Epigamia Nygren, 2004, gen. n.

Epigamia gen. n. Linnean name definition . Type species Autolytus noroi Imajima & Hartman, 1964. Node­based name definition . Epigamia refers to the least inclusive clade comprising E. noroi (Imajima & Hartman, 1964), and E. macrophtalma (Marenzeller, 1875). Apomorphies . Morphologically sup...

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Main Author: Nygren, Arne
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Published: Zenodo 2004
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Online Access:https://dx.doi.org/10.5281/zenodo.6273268
https://zenodo.org/record/6273268
id ftdatacite:10.5281/zenodo.6273268
record_format openpolar
institution Open Polar
collection DataCite Metadata Store (German National Library of Science and Technology)
op_collection_id ftdatacite
language unknown
topic Biodiversity
Taxonomy
Animalia
Annelida
Polychaeta
Phyllodocida
Syllidae
Epigamia
spellingShingle Biodiversity
Taxonomy
Animalia
Annelida
Polychaeta
Phyllodocida
Syllidae
Epigamia
Nygren, Arne
Epigamia Nygren, 2004, gen. n.
topic_facet Biodiversity
Taxonomy
Animalia
Annelida
Polychaeta
Phyllodocida
Syllidae
Epigamia
description Epigamia gen. n. Linnean name definition . Type species Autolytus noroi Imajima & Hartman, 1964. Node­based name definition . Epigamia refers to the least inclusive clade comprising E. noroi (Imajima & Hartman, 1964), and E. macrophtalma (Marenzeller, 1875). Apomorphies . Morphologically supported by one apomorphy (Fig. 4): 1) body ciliation as 2 trochs per segment (character 4), other most parsimonious reconstructions (MPRs) possible, character state change is a parallelism, later reversed within clade, character state unknown in E. labordai (San Martín & López, 2002). General description . Atokous form . Length 1.8–22 mm for 20–88 chaetigers; width, measured at level of proventricle and excluding parapodial lobes, 0.2–1.5 mm. Body shape, excluding parapodial lobes, cylindrical to rounded rectangular in transection, venter flattened; body width fairly constant with tapering end. Ciliation as 1 or 2 trochs per segment (unknown in some taxa). Prostomium usually rounded rectangular, in E. macrophtalma more rounded oval. Four eyes, with lenses, in trapezoid arrangement, anterior pair larger. Eyes confluent or separated; eye spots absent or present. Palps fused at base or completely fused; in dorsal view projecting 1 / 5 – 1 / 2 of prostomial length. Extension of nuchal epaulettes from end of chaetiger 1 to end of chaetiger 6. Prostomium with 3 antennae; median antenna inserted medially on prostomium, the lateral on anterior margin. Tentacular cirri 2 pairs. Dorsal cirri alternate in length, except in E. macrophtalma cirrophores equal; cirrophores shorter or equal in length to parapodial lobes. All appendages cylindrical except in E. macrophtalma with flattened dorsal cirri from chaetiger 3. Parapodial lobes generally large, rounded to rounded rectangular; in some taxa with slightly swollen dorsal part. Except for bayonet chaetae, all chaetae compounds with bidentate blades; serration present. Compounds with small or large distal tooth. Single thin bayonet chaetae, subdistally denticulated. Pharynx with single to multiple sinuations. Trepan with various types of denticulation, in 1–3 rings. Basal ring present; infradental spines absent or present. Proventricle with varying number of rows of square shaped muscle cells. Pygidium with 2 cirri (reported length compared to body width, excluding parapodial lobes, at level of proventricle, if not otherwise stated); median papilla absent. Epitokes . Male. Body divided into 3 regions, anterior with 11 (see E. noroi ) or 14 uniramous chaetigers (region a), median with c. 37 biramous chaetigers (region b), and posterior with 3–23 uniramous chaetigers (region c). Body widest in anteromedian half of region b; body width measured in region a, as body width excluding parapodial lobes, and in region b, at the widest part, as body width including parapodial lobes. Ciliation as in atokes. Prostomium rounded rectangular, wider than long, with straight or concave anterior margin. Eyes large, 2 pairs, with lenses; eyes situated on dorsal and ventral side of prostomium, ventral pair larger. Palps present, much smaller than in atokes. Nuchal epaulettes as in atokes. Large median antenna inserted medially on prostomium, lateral antennae inserted on anterior margin. Lateral antennae bifid, basal part c. 1 / 2 of total length; outer ventral rami equal or longer than inner dorsal rami. Basal part and inner dorsal rami segmented with abundant cilia. Pair