Africanized honeybee stings: how to treat them

INTRODUCTION: In 1956, Africanized honeybees (AHB) migrated from Brazil to other regions of the Western Hemisphere, including South, Central, and North America, except for Canada. Despite being productive, they are highly aggressive and cause fatal accidents. This study aimed to evaluate patients at the Clinical Hospital of Botucatu Medical School (HC-FMB) and to propose treatment guidelines. METHODS: From 2005 to 2006, the clinical and laboratorial aspects of 11 patients (7 male and 4 female) and the anatomopathological aspects of one patient who had died in 2003 were analyzed. RESULTS: The age of the surviving patients varied from 5 to 87 years, with a mean of 42.5 years. The majority of accidents occurred in the afternoon, and the number of stings ranged from 20 to 500. The principal signs and symptoms were pain and local inflammatory signs, nausea, tachycardia, and vomiting. Biochemical findings presented increased levels of creatine phosphokinase, lactate dehydrogenase, and aspartate/alanine aminotransferase. An 11-year-old male patient died upon entering the attic of a two-storey building where he was attacked by a swarm, receiving more than 1,000 stings. He was sent to HC-FMB where he was treated, but he died 24h later. Observed at the autopsy were erythematous-purpuric skin lesions besides necrosis at the sting locations, rhabdomyolysis, focal myocardial necrosis, tubular hydropic degeneration and focal tubular acute necrosis of the kidneys, myoglobinuria, and centrolobular necrosis in the liver. CONCLUSIONS: Accidents caused by multiple AHB stings always constitute a medical emergency. As there is no specific antivenom, we have developed guidelines, including first aid, drugs, and the proper removal of stingers.

Africanized honeybees in urban areas: a public health concern

IntroductionThis study aimed to investigate the occurrence of Africanized honeybees in Botucatu, São Paulo, Brazil, and to implement a program to remove such swarms.MethodsThe occurrences of Africanized honeybee swarms between 2010 and 2012 were studied and strategies to prevent accidents were developed.ResultsWe noted 1,164 cases of Africanized honeybee occurrences in the city, and 422 swarms were collected. The developed strategies to prevent accidents were disseminated to the population.ConclusionsWe contributed to reducing the risks represented by Africanized honeybee swarms in urban areas, by collecting swarms and disseminating strategic information for preventing accidents.

Espécies nectaríferas e poliníferas utilizadas pela abelha Melipona compressipes fasciculata (MELIPONINAE, APIDAE), no Maranhão

Este trabalho apresenta 79 espécies de plantas que fornecem néctar e/ou pólen para operárias de Melipona compressipes fasciculata, que é a abelha mais comum do Maranhão. A maioria dessas plantas são também visitadas por Apis mellifera. Sugere-se, com isso, o plantio de algumas espécies em estradas, cercas, ruas, avenidas e praças, a fim de melhorar a pasto apícola.

Aspectos sobre a polinizaçâo do "Dendezeiro" Elaeis guineensis Jacq. e do "Caiaué" Elaeis oleifera (H.B.K.) Cortés. (ARECACEAE).

Este trabalho tem como objetivo a identificação dos insetos visitantes e polinizadores das flores do "dendê" Elaeis guineensis Jacq., e do "caiaué" Elaeis oleifera (H.B.K) Cortés, atráves de coletas em locais e horários diferentes, quando as inflorescências masculinas das plantas encontravam-se em plena antese. Um total de 159 insetos foram observados tendo sido constatado dentre os diversos tipos de visitantes, os meliponídeos: Trigona sp. ("dendê" e "caiaué"), Apis mellifera adansonni e Partamona sp. ("dendê"). Constatou-se ainda a presença de uma quantidade razoável de insetos da família Curculionidae do gênero Elaeidobius, que voavam em torno das inflorescências, sendo evidente a sua participação na polinização das espécies estudadas. Além disso, verificou-se a presença de larvas de um coléoptero da família lycidae, junto as inflorescências das plantas.

