Horaeomorphus Schaufuss

Jałoszyński, Paweł, 2014, ' The curse of Horaeomorphus ': taxonomy of misplaced Australian Cyrtoscydmini (Coleoptera: Staphylinidae: Scydmaeninae), Zootaxa 3828 (1), pp. 1-76: 7-8

publication ID

http://dx.doi.org/10.11646/zootaxa.3828.1.1

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lsid:zoobank.org:pub:B2FEAE60-7E51-45FA-A38F-930A084A5AAA

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scientific name

Horaeomorphus Schaufuss
status

 

Horaeomorphus Schaufuss 

Horaeomorphus Schaufuss, 1889: 21  . Type species: Horaeomorphus eumicroides Schaufuss, 1889  (orig. des.). Anthicimorphus Franz, 1975: 175  syn. n. (as subgenus of Euconnus  ; not as new). Type species: Phagonophana anthicoides Lea, 1915  (monotypy). Also spelled Anticimorphus ( Franz 1975: 303), selected as incorrect original spelling by Newton & Franz (1998). Franz (1975) referred to Madagascan Anthicimorphus  , evidently having in mind a paper that has appeared in print much later ( Franz 1986 b), but presumably was supposed to be published as first.

Anthicimorphus Franz, 1986 b: 234  (as a new subgenus of Euconnus  ). Type species: Euconnus anthiciformis Franz, 1986 b  (preoccupied, nec Franz, 1967) (des. orig.).

Revised diagnosis. Body ( Figs. 1 –5View FIGURES 1 – 5, 22–23, 26– 28View FIGURES 22 – 28) strongly elongate; head ( Figs. 1 –5View FIGURES 1 – 5, 22–23, 26– 28View FIGURES 22 – 28) distinctly flattened, with vertex not projecting dorsocaudad, its posterior margin arcuate and distinctly concave; supraantennal tubercles prominent and in most cases accompanied posteriorly by a pair of shallow but distinct pits; frontoclypeal suture or groove absent; eyes located anteriorly and therefore tempora long and strongly curved toward occipital constriction; tempora, genae and postgenae with sparse and short thick bristles mostly located lateroventrally; 'neck region' ( Fig. 6View FIGURES 6 – 9) distinctly demarcated from anterior part of head capsule by constriction and much narrower than vertex; hypostomal ridges ( Fig. 6View FIGURES 6 – 9; hr) extending from cardines to posterior tentorial pits ( Fig. 6View FIGURES 6 – 9; ptp), which are elongate and located on anterior margin of transverse groove demarcating 'neck' ventrally; submentum ( Fig. 6View FIGURES 6 – 9; smn) without lateral sutures; each mandible with two subapical teeth ( Fig. 8View FIGURES 6 – 9; sat) and densely setose submedian mesal prostheca ( Fig. 8View FIGURES 6 – 9; pst); maxillary palpomeres III and IV ( Fig. 9View FIGURES 6 – 9; mxp 3–4) slender, strongly elongate; antennae ( Figs. 1 –5View FIGURES 1 – 5, 22–23, 26– 28View FIGURES 22 – 28) gradually thickening distally; pronotum ( Figs. 1 –5View FIGURES 1 – 5, 22–23, 26– 28View FIGURES 22 – 28) with odd (three or five) number of antebasal pits ( Fig. 10View FIGURES 10 – 14; lp, mp) often connected by transverse groove ( Fig. 10View FIGURES 10 – 14; tg); prosternum laterally demarcated from hypomera by pronotosternal sutures ( Fig. 11View FIGURES 10 – 14; nss), with distinct prosternal process ( Fig. 11View FIGURES 10 – 14; psp) developed as low and narrow carina; procoxal sockets ( Fig. 11View FIGURES 10 – 14; pcs) broadly closed; prothoracic hypomera ( Fig. 11View FIGURES 10 – 14; hy) with large internal (adcoxal) parts demarcated laterally by complete hypomeral ridges ( Fig. 11View FIGURES 10 – 14; hyr); sides of pronotum ( Fig. 11View FIGURES 10 – 14) with short and sparse thick bristles mostly located lateroventrally; mesoventrite with strikingly long asetose and reticulated anterior ridge ( Fig. 15View FIGURES 15 – 17; ar) with posterior median projection; mesoventral process ( Fig. 15View FIGURES 15 – 17; msvp) narrow and weakly expanding ventrally but distinct and clearly separating mesocoxae; ventro- and dorsolateral foveae absent; anterior metaventral process absent; metaventral intercoxal process ( Figs. 18–19View FIGURES 18 – 21; mtvp) narrowly separating metacoxae, with two long spines and deep median notch; each elytron with two distinct and asetose basal foveae ( Fig. 17View FIGURES 15 – 17; bef) connected by inversely Ushaped groove located on basal articulating lobe of elytron; aedeagus ( Figs. 21View FIGURES 18 – 21, 29– 36View FIGURES 29 – 32View FIGURES 33 – 36) with free and slender parameres ( Fig. 21View FIGURES 18 – 21; pm); spermatheca sclerotized and globular.