of small frontal processes inserted anterolaterally to dorsal pair of eyes. Tentacular cirri as in atokes. First dorsal cirri, larger than in atokes, equal in shape and size to median antenna. Achaetous knobs absent. Cirri with alternation in direction and size in region a, and c as in atokes; cirri in region b with less obvious alternation in both size and direction. However, this needs to be explored using a larger sample­size. Cirri length measured as body width excluding parapodial lobes in region a, and c; as body width including parapodial lobes in region b. Median antenna with large ceratophore, large cirrophores present on first dorsal cirri; cirrophores otherwise as in atokes. Appendages cylindrical, suspected to be flattened in epitokes of E. macrophtalma . Pharynx and proventricle disintegrates at some stage, and is totally absent in fully developed epitokes. Neuropodia as in atokes but generally larger and with enlarged, and prolonged dorsal part, especially in region b; in region b also with well­developed flattened notopodial lobes. Neuropodial aciculae as in atokes; notopodia in region b supported by c. 3 anterodorsal aciculae, and 3–4 thick and 3–5 thin posteroventral aciculae. Neuropodial chaetae as in atokes. Notopodial lobes with 20–50 swimming chaetae, in length equal to c. body width in region b including parapodial lobes. Pygidium as in atokes. Female . Body divided into 3 regions, anterior with 14 uniramous chaetigers (region a), median with 29–41 biramous chaetigers (region b), posterior with 16–33 uniramous chaetigers (region c). Body width fairly constant, slightly wider in region b; body width measured in region a, as body width excluding parapodial lobes, and in region b as body width including parapodial lobes. Ciliation as in atokes. Prostomium rounded rectangular, wider than long, with straight or concave anterior margin. Eyes large, 2 pairs, with lenses; eyes situated on dorsal and ventral side of prostomium, ventral pair larger. Palps present, much smaller than in atokes. Nuchal epaulettes as in atokes. Median antenna inserted medially on prostomium, lateral antennae inserted on anterior margin. Tentacular cirri as in atokes. Achaetous knobs absent. Cirri with alternation in direction as in atokes, except for cirri in region b with less obvious alternation; cirri length as in atokes or longer. Cirri length measured as body width excluding parapodial lobes in region a, and c; as body width including parapodial lobes in region b. Cirrophores as in atokes. Appendages cylindrical, suspected to be flattened in epitokes of E. macrophtalma . Pharynx and proventricle disintegrates at some stage, and is totally absent in fully developed epitokes. Neuropodia as in atokes but generally larger and with enlarged, and prolonged dorsal part, especially in region b; in region b also with notopodial lobes, not as developed as in male. Neuropodial aciculae as in atokes; notopodia in region b supported by 5–14 anterodorsal aciculae, and 6–8 thick and 6–9 thin posteroventral aciculae. Neuropodial chaetae as in atokes. Notopodial lobes with 25–50 swimming chaetae, in length equal to c. body width in region b including parapodial lobes. Pygidium as in atokes. Epigamia alexandri (Malmgren, 1867) comb. n. (Fig. 83 A–G) Autolytus alexandri Malmgren, 1867: 37, pl. 7, fig. 39, 39C–D; Langerhans 1879, 577; Verrill 1881, 292, pl. 12, fig. 8, 8A–C; Okada 1937; Hartman 1945: 17; Pettibone 1954: 246 –247; 1963: 147–148, fig. 37 F–G; Gidholm 1965: 36 –38; Hamond 1969 b; 1974; Hartmann­Schröder 1971: 176;? Qian & Chia 1989; San Martín 1994: 271 –272, fig. 1 A–D; Hartmann­Schröder 1996: 180 –181. Autolytus newtoni Malmgren, 1867: 36 –37. Stephanosyllis ornata Verrill, 1874 a: 132. 1874b: 361, pl. 4, fig. 1. Autolytus longigula Verrill, 1881: pl. 12, fig. 3, 3A–B. Autolytus longeferiens Saint­Joseph, 1887: 217 –219, pl. 10, fig. 95–97; Southern 1914: 39 –40; Fauvel 1923: 319 –320, fig. 122 H–K; Okada 1929 a; Cognetti 1961: 304; Gidholm 1966; 1967: 201 –203, figs 2 C, 7 G, 13 C, 27; Hartmann­Schröder 1971: 178; Kirkegaard 1992: 230 –231, fig. 112 A–C; Hartmann­Schröder 1996: 183; Nygren & Sundberg 2003: GenBank sequences, 16 S rDNA partial sequence AF 474262, and 18 S rDNA partial sequence AF 474308. Proceraea (Stephanosyllis) ornata Webster & Benedict 1887: 724. Autolytus longiferiens Elwes 1908: 202; Allen 1915: 604; McIntosh 1910: 245 –247, pl. 86, fig. 17, pl. 87, fig. 16. Autolytus paradoxus Saint­Joseph, 1887: 216 –217, pl. 10, fig. 92–94; Fauvel 1923: 318, fig. 122 E– F; Hartmann­Schröder 1971: 175. Autolytus verrilli