Hostname: page-component-76fb5796d-dfsvx Total loading time: 0 Render date: 2024-04-25T20:59:08.218Z Has data issue: false hasContentIssue false

Biased sex ratio and niche restriction in Baruscapillaria obsignata (Madsen 1945) (Nematoda, Capillariidae) from Columba livia (Aves, Columbidae)

Published online by Cambridge University Press:  18 October 2011

S. D'Ávila*
Affiliation:
Department of Zoology, Institute of Biological Sciences, Juiz de Fora Federal University, Minas Gerais, Brazil Malacological Museum Prof. Maury Pinto de Oliveira, Juiz de Fora Federal University, Minas Gerais, Brazil
E.C.A. Bessa
Affiliation:
Department of Zoology, Institute of Biological Sciences, Juiz de Fora Federal University, Minas Gerais, Brazil Malacological Museum Prof. Maury Pinto de Oliveira, Juiz de Fora Federal University, Minas Gerais, Brazil
S. Souza-Lima
Affiliation:
Department of Zoology, Institute of Biological Sciences, Juiz de Fora Federal University, Minas Gerais, Brazil
M.L.A. Rodrigues
Affiliation:
Department of Animal Parasitology, Veterinary Institute, Rio de Janeiro Federal Rural University, Brazil

Abstract

In the present study populations of the avian nematode species Baruscapillaria obsignata are described from Columba livia. Male and female individuals were obtained from 27 birds, fixed in alcohol/formalin/acetic acid (AFA) and preserved in 70% ethanol. Nematodes were identified and then counted under a stereoscopic microscope. Baruscapillaria obsignata were much more frequent in the anterior third of the small intestine, and females were more abundant than males in all infra populations. The prevalence was 55.6%, mean intensity was 11.8 (median 11.0; range 1–31) and abundance 6.56. In the present study, we observed an aggregated distribution of parasite infrapopulations, as demonstrated by the value of the exponent of the negative binomial distribution, K = 0.2773; by the discrepancy index, D = 0.656 and by the variance/mean ratio, 12.44. The female/male sex ratios found in all infrapopulations were always greater than 1, showing a bias in favour of female abundance. This tendency was especially marked in infrapopulations containing fewer individuals. The sizes of infrapopulations ranged from 5 to 31 individuals. The mean sex ratio observed was 2.69 ± 3.28 (median 1.83; range 0–11). In infrapopulations with 5–15 individuals, the sex ratios observed varied from 2.6 to 11, while in those with 17–31 individuals, the sex ratios were lower, ranging from 1.7 to 2.4. There was a negative correlation between the intensity of infection and the sex ratio of infrapopulations. Results are discussed in terms of possible factors influencing the processes that lead to niche restriction and biased sex ratios in parasite infrapopulations.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Amato, J.F.R., Boeger, W.A. & Amato, S.B. (1991) Protocolos para laboratório – coleta e processamento de parasitos do pescado. 81 pp. Seropédica, Imprensa Universitária Universidade Federal do Rio de Janeiro.Google Scholar
Bone, L.W. (1982) Nippostrongylus brasiliensis: female incubation, release of pheromone, fractionation of incubates. Experimental Parasitology 54, 1220.CrossRefGoogle ScholarPubMed
Bone, L.W. & Bottjer, K.P. (1985) Cuticular carbohydrates of three nematode species and chemoreception by Trichostrongylus colubriformis. Journal of Parasitology 71, 235238.CrossRefGoogle ScholarPubMed
