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1.
新疆北部鹅喉羚的食性分析   总被引:4,自引:2,他引:2  
2006年10月至2007年8月,作者采用粪便显微分析法研究了新疆卡拉麦里山有蹄类保护区鹅喉羚的四季食性以及冬季绵羊的食性.结果发现:鹅喉羚共采食16科47种植物;不同季节间鹅喉羚食性有明显变化,秋季采食7科24种植物,冬季采食6科17种植物,春季采食16科41种植物,夏季采食12科30种植物;藜科、禾本科植物是鹅喉羚全年的主要食物来源,占鹅喉羚总采食量的38.8~85.1%,非禾本科草本植物也在鹅喉羚食物组成中占有重要地位;春季短命和类短命植物对鹅喉羚有重要意义,占春季采食量的27%.针茅在四季都是鹅喉羚采食的主要植物;春季和夏季鹅喉羚采食较多的驼绒藜,秋季和冬季梭梭被较多采食.由于干旱胁迫,春季、夏季和秋季鹅喉羚喜食含水量较高的多根葱、骆驼蹄瓣、粗枝猪毛菜等非禾本科草本植物.冬季鹅喉羚与绵羊间的生态位宽度相近,食物重叠指数高达76.6%,绵羊与鹅喉羚之间食物竞争明显.  相似文献   

2.
陕西凤县林麝的冬、春季食性的初步研究   总被引:1,自引:0,他引:1  
张履冰  徐宏发  薛文杰  姜海瑞  孟秀祥 《四川动物》2008,27(1):110-114,F0004
利用粪便显微组织分析法对陕西凤县野生林麝冬季和春季的食性进行了研究.结果表明:林麝冬季主要取食常绿或半常绿灌木和乔木的落叶,经检验确认的有14科16种;春季主要以当年生枝条以及非禾草类草本植物为食,共确认17科18种.其中黄瑞香Daphne giraldii和色木槭Acer mono分别为冬季和春季主要食物,分别占该季食物的20.51%和11.16%.另外,林麝也取食禾草类植物,取食量从冬季的3.01%上升至春季的9.02%.  相似文献   

3.
食物是影响野生动物生存的关键因子之一,食性研究是了解野生动物与其生存环境关系的重要内容,也是评价动物生存状况和栖息地质量的基础工作。通过粪便显微分析法对内蒙古赛罕乌拉国家级自然保护区中华斑羚Naemorhedus griseus的食物季节性构成分析,发现中华斑羚全年取食植物16科27属31种,冬季取食植物种类与其他各季节的差异有高度统计学意义(χ~2=28.865,P0.001),食物种类明显低于其他3个季节。各季节取食乔木的比例均最低,且冬季取食乔木种类仅1种。全年取食非禾本科草本种类各季节的差异有高度统计学意义(χ~2=17.213,P0.001),冬季明显低于其他季节。Shannon-Wiener多样性指数和食物生态位宽度由高到低依次为夏季、秋季、春季、冬季,而Pielou均匀度指数由高到低依次为夏季、秋季、冬季、春季。本研究结果表明,中华斑羚的食物选择对栖息地的植被变化具有一定适应性,受植物丰富度和可食部位,以及自身的季节性活动范围和能量平衡等因素的综合影响。  相似文献   

4.
神农架川金丝猴冬春季节食性分析   总被引:4,自引:0,他引:4  
采用样方调查法和粪便显微组织学分析法研究了冬季和春季神农架地区川金丝猴的食性。结果表明:川金丝猴冬季取食的植物有7科9属15种,以蔷薇科、松萝科、松科和木樨科为主,春季取食的植物有25科37属48种,以蔷薇科、松萝科、四照花科、卫矛科、樟科、桦木科和木樨科为主;春季食物组成与食源植物相对高度、相对频度呈显著正相关,与相对生物量、相对丰富度呈极显著正相关;冬季食物组成与相对生物量呈显著正相关,与相对高度和相对丰富度呈正相关,与相对频度呈负相关,但相关性差异均不显著;神农架川金丝猴的食物组成中,松萝类植物所占比例冬季(16.51%)明显高于春季(5.69%),说明这类植物只是冬季食物较缺乏时的一种补救,并非是它们的主要食物。  相似文献   