Marenzeller, 1892: 416 –420, pl. 19, fig. 4; Wesenberg­Lund 1947: 33 –36, figs 14–15; 1950: 52, fig. 13. Proceraea rzhavskyi Britayev & San Martín, 2001: 105–113, fig. 1 A–E. Not figs 2–5. Material examined . Greenland : holotype (female epitoke) SMNH 2438, West Greenland, Davis Strait, 65 °N 60 °W, Swedish arctic expedition 1859. Norway : holotype (female epitoke) of Autolytus newtoni SMNH 2437, Spitsbergen, Storfjord, 78 ° 37 'N 19 °E, 21 Aug 1864. Russia : holotype ZMMSU 849, and 4 paratypes ZMMSU 850–853 of Proceraea rzhavskyi , Mednyy Island (Commander Islands), Gladkovskaya Bay, 54 ° 44 'N 167 ° 45 'E, 6 m, on hydroid Abietinaria turgida , 1986. Faroes : 35 spms (15 spms in formalin, 18 spms on slide, 2 spms in author's collection for DNA analyses), South of Vagar, 61 ° 56.8 'N 06° 59.5 'W, triangle­dredge, 76–78 m, hydroids, 27 Jun 1997; 7 spms (1 spm in formalin, 6 spms in author's collection for DNA analyses), East of Nolsøy, 62 °01.5'N 06° 31.9 W, triangle dredge, 41 m, bedrock, 27 Jul 1997; 29 spms (17 spms in formalin, 9 spms on slides (2 rear ends in author's collection for DNA analyses), 3 spms in author's collection for DNA analyses), East of Bordøy, 62 ° 24.6 'N 06° 26.3 'W, triangle dredge, 65–68 m, shellgravel with hydroids, 17 Jul 1997; 7 spms (6 spms on slides, 1 in author's collection for DNA analyses), East of Bordøy, 62 °08.4'N 06° 23.4 'W, triangle dredge, 77 m, shellgravel with hydroids, 17 Jul 1997. France : 11 syntypes of Autolytus longeferiens MNHN 1031–1041, Dinard, Jun–Aug 1872–1881; holotype of Autolytus paradoxus MNHN 1030, Dinard, 18 Jul 1887. USA : 8 spms (4 spms in formalin (2 rear ends in author's collection for DNA analyses), 2 spms on slides (rear ends in author's collection for DNA analyses), 2 spms in author's collection for DNA analyses), Rock Pt and López Island, 48 ° 29.6 'N 122 ° 56.9 'W, dredge, 75 m, Polycarpa sp., barnacles with rich hydroid fauna, few sponges, 24 Jan 2001. Diagnosis . Epigamia with a DDU­group posterior to chaetiger 27, a much convoluted pharynx, and a trepan with 1 large teeth alternating with 2–4 much smaller. Description . Length 4.5–17.2 mm for 27–88 chaetigers, width 0.20–0.72 mm. Live specimens from faint reddish or yellowish, sometimes with 3 faint red lines, to more intensely red anterior to proventricle, intestinal region orange to red­brown; anterior appendages red­tipped; eyes red. Preserved specimens without colours. Ciliation as 2 trochs per segment. Eyes confluent (Fig. 83 B); eye spots present. Palps in dorsal view projecting c. 1 / 3 of prostomial length. Nuchal epaulettes reaching between end of chaetiger 1 (small individuals), and end of chaetiger 2 (Fig. 83 A, B). Median antenna reaching chaetiger 7–15 (n= 10) in live specimens. Lateral antennae and dorsal tentacular cirri, length 1 / 2 – 2 / 3 of median antenna. Ventral tentacular cirri 1 / 3 – 1 / 2 as long as dorsal pair. First dorsal cirri as long as median antenna, second dorsal cirri as long as ventral tentacular cirri. From chaetiger 1–27 cirri with usual alternation in direction, followed by 1 DDU­groups, 1–3 DDUU­groups, and 1–13 DDU­groups (n= 6). Dorsal cirri from chaetiger 3, alternate in length (Fig. 83 A); short cirri equals 1 / 2 – 2 / 3 of body width, long cirri equal or slightly longer than body width. Cirrophores present on tentacular cirri, and all dorsal cirri. Cirrophores equal, cirrostyles unequal; short cirrostyles 1 / 2 – 2 / 3 in length of long cirrostyles; cirrophores shorter than parapodial lobes; cirrophores shorter than cirrostyles. All appendages cylindrical. Parapodial lobes large, rounded, slightly swollen dorsal to chaetal fascicle. 2–4 aciculae in anterior chaetigers, 1–2 in median and posterior. Chaetal fascicle with 9–18 compounds in anterior chaetigers, 3–13 in median and posterior. Compound chaetae with large distal tooth (Fig. 83 F); serration present. Single thin bayonet chaetae (Fig. 83 G), beginning between chaetiger 3–30. Pharynx with from one sinuation (small individuals) anterior to proventricle to multiple sinuations anterior and lateral to proventricle (Fig. 83 D). Trepan in chaetiger 1–4, with 34–44 unequal teeth, 9 large teeth and 25–35 smaller; 1 large alternating with 2–4 much smaller, in 2 rings, small teeth situated slightly inside large teeth (Fig. 83 E). Basal ring present; infradental spines present (Fig. 83 E). Proventricle equal in length to 2–4 segments in chaetiger 6–18 with 34–44 rows of muscle cells (n= 11). Anal cirri equal in length to 1– 2 times the body width. Reproduction . Epigamy (Fig. 83 C, D). Epitokous specimens caught