Homocopris williami Darling & Genier 2024, sp. nov.
Bibliographic record
Abstract
Homocopris williami Darling & Génier sp. nov. urn:lsid:zoobank.org:act: 94FAF15A-7945-460D-BF15-69FB3D05CBD0 Figs 11–12, 23–24, 30, 36, 55, 66 Pinotus torulosus – Lange 1947: 313 (distribution). Differential diagnosis Dorsal ocular width subequal to one-sixth interocular distance; anteromedial pronotal edge curvature tends to be continuous; posterior pronotal surface uniformly punctate; elytral interstriae punctation tends to be visible at 10 × magnification; metasternal depression divided anteriorly. ♂ pronotal ridge with two sets of distinct bilaterally paired tubercles in large individuals; paramere apex evenly rounded; FLP endophallite elongate, with two indentations along right edge. Etymology Williami is the Latin singular genitive form of William. This species is named in honour of the second author’s brother, William Darling. Name-bearing type data Holotype ♂ (MZSP) (Fig. 55): “ BRASIL: SÃO PAULO | 50km SE Mogi das Cruzes | Serra do Mar, Est. Biol. | Boracéia, 800-900m, 28-30. | IV.1997, F. Génier & S. Ide | ex. carrion trap, cloud forest”; “ WORLD | SCARAB. | DATABASE | WSD00035694” [barcode label]; “ HOLOTYPE ♂ | Homocopris | williami | Des. Darling & Génier, 2018” [on red card with black border]. Type locality Estação Biológica de Boracéia, 23°38′55″ S, 45°52′20″ W, 800–900 m, Salesópolis, Serra do Mar Mountains, São Paulo, Brazil. Type material Holotype BRASIL • ♂ (Fig. 55); São Paulo, Salesópolis, Estação Biológica de Boracéia, 50 km SE of Mogi das Cruzes, Serra do Mar; [23°38′55″ S, 45°52′20″ W]; 800–900 m; 28–30 Apr. 1997; F. Génier and S. Ide; cloud forest, dung trap; MZSP. Allotype BRASIL • ♀; same collection data as for holotype; MZSP. Other material examined (55 ♂♂, 32 ♀♀) Paratypes BRAZIL – Rio de Janeiro • 5 ♂♂; Nova Friburgo, Upper Macaé River (“ Haut Rio Macaé ”); [22°23′ S, 42°28′ W]; Apr. 1884; P. Germain; MNHN • 1 ♂; unspecified locality]: [no date]; [anonymous]; MNHN. – Rio Grande do Sul • 2 ♀♀; Nova Prata; [28°47′ S, 51°36′ W]; 30 Sep. 2001; C. Arioli; CEMT • 1 ♂, 4 ♀♀; São Francisco de Paula; [29°26′49″ S, 50°34′45″ W]; 14 Jan. 2008; L. Audino; human dung; CEMT. – Santa Catarina • 1 ♂, 2 ♀♀; Bom Jardim da Serra; [28°20′30″ S, 49°37′30″ W]; Dec. 2001; C. Arioli; CEMT • 3 ♂♂; same locality as for preceding; Jan. 2002; C. Arioli; CEMT • 1 ♂, 1 ♀; same locality as for preceding; 28 Dec. 2001; C. Arioli; CEMT • 4 ♀♀; same locality as for preceding; 3 Jan. 2002; C. Arioli; CEMT • 1 ♂; Campos Novo; [27°23′ S, 51°12′ W]; Feb. 2011; R.C. Campos; pitfall trap; CEMT • 1 ♂; same locality as for preceding; Feb. 2013; R.C. Campos; pitfall trap; CEMT • 1 ♂, 1 ♀; Monte Castelo; [26°43′ S, 50°19′ W]; 881 m; 6 Aug. 2012; A.L. Brandl; mata nativa, pitfall trap; CEMT • 1 ♂; Seara, Nova Teutônia; [27°11′ S, 52°23′ W]; [no date]; F. Plaumann; CAS • 1 ♂; same locality as for preceding; Jun.; F. Plaumann; CAS • 2 ♂♂; same locality as for preceding; Sep.; F. Plaumann; CAS • 1 ♂; same locality as for preceding; Nov.; F. Plaumann; CAS • 1 ♂; same collection data for preceding; GHCM • 1 ♂; Urubici; [27°59′ S, 49°35′ W]; 25 Nov. 2012; J.A. Bogoni; pitfall trap; CEMT • 1 ♂, 1 ♀; Urubici; [28°8′21″ S, 49°37′51″ W]; 1300 m; 17 Dec. 2015; P.G. da Silva; pitfall trap: human feces; CEMT • 1 ♀; Urubici; [28°9′32″ S, 49°37′49″ W]; 1600 m; 20 Nov. 2015; P.G. da Silva; pitfall trap: human feces; CEMT • 1 ♂; same locality as for preceding; 17 Dec. 2015; P.G. da Silva; pitfall trap: human feces; CEMT • 2 ♂♂; same locality as for preceding; 23 Apr. 2016; P.G. da Silva; pitfall trap: human feces; CEMT. – São Paulo • 1 ♂, 1 ♀; same collection data as for holotype; CEMT • 8 ♂♂, 2 ♀♀; same locality as for holotype; 28–30 Apr. 1997, F. Génier and S. Ide; cloud forest, carrion trap; CMNC • 12 ♂♂, 8 ♀♀; same locality as for holotype; 28–30 Apr. 1997; F. Génier and S. Ide; cloud forest, dung trap; CMNC • 1 ♂; same locality as for holotype; 28–30 Apr. 1997; F. Génier and S. Ide; cloud forest, feces trap; CMNC • 1 ♀; Salesópolis, Estação Biológica de Boracéia; [23°38′55″ S, 45°52′20″ W]; 22 Sep. 1965; [anonymous]; CEMT • 1 ♂; same locality as for preceding; 6 Oct. 1965; [anonymous]; dung; CEMT • 1 ♀; same locality as for preceding; 21 Sep. 2012; A. Díaz; Atlantic Forest, human feces; CEMT • 1 ♂; Santo André, Estação Biológica do Alto da Serra; [23°47′ S, 46°18′ W]; Apr. 1926; [anonymous]; MZSP • 1 ♂; São Miguel Arcanjo, Parque Estadual Carlos Botelho; [24°3′59″ S, 47°59′39″ W]; 580 m; 13 May 2012; M. Boutefeu; Tapirus feces; CEMT • 1 ♂; same locality as for preceding; 15 May 2012; M. Boutefeu; Tapirus feces; CEMT • 1 ♂; São Miguel Arcanjo, Parque Estadual Carlos Botelho; [24°3′40″ S, 47°58′44″ W]; 806 m; 29 Jan. 2012; E. Bovy (1); human feces; CEMT • 3 ♀♀; São Miguel Arcanjo, Parque Estadual Carlos Botelho; [24°3′46″ S, 47°58′44″ W]; 823 m; 29 Jan. 2012; E. Bovy (2); human feces; CEMT • 2 ♂♂; [no date]; [anonymous]; MNHN. Description Male holotype (Figs 11, 23, 30, 36) MEASUREMENTS. Body length 15.1 mm. HEAD. Clypeus bidentate with broad, rounded teeth. Anteroventral clypeal tooth broad. Clypeal and genal surface rugose, clypeogenal suture demarcated by shallow notch. Posterior genal angle obtuse. Frontal surface reduced, smooth. Dorsal ocular width subequal to one-sixth interocular distance. Interocular surface medially smooth. Cephalic horn emerging centrally from clypeofrontal surface, tapering apically, gently curved, 4.7 mm in length. PROTHORAX. Anteromedial pronotal edge curvature continuous. Lateral pronotal edge angular on anterior fourth in dorsal view. Anterior inclined pronotal surface with fine, transverse rugosities. Pronotal ridge with two sets of distinct bilaterally paired tubercles. Posterior pronotal surface uniformly punctate. Prosternal apex acutely tipped. ELYTRA. Glossy overall. Striae 1–6 widest anteriorly; narrowing posteriorly. Third and fourth striae posteriorly joined. Eighth stria absent throughout. Ninth stria effaced along anterior quarter of elytral length. Interstriae convex, finely punctate. HINDWING. Membrane edge between AP and AA sinuous. AP vein entire, converging with J. VENTRITES. Meso-metasternal suture straight. Surface of median metasternal lobe with uneven texture and deep, anteriorly divided impression. Lateral metasternal lobe densely setose. Fifth abdominal ventrite with sparse medial punctation. Pygidium coarsely punctate. PROTHORACIC LEGS. Anterior and posterior surfaces of profemur with dense row of long dark setae. Ventral profemoral surface finely punctate, sparsely setose. Protibia with three distinct teeth. Protibial forespur apically tapered, curving inward. MESOTHORACIC LEGS. Posterior surface of mesotrochanter with tuft of long dark setae. Anterior and posterior surfaces of mesofemur with sparse row of long dark setae. Outer surface of mesotibia serrate. Width at mesotibial apex one-third mesotibial length. METATHORACIC LEGS. Posterior surface of metatrochanter with tuft of long dark setae. Anterior and posterior surfaces of