Streptocephalus wolof, Sainz-Escudero & Alonso & Sánchez-Vialas, 2022
publication ID |
https://doi.org/ 10.11646/zootaxa.5213.4.4 |
publication LSID |
lsid:zoobank.org:pub:D84DB5A5-01C2-45DE-B246-8A0EE8769B23 |
DOI |
https://doi.org/10.5281/zenodo.7383581 |
persistent identifier |
https://treatment.plazi.org/id/8E7187A2-FFBB-FFC1-698B-5DDF9E88CD11 |
treatment provided by |
Plazi |
scientific name |
Streptocephalus wolof |
status |
sp. nov. |
Streptocephalus wolof sp. nov.
( Figs. 6–9 View FIGURE 6 View FIGURE 7 View FIGURE 8 View FIGURE 9 )
Etymology. The name wolof refers to the ethnic group native to Senegal, Gambia, and in a lesser extent, to Mauritania. Most of the known geographic range of the newly described species overlaps with the Wolof ethnic distribution. The name is a noun in genitive case.
Type material. Holotype. Male: Senegal, Tambacounda, 6 km west of Koutenabe , 93 m, 14 º 15′34.38″N, 12 º 35′42.38″W, 16-VIII-2015 (white label, printed); MNCN 20.04 About MNCN /20321 (white label, printed) GoogleMaps ; Holotypus, Streptocephalus wolof Sainz-Escudero, Alonso & Sánchez-Vialas , des. 2022 (white label printed).
Paratypes. 20males, 15 females: Senegal, Saint-Louis, 2 km north of Podor , 9 m, 16 º 40′17.43″N, 14 º 57′55.29″W, 18-VIII-2015 (white label, printed); MNCN 20.04 About MNCN /20269–20.04/20289 and 20.04/20327–20.04/20340 (white label, printed). Twenty-six males GoogleMaps , 50 females: Senegal, Ziguinchor, Diembéreng , 9 m, 12 º 28′00.61″N, 16 º 47′02.16″W, 13-VIII-2015 (white label, printed); MNCN 20.04 About MNCN /20290–20.04/20302 and 20.04/20341–20.04/20403 (white label, printed). Thirteen males GoogleMaps , 22 females: Senegal, Matam, 1.9 km south-east of Bokiladji, 30 m, 15 º 02′48.91″N, 12 º 43′49.78″W, 17-VIII-2015 (white label, printed); GoogleMaps MNCN 20.04 About MNCN /20303–20.04/20320 and 20.04/20404- 20.04/20420(white label,printed). Five males: Senegal, Tambacounda, 6km west of Koutenabe , 93 m, 14 º 15′34.38″N, 12 º 35′42.38″W, 16-VIII-2015 (white label, printed); GoogleMaps MNCN 20.04 About MNCN /20321–20.04/20326 (white label, printed). All paratypes labelled GoogleMaps : “ Paratypus, Streptocephalus wolof Sainz-Escudero, Alonso & Sánchez-Vialas , des. 2022 (white label printed) ( Table 2 View TABLE 2 ).
Description. Male. Head ( Fig. 6A View FIGURE 6 ) round. Nuchal organ visible. Eyes spherical with diameter as long as its corresponding eyestalk.
First antennae filiform, 2 times longer than basal joint of second antenna ( Fig. 6A View FIGURE 6 ). Distal end with 3 subdistal setae, approximately 2–2.5 times longer than antennular thickness ( Fig. 6B View FIGURE 6 ).
Frontal appendage ( Fig. 6C View FIGURE 6 ) consisting of 2 slightly curved long and pointed branches, reaching half-length of distal antennomere, with 2 small tips at inner margin, one close to base and other approximately in its half. Single acute basal projection in its ventral surface, whose length is about one-third of the latter.
