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85 results for “Apodemus”
Data from: Predation of wood mice (Apodemus sylvaticus) on hibernating bats
<p>In order to protect hibernating bats effectively, more knowledge about mortality factors is needed. This study proved the wood mouse (<em>Apodemus sylvaticus</em>) actively predates on bats. Fresh remains made by the wood mouse can be identified due to a typical pattern of lesions.</p> <p>This study was conducted in the province of Zuid-Holland, between the cities of Den Haag (The Hague), Leiden and the town of Wassenaar (between 52-070 and 52-090N, 4-180 and 4-210E). During a preliminary investigation with a trail camera, we were able to prove that wood mice actively searched for prey. Thereafter, remains of partially eaten bats have been collected and inspected in the laboratory. Bats which had not died of predation were excluded from the analysis. The remains that we found showed the typical pattern of lesions attributable to predation by wood mice. The skin of the victims is scraped clean. In the process of eating all the soft tissue, the skin is turned inside out, including the skin around the skull and hind legs. We found a total of 214 remains of predated bats during the 12 years. The resulting data are presented in this dataset.</p> <p> </p> <p>Files</p> <p><strong>Distance to entrance</strong></p> <p>Status: status of observation, this is a filter for fresh remains.</p> <p>Date: date of the observation of the remains. Note: observations were made each 2 weeks, not necessarily the date of death.</p> <p>Species: fresh remains of what bat species</p> <p>Location: name of hibernacula, location of observation</p> <p>N of animals: number of fresh remains</p> <p>Distance: distance to the exit (in meters)</p> <p> </p> <p><strong>Oak and predation</strong></p> <p>Winter: the period between September and April is defined as the winter of the year starting in January</p> <p>Predation: N of fresh remains found in one winter</p> <p>Cumulative N of bats: The cumulative population, based on the maximum population size of each site.</p> <p>Mast production of the common oak (kg): kg of acorns. We used annual data on the seed production of common oak collected by the ‘Vereniging Wildbeheer Veluwe’ in the province of Gelderland as a measure for the availability of acorns in our study area.</p> <p> </p> <p><strong>Predation and winter population</strong></p> <p>Winter: the period between September and April is defined as the winter of the year starting in January</p> <p>Predation: the Number of predated bats</p> <p>Max N: the maximum population size</p> <p>Location: the hibernacula</p>
Fig. 4 in Taxonomic Hierarchy And Evolutionary Scenario Of The Genus Group Apodemus S. L. (Muridae) Of The Palaearctic Based On Genetic Differentiation In The Gene
Fig. 4. Distribution of pairwise values of genetic distances amongst species with allopatric areas: 1 — for the Western Palearctic genus Sylvaemus; 2 — for the Eastern Palearctic genera Apodemus and Alsomys; 3 — for the Palearctic Muridae as a whole, including species of genera Micromys and Mus.
Fig. 3 in Taxonomic Hierarchy And Evolutionary Scenario Of The Genus Group Apodemus S. L. (Muridae) Of The Palaearctic Based On Genetic Differentiation In The Gene
Fig. 3. Distribution of pairwise intraspecies genetic distances within: 1 — the Western Palearctic genus Sylvaemus; 2 — the Eastern Palearctic genera Apodemus and Alsomys; 3 — in general for the Palearctic Muridae, including Micromys and Mus.
Fig. 2 in Taxonomic Hierarchy And Evolutionary Scenario Of The Genus Group Apodemus S. L. (Muridae) Of The Palaearctic Based On Genetic Differentiation In The Gene
Fig. 2. Phenogram of genetic distances (Tamura, Nei, 1993) calculated from cytb sequences amongst representatives of the genera/subgenera Alsomys, Apodemus and genera Micromys, Mus, Rattus, constructed using the UPGMA algorithm. Representatives of the Arvicolidae and Cricetidae as well as S. s. dichrurus, S. flavicollis, S. (K.) mystacinus and S. (K.) epimelas were taken as outgroups.
Fig. 5 in Taxonomic Hierarchy And Evolutionary Scenario Of The Genus Group Apodemus S. L. (Muridae) Of The Palaearctic Based On Genetic Differentiation In The Gene
Fig. 5. Distribution of pairwise genetic distances amongst taxa: 1 — Western Palearctic genus Sylvaemus, 2 — Eastern Palearctic genera Apodemus, Alsomys, 3 — Western Palearctic genus Sylvaemus and contrarily Eastern Palearctic genera Apodemus, Alsomys.