metafemur with sparse row of long dark setae. Outer surface of metatibia serrate. Width at metatibial apex one-third metatibial length. MALE GENITALIA. Aedeagus length: 3.5 mm. Medially paired sclerites of genital segment elongate, subequal in length to lateral sclerites. Paramere (Fig. 30) laterally flattened, slightly tapering from base to apex with apex evenly rounded. FLP endophallite (Fig. 36) elongate with two indentations along right edge. Female allotype (Figs 12, 24) Similar to male with the following exceptions: Body length 14.3 mm. Clypeofrontal carina transverse, centrally raised. Interocular surface chagrined. Anterior pronotal ridge low, followed by shallow concavity. Variation Body length 13–19 mm. Small males with medially projecting clypeofrontal ridge instead of cephalic horn. Anteromedial pronotal edge evenly curved more often than indented. Pronotal ridge in small males low, medially notched. Elytral interstriae finely punctate (visible at 10 ×) more often than minutely punctate (invisible at 10 ×). Distribution (Fig. 66) Serra do Mar and Serra Geral Mountains in the Brazilian states of Rio de Janeiro, São Paulo, Santa Catarina, and Rio Grande do Sul, with recorded elevations from 800 to 1600 m. Natural history Specimens with data were collected in cloud and sub-montane Atlantic Forest. Some specimens came to carrion and dung traps, pitfall traps baited with human faeces and faeces of Tapirus Brisson, 1762 at elevations between 580 m and 1600 m. Identification key to species of Homocopris Burmeister, 1846 and Andinocopris gen. nov. 1 Dorsal ocular width greater than one quarter of interocular distance; lateral pronotal carina and pronotal edge joined anteriorly and posteriorly, forming a closed ellipse in lateral view (Figs 13– 16); meso-metasternal suture posteriorly arcuate between mesocoxae (Fig. 60). Metasternum broadly flat (Fig. 42), some individuals with a narrow and shallow longitudinal sulcus. ♂ pronotal armament forming an overhanging ridge or bifurcating projection in large individuals (Figs 13, 15). Colombia, Ecuador, Peru .............................................................................................. Andinocopris gen. nov. 2 – Dorsal ocular width approximately one sixth of interocular distance; lateral pronotal carina and pronotal edge only joined anteriorly, forming an open ellipse in lateral view (Figs 17–24); meso-metasternal suture approximately straight between median coxae (Fig. 61); metasternum with a large median depression (Figs 43–45). ♂ pronotal armament forming bilaterally paired tubercles along an inclined ridge in large individuals (Figs 5, 7, 9, 11). Chile, Argentina, Brazil .................... .......................................................................................................... Homocopris Burmeister, 1846 3 2. Elytral interstriae flat (Fig. 46). Fifth abdominal ventrite with dense setigerous punctation. Body length: 20–34 mm. Colombia, Ecuador (Carchi) ...................
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How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.001 |
| Meta-epidemiology (narrow) | 0.001 | 0.001 |
| Meta-epidemiology (broad) | 0.001 | 0.000 |
| Bibliometrics | 0.002 | 0.002 |
| Science and technology studies | 0.002 | 0.001 |
| Scholarly communication | 0.001 | 0.002 |
| Open science | 0.001 | 0.001 |
| Research integrity | 0.001 | 0.001 |
| Insufficient payload (model declined to judge) | 0.016 | 0.015 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".