Second antennae ( Fig. 6D View FIGURE 6 ) reaching thoracopod IX or X when extending backwards. Proximal and distal antennomeres subcylindrical, similar in length, 2 times as long as broad. Inner longitudinal row of 12 or 13 small papillae (sp) from medial part of proximal antennomere to medial part of distal antennomere. Medial part of distal antennomere with transversal row of 5–7 small papillae. Small papillae consist of a conical base with 1 apical small sensory seta. Apical joint (aj) oriented ventrolaterally, at distal end of basal joint, approximately as long as distal antennomere. Hand (according to Maeda-Martínez et al. 1995b) with 2 sharp and smooth rami. Longest ramus (anterior primary ramus, “thumb) 2 times longer than distal antennomere, slightly curved at end of proximal third; small subtriangular blunt (spur) present in its proximal part. Shorter ramus (posterior ramus, “finger) 0.6 times of anterior primary ramus length, and dorsally bent; proximal part with a small rounded protruding structure followed by short thickening.
Labrum ( Fig. 6E View FIGURE 6 ) subtrapezoidal, without distal protuberances; terminal fleshy process straight, tapering distally. Two setulose pads placed ventrally midway and in the base of fleshy process.
Phyllopodia with gross structure, typical of the genus ( Figs. 7A–E View FIGURE 7 ). Eleven pairs of thoracopods. First thoracopod ( Fig. 7A View FIGURE 7 ) 2 times shorter than seventh thoracopod ( Fig. 7C View FIGURE 7 ); eleventh thoracopod ( Fig. 7E View FIGURE 7 ) 0.8 times longer than seventh thoracopod; rest of thoracopods subsimilar in size. Praepipodite (PE) oval, with serrated outline in all thoracopods. Epipodite (EP) wide, with undulated margin ( Figs. 7A, C View FIGURE 7 ) in the tenth anterior thoracopod; eleventh thoracopod epipodite elongated, with serrated extreme ( Fig. 7E View FIGURE 7 ). Exopodite (EX) oval, bordered by plumose marginal setae; first thoracopod small ( Fig. 7A View FIGURE 7 ), not sticking out from endopodite; rest of thoracopods ( Figs. 7C, E View FIGURE 7 ) of similar size to endopodite. Endopodite (EN) broad, covered by short plumose setae in its outer margin, and provided with a more or less marked depression in the middle ( Figs. 7A, C, E View FIGURE 7 ). Endites from first to tenth thoracopods: first endite with 2 submarginal spine-like setae on anterior surface, proximal one long and thin, provided with denticles, and distal one shorter, spiniform, with a basal tiny spine-like seta ( Figs. 7A, C View FIGURE 7 ); second endite with a long spiniform proximal seta, submarginal on anterior surface, with a basal tiny seta ( Figs. 7A, C View FIGURE 7 ); third endite with 2 unequal submarginal spinelike seta on anterior surface and three plumose setae on posterior surface ( Figs. 7B, D View FIGURE 7 ); 4 endite with 2 unequal submarginal spinelike seta on anterior surface and 2 plumose setae on posterior surface ( Figs. 7B, D View FIGURE 7 ); fifth endite with 3 unequal submarginal spinelike seta on anterior surface and 2 plumose setae on posterior surface ( Figs. 7B, D View FIGURE 7 ). Endites to eleventh thoracopod ( Fig. 7E View FIGURE 7 ): first endite with submarginal spine-like setae very reduced; second endite with 2 small spines on anterior surface and 3 plumose setae on posterior surface; third and fourth endites with 2 small spines in anterior surface and 2 plumose setae on posterior surface; fifth endite with 1 small spine in anterior surface and 2 plumose setae on posterior surface.
Abdominal segments ( Fig. 8A View FIGURE 8 ) typical of the genus. First, second, and third segments with 2 small cuticle projections, one at each side, close to posterior margin (pointed with arrow in Fig. 8A View FIGURE 8 ).