5.
利用粪便显微分析法对贺兰山高山麝冬春季的食性进行了研究。采集高山麝活动区域内粪样和植物样本,采用频率转换法对数据进行处理,得到高山麝冬春季的食性组成及比例。结果表明:高山麝冬季共取食植物19科30种(属),其中蔷薇科(17.16%)、忍冬科(16.64%)、豆科(15.64%)和莎草科(10.93%)组成了高山麝冬季的主要食物;春季共取食植物20科31种(属),其中蔷薇科(27.37%)、杨柳科(13.28%)和豆科(12.84%)为主要食物;秦氏黄芪(Astragalus chingianus)为冬春季共同的主要食物,分别占冬春季食物的11.33%和11.04%;此外,高山麝也取食乔木类植物,取食量从冬季的9.53%上升至春季的18.67%;根据高山麝粪样镜检结果,计算其取食植物的Shannon指数、均匀度指数、生态位宽度指数,分析高山麝食物组成及其多样性,结果显示,3种指数冬季均高于春季。  相似文献   

6.
2005 ~2008 年于陕西省青木川自然保护区使用瞬时扫描法观察了川金丝猴的食性。结果表明,川金丝猴冬季和夏季共取食42 种植物,可鉴定植物归属23 科34 属。川金丝猴食物类型包括果实、花、树叶、树皮、树芽。夏季取食21 种植物的果实或树叶;冬季取食25 种植物。树叶是其冬季主要食物,取食频次占总取食频次的73.0% ;夏季取食果实的频次占总取食频次的72.2% ,灯台树果实是其主要食物。啃食树皮行为主要发生在落叶阔叶林、针叶林与落叶阔叶混交林;在常绿和落叶阔叶混交林中,树皮啃食强度则相对较小。与其它地区金丝猴的食性比较,该地区川金丝猴食物谱较宽。蔷薇科和壳斗科植物在川金丝猴食物组成中最多,杨柳科、桦木科、山茱萸科、槭树科和忍冬科植物也取食较多。  相似文献   

7.
云南龙马山滇金丝猴(Rhinopithecus bieti)冬季食性分析   总被引:1,自引:0,他引:1  
2006年11月-2007年12月,对云南云龙县龙马山滇金丝猴(Rhinopithecus bieti)冬季食性进行了研究.采用粪便显微组织学分析技术分析龙马山滇金丝猴冬季采食植物的种类组成和比例,并测定了该猴群主要取食的15种植物(包括两种松萝科植物)(取食食物百分比>1%)和次要取食的10种植物(取食食物百分比<1%)的化学成分.研究结果表明,龙马山滇金丝猴冬季取食的植物共计26科45种,其中云龙箭竹、长松萝、花松萝、实竹、空心箭竹分别占19.78%、10.28%、8.37%、4.93%、4.46%,是滇金丝猴冬季主要取食的植物种类,占取食植物的47.99%.木本植物和草本植物的叶是滇金丝猴的主要食物,在冬季食物中所占百分比最高,达75%.冬季滇金丝猴比较喜欢采食P/F值较高、单宁含量较低的食物,其主要食物比次要食物含有较高的P/F值和较低的单宁(P<0.05).  相似文献   

8.
觅食是获取营养物质和能量的重要途经。对于栖息在四季分明地区的灵长类动物而言,低温以及食物资源相对匮乏的冬季是其生存和生长发育的瓶颈期。本研究以安徽黄山的野生藏酋猴(Macaca thibetana)天湖山群为对象,于2019年11月至2020年1月采用瞬时扫描取样法(Instantaneous scan sampling)采集猴群觅食行为数据,并分析其冬季食物组成及食物中各化学成分含量对取食的影响。结果显示,野生藏酋猴在冬季共取食23科31属34种植物,主要包括壳斗科(Fagaceae,21.62%)、樟科(Lauraceae,17.57%)、蔷薇科(Rosaceae,8.11%)的植物,取食部位以叶片(66.22%)和果实(种子)(24.32%)为主。不同取食部位的水分、总糖、淀粉、脂肪、单宁等成分存在显著差异。其中,叶片的水分含量高于果实(种子)、茎和芽,茎和果实(种子)含有较高的总糖,果实(种子)的淀粉和脂肪含量最高,芽的单宁含量最高。此外,取食植物中的总糖含量高于非取食植物。结果表明,野生藏酋猴适应寒冷冬季与食物匮乏的觅食策略是对植物种类、植物部位及其主要营养成分的综合结果。  相似文献   

