As yet, certain aspects of the Africanization process are not well understood, for example, the reproductive behavior of African and European honeybees and how the first Africanized swarms were formed and spread. Drone congregation areas (DCAs) are the ideal place to study honeybee reproduction under natural conditions since hundreds of drones from various colonies gather together in the same geographical area for mating. In the present study, we assessed the genetic structure of seven drone congregations and four commercial European-derived and Africanized apiaries in southern Brazil, employing seven microsatellite loci for this purpose. We also estimated the number of mother-colonies that drones of a specific DCA originated from. Pairwise comparison failed to reveal any population sub-structuring among the DCAs, thus indicating low mutual genetic differentiation. We also observed high genetic similarity between colonies of commercial apiaries and DCAs, besides a slight contribution from a European-derived apiary to a DCA formed nearby. Africanized DCAs seem to have a somewhat different genetic structure when compared to the European.

We collected 40 colonies of the wasp Polistes satan in November 1993 (Population A = 23 colonies) and October 1995 (Population B = 17 colonies) from the town of Delfinopólis in the Brazilian state of Minas Gerais. Pupae from these nests were used to assess allozyme variation and genetic relatedness among nestmates. Of the 24 gene loci sampled six showed allozyme polymorphism (Est-2, Pgm-1, 6Pgd, Hk-1, Idh and Pep-A) and all loci except Idh were at Hardy-Weinberg equilibrium. Populations A and B showed distinct intra-loci heterozygosities, but similar average heterozygosity over all loci. Significant inter-population differentiation (Fst = 0.051; p < 0.01) was detected, probably due to genetic drift driven by bottlenecking that occurred due to the first sampling. Mean intra-colony relatedness values between female broods (rA = 0,525 ± 0.063; rB = 0,456 ± 0.103) indicated that P. satan has a simple sociogenetic structure where one female takes on most of the reproductive tasks but, eventually, subordinates also reproduce in the colony.

São apresentados os resultados de um estudo de dois anos sobre o Symphyta neotropical Digelasinus diversipes. Esta espécie é univoltina e comum na Estação Ecológica Jataí, uma reserva de Cerrado no Estado de São Paulo. As larvas alimentam-se gregariamente em Eugenia glazioviana (Myrtaceae) de novembro a abril. Associações entre grupos de alimentação foram freqüentes. Após o período de alimentação, as larvas congregam-se e comunalmente constróem uma massa de casulos (105 casulos ± 60DP; n = 25) aderida ao tronco da planta hospedeira, permanecendo em diapausa como prepupas até o início da estação chuvosa, em outubro. O pico populacional foi observado em dezembro, quando 62% (n = 2.967) dos adultos emergiram. Em condições experimentais, foram observadas emergências das 6:30 às 15:00 h, mas 73,5% (n = 223) dos adultos emergiram entre 9:00 e 12:00 h. Não foi observado, durante a emergência, sequenciamento sexual, mas em um agregado de casulos os machos podem emergir de 20 a 40 dias antes das fêmeas. Após a emergência os machos podem (1) dispersar-se (no início e final do período de emergência; outubro e novembro, janeiro e fevereiro, respectivamente) ou (2) permanecer sobre ou próximo ao agregado de casulos e copular com as fêmeas recém-emergidas (durante o pico de emergência, em dezembro). As cópulas duraram 4,28 minutos (± 3,4DP; n = 28). Ao longo do dia, os machos podem copular com diferentes fêmeas (1-8; n = 5); contudo, as fêmeas copularam apenas uma vez. Em média, as fêmeas emergem com 76 (± 21DP; n = 19) ovos maduros e todos eles são ovipositados de uma só vez sob uma única folha da planta hospedeira. A guarda dos ovos pelas fêmeas durou apenas 2 dias (n = 12) dos 30 necessários para sua incubação. O repertório de comportamentos da fêmea contra potenciais inimigos foi menor do que o observado em outras espécies de Symphyta. Aparentemente, a fêmea induz um necrosamento do tecido foliar que cobre os ovos. Isto formaria uma proteção rígida para os ovos durante sua incubação. Em D. diversipes, adultos de ambos os sexos não se alimentaram (condição controlada) e tiveram vida curta (5,2 dias ± 1,7DP; mínimo 1, máximo 11; n = 179). A razão sexual média foi 2,83 (± 0,014EP) em favor de fêmeas. Os principais fatores de mortalidade foram falhas no desenvolvimento, falta de alimento devido à intensa herbivoria e ataque de parasitóides. Parasitóides criados, Lymeon dieloceri (Costa Lima, 1937) (Ichneumonidae), Conura (Spilochalcis) sp. (Chalcididae) e Perilampus sp. (Perilampidae).

