Publique nesta revista
Informação da revista
Vol. 62. Núm. 2.Abril - Junho 2018
Páginas 83-168
Baixar PDF
Mais opções do artigo
Vol. 62. Núm. 2.Abril - Junho 2018
Páginas 83-168
Systematics, Morphology and Biogeography
DOI: 10.1016/j.rbe.2018.01.001
Lopesia indaiensis (Diptera, Cecidomyiidae), a new species of gall midge feeding on Andira fraxinifolia Benth (Fabaceae), an endemic plant in Brazil
Valéria Cid Maiaa,
Autor para correspondência

Corresponding author.
, Lázaro Araújo de Oliveirab
a Museu Nacional, Quinta da Boa Vista, Rio de Janeiro, RJ, Brazil
b Faculdade de Filosofia, Ciências e Letras do Alto São Francisco, Departamento de Ciências Biológicas, Luz, MG, Brazil
Este item recebeu
Informação do artigo
Texto Completo
Baixar PDF
Tabelas (1)
Table 1. Insect galls in Andira fraxinifolia Benth (Fabaceae): characterization, locality and reference.

Lopesia indaiensis (Diptera, Cecidomyiidae), a new species of gall midge found causing galls on Andira fraxinifolia (Fabaceae), an endemic plant species in Brazil, is described based on larva, pupa, male and female. L. indaiensis galls were collected in Dores do Indaiá, State of Minas Gerais, Southeastern Brazil. Larvae were removed from the galls and pupae and adults were obtained by rearing. The specimens were mounted on slides and the most important morphological characters were illustrated. The new species was compared to the other species of Lopesia.

Insect–plant interaction
Texto Completo

Andira fraxinifolia Benth (Fabaceae) is a heliophytic, evergreen, woody plant, which is endemic in Brazil (Lorenzi, 1992). It occurs in the Atlantic forest, Cerrado and Caatinga and has been found from Rio Grande do Sul to Piauí States. Due to its good propagation and fast germination, this species has great importance for recovering disturbed areas (Backes and Irgang, 2004).

Four gall morphotypes have been recorded on this plant species. One of them (Fig. 1) is a vermiform leaf fold found in several areas of Atlantic forest (Southeastern Brazil: Bertioga/State of São Paulo, Mangaratiba and Maricá/State of Rio de Janeiro; Northeastern Brazil: Tamandaré/State of Pernambuco), as well as in a Cerrado area (Southeastern Brazil: Dores do Indaiá, State of Minas Gerais) (Table 1). This gall is induced by a new species of Lopesia Rübsaamen, 1908 (Diptera, Cecidomyiidae).

Fig. 1.

Galls of Lopesia indaiensis, sp. n., on leaf of Andira fraxinifolia Benth (Fabaceae), general aspect.

Table 1.

Insect galls in Andira fraxinifolia Benth (Fabaceae): characterization, locality and reference.

Galled organ  Gall shape  Galling insect  Locality  Domain phytogeopraphic  Reference 
LeafVermiformCecidomyiidi  Bertioga/SP  Atlantic forest  Maia et al. (2008) 
Lopesia sp.  Mangaratiba/RJ  Atlantic forest  Rodrigues et al. (2014) 
Cecidomyiidae  Tamandaré/PE  Atlantic forest  Santos et al. (2012) 
Lopesia indaiensis, sp. n.  Dores do Indaiá/MG  Cerrado  Present work 
LeafGloboidAsphondyliina  Bertioga/SP  Atlantic forest  Maia et al. (2008) 
Asphondylia sp.  Mangaratiba/RJ  Atlantic forest  Rodrigues et al. (2014) 
Asphondyliina  Santa Teresa/ES  Atlantic forest  Maia et al. (2014) 
StemFusiformCurculionidae  Bertioga/SP  Atlantic forest  Maia et al. (2008) 
Not determined  Tamandaré/PE  Atlantic forest  Santos et al. (2012) 
Curculionidae  Santa Teresa/ES  Atlantic forest  Maia et al. (2014) 
LeafLenticularMeunieriella sp.  Maricá  Atlantic forest  Maia et al. (2002) 
Meunieriella sp.  Araruama and Arraial do Cabo/RJ  Atlantic forest  Carvalho-Fernandes et al. (2016) 

Similar galls have been recorded on Andira sp. in Bahia (Northeastern) (Tavares, 1920) and Andira humilis Mart. ex Benth. in Mato Grosso (Midwestern), São Paulo and Bahia (Garcia et al., 2017). The former is induced by Andirodiplosis bahiensisTavares, 1920 (Cecidomyiidae) and the latter by Lopesia andirae Garcia, Lima, Calado and Urso-Guimarães, 2017.

