Abstract Abstract
Background
The checklist of the ascidian fauna (Tunicata: Ascidiacea) of Greece was compiled within the framework of the Greek Taxon Information System (GTIS), an application of the LifeWatchGreece Research Infrastructure (ESFRI) aiming to produce a complete checklist of species recorded from Greece. This checklist was constructed by updating an existing one with the inclusion of recently published records. All the reported species from Greek waters were taxonomically revised and cross-checked with the Ascidiacea World Database.
New information
The updated checklist of the class Ascidiacea of Greece comprises 75 species, classified in 33 genera, 12 families, and 3 orders. In total, 8 species have been added to the previous species list (4 Aplousobranchia, 2 Phlebobranchia, and 2 Stolidobranchia). Aplousobranchia was the most speciose order, followed by Stolidobranchia. Most species belonged to the families Didemnidae, Polyclinidae, Pyuridae, Ascidiidae, and Styelidae; these 4 families comprise 76% of the Greek ascidian species richness. The present effort revealed the limited taxonomic research effort devoted to the ascidian fauna of Greece, which is attributed to the lack of experts and low sampling effort. Therefore, major knowledge gaps on the ascidian diversity of Greece occur and further research in this field is needed.
Keywords: Sea-squirts, Aplousobranchia , Phlebobranchia , Stolidobranchia , Aegean Sea, Levantine Sea, Ionian Sea, eastern Mediterranean
Introduction
The class Ascidiacea (phylum Chordata, subphylum Tunicata) is globally represented by over 2,800 marine species (Shenkar and Swalla 2011, Shenkar et al. 2016b). Ascidians have been identified as a distinct zoological group since the ancient times; Aristotle was the first who described these peculiar animals, "Téthya", as the most extraordinary ones having a completely hidden body inside a leathery shell attached on rocks and with two openings some distance apart (Voultsiadou and Vafidis 2007). Their taxonomic classification proved to be challenging for zoologists. As members of the subphylum Tunicata, their close affinity to vertebrates has been recently confirmed by phylogenomic studies (Delsuc et al. 2006). Furthermore, the original classification of Lahille (1886), which classified the ascidian species into the orders Aplousobranchia, Phlebobranchia, and Stolidobranchia according to the structure of the branchial sac, is supported by molecular phylogeny and is currently accepted by most taxonomists (Shenkar and Swalla 2011). However, there are still different views on the placement of several families into orders, and the phylogenetic relationships within the ascidians remain fuzzy (Turon and López-Legentil 2004, Moreno et al. 2008, Pérez-Portela et al. 2009, Tsagkogeorga et al. 2009, Shenkar et al. 2016a).
The first list of Mediterranean ascidians (Pérès 1958, Pérès 1967) reported 132 species; since then, the relevant scientific research increased leading to 229 ascidian species at present (Coll et al. 2010, Shenkar and Swalla 2011). Most records are from the western Mediterranean (165 species), where much more effort has been devoted as opposed to the eastern basin, from which only 86 species have been reported (Koukouras et al. 1995). Among Mediterranean ascidians, 103 exclusive species are included and the entire basin has been recognized as an area of endemism, at least for this specific taxonomic group (Naranjo et al. 1998, Moreno et al. 2014).
In the Greek seas, however, only scattered records of ascidian species were available, either in relevant faunistic accounts (e.g. Hartmeyer 1904, Monniot and Monniot 1974, Koukouras and Siamidou-Efremidou 1978) or in general ecological publications (e.g. Pérès and Picard 1958, Kiseleva 1963, Vamvakas 1971). Koukouras et al. (1995) published the first checklist of the Aegean Ascidiacea, covering also the eastern Mediterranean basin and the Black Sea. So far, this work was the only comprehensive systematic account on the Greek ascidians, combining primary data with an exhaustive literature review. After this publication, a number of studies have been conducted covering various aspects of ascidian biology, such as population dynamics (Panagiotou et al. 2007, Panagiotou et al. 2008, Vafidis et al. 2008), reproduction (Panagiotou et al. 2008, Vafidis et al. 2008), fisheries (Antoniadou and Vafidis 2008), and ecology in general (Morri et al. 1999, Antoniadou et al. 2006, Antoniadou et al. 2013, Sini et al. 2014) or focusing on ascidian associations with other invertebrates (Voultsiadou et al. 2007, Voultsiadou et al. 2010). This research effort has led to some new records of ascidian species in the Aegean Sea (i.e. Morri et al. 1999, Sini et al. 2014), in parallel with additional biodiversity records (Thessalou-Legaki et al. 2012) and the presence of non-indigenous species (Kondilatos et al. 2010, Katsanevakis et al. 2014).
