Careocallus Cherman & Basílio & Clarkson & Agostinis & Smith & Vaz-De-Mello & Almeida 2024, gen. nov.
Bibliographic record
Abstract
Genus Careocallus Cherman, gen. nov. (Figs 8–11) ZooBank: urn:lsid:zoobank.org:act: 01587959-22AB-49A9- 835D-FF7DAD5DF8A2 Type species: Careocallus tehuelche. Diagnosis Careocallus is distinguished from all other Diplotaxini genera by the following combination of features: clypeus trapezoidal, coplanar with frons (2:0); anterior margin subemarginate (6:0) (Figs 8B, 10B); apex of mandible perpendicular to the axis, equal in length or slightly shorter than the labrum in frontal view (156:0) (Fig. 12A, D); antenna with 10 antennomeres (40:0); constriction between pro- and pterothorax (58:1); elytra coarsely punctate, punctures elongate (61:1); three elytral ridges; first gap of ridges on its distal half as wide as the innermost ridge (66:1); sutural ridge extending from the base of scutellum (65:0), not uniform in width along its length (64:1), and angulate on apex (157:1) (Fig. 14F); procoxa without scales on infracarinal surface (69:1); protarsomeres I– III combined as long as or longer than head (79:0); metatibia with apical spurs even in shape (97:0); protarsomere I as long as protarsomere II (80:0); in males all tarsi slender (Fig. 8C), protarsomeres I– III inconspicuously wider than the others (133:0); in females elytra strongly convex (Fig. 9B), hindwings brachypterous (Fig. 11C); subapical callus of elytron inconspicuous (Fig. 10F) or even absent in males (Fig. 8E), completely absent in females (Fig. 9C). Description Length: 6.5–14.7 mm; width: 3.5–7.2 mm. Body elongate in males, oval in females; body and elytra plum-coloured to brownish-red. Head: frons swollen; frons and clypeus coplanar; frontoclypeal division weak, outer margin of maxillae straight (14:0), galea with five teeth at the apex; distal palpomere oblong, apex more-or-less acuminate; sensorial surface forming a fovea deep or shallow, varying from not reaching the midline of the palpomere (Careocallus densicollis Cherman and Smith, sp. nov.) to extending past the midline or reaching the apex (C. tehuelche) (Fig. 8B); apex of mandible bifid, perpendicular to the mandible axis (Fig. 12D), and in frontal view equal in length or slightly shorter than the labrum (Fig. 12A); labium quadrate; ligula slightly concave anteriorly; length of ligula shorter than the excavation; labial palpomere I longer and narrower than palpomere II; labrum convex on upper margin and longer than clypeus in frontal view (Cherman et al. 2017, Fig. 13A); antenna with 10 antennomeres, club lighter in colour and slightly longer than the funicle. Prothorax: pronotum wider medially, forming a lateral convexity; pronotal posterior corners in obtuse angle or subangulate, sometimes weakly carinate (Fig. 8B); hypomeron setose, long bristles throughout and few scales on inner margin. Pterothorax: scutellum ogival variable in width; punctate; metaventrite sparsely bristled. Elytra: glabrous, shiny, coarsely punctate; sutural ridge weak around the scutellum and more marked towards its apex, wider along the medial portion; elevated or not, in general unicolorous with the elytron; three elytral ridges more-or-less noticeable, separated by gaps, the first gap equal to or narrower than the second gap; the first gap distally as wide as the innermost ridge, subapical callus of elytron inconspicuous in males, completely absent in females. Legs: procoxae conical, with scattered bristles; protibial surface with two medial longitudinal carinae (Figs 9A, 10B); protibial inner margin concave and the outer one with three teeth, the apical tooth slightly oblique to the tibial axis (see Cherman et al. 2016: fig. 3E), the basal tooth is always the smallest; the two other protibial teeth equal in size, the three teeth equally spaced; basal articular lobe of metacoxae produced beyond the outer margin of trochanter; mesotibiae cylindrical or subquadrate, with two transverse carinae bearing long setae, mesotibial setae longer than the spines of the apical crown (Cherman et al. 2017: figs 42–45), the apical carina on mesotibia complete, sometimes very strong forming a ring; pair of apical spurs on apex of mesotibia and metatibia; even or slightly uneven in length, the gap between spurs is equal to the base of one spur; protarsi long, slender; protarsomere I as long as protarsomere II or slightly shorter; all claws bifid and symmetrical, protarsal claws slightly longer than the others, up to one-half the length of the protarsomere V, inferior tooth reduced, raising from the midline of the superior tooth (Fig. 9D, E) or next to its base (Fig. 10E). Abdomen: propygidium slightly visible (Fig. 10F) or hidden by the elytra (especially in females) (Fig. 9C); sparsely bristled; pygidium flat, disc with bristles throughout or only at apex; varying from coarsely to weakly punctate; subquadrate or subtrapezoidal, pygidium twice the length of ventrite V; maximum width does not exceed the distance between the propygidial spiracles; apex of pygidium varies from quadrate, subquadrate to rounded. Dimorphism Female: Length: 9.1–12.3 mm; width: 4.7–7.1 mm. Size and body shape: strongly oval, shorter than males. Pterothorax: distance between mesocoxae and metacoxae very short, equal in length to metacoxae or shorter. Elytra: strongly convex, punctures coarser, elytral ridges wider, subapical