Laccomimus alvarengi, Toledo, Mario & Michat, Mariano C., 2015

Toledo, Mario & Michat, Mariano C., 2015, Description of Laccomimus gen. n. and eleven new species from the Neotropical region (Coleoptera, Dytiscidae, Laccophilinae), Zootaxa 3990 (3), pp. 301-354 : 317-319

publication ID

https://doi.org/ 10.11646/zootaxa.3990.3.1

publication LSID

lsid:zoobank.org:pub:378C0359-E0E4-4CCC-821D-649144E37A63

DOI

https://doi.org/10.5281/zenodo.5692052

persistent identifier

https://treatment.plazi.org/id/03EE87FE-FFE3-FFE6-91A6-F8B2FDCAA469

treatment provided by

Plazi

scientific name

Laccomimus alvarengi
status

sp. nov.

Laccomimus alvarengi View in CoL sp. n.

( Figs 3 View FIGURES 1 – 7. 1 ; 5; 11; 14–15; 28; 39; 57; 64; 69; 77–81; 94–102; 111; 118; 125; 128)

Type locality. Brazil, Mato Grosso, Jacaré, Xingu National Park.

Type material. Holotype male ( USNM): dissected for genitalia probably by Young; genitalia and last two abdominal ventrites glued on separate label under the holotype “ Brazil, Matto [sic] Grosso, Jacaré, P.N. Xingu, XI.1961, Alvarenga & Werner leg” [printed], “FIC” [small, pink, printed label]”, “ Laccomimus alvarengi Young ” [white label, handwritten by Young], “ HOLOTYPE Laccomimus alvarengi Toledo & Michat” [red, rectangular, printed label].

