Agnosthaetus thayerae Clarke, 2011
publication ID |
https://doi.org/ 10.1649/0010-065X-65.mo4.1 |
publication LSID |
lsid:zoobank.org:pub:0818A3A2-AB42-43D8-8F76-4F65F367C584 |
persistent identifier |
https://treatment.plazi.org/id/038787B5-FFA4-537A-46D0-BA6A857FFC24 |
treatment provided by |
Carolina |
scientific name |
Agnosthaetus thayerae Clarke |
status |
sp. nov. |
(27) Agnosthaetus thayerae Clarke View in CoL , new species
( Figs. 165 View Figs , 167–168 View Figs , Map 6 View Map 6 )
Type Material. Holotype. ♂, with three labels:
“ Ahuriri V., 761 m., Otago | 23.i.1966, J.I. Townsend ,
in| forest, moss 66/44/ FMNH-INS 0000 048 449 / HOLOTYPE Agnosthaetus thayerae Clarke , ♂, design. D. Clarke 2011”, in NZAC. Paratypes. 22 specimens (15♂ 7♀). NEW ZEALAND: South Island: CO: Danseys Pass , 44°58.566′S, 170°29.28′E [coord.= Danseys Pass], 9.xi.1968, 68/165, moss, J.I. Townsend, 2♀, FMNH-INS 38428–429 (in NZAC) GoogleMaps ; Danseys Pass , rd. summit, 915 m, 44°57.107′S, 170°22.312′E, 11.i.2009, moss & tussock litter, J.T. Nunn, 1♂, 1♀ (in JTNC) GoogleMaps ; Danseys Pass , summit, 900 m, 44°57.161′S, 170°22.31′E, 6.ii.2005, J.T. Nunn, 1♂, FMNH-INS 19723 (in JTNC) GoogleMaps ; CO/DN: Mt. Bitterness , 1219 m, 44°45.36′S, 170°18.18′E, 12.i.1971, 71/16, litter, J.S. Dugdale, 1♂ (in NZAC) GoogleMaps ; DN: Otago, Mt. Watkins, Waikouaiti , 44°29.64′S, 168°21.54′E [coord.= Watkins Hill], 5.ix.1968, 68/106, litter, J.S. Dugdale, 1♂ (in NZAC) GoogleMaps ; Silverpeaks, The Tunnels , 2.vi.2001, in moss and litter near stream, J.T. Nunn, 1♂, FMNH-INS 19715 (in JTNC) ; MK: Ahuriri Valley, Omarama , 762 m, 44°29′6″S, 169°57′16″E [coord.= Omarama], 23.i.1966, 66/46, moss, J.I. Townsend, 1♀ 1♂, 1♀, FMNH-INS 48447–448 (in NZAC) GoogleMaps ; Ohau Range, Ohau Skifield , 1480 m, 44°13.417′S, 69°46.738′E, 10.iii.2007, in damp streamside moss and turf, J.T. Nunn, 5♂, FMNH-INS 19373 (in JTNC) GoogleMaps ; 14.ii.2007, tussock litter, J.T. Nunn, 1♂, 1♀, FMNH-INS 48252–253 (in JTNC) ; OL: Hawea, Kidds Bush , 44°26.64′S, 169°16.08′E, 28.i.1973, 73/29, litter, J.C. Watt, 1♂, FMNH-INS 48450 (in NZAC) GoogleMaps ; Lake Hawea, Hunter Valley Rd., Sawyer Burn , 400 m, ANMT 737, 44°26′S, 169°16′E, Nothofagus solandri forest, 13.i.1985, FMHD#85-470, litter, forest, Berl., A. Newton & M. Thayer, 2♂, FMNH-INS 38435–436 (in FMNH) GoogleMaps ; SC: Mount Studholme , 1065 m, 44°38.528′S, 170°54.611′E, 1.ii.2007, tussock litter, J.T. Nunn, 1♀ (in JTNC) GoogleMaps .
Diagnosis. In addition to the characters mentioned in the diagnosis of the thayerae speciesgroup, A. thayerae may be distinguished from A. newtoni by the combination of labrum without distinct medial ridge, medial oblique labral setae present ( Fig. 20 View Figs , mo), and median lobe with rounded apex, without apicolateral teeth ( Fig. 167 View Figs , cf. Fig. 169 View Figs ).
