Creophilus albertisi, (FAUVEL)
publication ID |
https://doi.org/ 10.1111/j.1096-3642.2011.00725.x |
publication LSID |
lsid:zoobank.org:pub:FBFE9195-BE04-4AFE-9417-6E38BCE6AB84 |
persistent identifier |
https://treatment.plazi.org/id/039B414F-193C-FFB9-FF16-FD9B4990FEB2 |
treatment provided by |
Valdenar |
scientific name |
Creophilus albertisi |
status |
|
9. CREOPHILUS ALBERTISI (FAUVEL) View in CoL
( FIGS 1E, 4K View Figure 4 , 7E View Figure 7 , 28 View Figure 28 , 31 View Figure 31 )
Emus Albertisi Fauvel, 1879: 95 View in CoL , 94 (in key). Type locality: ‘Nouvelle-Guinée, Fly River’; Macleay, 1886: 142.
Creophilus Albertisi View in CoL ; Bernhauer & Schubert, 1914: 398; Scheerpeltz, 1971: 202.
Creophilus albertisi View in CoL ; Gressitt & Hornabrook, 1977: 26, pl. 5h; Herman, 2001b: 3315.
Type material: Emus Albertisi. Lectotype (here designated). ♂, ‘Nuova Guinea | Fly River| L.M.D’Albertis 1876–77/ Co Typus/ Museo Civico| di Genova/ FMNH-INS 0000 016 766/ [red] LECTO- TYPE | Emus | albertisi Fauvel, 1879 | designated by| D.J. Clarke 2008’ (in MCSN). Paralectotypes (15). All with same collecting data as lectotype and with label ‘[yellow] PARALECTOTYPE | Emus | albertisi Fauvel, 1879 | designated by| D.J. Clarke 2008’. Five specimens with label ‘Museo Civico| di Genova’: 2♂, ‘Co Typus/ FMNH-INS 0000 016 767’; ‘Co Typus/ FMNH-INS 0000 016 768’; 3♀, ‘Co Typus/ FMNH-INS 0000 016 769’; ‘Co Typus/ FMNH-INS 0000 016 770’; ‘Typus/ Albertisi| Fauvel./ C. Albertisi | FvL./ FMNH-INS 0000 016 765’ (in MCSN); five specimens with label ‘Ex-Typis’: 3♂, ‘albertisi| FvL./ R.I.Sc.N.B. 17.479| Coll. et det. A. Fauvel/ FMNH- INS 0000 016 760’; ‘Coll. et det. A. Fauvel| Creophilus | albertisi| Fauv.| R.I.Sc.N.B. 17.479/ FMNH-INS 0000 016 761’; ‘Coll. et det. A. Fauvel| Creophilus | Albertisi| Fauv./ R.I.Sc.N.B. 17.479/ FMNH-INS 0000 016 763’; 2♀, ‘Coll. et det. A. Fauvel| Creophilus | albertisi| Fauv.| R.I.Sc.N.B. 17.479/ FMNH-INS 0000 016 762’; ‘Coll. et det. A. Fauvel| Creophilus | Albertisi| Fauv./ R.I.Sc.N.B. 17.479/ FMNH-INS 0000 016 764’ (in IRSNB); ♀, ‘ Emus | albertisi| Fauvel/ coll. L.W.| Schaufauss/[red] SYNTYPUS | Emus | albertisi Fauvel, 1879 | labeled by MNHUB 2004/ FMNH-INS 0000 016 759’ (in ZMHB); 3 specimens on card: 2♂, FMNH-INS 0000 019 622; FMNH- INS 0000 019 623; 1♀, ‘[ Creophilus | albertisi| Fauvel/ FMNH-INS 0000 019 622’ (in MNHN); 1♂,
aedeagus on card, ‘ ♂ / Albertisi| Fauv./[blue] ex coll.| Klima/[blue] ex coll.| Scheerpeltz/ Albertisi| Fauv./ FMNH-INS 0000 012 299’ (in NMW). Fauvel’s description was based on numerous specimens collected by D’Albertis: ‘Nouvelle-Guinée, Fly River ; en nombre (L.M. D’Albertis).’ These were deposited in ‘ Collection de Musee Civique de Genes et la mienne’ ( MCSN and Fauvel’s collection) .
Other material examined: 59 specimens. See supporting information, Appendix S1.
Diagnosis: With characters of the erythrocephalus - group; head orange-red with subtriangular black spot on frons ( Fig. 7E View Figure 7 ), with distinct denticle at hind angles ( Fig. 31A, B View Figure 31 , vl); antennomeres 7–11 variably orange-brown to white; right mandible with two distinct teeth ( Fig. 31C View Figure 31 ); elytra metallic blue-green or violet; abdominal segments VIII –X orange; tergal chaetotaxic formula = 4-6-6-2-4-4.