Fig. 1 in Taxonomic Hierarchy And Evolutionary Scenario Of The Genus Group Apodemus S. L. (Muridae) Of The Palaearctic Based On Genetic Differentiation In The Gene
Fig. 1. Phenogram of genetic distances calculated from cytb sequences amongst representatives of the genera Sylvaemus, Rattus, constructed using the UPGMA algorithm, as mentioned above. Microtus arvalis (Arvicolidae) and Cricetus cricetus (Cricetidae) are used as outgroups.
Fig. 1. Collectionsitesfor 91 specimensfrom 29 locationsof Apodemusagrarius, usedin thisstudy. ThespecimennumberforeachlocationarelistedinTable 1 in Comparative Genetics Of Apodemus Agrarius (Rodentia: Mammalia) From Insular And Continental Eurasian Populations: Cytochrome B Sequence Analyses
Fig. 1. Collectionsitesfor 91 specimensfrom 29 locationsof Apodemusagrarius, usedin thisstudy. ThespecimennumberforeachlocationarelistedinTable 1, andminimum Jukes-Cantordistancesbetween 17 haplotypesfrommainlandKoreaandother 49 haplo- typesfromsevenregions (Taiwan, Jeju, northeasternChina, easternChina, centralChina, Far-easternRussia, andEurope) basedonthecytochrome b completesequencesaregiven
Fig. 4 in Spatial Organization And Home Range Of Apodemus Flavicollis And A. Agrarius On Mt. Avala, Serbia
Fig. 4. Least-squared corrected means of observed range length (ORL) values (four possible density combination showing the interaction effects): A = A. flavicollis, B = A. agrarius
Fig. 6 in Spatial Organization And Home Range Of Apodemus Flavicollis And A. Agrarius On Mt. Avala, Serbia
Fig. 6. Correspondence of vegetation cover (a) and capture frequency of both species (b, c) on the grid as an indicator of their habitat preferences
Fig. 1 in Spatial Organization And Home Range Of Apodemus Flavicollis And A. Agrarius On Mt. Avala, Serbia
Fig. 1. Population densities of A. flavicollis (A) and A. agrarius (B) during the study period. The base line indicates arbitrarily defined periods of high versus low density
Fig. 5 in Spatial Organization And Home Range Of Apodemus Flavicollis And A. Agrarius On Mt. Avala, Serbia
Fig. 5. Least-squared corrected means of home range (HR) area (four possible density combination showing the interaction effects): A = A. flavicollis, B = A. agrarius
Fig. 2. A in Morphometric And Biochemical Variation And The Distribution Of The Genus Apodemus (Mammalia: Rodentia) In Turkey
Fig. 2. A scatterplot of six Apodemus species based on CVA analysis on the pooled variance covariance matrix
Fig. 4. A in Morphometric And Biochemical Variation And The Distribution Of The Genus Apodemus (Mammalia: Rodentia) In Turkey
Fig. 4. A scatterplot of Sylvaemus species based on CVA analysis on the pooled variance covariance matrix
Fig. 1 in Morphometric And Biochemical Variation And The Distribution Of The Genus Apodemus (Mammalia: Rodentia) In Turkey
Fig. 1. Distribution map of the analyzed populations of the genus Apodemus in Turkey. 1 = Edirne, 2 = Velikaköprüsü (Kirklareli), 3 = Pınarhisar (Kirklareli), 4 = Büyükkarıştıran (Tekirdağ), 5 = Istanbul, 6 = Kemalpaşa (İzmir), 7 = Buharkent (Aydin), 8 = Balıkesir, 9 = Uludağ (Bursa), 10 = Çığlıkara (Antalya), 11 = Burdur, 12 = Beyşehir (Konya), 13 = Kütahya, 14 = Kocaeli, 15 = Akçakoca (Bolu), 16 = Bolu, 17 = Çaycuma (Zonguldak), 18 = Ankara, 19 = Konya, 20 = Sebil (Mersin), 21 = Niğde, 22 = Kayseri, 23 = Kırşehir, 24 = Yozgat, 25 = Samsun, 26 = Akkuş (Ordu), 27 = Sıvas, 28 = Göksun (K = Maraş), 29 = Kırıkhan (Hatay), 30 = Kilis-Gaziantep, 31 = Malatya, 32 = Nusasbin (Mardin), 33 = Efirli (Ordu), 34 = Bulancak (Giresun), 35 = Sümela (Trabzon), 36 = İkizdere (Rize), 37 = Ayder (Rize), 38 = Hopa (Artvin), 39 = Kutul (Artvin), 40 = Posof (Ardahan), 41 = Ardahan, 42 = Iğdır, 43 = Erzurum, 44 = Muş, 45 = Van