ABELHAS SOCIAIS (HYMENOPTERA : APIDAE) E SEUS RECURSOS FLORAIS EM UMA REGIÃO DE MATA SECUNDÁRIA, ALCÂNTARA, MA, BRASIL

De julho/1992 a junho/1993 foram feitas coletas em intervalos de ,28 a 30 dias em uma .área de vegetação secundária com 1.650m2, próxima ao rio Pepital, em Alcântara - MA, com o objetivo de conhecer a fauna apícola e suas relações com a flora local. Foram coletados sobre flores 1.076 indivíduos (1.073 fêmeas e 03 machos), pertencentes a 20 espécies e 11 gêneros da família Apidae. Trigona fulviventrís(42,2%), Apis mellifera(24,5%), Trigona pollens(12,5%), Trigona fuscipennis(10,0%), Tetragona clavipes(2,9%) e Melipona puncticollis(2,3%) foram as espécies mais abundantes. O menor número de indivíduos foi coletado em abril (mês chuvoso), e o mês com maior númerode indivíduos capturados foi julho. A maior frequência de Apidae foi observada entre 6:00 e 8:00 horas. As espécies de plantas que receberam o maior número de visitas foram: Borreria verticillata(Rubiaceae), Clusiasp. (Guttiferae), Hyptis atrorubens(Labiatae), Heliotropiumsp. (Boraginaceae) e Crotalaria refusa(Leguminosae). As espécies de Trigonavisitaram quase todas as plantas do local, preferencialmente aquelas das famílias Guttiferae, Rubiaceae e Boraginaceae.

Fenologia e produtividade do araçá-boi (Eugenia stipitata, Myrtaceae) na Amazônia Central

O araçá-boi (Eugenia stipitata McVaugh ssp. sororia McVaugh, Myrtaceae) é uma frutífera nativa da Amazônia Ocidental com potencial para a indústria de sucos e flavorizantes. Embora pouco plantada na Amazônia brasileira devido a sua acidez, é frequentemente cultivada na Amazônia peruana. O conhecimento de sua fenologia pode ajudar no planejamento do manejo do plantio e da comercialização dos frutos. A fenologia de dez plantas, crescendo num latossolo amarelo degradado, foi observada durante cinco anos. O araçá-boi geralmente floresceu e frutificou três vezes ao longo do ano e sempre teve pelo menos um pico de floração forte durante a estação seca (julho a setembro) e um pico de frutificação mais acentuado na estação chuvosa (janeiro a março). A floração é um evento complexo e demorado que pode durar de dois a três meses, embora o período entre o aparecimento do botão floral até a antese do flor é curto (~15 dias) e o período entre a antese e a maturação dos frutos dura 50 a 60 dias. As regressões múltiplas usadas para determinar o efeito das variáveis climáticas na floração e frutificação não apresentaram altos coeficientes de determinação, embora os modelos tenham sido significantes, provavelmente porque o araçá-boi floresce várias vezes durante o ano e ainda não se sabe qual o estímulo mais importante para iniciar o processo. O vingamento dos frutos variou de menos de 5% a aproximadamente 15%. O peso médio dos frutos avaliados em janeiro de 1988 foi 135 g, com 77% de polpa. Ao longo do período, estimou-se que as dez plantas produziram cm média 1000 frutos/ano, com uma mediana de 890 frutos/ano. Os insetos visitantes eram principalmente abelhas, especialmente Apis mellifera, Eulaema mocsaryi e Ptilotrigona lurida.

Levantamento da fauna de Abelhas silvestres (Hymenoptera, Apoidea) na região da "Baixada Maranhense": Vitória do Mearim, MA, Brasil

Estudou-se durante um ano a fauna de abelhas de uma região da Baixada maranhense em Vitória do Mearim — MA. Foram feitas coletas mensais com auxílio de redes entomológicas e armadilhas de cheiro, no período de um ano, totalizando 288 horas de amostragem. Um total de 839 indivíduos de 38 espécies de abelhas pertencentes às famílias Apidae, Megachilidae, Halictidae, Andrenidae e Colletidae foram coletadas nas flores e 72 indivíduos (11 espécies) de Euglossinae em armadilhas com iscas-odoríferas. Scaptotrigona flavisetis Μoure, Trigona pallens Cockerell e Apis mellifera Linnaeus foram as espécies mais abundantes na área. A sazonalidade foi variável de acordo com as diferentes espécies de abelhas. S. flavisetis foi observada em maior número em janeiro e outubro, T. pallens em janeiro e fevereiro e A. mellifera em abril. Das abelhas coletadas em armadilhas, Euglossa (E.) cordata e Ε. (E.) gr. modestior foram as mais abundantes e Eucaliptol foi a isca odorífera que recebeu maior número de visitas.

