Lepidocyrtus divisus , Mateos, 2025
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https://doi.org/10.11646/zootaxa.5717.3.6 |
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lsid:zoobank.org:pub:DDC329E4-C24D-4437-B67E-52E891F20165 |
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persistent identifier |
https://treatment.plazi.org/id/FB3FE532-FFF1-FFC5-668D-FE83FED7FC3F |
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Plazi |
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scientific name |
Lepidocyrtus divisus , Mateos |
| status |
sp. nov. |
Lepidocyrtus divisus, Mateos , sp. nov.
urn:lsid:zoobank.org:act:
Figs 2–23 View FIGURE 2 View FIGURES 3–4 View FIGURES 5–9. 5–7 View FIGURES 10–11 View FIGURES 12–14 View FIGURES 15–16 View FIGURES 17–21 View FIGURE 22 View FIGURE 23 , Tabs 1–2
Type material. Holotype: Female on slide code CRBA-113472, Cassine, Piemonte ( Italy), 200 m a.s.l., lat/long coordinates N44.76891 E8.49129 ( Fig. 1 View FIGURE 1 location 1), collected in grassland surrounded by forests using a modified leaf blower functioning as an aspirator (diameter of opening 14 cm), 07.v.2015, leg. B. Zhang. GoogleMaps Paratypes: 5 specimens on slides ( 1 female and 4 adults without visible genital plate) and 9 specimens preserved in absolute alcohol, same data as holotype GoogleMaps . Holotype and paratype female slide code CRBA-113473 saved in the collection of the Centre de Recursos de Biodiversitat Animal , Faculty of Biology , University of Barcelona (http://www.crba.ub.edu); other paratypes kept in the E. Mateos’ collection ( University of Barcelona, lot LP415 ) .
Other material. Three specimens on slides, Vernante , Piemonte ( Italy), 1175 m a.s.l., lat/long coordinates N44.20194 E7.50488 ( Fig. 1 View FIGURE 1 location 2), collected in grassland surrounded by forests using a modified leaf blower functioning as an aspirator (diameter of opening 14 cm), 07.v.2015, leg. B. Zhang, lot LP416 GoogleMaps . 2 specimens on slides, Pedavena , Veneto ( Italy), 925 m a.s.l., lat/long coordinates N46.04116 E11.84655 ( Fig. 1 View FIGURE 1 location 3), collected in grassland surrounded by forests using a modified leaf blower functioning as an aspirator (diameter of opening 14 cm), 04.v.2015, leg. B. Zhang, lot LP413 GoogleMaps . 5 specimens on slides and 5 specimens preserved in absolute alcohol, Orsomarso , Calabria ( Italy), 162 m a.s.l., lat/long coordinates N39.79414 E15.92726 ( Fig.1 View FIGURE 1 location 4), hand collected under logs and stones in forest environment, 21.iv.2017, leg. E. Mateos, lot LP481 GoogleMaps . 7 specimens on slides and 9 specimens preserved in absolute alcohol, Roybon , Dep. Isère, Region Ródano-Alpes ( France), 652 m a.s.l., lat/long coordinates N45.241130 E5.282241 ( Fig.1 View FIGURE 1 location 5), hand collected under logs and stones in forest environment, 02.xi.2012, leg. E. Mateos, lot LP315 GoogleMaps . All other material kept in the E. Mateos’ collection ( University of Barcelona) .
Diagnosis. Body length (without head nor furca) 2–3 mm ( Holotype 2.6). With dark purple pigment on ant. II–IV and coxae I–II, head with lateral and ventral light purple pigment, legs beyond coxae purple. Mesothorax projecting over head. Scales covering ant.I–IV, legs, ventral tube, and posterior face of manubrium. One pseudopore at the ventral apical end of ant.I. Ocular chaeta q present. Prelabral chaetae smooth. Labial chaetotaxy M 1m 2Rel1l2, M1 and R shortened. Dorsal cephalic macrochaetae formula A0[A2a]A2Pa5; dorsal body macrochaetae formula 0,0/0,1,0,1+3; lateral body macrochaetae formula 0,0/0,1,4,16. Fourth abdominal segment with chaeta s. With two short ciliated postlabial chaetae ( X and X’). Unguis with basal paired teeth and one unpaired tooth. Unguiculus lanceolate and with smooth or finely serrated outer margin. Lateral pseudopores present on abd.III–IV; abd.IV also with ventral pseudopores located on basal region. Dorsal pseudopores of th.II and abd.IV divided.
Etymology. The species name refers to the presence of divided pseudopores.
Description. Holotype body length (without head nor furca) 2.6 mm, paratypes 2.0–3.0 mm. Body color pattern ( Fig. 2 View FIGURE 2 ) with dark purple pigment on ant.II–IV and coxae I–II, head with lateral and ventral light purple pigment, legs beyond coxae purple, densely black pigmented ocular areas. Mesothorax projected over head.