in February to May in the North Atlantic (Hamond 1969 b). Transforming individuals observed in January in the North Pacific (pers. obs.). : Published as part of Nygren, Arne, 2004, Revision of Autolytinae (Syllidae: Polychaeta)., pp. 1-314 in Zootaxa 680 on pages 163-166, DOI: 10.5281/zenodo.157809 : {"references": ["Imajima, M. & Hartman, O. (1964) The polychaetous annelids of Japan part 1. Allan Hancock Foundation Publications. Occasional Paper, 26, 1 - 237.", "Marenzeller, E. (1875) Zur Kenntniss der adriatischen Anneliden. Zweiter Beitrag. (Polynoinen, Hesioneen, Syllideen). Sitzungsberichte der Kaiserliche Akademie der Wissenschaften, Wien, Mathematisch-Naturwissenschaftliche Klasse, 72, 1 - 43.", "San Martin, G. & Lopez, E. (2002) New species of Autolytus Grube, 1850, Paraprocerastea San Martin and Alos, 1989, and Sphaerosyllis Claparede, 1863 (Syllidae, Polychaeta) from the Iberian Peninsula. Sarsia, 87, 135 - 143.", "Malmgren, A. J. (1867) Annulata polychaeta Spetsbergiae, Gronlandiae, Islandiae et Scandinaviae hactenus cognita. Ofversigt af kongliga vetenskaps-akademiens forhandlingar nr. 4. Ex Officina Frenckelliana, Helsingfors.", "Langerhans, P. (1879) Die Wurmfauna von Madeira. Zeitschrift fur wissenschaftliche Zoologie, 32, 513 - 592.", "Verrill, A. E. (1881) New England Annelida. Pt 1. Historical sketch, with annotated lists of species hitherto recorded. Transactions of the Connecticut Academy of Arts and Sciences 4, 285 - 324.", "Okada, Y. K. (1937) La stolonisation et les caracteres sexuels du stolon chez les Syllidiens polychetes (Etudes sur les Syllidiens 3). Japanese Journal of Zoology, 7, 441 - 490.", "Hartman, O. (1945) The marine annelids of North Carolina. Duke University marine station bulletin, 2, 1 - 51.", "Pettibone, M. H. (1954) Marine polychaete worms from Point Barrow, Alaska, with additional records from the North Atlantic and North Pacific. Proceedings of the United States National Museum, 103, 203 - 356.", "Gidholm, L. (1965) On the morphology of the sexual stages, mating and egg-laying in Autolytus (Polychaeta). Zoologiska Bidrag fran Uppsala, 37, 1 - 44.", "Hamond, R. (1969 b) Aspects of the biology of Autolytus alexandri Malmgren 1867 (Polychaeta, Syllidae). Cahiers de Biologie marine, 10, 85 - 94.", "Hamond, R. (1974) The culture, experimental taxonomy, and comparative morphology of the planktonic stages of Norfolk autolytoids (Polychaeta: Syllidae: Autolytinae). Zoological Journal of the Linnean Society, 54, 299 - 320.", "Hartmann-Schroder, G. (1971) Annelida, Borstenwurmer, Polychaeta. VEB Gustav Fischer Verlag, Jena.", "Qian, P. J. & Chia, F. S (1989) Larval development of Autolytus alexandri Malmgren 1867 (Polychaeta, Syllidae). Invertebrate Reproduction and Development, 15, 49 - 56.", "San Martin, G. (1994) Autolytinae (Polychaeta, Syllidae) from Cuba and north American Atlantic Ocean. Memoires du Museum National d'Histoire Naturelle, 162, 269 - 277.", "Hartmann-Schroder, G. (1996) Annelida, Borstenwurmer, Polychaeta. 2 nd edition. VEB Gustav Fischer Verlag, Jena. Hartmann-Schroder, G. & Rosenfeldt, P. (1988) Die Polychaeten der \" Polarstern \" - Reise ANT III / 2 in die Antarktis 1984 Teil 1: Euphrosinidae bis Chaetopteridae. Mitteilungen aus dem Hamburgischen Zoologischen Museum und Institut, 85, 25 - 72.", "Verrill, A. E. (1874 a) Results of recent dredging expeditions on the coast of New England. American Journal of Science and Arts, 7, 131 - 138.", "Saint-Joseph, A. (1887) Les Annelides polychetes des cotes de Dinard. Premiere partie. Annales des sciences naturelles (Zoologie) (ser. 7), 1, 127 - 270.", "Southern, R. (1914) Clare Island Survey. Archiannelida and Polychaeta. Proceedings of the Royal Irish Academy, 31, 1 - 160.", "Fauvel, P. (1923) Polychetes errantes. Faune de France, 5, 1 - 488.", "Okada, Y. K. (1929 a) Regeneration and fragmentation in the syllidian polychaetes. Wilhelm Roux' Archiv fur Entwicklungsmechanik der Organismen, 115, 542 - 600.", "Cognetti, G. (1961) Les syllidiens des cotes de Bretagne. Cahiers de Biologie Marine, 2, 291 - 312.", "Gidholm, L. (1966) On epigamy in Autolytus (Polychaeta), and non-stolonic Sacconereis and Polybostrichus stages. Arkiv for Zoologi, 19, 135 - 142.", "Gidholm, L. (1967) A revision of Autolytinae (Syllidae, Polychaeta) with special reference to Scandinavian species, and with notes on external and internal morphology, reproduction and ecology. Arkiv for Zoologi, 19, 157 - 213.", "Kirkegaard, J. B. (1992) Havborsteorme 1. Danmarks fauna, 83, 1 - 416.", "Nygren, A. & Sundberg, P. (2003) Phylogeny and evolution of reproductive