Therefore, the aim of the present work is to compile an updated checklist of Ascidiacea of the Greek seas. For this purpose, the earlier list compiled by Koukouras et al. (1995) has been extended, updated, and annotated according to the recent literature and taxonomic status.
Materials and methods
The Checklist of Ascidiacea of Greece (Suppl. material 1) was compiled within the context of the Greek Taxon Information System (GTIS). GTIS is an application of the LifeWatchGreece Research Infrastructure (ESFRI) aiming to produce a complete inventory of the Greek biota, by joining relevant efforts. As a first step, the publication of Preliminary Checklists for each taxonomic group has been suggested (Bailly et al. 2016). The present checklist of ascidians has been based on the key-publication of Koukouras et al. (1995), who had compiled the ascidian species list of the Aegean Sea for the first time. In the course of the current study, all recent primary literature was also thoroughly searched and the relevant data were incorporated into the updated species list. New species additions are annotated in the checklist and cited along with the first literature reference reporting their presence in the Greek seas. Non-indigenous species (NIS) are also marked. A cross-checking of all species names and their higher classification was carried through the Ascidiacea World Database, AWD (Shenkar et al. 2016b); the classification followed in the present checklist is the one proposed by the AWD, which contains an updated list of all ascidian species, recursively revised by ascidian taxonomy experts (Shenkar and Swalla 2011).
Checklists
Checklist of Ascidiacea known to occur in Greek waters
Ascidiacea
Aplousobranchia
Clavelinidae
Clavelina dellavallei
(Zirpolo, 1825)
Clavelina lepadiformis
(Müller, 1776)
Didemnidae
Didemnum amourouxi
Lafargue, 1976
Didemnum coriaceum
(Drasche, 1883)
Didemnum drachi
Lafargue, 1975
Didemnum fulgens
(Milne Edwards, 1841)
Didemnum granulosum
(Drasche, 1883)
Didemnum maculosum
(Milne Edwards, 1841)
Didemnum peyrefittense
Brément, 1913
Diplosoma listerianum
(Milne Edwards, 1841)
Notes
Recorded by Morri et al. (1999)
Diplosoma spongiforme
(Giard, 1872)
Lissoclinum perforatum
(Giard, 1872)
Notes
Recorded by Thessalou-Legaki et al. (2012)
Polysyncraton bilobatum
Lafargue, 1968
Polysyncraton lacazei
(Giard, 1872)
Trididemnum cereum
(Giard, 1872)
Trididemnum inarmatum
(Drasche, 1883)
Polycitoridae
Cystodytes dellechiajei
(Della Valle, 1877)
Eudistoma costai
(Della Valle, 1877)
Polycitor crystallinus
(Renier, 1804)
Polyclinidae
Aplidium aegeaensis
(Hartmeyer, 1904)
Aplidium albicans
(Milne Edwards, 1841)
Aplidium asperum
Drasche, 1883
Aplidium conicum
(Olivi, 1792)
Aplidium elegans
(Giard, 1872)
Notes
Recorded by Sini et al. (2014)
Aplidium nordmanni
(Milne Edwards, 1841)
Aplidium pallidum
(Verrill, 1871)
Aplidium pseudolobatum
(Pérès, 1956)
Aplidium turbinatum
(Savigny, 1816)
Aplidium undulatum
Monniot & Gaill, 1978
Polyclinella azemai
Harant, 1930
Polyclinum aurantium
Milne Edwards, 1841
Notes
