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Genetic variation of Zoarces viviparus: six populations revisited after about 35 years

机译:Zoarces viviparus的遗传变异:大约35年后重新研究了六个种群

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摘要

Eelpout, Zoarces viviparus, has been used as study object for nearly 100 years by several Danish scientists. The advantage of eelpout is that it is viviparous which means that the genetic contribution from the parents to the offspring may be recognised and identified when the genotype of the female is known. Already in 1917 Schmidt published a work on the number of rays in the right pectoral fin, vertebrate number, number of hard rays in the dorsal fin and number of pigmentation spots along the dorsal fin. The first conclusion based on vertebrate number, hard rays and pigmentation spots was that environmental factors per se was not sufficient to explain the similarity between the female and the offspring, so a genetic component had to be involved in the determination of the four traits. Secondly, four major groups of eelpouts were recognised, i.e. one group living in the western part of the North Sea, one in the eastern part of the North Sea, one in the western part of the Baltic Sea encompassing the internal Danish waters, and one in the eastern part of the Baltic Sea. Thirdly, a gradient in the traits was found in four fjords. Mainly one of the fjords, Mariager Fjord, has been studied several times. Samples were analysed by using the analytic method described by Schmidt (1917) and by isozymes (Christiansen et al. 1981, 1988; Olsen et al. 2002). Christiansen et al. (1981, 1988) found that the morphological traits were nearly unchanged for at least 60 years and some of the isozymes showed the same gradient as the morphological traits which indicated that the fjord harboured at least two populations of eelpouts, one in the inner part and one in the outer part of the fjord. However, after a tremendous oxygen deficiency in 1998 where nearly all life in the fjord was destroyed, both the morphological traits and the isozymes were revealing gradients indicating that the fjord was re-colonised from the population located outside of the fjord (Olsen et al. 2002).During the 1970s a number of eelpouts were analysed by means of isozymes. The major conclusion was that the eelpouts in the Danish waters were divided into more groups than recognised by Schmidt (1917) (Christiansen et al. 1976; Simonsen and Christiansen 1985). By the end of last century and now, several studies on deformities among the larvae were published (Vetemaa et al. 1997; Strand et al. 2004; Gercken et al. 2006). Previous studies on eelpouts in the breeding season in the period 1969–1974 (Christiansen et al. 1977) collected close to Aarhus in the southern part of Kattegat revealed only a few dead individuals among the investigated litters and no deformities were observed (unpubl.). Furthermore, sampling in the breeding season 1975–1977 at a locality 30 km south of Aarhus did not reveal any deformities (unpubl.).The aim of the present study was to see if the genetic distribution in samples collected to day was deviating from the distribution found in the 1970s and if the lately recognised impaired larval development was reflected in the genotypic distribution among the eelpouts.
机译:近百年来,几位丹麦科学家一直将Eelpout(Zoarces viviparus)用作研究对象。出胚的优势在于它是胎生的,这意味着当已知雌性的基因型时,就可以识别并鉴定出父母对后代的遗传贡献。施密特早在1917年就发表了有关右胸鳍的射线数量,脊椎动物的数量,背鳍的硬射线数量以及背鳍沿色素沉着斑点数量的著作。基于脊椎动物的数量,硬射线和色素沉着斑点的第一个结论是,环境因素本身不足以解释雌性和后代之间的相似性,因此在确定这四个性状时必须涉及遗传因素。其次,确认了四大主要出水种群,其中一类生活在北海西部,一类生活在北海东部,一类生活在波罗的海西部,其中包括丹麦内部水域,一类生活在丹麦北部。在波罗的海东部。第三,在四个峡湾中发现了性状的梯度。主要的峡湾之一,Mariager峡湾,已经被研究了数次。使用Schmidt(1917)和同工酶(Christiansen等,1981,1988; Olsen等,2002)描述的分析方法对样品进行分析。 Christiansen等。 (1981,1988)发现至少60年以来形态特征几乎没有变化,一些同工酶的形态梯度与形态特征相同,这表明峡湾至少有两个种群的藻类,其中一个在内部,一个在内部。一个在峡湾的外部。然而,在1998年严重缺氧后,峡湾的几乎所有生命都被破坏了,形态特征和同工酶都显示出梯度,表明峡湾从位于峡湾以外的种群中重新定殖了(Olsen等。 2002)。在1970年代,通过同工酶分析了许多出汗。主要结论是,丹麦水域的出水被划分为更多的组,而不是Schmidt(1917)认识到的(Christiansen等,1976; Simonsen和Christiansen,1985)。到上世纪末和现在,有关幼虫畸形的一些研究已经发表(Vetemaa等,1997; Strand等,2004; Gercken等,2006)。先前在1969年至1974年繁殖季节的Kattegat南部奥尔胡斯附近收集的有关溢水的研究(Christiansen等人,1977年)显示,在所调查的垃圾中只有少数死亡个体,没有发现畸形(未发表)。 。此外,在1975年至1977年繁殖季节在奥胡斯以南30公里处进行的采样未发现任何畸形(未公布)。本研究的目的是要了解今天收集的样本中的遗传分布是否偏离了分布在1970年代,如果最近发现的幼虫发育受损,则反映在幼虫之间的基因型分布中。

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