In this study, we describe a new species of Lopesia that induces vermiform galls on leaves of A. fraxinifolia based on material from Minas Gerais. This genus is known from 25 described species, 20 of them from the Neotropics. The other species are Afrotropical (three spp.), Nearctic (one sp.) and Australasian (one sp.) (Gagné and Jaschhof, 2017; Maia and Monteiro, 2017).

Material and methods

Branches of A. fraxinifolia with leaf galls were collected at Porcos Farm (19°30′18.99″ S–45°41′00.88″ W), municipality of Dores do Indaiá, State of Minas Gerais (Southeastern Brazil), in April of 2009. Galls were found on an individual plant situated in the border of a Cerrado fragment. Most leaves were galled and leaflets hosted one to several galls. The presence of more than three galls on the same leaflet caused its distortion.

Galled branches were removed from the host plant and transported in plastic bags to the laboratory of the Departamento de Ciências Biológicas/Faculdade de Filosofia, Ciências e Letras do Alto São Francisco, where some galls were dissected under a stereoscopic microscope to obtain larvae and pupae. Other galled branches were wrapped in wet cotton at the basis and kept in plastic pots covered by a fine screening until adults’ emergence, when these pots were put in a refrigerator to cause insects’ lethargy. Then, midges were collected using a 70% ethanol soaked paintbrush.

All specimens were first preserved in 70% ethanol, then mounted on microscope slides, following the methods outlined by Gagné (1994) and deposited in the Entomological Collection of the Museu Nacional/Universidade Federal do Rio de Janeiro (MNRJ).

Samples of the host plant were pressed, dried, identified by Dr. Fernando Augusto de Oliveira e Silveira (Universidade Federal de Minas Gerais) and kept in his laboratory as a voucher material.


Lopesia indaiensis, sp. n. (Figs. 2–13)

Figs. 2–3.

Lopesia indaiensis, sp. n. 2. Larva, sternal spatula with adjacent papillae (ventral view). 3. Larva, terminal segments (dorsal view).

Figs. 4–5.

Lopesia indaiensis, sp. n. 4. Pupa, face (ventral view). 5. Pupa, anterior part (dorsal view). Scale bars in mm.

Figs. 6–10.

Lopesia indaiensis, sp. n. 6. Male head (frontal view). 7. Male flagellomere 5. 8. Male hindleg, tarsal claw and empodium. 9. Male abdominal segments 7–8 (lateral view). 10. Male terminalia (dorsal view). Scale bars in mm.

Figs. 11–13.

Lopesia indaiensis, sp. n. 11. Female flagellomere 5. 12. Female abdominal segments 7–8 (lateral view). 13. Ovipositor (ventral view). Scale bars in mm.

The new species was placed in Lopesia due to four-segmented palpi, R5 curved at its juncture with Rs, Rs situated near the midlength of R1, short female postabdomen and its cerci with many short, sensory setae, and larva with corniform terminal papillae, each on a terminal projection.

Diagnosis. Adults with 1st–11th antennal flagellomeres neck partially setulose in both sexes, 12th flagellomere with apical process entirely setulose in both sexes, four-segmented palpi, male circumfila with all loops similar in length, tarsal claw with two teeth, 8th male tergite narrow, elongated, with only basal pair of trichoid sensilla; pupa with antennal basis modified into anteriorly pointed projection, with inner margin slightly serrated, apical plate deeply bilobed, prothoracic spiracle long and abdominal dorsal spines absent; larva with spatula two-toothed and four pairs of corniform terminal papillae.

Larva. Fusiform and cylindrical body; 1.90–2.60mm long (n=05). Integument rough. Spatula (Fig. 2): 0.17–0.26mm long (n=05), two-toothed, apical teeth triangular, stalk long. Two groups of three lateral papillae on each side of spatula (two pairs setose and a single setose papilla in each group) (Fig. 2). Terminal segment (Fig. 3): four pairs of corniform papillae similar in length.