Recorded by Morri et al. (1999)
Pseudodistoma cyrnusense
Pérès, 1952
Phlebobranchia
Ascidiidae
Ascidia colleta
Monniot C. & Monniot F., 1970
Ascidia mentula
Müller, 1776
Ascidia muricata
Heller, 1874
Ascidia salvatoris
(Traustedt, 1885)
Ascidia virginea
Müller, 1776
Ascidiella aspersa
(Müller, 1776)
Ascidiella scabra
(Müller, 1776)
Phallusia fumigata
(Grube, 1864)
Phallusia mammillata
(Cuvier, 1815)
Phallusia nigra
Savigny, 1816
Notes
Recorded by Kondilatos et al. (2010); NIS
Cionidae
Ciona intestinalis
(Linnaeus, 1767)
Ciona roulei
Lahille, 1887
Notes
Recorded by Thessalou-Legaki et al. (2012)
Corellidae
Corella parallelogramma
(Müller, 1776)
Rhodosoma turcicum
(Savigny, 1816)
Diazonidae
Diazona violacea
Savigny, 1816
Rhopalaea neapolitana
Philippi, 1843
Perophoridae
Ecteinascidia turbinata
Herdman, 1880
Notes
Recorded by Monniot (1983)
Perophora listeri
Wiegman, 1835
Stolidobranchia
Molgulidae
Eugyra arenosa
(Alder & Hancock, 1848)
Molgula appendiculata
Heller, 1877
Molgula manhattensis
(De Kay, 1843)
Molgula occulta
Kupffer, 1875
Pyuridae
Halocynthia papillosa
(Linnaeus, 1767)
Herdmania momus
(Savigny, 1816)
Notes
Recorded by Katsanevakis et al. (2014); NIS
Microcosmus claudicans
(Savigny, 1816)
Microcosmus nudistigma
Monniot C., 1962
Microcosmus polymorphus
Heller, 1877
Microcosmus sabatieri
Roule, 1885
Microcosmus savignyi
Monniot, 1962
Microcosmus vulgaris
Heller, 1877
Pyura dura
(Heller, 1877)
Pyura microcosmus
(Savigny, 1816)
Pyura squamulosa
(Alder, 1863)
Pyura tessellata
(Forbes, 1848)
Styelidae
Botryllus schlosseri
(Pallas, 1766)
Botrylloides leachii
(Savigny, 1816)
Distomus variolosus
Gaertner, 1774
Polycarpa caudata
Monniot C. & Monniot F., 1974
Polycarpa fibrosa
(Stimpson, 1852)
Polycarpa gracilis
Heller, 1877
Polycarpa pomaria
(Savigny, 1816)
Styela canopus
(Savigny, 1816)
Styela plicata
(Lesueur, 1823)
Discussion
A total of 75 species classified, according to AWD, into 33 genera, 12 families and 3 orders, have been reported from the Greek seas. In addition, Ascidia conchilega, Müller, 1776 which is included in AWD and WoRMS databases is a doubtful record for the Greek seas because its original reference for the area is missing and thus it was not included in the list by Koukouras et al. (1995). Aplousobranchia and Stolidobranchia are the most speciose orders with 32 and 25 species, respectively. Aplousobranchia reach 36 species, if the families Diazonidae and Cionidae are included therein instead of Phlebobranchia, as suggested by various ascidian taxonomists based on morphological, developmental, and molecular data (Kott 1990, Turon and López-Legentil 2004, Shenkar and Swalla 2011, Shenkar et al. 2016a) but not currently adopted by AWD. The families Didemnidae (14 species), Polyclinidae (12 species), Pyuridae (12 species), Ascidiidae (10), and Styelidae (9 species) comprised the highest number of species, covering altogether 76% of the Greek ascidian species richness. The first two families have been identified as the most speciose ones across most Mediterranean longitudinal bands (Moreno et al. 2014).