9.
甘肃民勤治沙站纵纹腹小鸮食性的季节变化   总被引:1,自引:0,他引:1  
赵伟  宋森  邵明勤  刘迺发 《动物学报》2007,53(6):953-958
分析民勤治沙站纵纹腹小鸮(Athene noctua)食团405块,共鉴定猎物562只。以个体计,民勤小鸮主要取食昆虫,占64.23%;其次为小型哺乳类,占32.38%;也取食少量爬行类(1.96%)和雀形目鸟类(1.42%)。生物量贡献则以小型哺乳类为主,占93.34%。猎物种类组成存在显著的季节变异:取食小型哺乳类的频率存在显著季节差异,冬季最高94.59%,夏季最低17.75%,食物生物量贡献四季均在90%以上,季节变异不显著;昆虫成分出现在除冬季外的其他季节,且取食频率均在65%以上,季节差异显著;爬行类仅出现于夏季食谱中,仅秋季没有发现鸟类成分。分析秋、冬、春三季哺乳类猎物胫骨的量度发现,小鸮取食哺乳类的胫骨长度平均为16.22mm±4.72mm(n=112),主要取食Ⅰ(10.01mm-15.00mm)和Ⅱ(15.01mm-20.00mm)等级的猎物(分别58.04%和25.00%)。取食猎物的胫骨长度组成存在季节差异,平均长度以春季最大。民勤地区小鸮一年的食物生态位宽度为2.32,季节间存在变异,以冬季最高为2.99,夏季最低为1.64。一年的食物多样性为1.96,季节间存在变异,冬季最高为2.00。食物种类以夏季最多,秋季最少。  相似文献   

10.
短尾猴黄山鱼鳞坑群四季巢区的研究   总被引:4,自引:4,他引:0  
王岐山  熊成培 《兽类学报》1989,9(4):239-246
本文采用无线电发讯器和直接跟踪观察等方法,研究了短尾猴黄山鱼鳞坑群四季巢区的利用与环境的关系。鱼鳞坑群的春季巢区为2.75平方公里,夏季为1.62平方公里,秋季为3.62平方公里,冬季为2.5平方公里。四季巢区有重叠现象,总面积为6平方公里;巢区的季节性垂直迁移现象不明显,与分布在黄山的短尾猴整体情况有所差异,反映了短尾猴适应环境而表现的一种生活样式。  相似文献   

11.
卡拉麦里山自然保护区蒙古野驴的食性   总被引:3,自引:0,他引:3  
蒙古野驴(Equus hemionus hemionus),国家一级保护动物.由于人类活动的加剧,分布范围缩小,加之过度狩猎,目前已处于濒危状态.  相似文献   

12.
河南太行山自然保护区猕猴冬春季食性分析   总被引:1,自引:0,他引:1  
2008年11月-2009年4月,在太行山猕猴国家级自然保护区采集了40份太行山猕猴粪样和38科91种植物标本,用粪便显微组织学分析法研究了太行山猕猴的冬春季食性。结果表明:1)太行山猕猴在冬季采食植物13科21种,其中栓皮栎、青冈、羊胡草、露珠草、大叶榉是其冬季的主要采食植物,共占所采食植物总量的55.4%;小叶榉、千金榆、南蛇藤、君迁子等10种是常见采食植物,共占所采食植物总量的39.1%;第三类是少见采食植物,包括板栗、毛栗、辽东栎,蒙古栎、黄荆等5种,共占所采食植物总量的5.2%;2)共记录到猕猴春季采食植物24科37种,其中栓皮栎、青冈、早熟禾、大叶榉、小叶榉、千金榆、鹅耳枥、枳椇、构树、博落回等10种为主要采食植物,共占所采食植物总量的70.8%;唐松草、白丁香、紫丁香等14种是常见采食植物,共占所采食植物总量的23.4%,少见采食植物包括马齿苋、铁线莲、槐、胡枝子等16种,共占所采食植物总量的5.7%;3)部分植物在冬季和春季均被猕猴取食,但在2个季节所取食的部位有所不同,在冬季主要取食嫩芽和果实,在春季则主要取食花和叶。太行山猕猴在春季的取食植物比冬季更广泛。  相似文献   

