Marphysa adenensis Gravier 1900

Autor: Katsiaras, Nikolaos, Simboura, Nomiki, Koutsoubas, Drosos
Rok vydání: 2014
Předmět:
DOI: 10.5281/zenodo.5613403
Popis: Marphysa adenensis Gravier, 1900 Fig. 1 a���h, 2 a���d, 3, 4a���d, 5 a���d, Table 2 Marphysa adenensis Gravier 1900: 270, Plate 14 Figures 91���92; Text-figures 140���143; Day 1962: 644; Day 1967: 399, Figures 17.6 p���s Type material. Holotype (MNHN POLY TYPE 0531) from Aden Sea, 1900, 1 specimen, 45mm long and 0.75 width, 200 segments, posterior end missing, jaws removed. Non-type material. Lesvos Island, Gera Gulf 15 / 9 / 2009: 3 specimens (GP- 4 B): 76 segments 30 mm long and 2.5 mm wide, 62 segments 24 mm long and 2.5 mm wide, 74 segments 25 mm long and 1mm wide; 1 specimen (GP- 2 B): in the 25 segments 30 mm long and 4 mm wide; Methoni 24 / 4 / 2012: 3 specimens (1 /WFD 3 R 1): 54 segments 10.3 mm long and 1 mm wide, 43 segments 5 mm long and 1 mm wide, 35 segments 9 mm long and 1.5 mm wide; Lesvos Strait 29 / 3 / 2013: 1 specimens (3 /WFD 70 R 1): 42 segments 20 mm long and 1.7mm wide. Description. Holotype an anterior fragment of about 200 segments (Fig. 5 a). All 8 Mediterranean specimens anterior fragments; longest 30 mm long and 2.5 wide with 76 segments; shortest 5 mm long and 0.9 mm wide with 43 segments. Prostomium rounded anteriorly, as long as first peristomial ring, which is longer than second peristomial ring. Three antennae present and a pair of dorso-lateral palps. Antennae slightly longer than prostomium; median longer. Antennae arranged in slightly curved line and slightly articulated. Eyes present, positioned behind the lateral antennae. Jaws removed from holotype. Maxillary formula of Mediterranean material: I(1 + 1), II(5-7 + 7-8), III(6-7 +0), IV (4 + 8) (Fig. 3). Dorsal cirri cirriform in anterior body, more thin and slender after mid-body; slightly longer than the parapodium in anterior region, increasing in size up to twice as long after the first branchiae. Ventral cirri tongueshaped with rounded tips in anterior body, tips with a distal papilla in branchial segments, which gradually becomes less distinct after mid-body. Ventral cirri slightly shorter than the parapodium lobe. Post-chaetal lobes elongated and tongue-shaped, much longer than acicular lobe, gradually decreasing down to a similar length in posterior body. Pre-chaetal lobes always truncated and straight, shorter than acicular lobes. Branchiae present from chaetiger 10���17 until 16���32, depending on specimen size; all pectinate and have up to 10 filaments. Holotype: Superior setae in each fascicle consist of: (1) 3���5 long capillaries, (2) 4���9 relatively shorter capillaries, (3) 1���2 heterodont pectinate setae, marginal teeth longer and unequal to each other (twice as long) throughout the body, with 4���5 teeth in anterior region (Fig. 4 c, 5 c), increasing up to 7���8 towards the posterior end (Fig. 4 d). Inferior setae consist only of composite falcigers, bidentate and hooded (Fig. 4 b, 5 b). There are up to 20 in anterior body, but only up to 10 at the posterior part. No composite spinigers present. Towards the posterior body, the number and length of all setae is decreasing, except of pectinate which remains the same. The length of the falciger blades is relatively short (32���40 ��m in anterior chaetigers; decreasing down to 12���20 ��m in posterior) and about equal between falcigers of the same fascicle, but with a slight length gradation (from 90 ��m up to 140 ��m) in the branchial region (one and half times longer). Aciculae blunt and pale. Acicular setae, beginning from chaetiger 35; pale yellow, hooded and bidentate; teeth have almost 90 �� angle between them; subdistal almost twice as wide (Fig. 4 a, 5 d). Mediterranean material: Superior setae in each fascicle consist of: (1) 3���5 long serrated capillaries (Fig. 1 a), (2) 4���9 short serrated capillaries, (3) 1���2 heterodont pectinate setae, marginal teeth longer and unequal to each other (twice as long) throughout the body, with 4���8 teeth in total (Fig. 1 f���h, 2 c), regardless of specimen dimensions. Inferior setae consist only of serrated, bidentated and hooded composite falcigers. No composite spiniger present. In each fascicle of anterior body (Fig. 1 b, 2 b), or until the mid-body in older individuals (Fig. 1 c), there are 3���4 falcigers with notably longer and thinner blades (up to 160 ��m; 115.3 ��m average in older, 68 ��m average in younger specimens), more than twice as long as the other (up to 76 ��m; 55.3 ��m average in older, 34.6 ��m average in younger specimens). The length and the number of all setae decrease close to the posterior end (Fig. 1 d), except the pectinate which remains the same. Aciculae blunt, pale yellow at the edge and dark brown at base; 2���3 per parapodium in anterior body, only 1 after the first branchiae. Acicular setae, beginning from chaetiger 22���35 (depending on specimen dimensions) are pale yellow, hooded and bidentate; teeth have almost 90 �� angle between them; subdistal almost twice as wide (Fig. 1 e, 2 d). Distribution. Red Sea: Aden (Gravier 1900), Indian Ocean: Madagascar (Day 1962), Reunion Island (Bigot et al. 2008), Pacific Ocean: Hong Kong (Mak 1980), Andaman Sea (Aungtonya et al. 2002). Mediterranean Sea: Gera Gulf, Lesvos Island; Mytilene Strait (East Aegean Sea), Methoni (South Ionian Sea). Ecology. Soft mud (Madagascar), Muddy