Xiphocentron (Antillotrichia) muelleri, Vilarino & Bispo, 2020
publication ID |
https://doi.org/ 10.11646/zootaxa.4851.2.11 |
publication LSID |
lsid:zoobank.org:pub:3F1C604F-22B1-43AD-8520-0A1B47E25843 |
DOI |
https://doi.org/10.5281/zenodo.4407915 |
persistent identifier |
https://treatment.plazi.org/id/62AF1882-535C-419A-8745-1B1CC2A108D8 |
taxon LSID |
lsid:zoobank.org:act:62AF1882-535C-419A-8745-1B1CC2A108D8 |
treatment provided by |
Plazi |
scientific name |
Xiphocentron (Antillotrichia) muelleri |
status |
sp. nov. |
Xiphocentron (Antillotrichia) muelleri sp. nov.
Figs 10–17 View FIGURES 10–19 , 21 View FIGURES 20–26 , 39 View FIGURE 39
urn:lsid:zoobank.org:act:62AF1882-535C-419A-8745-1B1CC2A108D8
Diagnosis. Xiphocentron muelleri sp. nov. is similar to X. copacabana and X. maitea by the basal region of the inferior appendage with its ventral margin distinctly produced ( Figs 14, 17–19 View FIGURES 10–19 ). The new species can be differentiated from its congeners by the truncate basoventral margin of the inferior appendage, forming a right angle ( Figs 14, 17 View FIGURES 10–19 ) (overall rounded in X. maitea and X. copacabana , Figs 18–19 View FIGURES 10–19 ), and the presence of stout spines (very short spines in X. copacabana ) and a mesal sclerite with about three apical points (mesal sclerite absent in X. maitea and just a simple spine without apical points in X. copacabana ).
Description. Adult male. Forewing length 3.5–3.6 mm (n = 7); head and thorax pale brown in alcohol ( Fig. 21 View FIGURES 20–26 ). Legs pale yellow, tibia of hind leg darker. Maxillary palp in increasing order of length (I=II=III)-IV-V, segment IV as long as II+III. Spur formula 2, 4, 3; hind leg with unmodified apical spur. Forewing fork II and fork IV present; fork II sessile at discoidal cell; thyridial cell as long as discoidal cell; three anal veins present ( Figs 10, 11 View FIGURES 10–19 ). Hind wing fork II and fork V present ( Fig. 10 View FIGURES 10–19 ). Sternum V with pair of anteroventral cuticular reticulated regions.
Male genitalia. Tergum IX, in lateral view ( Fig. 14 View FIGURES 10–19 ), wider basally, narrower apically; in dorsal view ( Fig. 12 View FIGURES 10–19 ), anterior margin with a broad V-shaped incision; posterior margin produced as pair of small rounded lobes divided by incision nearly reaching transverse line of tergum IX. Sternum IX, in lateral view ( Fig. 14 View FIGURES 10–19 ), about 2x longer than tall, truncate at apex, anterior apodeme filiform, straight, tapering to slender flange; in ventral view ( Fig. 13 View FIGURES 10–19 ), almost round, posterior margin with shallow incision. Paraproct, in lateral view ( Fig. 14 View FIGURES 10–19 ), oblong, produced in narrow apicoventral lobe; in dorsal view ( Fig. 12 View FIGURES 10–19 ), wider basally, tapering apically, apex cleft about 1/2 its length, membranous, bearing sensilla. Preanal appendage about 2.5x as long as tergum IX, setose; in lateral view ( Fig. 14 View FIGURES 10–19 ), slightly curved caudad at basal third, width almost subequal throughout length, apex slightly crenulate; in dorsal view ( Fig. 12 View FIGURES 10–19 ), clavate, slightly produced basomesally, narrow just beyond base, enlarged apically. Inferior appendage less than 2x as long as tergum IX, setose, coxopodite and harpago completely fused; basal region broad, apical region slender, digitate; in lateral view ( Figs 14, 17 View FIGURES 10–19 ), apical region about as long as basal region, basal region apicoventrally produced, truncate apically, forming right angle; in dorsal and ventral views ( Figs 12, 13 View FIGURES 10–19 ), inner face with numerous spines. Mesal sclerite spine-like with 3 points. Phallus tubular, long, slender, weakly sclerotized, phallobase wide; in lateral view ( Fig. 15 View FIGURES 10–19 ), apex straight; in dorsal view ( Fig. 16 View FIGURES 10–19 ), apex enlarged.
Etymology. Named in honor of Fritz Müller, German biologist who emigrated to Brazil, living and doing most of his studies in the state of Santa Catarina where the holotype was collected.
Material examined. Holotype. BRAZIL— Santa Catarina: ♂ ( UFBA) Florianópolis: Córrego Pantanal; 13.vii.2012; sweeping net; LC Pinho leg.
Paratypes. BRAZIL— Santa Catarina: 1♂ ( UFBA), same data as holotype. 4♂♂, 1♀ ( MZSP) Grão Pará: Parque Estadual da Serra Furada ; 30.ix.2016; T Duarte, V Gomes leg. São Paulo: 1♂ ( MZSP) Iporanga: P.E. Intervales; i.2015; light trap; PC Bispo et al. leg .
Distribution. Brazil (Santa Catarina and São Paulo states) ( Fig. 39 View FIGURE 39 ).
Remarks. Xiphocentron muelleri sp. nov. together with X. copacabana ( Fig. 18 View FIGURES 10–19 ), and X. maitea ( Fig. 19 View FIGURES 10–19 ) have the ventral margin of the basal region of the inferior appendage distinctly produced, a character typical of genus Cnodocentron . However, the setal brush on the ventral margin of the coxopodite that also is typical for the Neotropical Cnodocentron (Caenocentron) is not present on those three species of Xiphocentron . Xiphocentron muelleri sp. nov., X. copacabana , and X. maitea are distributed along the Atlantic coast of Brazil. The presented records of Xiphocentron mulleri sp. nov. in Santa Catarina state ( Brazil) together with X. caenina Schmid 1982 and X. cuyensis Flint 1983 in Tucumán province ( Argentina) are the southernmost records of the genus in the Americas. They are also the most austral occurrence of the family together with Abaria electa Marlier 1960 in South Africa ( de Moor 1993).
MZSP |
Sao Paulo, Museu de Zoologia da Universidade de Sao Paulo |
T |
Tavera, Department of Geology and Geophysics |
V |
Royal British Columbia Museum - Herbarium |
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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