日本日光地区森林中梅花鹿的夏季巢区面积和内部利用

为了估算梅花鹿(Cervusnippon)巢区面积和内部利用以及雌雄个体间的比较,于1993-1997年在日本国日光国立公园使用无线电遥测定位法测定了8头成年雌鹿和4头雄鹿(包括1头亚成年)在森林生境中的活动定位点。按照当地梅花鹿离开和返回越夏地的日期,使用每年6月1日至10月25日的无线电遥测定位数据,采用定值核心法(Fixed kernel)计算了梅花鹿的夏季巢区面积和内部利用密度分布。梅花鹿雄鹿夏季巢区面积(192·5±50·5 hm2)显著大于雌鹿(115·7±56·7 hm2,P=0·017) ,其半家区面积(HRS0·50)和核心区面积(HRS0·25)也显著大于雌鹿(依次为P=0·027和P=0·042) ,但巢区内部利用集中度指标Ah(HRS0·50/HRS0·95)和Ac(HRS0·25/HRS0·50)在雌雄鹿之间没有显著性差异(依次为P=0·999和P=0·234)。在无线电遥测的12头梅花鹿中, 11头个体的巢区为单核心型,只有1头成年雄鹿的巢区为双核心型。11头梅花鹿个体的混合数据显示巢区面积和体重之间存在显著性相关(P=0·049) [动物学报52 (2) : 235 -241 , 2006]。     

啮齿动物巢区研究进展

巢区 (ｈｏｍｅｒａｎｇｅ)这一术语为生物学家们所使用是从 190 9年Ｓｅｌｔｏｎ开始的 ,直到 194 0年才由Ｂｕｒｔ定义为 :巢区是动物在其巢附近进行取食、生殖、育幼等日常活动的区域[54 ] 。此后 ,这一概念几乎没有争议 ,只是有些学者在与领域概念的使用上未加严格区分 ,而多数学者强调领域只是巢区中不允许同种其它个体侵入而受到严格保护的核心部分[2 ] 。近年Ｂｏｎｄ等[19] 提出最适巢区概念 ,为深入分析鼠类繁殖策略、进化及其巢区生态学功能提供了新思路 ,已成为巢区研究的一个重要方向。绝大多数啮齿动物营穴居生活 ,巢区研究对…     

动物巢区二维正态概率模型的探讨

本文根据二维正态分布的性质以及识别动物极端活动位点的技术建立了一种动物巢区二维正态概率模型。应用中,首先对动物活动位点进行二维正态分布检验,采用加权法消除了极端位点的影响。在二维正态分布条件下,动物巢区定义为由下列方程决定的椭圆区域d_β由下列方程组确定其中β为巢区所含活动位点百分比,a_i(i=1,2,…6)为常数。椭圆巢区两半轴长分别为d_β·面积为π·d_β·σ_x~2 ·椭圆的方向由坐标轴旋转角     

高原鼠兔家群空间领域的季节性动态格局

为探讨高原鼠兔家群空间领域的季节特征,分别于2005年和2006年的5～8月,在青海省玛沁县,采用标志重捕法和最小多边形面积法对其家群巢区和核域进行了研究.结果表明,不同季节,高原鼠兔巢区和核域面积存在显著差异.5、6月份,成体巢区面积显著大于幼体,但二者核域面积却无显著差异;7月份,成体与第1胎幼体巢区及核域面积均显著大于第2胎.5、6月份雄性成体巢区显著大于7、8月份,6、7月份雌性成体巢区显著大于5月和8月份.巢区及核域面积均与家群个体数呈极显著性正相关关系,说明季节和家群结构均可对高原鼠兔空间领域产生重要作用.     