Paratypes (200 exs all bearing red, printed label “ PARATYPE Laccomimus alvarengi Toledo & Michat”): Brazil: same data as holotype (10 exs USNM); same data as holotype except for “ XI.1965 ” (65 exs USNM –most of them without label); “Mato Grosso, Cuiabá, 30.III.1972, W.H. Withcomb” (8 exs USNM); idem but “ 9.IV.1972 ” (6 exs USNM); idem but “ 11.IV.1972 ” (3 exs USNM); idem but “ 21.IV.1972 ” (1 ex. USNM); idem but “ 22.IV.1972 ” (7 exs USNM –four of which without label); “Mato Grosso, Rio Bento Gomes (Pantanal), 1993– 1994, E. Stuhr leg.”, “Flussabschnitt bei [= section of river at] Periquito, 15°54' S, 56°33' W ” (1 ex. NMW); “Rondôna, 62 km SW Ariquemes, nr. fz. Rancho Grande, 8–20.IX.1994, JE Eger & C.W. O’Brien leg” (3 exs ZSM); “Minas Gerais, Prov. Cordisburgo, Faz. Pontinha, XII.1997, leg. F.Z. Vaz-de-Mello, coll. L. Hendrich” (16 exs ZSM); “Par. Curitiba, 28.VI.1969, leg. P.& P. Spangler” (1 ex. USNM). Argentina: “Prov. Corrientes, Mbrucuyá N.P., 15–17.I.2004, light trap, leg. M.C. Michat” (24 exs MCMC). Bolivia: “Beni, 40 km E San Borja, Estacion Biologica Beni, Estancia El Porvenir, 6–8.IX.1987, M. E. Steiner”, “At black light, open grass savanna and marsh” (7 exs USNM); “Guayaramerin, Beni, river bank, Soil Zoological Exp., Balogh, Mahunka, Zicsi”, “No. 428, beaten from vegetation, 2.XII.1966 ” (2 exs HNMB); “El Beni, Beni Station, NE of San Borja, 31. VII.1988 ”, “Robert W. Brooks ex., at lights, BIOLAT-SI/MAB” (2 exs VAIP); “El Beni, El Porvenir Station, NE of San Borja, 6–9.VIII.1988 ”, “Robert W. Brooks ex., at lights, BIOLAT-SI/MAB” (1 ex. VAIP); “Santa Crus, Sara, 2 km NW Santa Rosa, 21.II.1969, BLT A. Martinez & R.E. Woodruff” (5 exs USNM); idem “ 3 km S Santa Rosa, 22.II.1969 ” (7 exs USNM). Ecuador: “Esmeraldas, 9 km S San Lorenzo, 25.V.1979, ultraviolet light, Jos. J. Anderson”, “ Ecuador Peace Corps, Smithsonian Institution Aquatic Insects Survey” (3 exs USNM –one ex. without label); “Los Rios, Babahoyo, 21.VI.1975, Cohen, Langley & Monnig”, “ Ecuador Peace Corps, Smithsonian Institution Aquatic Insects Survey” (2 exs USNM). Panamá: “C. Z. [= Canal Zone], Albrook Forest site, 21–22.IX.1967, BLT RS Hutton” (1 ex. USNM). Perú: “Prov. Loreto, Rio Yarapa, Puerto Miguel”, “ 200 m, 16–23.XII.1994, T. Hàcz & G. Holzinger” (3 exs HNMB); “Loreto, Yacumama Lodge, 73.6°W, 4.8°S, nr. junction Rio Maranon - Rio Ucayali, 6–20.VIII.1994, Skelly leg., small light in wood, coll. L. Hendrich” (8 exs ZSM); “Colonia Calleria, Rio Calleria, 15 km E Ecayali, muddy river shore, 12–25.X.1961, B. Malkin” (2 exs USNM); “Madre de Dios, Rio Tambopata Res., 30 air km SW Pto. Maldonado, 290 m, 2–5.XI.1979, J. B. Heppner, subtropical moist forest” (3 exs USNM). Paraguay: “Jejuí-Mí, light trap, 18.XII.2003, leg. M.C. Michat” (2 exs MCMC); “Dep. Alto Paraguay, Campo Grande Farm, light trap, 7.XII.2002, leg. M.C. Michat” (2 exs MCMC); “Dep. Alto Paraguay, rd. to Fortín Patria, 3.XII.2002, light trap, leg. M.C. Michat” (4 exs MCMC); “Dep. Alto Paraguay, Defensores del Chaco N.P., Fortín Madrejón, 23.XI.2002, light trap, leg. M.C. Michat” (2 exs MCMC); “Dep. Cordillera, Arroyos y Esteros, 8.IX.1991, Ulf Drechsel leg., Coll. Hendrich” (1 ex. ZSM); “Dep. Central, Asuncion, Rio Paraguay, 2.XI.1990, Ulf Drechsel leg., Coll. Hendrich” (1 ex. ZSM). Suriname: “Paramaribo, Guest House of Museum, at light, 19–20. VII.1969, leg N. Nieser” (1 ex. NMW); idem except for “ 21–25.VIII.1969 ” (1 ex. NMW).

Diagnosis. Recognisable from most species of Laccomimus by aedeagal characters only, and from the very close L. pumilio (see above) by aedeagal characters and, frequently, by the more distinct pattern on elytra. Median lobe differentiated into basal and distal portion, divided by an angle or a curve ( Figs 94–102 View FIGURES 94 – 97 View FIGURES 98 – 102 ), with apex ending in small button-like expansion. The rounded tip of the prosternal process, which is very different from the acuminate tip of L. pumilio , is constant in this species. The average size is smaller with respect to L. pumilio .

Description. Habitus ( Fig. 64 View FIGURES 59 – 66 ). TL: 1.9–2.25 mm; MW: 0.95–1.2 mm (holotype: TL: 2.2 mm; MW: 1.1 mm); A-TL: 2.1 mm; A-MW: 1.1 mm (NUM: 47 exs); very similar to L. pumilio except for aedeagal characters, shape of prosternal process and, frequently, elytral colouration.

Colour. Variable. Pale patterns of elytra normally (but not always) more sharply defined on darker background and often more extended with respect to L. pumilio . Most commonly pale subbasal band of elytra fragmented in semicircular spots, although strong variability occurs (see below). Pronotum normally with narrower dark transversal band, more evidently bicolour; head, antennae, mouthparts, legs, and underside as in L. pumilio .

