Dietary separation in three species of shrew inhabiting water-cress beds

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%).     

Small mammal populations in relation to hedgerow structure in an arable landscape

The population ecology of small mammals in hedgerows in arable farmland in eastern England is described. Features of hedgerows of importance to individual species are examined. Some 97% of the total 3042 mammals captured were wood mouse Apodemus sylvaticus , yellow-necked mouse Apodemus flavicollis , bank vole Clethrionomys glareolus and common shrew Sorex araneus . Small numbers of harvest mice Micromys minutus , field voles Microtus agrestis , pygmy shrews Sorex minutus and water shrews Neomys fodiens were also caught. Wood mouse, the most numerous species, showed a typical pattern of large numbers in autumn and winter, followed by a simultaneous decline over all hedges in early spring. Population changes were less clear in yellow-necked mouse and bank vole but the yellow-necked mouse was more scarce in the second year of study. Common shrews were most numerous in summer and declined rapidly in autumn. Hedgerow coppicing had a marked effect on yellow-necked mouse numbers but not on wood mouse. In an extensive survey of mammal numbers in relation to hedgerow features, ground cover was found to be the single largest factor influencing size of bank vole populations. Hedgerow condition (lack of gaps) was important to yellow-necked mice, which thrived only in well-established hedgerows. Wood mice appeared little influenced by the characteristics of the hedge. Common shrews were more abundant in hedgerows with adjacent permanent water.     

Habitat occurrence and prey distribution of a multi-species community of shrews in the Siberian taiga

The habitat occurrence and invertebrate prey distribution of nine species of shrew in the mid-taiga of central Siberia were investigated. Species richness ranged from 4–9 shrews per habitat. Sorex araneus and S. caecutiens were numerically dominant in all seven habitats (44 and 36% of the total catch, respectively) while Sorex minutus, S. tundrensis, S. isodon , and S. roboratus each constituted 4–6% and Sorex minutissimus, S. daphaenodon , and Neomys fodiens were rare (< 1% each). There was no overall correlation between abundance of shrews and invertebrate prey, but flood-plain habitats supported the greatest abundance and species richness of shrews, and high density and biomass of prey. Oligochaete-eating shrews were twice as numerous here as in other habitats, coincident with high abundance of oligochaetes. The large, earthworm-feeding Sorex roboratus occurred only here. The more acid, typical taiga habitats had lower adundance and species richness of shrews. They had the lowest density and biomass of prey, particularly oligochaetes, and far fewer oligochaete-eating shrews. The relative paucity of shrews in bush-meadow habitats, despite abundant prey, implied that habitat structure influences shrew distribution. Differential numbers of certain species in the presence or absence of larger congeners also suggested that interspecific competitive effects influence habitat selection by shrews. The high species richness of shrews here in the mid-taiga may be accounted for by the heterogeneous nature of the constituent habitats which provide niches for small and large species of shrew with a range of feeding habits.     

Studies on the helminth parasites of voles and shrews from Wales

The incidence and degree of infestation of the Bank vole, Clethrionomys glareolus , the Skomer vole, C. skomerensis , the Common shrew, Sorex araneus and the Pygmy shrew, S. minutus have been studied from a rough grassland and woodland area, Aberystwyth and from Skomer Island in Wales. In addition, small numbers of the Short-tailed vole, Microtus agrestis and the Water shrew, Neomys fodiens were examined for helminth parasites, when they became available. Seven new host records and six new British records are listed. The number of species of helminths in shrews, which consisted largely of digeneans and cestodes, was greater than that in voles. This is undoubtedly linked with differences in the feeding habits of the two hosts.
In Aberystwyth, where the composition of the helminth fauna was found to be more varied than that from Skomer Island, one species of nematode showed evidence of seasonal variation in the degree of infestation of Clethrionomys glareolus and four species, one digenean, two cestodes and one acantocephalan in Sorex araneus. The factors affecting this seasonal fluctuation in parasite numbers are discussed.     