Diversidade de abelhas (Hymenoptera: Apoidea) em uma área de transição Cerrado-Amazônia

A comunidade de abelhas em uma área de transição cerrado-amazônia, localizada na região do Bico-do-Papagaio, Estado do Tocantins, foi estudada entre novembro de 1999 e novembro de 2000, por meio da amostragem sistemática dos espécimes nas plantas em floração, com o objetivo de obter informações sobre a sua composição. Um total de 5.534 indivíduos, distribuídos em 83 espécies e 38 gêneros foram coletados. A maior abundância de indivíduos e riqueza de espécies foi encontrado na família Apidae sensu Roig-Alsina & Michener. Os gêneros com maior riqueza foram Trigona (8), Megachile (7), Centris (6), Augochloropsis (5), Coelioxys (5), Paratetrapedia (5) e Xylocopa (5), enquanto que a espécie mais freqüente foi Apis mellifera. A comunidade seguiu o padrão geral encontrado nos neotrópicos, apresentando muitas espécies com poucos indivíduos e poucas espécies com muitos indivíduos. A freqüência, constância e dominância das espécies são discutidas e os índices de abundância, diversidade, eqüitabilidade e dominância são apresentados.

Biologia floral e sistema reprodutivo de Byrsonima coccolobifolia (Kunth) em uma savana amazônica

A biologia reprodutiva de Byrsonima coccolobifolia, foi avaliada em uma população de savana do Estado de Roraima. A espécie é constituída de arbustos e arvoretas com altura inferior a 3m, de flores hermafroditas zigomorfas, pentâmeras, reunidas em inflorescências do tipo racemo terminal, produzidos em brotações novas, o cálice é composto por cinco sépalas, que apresentam um par de glândulas produtoras de óleo. A corola é formada por cinco pétalas albo-róseas e unguiculadas, o androceu é composto por dez estames com anteras de coloração amarela. A antese pode ser noturna ou diurna, estende-se por um período médio de 12 horas e as flores costumam ficar abertas e vistosas por um período adicional de 15 horas, quando se inicia a senescência. Foram registrados dois episódios de floração e o fogo parece ser um fator ambiental estimulador desta fenofase. Os visitantes florais predominantes foram abelhas das famílias Anthophoridae (Centris sp. e Xylocopa sp.) e Apidae (Apis mellifera e Bombus sp.). Os resultados das polinizações controladas e o cálculo do índice de auto-incompatibilidade (ISI) indicam que a espécie apresenta comportamento protogínico e é autocompatível, produzindo frutos em todos os tratamentos de autopolinização em proporções semelhantes à polinização natural, não sendo confirmada a produção de frutos apomíticos. Entretanto, os percentuais de frutos formados nos tratamentos de xenogamia foram significativamente superiores aos tratamentos de autofertilização, indicando que B. coccolobifolia apresenta um sistema reprodutivo misto com níveis elevados de alogamia e autogamia.

Formação das castas no gênero Melípona (Illiger, 1806)