Most ascidian species included in the present checklist were already known as elements of the Greek fauna (Koukouras et al. 1995), while 8 new additions were made in the course of this compilation. These additions include: 4 species of Aplousobranchia, namely Aplidium elegans, Diplosoma listerianum, Lissoclinum perforatum, and Polyclinum aurantium; 2 species of Phlebobranchia, namely Ciona roulei and Ecteinascidia turbinata; and 2 species of Stolidobranchia, namely Herdmania momus and Phallusia nigra. Although the latter species may need additional confirmation because of the identification uncertainty between the 3 darkly pigmented Phallusia species when based on exclusively external features (Vandepas et al. 2015), we consider its presence as valid since it has been reported from the south sector of the Aegean Sea by multiple authors (Kondilatos et al. 2010, Çinar 2014).
The Greek ascidian fauna is mainly composed by species of Atlanto-Mediterranean origin (44.4%) or by endemic species (40.3%), as previously suggested (Koukouras et al. 1995). Among the newly added species, C. roulei is a Mediterranean endemic, whereas Phallusia nigra and Herdmania momus are considered non-indigenous species (NIS) of circum(sub)tropical and Indo-pacific origin, respectively (Gerovasileiou et al. 2016); both species have been probably introduced through shipping (Galil et al. 2016). Another three species, i.e. Molgula occidentalis Traustedt, 1883, Pycnoclavella nana (Lahille, 1890), and Microcosmus exasperatus Heller, 1878, have been recently reported from the Turkish coasts of the Aegean (Çinar 2014); this may imply their presence in the nearby Greek coasts, since they are part of the same ecoregion, the Aegean Archipelago (Spalding et al. 2007) and also part of the Levantine cluster, i.e. areas highly impacted by Erythraean species migration (Galil et al. 2016). Finally, we should mention the presence of Symplegma brakenhielmi (Michaelsen, 1904) in the Turkish levantine coasts (Çinar et al. 2006). Since several non-indigenous ascidians, such as P. nigra and H. momus, have invaded the Greek waters few years after their first record in Turkish waters, it is reasonable to expect them to be reported from south Greece as well, within next few years.
The present updated checklist of Ascidiacea of the Greek seas summarizes the status of the current knowledge. However, a major gap in our knowledge on ascidian diversity of the Greek seas is obvious when the number of species is compared to those known from the western Mediterranean. This can be attributed to two main reasons: (i) the absence of ascidian expertise in Greece and, (ii) the fact that the entire literature on Greek ascidians refers almost exclusively to the Aegean Sea. The necessity for further research on ascidian diversity becomes therefore obvious and expands to the Ionian and Levantine coasts of Greece, from which the ascidian fauna has practically not at all been studied so far.
Supplementary Material
Checklist of the ascidian fauna (Tunicata: Ascidiacea) of Greece
Chryssanthi Antoniadou, Vasilis Gerovasileiou, Nicolas Bailly
Data type: Taxonomic checklist
Brief description: Taxonomic checklist of Ascidiacea known to occur in Greek waters.
File: oo_97915.xls
Acknowledgements
This work was supported by the LifeWatchGreece infrastructure (MIS 384676), funded by the Greek Government under the General Secretariat of Research and Technology (GSRT), ESFRI Projects, National Strategic Reference Framework (NSRF). We would like to thank Dr. Xavier Turon and anonymous reviewers for their constructive comments.