Quantitative estimation of population numbers of shrews (mammalia,insectivora) after wintering

Autumn-winter mortality in shrews (Sorex araneus, S. caecutiens, S. minutus) was estimated on the basis of long-term (12 years) live-trapping on the permanent transect lines in Tver oblast. Relative as well as absolute population numbers were estimated. Lesser shrew (S. minutus) has permanently low population numbers. Fall in this species made 40.1%, and it was scattered through this term. Common shrew (Sorex araneus) lose 89.3% of population and in masked shrew (S. caecutiens) those lost was 73.6%. The most lost was found in autumn and winter fall was as least as 38,2% and 30.4% in the latter two species. The mortality is positively dependent on population density in preceding summer and with severity of winter.     

The occurrence of Centrorhynchus (Acanthocephala) in shrews (Sorex araneus and Sorex minutus) in the United Kingdom

Encysted acanthocephalans belonging to the genus Centrorhynchus were found in the body cavities of Sorex araneus (common shrew) and Sorex minutus (pygmy shrew) from Boxworth, Cambridgeshire, U.K. Fifty percent of the male S. araneus and 67% of the male S. minutus examined were found to be infected, with the mean intensity (+/-SD) being 54.3 +/- 91.3 and 14.7 +/- 18.4, respectively. The species of Centrorhynchus in the shrews may be Centrorhynchus aluconis, which is distributed widely in tawny owls, Strix aluco, in the United Kingdom. Shrews appear to serve as paratenic hosts for C. aluconis.     

Fiber capillarization relative to mitochondrial volume in diaphragm of shrew.

The objective was to examine fiber capillarization in relation to fiber mitochondrial volume in the highly aerobic diaphragm of the shrew, the smallest mammal. The diaphragms of four common shrews [Sorex araneus; body mass, 8.2 +/- 1.3 (SE) g] and four lesser shrews (Sorex minutus, 2.6 +/- 0.1 g) were perfusion fixed in situ, processed for electron microscopy, and analyzed by morphometry. Capillary length per fiber volume was extremely high, at values of 8,008 +/- 1,054 and 12,332 +/- 625 mm(-2) in S. araneus and S. minutus, respectively (P = 0.012), with no difference in capillary geometry between the two species. Fiber mitochondrial volume density was 28.5 +/- 2.3% (S. araneus) and 36.5 +/- 1.4% (S. minutus; P = 0.025), yielding capillary length per milliliter mitochondria values (S. araneus, 27.8 +/- 1.5 km; S. minutus, 33.9 +/- 2.2 km; P = 0.06) as high as in the flight muscle of the hummingbird and small bats. The size of the capillary-fiber interface (i.e., capillary surface per fiber surface ratio) per fiber mitochondrial volume in shrew diaphragm was also as high as in bird and bat flight muscles, and it was about two times greater than in rat hindlimb muscle. Thus, whereas fiber capillary and mitochondrial volume densities decreased with increased body mass in S. araneus compared with S. minutus Soricinae shrews, fiber capillarization per milliliter mitochondria in both species was much higher than previously reported for shrew diaphragm, and it matched that of the intensely aerobic flight muscles of birds and mammals.     

Water and fat contents of British shrews and their role in the seasonal changes in body weight

Water and fat contents of wild and captive Sorex araneus, S. minutus and Neomys fodiens were determined. The influence of sex, locality, body weight and age on water and fat contents of wild shrews are discussed. A seasonal cycle in both water and fat content of wild shrews is demonstrated. An investigation of captive shrews revealed fat contents to be considerably greater than in wild shrews. It is concluded that the seasonal differences in water and fat contents found in this study are of insufficient magnitude to account for the loss in body weight of wild shrews in winter or to be of any great survival value to them.     