Description. Color: Reddish brown, with abdominal segments VI and VII sometimes darker. Head: Frontal ridge absent. Dorsum sparsely punctate; with punctures distributed over entire surface except for small medial impunctate region. Punctures deep, well-defined; diameter subequal to or slightly greater than diameter of eye facet; interpuncture distance mostly less than half puncture diameter. Dorsal microsculpture present on entire or most of surface; distinctly reticulate, fainter posteriorly. Dorsal tentorial sulcus (cf. Figs. 10–11 View Figs , dt) distinctly slit-like; width subequal to or less than puncture diameter. Sublongitudinal ridge (cf. Fig. 10 View Figs , sr) distinct; confused by punctures; crest at antennal tubercle with distinct microsculpture. Area above and behind antenno-ocular carina ( Figs. 10–11 View Figs , arrow) with single subsidiary carina formed by confluent punctures. Antenno-ocular carina joining eye at about middle. Temple ( Fig. 11 View Figs , tm) short, less than 50% EYL. Subocular surface more or less evenly microsculptured (cf. Fig. 65 View Figs ). Labrum with medial blunt carina; distinctly sexually dimorphic ( Fig. 165 View Figs ). Apical labral margin in males broadly convex, smooth mesially, dentate only laterally, with 6–11 teeth (n =7), all teeth normal, projecting more or less anteriorly. Apical labral margin in females broadly convex, not emarginate medially; with 19–23 teeth (n =2), all teeth subequal in length. Medial oblique labral setae (cf. Fig. 20 View Figs ) present. Adoral labral surface in males with subapical transverse ridge ( Fig. 165 View Figs , arrow). Mandible sexually dimorphic; males with 2 mesal teeth, 1 directed dorsally and 1 mesially (cf. Fig. 189 View Figs , arrow), without preapical spur (cf. Fig. 189 View Figs ); females with single, mesially projecting tooth, without spur. Labium angulate anterolaterally. Prothorax: Pronotum with distinctly reticulate microsculpture. Medial pronotal sulci anteriorly separate from and terminating posterior to anterior punctures. Distance between medial sulci subequal along entire length, or slightly greater posteriorly. Pronotal basolateral carina present, distinct (cf. Fig. 73 View Figs , bp). Pronotal macrosetal punctures distinct (cf. Fig. 73 View Figs ). Medial pronotal seta subequidistant from medial and lateral sulci (cf. Fig. 73 View Figs , mu). Pronotal hypomeron ( Fig. 24 View Figs , hy) with distinct reticulate microsculpture. Prosternum with faintly reticulate microsculpture. Pterothorax: Elytron ( Fig. 23 View Figs , e) with distinct microsculpture; with 2 macrosetae, set in distinct punctures; laterally with two ridges (cf. Fig. 88 View Figs , ek, mr). Mesothoracic epimeral region ( Fig. 24 View Figs , mer) with distinct microsculpture. Metathoracic pleural region ( Fig. 24 View Figs , m) with distinct reticulate microsculpture. Metathoracic pleural ridge present (cf. Fig.88 View Figs , mp), fully developed; metathoracic pleural groove ( Fig. 24 View Figs , gr) incomplete posteriorly, forming elongate oval punctiform impression. Abdomen: Abdominal vestiture short, somewhat appressed, dorsally more or less evenly projecting posteriorly but with middle setae directed posteromedially. Abdominal sternite IV of male with surface glabrous and slightly impressed apicomedially; V with surface glabrous and impressed apicomedially, flanked by coarse acuminate setae; VI with surface subglabrous apicomedially. Aedeagus ( Fig. 167 View Figs ): “ Type B” (see description on p. 8). Apical part of median lobe gradually curving to small medial tooth at apex.Apicolateral setae small; apicomedial setae up to 5X longer than apicolateral setae ( Fig. 168 View Figs ). Paramere extending to about level of median lobe apex; in lateral view produced apically into lobe; with apical part perpendicular to median lobe; in dorsal view with outer side gently convex; with 4 small setae arranged in a line subapically.
Etymology. The name thayerae is a noun in the genitive case, honoring Margaret Thayer in recognition of her contributions to rove beetle systematics and evolution, particularly in the omaliine group of subfamilies, and also for her personal contributions to the intellectual development of the author.
Distribution. ( Map 6 View Map 6 ). South Island: CO; MK; OL; SC.
Biology and Ecology. Habitat: Nothofagus forest. Specimens have been taken from moss and a variety of leaf litter. Phenology: September–March. Elevation: 400–1,480 m.
Remarks. Though available specimens are all more or less uniformly light brown, not as large as A. newtoni , and with much shorter, non-swirled, and more appressed abdominal vestiture, these characters are not generally reliable as they overlap with that species or can be difficult to interpret without A. newtoni specimens on hand. Additionally, the medial pronotal sulcus is much straighter than in A. newtoni (and the inter-sulcus distance subequal along entire length of sulci). In the absence of the observable labral characters, this species can be distinguished from A. newtoni by the remarkable and many aedeagal differences (cf. Figs. 167–170 View Figs View Figs ).
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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