Genital segments ( Fig. 8B View FIGURE 8 ) slightly expanded and partially fused. First segment ventrally smooth. Second segment with linguiform outgrowths 2 times shorter than basal part of gonopods, placed posterolaterally on ventral surface. Basal part of gonopods non-retractile, reaching the end of third abdominal segment; spinulated appendix located in its basal inner side and 2 rounded expansions in its distal end. Everted part of gonopods twice longer than basal part, provided with longitudinal rows of spines.
Cercopods ( Fig. 8C View FIGURE 8 ) of the type “spinose cercopods sensu Maeda-Martínez (1995b), sclerotized, with short spine-like setae replacing the marginal plumose setae on the distal half. Cercopods as long as the last 4 abdominal segments. Anus terminal.
Female. First antennae ( Fig. 9A View FIGURE 9 ) filiform 4 times longer than eye diameter, and 2 and a half longer than second antenna. Distal end as in male.
Second antennae ( Fig. 9A View FIGURE 9 ) broad with rounded end, little longer than eye plus stalk. Distal surface and margins bearing short setae. One small marginal beak on anterior edge close to distal end.
Thoracopods as in male.
Abdominal segments ( Fig. 9C View FIGURE 9 ) with smooth surface. Some of them bearing warty outgrowths provided with sensillae (in fourth and sixth segments in the figure).
Genital segments ( Fig. 9C View FIGURE 9 ) completely fused. Brood pouch elongate, fusiform extending to middle of fourth abdominal segment; end provided with an angular flat expansion directed posteriorly ( Fig. 9D View FIGURE 9 ).
Eggs subspherical; surface covered by wide protruding keeled ribs delimiting polygonal fields ( Fig. 3A View FIGURE 3 ). Diameter around 200 µm.
Cercopods ( Fig. 9E View FIGURE 9 ) broad in the base, margined on both sides by feathery setae gradually shortening to their acute end. Length as last four abdominal segments plus telson.
Size. Total body length of the holotype (MNCN 20.04/20321), (including cercopods setae): 7.48 mm. Largest female specimen recorded: 10.56 mm.
Geographic distribution. Streptocephalus wolof is known from the following localities in Senegal: 2 km north of Podor, Diembéreng, 1.9 km south-east of Bokiladji, 6 km east of Koutenable and Diabal ( Table 2 View TABLE 2 ). Future studies could likely extend its distribution to the neighboring countries Mauritania, Gambia, Mali, Guinea, and Guinea-Bissau. The previous recorded populations identified as S. zeltneri in Senegal [Lingure and Palagu ( Monod 1969; Hamer et al. 1994b; Maeda-Martínez et al. 1995b)] require revision as they were not examined by us, and therefore, we were unable to confirm its taxonomic identity. However, we tentatively treated these records as S. zeltneri until additional studies confirm its identity ( Fig. 1 View FIGURE 1 ).
Remarks. The new species is closely related to Streptocephalus zeltneri . Both species cannot be distinguished based on adult morphological characters, and consequently they can be considered as cryptic species ( Marrone et al. 2017). However, they differ on the basis of the eggs macrosculpture. Eggs of S. wolof present their surface covered with carinated ribs, delimiting polygons of variable number of sides ( Fig. 3A View FIGURE 3 ). This trait was consistent in each revised population that contained mature females.
Streptocephalus wolof is the most commonly found and widespread Anostraca species in Senegal, occurring in several ecoregions (including the Sahelian and Sudanian savannas, and the Guinean forest savanna close to the Guinean forest) ( Fig. 1 View FIGURE 1 ). The studied specimens of S. wolof were found during the rainy season in temporary ponds, both with transparent and turbid waters, often in syntopy with amphibian larvae, as Sclerophrys xeros ( Tandy, Tandy, Keith & Duff-MacKay, 1976), Kassina senegalensis ( Duméril & Bibron, 1841) , K. fusca Schiøtz, 1967 , Ptychadena bibroni ( Hallowell, 1845) , and Phrynobatrachus francisci Boulenger, 1912 ( Fig. 5 View FIGURE 5 ).
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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