Structures and sculpture. Mostly as in L. pumilio , but prosternal process rounded at tip and elevated, not carinate ( Figs 28 View FIGURES 26 – 31 ; 69); iridescence on pronotum and mainly on elytra often more intense.

Male. Last abdominal ventrite as in L. pumilio . Outer claw of forelegs scimitar-shaped, variable in shape, often with denticles on ventral margin ( Figs 77–81 View FIGURES 67 – 83 ). Median lobe of aedeagus in dorsal view as in Fig. 111 View FIGURES 107 – 115 ; same as in L. pumilio (see description above). In left lateral view variable ( Figs 94 View FIGURES 94 – 97 a; 95a, 96a; 97a; 98a; 99a; 100a; 101a; 102a): in holotype ( Fig. 94 View FIGURES 94 – 97 a) base and distal portion forming a curve instead of an angle, distal portion less elongate with respect to L. pumilio and more uniformly wide along its length, although visibly sinuate on apical half. Left paramere ( Figs 94 View FIGURES 94 – 97 c; 95c; 96c; 97c; 98c; 101c; 102c) strongly sinuate apically, expanded and thickened.

Female. Often duller than males, with more intense iridescence. Genital pieces ( Fig. 118 View FIGURES 116 – 121 ) as in L. pumilio .

Distribution. Laccomimus alvarengi is one of the most widespread and variable member of Laccomimus : Argentina, Bolivia, Brazil, Ecuador, Panamá, Paraguay, Perú, Suriname ( Figs 125 View FIGURES 122 – 125 ; 128). It has not been recorded from Venezuela, however, in spite of VAIP’s intensive collections during the last decade.

Etymology. Frank N. Young and Paul J. Spangler named, in litteris, this taxon “ Laccomimus alvarengi n. sp. ”, in honour of the collector Moacir Alvarenga (cf. Young 1974: 2, 3). The specific epithet is a noun in the genitive case.

Notes on variability. L. alvarengi is more variable than L. pumilio . Except for the striking differences in the prosternal process, morphological separation of the two species is often difficult. The visibly sinuate and expanded apex of the left paramere and the less broadened distal portion of the median lobe seem to be constant diagnostic characters of L. alvarengi with respect to L. pumilio . In other features the median lobe is very variable, and this variability has been observed in different populations. Intermediate forms between the holotype of L. alvarengi and Florida specimens of L. pumilio have been observed frequently, even in exemplars from the same locality (see for example Fig. 97 View FIGURES 94 – 97 ). In most cases, however, the aedeagus is distinctive with respect to L. pumilio , particularly in the angulated separation between the base and distal portion and the somewhat widened distal portion. An aberrant median lobe was found dissected from a specimen collected at the type locality ( Fig. 95 View FIGURES 94 – 97 ). Colouration is also very variable. Normally the elytral patterns in L. alvarengi are more defined than in L. pumilio , and some populations exhibit very bright elytral patterns, including large and complete pale subbasal bands ( Fig. 64 View FIGURES 59 – 66 a, b).We have observed, however, specimens (especially from Brazil) with obscure or reduced pale markings, similar to L. pumilio . Uniformly dark-chestnut elytra occur in few specimens from Brazil and Paraguay. Since the shape of the prosternal process unambiguously separates L. alvarengi from L. pumilio , and a visibly sinuate and expanded apex of the left paramere and a less broadened distal portion of the median lobe are also apparently constant differences, we decided to describe L. alvarengi as a distinct species and not as a subspecies within L. pumilio .

Remarks. See under L. pumilio .

USNM

Smithsonian Institution, National Museum of Natural History

NMW

Naturhistorisches Museum, Wien

ZSM

Bavarian State Collection of Zoology

MCMC

Museo de Historia Natural de la Ciudad de Mexico

BLT

Belfast Natural History and Philosophical Society

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Coleoptera

Family

Dytiscidae

Genus

Laccomimus

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