Pseudosinella orba Christiansen 1961

• Main Author: Soto-Adames, Felipe N.
• Format: Text
• Language: unknown
• Published: Zenodo 2010
• Subjects: Biodiversity; Taxonomy; Animalia; Arthropoda; Entognatha; Collembola; Entomobryidae; Pseudosinella; Pseudosinella orba; Mercer; Seta; Fennoscandia
• Online Access: https://dx.doi.org/10.5281/zenodo.6208555; https://zenodo.org/record/6208555

Pseudosinella orba Christiansen, 1961 Figs 88–104, Table 6 Material Examined . West Virginia, MERCER Co., Honacker Cave, 2 individual on one slide and 2 others in alcohol; Chris’s Last Look, 2 individual on one slide and 2 others in alcohol. Virginia , SMYTHE Co., Dead Air Cave, water pool, 16 March 2000, 3 individuals on one slide. Descriptive notes. Length to 2.4mm; color in alcohol white, without trace of pigment. Subapical sense organ weakly clavate (Fig. 87). Ant. 3 sense organ formed by two thin walled rods in shallow pits (Fig. 88); the segment has additional basally-swollen, thin walled setae and conic sensilla near the usual sense organ. Dorsal head chaetotaxy (Fig. 93) includes 6–7 macrosetae along antennal base, and macrosetae A0 , A 2 , A 3 , M 1 /S 1 , S 2 , S 3 and Pa 5 A 1 ciliate, all other dorsal microsetae smooth; seta S0 closer to S 2 than S 3 M 1 /S 1 just posterior to M 2 . Eyes absent. Prelabral and all labral setae smooth. Labral papillae obscured. Peristomal setae (Fig. 89) pss0 ciliate, pss 1–2 smooth, pleural fold setae smooth. Ungulum of maxilla with 3 teeth. Labial papilla E (Fig. 92) with lateral process curved inwards and not reaching tip of papilla. Labial palp with proximal seta Z distinctly shorter than seta Y (Fig. 90). Labial chaetotaxy M 1 M 2 oEL 1 L 2 A 1–5 in some individuals r visible as a translucent conic sensilla barely protruding beyond socket. Postlabial chaetotaxy (Fig. 90) with 4 + 4 setae along ventral groove, seta I 1 always smooth, I 4 always ciliate, I 2–3 variable, either ciliate or smooth; C 1 smooth, and 5–8 posterior ciliate setae not organized into a column; E 1 smooth, E 2 ciliate; L 1 smooth, L 2 ciliate but not modified; O 1 modified into a conic microsetae similar to but longer than labial r , O 2 smooth or ciliate. Inner macrochaetotaxy of body as 32 /0100+ 3. Mesothoracic macrosetae p 2 , p 3 and p 5 present (Fig. 95). Metathorax (Fig. 97) with macroseta p 2 and p 3 . Abd. 1 seta a 6 absent, a 3 and/or a 5 , displaced anteriorly out of the row (Fig. 98). Chaetotaxy of Abd. 2 (Fig. 99) with a 6 and all supplementary setae fan-shaped; a 2 ciliate, a 2 p absent; a 3 fan-shaped, external to as , and surpassing tip of as as not reaching socket of macroseta m 3 m 3 e not reaching socket of as socket of m 5 modified as a normal macroseta, but seta itself subequal or shorter than seta p 5 p p 5 p a short, ciliate mesoseta. Abd. 3 (Fig. 100) with a 2 , a 6 , am 6 , a 7 and all supplementary setae fan-shaped or ciliate; mi shorter than ml a 3 ciliate, anterior to and far from as as reaching m 3 , nearly half the length of m 3 d 2 reaching p 5 a 7 inserted close to, longer than, and reaching am 6 m 7 a normal microseta inserted anterior to p 6 p 7 a long microseta; m 7 a macroseta; 1–2 additional acuminate macrosetae present posterior to p 7 . Abd. 4 bothriotrichal complex as in Fig. 101: s absent; a , m, D 1 , Pi and Pe fan-shaped; C 1 p , T 3 and D 1 p ciliate; T 3 and D 1 p almost forming a row, T 3 and D 1 p reaching Pi and Pe respectively. General chaetotaxy of Abd. 4 (Fig. 102) with macrosetae B 4, B 5, B 6, T 6 , T 7, D 2 , E 1, D 3, E 2, E 3 , F 1 and F 3 microseta posterior to E 3 present; macroseta B 5 anterior to a line drawn between A 5 and C 2 . Posterior setae on Abd. 4 usually 3 + 3. Trochanteral organ with 17–18 setae. Metathoracic femora with three blunt macrosetae inserted near the middle of the segment. Tenet hair (Fig. 103) acuminate, slightly shorter than unguiculus; unguiculus lanceolate with a small basal swelling and weakly truncate on third pair of legs; posterior lamella of all legs with small, clear tooth in the two largest individuals, but smooth on smaller specimens, all other lamellae smooth (Fig. 104). Unguis with three teeth (Fig. 103): basal pair clearly unequal in size, shortest member of the pair smaller than distal unpaired tooth; unpaired tooth prominent; outer teeth short, not nearly attaining basal inner teeth, clearly seen only on pro- and mesothoracic legs, metathoracic claws apparently lacking outer teeth. Collophore with