Pupa. Body length: 3.10–4.40mm (n=17). Head (Fig. 4): apical setae 0.07–0.13mm long (n=11); vertical plate deeply bilobed at upper margin, antennal projections slightly serrated, 0.10–0.17mm long (n=17) (from apex to the upper antennal margin); two pairs of lower facial papillae (one asetose and the other setose), three pairs of lateral facial papillae, one pair setose and two without seta. Prothoracic spiracle (Fig. 4) elongate 0.25–0.35mm long (n=17), sclerotized. Prothoracic integument partially rough (Fig. 5). Abdominal segments 2–8 without dorsal spines.

Male. Body length 2.70–3.80mm long (n=12) (including terminalia). Head (Fig. 6): apical process absent. Eye facets circular, all closely approximated. Antenna (n=05): scape obconical, pedicel globose, flagellomeres binodal and tricircumfilar; nodes and internodes setulose, necks partially setulose; three circumfila of each flagellomere with loops regular in length (Fig. 7); 1st and 2nd flagellomeres connate, 12th flagellomere 0.20mm long (n=5), with apical process entirely setulose. Frontoclypeus with 10–12 setae (n=10). Labrum triangular, long-attenuate, with 3 pairs of ventral sensory setae. Hypopharynx with anteriorly directed lateral setulae. Labella elongate-convex, each with long lateral setae and three pairs of short mesal sensory setae. Palpus (n=07) with four segments, all cylindrical with setae, 1st segment shorter than the others, 0.03–0.04mm long, 2nd segment 0.08–0.09mm long, 3rd segment 0.08mm long, and 4th segment 0.08mm long.

Thorax. Wings: length: 2.40–2.70mm (n=12). Venation: R5 and Rs as in the genus diagnosis, CuA forked, M3+4 present. Scutum with 4 longitudinal rows of setae with a few scales intermixed, the 2 dorsocentral rows broadest anteriorly, forming a single row posteriorly, and the 2 lateral as a single row. Scutellum with several setae. Anepisternum bare. Anepimeron with setae. Tarsal claws bent near base and two-toothed, tooth basal shorter than the distal; empodium short, not reaching bent in claws (Fig. 8).

Abdomen (Fig. 9): 1st–6th tergites sclerotized, rectangular, with a single distal row of setae, few setae mesally and laterally, basal pair of trichoid sensilla, and scattered scales; 7th tergite sclerotized, rectangular, with a double distal row of setae, few setae mesally and laterally, basal pair of trichoid sensilla, and scattered scales; 8th tergite sclerotized, narrow, elongated, with only basal pair of trichoid sensilla. 2nd–7th sternites sclerotized, rectangular, with a single distal row of setae, many setae mesally and laterally, basal pair of trichoid sensilla, and scattered scales; 8th sternite sclerotized, with scattered setae at ½ distal, lateral setae, basal pair of trichoid sensilla and scattered scales. Terminalia (Fig. 10): gonocoxite partially setose, 0.21–0.22mm long, 0.07–0.08mm wide (n=07), with setulose rounded mesobasal lobe; gonostylus setulose basally, striated beyond basis, 0.11–0.12mm long, 0.02–0.03mm wide (n=07); cerci apically rounded with setae and setulae, cercal lobes convergent; hypoproct deeply bilobed, with setae and setulae, lobes widely separated and rounded apically; hypoproct much longer than cercus; aedeagus accentuately longer than hypoproct, wider than gonostylus, tapered to apex, rounded apically, bearing several asetose papillae.

Female. Body length 3.90–4.20mm long (n=8) (including ovipositor). Antenna: scape and pedicel as in male, flagellomeres cylindrical; nodes entirely setulose and necks partially setulose; circumfila made of two rings, connected horizontally, slightly sinuous (Fig. 11), 12th flagellomere 0.11–0.13mm long (n=6), entirely setulose, apical process 0.05–0.07mm long (n=6) with basal node 0.02mm long (n=6). Frontoclypeus with 10–14 setae (n=9). Palpus (n=9): 1st segment shorter than the others, 2nd–4th segments subequal in length, 1st segment 0.04–0.05mm long, 2nd segment 0.09–0.10mm long, 3rd segment 0.08–0.09mm long, 4th segment 0.09–0.10mm long.

