Plecia sp.

Schelesky-Prado, Daniel de Castro & Falaschi, Rafaela Lopes, 2023, Notes on presumed Neotropical records and species of Hesperinus Walker, 1848 (Diptera: Bibionidae), EntomoBrasilis (e 1059) 16, pp. 1-6 : 2

publication ID

https://doi.org/10.12741/ebrasilis.v16.e1059

DOI

https://doi.org/10.5281/zenodo.15878913

persistent identifier

https://treatment.plazi.org/id/282C8782-FFCF-F066-FEF4-F8BC5FE5F872

treatment provided by

Felipe

scientific name

Plecia sp.
status

 

Plecia sp. ( Figures 1 View Figure 1 A-C, 2)

Material examined. 1 male [ BRASIL, São Paulo] Monte Alegre [do Sul], Fazenda Sta. [Santa] Maria , Alt. [Altitude] 1.100 mts. [1,100 m], 24-30.XI.1942, F. Lane col. ( MZUSP) ; 1 male, label 1: BRASIL - SÃO PAULO, Monte Alegre [do Sul], Faz. [Fazenda] N.S. [Nossa Senhora] [Da] Incarnação [Encarnação], 750 ms. [m] 14.27- X-1942, L. Trav. F. & Almeida; label 2: Hesperinus sp ., ♂, M. CARRERA DET. 1943 ( MZUSP) .

Comments. CARRERA (1944) reported three specimens of Hesperinus sp. from the municipality of Monte Alegre do Sul , state of São Paulo, Brazil. He mentioned one male and one female from Faz. [Fazenda] N. S. [Nossa Senhora] [Da] Encarnação (750 mts. [m]), 14/27-X-42, L. Trav. F. & Almeida col., and one male from Faz. [Fazenda] Sta. [Santa] Maria (1.100 mts. [1,100 m]), 24/ 30-XI-1942, F. Lane col. Only the two male specimens were located in the MZUSP collection.

The specimens are not Hesperinus . Firstly, the male eyes are holoptic ( Figure 1C View Figure 1 ), while they are dichoptic in Hesperinus (see HARDY 1981, p. 219, Figure 13.2). Secondly, the antennal flagellomeres are compact and compressed, except for the first flagellomere ( Figure 1A View Figure 1 ). This contrasts with the filiform flagellomeres of Hesperinus , in which each article is longer than wide, excluding the apical segment (see HARDY 1981, p. 219, Figure 13.2). Thirdly, the vein R 2+3 is relatively short (less than a third of the length of R 4+5) and slightly oblique with respect to R 4+5, and has a distinct basal bend ( Figure 1B View Figure 1 ), unlike the relatively medium length (almost half the length of R 4+5), more distinctly oblique with respect to R 4+5, and without a distinct basal bend as in Hesperinus (see HARDY 1981, p. 220, Figure 13.8). Additionally, the R 2+3 is not sinuous ( Figure 1B View Figure 1 ), unlike Hesperinus , which may present a slight (see HARDY 1981, p. 220, Figure 13.8) or prominent (see KURINA 2013, p. 3, Figure 2b View Figure 2 ) sinuosity. Lastly, the apex of R 4+5 is only slightly arched posteriorly ( Figure 1B View Figure 1 ), rather than being distinctly arched posteriorly as in Hesperinus (see HARDY 1981, p. 220, Figure 13.8) ( FITZGERALD 2004).

A synapomorphic character of Bibionidae , excluding Hesperinus , is the presence of holoptic eyes in males ( PINTO & AMORIM 2000; FITZGERALD 2004). However, in a few species such as Penthetria funebris Meigen, 1804 and P. conjungens , males are dichoptic ( HARDY 1967; FITZGERALD 2004). Hesperinus consistently exhibits dichoptic eyes, usually widely separated, as seen in H. brevifrons and H. nigratus , although it can be weakly dichoptic, as seen in H. macroculatus ( FITZGERALD 2004; SKARTVEIT 2009; PAPP 2010). Another synapomorphy of Bibionidae , excluding Hesperinus , is the presence of compressed antennal flagellomeres in males ( FITZGERALD 2004). The R 2+3 of Plecia is relatively short and can be oblique, curved, straight, or even with a distinct basal bend ( FITZGERALD 2004). In Hesperinus , R 2+3 is relatively medium in length (usually longer than Plecia and shorter than Penthetria ) and oblique ( FITZGERALD 2004). However, in fossils of Hesperinus the length of R 2+3 can be more variable than in extant species, i.e., shorter or longer with respect to R 4+5 ( SKARTVEIT 2009). The distinctly arched posterior apex of R 4+5 is a synapomorphy of Hesperinus ( FITZGERALD 2004) . Based on our observations, it is evident that the specimens do not belong to Hesperinus . They can also not be Bibioninae, as the vein R 2+3 is present and the fore tibia lacks a strong apical spine seen in Bibionini or the sets of spines seen in Dilophus Meigen, 1803 ( FITZGERALD 2004). The remaining options are Penthetria and Plecia . The specimens have a diagnostic feature of Plecia , which is a short R 2+3 and subparallel to R 4+5 (diagnosis for Penthetria ) ( FITZGERALD 2004). Hence, they do not belong to Penthetria , but to Plecia .

Since Carrera identified these specimens only to genus, we decided here to correct his genus misidentification and assign it to Plecia rather than Hesperinus . This material can be identified at the species level or even described as a new species in a further study, which is not the scope of the present study.

MZUSP

Museu de Zoologia da Universidade de Sao Paulo

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Diptera

Family

Bibionidae

Genus

Plecia

GBIF Dataset (for parent article) Darwin Core Archive (for parent article) View in SIBiLS Plain XML RDF