HEAD. Dorsal cephalic macrochaetae A0, A2, Pa5, with pair of smaller supplementary macrochaetae A2a between A0 and A2 (reduced formula= A0[A2a]A2Pa5); maximum number of macrochaetae An on head 22+22 ( Fig. 3 View FIGURES 3–4 ). Interocular chaetotaxy with s, t, p, q ciliated chaetae and 2 scales.Eyes 8+8; eyes A to F subequal, G and H slightly smaller, ratio F/G and C/H ≈ 1.7 ( Fig. 4 View FIGURES 3–4 ).
Clypeus ( Fig. 5 View FIGURES 5–9. 5–7 ) prefrontal area with three chaetae (1 pf0 and 2 pf1) and eight scales, facial area with two chaetae ( f) and three scales, lateral area with 1+1 L1 and 1+1 L2 chaetae; all these chaetae and scales ciliated.
Labrum ( Fig. 6 View FIGURES 5–9. 5–7 ) with 5/5/4 smooth and pointed chaetae on rows p/m/a, respectively; two rounded labral papillae with pointed apex; four prelabral chaetae ( pl) smooth and pointed.
Maxillary palp outer lobe ( Fig. 7 View FIGURES 5–9. 5–7 ) with apical appendage and basal chaeta smooth and equal in size, sublobal plate with three smooth chaeta-like appendages.
Labial and postlabial chaetotaxy as in Fig. 8 View FIGURES 5–9. 5–7 ; with five smooth proximal chaetae at the base of labial palp; labial anterior row with five smooth chaetae ( a1–a5); posterior row with m2, e, l1 and l2 smooth and M1 and R ciliated, reduced formula M 1m 2Rel1l2 ( one paratype with one ciliated chaeta M1 and one smooth chaeta m1, another paratype with ciliated chaeta E); chaetae m2 e l1 and l2 smooth, chaetae M1 and R ciliated and shorter, ratio m2/ M1 = 3.6, ratio m2/ R = 3.2; postlabial chaetotaxy with all chaetae ciliated, with four chaetae along ventral cephalic groove, and with two X chaetae ( X and X’) shorter, ratio G3/X = 2.8. Lateral process of outer labial papilla fingershape, slightly curved and reaching apex of papilla ( Fig. 9 View FIGURES 5–9. 5–7 ) .
BODY. Dorsal macrochaetae formula 00/0101+3, lateral macrochaetae formula 0,0/0,1,4,16. Dorsal chaetotaxy of th.II–III as in Figs 10–11 View FIGURES 10–11 . Mesothorax polychaetotic, covered by numerous small smooth microchaetae interspersed among scales, with 2 lateral S-chaetae ( al and ms), without dorsal nor lateral macrochaetae. Metathorax with a lateral sensillum ( al) close to several ciliated chaetae, without dorsal nor lateral macrochaetae. Chaetotaxy of abd.I– III as in Figs 12–14 View FIGURES 12–14 . Abd.I with a lateral S-microchaeta ( ms) external to a6, without dorsal nor lateral macrochaetae. Second abdominal segment with dorsal macrochaeta m3 (lsM) and lateral macrochaeta m5 (lsM); m3 socket 1.5 times larger than m5 socket. Third abdominal segment with lateral macrochaetae pm6 and p6 (lsM both), with chaeta d3 between these two macrochaetae, with lateral macrochaetae a8 and p8 (ssM both), and with S-chaetae as and ms. All chaetae associated with the trichobothria on abd.II–III fan-shaped ( Figs 13–14 View FIGURES 12–14 ). Chaetotaxy of abd. IV as in Fig. 15 View FIGURES 15–16 ; dorsal macrochaetae Sm, B4, B5, B6, and lateral macrochaetae D3, E2, E3, E4, F1, F2, F3 with large socket (lsM); lateral macrochaetae T6, T7, D2, D3p, De3, E1, E4p, Fe4, Fe5 longer or shorter but always with small socket (ssM); macrochaeta F2 inserted at the same level of macrochaeta E3; the ratio of distances between macrochaetae Sm–B4 / B4–B6 as 0.35–0.43; ratio of distances between macrochaetae B4–B5 / B5–B6 as 1.0–1.2; accessory chaeta s associated with trichobothrium T2 present; chaetae a, D1, m, s, pe and pi associated with trichobothria T2 and T4 fan-shaped; sens chaetotaxy composed of three anterior dorsomedial elongate S-chaetae, and short chaetae as and ps.; posterior margin with 9+9 smooth mesochaetae; with 8–19 pseudopores located externally to the lateral suture and 4–8 in the ventral region; BP4 without pseudopores. Dorsal chaetotaxy of abd.V ( Fig. 16 View FIGURES 15–16 ) with S-chaetae as, acc.p4 and acc.p5.
APPENDAGES. Antennal segments I–III and basal portion of ant.IV with scales on dorsal and ventral faces ( Fig. 17 View FIGURES 17–21 ). Ratio antenna:cephalic diagonal ≈ 1.9 (head diagonal measured from cervical edge to apex of mouth part); ratio ant.I:II:III:IV as 1:1.9:1.8:3.9. Proximal margin of ant.I dorsally with three microchaetae arranged in triangle (ant.I-organ); ventro-distal membranous margin of ant.I with a short-curved S-chaeta. Ant.III organ composed of two subcylindrical, slightly curved sensory rods of equal length. Ant.IV without apical bulb.