河北唐海湿地四种鹭的种群动态和繁殖空间生态位

2004年8月—2005年7月对河北唐海湿地夜鹭(Nycticorax nycticorax)、白鹭(Egtetta garzetta)、池鹭(Ardeola bacchus)、大白鹭(Casmerodius albus)的种群动态和繁殖行为进行了观察，并对巢群关系进行了研究。统计了4种鹭垂直和水平巢位的巢密度，计算了不同种鹭巢的生态位重叠、生态位宽度值。结果：4种鹭在唐海数量最多月份为4—9月，最大量达到了近5 800只。共有Ⅰ、Ⅱ两个巢区，迁来Ⅱ区时间较Ⅰ区晚半个月左右。除池鹭外，3种鹭之间均有争巢现象，后期趋于稳定。迫于密度压力和竞争，部分白鹭和池鹭取食范围较广。除大白鹭外，其他3种鹭同种间均有混交现象。 在混巢区，夜鹭迁来最早，数量最大，为优势种，多数占据中心区的顶巢；大白鹭数量最少，亦占据中心区的顶巢；白鹭迁来较晚，占据中位巢；池鹭迁来最晚，数量较白鹭少，多数在边缘区单独筑巢，少数在中心区占下位巢。白鹭巢的垂直生态位最宽；夜鹭巢的水平生态位最宽；池鹭巢的综合空间生态位最宽。池鹭和夜鹭巢位的空间格局最为相似，池鹭和白鹭的生态位重叠较大。夜鹭的数量最多、大白鹭的个体最大，导致其处于优势；白鹭和池鹭数量少、个体小，导致其处于劣势。唐海湿地内丰富的食物和适宜的林带是鹭鸟密度较大的主要原因。此外，鹭类只筑巢在散布的、双行杨树林带均高为22 m以上区域，是该地鹭类巢区的主要特点。     

种群外部及内部因子对东方田鼠巢区大小的效应

在野外围栏条件下, 采用重复的2×2×2析因实验, 测定外部和内部因子对东方田鼠(Microtus fortis)巢区大小的作用模式。研究结果表明, 雄体巢区大小显著大于雌体巢区大小。雄体巢区大小与体重存在显著的正相关, 而雌体巢区大小与体重的相关不显著; 雄体和雌体巢区大小与种群数量均呈显著的线性负相关。外部因子对东方田鼠雄体和雌体巢区大小的作用不一致。在排除内部因子种群数量及体重对雄体巢区大小作用的条件下, 食物对雄体巢区大小的作用显著; 而捕食及种间竞争的独立作用及其交互作用, 以及3 种外部因子的交互作用均不显著; 在排除种群数量对巢区大小作用的条件下, 食物与捕食的独立作用及3 种外部因子的交互作用对雌体巢区大小的效应均达到显著水平, 食物与种间竞争的交互作用接近显著, 而种间竞争的独立作用、食物和捕食的交互作用, 以及捕食与种间竞争的交互作用对雌体巢区大小的效应均不显著。本文结果验证了种群外部因子食物、捕食及种间竞争、种群内部因子种群数量及个体体重对田鼠种群巢区大小具有独立和交互作用的假设。     

河北唐海湿地四种鹭的种群动态和繁殖空间生态位

2004年8月—2005年7月对河北唐海湿地夜鹭(Nycticoraxnycticorax)、白鹭(Egtettagarzetta)、池鹭(Ardeolabacchus)、大白鹭(Casmerodiusalbus)的种群动态和繁殖行为进行了观察,并对巢群关系进行了研究。统计了4种鹭垂直和水平巢位的巢密度,计算了不同种鹭巢的生态位重叠、生态位宽度值。结果4种鹭在唐海数量最多月份为4—9月,最大量达到了近5800只。共有Ⅰ、Ⅱ两个巢区,迁来Ⅱ区时间较Ⅰ区晚半个月左右。除池鹭外,3种鹭之间均有争巢现象,后期趋于稳定。迫于密度压力和竞争,部分白鹭和池鹭取食范围较广。除大白鹭外,其他3种鹭同种间均有混交现象。在混巢区,夜鹭迁来最早,数量最大,为优势种,多数占据中心区的顶巢;大白鹭数量最少,亦占据中心区的顶巢;白鹭迁来较晚,占据中位巢;池鹭迁来最晚,数量较白鹭少,多数在边缘区单独筑巢,少数在中心区占下位巢。白鹭巢的垂直生态位最宽;夜鹭巢的水平生态位最宽;池鹭巢的综合空间生态位最宽。池鹭和夜鹭巢位的空间格局最为相似,池鹭和白鹭的生态位重叠较大。夜鹭的数量最多、大白鹭的个体最大,导致其处于优势;白鹭和池鹭数量少、个体小,导致其处于劣势。唐海湿地内丰富的食物和适宜的林带是鹭鸟密度较大的主要原因。此外,鹭类只筑巢在散布的、双行杨树林带均高为22m以上区域,是该地鹭类巢区的主要特点。     

