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15 results for “Cervus nippon”
Рис. 4. Карта-схема мест встреч пятнистого оΛеня в Нижнем Приамурье в 1979–2021 гг. КваΑраты — места фоторегистрации: 1 — верховья рр. Обор и Àурмин; 2, 3 — Анюйский национаΛьный парк; круги — места встреч по Λитературным и опросным Αанным: 1 — окрестности с. Кутузовка (место первой регистрации в 1979 г.); 2 — верховья р. СиΑима; 3 — устье р. Нижняя Буге; 4 — бассейн р. Мухен; 5–8 — Анюйский национаΛьный парк (соответственно, р. Пихца, урочище Сира, окрестности с. Арсеньево, устье р. СоΛоми); 9 — среΑнее течение р. СоΛоми; 10 — 76 км трассы ΔиΑога — Ванино; 11 — бассейн р. Кия; 12 — бассейн р. ХойΑур; 13 — бассейн р. Нюра Fig. 4. A schematic map of sika deer sightings in the Lower Amur Region in 1979-2021. Squares designate sites of photo recording: 1 — upper reaches of the rivers Obor and Durmin; 2, 3 — Anyui National Park; circles designate sightings sites according to the literature and the survey data: 1 — vicinity of the village Kutuzovka (the place of the first registration in 1979); 2 — upper reaches of the river Sidima; 3 — the mouth of the river Lower Buge; 4 — the Mukhen River basin; 5-8 —Anyui National Park (respectively, the Pikhtsa River, the Sira tract, the vicinity of the village Arsenyevo, the mouth of the Solomi River); 9 — the middle course of the Solomi River; 10 — 76 km of the Lidoga-Vanino Highway; 11 — the Kiya River basin; 12 — the Khoydur River basin; 13 — the Nyura River basin in New data on the distribution of sika deer Cervus nippon Temminck, 1838 in the Lower Amur Region
Рис. 4. Карта-схема мест встреч пятнистого оΛеня в Нижнем Приамурье в 1979–2021 гг. КваΑраты — места фоторегистрации: 1 — верховья рр. Обор и Àурмин; 2, 3 — Анюйский национаΛьный парк; круги — места встреч по Λитературным и опросным Αанным: 1 — окрестности с. Кутузовка (место первой регистрации в 1979 г.); 2 — верховья р. СиΑима; 3 — устье р. Нижняя Буге; 4 — бассейн р. Мухен; 5–8 — Анюйский национаΛьный парк (соответственно, р. Пихца, урочище Сира, окрестности с. Арсеньево, устье р. СоΛоми); 9 — среΑнее течение р. СоΛоми; 10 — 76 км трассы ΔиΑога — Ванино; 11 — бассейн р. Кия; 12 — бассейн р. ХойΑур; 13 — бассейн р. Нюра Fig. 4. A schematic map of sika deer sightings in the Lower Amur Region in 1979-2021. Squares designate sites of photo recording: 1 — upper reaches of the rivers Obor and Durmin; 2, 3 — Anyui National Park; circles designate sightings sites according to the literature and the survey data: 1 — vicinity of the village Kutuzovka (the place of the first registration in 1979); 2 — upper reaches of the river Sidima; 3 — the mouth of the river Lower Buge; 4 — the Mukhen River basin; 5-8 —Anyui National Park (respectively, the Pikhtsa River, the Sira tract, the vicinity of the village Arsenyevo, the mouth of the Solomi River); 9 — the middle course of the Solomi River; 10 — 76 km of the Lidoga-Vanino Highway; 11 — the Kiya River basin; 12 — the Khoydur River basin; 13 — the Nyura River basin
Рис. 2. МоΛоΑая особь; 01.06.2017. 19:45. Фото В. В. Пронкевича Fig. 2. A juvenile; 06.01.2017. 19:45. Photo by V. V. Pronkevich in New data on the distribution of sika deer Cervus nippon Temminck, 1838 in the Lower Amur Region
