Anaballetus, Newton & Švec & Fikáček, 2017
publication ID |
https://doi.org/ 10.1515/aemnp-2017-0061 |
DOI |
https://doi.org/10.5281/zenodo.6470533 |
persistent identifier |
https://treatment.plazi.org/id/03AADA7A-E607-7C2A-FE75-396BFBA1FA80 |
treatment provided by |
Marcus |
scientific name |
Anaballetus |
status |
gen. nov. |
Anaballetus View in CoL gen. nov.
Type species. Anaballetus chilensis View in CoL sp. nov.
Diagnosis. Anaballetus gen. nov. is defined by the following characters: (1) body moderately large (3.3–3.6 mm), highly convex, ovoid with elytra almost parallel-sided ( Figs 1A–B View Fig ); (2) head moderately broad with anterior margin of clypeus straight, margined by a distinct fine carina that extends laterally over the antennal insertions and inner margin of the eyes ( Fig. 1C View Fig ); (3) epistomal suture present internally, broadly curved, indistinctly indicated externally by fine groove; (4) labrum shallowly emarginate, the emargination deeper than one fifth of the labral width ( Fig. 1C View Fig ); (5) eyes bulging, almost hemisphaerical; (6) antennae 11-segmented with interrupted five-segmented club ( Figs 1H View Fig , 2B,D View Fig ), AVII, AIX and AX each with a shallow periarticular gutter, AIX and AX also with additional invaginations (shallow anteriorly but forming a deep two-chambered sensory vesicle posteriorly); (7) mandibles broad at base but without contiguous molae, with simple tips, left mandible with medial blade without tooth but with feeble emargination in the middle, right mandible with strong tooth proximally just beyond middle of blade ( Fig. 1E View Fig ); (8) galea narrow, its setose brush small and poorly developed, lacinia with apical tooth and long densely setose brush along mesal edge ( Fig. 1G View Fig ); (9) maxillary palpi 4-segmented, apical palpomere about twice as long as and slightly narrower than penultimate palpomere ( Figs 1G View Fig , 2C View Fig ); (10) labial palpi 3-segmented, short, apical palpomere approximately as long as thickened penultimate palpomere ( Fig. 2C View Fig ); (11) mentum trapezoidal, apex bordered and about half as wide as base ( Fig. 2C View Fig ); (12) gular sutures widely separated, only partially evident externally ( Fig. 2A View Fig ); (13) pronotal base not bordered ( Figs 1A–B View Fig ); (14) scutellum distinct, triangular ( Fig. 1A View Fig ); (15) pair of large abdominal-elytral binding patches consisting of rows of very fine teeth on either side of the mid-line of tergites VI and VII (next to last visible tergite) occupying more than half of tergite VII ( Figs 4A–E View Fig ), and on the corresponding area on the underside of elytra ( Figs 4F–H View Fig ); (16) anterior tibiae with long distinct tarsal groove dorsally ( Fig. 3B View Fig , trgr); (17) anterior coxae touching each other ( Fig. 3B View Fig ); (18) procoxal cavities nearly closed behind by notal process and proventrite that meet but are not fused to each other ( Fig. 3B View Fig ); (19) mesocoxae distant ( Figs 3A,C View Fig ); (20) mesoventrite nearly vertical between the mesocoxae and with low short longitudinal carina ( Figs 3C–D View Fig , msvc); (21) anterior process of metaventrite broadly rounded and bordered between mesocoxae ( Figs 3A, C View Fig ); (22) abdomen with five visible ventrites ( Fig. 3H View Fig ).
Etymology. The name of the genus is derived from Greek αναβάλλεται (= anaválletai) meaning postponed, because the genus had been discovered and mentioned many years ago by NEWTON (1985, 1998) and others; subsequently Z. Švec recognized the new taxon while examining a single female not suitable for description due to its sex (in litt. to Newton, 2002). Masculinum.
Discussion. The new genus can be easily differentiated from similar genera of Sogdini by the combination of the characters given in the key above. The abdominal-elytral binding patches are unique among described genera of Sogdini , but are similar to structures that occur in some members of the related family Agyrtidae ( NEWTON 1997: Figs 24–25). These patches should not be confused with the normal patches of much larger “wing folding setae” (actually unarticulated setiform projections: HAMMOND 1979) found on the dorsum of the abdomen in most flying beetles, which are present in Anaballetus gen. nov. at the sides of tergites V–VII ( Figs 4B–E View Fig ). This new genus and its single included species were previously referred to in publications as “Hydnobiini Genus D” in NEWTON (1985: 192) and NEWTON (1998: 83), “ Sogdini Undescribed Genus 3” in PECK et al. (2000: 45), and “ Sogdini Género 3 no descrito” in SOLERVICENS ALESSANDRINI (2014: 74), in all these cases identified by A. Newton. According to Mario Elgueta (in lit. to Newton, May 2016), this genus and species is also the “ Sogdini sp.” of GREZ et al. (2003: 16), and was also referred to by the manuscript name Hydnobius globulosus by GERMAIN (1911: 62) and JEANNEL (1957: 55). NEWTON (1985) noted that the genus was closely allied to three other genera of Sogdini , also undescribed, and referred to by him collectively as the “BCDE” group, with two genera in Australia (B, C) and one in New Zealand (E) in addition to the Chilean genus (D). He considered these genera to form a monophyletic group because they “have retained molar lobes on their mandibles (reduced in all other Hydnobiini [= Sogdini ]) and have unique elytral-abdominal interlocking patches”. Anaballetus gen. nov. is the first of these genera to be described, and does not strictly fit the above description because the mandibles do not have contiguous molar lobes like the other three genera, although the mandibular bases are broader than in other Sogdini . Clearly, further study and description of the other three new genera is needed to fully understand and document the origin and status of this group, but at present it can be said that the relationships of Anaballetus gen. nov. are to these other southern temperate genera from Australia and New Zealand, rather than to the two other Chilean genera or the numerous northern hemisphere genera of Sogdini .
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Sogdini |