The present work is destinated to prove that the castes : workers and queens, in Melipona bees are due to genetic factors and not to differences in food. 2) Material used: Hives of Melipona quadri-fasciata anthidioides (Lep. 1836), M. schenki schenki (Gribodo, 1893), M. fasciata rufiventris (Lep. 1836), M. quadri-fasciata vicina (Lep. 1836), M. marginata marginata (Lep. 1836), Apis mellifera (L. 1758). 3) It should be pointed out that in Melipona bees there are no royal cells for the queens, but all the cells are of the same size independently of being destinated for workers, queens or drones. The numerous queens which are born are killed soon after emerging from their cells. 4) Changes of feeding in quality and in quantity caused no variation of castes. The only variable factor is the size, which becomes bigger when the bee is well nourished. 5) The offsprings of 5 hives were examined : 3 of M. quadri-fasciata anthidioides (n.o 1, n.o 2 and n.o 3), 1 of M. quadri-fasciata vicina (n.o 4) and 1 of M. marginata marginata (n.o 5). Combs of about 40 cells were taken into laboratory and the type of bee registered immediately after emerging. The results of the counts were: BOX COMB WORKER QUEEN PERCENTAGE Σ X2 to 12,5% Nº 1 1th 69 8 10,4% 0, 3139 " 1 2nd 144 18 11,1% 0, 2856 " 2 1th 52 8 13,3% 0, 0384 " 3 1th 45 10 18,2% 1, 6736 " 4 1th 56 4 6,7% 1, 8686 " 4 2nd 29 4 12,1% 0,00432 Σ X2 to 25% " 5 1th 34 14 29,2% 0,44444 "5 2nd 83 27 24,5% 0, 0121 In the 4 first boxes there is a percentage of 11,63% queens and in the last there is a percentage of 25,95%. 6) These percentages are very near two genetical ratios: 12,5% or 7:1, and 25% or 3:1, which correspond to a trifactorial and a bifactorial back-cross. Carrying out a X² test no significant deviations were found ( X² to 12,5% and to 25% and table 1 to 4). 7) We suppose that the formula for the queen in the first case (11,65%) is: AaBbCc. Since the Melipona bees are arrhenotokous hymenopteres, the drones are haploid and may have any one of the following eight formulas, corresponding to the gonic segregation of the queem : ABC, ABc, Abc, Abc, AbC, aBC, aBc, abC, abc. Anyone combination of these males with the queen will give a segregation of 7 workers to 1 queen, since there is always only one triple heterozygote among the eight possible segregates (table 5). 8) In order to explain the second case, it is suffient to assume that in this species there are only two pairs of factors, the queen being the double heterozygote : AaBb, while the drones may have any one of the following constitutions: AB, Ab, aB and ab. Workers are again all diploids which are homozygous for one or both factors, for instance: AABB, AABb, AaBB, aaBb, AAbb, etc. (table 6). 9) It is suggested that the genus Melipona is an intermediary type between the solitary bees, where all females are fertile independently of their feeding, and the genera Apis and Trigona, where without special feeding all females are born sterile, while only specially fed females develop into fertile queens. 10) No speculations are put forward with regards to the evolutionary mechanism which may have been responsible for the development of the genetical determination of castes in Melipona, since it seems advisable point to extend the studies to other insects with complicated caste systems.

Bases para o estudo da genética de populações dos Hymenoptera em geral e dos Apinae sociais em particular