Рис. 2. МоΛоΑая особь; 01.06.2017. 19:45. Фото В. В. Пронкевича Fig. 2. A juvenile; 06.01.2017. 19:45. Photo by V. V. Pronkevich
Рис. 3. Самка; правый берег р. Анюй, окрестности корΑона «ТаΛый», 11.08.2021. 09:50. Фото А. В. Готванского Fig. 3. A female; right bank of the river Anyui, vicinity of the Taly ranger station, 11.08.2021. 09:50. Photo by A. V. Gotvansky in New data on the distribution of sika deer Cervus nippon Temminck, 1838 in the Lower Amur Region
Рис. 3. Самка; правый берег р. Анюй, окрестности корΑона «ТаΛый», 11.08.2021. 09:50. Фото А. В. Готванского Fig. 3. A female; right bank of the river Anyui, vicinity of the Taly ranger station, 11.08.2021. 09:50. Photo by A. V. Gotvansky
Рис. 5. Пятнистый оΛень неоΑнократно снят фотоΛовушками в бассейнах рек Обор и Àурмин. 15.10.2020. 14.49. Фото А. С. БатаΛова Fig. 5. Sika deer repeatedly photographed by camera traps in the basins of the rivers Obor and Durmin; 15.10.2020. 14:49. Photo by A. S. Batalova in New data on the distribution of sika deer Cervus nippon Temminck, 1838 in the Lower Amur Region
Рис. 5. Пятнистый оΛень неоΑнократно снят фотоΛовушками в бассейнах рек Обор и Àурмин. 15.10.2020. 14.49. Фото А. С. БатаΛова Fig. 5. Sika deer repeatedly photographed by camera traps in the basins of the rivers Obor and Durmin; 15.10.2020. 14:49. Photo by A. S. Batalova
Рис. 1. Самец пятнистого оΛеня на берегу р. Анюй; 01.06.2017. 19:44. Фото В. В. Пронкевича Fig. 1. A male of a spotted deer on the bank of the river Anyui; 06.01.2017. 19:44. Photo by V. V. Pronkevich in New data on the distribution of sika deer Cervus nippon Temminck, 1838 in the Lower Amur Region
Рис. 1. Самец пятнистого оΛеня на берегу р. Анюй; 01.06.2017. 19:44. Фото В. В. Пронкевича Fig. 1. A male of a spotted deer on the bank of the river Anyui; 06.01.2017. 19:44. Photo by V. V. Pronkevich
Fig. 2 in Morphological and molecular characteristics of seven Sarcocystis species from sika deer (Cervus nippon centralis) in Japan, including three new species
Fig. 2. Light microscopic appearance of sarcocysts isolated from sika deer from Gifu Prefecture, Central Japan. a-d Thumb-like (a, b) and elongated finger-like (c, d) protrusions (P) of S. japonica. e, f Finger-like protrusions in S. cf. tarandi (e) and S. matsuoae (f). g, h Hair-like protrusions in S. pilosa (g) and S. gjerdei (h). i Indistinct protrusions on cyst S. cf. taeniata. j, k Oval sarcocyst of S. ovalis (j); cyst surrounded by fibrous layer (FL), making the slanting tongue-like protrusions (arrow) nearly invisible (k).
Fig. 1 in Morphological and molecular characteristics of seven Sarcocystis species from sika deer (Cervus nippon centralis) in Japan, including three new species
Fig. 1. Phylogenetic tree based on 322 partial sequences of cox1 of 61 taxa, including the seven Sarcocystis species (types 1–7) from this study and inferred using the neighbour-joining method and with evolutionary distances computed using the p-distance method. Bootstrap support (1000 replicates) is shown at each node. Subtrees formed by two or more haplotypes of the same species have been collapsed. The number of haplotypes included is given in parentheses. The number of sequences of each Sarcocystis species used in this analysis and their GenBank accession numbers are shown in Table S3.