Small mammals and their ectoparasites from the Scottish islands of Handa (Sutherland), Muck, Pabay, Scalpay and Soay (Inner Hebrides)

Small mammals were trapped on five islands for short periods during the summers of 1964 and 1965, with the following results:
Handa: Rattus norvegicus only, probably no other species present.
Muck: Sorex araneus, S. minutus, Apodemus sylvaticus and Microtus agrestis; R. norvegicus also present.
Pabay: S. minutus and Neomys fodiens ; probably no other species present.
Scalpay: S. araneus, S. minutus and M. agrestis.
Soay: S. araneus and S. minutus ; rodents almost certainly absent.
Ectoparasites (fleas and Acarina) collected from these small mammals are tabulated.     

The occurrence of the Pigmy shrew Sorex minutus on moorland, and the implications for its presence in Ireland

Throughout most of its range in western Europe, the Pigmy shrew Sorex minutus is sympatricwith the Common shrew Sorex araneus but greatly outnumbered by it. This makes it difficult to explain the presence of the Pigmy shrew, in the absence of its congener, in Ireland. A limited pitfall trapping exercise in England has shown that in moorland on deep peat, the Pigmy shrew may in fact outnumber the Common shrew. Reference to the literature on the ecology of the two shrews shows that this result is readily explained by existing knowledge of their diet; earthworms are a major prey for Common shrews and are absent from waterlogged, acidic, peats. Further, evidence on the nature of the possible land bridge from Scotland to Ireland suggests that it was at best low-lying, and probably partly flooded. By analogy with moorland, such a land bridge might have been suitable for Pigmy shrews but not for Common shrews.     

Population dynamics of shrews on small islands accord with the equilibrium model

Three of the six species of shrew in Finland, Sorex araneus, S. caecutiens, and S. minutus , are common on the mainland and widespread on islands in lakes. The islands range from 0.01 to 500 ha in area, and from 10 to 3000 m in isolation (distance from the mainland). The species-area relationship, the lack of importance of habitat diversity, the increasing frequency of unoccupied small islands with isolation, and direct observations of small populations, all suggest that populations on small islands have a high extinction rate. Demographic stochasticity is the main cause of extinctions in the superior competitor, S. araneus , which occurs consistently on islands greater than 2 ha. The small species, S. caecutiens and S. minutus , are more sensitive to environmental stochasticity than is S. araneus , and are inferior to it in interspecific competition; these factors probably contribute to the absence of the small species from many islands tens of hectares in area. Frequent colonization of islands less than 500 m from the mainland is indicated by large numbers of shrews trapped from tiny islets where breeding is not possible, by increasing epigenetic divergence of island populations with isolation, and by observations of dispersal to and colonization of islands. Dispersal ability decreases with decreasing individual size, which may partly explain the absence of the small shrews from many relatively large islands. The shrew populations persist in a dynamic equilibrium on the islands. Epigenetic morphological variation is a useful tool in ecological studies of island populations.     

Seasonal dynamics of a flea number (Siphonaptera) on the common shrew (Sorex araneus) in the north part of the Novgorod oblast

In the course of 5-year stationary investigations of the common shrew Sorex araneus in the north part of the Novgorod oblast, 12 flea species have been recorded on this host. Among them, Palaeopsylla soricis and Doratopsilla dasycnema are specific parasites of small insectivores, including the common shrew. Hystrichopsylla talpae is a polyxenous species, parasitizing both rodents and insectivores. Other 9 flea species are not common parasites of S. araneus and apparently have come to this host from other mammal species inhabiting the forest biotopes in the area of investigation. P. soricis and D. dasycnema have similar phenology of parasitism. These fleas appear in spring (April), are present during summer and autumn and disappear in winter. During a year, the abundance of these species shows three pikes, which correspond to three generations: spring (April), summer (June-July) and autumn (September-October) generation. The first species dominates in spring (April-May) and in the autumn-winter period, while the second species predominates in summer. These two species comprise over 90% of total number of fleas collected and determine general dynamics of the flea number on the shrews; during the year the flea number has a sinusoidal increasing from spring to autumn and minimum in winter.     