References
- Antoniadou C., Vafidis D. First assessment of Microcosmus sabatieri (Tunicata: Ascidiacea) small-scale artisanal fishery in the South Aegean Sea (eastern Mediterranean) Cahiers de Biologie Marine. 2008;49:97–100. [Google Scholar]
- Antoniadou C., Voultsiadou E., Chintiroglou C. Sublittoral megabenthos along cliffs of different profile (Aegean Sea, eastern Mediterranean) Belgian Journal of Zoology. 2006;136:69–79. [Google Scholar]
- Antoniadou Chryssanthi, Voultsiadou Eleni, Rayann Abdalnasser, Chintiroglou Chariton. Sessile biota fouling farmed mussels: diversity, spatio-temporal patterns, and implications for the basibiont. https://doi.org/10.1017/s0025315412001932. Journal of the Marine Biological Association of the United Kingdom. 2013;93(6):1593–1607. doi: 10.1017/s0025315412001932. [DOI] [Google Scholar]
- Bailly N., Gerovasileiou V., Arvanitidis C., Legakis A. Introduction to the Greek Taxon Information System (GTIS) in LifeWatchGreece: the construction of the Preliminary Checklists of species of Greece. Biodiversity Data Journal. 2016;LifeWatchGreece: Research infrastructure (ESFRI) for biodiversity data and data observatories:in press. doi: 10.3897/BDJ.4.e7959. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Çinar M. E. Checklist of the phyla Platyhelminthes, Xenacoelomorpha, Nematoda, Acanthocephala, Myxozoa, Tardigrada, Cephalorhyncha, Nemertea, Echiura, Brachiopoda, Phoronida, Chaetognatha, and Chordata (Tunicata, Cephalochordata, and Hemichordata) from the coasts of Turkey. https://doi.org/10.3906/zoo-1405-70. Turkish Journal of Zoology. 2014;38:698–722. doi: 10.3906/zoo-1405-70. [DOI] [Google Scholar]
- Çinar M. E, Bilecenoglu M., Öztürk B., Can A. New records of alien species on the Levantine coast of Turkey. https://doi.org/10.3391/ai.2006.1.2.6. Aquatic Invasions. 2006;1(2):84–90. doi: 10.3391/ai.2006.1.2.6. [DOI] [Google Scholar]
- Coll Marta, Piroddi Chiara, Steenbeek Jeroen, Kaschner Kristin, Rais Lasram Frida Ben, Aguzzi Jacopo, Ballesteros Enric, Bianchi Carlo Nike, Corbera Jordi, Dailianis Thanos, Danovaro Roberto, Estrada Marta, Froglia Carlo, Galil Bella S., Gasol Josep M., Gertwagen Ruthy, Gil João, Guilhaumon François, Kesner-Reyes Kathleen, Kitsos Miltiadis-Spyridon, Koukouras Athanasios, Lampadariou Nikolaos, Laxamana Elijah, la Cuadra Carlos M. López-Fé de, Lotze Heike K., Martin Daniel, Mouillot David, Oro Daniel, Raicevich Saša, Rius-Barile Josephine, Saiz-Salinas Jose Ignacio, Vicente Carles San, Somot Samuel, Templado José, Turon Xavier, Vafidis Dimitris, Villanueva Roger, Voultsiadou Eleni. The Biodiversity of the Mediterranean Sea: Estimates, Patterns, and Threats. https://doi.org/10.1371/journal.pone.0011842. PLoS ONE. 2010;5(8):e11842. doi: 10.1371/journal.pone.0011842. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Delsuc Frédéric, Brinkmann Henner, Chourrout Daniel, Philippe Hervé. Tunicates and not cephalochordates are the closest living relatives of vertebrates. https://doi.org/10.1038/nature04336. Nature. 2006;439(7079):965–968. doi: 10.1038/nature04336. [DOI] [PubMed] [Google Scholar]
- Galil Bella S., Marchini Agnese, Occhipinti-Ambrogi Anna. East is east and West is west? Management of marine bioinvasions in the Mediterranean Sea. https://doi.org/10.1016/j.ecss.2015.12.021. Estuarine, Coastal and Shelf Science. 2016;in press:1–10. doi: 10.1016/j.ecss.2015.12.021. [DOI] [Google Scholar]
