Neolindus yotokae Guzman, Tokareva & Żyła, 2024
publication ID |
https://doi.org/ 10.5852/ejt.2024.942.2581 |
publication LSID |
lsid:zoobank.org:pub:DF991BC4-1761-4C5D-96E5-EFC62F8F7D1A |
DOI |
https://doi.org/10.5281/zenodo.12570659 |
persistent identifier |
https://treatment.plazi.org/id/F2E11144-A406-413E-9DBF-465E1B0252DB |
taxon LSID |
lsid:zoobank.org:act:F2E11144-A406-413E-9DBF-465E1B0252DB |
treatment provided by |
Plazi |
scientific name |
Neolindus yotokae Guzman, Tokareva & Żyła |
status |
sp. nov. |
Neolindus yotokae Guzman, Tokareva & Żyła sp. nov.
urn:lsid:zoobank.org:act:F2E11144-A406-413E-9DBF-465E1B0252DB
Fig. 24 View Fig ; Supp. file 2
Diagnosis
Among species with two pairs of head trichobothria, N. yotokae Guzman, Tokareva & Żyła sp. nov. resembles N. paralellus with a wide midlongitudinal invagination in sternite VIII and the structure of aedeagus. However, in contrast to N. paralellus , this invagination is glabrous (without setation), and the concave deep emargination of the posterior margin of sternite VIII is covering the whole width and has acute lateral ends ( Herman 1991: fig. 88; Fig. 24E View Fig ). Moreover, tergite VIII has a rounded posterior margin, compared to straight margin in N. paralellus ( Herman 1991: fig. 87; Fig. 24D View Fig ), and the aedeagus of N. yotokae has shorter apical invagination on the parameral side compared to these structures in N. paralellus ( Herman 1991: fig. 85; Fig. 24F–G View Fig ).
Etymology
The name is dedicated to Dr Karla Yotoko, evolutionary biologist, and Camilo Guzman’s PhD advisor. An adjective.
Type material
Holotype VENEZUELA • ♂; “ Neolindus yotokae Guzman, Tokareva & Żyła 2024 HOLOTYPE [red label] \\ Aragua, [Mario Briceño Iragorry, Henri Pitttier National Park] Rancho Grande Biological Station ; 10°21’38’’N, 67°41’38’’W; 1550 m [m a.s.l.]; 14 May 1998; R. Anderson Leg.; VEN1A98 008A; ex: cloud forest litter \\ SM0129897 KUNHM-ENT [barcode]”; KUNHM-ENT. GoogleMaps
Paratypes VENEZUELA • 1 ♂; “ Neolindus . yotokae Guzman, Tokareva & Żyła 2024 PARATYPE [yellow label] \\ same data as for holotype \\ 1550 m; 10°21’38’’N, 67°41’38’’W; 14 May 1998; VEN1A98 007E \\ [barcode] SM0112571 KUNHM-ENT ”; KUNHM-ENT GoogleMaps • 1 ♂; same data as for preceding; “ 1100–1300 m; 10°21’32’’N, 67°40’46’’W; 14 MAY 1998; J. Ashe, R. Anderson Leg.; VEN1ABH98 009; ex: fungus log \\ SM0334139 KUNHM-ENT [barcode]”; KUNHM-ENT GoogleMaps .
Description
MEASUREMENTS. BL (5.7), H (0.34, 0.5), A (0.77), a1 (0.2, 0.06), a2 (0.09, 0.05), a3 (0.07, 0.05), a4 (0.06, 0.05), a5 (0.05, 0.05), a6 (0.05, 0.06), a7 (0.06, 0.06), a8 (0.06, 0.07), a9 (0.06, 0.07), a10 (0.06, 0.08), a11 (0.01, 0.08), NKW (0.33), GL (0.20), P (0.8, 0.7), E (0.06, 0.62), PC (0.32, 0.13), PF (0.57, 0.3), PT (0.3, 0.1), MSC (0.4, 0.25), MSF (0.6, 0.2), MST (0.4, 0.1), MTC (0.26, 0.21), MTF (0.38, 0.22), MTT (0.4, 0.07).
COLOURATION. Head and pronotum brown; legs light brown; abdomen brown.
HEAD. Head capsule wider than long; anterior margin sinuate, dorsoventrally deflexed, slightly elevated; posterior margin rounded with emargination in front of neck; posterior angles round; setation with 2 pairs of PCS and 1 row with 8 setae of PMS, central PMS wide apart, setae near neck longer than others. Epicranium with low-density micropunctuation, setation with 1 pair of OS; IOS and SAS displaced towards second and third parts of head. Gena with smooth surface, with depression from mandibular base to posterior margin of head, setation with 2 trichobothria, MS, 1 POS, and 1 PTOS between margin of eye and POT. Postgena with row of 3 setae in line from eye to gular suture; gular sutures reaching posterior margin of head joining neck pits; anterior part of gula without setae, with lateral depressions; midlength of gula with 2 setae; posterior margin of head with 2 setae close to gular sutures. Antenna moniliform from antennomere 3, shorter than head and pronotum combined; antennomeres 1–7 longer than wide, antennomeres 8–11 wider than long, tomentose pubescence starting from antennomere 5; antennomere 1 as long as antennomeres 2 and 3 combined, antennomere 2 longer than 3. Labrum bilobed, with wide quadrate emargination ( Fig. 24A View Fig , Supp. file 2).
THORAX. Pronotum slightly longer than wide, with umbilicate randomly distributed micropunctures. Prosternal basisternum with longitudinal carina and smooth surface. Mesosternum with scutiform basisternum with scarce tuberculate micropunctuation. Metasternal intercoxal process with 1 pair of rounded processes. Elytron wider than long, shorter than pronotum; surface of elytra with umbilicate micropunctures in 4–6 moderately dense longitudinal rows ( Fig. 24A View Fig , Supp. file 2).
LEGS. Protibia with 3 well-developed combs of setae; mesotibial apical ctenidium on both sides, inner longer than outer, outer spine-like; mesotarsomeres 1, 2 and 3 as long as mesotarsomere 5 as longer than mesotarsomeres 1, 2, 3 and 4 combined; inner ctenidium of metatibia longer than outer; metatarsomeres 1, 2, 3 and 4 subequal, metatarsomere 5 as long as metatarsomeres 1–3 combined.
ABDOMEN. Male: tergites with moderate density of micropunctuation. Posterior margin of tergite VII straight( Fig.24B View Fig ).Posterior margin of sternite VII sinuate, with moderately shallow midline emargination, area around emargination invaginated ( Fig. 24C View Fig , Supp. file 2). Posterior margin of tergite VIII elongate, rounded ( Fig. 24D View Fig ). Posterior margin of sternite VIII with midline concave emargination as long as posterior margin width, with wide longitudinal glabrous stripe throughout entire segment, lateral angles rounded ( Fig. 24E View Fig , Supp. file 2). Posterior margin of tergite IX with midlongitudinal deep emargination in ⅓ of segment length, fused; aedeagus, in parameral view, median lobe of uniform width along sides, apex of median lobe with 2 lateral flattened rounded processes. pPMS and pLS absent. APS short, triangular, flattened, no longer than median lobe, partially covering median foramen ( Figs. 24F–I View Fig ). Female: unknown.
Distribution
The species is known from the type locality in Venezuela (Aragua, Rancho Grande Biological Station). It was collected in the cloud forest at high altitude (1550 m a.s.l.) by sifting leaf litter.
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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