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531.
Cristina Nava Verónica C. Neves Malvina Andris Marie-Pierre Dubois Philippe Jarne Mark Bolton Joël Bried 《Die Naturwissenschaften》2017,104(11-12):103
Bottleneck episodes may occur in small and isolated animal populations, which may result in decreased genetic diversity and increased inbreeding, but also in mating strategy adjustment. This was evaluated in the vulnerable and socially monogamous Monteiro’s Storm-petrel Hydrobates monteiroi, a seabird endemic to the Azores archipelago which has suffered a dramatic population decline since the XVth century. To do this, we conducted a genetic study (18 microsatellite markers) in the population from Praia islet, which has been monitored over 16 years. We found no evidence that a genetic bottleneck was associated with this demographic decline. Monteiro’s Storm-petrels paired randomly with respect to genetic relatedness and body measurements. Pair fecundity was unrelated to genetic relatedness between partners. We detected only two cases of extra-pair parentage associated with an extra-pair copulation (out of 71 offspring). Unsuccessful pairs were most likely to divorce the next year, but genetic relatedness between pair mates and pair breeding experience did not influence divorce. Divorce enabled individuals to improve their reproductive performances after re-mating only when the new partner was experienced. Re-pairing with an experienced partner occurred more frequently when divorcees changed nest than when they retained their nest. This study shows that even in strongly reduced populations, genetic diversity can be maintained, inbreeding does not necessarily occur, and random pairing is not risky in terms of pair lifetime reproductive success. Given, however, that we found no clear phenotypic mate choice criteria, the part played by non-morphological traits should be assessed more accurately in order to better understand seabird mating strategies. 相似文献
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Anne Pinton Julia Boubnova François Becmeur Pierre Kuhn Marie-Victoire Senat Julien Stirnemann Marianne Capelle Jonathan Rosenblatt Jérôme Massardier Pascal Vaast Gwenaelle Le Bouar Amélie Desrumaux Laure Connant Laetitia Begue Benoit Parmentier Franck Perrotin Alain Diguet Guillaume Benoist Charles Muszynski Aurélien Scalabre Norbert Winer Jean-Luc Michel Florence Casagrandre-Magne Jean-Marie Jouannic Denis Gallot Perrine Coste Mazeau Emmanuel Sapin Alexis Maatouk Anne-Hélène Saliou Loïc Sentilhes Florence Biquard Nicolas Mottet Romain Favre Alexandra Benachi Nicolas Sananès 《黑龙江环境通报》2020,40(8):949-957
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Hélène Duval Laurence Michel-Calemard Marie Gonzales Philippe Loget Claire Beneteau Annie Buenerd Madeleine Joubert Marielee Denis-Musquer Alix Clemenson Anne-Laure Chesnais Sophie Blesson Isabelle De Pinieux Anne-Lise Delezoide Gheorghe Bonyhay Christine Bellanné-Chantelot Laurence Heidet Florence Dupré Sophie Collardeau-Frachon 《黑龙江环境通报》2016,36(8):744-751
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Martin B. Delatycki Fowzan Alkuraya Alison Archibald Carlo Castellani Martina Cornel Wayne W. Grody Lidewij Henneman Adonis S. Ioannides Edwin Kirk Nigel Laing Anneke Lucassen John Massie Juliette Schuurmans Meow-Keong Thong Irene van Langen Joël Zlotogora 《黑龙江环境通报》2020,40(3):301-310
Reproductive carrier screening started in some countries in the 1970s for hemoglobinopathies and Tay-Sachs disease. Cystic fibrosis carrier screening became possible in the late 1980s and with technical advances, screening of an ever increasing number of genes has become possible. The goal of carrier screening is to inform people about their risk of having children with autosomal recessive and X-linked recessive disorders, to allow for informed decision making about reproductive options. The consequence may be a decrease in the birth prevalence of these conditions, which has occurred in several countries for some conditions. Different programs target different groups (high school, premarital, couples before conception, couples attending fertility clinics, and pregnant women) as does the governance structure (public health initiative and user pays). Ancestry-based offers of screening are being replaced by expanded carrier screening panels with multiple genes that is independent of ancestry. This review describes screening in Australia, Cyprus, Israel, Italy, Malaysia, the Netherlands, Saudi Arabia, the United Kingdom, and the United States. It provides an insight into the enormous variability in how reproductive carrier screening is offered across the globe. This largely relates to geographical variation in carrier frequencies of genetic conditions and local health care, financial, cultural, and religious factors. 相似文献