callus absent (Fig. 9C), hindwings brachypterous (Fig. 11C). Legs: protibia shorter and wider, teeth of outer margin wider; mesotibia sometimes noticeably enlarged towards apex; apical transverse carina on mesotibia and metatibia commonly complete and proeminent; metatibia wider and shorter; protarsomeres as wide as in the other legs. Abdomen: the pygidium may differ from the male in shape, being narrower and slightly longer. Male: Length: 6.5–14.7 mm; width: 3.5–7.2 mm. Head: club of antenna longer. Pterothorax: distance between mesocoxae and metacoxae longer than the metacoxae. Elytra: slightly convex or flattened dorsally, subapical callus unnoticeable, hindwings normal in size (Fig. 11A, B). Legs: inner margin of metatibia carinate from the medial portion towards apex, depending on the species uniformly straight (C. tehuelche) (Fig. 8D) or expanded from subapical portion (C. densicollis) (Fig. 10D); apex barely setose along the inner surface; two transverse carinae present posteriorly; the basal carina sometimes very weak, the apical carina incomplete or complete (that is crossing the disc of metatibia), pair of apical spurs even or uneven in length; protarsomeres I and II slightly wider than the others, in C. densicollis also the protarsomere III. Abdomen: more concave than in females. Parameres: basal region (BR) sulcate at its longitudinal midline (Figs 8F, 10G), lateral margin, on a plane below expanded (Fig. 10G) or not (Fig. 8F); parameral split on the basal third (Fig. 10G) or in the second third (Fig. 8F); inner margins of parameres straight or convergent at the apex; apex spatulate, with margins rounded or subangulate; in lateral view parameres straight, coplanar with BR or not, sloped from subapical region and flattened on apex (Figs 8G, 10H). Remarks on hindwings Radial sector of the hindwings is more sclerotized in C. densicollis (Fig. 11A), while it is reduced in females of C. tehuelche (Fig. 12A, B). The radial sector is the most important during the flight activity. Moreover, the fold mechanism that involve the RA1 + 2, the RP loop and the MP veins, which is also responsible for the flight (Kukalová-Peck and Lawrence 1993, 2004), is also reduced in hindwings of C. tehuelche females. This reduction possibly indicates that females of C. tehuelche do not fly. Etymology From Latin ‘ careo ’ (be deprived of); ‘ callus ’, (hard skin). The name refers to the absence of the subapical callus from the elytra. Masculine in gender. Composition: Careocallus tehuelche and Careocallus densicollis. Distribution and habitats Careocallus occurs in southern Argentina, from San Luis province (northernmost record 35°34ʹS 65°19ʹW) up to Chubut (42°46ʹS 64°59ʹW). Its distribution encompasses the southernmost part of Pampas and mainly the Patagonian region, from the eastern Andes with wet winters towards the Atlantic dry region. Careocallus and the other genera Among all genera of Neotropical Diplotaxini, Careocallus and Liogenys exclusively share the longitudinal inner margin of male metatibia produced [except the clade (L. tarsalis + L. forcipata)] (143:0),andcoveredwithsetaeoninnersurface(144:0)(variable among Liogenys species). Among the Neotropical Diplotaxini, Careocallus could be morphologically mistaken with Liogenys or Pachrodema. Compared to Liogenys, Careocallus is similar in size, colour, and number of antennomeres (10, as in most Liogenys). The anterior margin of clypeus is subemarginate in Careocallus, which is uncommon among Liogenys species, though present in L. niger, L. unicolor Evans, and L. rufocastanea Moser (Cherman et al., 2019). Careocallus differs from Liogenys mainly in the clypeus trapezoidal (Fig. 8B), without lateral impressions; frons and clypeus coplanar; ocular canthus narrow distally and gradually wider towards the proximal region, at the junction with clypeus (head in shape most similar to Pachrodema); apex of mandible perpendicular to the axis and almost as long as the labrum (156:0) (in Liogenys and Homalochilus the apex of mandible is in oblique plane to the axis) (Fig. 13E, F); anterior margin of labium with emargination wider than in Liogenys; labial palpomere I narrower and longer than palpomere II (in Liogenys palpomere I slightly wider and shorter than palpomere II); labrum longer than clypeus in frontal view (39:0) (Fig. 13A) (in Liogenys it is shorter; Fig. 13C); pronotum narrower posteriorly than in Liogenys; and mesotibial setae longer than the spines of the apical crown (as long as or shorter in Liogenys) (see Cherman et al. 2016:: fig. 3). In addition to most of the previous features, Careocallus resembles Pachrodema in the head in shape; frons swollen, not forming a concavity with clypeus;
Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.
How this classification was reachedexpand
Full frame distilled prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.
Codex and Gemma teacher scores by category
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.001 | 0.000 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.000 | 0.001 |
| Science and technology studies | 0.002 | 0.000 |
| Scholarly communication | 0.001 | 0.000 |
| Open science | 0.001 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.100 | 0.062 |
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; both teacher heads agree on what is shown here.
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".