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.

Estudos sôbre a alimentação mineral do cafeeiro, X: extração de macronutrientes na colheita pelas variedades "Mundo Novo", "Caturra" e "Bourbon Amarelo"

This paper deals with the determination of the content of macronutrients in pulp and beans of three coffee varieties, namely 'Mundo Novo', 'Caturra Amarelo' and 'Bourbon Amarelo'. Samples were collected in plantations located in the three types of soils herein most of S. Paulo, Brazil, coffee is grown, that is, "terra roxa legítima" (Ribeirão Preto), "massapé-salmourão" (Mocóca), and "arenito de Bauru" (Pindorama). The following main conclusions were drawn after statistical analysis of data obtained hereby. There is no statistical difference among the three varieties . Average contents of macronutrients, as per cent of the dry matter, are the following: N P K Ca Mg S bean 1,71 0,10 1,53 0,27 0,15 0,12 pulps 1.78 0,14 3,75 0,41 0,13 0,15 Samples collected in Mocóca ("massapé-salmourão") had lower N and K contents, probably due to lack of availability of these elements in the soil, as suggested by its analysis. Results obtained in this work are in good agreement with data described elsewhere. Out of the total of elements contained in the whole fruit the following proportions are exported as clean coffee: N - 2/3, P and K - 1/2, Ca, Mg and S - 1/3. It is clear therefore that a substantial amount of elements absorbed from the soil remains in the pulp or in the dry hulls which result from processing. From this fact raises the interest of using these residues as fertilizer in the coffee plantations.

Arroz: ensaio fatorial variedade x espaçamento x densidade

In this experiment it was attempted to find better row spacing (0,20 m, 0,40 m and 0,60 m) and seed rate (3 and 6 grams of seeds/m) to be used in rice. The ordinary flooding was used as irrigation. Four varieties with different flowering periods were used: "Pratão" and "Iguape Agulha" are late varieties (150 days); "Batatais", "Dourado Precoce" early varieties (100 days). These two early varieties produce two harvests by ratooning. The data showed that the late varieties gave a better yeld on a single crop, but the greatest annual yeld by area was obtained when the ratooning was used. As far as amount of seed is concerned the data showed that the better yelds were obtained with 3 grams of seeds.

Fixação de fósforo por um latossolo e determinação do valor «X»

Este trabalho se refere a um ensaio conduzido em laboratório para avaliar a capacidade de fixação de fosfato dos horizontes A1 (0.22cm), A3 (22-56cm) e B22 (155-200cm) de Lotossolo Roxo Distrófico. Foi, também, determinado o valor "X" de WAUGH & FITTS (1966) dos três horizontes. Os principais resultados são apresentados a seguir: 1 - O horizonte B22 foi o que apresentou maior capacidade de fixação de fósforo, seguido pelo A3 e, finalmente, pelo A1 . 2 - Os valores "X" encontrados foram: 350 ppm, 225 ppm e 175 ppm para os horizontes B22 , A3 e A2, respectivamente. 3 - Houve uma relação muito estreita entre as quantidades de R adicionadas e as fixadas pelos três horizontes.

Uso da espectrografia de raio X na determinação do cálcio e do potássio em solos

Foi estudado por espectrografia de raio X a distribuição do Ca e K na fração areia e no solo total em oito pedons representativos de uma topossequência de solos da região de São Pedro no Estado de São Paulo. As principais conclusões foram as seguintes: - Com exceção dos Pedons 1 e 3 os teores de K e Ca são muito baixos. Os elevados teores de K encontrados nos Pedons 1 e 3 indicam que os materiais das superfícies I e III são menos intemperizados e portanto de origem mais recente. - A fração areia dos solos estudados, com exceção dos Pedons 1 e 3, possue baixíssimos valores de K e Ca, consequentemente de minerais contendo tais elementos. - Com exceção do Pedon 3 os solos não possuem reserva mineral na fração areia. - De todos os solos estudados os Pedons 6, 7 e 8, localizados nas superfícies mais antigas, são os mais intemperizados.

Dois processos para a determinação do valor X de Waugh & Fitts (1966), modificado

São apresentados dois processos para a determinação das quantidades de P a serem adicionadas a amostras de 10 g de terra de modo que, após um período de incubação de 4 dias, 30 ppm de P permaneçam solúveis em 100 ml de solução 0,05 N em HCl e 0,025N em H2SO4. Os processos são os seguintes: a. Baseado na correlação entre as quantidades de P adicionadas as amostras e as extraídas pelo estrator citado; b. Baseado na semelhança dos triângulos obtidos a partir das coordenadas retangulares dos pontos representativos de 30 ppm de P extraído e adicionado e dos pontos imediatamente inferiores e superiores a esse valor. Concluiu-se que os dois processos fornecem resultados equivalentes, sendo indiferente o uso de um ou de outro.

