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10 results for “Microtus agrestis”

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zenodo40/100

Text-fig. 6. Molars of Microtus from Mikhailovka-5. Microtus ex gr. agrestis LINNAEUS, 1761: a–l: M2, m–s: M3; Microtus (Terricola) ex gr. subterraneus (SELYS-LONGCHAMPS, 1836): t–z: m1, aa–ab: m2, ac–ag: M3. in Late Pleistocene (Eemian) Mollusk And Small Mammal Fauna From Mikhailovka-5 (Kursk Oblast, Central Russia)

Text-fig. 6. Molars of Microtus from Mikhailovka-5. Microtus ex gr. agrestis LINNAEUS, 1761: a–l: M2, m–s: M3; Microtus (Terricola) ex gr. subterraneus (SELYS-LONGCHAMPS, 1836): t–z: m1, aa–ab: m2, ac–ag: M3.

opencc-by-4.0Nov 2020View details →
zenodo40/100

Text-fig. 5. Molars of Microtus ex gr. agrestis LINNAEUS, 1761 from Mikhailovka-5. a–l: m1, m–r: M1. in Late Pleistocene (Eemian) Mollusk And Small Mammal Fauna From Mikhailovka-5 (Kursk Oblast, Central Russia)

Text-fig. 5. Molars of Microtus ex gr. agrestis LINNAEUS, 1761 from Mikhailovka-5. a–l: m1, m–r: M1.

opencc-by-4.0Nov 2020View details →
zenodo32/100

FIGURE 15. Eurotaenia gracilis. A. Scolex and neck from Microtus agrestis from Finland. B in Phylogenetic relationships and taxonomic revision of Paranoplocephala Lühe, 1910 sensu lato (Cestoda, Cyclophyllidea, Anoplocephalidae)

FIGURE 15. Eurotaenia gracilis. A. Scolex and neck from Microtus agrestis from Finland. B. Mature proglottid from Dinaromys bogdanovi from Bosnia.

opennotspecifiedDec 2014View details →
zenodo32/100

FIGURE 6. Paranoplocephala omphalodes from Microtus agrestis from Finland. A. Scolex and neck. B in Phylogenetic relationships and taxonomic revision of Paranoplocephala Lühe, 1910 sensu lato (Cestoda, Cyclophyllidea, Anoplocephalidae)

FIGURE 6. Paranoplocephala omphalodes from Microtus agrestis from Finland. A. Scolex and neck. B. Mature proglottid.

opennotspecifiedDec 2014View details →
zenodo32/100

On following pages: 115. Reed Vole (Alexandromys fortis); 116. Sakhalin Vole (Alexandromys sachalinensis); 117. Mongolian Vole (Alexandromys mongolicus); 118. Middendorff's Vole (Alexandromys middendorffii; 119. Gromov's Vole (Alexandromys gromovi); 120. Lacustrine Vole (Alexandromys limnophilus); 121. Root Vole (Alexandromys oeconomus); 122. Taiwan Vole (Alexandromys kikuchii); 123. Japanese Grass Vole (Alexandromys montebell); 124. Afghan Vole (Microtus afghanus); 125. Bucharian Vole (Microtus bucharensis); 126. Juniper Vole (Microtus juldaschi); 127. Short-tailed Field Vole (Microtus agrestis); 128. Mediterranean Field Vole (Microtus lavernedii): 129. Portuguese Field Vole (Microtus rozianus); 130. Insular Vole (Microtus abbreviatus); 131. Singing Vole (Microtus miurus); 132. Rock Vole (Microtus chrotorrhinus); 133. Zempoaltepec Vole (Microtus umbrosus); 134. Tarabundi Vole (Microtus oaxacensis); 135. Guatemalan Vole (Microtus guatemalensis); 136. Woodland Vole (Microtus pinetorum); 137. Jalapan Vole (Microtus quasiater); 138. California Vole (Microtus californicus): 139. Beach Vole (Microtus brewer); 140. Mexican Vole (Microtus mexicanus); 141. Mogollon Vole (Microtus mogollonensis); 142. Prairie Vole (Microtus ochrogasten; 143. Taiga Vole (Microtus xanthognathus); 144. Cabrera''s Vole (Microtus cabrerae); 145. North American Water Vole (Microtus richardson); 146. Gray-tailed Vole (Microtus canicaudus). in Cricetidae