樟巢螟成虫的求偶及交配行为

在光周期14 L∶〖KG-*2〗10 D、温度（27±1） ℃、相对湿度（60±10）%的室内条件下,研究了樟巢螟成虫的求偶及交配行为.结果表明：樟巢螟雌蛾在光期不求偶,进入暗期后少数个体开始求偶,暗期5 h求偶个体百分率明显增加,暗期6～7 h达求偶高峰期;不同日龄雌蛾的求偶率不同,以2～3日龄雌蛾较高,高峰期求偶率达70%以上;樟巢螟雌雄蛾的交配行为依时间顺序可分为求偶和交配2个过程;雌雄蛾间的交配主要发生在暗期5～9 h,交配高峰期在暗期6～7 h,与雌蛾的求偶高峰期一致;樟巢螟雌蛾一生只交配1次;雌雄比1∶1处理的雌蛾交配率显著低于雌雄比1:2处理,但前者的交配持续时间明显高于后者.     

黑线仓鼠巢区的研究

1987年6—9月用标志重捕流放法在呼和浩特地区对黑线仓鼠的巢区进行了研究,雌、雄性的巢区分别为2720.6±576.0平方米和7684.1±1736.6平方米,活动距离分别为95.5±14.4米和135.9±12.4米。黑线仓鼠巢区和活动距离季节变化不明显,雄鼠巢区6—9月全部重叠,雌鼠巢区只有9月份不重叠,雌、雄性巢区彼此重叠。     

香鼬的活动节律和巢区

本文采用无线电遥测技术对栖息在自然环境中香鼬（Ｍｕｓｔｅａｌａｌｔａｉｃａ）的活动节律及其巢区进行了较为系统的研究。结果表明,香鼬多营独居生活．除繁殖期外,无论雌雄个体均无长期稳定的巢穴,经常更换活动的位置。香鼬的每日活动主要为玩耍、自身的修饰、光浴、探视和取食,在繁殖期还有育幼及对幼鼬的保护。在不同时期香鼬日活动高峰和巢区大小均有不同。幼鼬出洞活动前,其亲体雌性成鼬活动呈现两个明显的高峰,１１：００～１３：００和１６：００～１７：００,雄性成鼬则只有一个活动高峰在１１：００左右;在这一时期,成体香鼬的地面活动高峰与其食物──高原鼠兔的地面活动高峰不相吻合,雌性成鼬的巢区面积为７．２１ｈａ,雄性成鼬的巢区面积为１１．７ｈａ。幼鼬出洞活动后,雌性成鼬的活动高峰为８：００～９：００和１７：００～１９：００,巢区面积平均为８２．７２ｈａ。幼鼬扩散期间;雌性成鼬的活动高峰期分别为８：００～９：００和１５：００～２０：００。在这两个时期。成体香鼬的地面活动高峰与高原鼠兔的地面活动高峰趋于一致。影响香鼬活动和巢区大小的主要因素是食物的丰富度、猎物的活动性和繁殖行为,同时种群密度也是主要因素之一。     

农田黑线姬鼠与臭鼩的巢区及种间关系的研究

通过为期一年的标志重捕研究,获得了农田优势种黑线姬鼠与臭聃的巢区、活动距离、领域性等资料,分析了种间领域性及空间分布的关系。并观察到随着捕获突数增多,对动物的可捕性产生影响,再结合对重捕期体重变化的分析,发现长期标志重捕对两种动物产生了正与负的效应。     

Social organization,survival, and dispersal of cape foxes (Vulpes chama) in South Africa