Fig. 1 in Demographic And Morphometric Parameters Of The Yellow-Necked Mouse (Apodemus Flavicollis) In Late Autumn-Early Spring In Lithuania
Fig. 1. Dynamics of the age structure of A. flavicollis population in October–April 2004–2009. RESULTS
Fig. 1 in Short communication Arboreal behaviour of the wood mouse Apodemus sylvaticus (Rodentia: Muridae): a study in the Venetian plain
Fig. 1 - Averages and confidence intervals of the heights of the hair tubes used by the wood mouse during the sampling sessions. / Valori medi e relativi intervalli di confidenza delle altezze degli hair tube utilizzati dal topo selvatico durante le sessioni di campionamento.
Fig. 2 in Short communication Arboreal behaviour of the wood mouse Apodemus sylvaticus (Rodentia: Muridae): a study in the Venetian plain
Fig. 2 - Medulla (above) and cuticle (below) of wood mouse hair seen under an optical microscope. / Midollo (sopra) e cuticola (sotto) di peli di topo selvatico visti al microscopio ottico.
Рис. 1. ФиΛогенетические Αеревья хантавируса AMRV и его прироΑного носитеΛя восточноазиатской мыши Apodemus peninsulae Thomas, 1906. А. ФиΛогенетическое Αерево восточноазиатской мыши Apodemus peninsulae, построенное метоΑом «максимаΛьного правΑопоΑобия» (ML) и поΛученное на основе анаΛиза участка гена цитохрома b мтΔНК (744 п.н.). В узΛах ветвΛения указаны бутстреп-поΑΑержки, рассчитанные ΑΛя 1000 повторов. Цветными Λиниями обозначены фиΛогенетические Λинии: Αве Китайские (зеΛеный), Корейская «Korea» (синий), Амурская «Amur» (красный). ПоΛужирным шрифтом выΑеΛены собственные образцы. Названия образцов из GenBank/NCBI быΛи сокращены; B. ФиΛогенетическое Αерево из работы Α. Н. Яшиной с ΑопоΛнениями, построенное метоΑом «бΛижайшего сосеΑа» (NJ) на основе посΛеΑоватеΛьностей фрагмента М-сегмента (2737–2980 н.п.) генома хантавирусов. В узΛах ветвΛения указаны бутстреппоΑΑержки, рассчитанные ΑΛя 1000 повторов. Жирным выΑеΛены иссΛеΑованные РНК изоΛяты (Яшина 2012; Яшина и Αр. 2019) Fig. 1. Phylogenetic trees of AMRV and its natural reservoir host — the Korean field mouse Apodemus peninsulae Thomas, 1906. A. Phylogenetic tree of the Korean field mouse Apodemus peninsulae constructed by the "maximum likelihood" method (ML). The data are obtained from the analysis of the cytochrome b mtDNA gene fragments (744 bp). Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. Colored lines indicate phylogenetic lines: two Chinese (green), Korea (blue), and Amur (red). Own samples are highlighted in bold. The names of the samples from GenBank/NCBI have been shortened; B. Phylogenetic tree from L. N. Yashina's work with additions constructed by the neighbour joining method (NJ). It is based on the sequences of an M-segment fragment (2737–2980 bp) of the hantavirus genome. Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. The researched RNA isolates are highlighted in bold (Yashina 2012; Yashina et al. 2019) in Variability of the gene cyt b in the Korean field mouse Apodemus peninsulae Thomas, 1906 - a reservoir host of AMRV in the Khasansky District of Primorsky Krai