On following pages: 115. Reed Vole (Alexandromys fortis); 116. Sakhalin Vole (Alexandromys sachalinensis); 117. Mongolian Vole (Alexandromys mongolicus); 118. Middendorff's Vole (Alexandromys middendorffii; 119. Gromov's Vole (Alexandromys gromovi); 120. Lacustrine Vole (Alexandromys limnophilus); 121. Root Vole (Alexandromys oeconomus); 122. Taiwan Vole (Alexandromys kikuchii); 123. Japanese Grass Vole (Alexandromys montebell); 124. Afghan Vole (Microtus afghanus); 125. Bucharian Vole (Microtus bucharensis); 126. Juniper Vole (Microtus juldaschi); 127. Short-tailed Field Vole (Microtus agrestis); 128. Mediterranean Field Vole (Microtus lavernedii): 129. Portuguese Field Vole (Microtus rozianus); 130. Insular Vole (Microtus abbreviatus); 131. Singing Vole (Microtus miurus); 132. Rock Vole (Microtus chrotorrhinus); 133. Zempoaltepec Vole (Microtus umbrosus); 134. Tarabundi Vole (Microtus oaxacensis); 135. Guatemalan Vole (Microtus guatemalensis); 136. Woodland Vole (Microtus pinetorum); 137. Jalapan Vole (Microtus quasiater); 138. California Vole (Microtus californicus): 139. Beach Vole (Microtus brewer); 140. Mexican Vole (Microtus mexicanus); 141. Mogollon Vole (Microtus mogollonensis); 142. Prairie Vole (Microtus ochrogasten; 143. Taiga Vole (Microtus xanthognathus); 144. Cabrera''s Vole (Microtus cabrerae); 145. North American Water Vole (Microtus richardson); 146. Gray-tailed Vole (Microtus canicaudus).

opennotspecifiedNov 2017View details →
dryad32/100

Microtus agrestis microbiome reads, taxonomy and related animal metadata

<p class="MsoNormal">Mammalian gastrointestinal microbiomes are highly variable, both within individuals and across populations, with changes linked to time and ageing being widely reported. Discerning patterns of change in wild mammal populations can therefore prove challenging. We used high-throughput community sequencing methods to characterise the microbiome of wild field voles (<em>Microtus agrestis</em>) from faecal samples collected across 12 live-trapping field sessions, and then at cull. Changes in α- and β-diversity were modelled over three timescales. Short-term differences (following 1–2 days captivity) were analysed between capture and cull, to ascertain the degree to which the microbiome can change following a rapid change in environment. Medium-term changes were measured between successive trapping sessions (12–16 days apart), and long-term changes between the first and final capture of an individual (from 24 to 129 days). The short period between capture and cull was characterised by a marked loss of species richness, while over medium- and long-term in the field, richness slightly increased. Changes across both short and long timescales indicated shifts from a Firmicutes-dominant to a Bacteroidetes-dominant microbiome. Dramatic changes following captivity indicate that changes in microbiome diversity can be rapid, following a change of environment (food sources, temperature, lighting etc.). Medium- and long-term patterns of change indicate an accrual of gut bacteria associated with ageing, with these new bacteria being predominately represented by Bacteroidetes. While the patterns of change observed are unlikely to be universal to wild mammal populations, the potential for analogous shifts across timescales should be considered whenever studying wild animal microbiomes. This is especially true if studies involve animal captivity, as there are potential ramifications both for animal health, and the validity of the data itself as a reflection of a 'natural' state of an animal.</p>

opencc-zeroFeb 2023View details →
dryad32/100

Microtus agrestis microbiome reads, taxonomy and related animal metadata

Open the record for dataset details and reuse information.

publicApr 2025View details →
dryad32/100

Data from: From the animal house to the field: are there consistent individual differences in immunological profile in wild populations of field voles (Microtus agrestis)?

Open the record for dataset details and reuse information.

publicJul 2018View details →
dryad32/100

Data from: Gene flow and population structure of a common agricultural wild species (Microtus agrestis) under different land management regimes

Open the record for dataset details and reuse information.

publicJun 2013View details →
dryad32/100

Data from: Evidence for selection at cytokine loci in a natural population of field voles (Microtus agrestis)

Open the record for dataset details and reuse information.

publicDec 2011View details →

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