Bees of the genus Megachile Latreille are popularly known as leaf cutters, and females utilize leaves and petals for construction of their nest cells. Their cavity-nesting behavior probably developed from Megachile ancestors that nested in the ground (Eickwort et al., 1981). This genus is large, with around 1320 known species (Michener, 2000) of which 161 occur in Brazil (Silveira et al., 2002). Further information about these insects is sparse (Almeida et al., 1997). From November 2006 to February 2010 trap nests (made of cardboard tubes inside plastic bottles and black cardboard tubes inside wooden blocks) were placed horizontally on the ground along a boundary of a semi-deciduous secondary forest in a in Itacolomi State Park in the city of Ouro Preto, Minas Gerais, Brazil. Trap nests were uniform in length (120 mm) but varied in their inner diameters (6–12 mm). They were inspected twice a month for Megachile spp., and completed nests were removed to the laboratory for analysis. Fifty-seven nests of Megachile (Moureapis) anthidioides Radoszkowski were built in trap-nests not previously used by other species. The diameter of trap-nests that were occupied ranged from 6 to 12 mm (8.49 6 1.25; median 6 standard deviation). Nest diameter preferences vary from species to species; according to Aguiar and Martins (2002) the bees prefer diameters that best accommodate their bodies within the cells. A cavity of large diameter makes the bee expend more energy to fill the excess space with construction material. During the end of dry season (August and September of 2007) M. anthidiodes occupied almost 30% (n 5 16) of the trap-nests. This high nesting rate at the end of the dry season may be related to the availability of food that the females use to feed their offspring. The nest cells were built with leaves, and we found an average of 5.06 6 2.22 cells per nest. The construction of cells followed the pattern reported by Krombein (1967) for other species of Megachile that made 1 to 9 cells per nest. Of the 226 emerged adults, 144 were males and 82 females, resulting in a sex ratio of 1:0.56. The male/female difference was statistically significant (x 5 13.154; P , 0.05). In general, the adults emerged 4 to 8 weeks after the female closed the main entrance. There was parasitism in 14.28% (N 5 8) of the occupied trap-nests, and two parasitic species emerged from them: Coelioxys (Acrocoelioxys) sp., from three nests, and Melittobia sp., from one nest. The presence of parasitic bees of the genus Coelioxys in Megachile nests is widely known from literature. These bees are the principal parasites found in Megachile nests, but some species also parasitize nests of other solitary bees mentioned in literature on trap-nests (e.g., Aguiar and Martins, 2002; Alves-dos-Santos, 2003; Aguiar et al., 2005; Aguiar et al., 2006). This is the first record of M. anthidioides in trap nests. To date, there have only been reports of collecting this species (e.g., Silveira and Cure, 1993; Silveira et al., 1993; Silveira and Campos, 1995; Goncalves and Melo, 2005). The abundance of M. anthidioides in the trap-nests could indicate the scarcity of appropriate sites for nesting by this species in the study area, since that area has already suffered a substantial anthropogenic impact.
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