Fig. 2 in Effects of introduced sika deer (Cervus nippon) and population control activity on the distribution of Haemaphysalis ticks in an island environment
Fig. 2. Seasonal changes in tick abundance of the dominant species (A) H. megaspinosa, (B) H. longicornis, and (C) H. cornigera on Niijima Island. (Broken line with black dot: Larvae, Dotted-dashes line with back triangles: Nymphs, Solid line with crosses: Adults).
Fig. 3 in Effects of introduced sika deer (Cervus nippon) and population control activity on the distribution of Haemaphysalis ticks in an island environment
Fig. 3. Statistical summary of the abundances of H. megaspinosa larvae. (A) Days since the last sika deer was captured in August–November, (B) days since the last sika deer was captured in August–November for the high sika deer group, and (C) days since the last sika deer was captured in August–November for the low sika deer group. (X mark inside box: mean, lower and upper side of the box: first and third quartiles, line inside box: median, lower and upper error lines 10th and 90th percentiles, respectively, circles: data falling outside 10th and 90th percentiles).
Fig. 1 in Effects of introduced sika deer (Cervus nippon) and population control activity on the distribution of Haemaphysalis ticks in an island environment
Fig. 1. Map of Niijima Island, with locations of foot snare traps (black circle), and tick collection routes for the tick survey conducted June, August, and November of 2018 and February of 2019 (orange area). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Figure 1 in The complete mitochondrial genome of the Chinese Sika deer (Cervus nippon Temminck, 1838), and phylogenetic analysis among Cervidae, Moschidae and Bovidae
Figure 1. Molecular phylogenetic tree derived from complete DNA sequence of 12 mitochondrial protein-coding genes using Bayesian inference and maximum parsimony analysis. The numbers beside the nodes are Bayesian posterior probabilities and bootstrap proportions. Equus asinus and Equus caballus were set as out-groups.
Data for: Seasonal home range and habitat selection patterns of sika deer Cervus nippon in southern Hokkaido, Japan
<p>In 1980 and 1981, eight and nine individual sika deer <em>Cervus nippon</em> were reintroduced in southern Hokkaido, Japan, respectively, to address population declines in this species during 1900s. As recent population growth has led to human–wildlife conflicts, this study investigated the responses of sika deer to resource availability and geomorphic factors during the summer and winter seasons in southern Hokkaido. Global positioning system-collared data collected from 2016 to 2018 were used to assess the home range patterns and habitat selection of 14 female sika deer located in Mount Esan and Shiriuchi. The core home range size was defined using a 50% kernel density estimation that indicated a larger home range in winter than summer for all deer. Habitat selection was assessed using generalized linear mixed models. The results showed variation in habitat selection between resident deer of Mount Esan and Shiriuchi, as well as migratory deer in Shiriuchi during summer. Resident deer in Mount Esan and Shriuchi preferred areas closer to crops during summer. Interaction effects revealed that migratory deer utilized natural grassland close to forest edge habitat in Shiriuchi. By contrast, resident deer in Shiriuchi selected forest edge habitat and natural grasslands close to crops. In winter, low elevation was the most important habitat factor for all deer across the study area. Thus, sika deer habitat selection depends on resource availability in summer and topographic factors in the winter.</p>
Data for: Seasonal home range and habitat selection patterns of sika deer Cervus nippon in southern Hokkaido, Japan
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Supplementary material 1 from: Wang D, Hu X, Li M, Liu J, Tang M, Liu W, Zhan J, Xu Y, Zhang W (2023) Diet composition and interspecific niche of Taohongling Sika deer (Cervus nippon kopschi) and its sympatric Reeve's muntjac (Muntiacus reevesi) and Chinese hare (Lepus sinensis) in winter (Animalia, Mammalia). ZooKeys 1149: 17-36. https://doi.org/10.3897/zookeys.1149.96936
Dietary of Sika deer, Reeves՚ muntjac and Chinese hare
Data from: Comparing two classes of alpha diversities and their corresponding beta and (dis)similarity measures, with an application to the Formosan sika deer (Cervus nippon taiouanus) reintroduction program
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