Shrews on small islands: epigenetic variation elucidates population stability

Three large (4 to 8 ha) and 14 small islands (0.3 to 2 ha) in a lake in eastern Finland, all situated less than 0.5 km from the mainland, were surveyed for small mammals. Three species of shrew and two species of vole were resident in July 1982: Sorex araneus on 10, S. caecutiens on 2, S. minutus on 5, Microtus agrestis on 12 and Clethrionomys glareolus on 4 islands. Immigrants were trapped from tiny islets, and the data indicate that S. caecutiens and M. agrestis are better dispersers than S. minutus and C. glareolus , respectively. Microtus agrestis, S. araneus and C. glareolus occurred non-randomly, on subsets of the larger islands, while the two small Sorex species occurred more erratically, possibly because of competition with S. araneus . Juvenile sex ratio was male-biased on the mainland but female-biased on large islands, possibly because juvenile males move more and are more likely to emigrate from an island than juvenile females.
Metrical and non-metrical (epigenetic) cranial traits gave similar patterns of population differentiation in S. araneus . Two of the three large-island populations have differentiated from the mainland populations and from each other, suggesting that the populations are relatively stable. Small-island populations, which are often less than 10 individuals in size, showed little differentiation but had more epigenetic traits fixed than large-island and mainland populations (founder effect). This suggests that the small-island populations are unstable, have a high extinction rate.     

Spatial Variability of Resident and Nonresident Populations of Small Mammals on a Forest Plot

Biology Bulletin - Abstract—The resident population density and the numbers of nonresident common shrew (Sorex araneus), Laxmann’s shrew (S. caecutiens), and the bank vole...     

The helminth fauna of the shrew genus Sorex (Insectivora: Soricidae) in the Kandalksha nature reserve

The helminth fauna of shrews (Sores araneus, S. caecutiens, S. minutus, S. minutissimus) from the Karelian coast and islands of the Kandalaksha nature reserve was studied. 18 helminth species belonging to 3 taxonomic groups, Trematoda (3), Cestoda (8), and Nematoda (7) were found. The main body of the helminth fauna of shrews is represented by the nematodes species Longistriata codrus, L. didas, and the cestode species Ditestolepis diaphana. Inhabiting of shrews in the insular localities leads to the decrease of the species diversity and the abundance of their helminths. The distribution ranges of the shrew parasites have been outlined more accurately.     

Structure and seasonal dynamics of an ectoparasite community on the common shrew (Sorex araneus) in the Il'men'-Volkhov lowland

Species composition, seasonal dynamics, and a load of ectoparasites per individual and population of the common shrew Sorex araneus have been examined in coniferous and mixed forests of the Ilmen'-Volkhov lowland (a neighbourhood of Oskuy village, Chudovo district, Novgorod Province) during the period 1999-2003. Trapping of mammals was carried monthly, with exception of few accidental gaps. The Gero traps were used for catching micromammalian hosts. The lines of trap were checked 2 times a day, places of lines changed each 3-5 day. Total number of micromammalians collected during the period of study is 3215, including 1115 specimens of the common shrew S. araneus and 246 ones of the pigmy shrew S. minutus. Parasite fauna on the common shrew included 23 ectoparasite species: fleas--12, ixodid ticks--2, gamasid mites--7, and myobiid mites--2 species. Among recorded species, 9 fleas species and some gamasid species are accidental parasites. These accidental ectoparasite species are common to the bank vole Clethrionomys glareolus in the territory investigated. Species composition, occurrence and abundance indices of parasites changed during the year. In total, about 55% shrew specimens are infected with ectoparasites. The infracommunity of ectoparasites on the common shrew usually consists of 6 species or less. Mean number of all ectoparasite individuals per one host specimens varies from 4 to 83. The greatest number of parasites (50 and 83) was recorded on the shrews, which carried 5 and 4 parasites species, respectively. Biodiversity of parasite species in the ectoparasite community on the common shrew and the load of parasites per one host specimen are lower than those in the bank vole. In forest biotopes explored, the most part of temporary ectoparasite species found on the common shrew was also recorded on other small mammals, which could have contacts with this host. It is possible to conclude that among the parasite supracommunity in the explored ecosystem, the temporary ectoparasites represent a "fond" of temporary parasites, which are common for most small mammal species. A role of different shrew and rodent species as main of additional hosts changes depending on a population density of potential mammalian hosts and other environment factors.     