modes in Autolytinae (Syllidae, Annelida). Molecular phylogenetics and evolution, () 29, 235 - 249.", "Webster, H. E. & Benedict, J. E. (1887) The Annelida Chaetopoda from Eastport, Maine. The Annual Report of theCommissioner of Fish and Fisheries, 1885, 707 - 755.", "Elwes, E. V. (1908) Notes on littoral Polychaeta of Torquay. Journal of the Marine Biological Association of the United Kingdom, 8, 197 - 206.", "Allen, E. J. (1915) Polychaeta of Plymouth and the South Devon coast including a list of the Archiannelida. Journal of the Marine Biological Association of the United Kingdom, 10, 592 - 646.", "McIntosh, W. C. (1910) A monograph of the British Annelids. Polychaeta. Syllidae to Ariciidae. Ray Society, London, 233 - 524.", "Marenzeller, E. (1892) Zoologische Ergebnisse der im Jahre 1889 auf Kosten der Bremer Geographishcen Gesellschaft von Dr. Willy Kukenthal und Dr. Alfred Walter ausgefurthen Expedition nach Ostspitzbergen. Zoologische Jahrbucher, Abteilung fur Systematik, Geographie und Biologie der Tiere, 6, 397 - 434.", "Wesenberg-Lund, E. (1947) Syllidae (Polychaeta) from Greenland waters. Meddelelser om Gronland, 134, 1 - 38.", "Britayev, T. A. & San Martin, G. (2001) Description and life-history traits of a new species of Proceraea with larvae infecting Abietinaria turgida (Polychaeta, Syllidae & Hydrozoa, Sertulariidae) Ophelia, 54, 105 - 113."]}
format Text
author Nygren, Arne
author_facet Nygren, Arne
author_sort Nygren, Arne
title Epigamia Nygren, 2004, gen. n.
title_short Epigamia Nygren, 2004, gen. n.
title_full Epigamia Nygren, 2004, gen. n.
title_fullStr Epigamia Nygren, 2004, gen. n.
title_full_unstemmed Epigamia Nygren, 2004, gen. n.
title_sort epigamia nygren, 2004, gen. n.
publisher Zenodo
publishDate 2004
url https://dx.doi.org/10.5281/zenodo.6273268
https://zenodo.org/record/6273268
long_lat ENVELOPE(-67.133,-67.133,-68.117,-68.117)
ENVELOPE(-63.567,-63.567,-64.850,-64.850)
ENVELOPE(168.683,168.683,-77.517,-77.517)
ENVELOPE(-66.585,-66.585,-66.157,-66.157)
ENVELOPE(-66.117,-66.117,-65.750,-65.750)
ENVELOPE(70.203,70.203,-49.626,-49.626)
ENVELOPE(166.286,166.286,54.909,54.909)
ENVELOPE(25.125,25.125,70.314,70.314)
geographic Arctic
Greenland
Pacific
Norway
San Martín
Lopez
McIntosh
Benedict
Malmgren
Gronland
Gladkovskaya
Nygren
geographic_facet Arctic
Greenland
Pacific
Norway
San Martín
Lopez
McIntosh
Benedict
Malmgren
Gronland
Gladkovskaya
Nygren
genre Antarktis*
Arctic
Barrow
Davis Strait
Faroes
Greenland
North Atlantic
Point Barrow
Alaska
Spitsbergen
genre_facet Antarktis*
Arctic
Barrow
Davis Strait
Faroes
Greenland
North Atlantic
Point Barrow
Alaska
Spitsbergen
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cc0-1.0
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op_doi https://doi.org/10.5281/zenodo.6273268
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spelling ftdatacite:10.5281/zenodo.6273268 2023-05-15T14:15:11+02:00 Epigamia Nygren, 2004, gen. n. Nygren, Arne 2004 https://dx.doi.org/10.5281/zenodo.6273268 https://zenodo.org/record/6273268 unknown Zenodo http://publication.plazi.org/id/FFF4CE5ECC774E20FFE07D31881E806B http://zoobank.org/471A4E52-4C92-44F8-AB38-CD03071C0067 https://zenodo.org/communities/biosyslit https://dx.doi.org/10.5281/zenodo.157809 http://publication.plazi.org/id/FFF4CE5ECC774E20FFE07D31881E806B https://dx.doi.org/10.5281/zenodo.157813 http://zoobank.org/471A4E52-4C92-44F8-AB38-CD03071C0067 https://dx.doi.org/10.5281/zenodo.6273267 https://zenodo.org/communities/biosyslit Open Access Creative Commons Zero v1.0 Universal https://creativecommons.org/publicdomain/zero/1.0/legalcode cc0-1.0 info:eu-repo/semantics/openAccess CC0 Biodiversity Taxonomy Animalia Annelida Polychaeta Phyllodocida Syllidae Epigamia article-journal ScholarlyArticle Taxonomic treatment Text 2004 ftdatacite https://doi.org/10.5281/zenodo.6273268 https://doi.org/10.5281/zenodo.157809 https://doi.org/10.5281/zenodo.157813 https://doi.org/10.5281/zenodo.6273267 2022-04-01T12:37:00Z Epigamia gen. n. Linnean name definition . Type species Autolytus noroi Imajima & Hartman, 1964. Node­based name definition . Epigamia refers to the least inclusive clade comprising E. noroi (Imajima & Hartman, 1964), and E. macrophtalma (Marenzeller, 1875). Apomorphies . Morphologically supported by one apomorphy (Fig. 4): 1) body ciliation as 2 trochs per segment (character 4), other most parsimonious reconstructions (MPRs) possible, character state change is a parallelism, later reversed within clade, character state unknown in E. labordai (San Martín & López, 2002). General description . Atokous form . Length 1.8–22 mm for 20–88 chaetigers; width, measured at level of proventricle and excluding parapodial lobes, 0.2–1.5 mm. Body shape, excluding parapodial lobes, cylindrical to rounded rectangular in transection, venter flattened; body width fairly constant with tapering end. Ciliation as 1 or 2 trochs per segment (unknown in some taxa). Prostomium usually rounded rectangular, in E. macrophtalma more rounded oval. Four eyes, with lenses, in trapezoid arrangement, anterior pair larger. Eyes confluent or separated; eye spots absent or present. Palps fused at base or completely fused; in dorsal view projecting 1 / 5 – 1 / 2 of prostomial length. Extension of nuchal epaulettes from end of chaetiger 1 to end of chaetiger 6. Prostomium with 3 antennae; median antenna inserted medially on prostomium, the lateral on anterior margin. Tentacular cirri 2 pairs. Dorsal cirri alternate in length, except in E. macrophtalma cirrophores equal; cirrophores shorter or equal in length to parapodial lobes. All appendages cylindrical except in E. macrophtalma with flattened dorsal cirri from chaetiger 3. Parapodial lobes generally large, rounded to rounded rectangular; in some taxa with slightly swollen dorsal part. Except for bayonet chaetae, all chaetae compounds with bidentate blades; serration present. Compounds with small or large distal tooth. Single thin bayonet chaetae, subdistally denticulated. Pharynx with single to multiple sinuations. Trepan with various types of denticulation, in 1–3 rings. Basal ring present; infradental spines absent or present. Proventricle with varying number of rows of square shaped muscle cells. Pygidium with 2 cirri (reported length compared to body width, excluding parapodial lobes, at level of proventricle, if not otherwise stated); median papilla absent. Epitokes . Male. Body divided into 3 regions, anterior with 11 (see E. noroi ) or 14 uniramous chaetigers (region a), median with c. 37 biramous chaetigers (region b), and posterior with 3–23 uniramous chaetigers (region c). Body widest in anteromedian half of region b; body width measured in region a, as body width excluding parapodial lobes, and in region b, at the widest part, as body width including parapodial lobes. Ciliation as in atokes. Prostomium rounded rectangular, wider than long, with straight or concave anterior margin. Eyes large, 2 pairs, with lenses; eyes situated on dorsal and ventral side of prostomium, ventral pair larger. Palps present, much smaller than in atokes. Nuchal epaulettes as in atokes. Large median antenna inserted medially on prostomium, lateral antennae inserted on anterior margin. Lateral antennae bifid, basal part c. 1 / 2 of total length; outer ventral rami equal or longer than inner dorsal rami. Basal part and inner dorsal rami segmented with abundant cilia. Pair of small frontal processes inserted anterolaterally to dorsal pair of eyes. Tentacular cirri as in atokes. First dorsal cirri, larger than in atokes, equal in shape and size to median antenna. Achaetous knobs absent. Cirri with alternation in direction and size in region a, and c as in atokes; cirri in region b with less obvious alternation in both size and direction. However, this needs to be explored using a larger sample­size. Cirri length measured as body width excluding parapodial lobes in region a, and c; as body width including parapodial lobes in region b. Median antenna with large ceratophore, large cirrophores present on first dorsal cirri; cirrophores otherwise as in atokes. Appendages cylindrical, suspected to be flattened in epitokes of E. macrophtalma . Pharynx and proventricle disintegrates at some stage, and is totally absent in fully developed epitokes. Neuropodia as in atokes but generally larger and with enlarged, and prolonged dorsal part, especially in region b; in region b also with well­developed flattened notopodial lobes. Neuropodial aciculae as in atokes; notopodia in region b supported by c. 3 anterodorsal aciculae, and 3–4 thick and 3–5 thin posteroventral aciculae. Neuropodial chaetae as in atokes. Notopodial lobes with 20–50 swimming chaetae, in length equal to c. body width in region b including parapodial lobes. Pygidium as in atokes. Female . Body divided into 3 regions, anterior with 14 uniramous chaetigers (region a), median with 29–41 biramous chaetigers (region b), posterior with 16–33 uniramous chaetigers (region c). Body width fairly constant, slightly wider in region b; body width measured in region a, as body width excluding parapodial lobes, and in region b as body width including parapodial lobes. Ciliation as in