Acúmulo de nitrogênio, fósforo, potássio, cálcio, magnésio e enxofre pela videira (Vitis labrusca L. X Vitis vinifera L.) cv. 'Niágara rosada', durante um ciclo vegetativo

Ensaio foi conduzido com videiras de cultivar 'Niagara Rosada' (Vitis labrusca L. X Vitis vinifeva L.) com 7 anos de idade, no município de Jundiaí, SP (23°12' de latitude sul e 46º33' de longitude oeste e 715 m de altitude), situadas sobre um Regossolo unidade Currupira, com os objetivos de: (1) analisar o crescimento (produção de materia seca); (2) determinar as quantidades de nutrientes absorvidos pela videira nos diferentes estádios de desenvolvimento e (3) avaliar a exportação de nutrientes pela cultura durante o ciclo vegetativo. Após a brotação da videira, foram realizadas 17 coletas quinzenais de material. Foram coletadas e separadas as folhas das partes terminal e basal, sarmentos das partes terminal e basal e cachos. No material coletado foram determinados os teores de N, P, K, Ca, Mg e S. Curvas representativas dos acúmulos de matéria seca e das concentrações dos nutrientes nas partes da planta, em função da idade, foram obtidas a partir dos dados calculados através de equações de regressão. Pelos pontos de máximo estimaram-se a produção maxima de matéria seca e as quantidades de nutrientes extraídos. Conclui-se que: . A produção maxima de materia seca ocorre aos 148 dias. . A concentração dos nutrientes é sempre maior nas folhas do que nos sarmentos e existem diferenças nas concentrações de nutrientes das folhas, sarmentos e cachos, em função da idade. . Os acúmulos máximos de nutrientes nas folhas, sarmentos e cachos ocorrem nas seguintes idades.

Acúmulo de boro, cobre, ferro, manganês e zinco pela videira (Vitis labrusca L. X Vitis vinifera L.) CV.'niagara rosada' durante um ciclo vegetativo

Ensaio foi conduzido com viderias da cultivar 'Niagara Rosada' (Vitis labrusca L. X Vitis vinifera L.) com 7 anos de idade, no município de Jundiaí, SP, (23°12' de latitude sul e 46°33' de longitude oeste e 715 m de altitude), situadas sobre um Regossolo unidade Currupira, com os objetivos de: (1) determinar as quantidades de nutrientes absorvidos pela videira nos diferentes estádios de desenvolvimento; (2) avaliar a exportação de nutrientes pela cultura durante um ciclo vegetativo. Após a brotação da videira, foram realizadas 17 coletas quinzenais de material. Foram coletadas e separadas as folhas das partes terminal e basal, sarmentos das partes terminal e basal e cachos. No material coletado foram determinados os teores de micronutrientes, com exceção do molibdênio e cloro. Curvas representativas das concentraçoes dos nutrientes nas partes da planta, em função da idade, foram obtidas a partir dos dados calculados através de equações de regressão. Pelos pontos de máximo estimaram-se as quantidades máximas de nutrientes extraídos. Concluiu-se que: - A concentração dos nutrientes é sempre maior nas folhas do que nos sarmentos e existem diferenças nas concentrações de nutrientes das folhas, sarmentos e cachos, em função da idade. - Os acúmulos máximos de nutrientes nas folhas, sarmentos e cachos ocorrem nas seguintes idades: - A exportação de nutrientes em mg por planta pelos cachos e sarmentos removidos pelas colheitas e poda é a seguinte.

Nutrição mineral de plantas ornamentais: X-nutrição de Anthurium andraeanum

Plantas de Anthurium andraeanum foram cultivadas em soluções nutritivas carentes em N, P, K, Ca, Mg, S e B, afim de se obter o quadro sintomatológico das carências, assim como os níveis analíticos dos elementos nas folhas, caule e raiz. Os sintomas de carência foram obtidos para os nutrientes na seguinte ordem decrescente: N, Ca, Mg, S, B, P e K. Os teores porcentuais dos nutrientes na matéria seca foram, em folhas sadias e afetadas, respectivamente; N% -1,56-1,25; P % 0,37-0,25; K % - 3,37-0,53; Ca %-1,44-0,65; Mg % - 0,37-0,28; S % - 0,18-0,16. Para B, os valores foram de 86 e 47 ppm respectivamente. A fim de aquilatar as quantidades de nutrientes extraídas pelo antúrio, plantas com um, dois e três anos foram colhidas e separadas em folhas, caule, raize e flor e analisadas para os macro e macronutrientes, com exceção do Mo. Observou-se que a extração e sensivelmente aumentada na passagem do segundo para o terceiro ano. Plantas com três anos contém: N-434 mg; P-61 mg; Ca-327 mg; Mg-224 mg; S-45 mg; B-2434 µg; Cu-204 µg; Fe-7851 µg;Mn-7842 µg; e Zn-237 µg.

Estudos sobre a nutrição mineral do arroz: X. marcha de absorção de micronutrientes pela variedade IAC-25

Em condições controladas estudaram-se: acumulação de micronutrientes e produção de materia seca pela variedade de arroz IAC-25. A curva que descreve a produção de matéria seca total em função do tempo apresentou a tendência a sigmóide. Com respeito a acumulação global de micronutrientes, entretanto, o mesmo foi observado somente no caso do ferro.