Thorax. Wings: length: 3.00–3.30mm (n=8).

Abdomen (Fig. 12): 1st–7th tergites as in male; 8th tergite not sclerotized, with basal pair of trichoid sensilla and distal row of setae. 2nd–7th sternites as in male, 8th sternite not sclerotized, with basal pair of trichoid sensilla and a row of distal setae.

Ovipositor (Fig. 13) barely protrusible, 0.18–0.21mm long (from basal margin of segment 9 to cerci apex) (n=3), cerci separate elongate-ovoid, 0.07–0.08mm long (n=4) and setose, hypoproct wide with setae and setulae.

Etymology. The name indaiensis refers to the type locality.

Material examined. Holotype male. Brazil, Minas Gerais: Dores do Indaiá, IV.2009, L. Oliveira col., MNRJ. Paratypes, data as holotype– 10 males, 9 females, 18 pupal exuviae and 06 larvae, MNRJ.

Distribution. Brazil: Pernambuco (Tamandaré), Rio de Janeiro (Mangaratiba) and São Paulo (Bertioga) in Atlantic forest areas, and Minas Gerais (Dores do Indaiá) in Cerrado areas.

Comments.Lopesia includes adults with bare or setulose flagellomere necks. The new species has setulose flagellomeres neck as in L. andirae, L. brasiliensis Rübsaamen, 1908; L. caulinaris Maia, 2003; L. conspicua Maia, 2003; L. davillae Maia, 2017; L. eichhorniae Urso-Guimarães, 2014; L. elliptica Maia, 2013; L. erythroxyli Rodrigues & Maia, 2010; L. linearis Maia, 2003; L. marginalis Maia, 2001; L. maricaensis Rodrigues & Maia, 2010; L. similis Maia, 2004; L. simplex Maia, 2002; and L. tibouchinae Maia, 2004. Among them, nine species have male flagellomeres with basal and distal circumfila with well developed loops and midcircumfila with shorter loops or without loops (linear circumfila), namely: L. andirae, L. conspicua, L. davillae, L. eichhorniae Urso-Guimarães, 2014, L. linearis, L. marginalis, L. similis, L. simplex and L. tibouchinae; two have gynecoid circumfila (L. caulinaris and L. elliptica), three including the new species have all circumfila with developed loops (L. erythroxyli, L. brasiliensis and the new species) and a single one, L. maricaensis, has all circumfila with reduced loops.

Adults of the new species differ from those of L. erythroxyli and L. brasiliensis mainly by the shape of male terminalia. Gonocoxites, gonostyli and aedeagus are wider in L. indaiensis than in the others; the hypoproct of the new species has longer lobes than those of the others, and its cercal lobes are convergent (divergent in the two other species). Pupae differ mainly in the shape and length and of the antennal projections (slightly serrated and conspicuously longer in L. indaiensis, not serrated and shorter in the others), shape of the apical plate (deeply bilobed only in the new species), and number of abdominal dorsal spines (none in L. indaiensis, several in L. brasiliensis and L. erythroxyli). Besides, the prothoracic spiracles are clearly shorter in the new species than in L. brasiliensis.

As L. andirae and L. indaiensis are the only two congeneric species associated with Andira Lam., both are compared: larva – the spatula teeth of L. andirae are far apart from each other, while those of L. indaiensis are more closely approximated and the spatula basis of the former is narrow while in the latter is anchor-shaped; pupa – the vertical plate conspicuously more deeply bilobed at upper margin in L. indaiensis, the antennal projections have serrated inner margin only in the new species, the prothoracic spiracle is clearly longer in the new species (0.16mm in L. andirae and 0.25–0.35mm in L. indaiensis), as well as the apical setae (0.06mm in L. andirae and 0.07–0.13mm in L. indaiensis); male – the medial circumfilum has short whorls while in the new species they are long, the 8th tergite of L. andirae is setose whereas that of L. indaiensis has no setae, the cercus of L. andirae is more acute than that of the new species and the hypoproct has sinuous margin while in L. indaiensis its margin is rounded; and female – the circunfila of L. andirae are more sinuous than that of the new species, the 8th tergite of L. andirae has no setae whereas that of L. indaiensis has a distal row of setae and a basal pair of trichoid sensilla (not described in L. andirae).