We monitored 20 cape foxes (Vulpes chama) to determine the social organization, survival, and dispersal of this species on two sites in South Africa from 2005 to 2008. Cape foxes were socially monogamous and territorial, with annual home ranges of mated pairs (n = 8) overlapping 80% on average, compared to a mean overlap of 3% between foxes in adjacent ranges. At least 2 pairs remained associated for >1 breeding season, and both sexes exhibited strong site fidelity, as home ranges in consecutive years overlapped 58–98%. Members of mated pairs never foraged together, however they used the same or nearby (<100 m apart) day rests 81% of the time when pups were 0–4 months of age, but only 28% of the time during other months of the year. Dispersal was male biased, as all juvenile males (n = 6) dispersed when 9–11.5 months old, whereas 3 of 4 juvenile females remained philopatric as either breeders or non-breeding associates. At least 6 foxes bred as yearlings (3 F, 3 M), indicating cape foxes have high reproductive potential. Two adult females maintained their territories after their mates died, whereas two adult males dispersed soon after their mates died, indicating cape foxes likely have a female-based social organization. Annual survival was 0.64, and predation from larger carnivores, primarily black-backed jackals (Canis mesomelas), was responsible for 71% of mortalities. Our results provided empirical support for previous hypotheses regarding the relationship between body size and life-history patterns in Canidae, as several ecological parameters of cape foxes were similar to that of other small (<6 kg) canid species, especially Vulpes species inhabiting arid and semi-arid environments.     

臭鼩的繁殖和种群年龄结构

对浙江萧山瓜沥区农田臭鼩的研究,发现种群性比不等,存在明显的两性异型。分析了雄体的性成熟率和雌体的怀孕率及性活动率的变化规律。一年中存在两个繁殖高峰期。以齿长指数为指标．臭鼩种群可划分为4个年龄组。探讨了种群年龄结构的季节变化及其自然寿命。     

Habitat selection and home range in the Blanford's fox,Vulpes cana: compatibility with the resource dispersion hypothesis

Summary This paper presents analyses of habitat-use and home range size in the Blanford's fox. We predicted, from the resource dispersion hypothesis (RDH), that home ranges would encompass similar areas of combined fruitful habitats, but widely different areas of useless habitats, and thus that home ranges would be larger where such fruitful patches are fragmented and widely dispersed. Home range estimates of 0.5–2.0 km² were calculated for 16 adult Blanford's foxes, using three different methods. There were no significant differences in home range size between sexes or study sites. One habitat, dry creekbed, was the most frequently visited in all home ranges. Dry creekbed provided abundant prey for the foxes and only sparse cover for their predators. Both the available area of creekbed in each range, and the area of creekbed patches that was used by the foxes, were independent of home range size. However, the variance in home range size was explained by the mean distance between the main denning area and the most frequently used patches of creekbed. These results are in accord with some predictions of the resource dispersion hypothesis.     

中华姬鼠巢区的研究

中华姬鼠是亚热带山地常绿阔叶林内的优势种。本文报道了用标志重捕流放法,研究该鼠不同个体的巢区大小、相互关系以及在样地上的分布等一些生态学资料。     

Home range and movements of arctic foxes Alopex lagopus in Svalbard

Summary Movements and home ranges of arctic foxes Alopex lagopus were studied in two regions of Svalbard by means of radio tracking (n= 17), ear tagging (n= 192) and visual observations. The movements of radio collared foxes were highly variable, and most foxes roamed over wide areas at least during periods of the year. Home range size was estimated for 11 foxes when more stationary and for three other less stationary foxes, and were in the range 5–120km². During non-stationary periods several foxes roamed over areas 500–1000 km² or more. These movements may more correctly be classified as nomadic, and should not be termed home ranges. Only 3 of 12 radio collarec. foxes that disappeared from an area, returned later. Seven of the 17 foxes were relocated to the same area in more than one season. Overlap of home ranges was extensive, even more so when a number of non-tagged foxes in the regions were included. The heavier juveniles and adults were more sedentary than those of weight lower than median.     