Nutrição mineral de seringueira (Hevea spp). X. Quantidade de al no substrato afetando a concentração e o acúmulo de Fe, Mn e Zn

Com o propósito de comparar os efeitos de doses crescentes de Al sobre a concentração e acúmulo de Fe, Mn e Zn conduziu-se um experimento usando-se separadamente solução nutritiva usada por BOLLE-JONES e soluções de doses de Al que consistiram de 0, 5, 10, 15 20 e 25ppm, em que as plantas passaram vinte e quatro horas na solução nutritiva (sem Al) e vinte e quatro horas nas soluções de Al. Após noventa e cinco dias de tratamento as plantas foram coletadas e separadas em raiz, caule, folhas dos verticilos inferiores e folhas do último verticilo. Determinou-se as concentrações de Fe, Mn e Zn no material coletado. Observou-se que o Al estimula a concentração de Fe e Mn em todos os níveis de Al enquanto que o acúmulo desses micronutrientes é afetado a partir de 20ppm de Al na solução. A concentração de Zn na raiz e folhas do último verticilo é afetado a partir de 15ppm de Al na solução e o acúmulo deste nutriente é afetado a partir de 20ppm de Al na solução.

Anatomia foliar e do pedúnculo floral de plantas de morangueiro (Fragaria x ananassa) "Sequoia" tratadas com fitoreguladores

O presente estudo teve por objetivo descrever a anatomia foliar e do pedúnculo floral do morangueiro "Sequóia" a fim de verificar os efeitos dos reguladores vegetais, ácido giberélico (GA3) e ácido naftalenoacético (NAA), e dos bioestimulantes Ergostim e Atonik, sobre as características anatômicas das plantas tratadas. A dose total empregada dos quatro produtos foi de 30 ppm, parcelada em três pulverizações, iniciadas após o início do florescimento. Foram analisadas amostras de folhas (limbo e pecíolo) e o pedúnculo floral de 3 repetições. As análises histológicas foram feitas mediante o preparo e observação de lâminas de material fresco ou fixado. A análise da folha adulta revela a presença de hidatódios nas extremidades denteadas do limbo. A lâmina foliar é anfiestomática, com estômatos do tipo anomocítico. Ocorrem dois tipos de tricomas: tectores e glandulares. Na epiderme abaxial podem estar presentes estruturas semelhantes à lenti-celas. O mesofilo é dorsiventral. O padrão de venação é do tipo nervatio camptodroma arqueada típica. O pecíolo apresenta estômatos e tricomas cujas características se assemelham ao do limbo; abaixo da epiderme há um colênquima do tipo anelar; no parênquima fundamental há idioblastos contendo drusas e outros que contém compostos fenólicos; o cilindro vascular é descontínuo formando um arco, constituído de feixes do tipo colateral aberto envolvido por uma bainha parenquimática amilífera. Os elementos traqueais do xilema são espiralados. O pedúnculo floral apresenta epiderme com tricomas, colênquima do tipo anelar, um anel contínuo de fibras perivasculares e cilindro vascular descontínuo interrompido por raios medulares estreitos. Os produtos testados não alteraram a estrutura anatômica dos morangueiros "Sequóia", na dose empregada.

Cytogenetic study in natural hybrids of Callithrix (Callitrichidae: Primates) in the Atlantic forest of the state of Rio de Janeiro, Brazil

In the Atlantic forest of Rio de Janeiro, Callithrix aurita (É. Geoffroy in Humboldt, 1812) is a native species vulnerable to extinction and C. jacchus (Linnaeus, 1758) and C. penicillata (É. Geoffroy, 1812) are invasive species. The major threats to the native species are habitat degradation and hybridization, although there are currently no genetic data about natural hybrids available. Previous studies have revealed that species of the Callithrix genus are extremely homogeneous in their karyotypes with the exceptions of the morphology and size of the Y chromosome and its nucleolar organizer region (NOR) banding pattern. Three male marmosets captured in the wild in Guapimirim municipality, Rio de Janeiro, Brazil, considered as possible hybrids between C. aurita and C. jacchus or C. penicillata on the basis of pelage pattern, were cytogenetically studied. Metaphase chromosomes were obtained by using short-term lymphocyte cultures and Ag-NOR staining was performed. The hybrids karyotypes were 2n=46, 14 uni- and 30 bi-armed autosomes, a median size submetacentric X and NOR bearing autosomes, being compatible with that observed for the genus. In the three individuals studied, Y chromosomes were similar to those found for C. aurita, without NORs. The data obtained suggest the involvement of C. aurita in natural hybridization with one of the invasive species. We discuss the possible consequences of this hybridization.

External morphology of the immature stages of Neotropical heliconians: X. Heliconius sara apseudes (Lepidoptera, Nymphalidae, Heliconiinae)

ABSTRACT The biology and morphology of the immature stages of Heliconius sara apseudes (Hübner, [1813]) are still little known. External features of the egg, larvae and pupa of H. sara apseudes are described and illustrated, based upon light and scanning electron microscopy. Eggs with smooth carina, first instar larva with scaly setae, and body of second to fifth instars covered with scattered pinnacles distinguish H. sara apseudes from other heliconiine species.