Conflicts of interest

The authors declare no conflicts of interest.


We are grateful to Dr. Fernando Augusto de Oliveira e Silveira (UFMG) for plant identification.

[Backes and Irgang, 2004]
P. Backes,B. Irgang
Mata atlântica: as árvores e a paisagem
Paisagem do Sul, (2004)
[Carvalho-Fernandes et al., 2016]
S.P. Carvalho-Fernandes,S. Ascendino,V.C. Maia,M.S. Couri
Diversity of insect galls associated with coastal shrub vegetation in Rio de Janeiro, Brazil
An. Acad. Bras. Ciênc., 88 (2016), pp. 1407-1418
[Gagné, 1994]
R.J. Gagné
The Gall Midges of the Neotropical Region
Cornell University Press, (1994)
[Gagné and Jaschhof, 2017]
R.J. Gagné,M. Jaschhof
A Catalog of the Cecidomyiidae (Diptera) of the World. Digital Version
4th edition, (2017)
[Garcia et al., 2017]
C. Garcia,A. de,V.P. Lima,D.C. Calado,M.V. Urso-Guimarães
New species of Lopesia Rübsaamen (Diptera: Cecidomyiidae) associated with Andira humilis Mart. ex Benth. (Fabaceae)
Rev. Bras. Entomol., 61 (2017), pp. 239-242
[Lorenzi, 1992]
H. Lorenzi
Árvores brasileiras: manual de identificação e cultivo de plantas arbóreas nativas do Brasil
Editora Plantarum, (1992)
[Maia and Monteiro, 2017]
V.C. Maia,R.F. Monteiro
Lopesia davillae (Diptera. Cecidomyiidae), a new species of gall midge from Brazil associated with Davilla rugosa (Dilleniaceae)
[Maia et al., 2002]
V.C. Maia,M.A.P. Azevedo de,M.S. Couri
New contribution to the knowledge of the gall midges (Diptera, Cecidomyiidae) from the restinga of Barra de Maricá (Rio de Janeiro, Brazil)
Stud. Dipterol., 9 (2002), pp. 447-452
[Maia et al., 2008]
V.C. Maia,M.A.G. Magenta,S.E. Martins
Ocorrência e caracterização de galhas de insetos em áreas de restinga de Bertioga (São Paulo, Brasil)
Biota Neotrop., 8 (2008), pp. 167-197
[Maia et al., 2014]
V.C. Maia,L.J.T. Cardoso,J.M.A. Braga
Insect galls from Atlantic Forest areas of Santa Teresa, Espírito Santo, Brazil: characterization and occurrence
Bol. Mus. Biol. Mello Leitão, 33 (2014), pp. 47-129
[Rodrigues et al., 2014]
A.R. Rodrigues,V.C. Maia,M.S. Couri
Insect galls of restinga areas of Ilha da Marambaia, Rio de Janeiro, Brazil
Rev. Bras. Entomol., 58 (2014), pp. 173-197
[Santos et al., 2012]
J.C. Santos,J.S. Almeida-Cortez,G.W. Fernandes
Gall-inducing insects from Atlantic forest of Pernambuco, Northeastern Brazil
Biota Neotrop., 12 (2012), pp. 197-213
[Tavares, 1920]
J.S. Tavares
Cecidologia brazileira. Cecídias que se criam em plantas das famílias das Leguminosae, Sapotaceae, Lauraceae, Myrtaceae, Punicaceae, Aurantiaceae, Malpighiaceae, Sapindaceae, Umbelliferae, Loranthaceae, Apocynaceae, Urticaceae, Salicaceae e Graminae
Brotéria (Zool.), 18 (1920), pp. 82-125
Copyright © 2018. Sociedade Brasileira de Entomologia
Revista Brasileira de Entomologia

Receba nossa Newsletter

Opções de artigo
Política de cookies
Utilizamos cookies próprios e de terceiros para melhorar nossos serviços e mostrar publicidade relacionada às suas preferências, analisando seus hábitos de navegação. Se continuar a navegar, consideramos que aceita o seu uso. Você pode alterar a configuração ou obter mais informações aqui.