up to 11 distolateral setae; anterior face with 7–8 setae; posterior face with 3 + 3 distal setae. Dens with distal uncrenulate section at least 4 x length of mucro (Fig. 91). Manubrial plate with 2 outer and 2 inner setae separated by 2 pseudopores. Apical mucronal tooth longer and narrower than basal tooth (Fig. 91). Remarks . I have examined three individuals from Dead Air Cave in Smythe Co. Virginia kindly sent to me by Kenneth Christiansen and they differ from the material from West Virginia (Table 6) in the structure of labial seta m 1 , number and structure of setae in postlabial row O (Fig. 96) and in that Abd. 4 B 4 is a micro-, instead of a macroseta (Fig. 102, arrow). Some of this variation (e. g., number of setae on postlabium, Th. 2 and Abd. 4) may be attributed to differences in body size between locations given that the smallest specimen from Mercer Co. is 1.8mm long whereas the largest specimen seen from Smythe Co. is just 1.3mm long. However, populations considered by Christiansen and Bellinger (1998) as con-specific with P. o r b a also vary in details of the chaetotaxy of the head (dorsal), labium, postlabium, Th. 2, Th. 3 and Abd. 4 as shown in Table 6. These different ‘populations’ may in fact represent isolated species in a species complex, but a detailed analysis of the geographic distribution of the variation must be completed before reaching a conclusion. In addition, the chaetotaxy of the types from Tennessee needs description. Head Labium m 1 Postlabium Th. 2 Macrosetae Th. 3 Abd. 4 Abd. 4 Macroseta S 2 Column O Macrosetae Macroseta C 1 Medial ‘Population’ Macrosetae Material Examined. GREENBRIER Co ., Water Trough Cave, 3 on slides, 7 in alcohol; Tin Cave, 9 June 2004, 1 on slide. Descriptive notes. The dorsal chaetotaxy of the head includes 5–6 macrosetae along the base of the antenna and posterior to needle-shaped smooth setae (Fig. 105); A0 and Pa 5 are the only macrosetae present, all other setae in series A (except A 1 , which is ciliate), M, S and Ps are short and smooth; anterior to A0 there is a conic sensilla (not shown in Fig. 105); M0 absent. Macroseta Pa 5 and postocular bothriotricha ( Pa 6) distinctly displaced medially and inserted closer to seta Ps 3 than Ps 5 (cf. Figs. 105 and 4). Pleural and peristomal setae smooth and undifferentiated. Lateral appendage of labial palp papilla E curved internally and surpassing tip of papilla. Three of the four individuals examined have labial chaetotaxy as M 1 M 2 rEL 1 L 2 (Fig. 106), one individual with m 1 shorter than M 2 . All postlabial setae smooth in three of the four individuals examined, in one individual from Water Through Cave most setae are very weakly, but noticeably ciliate: columns I, C, E, L and O with 4, 2, 2, 3, 2 setae; L 2 and O 1 are conic to weakly blunt sensilla (Fig. 106). Ungulum of maxilla with three teeth (Fig. 112). Formula for inner macrochaetotaxy of body as 00/ 0300+ 2. Seta a 6 on Abd. 1 present. Abd. 2 (Fig. 110) with a 6 , a 3 and all supplementary setae around bothriotricha fan-shaped; a 2 p ciliate or smooth; macrosetae a 2 , m 3 , m 3 e , m 5 and p 5 p present. Abd. 3 (Fig. 111) with a 2 , a 6 and all supplementary setae around bothriotricha fan-shaped; a 3 ciliate, displaced posteriorly as to almost form a row with m 3 and as a 7 ciliate, anterior to and reaching am 6 d 2 absent; p 6 posterior to p 5 and m 7 m 7 a a macroseta. Bothriotrichal complex of Abd. 4 (Fig. 113) with T 3 ciliate, all other setae fanshaped; s absent; T 3 and D 1 p almost aligned into a row; D 1 p reaching Pe a supplementary fan-shaped seta present between Pe and T 5 (arrow, Fig. 113). General chaetotaxy of Abd. 4 (Fig. 114) with macrosetae B 5 , B 6 , T 7, F 2, D 2 , D 3 , E 2 , E 3 , F 1 , F 3 , and two others probably belonging to series Fe present, B 5 anterior to a line drawn between A 5 and C 2 C 1 a ciliate microseta; a supplementary microseta present between E 1 and E 2 . Abd. 4 Posterior setae 4 + 4. All individuals have claws with three inner teeth, with one of the basal teeth clearly larger than the other, unguiculus with a large posterior tooth. In the individuals from Water Trough Cave the difference in size between the basal paired teeth is less marked than in the specimen from Tin cave (cf. Figs 115, 116). In addition, the posterior unguicular tooth is longer in the individual from Tin cave than in those from Water Trough Cave. Anterior face of ventral tube with 1 + 1 distal macrosetae and