Bone, L.W. & Shorey, H.H. (1977a) Interactive influences of male- and female-produced pheromones on male attraction to female Nippostrongylus brasiliensis. Journal of Parasitology 63, 845848.CrossRefGoogle Scholar
Bone, L.W. & Shorey, H.H. (1977b) Disruption of sex pheromone communication in a nematode. Science 197, 694695.CrossRefGoogle Scholar
Bone, L.W., Bjostad, L.B., Shorey, H.H. & Gaston, L.K. (1977) Nippostrongylus brasiliensis: age and time of day effects on pheromone production and response. Experimental Parasitology 42, 8286.CrossRefGoogle ScholarPubMed
Bone, L.W., Shorey, H.H. & Gaston, L.K. (1978) Nippostrongylus brasiliensis: factors influencing movement of males toward a female pheromone. Experimental Parasitology 44, 100108.CrossRefGoogle Scholar
Bush, A.O., Lafferty, K.D., Lotz, J.M. & Shostak, A.W. (1997) Parasitology meets ecology on its own terms: Margolis et al. revisited. Journal of Parasitology 83, 575583.CrossRefGoogle Scholar
Carneiro, J.R., Lustosa, E.S., Pereira, E., Carvalho, E.D. & Nápoli, M.A. (1975) Incidência de ecto e endoparasitos de pombos (Columba livia domestica) em Goiânia. Revista de Patologia Tropical 4, 3941.Google Scholar
Combes, C. & Théron, A. (2000) Metazoan parasites and resource heterogeneity: constraints and benefits. International Journal for Parasitology 30, 299304.CrossRefGoogle ScholarPubMed
Costa, H.M.A. & Freitas, M.G. (1970) Lista de helmintos parasitos dos animais domésticos do Brasil. Arquivos da Escola de Veterinária 22, 3393.Google Scholar
Costa, H.M.A., Leite, A.C.R., Guimarães, M.P. & Lima, W.S. (1986) Distribuição de helmintos parasitos de animais domésticos no Brasil. Arquivos Brasileiros de Medicina Veterinária e Zootecnia 38, 465579.Google Scholar
Dezfuli, B.S., Volponi, S., Beltrami, L. & Poulin, R. (2002) Intra- and interspecific density-dependent effects on growth in helminth parasite of the cormorant. Phalacrocorax carbo sinensis. Parasitology 124, 537544.Google ScholarPubMed
Eveland, L.K., Fried, B. & Cohen, L.M. (1982) Schistosoma mansoni: adult worm chemoattraction with and without barriers. Experimental Parasitology 54, 271276.CrossRefGoogle ScholarPubMed
Eveland, L.K., Fried, B. & Cohen, L.M. (1983) Schistosoma mansoni: adult worm chemoattraction with barriers of specific molecular weight exclusions. Experimental Parasitology 56, 255258.CrossRefGoogle ScholarPubMed
Freitas, J.F. & Lins De Almeida, J. (1935) O gênero ‘Capillaria’ Zeder, 1800 (‘Nematoda – Trichuroidea’) e as capillarioses nas aves domésticas. Revista do Departamento Nacional de Produção Animal 2, 311363.Google Scholar
Graybill, H.W. (1924) Capillaria columbae (Rud.) from the chicken and turkey. Journal of Parasitology 10, 205207.CrossRefGoogle Scholar
Guyatt, H.L. & Bundy, D.A.P. (1993) Estimation of intestinal nematode prevalence: influence of parasite mating patterns. Parasitology 107, 99106.CrossRefGoogle ScholarPubMed
Holmes, J.C. (1990) Competition, contacts and other factors restricting niches of parasitic helminthes. Annals de Parasitologie Humaine et Compareé 65, 6972.CrossRefGoogle Scholar
Levine, N.D. (1980) Nematode parasites of domestic animals and of man. 477 pp. Minneapolis, Burges Publishing.Google Scholar
Madsen, H. (1950) Notes on the species of Capillaria Zeder, 1800 known from gallinaceous birds. Journal of Parasitology 37, 257265.CrossRefGoogle Scholar
May, M.R. & Woolhouse, M.E.J. (1993) Biased sex ratios and parasite mating probabilities. Parasitology 107, 287295.CrossRefGoogle ScholarPubMed