This paper deals with problems on population genetics in Hymenoptera and particularly in social Apidae. 1) The studies on populations of Hymenoptera were made according to the two basic types of reproduction: endogamy and panmixia. The populations of social Apinae have a mixed method of reproduction with higher percentage of panmixia and a lower of endogamy. This is shown by the following a) males can enter any hive in swarming time; b) males of Meliponini are expelled from hives which does not need them, and thus, are forced to look for some other place; c) Meliponini males were seen powdering themselves with pollen, thus becoming more acceptable in any other hive. The panmixia is not complete owing to the fact that the density of the breeding population as very low, even in the more frequent species as low as about 2 females and 160 males per reproductive area. We adopted as selection values (or survival indices) the expressions according to Brieger (1948,1950) which may be summarised as follows; a population: p2AA + ²pq Aa + q2aa became after selection: x p2AA + 2pq Aa + z q²aa. For alge-braics facilities Brieger divided the three selective values by y giving thus: x/y p2 AA + y/y 2 pq Aa + z/y q²aa. He called x/y of RA and z/y of Ra, that are survival or selective index, calculated in relation to the heterozygote. In our case all index were calculated in relation to the heterozygote, including the ones for haploid males; thus we have: RA surveval index of genotype AA Ra surveval index of genotype aa R'A surveval index of genotype A R'a surveval index of genotype a 1 surveval index of genotype Aa The index R'A ande R'a were equalized to RA and Ra, respectively, for facilities in the conclusions. 2) Panmitic populations of Hymenoptera, barring mutations, migrations and selection, should follow the Hardy-Weinberg law, thus all gens will be present in the population in the inicial frequency (see Graphifc 1). 3) Heterotic genes: If mutation for heterotic gene ( 1 > RA > Ra) occurs, an equilibrium will be reached in a population when: P = R A + Ra - 2R²a _____________ (9) 2(R A + Ra - R²A - R²a q = R A + Ra - 2R²A _____________ (10) 2(R A + Ra - R²A - R²a A heterotic gene in an hymenopteran population may be maintained without the aid of new mutation only if the survival index of the most viable mutant (RA) does not exced the limiting value given by the formula: R A = 1 + √1+Ra _________ 4 If RA has a value higher thah the one permitted by the formula, then only the more viable gene will remain present in the population (see Graphic 10). The only direct proof for heterotic genes in Hymenoptera was given by Mackensen and Roberts, who obtained offspring from Apis mellefera L. queens fertilized by their own sons. Such inbreeding resulted in a rapid loss of vigor the colony; inbred lines intercrossed gave a high hybrid vigor. Other fats correlated with the "heterosis" problem are; a) In a colony M. quadrifasciata Lep., which suffered severely from heat, the percentage of deths omong males was greater .than among females; b) Casteel and Phillips had shown that in their samples (Apis melifera L). the males had 7 times more abnormalities tian the workers (see Quadros IV to VIII); c) just after emerging the males have great variation, but the older ones show a variation equal to that of workers; d) The tongue lenght of males of Apis mellifera L., of Bombus rubicundus Smith (Quadro X), of Melipona marginata Lep. (Quadro XI), and of Melipona quadrifasciata Lep. Quadro IX, show greater variationthan that of workers of the respective species. If such variation were only caused by subviables genes a rapid increasse of homozigoty for the most viable alleles should be expected; then, these .wild populations, supposed to be in equilibrium, could .not show such variability among males. Thus we conclude that heterotic genes have a grat importance in these cases. 4) By means of mathematical models, we came to the conclusion tht isolating genes (Ra ^ Ra > 1), even in the case of mutations with more adaptability, have only the opor-tunity of survival when the population number is very low (thus the frequency of the gene in the breeding population will be large just after its appearence). A pair of such alleles can only remain present in a population when in border regions of two races or subspecies. For more details see Graphics 5 to 8. 5) Sex-limited genes affecting only females, are of great importance toHymenoptera, being subject to the same limits and formulas as diploid panmitic populations (see formulas 12 and 13). The following examples of these genes were given: a) caste-determining genes in the genus Melipona; b) genes permiting an easy response of females to differences in feeding in almost all social Hymenoptera; c) two genes, found in wild populations, one in Trigona (Plebéia) mosquito F. SMITH (quadro XII) and other in Melipona marginata marginata LEP. (Quadro XIII, colonies 76 and 56) showing sex-limited effects. Sex-limited genes affecting only males do not contribute to the plasticity or genie reserve in hymenopteran populations (see formula 14). 6) The factor time (life span) in Hymenoptera has a particular importance for heterotic genes. Supposing one year to be the time unit and a pair of heterotic genes with respective survival indice equal to RA = 0, 90 and Ra = 0,70 to be present; then if the life time of a population is either one or two years, only the more viable gene will remain present (see formula 11). If the species has a life time of three years, then both alleles will be maintained. Thus we conclude that in specis with long lif-time, the heterotic genes have more importance, and should be found more easily. 7) The colonies of social Hymenoptera behave as units in competition, thus in the studies of populations one must determine the survival index, of these units which may be subdivided in indice for egg-laying, for adaptive value of the queen, for working capacity of workers, etc. 8) A study of endogamic hymenopteran populations, reproduced by sister x brother mating (fig. 2), lead us to the following conclusions: a) without selection, a population, heterozygous for one pair of alleles, will consist after some generations (theoretically after an infinite number of generation) of females AA fecundated with males A and females aa fecundated with males a (see Quadro I). b) Even in endogamic population there is the theoretical possibility of the presence of heterotic genes, at equilibrium without the aid of new mutations (see Graphics 11 and 12), but the following! conditions must be satisfied: I - surveval index of both homozygotes (RA e Ra) should be below 0,75 (see Graphic 13); II - The most viable allele must riot exced the less viable one by more than is permited by the following formula (Pimentel Gomes 1950) (see Gra-fic 14) : 4 R5A + 8 Ra R4A - 4 Ra R³A (Ra - 1) R²A - - R²a (4 R²a + 4 Ra - 1) R A + 2 R³a < o Considering these two conditions, the existance of heterotic genes in endogamic populations of Hymenoptera \>ecames very improbable though not - impossible. 