TL;DR: This study explored functional relationships between the morphology of contrasting orb—weaver species and their prey—specific attack capabilities and found that each spider species is found most often in sites where its more successfully captured prey type is relatively more abundant.
Abstract: Previous studies indicate prey—specific attack behaviors in orb—weaving spiders. This study explored functional relationships between the morphology of contrasting orb—weaver species and their prey—specific attack capabilities. Araneus trifolium and Argiope trifasciata were observed attacking acridid Orthoptera, calyptrate Diptera, and Lepidoptera in the laboratory. Diets and habitat use of spiders in the field were determined by surveys. Distributions of prey types were determined by trapping. Araneus captured Orthoptera more quickly than did Argiope, but Argiope was more successful in capturing this prey type. There were no attack time differences between spider species on dipterans and lepidopterans, but Araneus captured these types more successfully. Attack times do not appear to limit prey intake rates in the field. Spider morphology and web design appear to interact in causing the above behavioral differences. Araneus builds its web in high, open sites, usually in herbaceous vegetation. Argiope tends to build its web in low sites in both grassy and herbaceous vegetation. Prey distributions are such that each spider species is found most often in sites where its more successfully captured prey type is relatively more abundant. Predation and physiological stress may also select for these differences in habitat use. If these results are extended to other species, the following predictions arise. Spiders with relatively short, stout legs, large fangs, and high, simple, open—meshed webs (such as Araneus) should specialize on innocuous, rapidly escaping prey types (Diptera and Lepidoptera). Spiders with relatively long legs, small fangs, and low, densely meshed, ornamented webs (such as Argiope) should specialize on dangerous, slowly escaping insects (Orthoptera, Homoptera, Hymenoptera).
TL;DR: The shrews of the Sorex araneus group have undergone a spectacular chromosome evolution, and available data suggest that the impressive chromosome polymorphism of this group is quite a recent phenomenon.
Abstract: The shrews of the Sorex araneus group have undergone a spectacular chromosome evolution. The karyotype of Sorex granarius is generally considered ancestral to those of Sorex coronatus and S. araneus. However, a sequence of 777 base pairs of the cytochrome b gene of the mitochondrial DNA (mtDNA) produces a quite different picture: S. granarius is closely related to the populations of S. araneus from the Pyrenees and from the northwestern Alps, whereas S. coronatus and S. araneus from Italy and the southern Alps represent two well-separated lineages. It is suggested that mtDNA and chromosomal evolution are in this case largely independant processes. Whereas mtDNA haplotypes are closely linked to the geographical history of the pop- ulations, chromosomal mutations were probably transmitted from one population to another. Available data suggest that the impressive chromosome polymorphism of this group is quite a recent phenomenon.
TL;DR: Measurements of the web height and counts of the number of webs on randomly selected plots in lespedeza fields reveal that immature Argiope aurantia and Argiopes trifasciata, very large araneid spiders, place their webs at different heights, while in late summer this vertical stratification disappears, while the numbers of the two species on plots become positively correlated.
Abstract: Measurements of the web height and counts of the number of webs on randomly selected plots in lespedeza fields reveal that immature Argiope aurantia and Argiope trifasciata, very large araneid spiders, place their webs at different heights. In late summer this vertical stratification disappears, while the numbers of the two species on plots become positively correlated. Coexistence of the two spider species may depend in part upon the usual occurrence of high mortality during the immature stages. Invasion of webs by araneids is reported as possible competitive interference. The two largest species of European araneids also show vertical stratification only as immatures. However, the niches of most Polish Araneus species in fields seem differentiated by parameters related to prey size: season of breeding and size differences between species.
TL;DR: A G-band composite karyotype has been prepared for the common shrew that includes multiple cut-outs of each chromosome arm derived from chromosome spreads prepared by a variety of methods by the different authors.
Abstract: A G-band composite karyotype has been prepared for the common shrew (Sorex araneus Linnaeus, 1758). This includes multiple cut-outs of each chromosome arm (in different stages of contraction) derived from chromosome spreads prepared by a variety of methods by the different authors. The important features of each chromosome arm are described. The nomenclature for the chromosome arms follows that of Halkka et al. (1974) as clarifi ed by Fredga, Nawrin (1977) and subsequent authors, i.e. italicised letters of the alphabet are used with a as the largest chromosome arm. Different authors have used a variety of methods to describe the karyotype of (a) individuals and (b) the pattern of variation within populations. Also, defi nitions of chromosomal ‘race’ differ. We suggest a standardised scheme for the description of individuals, populations and chromosomal races.
TL;DR: The diets of three species of shrew (Neomys fodiens, Sorex araneus and S. minutus) living sympatrically in an area of water-cress beds were investigated over a two-year period by faecal analysis of live-trapped animals.
Abstract: The diets of three species of shrew (Neomys fodiens, Sorex araneus and S. minutus) living sympatrically in an area of water-cress beds were investigated over a two-year period by faecal analysis of live-trapped animals. Thirty-eight different prey types were identified in the diet of N. fodiens, 25 in the diet of S. araneus and 18 in S. minutus. The most important prey items of N. fodiens in all months were freshwater crustaceans and cased trichopteran larvae. Other important items were terrestrial gastropods, coleopterans and dipterans. Neomys fodiens foraged underwater throughout the year and 33–67% of its prey were of aquatic origin. Major prey items of S. araneus throughout the year were lumbricids, terrestrial gastropods and coleopterans. Araneids, isopods and coleopterans were the dominant dietary items of S. minutus. All terrestrial prey items were taken in greater proportions by S. araneus and S. minutus than by N. fodiens, excepting lumbricids which were never eaten by S. minutus. Dietary overlap was greatest between S. araneus and S. minutus at 57%, followed by N. fodiens and S. araneus (44%) and least similar were N. fodiens and S. minutus (36%).