The results of a two-year study of the Neotropical sawfly Digelasinus diversipes are presented. This species is univoltine and common in Estação Ecológica Jataí, a nature reserve of Cerrado vegetation in São Paulo State, Brazil. The larvae feed gregariously on Eugenia glazioviana (Kiaersk.) D. Legrand (Myrtaceae) from November through April. Fusions of different feeding groups were frequent. After the feeding period, larvae congregate and communally construct a cocoon mass (105 cocoons ± 60SD; n = 25) attached to the trunk of the host plant, entering in diapause as prepupae until the beginning of the rainy season in October. The population peak was in December when 62% (n = 2,967) of adult emergence occurred. In experimental conditions, emergence was observed from 6:30 a.m. until 15:00 p.m., but 73.5% (n = 223) of the adults appeared between 9:00 a.m. and 12:00 h. Sex sequence was not observed during emergence but, in a single cocoon mass, males may appear 20 to 40 days earlier than females. After emergence, males may either (1) disperse (early and late in the emergence period; October and November, January and February, respectively) or (2) remain on or near the cocoon mass and mate with newly emerged females (during the emergence peak in December). Copulation lasts 4.28 minutes (±3.4SD; n = 28), and during the day, males may mate with different females (1-8; n = 5); however, females mate only once. Newly emerged females have a mean of 76 mature eggs (± 21SD; n = 19) and oviposited all of them underneath of a single leaf of the host plant. Egg guarding by females lasted only 2 (n = 12) of the 30 days of egg incubation. The female's behavioral repertoire against potential enemies was shorter than that reported for some other sawfly species. Apparently, the female induces necrosis of the leaf tissue that covers the eggs, which forms a hard shelter for the eggs during incubation. Both sexes of D. diversipes do not feed as adults (controlled condition) and have a short life span (5.2 days ± 1.7SD; minimum 1, maximum 11; n = 179). The mean sex ratio was 2.83 (± 0.014SE) in favor of females. Main mortality factors were development defects, lack of food due to intense herbivory, and attack of parasitoids. Parasitoids reared, Lymeon dieloceri (Costa Lima, 1937) (Ichneumonidae), Conura (Spilochalcis) sp. (Chalcididae) and Perilampus sp. (Perilampidae).

Two populations of the wasp Trypoxylon rogenhoferi Kohl, 1884 from São Carlos and Luís Antônio, State of São Paulo, Brazil, were observed and sampled from May 1999 to February 2001 using trap-nests. This mass-provisioning wasp was used to test some aspects of optimal sex allocation theory. Both populations fit all the predictions of the models of Green and Brockmann and Grafen. Maternal provisions determined the size of each offspring, and females allocated well-stocked brood cells to daughters, the sex that benefits most being large. This strategy resulted in a difference in size between the sexes. In São Carlos, female weight at emergence was 1.18 times that of males, in Luís Antônio this value was 1.13. The brood cell volume was correlated with both wing length and weight at emergence in both sexes, and the chance that a given brood cell contained a male offspring decreased with increased brood cell volume. In T. rogenhoferi female body size was related to fitness. Larger females were able to collect more mass of spiders per day, the spiders they captured were heavier, and they provisioned more brood cells per day. They also produced larger daughters. For males, no relationship between body size and fitness was found, but the data were scarce. Since the patterns of provisioning were variable among different females in both study sites, it is possible that the females not follow a unique strategy for sex allocation. The sex ratio and/or investment ratio in the São Carlos population was female-biased and in Luís Antônio, male-biased. In spite of the influence of trap-nests diameters on male production in Luís Antônio, there is some evidence that in São Carlos population the local availability of prey and/or lower rate of parasitism may be major forces in determining the observed sex ratio, but further studies are necessary to verify such hypothesis.

Twenty-two nests of Trypoxylon asuncicola were sampled in Viçosa, State of Minas Gerais, Brazil, in January 2000 and the occupants' behavior of three nests was registered in 2h of direct observation. 528 brood cells were excavated (24±13.84 SD cells per nest), 129 were reused cells, some of them for seven times (meconium deposit count). The mean number of total cells, mean number of open and closed cells, parasitism rate and mean number of reused cells per nest were similar between old and new nests. Parasitism rate and cell reuse were associated with the number of building cells in the nest, but nest aggregate in the sampled area may play some role in the parasitism rate. Brachymeria sp. (Chalcididae) was the most important agent of brood mortality (80%). Other parasites were Melittobia sp. (Eulophidae) (17%) and a species of Icheumonidae (3%). The number of closed cells with immature individuals per nest was 4±4.2SD (N=17) and the mean reproductivity per female was 3±2.4SD (N=5). New nests produced more offspring (0 a 35%) than old nests (0 to 11%). Females and males can be found resting in the nest but copula or guarding behavior by the male was not observed. There is some evidence that in the sampled area the switch of nests by females is great and agonistic behavior between a nest owner and a visitor was not evident. Females were larger (3.9±0.4SD mm) than males (3.1±0.3SD mm) (measured as forewing length). The secondary sex ratio was 1.26 (±0.07 SE) in favor of females, which was not different from 1:1 ratio. The majority (97%) of the sampled larvae of T. asuncicola showed diapause. Some (5.1%) 'anomalous cells' were found.