- Gerovasileiou Vasilis, Voultsiadou Eleni, Issaris Yiannis, Zenetos Argyro. Alien biodiversity in Mediterranean marine caves. https://doi.org/10.1111/maec.12268. Marine Ecology. 2016;37(2):239–256. doi: 10.1111/maec.12268. [DOI] [Google Scholar]
- Hartmeyer R. Tunicaten von Aegina. Ein Beitrag zur Kenntnis der Fauna des östlichen Mittelmeeres. Zoologischer Anzeiger. 1904;27:321–327. [Google Scholar]
- Katsanevakis S., Acar Ü., Ammar I., Balci B. A., Bekas P., Belmonte M., Chintiroglou C. C., Consoli P., Dimiza M., Fryganiotis K., Gerovasileiou V., Gnisci V., Gülşahin N., Hoffman R., Issaris Y., Izquierdo-Gomez D., Izquierdo-Muñoz A., Kavadas S., Koehler L., Konstantinidis E., Mazza G., Nowell G., Önal U., Özen M. R., Pafilis P., Pastore M., C. Perdikaris, Poursanidis D., Prato E., Russo F., Sicuro B., Tarkan A. N., Thessalou-Legaki M., Tiralongo F., Triantaphyllou M., Tsiamis K., Tunҫer S., Turan C., Türker A., Yapici S. New Mediterranean Biodiversity Records (October, 2014) Mediterranean Marine Science. 2014;15:675–695. [Google Scholar]
- Kiseleva M. I. Répartition qualitative du benthos de la Mer Egée. Trudy Sevastopol’skoi Biologicheskoi Stantsii. 1963;14:192–200. [Google Scholar]
- Kondilatos Gerasimos, Corsini-Foka Maria, Pancucci-Papadopoulou M. A., Occurrence of the first non-indigenous ascidian Phallusia nigra Savigny, 1816 (Tunicata: Ascidiacea) in Greek waters. https://doi.org/10.3391/ai.2010.5.2.08. Aquatic Invasions. 2010;5(2):181–184. doi: 10.3391/ai.2010.5.2.08. [DOI] [Google Scholar]
- Kott P. The Australian Ascidiacea. Part 2, Aplousobranchia (1) Memoirs of the Queensland Museum. 1990;29:1–266. [Google Scholar]
- Koukouras A., Siamidou-Efremidou O. Benthic fauna of the North Aegean Sea. I. Cionidae and Ascidiidae (Tunicata, Ascidiacea) Vie et Milieux. 1978;28-29:635–646. [Google Scholar]
- Koukouras A., Voultsiadou-Koukoura E., Kevrekidis T., Vafidis D. Ascidian fauna of the Aegean Sea with a check list of the eastern Mediterranean and Black Sea species. Annales de l’Institut Océanographique. 1995;71:19–34. [Google Scholar]
- Lahille M. F. Sur la classification des Tuniciers. Comptes Rendus de l’Académie des Sciences Paris. 1886;102:1573–1575. [Google Scholar]
- Monniot C. Ascidies littorales de Guadeloupe. II. Phlébobranches. Bulletin du Muséum national d’Histoire Naturelle Paris. 1983;5:51–71. [Google Scholar]
- Monniot C., Monniot F. Ascidies abyssales de Méditerranée récoltées par le “Jean Charcot” (campagnes Polymède) Bulletin du Muséum national d’Histoire Naturelle Paris. 1974;251:1353–1360. [Google Scholar]
- Moreno T. R., de Faria S. B., Rocha R. M. Phylogeny of the Aplousobranchia (Tunicata: Ascidiacea) https://doi.org/10.1590/s0101-81752008000200016. Revista Brasileira de Zoologia. 2008;25:269–298. doi: 10.1590/s0101-81752008000200016. [DOI] [Google Scholar]
- Moreno T. R., de Faria S. B., Rocha R. M. Biogeography of Atlantic and Mediterranean ascidians. https://doi.org/10.1007/s00227-014-2483-x. Marine Biology. 2014;161:2023–2033. doi: 10.1007/s00227-014-2483-x. [DOI] [Google Scholar]
- Morri C., Bianchi C. N., Cocito S., Periano A., DeBiase A. M., Aliani S., Pansini M., Boyer M., Ferdeghini F., Pestarino M., Dando P. Biodiversity of marine sessile epifauna at an Aegean island subject to hydrothermal activity: Milos, eastern Mediterranean Sea. Marine Biology. 1999;135:729–739. doi: 10.1007/s002270050674. [DOI] [Google Scholar]
