Leptognathia microcephala Kudinova-Pasternak, 1977
Bird, Graham J, 2007, Family incertae cedis *, Zootaxa 1599, pp. 121-149 : 144-146
publication ID |
https://doi.org/ 10.5281/zenodo.178710 |
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https://doi.org/10.5281/zenodo.4668940 |
persistent identifier |
https://treatment.plazi.org/id/03F187A3-FFFB-0375-FF57-FDE211C2FEEA |
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Leptognathia microcephala Kudinova-Pasternak, 1977 |
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Leptognathia microcephala Kudinova-Pasternak, 1977 View in CoL
Figures 17–18 View FIGURE 17 View FIGURE 18
Leptognathia microcephala Kudinova-Pasternak, 1977: 122 View in CoL –124, figs 4–5. Larsen & Shimomura, 2007: 15.
Material examined. 1 preparatory male, two mancae-III, station XR12, 41°37.67’– 41°37.08’N, 146°54.19’– 146°52.72’E. 5473–5484 metres, 22–23 September 2001.
Remarks. The three specimens from the present study agree with Kudinova-Pasternak’s description of L. microcephala , rather than L. birsteini (see above) especially with regard to cephalothorax and pereonite proportions ( Fig. 17 View FIGURE 17 A) and the shape of the pleotelson ( Fig. 17 View FIGURE 17 B). The species (and its probable ‘congeners’) appears to be one of the most morphologically complex tanaidomorphans, with possible exception of the paratanaid genus Bathytanais Beddard, 1886 . Of particular interest, the antennule is distinctly five-articled, with a small terminal article that could have been overlooked in previous studies. This is not homologous with the Paraleptognathia-Chauliopleona-Akanthophoreus configuration and is not linked to sexual development: although the preparatory male (length 3.48 mm) ( Fig. 17 View FIGURE 17 A) has stout and broad antennules ( Fig. 17 View FIGURE 17 C), the two mancae (1.92–2.18 mm) ( Fig. 17 View FIGURE 17 E) also have five-articled antennules, which are slender ( Fig. 17 View FIGURE 17 F). Unusual sensory setae on article 1 of antennule ( Fig. 17 View FIGURE 17 D) have a pedestal and articulated basal element.
Other notable characters include: the pleotelson ( Fig. 17 View FIGURE 17 B) with slightly tapering lateral margins and with long apical process; the cheliped ( Fig. 18 View FIGURE 18 A) carpus has a large free posterio-dorsal margin, so that the appearance of the cheliped is almost malleolate; the cheliped fixed-finger spine, incisive margin and dactylus are heavily sclerotised; all pereopods, especially pereopod 1 ( Fig 18 View FIGURE 18 C) are very slender and elongate; the pereopod 1 carpus has a small spatulate seta ( Fig. 18 View FIGURE 18 D); the uropods ( Fig. 18 View FIGURE 18 E) are slender, both articles are twoarticled, the exopod reaching half length of endopod article 2.
To confirm the true generic position of this species, and that of L. birsteini , it is desirable that material of Latitanais beklemishevi Kudinova-Pasternak, 1987 (type-locality Madagascar Basin, 5040–5069 metres) is obtained to check the number of antennule articles. In addition, new and irrefutable specimens of L. birsteini would help clarify distinctions between it and L. microcephala .
Distribution. Recorded from the Izu-Ogasawara Trench, 6330 metres ( Kudinova-Pasternak 1978) and the Kurile-Kamchatka Trench, 5473–5484 metres in the present study.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Leptognathia microcephala Kudinova-Pasternak, 1977
Bird, Graham J 2007 |
Leptognathia microcephala
Larsen 2007: 15 |
Kudinova-Pasternak 1977: 122 |