9) Genie mutation offects more hymenopteran than diploid populations. Thus we have for lethal genes in diploid populations: u = q2, and in Hymenoptera: u = s, being u the mutation ratio and s the frequency of the mutant in the male population. 10) Three factors, important to competition among species of Meliponini were analysed: flying capacity of workers, food gathering capacity of workers, egg-laying of the queen. In this connection we refer to the variability of the tongue lenght observed in colonies from several localites, to the method of transporting the pollen in the stomach, from some pots (Melliponi-ni storage alveolus) to others (e. g. in cases of pillage), and to the observation that the species with the most populous hives are almost always the most frequent ones also. 11) Several defensive ways used for Meliponini to avoid predation are cited, but special references are made upon the camouflage of both hive (fig. 5) and hive entrance (fig. 4) and on the mimetism (see list in page ). Also under the same heading we described the method of Lestrimelitta for pillage. 12) As mechanisms important for promoting genetic plasticity of hymenopteran species we cited: a) cytological variations and b) genie reserve. As to the former, duplications and numerical variations of chromosomes were studied. Diprion simile ATC was cited as example for polyploidy. Apis mellife-ra L. (n •= 16) also sugests polyploid origen since: a) The genus Melipona, which belongs to a" related tribe, presents in all species so far studied n = 9 chromosomes and b) there occurs formation of dyads in the firt spermatocyte division. It is su-gested that the origin of the sex-chromosome of Apis mellifera It. may be related to the possible origin of diplo-tetraploidy in this species. With regards to the genie reserve, several possible types of mutants were discussed. They were classified according to their survival indices; the heterotic and neutral mutants must be considered as more important for the genie reserve. 13) The mean radius from a mother to a daghter colony was estimated as 100 meters. Since the Meliponini hives swarm only once a year we may take 100 meters a year as the average dispersion of female Meliponini in ocordance to data obtained from Trigona (tetragonisca) jaty F. SMITH and Melipona marginata LEP., while other species may give different values. For males the flying distance was roughly estimated to be 10 times that for females. A review of the bibliography on Meliponini swarm was made (pg. 43 to 47) and new facts added. The population desity (breeding population) corresponds in may species of Meliponini to one male and one female per 10.000 square meters. Apparently the males are more frequent than the females, because there are sometimes many thousands, of males in a swarm; but for the genie frequency the individuals which have descendants are the ones computed. In the case of Apini and Meliponini, only one queen per hive and the males represented by. the spermatozoos in its spermateca are computed. In Meliponini only one male mate with the queen, while queens of Apis mellijera L. are fecundated by an average of about 1, 5 males. (Roberts, 1944). From the date cited, one clearly sees that, on the whole, populations of wild social bees (Meliponini) are so small that the Sewall Wright effect may become of great importance. In fact applying the Wright's formula: f = ( 1/aN♂ + 1/aN♀) (1 - 1/aN♂ + 1/aN♀) which measures the fixation and loss of genes per generation, we see that the fixation or loss of genes is of about 7% in the more frequent species, and rarer species about 11%. The variation in size, tergite color, background color, etc, of Melipona marginata Lep. is atributed to this genetic drift. A detail, important to the survival of Meliponini species, is the Constance of their breeding population. This Constance is due to the social organization, i. e., to the care given to the reproductive individuals (the queen with its sperm pack), to the way of swarming, to the food storage intended to control variations of feeding supply, etc. 14) Some species of the Meliponini are adapted to various ecological conditions and inhabit large geographical areas (e. g. T. (Tetragonisca jaty F. SMITH), and Trigona (Nanno-trigona testaceicornis LEP.) while others are limited to narrow regions with special ecological conditions (e. g. M. fuscata me-lanoventer SCHWARZ). Other species still, within the same geographical region, profit different ecological conditions, as do M. marginata LEP. and M. quadrifasciata LEP. The geographical distribution of Melipona quadrifasciata LEP. is different according to the subspecies: a) subsp anthidio-des LEP. (represented in Fig. 7 by black squares) inhabits a region fron the North of the S. Paulo State to Northeastern Brazil, ,b) subspecies quadrifasciata LEP., (marked in Fig. 7 with black triangles) accurs from the South of S. Paulo State to the middle of the State of Rio Grande do Sul (South Brazil). In the margined region between these two areas of distribution, hi-brid colonies were found (Fig. 7, white circles); they are shown with more details in fig. 8, while the zone of hybridization is roughly indicated in fig. 9 (gray zone). The subspecies quadrifasciata LEP., has 4 complete yellow bands on the abdominal tergites while anthidioides LEP. has interrupted ones. This character is determined by one or two genes and gives different adaptative properties to the subspecies. Figs. 10 shows certains meteorological isoclines which have aproximately the same configuration as the limits of the hybrid zone, suggesting different climatic adaptabilities for both genotypes. The exis-tance of a border zone between the areas of both subspecies, where were found a high frequency of hybrids, is explained as follows: being each subspecies adapted to a special climatic zone, we may suppose a poor adaptation of either one in the border region, which is also a region of intermediate climatic conditions. Thus, the hybrids, having a combination of the parent qualities, will be best adapted to the transition zone. Thus, the hybrids will become heterotic and an equilibrium will be reached with all genotypes present in the population in the border region.