- Naranjo Santiago, Carballo José Luis, García-Gómez José Carlos. Towards a knowledge of marine boundaries using ascidians as indicators: characterising transition zones for species distribution along Atlantic-Mediterranean shores. https://doi.org/10.1111/j.1095-8312.1998.tb01539.x. Biological Journal of the Linnean Society. 1998;64(2):151–177. doi: 10.1111/j.1095-8312.1998.tb01539.x. [DOI] [Google Scholar]
- Panagiotou Magdalini, Antoniadou Chryssanthi, Chintiroglou Chariton. Population dynamics and reproductive status of Microcosmus savignyi Monniot, 1962 (Thermaikos Gulf, Eastern Mediterranean): a preliminary assessment. https://doi.org/10.1080/00222930701835522. Journal of Natural History. 2008;42:545–558. doi: 10.1080/00222930701835522. [DOI] [Google Scholar]
- Panagiotou M., Antoniadou C., Krestenitis Y., Chintiroglou C. Stock assessment of the dominant ascidians: Microcosmus savignyi, Styela plicata and Phallusia mammillata, in Thessaloniki Bay (Thermaikos Gulf) Fresenius Environmental Bulletin. 2007;16:1012–1019. [Google Scholar]
- Pérès J. M. Origine et affinités du peuplement en ascidies de la Méditerranée. Rapports et Procès Verbaux de la CIESM. 1958;14:493–502. [Google Scholar]
- Pérès J. M. The Mediterranean Benthos. Oceanography and Marine Biology: An Annual Review. 1967;5:449–533. [Google Scholar]
- Pérès J. M., Picard J. Recherches sur les peuplements benthiques de la Méditerranée nord-orientale. Annales de l’Institut Océanographique Monaco. 1958;34:213–291. [Google Scholar]
- Pérez-Portela R., Bishop J. D.D., Davis A. R., Turon X. Phylogeny of the families Pyuridae and Styelidae (Stolidobranchiata, Ascidiacea) inferred from mitochondrial and nuclear DNA sequences. https://doi.org/10.1016/j.ympev.2008.11.014. Molecular Phylogenetics and Evolution. 2009;50(3):560–570. doi: 10.1016/j.ympev.2008.11.014. [DOI] [PubMed] [Google Scholar]
- Shenkar Noa, Swalla B. J. Global Diversity of Ascidiacea. https://doi.org/10.1371/journal.pone.0020657. PLoS ONE. 2011;6(6):e20657. doi: 10.1371/journal.pone.0020657. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shenkar N., Koplovitz G., Dray L., Gissi C., Huchon D. Back to solitude: Solving the phylogenetic position of the Diazonidae using molecular and developmental characters. https://doi.org/10.1016/j.ympev.2016.04.001. Molecular Phylogenetics and Evolution. 2016;100:51–56. doi: 10.1016/j.ympev.2016.04.001. [DOI] [PubMed] [Google Scholar]
- Shenkar N., Gittenberger A., Lambert G., Rius M., Moreira Da Rocha R., Swalla B. J., Turon X. Ascidiacea World Database. http://www.marinespecies.org/ascidiacea/
- Sini M., Garrabou J., Koutsoubas D. Diversity and structure of coralligenous assemblages dominated by Eunicella cavolini (Koch, 1887) in the Aegean Sea. In: Bouafif C., Langar H., Ouerghi A., editors. Proceedings of the second Mediterranean Symposium on the conservation of Coralligenous and other Calcareous Bio-Concretions. RAC/SPA; Tunis: 2014. [Google Scholar]
- Spalding M. D., Fox H. E., Allen G. R., Davidson N., Ferdaña Z. A., Finlayson M., Halpern B. S., Jorge M. A., Lombana A., Lourie S. A., Martin K. D., McManus E., Molnar J., Recchia C. A., Robertson J. Marine Ecoregions of the World: A Bioregionalization of Coastal and Shelf Areas. https://doi.org/10.1641/b570707. BioScience. 2007;57(7):573. doi: 10.1641/b570707. [DOI] [Google Scholar]