Description: Measurements (N = 10♂, 10♀). Forebody length: ♂ 6.3–9.7 mm, ♀ 6.8–8.4 mm. See supporting Table S5 for comparison of ranges of male and female ratios. Head ( Fig. 27A, B View Figure 27 ) orange-red, narrowly black around mouthparts and antennal fossae, frons with subtriangular black spot usually extending to frontoclypeal margin, and concealing dorsal tentorial pits on vertex or not; very slightly trapezoidal to subquadrate in large males, suborbicular in females and smaller males; HW/HL = 1.14–1.55; hind angles sharply delimited ( Fig. 31A View Figure 31 ); surface dull, with distinctive micropunctate microsculpture and very shallow indistinct and moderately dense impressions (as in Fig. 9A, B); ventrolateral carina present in both sexes ( Fig. 31B View Figure 31 , vl), also visible dorsally ( Fig. 31A View Figure 31 ), developed into distinct anteriorly projecting denticle; postgenal ridge obsolete medially ( Fig. 31B View Figure 31 , pgr); eyes large, protruding ( EYL /HL = 0.47–0.68), lateral to dorsolateral in large males; lateral margins of head usually obscured by eye in dorsal view; HL1/HL2 greater in females than males (♂ = 1.46–2.88, ♀ = 2.29–3.40); antennae as in Figure 31G View Figure 31 , antennomeres 1–6 black, 7–11 yellowish-white to mottled orange-brown ( Fig. 1E), 11 elongate, as long or longer than 9–10 together; mandibles as in Figure 31C View Figure 31 , moderately longer than head in large males, shorter than head in females ( ML /HL ♂ = 0.78–1.27, ♀ = 0.74– 0.92), right mandible with two teeth, T 1 absent, T 3 largest. Thorax and abdomen. Pronotum ( Fig. 31F View Figure 31 ) slightly transverse ( PW / PL = 1.03–1.26); PL 1.09– 1.29 ¥ ESL; with basolateral margins slightly emarginate; hind angles distinct; with sparse peripheral setae, longer sparse vestiture on lower anterolateral declivities, and long medially directed basal setae; small transverse basolateral impressions present, smooth and asetose, with transverse line of tiny punctules; elytra distinctly widened posteriorly, brightly coloured metallic blue-green or violet ( Fig. 1E), sparsely and finely setose, without sculpture; humeri sparsely punctate, narrowly glabrous laterally, not callused; disc shallowly impressed in middle; wings fully developed, clear yellowish-brown, without black spot in medial field between MP 3 and MP 4 veins; abdomen with segments III – VII shining black, VIII –X orange ( Fig. 1E); vestiture fine, moderately dense; microsculpture extremely fine, producing weak iridescent reflection, particularly on ventral side; tergite VII with well-developed palisade fringe. Male genitalia and secondary sexual characters. Sternite IV with densely setose posteromedial emargination of transverse fold (most obvious in larger specimens), and sternites V – VII with sparsely distributed micropores near middle of sternites. Aedeagus as in Figure 31E View Figure 31 ; median lobe distinctly yellowish, not produced apically, with minute projection dorsoapically ( Fig. 31E View Figure 31 , arrow), without lateral recurved teeth, with paired apicolateral sclerites (as) separated from sclerotized median lobe by membranous strip. Paramere nearly as wide as median lobe, with very long apicolateral setae ( Fig. 31J View Figure 31 ). Internal sac inverted as in Figure 31E View Figure 31 , everted as in Figure 31D View Figure 31 ; with ventromedian spiculose strip (vr) reduced, shorter than ventral sclerite (vs), flanked by very large paired basoventral spiculose regions ( Fig. 31D View Figure 31 , sr), with additional lateral spiculose regions ( Fig. 31D View Figure 31 , lr); ventral sclerite expanded distally ( Fig. 31H View Figure 31 ); copulatory piece (cp) completely surrounded by distinctly spiculose membranous sheath (sh). Female internal genitalia. Internal female genitalia as in Figure 31I View Figure 31 ; vaginal plate (vp) small, paired lateral sclerites fused posteriorly to form narrowly sclerotized ring; vaginal fold with medial sclerotized strip proximally ( Fig. 31I View Figure 31 , vf, arrow), and with diffuse patch of minute teeth distally. Chaetotaxy. Basiantennal, parasutural 1, and posterior epipleural macrosetae absent; elytral discal series with three macrosetae; metaventrital macroseta absent or undetected; tergal chaetotaxic formula = 4-6-6-2-4-4, inner lateral macrosetae absent on tergites VI – VIII, medial macrosetae absent on tergites III and VI.
Distribution ( Fig. 28 View Figure 28 , circles): Papua New Guinea, Indonesia: Irian Jaya. Scheerpeltz (1971) notes it is common throughout New Guinea and in (unspecified) neighbouring islands, but I have not seen any specimens from outside mainland New Guinea.
Biology and ecology: Rare in collections; most specimens without habitat or collection data. Fifteen collections are from light traps (mercury vapour, black light), two from carrion. Habitat: unknown, but probably intact forest. Altitude: 60–1700 m. Phenology: throughout the year. Gressitt & Hornabrook (1977: 26) gave the only known published biological observations, noting that C. albertisi ‘occasionally comes to light’ and ‘can discharge a peculiar pungent scent when frightened’. Other biology and life-history characteristics are unknown. Larvae and pupae are unknown.
Remarks: Last (1987) recorded Creophilus from New Guinea, but did not list the species, nor did he provide any records.
MCSN |
Museo Civico di Storia Naturale, Verona |
R |
Departamento de Geologia, Universidad de Chile |
IRSNB |
Institut Royal des Sciences Naturelles de Belgique |
MNHN |
Museum National d'Histoire Naturelle |
NMW |
Naturhistorisches Museum, Wien |
ML |
Musee de Lectoure |
T |
Tavera, Department of Geology and Geophysics |
PW |
Paleontological Collections |
PL |
Západoceské muzeum v Plzni |
MP |
Mohonk Preserve, Inc. |
V |
Royal British Columbia Museum - Herbarium |
VI |
Mykotektet, National Veterinary Institute |
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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Creophilus albertisi
Clarke, Dave J. 2011 |
Creophilus albertisi
Herman LH 2001: 3315 |
Gressitt JL & Hornabrook RW 1977: 26 |
Creophilus Albertisi
Scheerpeltz O 1971: 202 |
Bernhauer M & Schubert K 1914: 398 |
Emus Albertisi
MacLeay WJ 1886: 142 |
Fauvel A 1879: 95 |