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Flavonoid wing pigments increase attractiveness of female common blue (Polyommatus icarus) butterflies to mate-searching males 总被引:1,自引:0,他引:1
Common blue butterflies (Polyommatus icarus) sequester flavonoids from their larval host plants and allocate these UV-absorbing pigments to the wings. In field experiments
using dummies constructed from female butterflies, mate-searching males inspected flavonoid-rich dummies more intensively
than those with little or no flavonoids. Flavonoid content as signalled by UV-wing pattern may indicate ontogenetically determined
female quality or enhance detectability to males.
Received: 21 March 2000 / Accepted in revised form: 17 May 2000 相似文献
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Niels Gregersen Vibeke Winter Peter K. A. Jensen Anni Holmskov Steen Kølvraa Brage S. Andresen Ernst Christensen Peter Bross Jytte B. Lundemose Dr Markil Gregersen 《黑龙江环境通报》1995,15(1):82-86
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is a potentially fatal inherited disease with a carrier frequency of approximately 1:100 in most Caucasian populations. The disease is implicated in sudden unexpected death in childhood. A prevalent disease-causing point mutation (A985G) in the MCAD gene has been characterized, thus rendering diagnosis easy in the majority of cases. Since the clinical spectrum of MCAD deficiency ranges from death in the first days of life to an asymptomatic life, there are probably other genetic factors—in addition to MCAD mutations—involved in the expression of the disease. Thus, families who have experienced the death of a child from MCAD deficiency might have an increased risk of a seriously affected subsequent child. In such a family we have therefore performed a prenatal diagnosis on a chorionic villus sample by a highly specific and sensitive polymerase chain reaction (PCR) assay for the G985 mutation. The analysis was positive and resulted in abortion. We verified the diagnosis by direct analysis on blood spots and other tissue material from the aborted fetus and from family members. 相似文献
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Consanguineous partners had a boy with campomelic dysplasia who died of increasing respiratory distress soon after birth. The next pregnancy was monitored frequently by ultrasonography and a healthy male infant was born at term. During a further pregnancy, ultrasonography suggested campomelic dysplasia in the 16th week of gestation. This was confirmed in the 18th week. The pregnancy was terminated and the fetus showed the typical radiological, anatomical and histological findings. 相似文献
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