- Thessalou-Legaki M., Aydogan O., Bekas P., Bilge G., Boyaci Y. O., Brunelli E., Circosta V., Crocetta F., Durucan F., Erdem M., Ergolavou A., Filiz H., Fois F., Gouva E., Kapiris K., Katsanevakis S., Kljajic Z., Konstantinidis E., Konstantinou G., Koutsogiannopoulos D., Lamon S., Macic V., Mazzette R., Meloni D., Mureddu A., Paschos I., Perdikaris C., Piras F., Poursanidis D., Ramos-Espla A. A., Rosso A., Sordino P., Sperone E., Sterioti A., Taskin E., Toscano F., Tripepi S., Tsiakkiros L., Zenetos A. New Mediterranean Biodiversity Records (December 2012) https://doi.org/10.12681/mms.313. Mediterranean Marine Science. 2012;13(2):312–327. doi: 10.12681/mms.313. [DOI] [Google Scholar]
- Tsagkogeorga G., Turon X., Hopcroft R. R., Tilak M., Feldstein T., Shenkar N., Loya Y., Huchon D., Douzery J. P., Delsuc F. An updated 18S rRNA phylogeny of tunicates based on mixture and secondary structure models. BMC Evolutionary Biology. 2009;9:187. doi: 10.1186/1471-2148-9-187. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Turon X., López-Legentil S. Ascidian molecular phylogeny inferred from mtDNA data with emphasis on the Aplousobranchiata. https://doi.org/10.1016/j.ympev.2004.06.011. Molecular Phylogenetics and Evolution. 2004;33:309–320. doi: 10.1016/j.ympev.2004.06.011. [DOI] [PubMed] [Google Scholar]
- Vafidis Dimitris, Antoniadou Chryssanthi, Chintiroglou Chariton. Population dynamics, allometric relationships and reproductive status of Microcosmus sabatieri (Tunicata: Ascidiacea) in the Aegean Sea. https://doi.org/10.1017/s0025315408001811. Journal of the Marine Biological Association of the UK. 2008;88(5):1043–1051. doi: 10.1017/s0025315408001811. [DOI] [Google Scholar]
- Vamvakas C. Contribution to the study of soft substrata benthic biocoenoses of Greek seas area W. Saronikos Gulf. Hellenic Oceanology and Limnology. 1971;10:1–152. [Google Scholar]
- Vandepas L. E., Oliveira L. M., Lee S. S.C., Hirose E., Rocha R. M., Swalla B. J. Biogeography of Phallusia nigra: is it really black and white? Biological Bulletin. 2015;228:52–64. doi: 10.1086/BBLv228n1p52. [DOI] [PubMed] [Google Scholar]
- Voultsiadou E., Vafidis D. Marine invertebrate diversity in Aristotle’s zoology. Contributions to Zoology. 2007;76:103–120. [Google Scholar]
- Voultsiadou Eleni, Pyrounaki Maria-Myrto, Chintiroglou Chariton. The habitat engineering tunicate Microcosmus sabatieri Roule, 1885 and its associated peracarid epifauna. https://doi.org/10.1016/j.ecss.2007.04.003. Estuarine, Coastal and Shelf Science. 2007;74:197–204. doi: 10.1016/j.ecss.2007.04.003. [DOI] [Google Scholar]
- Voultsiadou Eleni, Kyrodimou Marianthi, Antoniadou Chryssanthi, Vafidis Dimitris. Sponge epibionts on ecosystem-engineering ascidians: The case of Microcosmus sabatieri. https://doi.org/10.1016/j.ecss.2009.11.035. Estuarine, Coastal and Shelf Science. 2010;86(4):598–606. doi: 10.1016/j.ecss.2009.11.035. [DOI] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Checklist of the ascidian fauna (Tunicata: Ascidiacea) of Greece
Chryssanthi Antoniadou, Vasilis Gerovasileiou, Nicolas Bailly
Data type: Taxonomic checklist
Brief description: Taxonomic checklist of Ascidiacea known to occur in Greek waters.
File: oo_97915.xls