Miller, M.J. (1937) The parasites of pigeons in Canada. Canadian Journal of Veterinary Research 15, 91103.CrossRefGoogle Scholar
Moravec, F. (1982) Proposal of a new systematic arrangement of nematodes of the family Capillariidae. Folia Parasitologica 29, 119132.Google ScholarPubMed
Moravec, F. (1987) The biology of nematodes of the family Capillariidae Neveu-Lemaire, 1936. Folia Parasitologica 34, 3956.Google ScholarPubMed
Morgan, D.O. (1932) On three species of the genus Capillaria from the English domestic fowl. Journal of Helminthology 10, 183194.CrossRefGoogle Scholar
Pinto, R.M., Tortelly, R., Menezes, R.C. & Gomes, D.C. (2004) Trichurid nematodes in ring-necked pheasants from backyard flocks of the state of Rio de Janeiro, Brazil: frequency and pathology. Memórias do Instituto Oswaldo Cruz 99, 721726.CrossRefGoogle Scholar
Poulin, R. (1993) The disparity between observed and uniform distributions: a new look at parasite aggregation. International Journal for Parasitology 23, 937944.CrossRefGoogle Scholar
Poulin, R. (1997) Population abundance and sex ratio in dioecious helminth parasites. Oecologia 111, 375380.CrossRefGoogle ScholarPubMed
Roche, M. & Patrzec, D. (1966) The female to male ratio (FMR) in hookworm. Journal of Parasitology 52, 117121.CrossRefGoogle ScholarPubMed
Rohde, K. (1979) A critical evaluation of intrinsic and extrinsic factors responsible for niche restriction in parasites. American Naturalist 114, 648671.CrossRefGoogle Scholar
Rohde, K. (1994) Niche restriction in parasites: proximate and ultimate causes. Parasitology 109, S69S84.CrossRefGoogle ScholarPubMed
Salm, R.W. & Fried, B. (1973) Heterosexual chemical attraction in Camallanus sp. (Nematoda) in the absence of worm mediated tactile behavior. Journal of Parasitology 59, 434436.CrossRefGoogle ScholarPubMed
Schirazian, D. & Schiller, E.L. (1982) Mating recognition by Schistosoma mansoni in vitro. Journal of Parasitology 68, 650652.CrossRefGoogle Scholar
Silva, C.C. (1990) Helmintos parasitos de Columba livia (Gm) no município de São Gonçalo, Rio de Janeiro. Arquivos Brasileiros de Medicina Veterinária e Zootecnia 42, 391394.Google Scholar
Simková, A., Desdevises, Y., Gelnar, M. & Morand, S. (2000) Co-existence of nine gill ectoparasites (Dactylogyrus: Monogenea) parasitising the roach (Rutilus rutilus L.): history and present ecology. International Journal of Parasitology 30, 10771088.CrossRefGoogle ScholarPubMed
Stien, A., Halvorsen, O. & Leinaas, H.-P. (1996) Density-dependent sex ratio in Echinomermella matsi (Nematoda) a parasite of the sea urchin Strongylocentrotus droebachiensis. Parasitology 112, 105112.CrossRefGoogle Scholar
Sukhdeo, M.V.K. & Sukhdeo, S.C. (1994) Optimal habitat selection by helminths within the host environment. Parasitology 109, S41S55.CrossRefGoogle ScholarPubMed
Tingley, G.A. & Anderson, R.M. (1986) Environmental sex determination and density dependent population regulation in the entomogenous nematode Romanomermis culicivorax. Parasitology 92, 431449.CrossRefGoogle Scholar
Travassos, L. (1915) Contribuições para o conhecimento da fauna helminthologica brasileira. V. Sobre as espécies brasileiras do gênero Capillaria Zeder, 1800. Memórias do Instituto Oswaldo Cruz 7, 146172.CrossRefGoogle Scholar
Von Zuben, C.J. (1997) Implicações da agregação espacial de parasitos para a dinâmica populacional na interação hospedeiro-parasita. Revista de Saúde Pública 31, 115.CrossRefGoogle Scholar