sand with sea-shells (Andaman Sea), coral communities (Hong Kong). P. oceanica beds and two individuals have been found especially in shoot sheaths micro-habitat (Greece). Remarks. Marphysa adenensis is the first species of the genus described as having present only composite falcigers in inferior setae and branchiae limited to the anterior body. Although the blades of the falcigers are referred as ���long and narrow��� both in the original description and the subsequent description by Day (1963), no remarks are made for the presence of length gradation among the blades. The re-examination of the holotype in the present study showed that there is a length gradation in the branchial region. The Mediterranean specimens differ from the holotype by having a stronger gradation of falciger blades-length (more than twice as long, rather than one and half). However, there are a lot of falcigers missing blades in the holotype, after a century of preservation, especially in the first segments. Maxillary apparatus has been dissected out from the holotype, but the maxillary formula of the Mediterranean specimens differ from the published formula by Day (1967). In particular, the latter have more teeth in maxillary IV (4 + 8 in the Mediterranean specimens, than 7 + 11 in the holotype), as well as a slight variation in MxII (5-7 + 7-8 in the Mediterranean specimens, than 7 + 8 in the holotype) and in MxIII (6-7 +0 in the Mediterranean specimens, than 7 +0 in the holotype), varying according to body size. However, the published formula could be considered inadequate, since it seems to be based only on 3 individuals in total (the holotype from Aden; Gravier 1900 and two individual collected from Madagascar; Day 1962) and this number should not be enough to cover the interspecies variation. Besides the above differences, the Mediterranean specimens show important similarities with the holotype, namely in having: a) 1���2 pectinate setae all along the body, up to eight teeth, b) pale yellow acicular setae, hooded and bidentate with teeth that have almost 90 �� angle between them and the subdistal only slightly longer than the distal, but twice as wide. Marphysa adenensis is very similar to M. sp. A from the Gulf of Mexico. Although the personal examination of this species��� type materials was not possible, according to the published description (Gathof 1984) the two species are very similar in terms of strong falciger blades-length gradation (twice as long in figure 40 - 14 e���f), acicular shape (bidentate, hooded, 90 �� angle between the teeth and subdistal is wider than distal in figure 40 - 14 h) and maxillary formula close to the interspecies variation (I: 1 + 1, II: 5-6 + 7, III: 5-7 +0, IV: 2-4 + 5-12). The relation of ��. sp. A to M. adenensis has to be defined in a future study, since there is a possibility to be a synonym species. Finally, it differs from the other species of Group C 1 from America, M. conferta, mainly in having pectinate setae of fewer teeth (based on published description).
Published as part of Katsiaras, Nikolaos, Simboura, Nomiki & Koutsoubas, Drosos, 2014, The rare subgroup C 1 of Marphysa (Polychaeta, Eunicidae): re-description of species and first records in the Mediterranean Sea, pp. 201-217 in Zootaxa 3873 (3) on pages 203-206, DOI: 10.11646/zootaxa.3873.3.1, http://zenodo.org/record/228641
{"references":["Gravier, C. (1900) Contribution a l' etude des Annelides Polychaetes de la Mer Rouge. Premiere partie. Nouvelles Archives du Museum d' Historie Naturelle Paris, Series 4, 2 (2), 137 - 282.","Day, J. H. (1962) Polychaeta from several localities in the Western Indian Ocean Proceeding of the Zoological Society of London, 139 (4), 627 - 656. http: // dx. doi. org / 10.1111 / j. 1469 - 7998.1962. tb 01597. x","Day, J. H. (1967) A monograph on the polychaeta of southern Africa. Part I. Errantia. British Museum (Natural History), London, 458 pp.","Bigot, L., Gremare, A., Amoroux, J. M., Frouin, P., Maire, O. & Gaertner, J. C. (2008) Assessment of the ecological quality status of soft-bottoms in Reunion Island (tropical southwest Indian Ocean) using AZTI marine biotic indices. Marine Pollution Bulletin, 56, 704 - 722. http: // dx. doi. org / 10.1016 / j. marpolbul. 2007.12.020","Mak, P. M. S. (1980) The coral associated polychaetes of Hong Kong, with special references to the serpulids. In: Morton, B. & Tseng, C. K. (Eds.), Proceedings of the First International Marine Biological Workshop: The Marine Flora and Fauna of Hong Kong and Southern China, Hong Kong. Hong Kong University Press, Hong Kong, pp. 595 - 617.","Aungtonya, C., Thaipal, S. & Bussarawit, S. (2002) A list of Polychaetes (Annelida) in the reference collection database of the phuket marine biological center, Thailand. Phuket Marine Biological Center Special Publication, 24, 21 - 32.","Day, J. H. (1963 a) The polychaete fauna of South Africa. Part 8: New species and records from grab samples and dredgings. Bulletin of the British Museum of Natural History Zoology, 10 (7), 383 - 445.","Gathof, J. M. (1984) Chapter 40 Eunicidae. In: Uebelacker, J. M. & Johnson, P. G. (Eds.), Taxonomic guide to the polychaetes of the northern Gulf of Mexico. Vol. 6. Final Report to the Minerals Management Service, contract 14 - 12 - 001 - 29091. Barry A. Vittor & Assoc. Inc. Mobile, Alabama, pp. 1 - 31. [pp. 40.1 - 40.30]"]}
Databáze: OpenAIRE