Рис. 1. ФиΛогенетические Αеревья хантавируса AMRV и его прироΑного носитеΛя восточноазиатской мыши Apodemus peninsulae Thomas, 1906. А. ФиΛогенетическое Αерево восточноазиатской мыши Apodemus peninsulae, построенное метоΑом «максимаΛьного правΑопоΑобия» (ML) и поΛученное на основе анаΛиза участка гена цитохрома b мтΔНК (744 п.н.). В узΛах ветвΛения указаны бутстреп-поΑΑержки, рассчитанные ΑΛя 1000 повторов. Цветными Λиниями обозначены фиΛогенетические Λинии: Αве Китайские (зеΛеный), Корейская «Korea» (синий), Амурская «Amur» (красный). ПоΛужирным шрифтом выΑеΛены собственные образцы. Названия образцов из GenBank/NCBI быΛи сокращены; B. ФиΛогенетическое Αерево из работы Α. Н. Яшиной с ΑопоΛнениями, построенное метоΑом «бΛижайшего сосеΑа» (NJ) на основе посΛеΑоватеΛьностей фрагмента М-сегмента (2737–2980 н.п.) генома хантавирусов. В узΛах ветвΛения указаны бутстреппоΑΑержки, рассчитанные ΑΛя 1000 повторов. Жирным выΑеΛены иссΛеΑованные РНК изоΛяты (Яшина 2012; Яшина и Αр. 2019) Fig. 1. Phylogenetic trees of AMRV and its natural reservoir host — the Korean field mouse Apodemus peninsulae Thomas, 1906. A. Phylogenetic tree of the Korean field mouse Apodemus peninsulae constructed by the "maximum likelihood" method (ML). The data are obtained from the analysis of the cytochrome b mtDNA gene fragments (744 bp). Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. Colored lines indicate phylogenetic lines: two Chinese (green), Korea (blue), and Amur (red). Own samples are highlighted in bold. The names of the samples from GenBank/NCBI have been shortened; B. Phylogenetic tree from L. N. Yashina's work with additions constructed by the neighbour joining method (NJ). It is based on the sequences of an M-segment fragment (2737–2980 bp) of the hantavirus genome. Bootstrap supports calculated for 1,000 repeats are indicated in the branching nodes. The researched RNA isolates are highlighted in bold (Yashina 2012; Yashina et al. 2019)
Fig. 2 in Molecular confirmation of Hymenolepis hibernia in field mice (Apodemus sylvaticus) from St Kilda has potential to resolve a host-parasite relationship
Fig. 2. The Sanger sequence of 385 bp of mt-Cox-1 fragments of cyclophyllidean DNA generated from eggs recovered from mouse 9 and faeces X (6. H-HA25), aligned with 5 corresponding H. hibernia sequences published in the NCBI Genbank database. There are 12 intraspecific SNPs at positions 5, 60, 78, 84, 90, 156, 216, 219, 252, 262, 291 and 318. GeneBank submission ID: 2151861.
Fig. 1 in Molecular confirmation of Hymenolepis hibernia in field mice (Apodemus sylvaticus) from St Kilda has potential to resolve a host-parasite relationship
Fig. 1. Examples of cyclophyllidean tapeworms and eggs recovered from Apodemus sylvaticus viscera and faeces. A: Unarmed scolex of an intact tapeworm - mouse 5. B: Anoplocephalid tapeworm egg - mouse 8. C: Hymenolepidid egg cropped without changing dimensions from the same image as B, for comparison - mouse 8. D: Anoplocephalid tapeworm egg - mouse X (faeces from a cleat). E: Anoplocephalid onchosphere released after squashing an egg under a cover slip - mouse X (faeces from a cleat). F: Tapeworm from mouse 8 (scolex not intact). G: hymenolepidid tapeworm egg - mouse X (faeces from a cleat). H: Hexacanth onchosphere surrounded by an onchospheral membrane and inner zone of the embryophore, which has swollen, having been released from the egg shell by squashing under a cover slip - mouse 9. I: Hymenolepidid tapeworm egg - mouse 7. J: Hexacanth onchosphere surrounded by an intact onchospheral membrane and inner and outer zones of the embryophore, being released from a cracked egg shell by squashing under a cover slip - mouse 7. K: Hymenolepidid tapeworm egg - mouse 8. L: Hexacanth onchosphere surrounded by an onchospheral membrane and inner zone of the embryophore, which has swollen, having been released from the egg shell by squashing under a cover slip - mouse 8.
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