Schaefer Matthias
Lehrstuhl für Ökologie, Zoologisches Institut der Universität Kiel, Kiel, Deutschland.
Oecologia. 1972 Jun;9(2):171-202. doi: 10.1007/BF00345881.
In a coastal landscape at the Baltic Sea the distribution of the Lycosidae was analysed, mainly by pitfall traps. 11 dominant species occurred in the 17 different types of habitat-belonging to salt meadows, dry heath, and dunes-and were isolated with only a few exceptions. Isolation of the species was observed 1. in the macrospatial distribution, 2. in the microspatial horizontal distribution, 3. in the microspatial vertical distribution, 4. in fluctuations of population density during a period of 6 years, 5. in the seasonal periodicity, 6. in the diurnal activity.In some cases the distributional pattern overlapped in such a way that biotic relations between lycosid spiders of comparable dominance were possible. In a model study such pairs of species were observed in glass jars in the laboratory as mixed and unmixed populations with a high density (Pirata piraticus-Pardosa purbeckensis, Pardosa purbeckensis-Pardosa pullata, Alopecosa pulverulenta-Pardosa pullata). In comparison with the unmixed populations the death rate of one species in the mixed populations was higher, so that this species became extinct after a period shorter than 30 days. The factors of mortality were: 1. interference (spatial competition)-in some cases the rival was even killed (without being eaten); 2. competitive exploitation of food; 3. predator-prey-relations. These components were not clearly seperated. As this is also true for interference and predation, the predator-prey-relations should be part of the definition of "competition", at least for predatory groups. In the natural habitats only predator-prey-relations between species of lycosids not being isolated may have played a certain role.The quantitative spatial distribution of the lycosids in the 17 habitats was expressed as biovolume of the catches of one pitfall trap. It was clearly correlated with a "prey index" calculated from the biovolume of catches of collemboles, leafhoppers, and flies (r=+0.86). In contrast the Carabidae did not show any correlation with the prey index. There were "vacant niches" in the spatial and temporal distribution of predators with the same potential prey as the lycosids (in addition mainly carabids). Lycosids and carabids scarcely overlapped in their seasonal periodicity. When, in spring, both groups occurred together, obviously interference did not play an important role.Abiotic factors obviously were most important in limiting the abundance of those lycosid spiders that attained only low densities in some types of habitat. The possibility of competitive displacement of one lycosid by another was analysed on the basis of ecological data concerning the North German species. It was considered to be improbable in most cases.To sum up, the distributional pattern of the lycosids in the investigated area and their relation to other predators depend much more on endogenous factors (e.g. environmental requirements, periodicity) than on competition.
在波罗的海沿岸的一处景观中,主要通过陷阱诱捕法对狼蛛科的分布情况进行了分析。在属于盐沼、干燥石南荒原和沙丘的17种不同类型的栖息地中,出现了11种优势物种,且这些物种几乎都是孤立分布的,仅有少数例外。物种的孤立现象在以下几个方面有所体现:1. 宏观空间分布;2. 微观空间水平分布;3. 微观空间垂直分布;4. 6年间种群密度的波动;5. 季节周期性;6. 昼夜活动规律。在某些情况下,分布模式相互重叠,使得具有相当优势的狼蛛科蜘蛛之间可能存在生物关系。在一项模型研究中,在实验室的玻璃罐中观察到了这样的物种对,它们以高密度混合和非混合种群的形式存在(盗蛛 - 珀伯克豹蛛、珀伯克豹蛛 - 拉氏豹蛛、粉状肥腹蛛 - 拉氏豹蛛)。与非混合种群相比,混合种群中一个物种的死亡率更高,以至于该物种在不到30天的时间内就灭绝了。死亡因素包括:1. 干扰(空间竞争)——在某些情况下,对手甚至会被杀死(未被吃掉);2. 对食物的竞争性利用;3. 捕食者 - 猎物关系。这些因素并没有明显区分开来。由于干扰和捕食的情况也是如此,捕食者 - 猎物关系至少对于捕食性群体来说,应该是“竞争”定义的一部分。在自然栖息地中,可能只有未被孤立的狼蛛科物种之间的捕食者 - 猎物关系起到了一定作用。狼蛛科在17种栖息地中的数量空间分布,用一个陷阱诱捕器捕获量的生物量来表示。它与根据弹尾虫、叶蝉和苍蝇捕获量的生物量计算出的“猎物指数”明显相关(r = +0.86)。相比之下,步甲科与猎物指数没有任何相关性。在与狼蛛科有相同潜在猎物的捕食者(此外主要是步甲科)的时空分布中存在“空生态位”。狼蛛科和步甲科在季节周期性方面几乎没有重叠。当在春季这两个群体同时出现时,显然干扰并没有起到重要作用。非生物因素显然在限制某些栖息地中密度较低的狼蛛科蜘蛛数量方面最为重要。根据有关德国北部物种的生态数据,分析了一种狼蛛被另一种狼蛛竞争性取代的可能性。在大多数情况下,这种可能性被认为是不大的。总之,在所研究区域内狼蛛科的分布模式及其与其他捕食者的关系,更多地取决于内生因素(如环境需求、周期性),而不是竞争。