All legs segments with scales. Trochanteral organ with about 60 spine-like chaetae, 9 on posterior arm, 10 on ventral arm, 34 internal, 6 external and 1 apical ( Fig. 18 View FIGURES 17–21 ). Unguis on all legs ( Fig. 19 View FIGURES 17–21 ) with basal pair of teeth at 47% from base of inner edge and with one unpaired tooth at 69% from base of inner edge; one external tooth and a pair of lateral teeth also present. Unguiculus lanceolate with smooth or finely serrated outer margin. Tenent hair spatulate, smooth and a little longer than claw (ratio tenent hair/claw ≈ 1.1); ratio of supra-empodial chaeta (smooth chaeta on tibiotarsus III opposite to tenent hair)/unguiculus ≈ 1.5.
Ventral tube with 11+11 ciliated chaetae on anterior side ( Fig. 20 View FIGURES 17–21 ) and 9+9 ciliated chaetae on posterior side; scales present on anterior and posterior sides; lateral flaps with a maximum of 45 laterodistal chaetae (38 ciliated and 7 smooth).
Manubrium with scales on anterior and posterior surfaces, with 2+2 ciliated apical chaetae on anterior side. Ratio manubrium:dens:mucro as 17:17:1. Manubrial plate ( Fig. 21 View FIGURES 17–21 ) with two pseudopores, three inner chaetae, and a maximum of 30 outer chaetae. Dental tubercle absent. Mucro with two subequal teeth, basal spine smooth (without spinelet).
PSEUDOPORES. Pseudopores distribution on dorsal, lateral and ventral regions of head, body, and appendages as in Fig. 22 View FIGURE 22 and Table 1. The dorsal pseudopores of th.II and abd.IV are divided in all the specimens studied, in the other segments, dorsal pseudopores may or may not be divided depending on the specimen. The antennal, coxal, furcal, and body ventral pseudopores, with few exceptions, are not divided. Divided pseudopores may be formed by two, three or four subunits, and some undivided pseudopores have an elongated shape ( Fig. 23 View FIGURE 23 ).
Ecology and distribution. The specimens were hand collected under logs and stones in forests and small grasslands surrounded by forest. The new species is only known from the localities indicated in the description.
Discussion. There are two different published nomenclatures that code for postlabial chaetae in Entomobryidae, Chen & Christiansen (1993) and Soto-Adames (2010). According to Soto-Adames (2010), the short ciliated chaetae X and X’ that we have observed in L. divisus sp nov. correspond to O1 and L2 respectively, while in the scheme of Chen & Christiansen (1993,) the O1 chaeta is X, and the L2 chaeta has no equivalent and is named X’ in the present paper ( Fig. 8 View FIGURES 5–9. 5–7 ).
*pse always divided; + pse divided or not divided depending on the specimens; (#) group of pse in central position of the tergum.
The new species belongs to the L. curvicollis -group by the following characters ( Mateos & Petersen 2012): presence of scales on the antennae, legs and dorsal side of manubrium; mesothorax protruded over the head; labial chaeta M1 shorter than M2; presence of chaeta s on abd.IV; dorsal macrochaetae formula A0A2Pa5/00/0101+3. The best diagnostic character of the Lepidocyrtus divisus sp. nov. is the presence of divided pseudopores in the dorsomedial position of some tergites. This character differentiates the new species from all other species of the L. curvicollis -group. Another three important diagnostic characters of the new species are:
1—Presence of smooth chaetae at the base of the labium. Within the L. curvicollis -group the only species described so far with smooth labial chaetae is L. curvicollis , and it is differentiated from the new species by presenting many dorsal pseudopores in abd.IV and not presenting lateral or ventral pseudopores in this segment.
2—Presence of pseudopores on abd.IV located externally to the lateral suture. Within the L. curvicollis -group, L. mariani Traser & Danyi, 2008 is the only species described so far with lateral pseudopores in abd.IV and it is differentiated from the new species by also having lateral pseudopores from th.III to abd.III, and for having all chaeta at base of labium ciliated (although not typical, occasionally also L. mariani can have smooth labial chaetae m1, r, l1 and l2, see Winkler & Mateos 2018).
3—Presence of ventral pseudopores in abd.IV located at the base of the inner edge of BP4. The presence of ventral pseudopores in abd.IV is observed in four species of the L. curvicollis -group, but in different positions depending on the species. In L. flexicollis these pseudopores are distributed forming a line along the inner edge of BP4 (see Mateos et al. 2021 Fig.S3 View FIGURES 3–4 ), while in the species L. divisus sp. nov, L. mariani and L. montseniensis these pseudopores are located grouped at the base of the inner edge of BP4 ( Fig. 21B View FIGURES 17–21 ).
Other characters that differentiate the new species from the rest of the species of the L. curvicollis -group are indicated in Table 2.
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Departamento de Geologia, Universidad de Chile |
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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