Studies on the biology of the Pygmy shrew Sorex minutus in the West of Ireland

Pygmy shrews were snap-trapped over one year in grassland and occasionally in other habitats. The bodies yielded data on tooth-wear, body and skull dimensions, moulting, reproduction, food and parasites. The shrews appeared equally abundant in grassland and woodland and were more active in the day. The breeding season, population turnover, and winter body and skull regression were similar to those of other Sorex species. However, cranial regression was more marked: this may be associated with the animal's exceptionally small size. Moulting extended in autumn from August to November, and in spring from March to May, the latter in males starting earlier and perhaps lasting longer. Simultaneous and patch moults were also recorded. The litter size dropped as the breeding season progressed. The main foods were beetles, woodlice, Diptera and insect larvae; all except Diptera were eaten consistently over the year. There was a wide variety of other foods, many showing seasonal fluctuations. The commonest flea was Doratopsylla dasycnema. Palaeopsylla soricis, a common shrew-flea, widespread in the British Isles, is at least locally absent. Pygmy shrews may be the principal host of Hystrichopsylla talpae in Ireland. Rates of infestation by the trematodes and one cestode appeared to increase as the hosts aged. The tapeworm Hymenolepis scutigera, however, was commonest in juveniles. It is postulated that Doratopsylla dasycnema is its intermediate host, allowing infection of young before they leave the nest. Sorex araneus is sympatric with Sorex minutus over most of its range, but not in Ireland. In its absence, S. minutus may have been able to exploit its niche, the apparent abundance of the latter in woodland and wider variety of food consumed providing grounds for such a hypothesis.     

Cases of coat colour anomalies in the common shrew, Sorex araneus L

Coat colour anomalies in the common shrew, Sorex araneus L., in the geographical range of this species, including Poland, are extremely rare. This study describes atypically coloured common shrews. Light colouration of the coat is a result of lack ofpigment in the entire hair or hair fragments. It appears that atypically coloured shrews occur more often in isolated populations whose gene transfer with neighboring populations is limited.     

Evidence for echolocation in the common shrew, Sorex araneus

In this laboratory experiment it is shown that, like four North American soricid shrew species, the European common shrew Sorex araneus L. is able to use echolocation to identify open and closed tubes at a distance of 200 mm.
Three common shrews captured in Sweden were used for the experiments, which were carried out in darkness and within a sound-proof box. The experimental set-up eliminated orientation using sight, sound or scent from outside the experimental cage. Echolocation calls consisted of broadband ultrasonic clicks at low sound pressure. These were recorded using an ultrasound detector.
The ecological significance of echolocation in shrews is discussed. It is proposed that common shrews use echolocation to locate protective cover, thus minimizing the risk to be taken by, e.g. owls.
Echolocation may also be used for detecting obstacles in subterranean tunnels. Hence, echolocation could be of certain importance when abandoned burrows in the periphery of the tunnel system are restored during periods of increasing population densities. Since density peaks in most populations occur regularly each summer, and may reach extreme magnitudes in cyclic populations, the ecological significance of echolocation in shrews may be considerabl.     

Morphometric distances and population structuring in the common shrew <Emphasis Type="Italic">Sorex araneus</Emphasis> L. (Lipotyphla: Soricidae)

The skulls of shrews of genus Sorex from eight samplings from the European part of Russia and two from the vicinity of Novosibirsk were compared. The characteristics were identified using 22 marks on the axial skull. It was found that the centroid size differs significantly in the common and Laxmann’s shrews S. caecutiens and the pygmy shrew S. minutus, while for selected marks, the common and Laxmann’s, as well as pygmy, shrews were significantly different in form, but the differences were very small between Laxmann’s and pygmy shrews. The characteristic features of the biology of the shrews Sorex are discussed, which may contribute to understanding the general laws of the morphological evolution of the genus.