. pmid:14530136
- 56. Guindon S, Lethiec F, Duroux P, Gascuel O. PHYML Online—a web server for fast maximum likelihood-based phylogenetic inference. Nucleic acids research. 2005; 33 (suppl 2): W557–W559.
- 57.
Swofford D. PAUP: Phylogenetic Analysis Using Parsimony (*and other methods), version 4.0 Sinauer Associates, Sunderland, Massachusetts. 2002.
- 58. Zuker M, and Stiegler P. Optimal computer folding of large RNA sequences using thermodynamics and auxiliary information Nucleic Acid Res. 1981; 9(1): 133–148. pmid:6163133
- 59. Zuker M. Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res. 2003; 31: 3406–3415. pmid:12824337
- 60. Voigt O, Erpenbeck D, Wörheide G. Molecular evolution of rDNA in early diverging Metazoa: first comparative analysis and phylogenetic application of complete SSU rRNA secondary structures in Porifera. BMC Evol Biol. 2008; 8: 69. pmid:18304338
- 61. Gazave E, Carteron S, Chenuil A, Richelle-Maurer E, Boury-Esnault N et al. Polyphyly of the genus Axinella and of the family Axinellidae (Porifera: Demospongiae). Mol Phylogenet Evol. 2010; 57: 35–47. pmid:20541021
- 62. Gazave E, Lavrov DV, Cabrol J, Renard E, Rocher C, Borchiellini C. Systematics and molecular phylogeny of the family Oscarellidae (Homoscleromorpha) with description of two new Oscarella species. PLoS One. 2013; 8(5): e63976. pmid:23737959
- 63. Erpenbeck D, Hooper JNA, Worheide G. CO1 phylogenies in diploblasts and the ‘Barcoding of Life’—are we sequencing a suboptimal partition? Mol Ecol Notes. 2006; 6: 550–553.
- 64. Cárdenas P, Xavier JR, Reveillaud J, Schander C, Rapp HT. Molecular Phylogeny of the Astrophorida (Porifera, Demospongiae) Reveals an Unexpected High Level of Spicule Homoplasy. PLoS ONE. 2011; 6(4): e18318. pmid:21494664
- 65. Vacelet J, Bitar G, Carteron S, Zibrowius H, Perez T. Five new sponge species (Porifera: Demospongiae) of subtropical or tropical affinities from the coast of Lebanon (eastern Mediterranean). J Mar Biol Ass U.K. 2007; 87: 1539–1552.
- 66.
Lévi C, Laboute P, Bargibant G. and Menou JL. Sponges of the New Caledonian Lagoon, Paris: ORSTOM éditions; 1998.
- 67. Schröder HC, Efremova SM, Itskovich VB, Belikov S, Masuda Y, Krasko A et al. Molecular phylogeny of the freshwater sponges in Lake Baikal. J Zool Sys Evol Res. 2003; 41(2): 80–86.
- 68. Addis JS, Peterson KJ. Phylogenetic relationships of freshwater sponges (Porifera, Spongillina) inferred from analyses of 18S rDNA, COI mtDNA, and ITS2 rDNA sequences. Zool Scripta. 2005; 34: 549–557.
- 69.
Heim I, Nickel M, Brummer F. Cytochrome oxidase subunit I—Opportunities and limits for molecular species discrimination. In: Custodio MR, Lobo-Hajdu G, Hajdu E, Muricy G, editors. Biodiversity, innovation, sustainability: book of 66 abstracts/7th International Sponge Symposium, Armação de Búzios, Rio de Janeiro, Brazil, 7–13 May 2006. Museu Nacional, Rio de Janeiro; 2006. pp. 286.
- 70. Cárdenas P, Rapp HT. A review of Norwegian streptaster-bearing Astrophorida (Porifera: Demospongiae: Tetractinellida), new records and a new species. Zootaxa. 2012; (3253): 1–53
- 71. Vargas SR, Dohrmann M, Goecke C, Janussen D, Woerheide G. Nuclear and mitochondrial phylogeny of Rossella (Hexactinellida: Lyssacinosida, Rossellidae): a species and a species flock in the Southern Ocean. 2015; PloS One bioRxiv doi: https://doi.org/http://dx.doi.org/10.1101/0374
- 72.
Barthel D, Tendal OS. Antarctic Hexactinellida. Synopses of the Antarctic Benthos, 6.Koeltz Scientific Books; 1994.
- 73. López-Legentil S, Pawlik JR. Genetic structure of the Caribbean giant barrel sponge Xestospongia muta using the I3-M11 partition of COI. Coral Reefs. 2009; 28(1): 157–165.
- 74. Reveillaud J, Van Soest R, Derycke S, Picton B, Rigaux A, Vanreusel A. Phylogenetic relationships among NE Atlantic Plocamionida Topsent (1927) (Porifera, Poecilosclerida): under-estimated diversity in reef ecosystems. PloS One. 2011; 6(2): e16533. pmid:21347368
- 75. Solé-Cava AM, Boury-Esnault N. Levels of inter and intraspecific differentiation in marine sponges. Mem Queensl Mus. 1999; 44: 591–602.
- 76. Sollas WJ. Preliminary account of the Tetractinellid sponges Dredged by H.M.S. ‘Challenger’ 1872–76. Part I. The Choristida. Sci Proc R Dublin Soc (new series). 1886a; 5: 177–199.
- 77. Sollas WJ. Report on the Tetractinellida collected by H.M.S. Challenger, during the years 1873–1876. Report on the Scientific Results of the Voyage of H.M.S. Challenger, 1873–1876. Zoology. 1888; 25(63): 1–458, pls I-XLIV, 1 map.
- 78.
Schmidt O. Die Spongien des Meerbusen von Mexico (Und des caraibischen Meeres). Heft II. Abtheilung II. Hexactinelliden. Abtheilung III. Tetractinelliden. Monactinelliden und Anhang. Nachträge zu Abtheilung I (Lithistiden). In: Reports on the dredging under the supervision of Alexander Agassiz, in the Gulf of Mexico, by the USCSS ‘Blake’. (Gustav Fischer:Jena); 1880b. pp. 33–90, pls V-X.
- 79. Hentschel E. Kiesel und Hornschwämme der Aru und Kei-lnseln. Abhandl. senckenb. naturf. Ges. 1912; 34(3): 293–448.
- 80. Topsent E. Spongiaires de la Baie d’Amboine. (Voyage de MM. M. Bedot et C. Pictet dans l’Archipel Malais). Rev Suisse Zool. 1897a; 4: 421–487, pls 18–21.
- 81. Downey RV, Griffiths HJ, Linse K, Janussen D. Diversity and Distribution Patterns in High Southern Latitude Sponges. PLoS One. 2012; 7(7): e41672. pmid:22911840
- 82.
Rodriguez PR, Muricy G. A new species of Cinachyra (Demospongiae: Tetillidae) collected by Project REVIZEE off Espírito Santo State, SE Brazil. MR Custódio; G. Lôbo-Hajdu. 2007; 547–553.
- 83. Cárdenas P, Pérez T, Boury-Esnault N. Sponge systematics facing new challenges. Adv Mar Biol. 2012; 61: 79–209. pmid:22560778
- 84. Morrow C, Cárdenas P. Proposal for a revised classification of the Demospongiae (Porifera). Front Zool. 2015; 12(1): 7.