atokes. Prostomium rounded rectangular, wider than long, with straight or concave anterior margin. Eyes large, 2 pairs, with lenses; eyes situated on dorsal and ventral side of prostomium, ventral pair larger. Palps present, much smaller than in atokes. Nuchal epaulettes as in atokes. Median antenna inserted medially on prostomium, lateral antennae inserted on anterior margin. Tentacular cirri as in atokes. Achaetous knobs absent. Cirri with alternation in direction as in atokes, except for cirri in region b with less obvious alternation; cirri length as in atokes or longer. Cirri length measured as body width excluding parapodial lobes in region a, and c; as body width including parapodial lobes in region b. Cirrophores as in atokes. Appendages cylindrical, suspected to be flattened in epitokes of E. macrophtalma . Pharynx and proventricle disintegrates at some stage, and is totally absent in fully developed epitokes. Neuropodia as in atokes but generally larger and with enlarged, and prolonged dorsal part, especially in region b; in region b also with notopodial lobes, not as developed as in male. Neuropodial aciculae as in atokes; notopodia in region b supported by 5–14 anterodorsal aciculae, and 6–8 thick and 6–9 thin posteroventral aciculae. Neuropodial chaetae as in atokes. Notopodial lobes with 25–50 swimming chaetae, in length equal to c. body width in region b including parapodial lobes. Pygidium as in atokes. Epigamia alexandri (Malmgren, 1867) comb. n. (Fig. 83 A–G) Autolytus alexandri Malmgren, 1867: 37, pl. 7, fig. 39, 39C–D; Langerhans 1879, 577; Verrill 1881, 292, pl. 12, fig. 8, 8A–C; Okada 1937; Hartman 1945: 17; Pettibone 1954: 246 –247; 1963: 147–148, fig. 37 F–G; Gidholm 1965: 36 –38; Hamond 1969 b; 1974; Hartmann­Schröder 1971: 176;? Qian & Chia 1989; San Martín 1994: 271 –272, fig. 1 A–D; Hartmann­Schröder 1996: 180 –181. Autolytus newtoni Malmgren, 1867: 36 –37. Stephanosyllis ornata Verrill, 1874 a: 132. 1874b: 361, pl. 4, fig. 1. Autolytus longigula Verrill, 1881: pl. 12, fig. 3, 3A–B. Autolytus longeferiens Saint­Joseph, 1887: 217 –219, pl. 10, fig. 95–97; Southern 1914: 39 –40; Fauvel 1923: 319 –320, fig. 122 H–K; Okada 1929 a; Cognetti 1961: 304; Gidholm 1966; 1967: 201 –203, figs 2 C, 7 G, 13 C, 27; Hartmann­Schröder 1971: 178; Kirkegaard 1992: 230 –231, fig. 112 A–C; Hartmann­Schröder 1996: 183; Nygren & Sundberg 2003: GenBank sequences, 16 S rDNA partial sequence AF 474262, and 18 S rDNA partial sequence AF 474308. Proceraea (Stephanosyllis) ornata Webster & Benedict 1887: 724. Autolytus longiferiens Elwes 1908: 202; Allen 1915: 604; McIntosh 1910: 245 –247, pl. 86, fig. 17, pl. 87, fig. 16. Autolytus paradoxus Saint­Joseph, 1887: 216 –217, pl. 10, fig. 92–94; Fauvel 1923: 318, fig. 122 E– F; Hartmann­Schröder 1971: 175. Autolytus verrilli Marenzeller, 1892: 416 –420, pl. 19, fig. 4; Wesenberg­Lund 1947: 33 –36, figs 14–15; 1950: 52, fig. 13. Proceraea rzhavskyi Britayev & San Martín, 2001: 105–113, fig. 1 A–E. Not figs 2–5. Material examined . Greenland : holotype (female epitoke) SMNH 2438, West Greenland, Davis Strait, 65 °N 60 °W, Swedish arctic expedition 1859. Norway : holotype (female epitoke) of Autolytus newtoni SMNH 2437, Spitsbergen, Storfjord, 78 ° 37 'N 19 °E, 21 Aug 1864. Russia : holotype ZMMSU 849, and 4 paratypes ZMMSU 850–853 of Proceraea rzhavskyi , Mednyy Island (Commander Islands), Gladkovskaya Bay, 54 ° 44 'N 167 ° 45 'E, 6 m, on hydroid Abietinaria turgida , 1986. Faroes : 35 spms (15 spms in formalin, 18 spms on slide, 2 spms in author's collection for DNA analyses), South of Vagar, 61 ° 56.8 'N 06° 59.5 'W, triangle­dredge, 76–78 m, hydroids, 27 Jun 1997; 7 spms (1 spm in formalin, 6 spms in author's collection for DNA analyses), East of Nolsøy, 62 °01.5'N 06° 31.9 W, triangle dredge, 41 m, bedrock, 27 Jul 1997; 29 spms (17 spms in formalin, 9 spms on slides (2 rear ends in author's collection for DNA analyses), 3 spms in author's collection for DNA analyses), East of Bordøy, 62 ° 24.6 'N 06° 26.3 'W, triangle dredge, 65–68 m, shellgravel with hydroids, 17 Jul 1997; 7 spms (6 spms on slides, 1 in author's collection for DNA analyses), East of Bordøy, 62 °08.4'N 06° 23.4 'W, triangle dredge, 77 m, shellgravel with hydroids, 17 Jul 1997. France : 11 syntypes of Autolytus longeferiens MNHN 1031–1041, Dinard, Jun–Aug 1872–1881; holotype of Autolytus paradoxus MNHN 1030, Dinard, 18 Jul 1887. USA : 8 spms (4 spms in formalin (2 rear ends in author's collection for DNA analyses), 2 spms on slides (rear ends in author's collection for DNA analyses), 2 spms in author's collection