Eutrichodesmus communicans Golovatch, Geoffroy, Mauriès & VandenSpiegel, 2009
publication ID |
https://doi.org/ 10.3897/zookeys.7.117 |
publication LSID |
lsid:zoobank.org:pub:67B4D2EC-2C6D-4226-847D-0BA2B2777AE3 |
DOI |
https://doi.org/10.5281/zenodo.3792486 |
persistent identifier |
https://treatment.plazi.org/id/8293BC13-BF5A-4E2F-BCEE-0711CFC4C86E |
taxon LSID |
lsid:zoobank.org:act:8293BC13-BF5A-4E2F-BCEE-0711CFC4C86E |
treatment provided by |
Plazi |
scientific name |
Eutrichodesmus communicans Golovatch, Geoffroy, Mauriès & VandenSpiegel |
status |
sp. nov. |
Eutrichodesmus communicans Golovatch, Geoffroy, Mauriès & VandenSpiegel View in CoL , sp. n.
urn:lsid:zoobank.org:act:8293BC13-BF5A-4E2F-BCEE-0711CFC4C86E
Figs 9-13 View Figure 9 View Figure 10 View Figure 11 View Figure 12 View Figure 13 .
Type material. Vanuatu, Espirito Santo, Malo Island, Avorani , forest litter, Berlese extraction, 15.IX.2006, leg. L. Deharveng & A. Bedos ( SK06-15/06 ), holotype ♂ ( MNHN JC 311 ), paratypes: 1 ♂, 4 ♀♀ ( MNHN JC 311 ), 1 ♂, 1 ♀ ( ZMUM), 1 ♀ ( NMNHS), 1 ♀ ( MCSNV), 1 ♀ ( ZMUC) ; same place, date and collectors ( SK06- 15/13 ), 1 ♂, 1 ♀, 1 juv. ( MNHN JC 311 ) ; Espirito Santo, Fapon doline 3, 5.IX.2006, leg. L. Deharveng & A. Bedos ( SK06-15/18 ), 5 ♀♀, 4 juv. ( MNHN JC 311 ), 1 ♂ ( SEM) ; Espirito Santo, very humid forest at Boutmas Pass , 27.IX.2006, leg. L. Deharveng & A. Bedos ( SK06-27/12 ), 1 ♂ ( MNHN JC 311 ) ; Espirito Santo, Boutmas, forest above Jourdain River , Berlese extraction of litter, 27.IX.2006, leg. L. Deharveng & A. Bedos ( SK06-27/09 ), 1 ♂ ( MNHN JC 311 ) ; Espirito Santo, Boutmas, Fapon doline 2, 5.IX.2006, leg. L. Deharveng & A. Bedos ( SK06-05/12 ), 2 ♀♀ ( MNHN JC 311 ) ; Espirito Santo, Funatus, Katae Cave , Berlese extraction of guano, 18.09.2006, leg. J. Lips ( SK06-18/07 , Katae 4gu), 1 ♂, 2 juv. ( ZMUC) .
Name. To emphasize a superficial transition from a still non-volvatory “haplodesmid” condition to the typical, fully volvatory “doratodesmid” one.
Diagnosis. Differs from congeners by the tergal trichome being composed of only very long, bisegmented, tactile setae, coupled with the gonopod telopodite having a peculiar, dentate-microtuberculate, lateral process at midway and a lobiform, slightly coiled distal part.
Description. Length of adults of both sexes ca 3.5-4.2 mm, width 0.6-0.75 mm, body broadest at segment 3 or 4; ♂♂ usually a little smaller than ♀♀. Holotype ca 3.8 mm long and 0.65 mm wide. Coloration uniformly pallid, ranging from white to light yellow or pink.
Adults with 19 segments, body subcylindrical ( Figs 9 View Figure 9 ; 10A View Figure 10 ), pattern of conglobation typical of “ Doratodesmidae ”, but volvation itself barely complete, poorly concealing at least legs of several caudal segments. Head ( Figs 10E, F View Figure 10 ; 11A, B) slightly transverse, rather densely pilose, microgranular; isthmus between antennal sockets very narrow. Antennae ( Figs 11C, D View Figure 11 ) very short and stout; antennomere 6 longer than 5, dorsoapically with an evident pit containing minute bacilliform sensilla; antennomere 8 with usual four sensory cones apically. Collum rather large, even and convex, not covering the head from above, very densely and irregularly setose, setae bisegmented, tactile ( Fig. 10F View Figure 10 ). Prozona very finely alveolate, collum and metaterga covered with a rather even cerotegumental crust held by microvilli, this crust, like on collum, being perforated only by dense, irregularly arranged, tactile, bisegmented setae; stricture between pro- and metazona broad and shallow, even more finely alveolate than prozona; limbus entire, not
hidden by sparse microvilli ( Figs 11F View Figure 11 ; 12 View Figure 12 A-C). Paraterga subvertical and rather narrow, weakly set off by 1-2 shallow depressions or sulci, slightly bisinuate caudally at base ( Figs 10E View Figure 10 ; 11E); paraterga 2 strongly enlarged, schism and hyposchism very small; paraterga
3 and 4 shorter than others ( Figs 9 View Figure 9 ; 10A, E View Figure 10 ), following paraterga broadly rounded, overlap typical. Pore formula normal, ozopores located near ventral margin, progressively closer to caudal corner of paraterga. Pleurotergal ridges very small, microgranular like entire ventral surface ( Fig. 11E View Figure 11 ). Epiproct short, slightly uneven, directed ventrocaudad, below tip with the usual four cones; para- and hypoproct as in Figs 10C, D View Figure 10 .
Sterna usually with a minute middle knob separating bases of nearly contiguous coxae ( Fig. 12D View Figure 12 ), only sterna between coxae 6, 7 and 9 much wider ( Fig. 12E View Figure 12 ). Gonopod aperture transverse-oval, relatively small, far from reaching lateral sides of segment 7, as in Fig. 12E View Figure 12 . Legs relatively short; coxae and prefemora microgranular; tarsal segment longest; claw usual, simple, very slightly curved ventrad; some setae very sparsely microdenticulate ( Fig. 12D View Figure 12 ). Coxae 1 of ♂ with a distinct distomedial spine, coxae 2 of ♂ perforated by vas deferens ( Fig. 11B View Figure 11 ).
Gonopods ( Figs 12E, F View Figure 12 ; 13 View Figure 13 ) rather complex. Coxae subquadrate, very large, scaly, with only a few setae ventrolaterally.Telopodite only slightly longer than coxite, its basal part setose and slender, with a conspicuous, densely dentate-tuberculate, distofemoral outgrowth (dp) at about midway, more distally with an expanded, somewhat folded, coiled, broadly trifid lobe, carrying a very short solenomere branchlet laterally.
Remarks. This remarkable species partly bridges the former Haplodesmidae and Doratodesmidae in showing the tergal trichome of peculiar, bisegmented setae so characteristic of Cylindrodesmus (in which, however, it is mixed with usual setation), also shared with several true “doratodesmids”, on the one hand, and the body and gonopod structure of a rather typical “doratodesmid”, on the other.
MNHN |
France, Paris, Museum National d'Histoire Naturelle |
ZMUM |
Russia, Moscow, Moscow State University |
NMNHS |
NMNHS |
MCSNV |
MCSNV |
ZMUC |
Denmark, Kobenhavn [= Copenhagen], University of Copenhagen, Zoological Museum |
MNHN |
Museum National d'Histoire Naturelle |
ZMUM |
Zoological Museum, University of Amoy |
ZMUC |
Zoological Museum, University of Copenhagen |
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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