Remarks. Although Horaeomorphus  is highly diverse and includes species small and large, flattened and strongly convex, with the pronotum strongly elongate or nearly circular, with or without antebasal transverse groove, yet with some experience it is easy to identify the genus even without examining the ventral characters. Independently of the variable body shape, the general shape of the head is nearly identical in all species of Horaeomorphus  : always flattened, with the vertex never projecting dorsocaudad and its posterior margin concave; the bristles on tempora, genae and postgenae are sparse and inconspicuous in dry-mounted specimens, visible only in transparent mounts under high magnifications of a compound microscope; the supraantenal tubercles always prominent and in nearly all species accompanied posteromesally by a pair of distinct pits (absent only in H. calcarifer (Franz)  and barely discernible in some specimens of H. sarawakensis Franz  (Jałoszyński 2012 a)). All Australian specimens seen by the author have these pits. Another unique character of Horaeomorphus  is the inversely U-shaped groove connecting a pair of basal foveae on each elytron; the groove extends from each fovea anteriorly onto the elytral articulating lobe overlapped by the pronotal base, but is usually partly visible in intact specimens. Many species of Horaeomorphus  show a distinct sexual dimorphism, frequently expressed in elongated metatrochanters of males, sometimes to such extent that the distal part of trochanter forms a long rod-like projection exceeding half length of femur (examples are shown in Figs. 2, 4– 5View FIGURES 1 – 5, and details in Fig. 20View FIGURES 18 – 21). In two species males differ from females in metafemora with a small ventral tooth. Australian species, at least those known from males, do not have any modifications of the legs.

A character previously unknown was discovered during the present study. Horaeomorphus sakishimanus  has the mesocoxae with dense and relatively long setae on the dorsal surface ( Figs. 12–13View FIGURES 10 – 14), and bunches of two-nine setae are inserted on small papillae ( Fig. 14View FIGURES 10 – 14). Examination of 15 species of Oriental Horaeomorphus  (cPJ) revealed that all of them have densely setose dorsal surface of mesocoxae. Among Australian Cyrtoscydmini  bunches of setae on the dorsal surface of mesocoxae were found only in Scydmaenozila  gen. n. ( Fig. 66View FIGURES 62 – 66), but in this genus there are two groups of setae, each seta inserted separately, the surface of coxa is not papillate, and there are numerous pores visible on the coxal cuticle.

Composition and distribution. Thirty-nine species (including those redescribed and described in the present paper) can be unambiguously placed in Horaeomorphus  . Thirty six are Asian (Oriental, Himalayan and Far Eastern), one Melanesian (from Fiji) and two Australian. Numerous additional undescribed species were seen by the author, mostly represented by unidentifiable females, from SE Asia (including the Indonesian New Guinea), and two more undescribed species (known from females) occur in Australia. Australian findings ( Fig. 193View FIGURES 193 – 198) are located near the eastern coastline and fill a distributional gap between SE Asia / New Guinea and eastern Melanesia.

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Coleoptera

Family

Staphylinidae

Loc

Horaeomorphus Schaufuss

Jałoszyński, Paweł 2014

2014
Loc

Horaeomorphus

Franz 1975: 175Franz 1975: 303Schaufuss 1889: 21

Loc

Anthicimorphus

Franz 1986: 234