seven other basal setae (Fig. 108); posterior face with 1 + 1 distal and 5 basal setae (Fig. 109); lateral vesicles view obstructed in all specimens examined. The three individuals from Water Trough Cave have one smooth seta on the dorsodistal row of the manubrium (Fig. 107), 1 internal and 1 external setae on the manubrial plate and short spatulate tenet hairs on all feet (fig. 115), whereas in the individual from Tin Cave all manubrial setae are ciliate, the manubrial plate has two external setae and all tenent hairs are acuminate (fig. 116). Remarks . Christiansen and Culver (1969) dealt with the extensive variation seen in this species across North America. The descriptive notes presented above are provided to place the West Virginian collections in the context of the geographic variation of the species and to add some characters not considered by previous authors. Pseudosinella violenta is distinguished from other blind North American Pseudosinella by a combination of characters which include having the postocular bothriotricha and macroseta Pa 5 displaced dorsomedially on the head, having a large posterior unguicular tooth, all posterior setae on labial triangle, and the anterior row of postlabial setae smooth, Abd. 2 with five macrosetae, Abd. 3 with setae a 3 , as and m 3 forming an irregular row and macroseta p 6 displaced posteriorly as to be inserted between p 5 and p 7 , Abd. 4 with macroseta B 5 displaced interiorly, closer to C 1 than B 6 , and supplementary setae between Pe–T 5 and E 1 –E 2 . absent 1 Enlarged and roughly ciliate, but not a macroseta in the sense used here for Abd. 4 setae in series B. The characteristic displacement of the cephalic bothriotricha and macrosetae Pa 5 is rare among Pseudosinella species, were it has been reported (to my knowledge) only in P. rolfsi Mills, 1932, P . folsomi (Mills, 1931), P . ashmoleorum Gama, 1988, P . gamae Gisin, 1967, and P . halophila Bagnall, 1939 ( sensu Fjellberg 2008). These six species, plus P . bellingeri Wang, Chen & Christiansen, 2002 (relative position of the postocular bothriotricha unknown) have been considered as part of an informally defined species group (e.g., Wang et al. 2004). Of the seven species, P . bellingeri and to some extent P . folsomi and P . rolfsi can be unambiguously distinguished, but the separation between the European forms ( ashmoleorum , gamae and halophila ) from P. v i o l e n t a as circumscribed by Christiansen & Bellinger (1998) is not clear. Table 7 presents a list of characters used to separate species in this group. According to Christiansen and Culver (1969) P . violenta from Central Texas and south through Mexico and South America have Abd. 4 seta s , whereas in North American populations north of Texas, seta s is absent. Christiansen and Culver (1969) also report great variation in claw complex structure, with some individuals having three inner teeth while others only having two teeth. This circumscription of P. v i o l e n t a, leads me to concluded that P . gamae is a junior synonym of P. violenta (Central and South American populations), P . ashmoleorum is a junior synonym of P. halophila ( sensu Fjellberg 2007), which in turn differs from some North American populations of P. v i o l e n t a only in the absence of one inner ungual tooth. I refrain from proposing a formal synonymization of these names until I have the opportunity to study types or topotypical material of each species. In any case, it is possible that the great interpopulation variation reported for P. violenta in the Americas masks a species complex, and that some of the names applied to European populations may be available to identify particular lineages within the complex. : Published as part of Soto-Adames, Felipe N., 2010, Two new species and descriptive notes for five Pseudosinella species (Hexapoda: Collembola: Entomobryidae) from West Virginian (USA) Caves, pp. 1-34 in Zootaxa 2331 on pages 25-30, DOI: 10.5281/zenodo.275457 : {"references": ["Christiansen, K. (1961) The genus Pseudosinella in caves of the United States. Psyche, 67 (1960), 1 - 25.", "Christiansen K. & Bellinger P. (1998) The Collembola of North America north of the Rio Grande; A taxonomic analysis. Grinnell College, Grinnell, Iowa, 1518 pp.", "Christiansen, K. & Culver, D. (1969) Geographical variation and evolution in Pseudosinella violenta (Folsom). Evolution, 23, 602 - 621.", "Mills, H. B. 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