Os insetos como agentes polinizadores da mangueira

The authors study the insect population that visit the mango trees and search for their pollinizing activity. Prior operations showed that very few bees (Apis mellifera) visited the flowers of mango trees. It was known that the percentage of fecundation is low (Simão 1955), Popenoe (1929), Spencer and Kennard (1955), Lynch and Mustard (1955), Ruehle and Ledin (1955), so that the authors wented to Know if insects could be responsible for this. Insects were collected from mango trees, belonging to 10 orders, which, on the whole are not pollinizing agents. Bees were not collected, 21% were Hymenoptera, 20% were Diptera, 13% Hemiptera, 10% Coleoptera, 3% Blattariae and smoller percentages belonged to other orders.

Polinização da aboboreira

Os autores planejaram um experimento com a finalidade de esclarecer vários problemas ligados com a polinização da aboboreira. Para êsse fim, foi organizada uma cultura com a variedade Brasileira. O campo constou de 48 covas, cada qual com uma planta, distanciadas de 2m. As plantas foram conduzidas em caramanchões de 1m de altura, separados por corredores de 3 m. Cada caramanchão abrangeu 4 plantas. Com a finalidade de se estudar a polinização na ausência de insetos, três caramanchões foram cobertos com telas de "nylon". Os resultados das pesquisas, foram os seguintes: 1.° - A proporção de flôres femininas e masculinas abertas no mesmo dia foi de 1:17,7. 2.° - A abertura das flôres se dá em plena madrugada. 3.° - As abelhas Irapuás (Trigona (Trigona) ruficrus Latr.) e as Apis mellifera L. constituiram os principais insetos polinizadores da aboboreira. 4.° - Não foi constatado o fenômeno partenocárpico na aboboreira. 5.° - As concentrações médias dos sólidos do néctar das flôres de abóbora, em dois dias, de medições com o refratômetro de campo Huet foram, respectivamente, de 39,7% e 40,6%. 6.° - Foi constatado que na ausência de insetos não houve frutificação. Os frutos provenientes de flôres polinizadas pelos insetos alcançaram um rápido desenvolvimento, estando em condições de serem consumidos como aboborinhas, após o quarto dia de formação.

Morfologia do polém de algumas compostas apícolas

Apresentamos neste trabalho a descrição e estudos das características morfológicas dos grãos de pólem de 14 Compostas apícolas, mais frequentes nas análises polínicas de méis de abelhas, e do pólem coletado pelas abelhas Apis mellifera L., por nos verificados. Através do resultado das características de tamanho e forma do grão de pólem, do Amb (contorno do grão de pólem em Vista Polar), área polar, espessura da exina, comprimento dos espículos e número dos contornos em vista polar, pudemos elaborar uma Chave para identificação das espécies estudadas.

Organization of the cysts in bee (Hymenoptera, Apidae) testis: number of spermatozoa per cyst

The morphology of the cyst cells in Apis mellifera Linné, 1758, Scaptotrigona postica Latreille, 1804, and Melipona bicolor bicolor Lepeletier, 1836 testis, as well as the average number of spermatic cells are reported. The data indicates a supporting and nourrishing role of the cyst cells to the developing cystocytes. The counts of immature spermatozoa in the cysts show an average of 202.8 ± 21.2 spermatozoa for A. mellifera, 117.4 ± 8.68 for S. postica and 88.8 ± 15.57 for M. bicolor, which predict the occurrence of 8 mitotic cycles in the cystocytes of A. mellifera and 7 in the meliponines, considering that only one spermatozoom originates of each final spermatogonium.