Space use and resting site selection of red foxes (<Emphasis Type="Italic">Vulpes vulpes</Emphasis>) living near villages and small towns in Southern Germany

In 2005–2008, we radio-tracked 17 foxes in rural areas of Southern Germany. The mean home range size was 76.6 ha (95% MCP) or 138.9 ha (95% fixed kernel), and the built-up area formed an integral part of the home range. Home ranges of juvenile foxes were significantly smaller than home ranges of adult foxes. Gender-specific differences among adult foxes were not established. A minimum population density of 2.7 foxes per km² and summer densities of up to 13.4 foxes per km² were calculated. Therefore, the fox density was three to eight times higher than that of strictly rural foxes. Daytime resting sites of foxes were mostly found in forests (62.2%) and reedbed areas (20.6%). Of the resting sites, 14.8% were situated inside settlements, in fallow gardens or gardens of residents. During the day, foxes exhibited habitat preferences for forests and reedbed areas. A habitat structure that offers plenty of cover or dense vegetation is essential for its selection as a safe resting site. If this basic requirement is fulfilled, foxes also choose resting sites within settlements, and are not disturbed by human presence.     

Influence of Population Reduction on Predator Home Range Size and Spatial Overlap

ABSTRACT The increasing populations of red foxes (Vulpes vulpes), raccoons (Procyon lotor), and striped skunks (Mephitis mephitis) in the Intermountain West have contributed to low waterfowl recruitment in recent decades. This effect prompted the need for predator removal at many waterfowl refuges, such as the Bear River Migratory Bird Refuge (BRMBR) in the Great Salt Lake ecosystem. Our study examined the effects of the removal of predatory mammals at the BRMBR on the home range size and spatial overlap of the remaining populations of red foxes, raccoons, and striped skunks. The removal of predators through traps, snares, and night-shooting created a lower predator population during the predators' rearing and dispersal seasons. Predator removal did not result in a change of home range size for red foxes, raccoons, or striped skunks. In all species, home ranges were of similar size during the rearing and dispersal seasons and there were no differences among sexes. After predator removal, the proportion of a home range that overlapped with that of another conspecific decreased in foxes but increased in raccoons. However, predator removal did not change the proportion of inter-specific home range overlap between foxes and raccoons. These findings indicate that home range sizes of these mammalian predators were not constrained by their population densities prior to predator management. In this situation, predator control may be only temporarily successful in reducing predator populations. Managers may achieve more permanent reduction in predator population by decreasing food and shelter resources, thereby reducing the carrying capacity of the landscape.     

A division between foraging range and territory related to food distribution in the red fox

Spatial organization of the red fox (Vulpes vulpes schrencki) was investigated on the basis of seasonal food distribution in the Shiretoko National Park, Hokkaido from 1992 to 1994. Four periods were recorded pertaining to the distribution of 2 kinds of food resources: human food and spawning salmonid carcasses. The home range utilizations of radio-collared foxes were compared for the periods. In the periods when food was not spatially concentrated, resident foxes were territorial, showing exclusive distribution of home ranges between families, defense against intruding foxes at the edge of home ranges, and site specific dominance over intruding foxes. In contrast, during periods when food distribution was concentrated, home ranges overlapped. In the latter periods, foxes made round trips of up to 8 km from their territories to the localized concentration of food, the distance that foxes can travel within a day. This suggests that red foxes in this area have unique foraging ranges that include some seasonally available food outside their territories, and that these ranges depend on fluctuating food distribution caused by humans.     

Home range and habitat use by the sable<Emphasis Type="Italic"> Martes zibellina brachyura</Emphasis> in a Japanese cool-temperate mixed forest

Home range and habitat use of the sable Martes zibellina brachyura were studied in a cool-temperate mixed forest in northernmost Japan. In both sexes, some sables showed a wide range of migration without establishing home ranges and the others had home ranges of 0.50–1.78 km² (mean: 1.12±SD 0.495 km², n =6) which were not significantly correlated with body weight or age. The analysis of canine tooth annuli revealed that the maximum age was 5.5 years. The home ranges of some sables overlapped so extensively that the home ranges and even the core areas did not appear exclusive to other sables. We determined resting sites and foraging routes in snow in winter. Comparison of vegetation at the resting sites and foraging routes with habitat availability suggested that the sables preferred resting in dense-tree forests with many tree species and debris probably in order to avoid predators (red foxes) and strong wind and foraging in forests of climax succession which are usually rich in their prey such as voles and mice.