for DNA analyses), Rock Pt and López Island, 48 ° 29.6 'N 122 ° 56.9 'W, dredge, 75 m, Polycarpa sp., barnacles with rich hydroid fauna, few sponges, 24 Jan 2001. Diagnosis . Epigamia with a DDU­group posterior to chaetiger 27, a much convoluted pharynx, and a trepan with 1 large teeth alternating with 2–4 much smaller. Description . Length 4.5–17.2 mm for 27–88 chaetigers, width 0.20–0.72 mm. Live specimens from faint reddish or yellowish, sometimes with 3 faint red lines, to more intensely red anterior to proventricle, intestinal region orange to red­brown; anterior appendages red­tipped; eyes red. Preserved specimens without colours. Ciliation as 2 trochs per segment. Eyes confluent (Fig. 83 B); eye spots present. Palps in dorsal view projecting c. 1 / 3 of prostomial length. Nuchal epaulettes reaching between end of chaetiger 1 (small individuals), and end of chaetiger 2 (Fig. 83 A, B). Median antenna reaching chaetiger 7–15 (n= 10) in live specimens. Lateral antennae and dorsal tentacular cirri, length 1 / 2 – 2 / 3 of median antenna. Ventral tentacular cirri 1 / 3 – 1 / 2 as long as dorsal pair. First dorsal cirri as long as median antenna, second dorsal cirri as long as ventral tentacular cirri. From chaetiger 1–27 cirri with usual alternation in direction, followed by 1 DDU­groups, 1–3 DDUU­groups, and 1–13 DDU­groups (n= 6). Dorsal cirri from chaetiger 3, alternate in length (Fig. 83 A); short cirri equals 1 / 2 – 2 / 3 of body width, long cirri equal or slightly longer than body width. Cirrophores present on tentacular cirri, and all dorsal cirri. Cirrophores equal, cirrostyles unequal; short cirrostyles 1 / 2 – 2 / 3 in length of long cirrostyles; cirrophores shorter than parapodial lobes; cirrophores shorter than cirrostyles. All appendages cylindrical. Parapodial lobes large, rounded, slightly swollen dorsal to chaetal fascicle. 2–4 aciculae in anterior chaetigers, 1–2 in median and posterior. Chaetal fascicle with 9–18 compounds in anterior chaetigers, 3–13 in median and posterior. Compound chaetae with large distal tooth (Fig. 83 F); serration present. Single thin bayonet chaetae (Fig. 83 G), beginning between chaetiger 3–30. Pharynx with from one sinuation (small individuals) anterior to proventricle to multiple sinuations anterior and lateral to proventricle (Fig. 83 D). Trepan in chaetiger 1–4, with 34–44 unequal teeth, 9 large teeth and 25–35 smaller; 1 large alternating with 2–4 much smaller, in 2 rings, small teeth situated slightly inside large teeth (Fig. 83 E). Basal ring present; infradental spines present (Fig. 83 E). Proventricle equal in length to 2–4 segments in chaetiger 6–18 with 34–44 rows of muscle cells (n= 11). Anal cirri equal in length to 1– 2 times the body width. Reproduction . Epigamy (Fig. 83 C, D). Epitokous specimens caught in February to May in the North Atlantic (Hamond 1969 b). Transforming individuals observed in January in the North Pacific (pers. obs.). : Published as part of Nygren, Arne, 2004, Revision of Autolytinae (Syllidae: Polychaeta)., pp. 1-314 in Zootaxa 680 on pages 163-166, DOI: 10.5281/zenodo.157809 : {"references": ["Imajima, M. & Hartman, O. (1964) The polychaetous annelids of Japan part 1. Allan Hancock Foundation Publications. Occasional Paper, 26, 1 - 237.", "Marenzeller, E. (1875) Zur Kenntniss der adriatischen Anneliden. Zweiter Beitrag. (Polynoinen, Hesioneen, Syllideen). Sitzungsberichte der Kaiserliche Akademie der Wissenschaften, Wien, Mathematisch-Naturwissenschaftliche Klasse, 72, 1 - 43.", "San Martin, G. & Lopez, E. (2002) New species of Autolytus Grube, 1850, Paraprocerastea San Martin and Alos, 1989, and Sphaerosyllis Claparede, 1863 (Syllidae, Polychaeta) from the Iberian Peninsula. 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A. & San Martin, G. (2001) Description and life-history traits of a new species of Proceraea with larvae infecting Abietinaria turgida (Polychaeta, Syllidae & Hydrozoa, Sertulariidae) Ophelia, 54, 105 - 113."]} Text Antarktis* Arctic Barrow Davis Strait Faroes Greenland North Atlantic Point Barrow Alaska Spitsbergen DataCite Metadata Store (German National Library of Science and Technology) Arctic Greenland Pacific Norway San Martín ENVELOPE(-67.133,-67.133,-68.117,-68.117) Lopez ENVELOPE(-63.567,-63.567,-64.850,-64.850) McIntosh ENVELOPE(168.683,168.683,-77.517,-77.517) Benedict ENVELOPE(-66.585,-66.585,-66.157,-66.157) Malmgren ENVELOPE(-66.117,-66.117,-65.750,-65.750) Gronland ENVELOPE(70.203,70.203,-49.626,-49.626) Gladkovskaya ENVELOPE(166.286,166.286,54.909,54.909) Nygren ENVELOPE(25.125,25.125,70.314,70.314)