13.
The newly described Arunachal macaque Macaca munzala occurs largely in sub‐tropical to temperate environments at elevations of c. 1,800–3,000 m in Arunachal Pradesh, northeastern India. We studied its over‐wintering strategy by comparing the diet, ranging, and behavior of a troop of 24 individuals during winter and spring (December 2005 to May 2006) through instantaneous scan sampling (3,002 records, 448 scans, 112 hr of observation). We also monitored the phenology of food plants. The macaques spent more time (41–66%) feeding in the winter than in spring (33–51%), whereas time spent moving and resting was greater in spring. The diet composed largely of plants, with animal matter being eaten rarely. The number of plant species in the diet increased from 18 to 25 whereas food types rose from 18 to 36 from winter to spring, respectively. Although only two species formed 75% of the winter diet, seven species comprised this proportion in spring. Availability of fruits and young leaves increased in spring; the troop moved more and utilized a larger part of its range during this time. Seasonal changes in behavior could be explained by the scarcity of food and the costs of thermoregulation in winter. Our study suggests that the Arunachal macaque inhabits a highly seasonal environment and has an over‐wintering strategy that includes subsisting on a high‐fiber diet by increasing the time spent feeding, and minimizing energy expenditure by reducing the time spent moving. Am. J. Primatol. 71:939–947, 2009. © 2009 Wiley‐Liss, Inc.  相似文献   

14.
We collected data on diet and daytime activity budget, and investigated the phenology of food trees and food abundance for a group of Rhinopithecus roxellana on the East Ridge of Yuhuangmiao in the Qinling Mountains from November 2001 to December 2003. We calculated the seasonal activity budget using data collected by scan sampling from 84 full-day observations (winter 16, spring 18, summer 28, autumn 22 days). During scan sampling we recorded behavioral states, and the food items and species consumed. The subjects consumed 84 plant species, including trees and shrubs of 29 families, and lichens. Food species varied seasonally. The overall diet of R. roxellana consisted of 29.4% fruit/seeds, 29.0% lichens, 24.0% leaves, 11.1% bark, 4.2% buds, 1.3% twigs and 1.0% unidentified items. Because the abundance of different food items varied seasonally, the monkeys had to shift their major food items seasonally. The annual activity budget of R. roxellana was 36.2% time spent resting, 35.8% feeding, 22.9% moving, and 5.1% other behavior. Seasonal changes in activity budget were observed. R. roxellana spent more time moving in autumn, when the quality of the food might be highest, and least time moving in winter when the food quality might be lowest. Thus, this type of monkey has a passive foraging strategy.  相似文献   

15.
We studied the food habits of the Formosan rock macaques (Macaca cyclopis) in Jentse via fecal analysis and direct field observation from October 1991 to September 1992, and recorded macaques eating 51 plant species and insects of 5 orders. Macaques in Jentse spent more time feeding on fruits than on other plant parts or insects. However, there was seasonal variation in their food habits, i.e., they spent a higher proportion of time feeding on fruits and insects in summer, and on leaves and stems in winter. The major plant species consumed and the patterns of seasonal variation in the macaque diets identified by fecal analysis and field observation are similar. However, there are discrepancies between results from the two methods in some of the finer details of estimated dietary composition.  相似文献   

16.
A small geographically isolated population of the Barbary macaque inhabits a high-altitude fir forest habitat ( Abies pinsapo ) in the Ghomaran region of the Rif mountains of northern Morocco. The climate of this region is Mediterranean, but the altitude (1600–2100 m) causes winters to be cold (as low as -8.0 C) with snow occurring from November to May (snowfall as deep as 1.5 m). The primary winter feeding adaptation is the ability to ingest high quantities of fir foliage; in spring, the macaques took a high diversity of leafy food items from all vegetation layers; in summer, the macaques foraged terrestrially for a high diversity of food items including seeds, small fruits, bulbous geophytes, and animal foods (including tadpoles from small streams); in autumn, the macaques returned to arboreal foraging, primarily feeding on oak acorns ( Quercus ilex ), fir seeds and yew fruit ( Taxus baccata ). The macaques were capable of ingesting 100 of 195 (51%) of all identified plant species in the region, although during the four-month winter, the macaques only averaged 12.5 common food items. A comparison of the study area with the prime habitat of the Barbary macaque-the high-altitude cedar forests of the Moroccan Moyen Atlas-indicates that climate and vegetation physiognomy are highly similar in both regions. Correspondingly, there is a high degree of similarity in macaque diet in both regions in terms of feeding behaviour by season, food diversity and specific feeding techniques. In the Ghomara, the winter feeding adaptation of fir foliage eating parallels that of the Barbary macaque in cedar forest (winter foraging for cedar foliage). This enables the Barbary macaque to exploit the Ghomaran fir forest habitat during the cold, snowy winters much the same as it does cedar forest habitat throughout a major portion of its geographical range.  相似文献   

17.
洞庭湖区东方田鼠的食物组成调查   总被引:22,自引:5,他引:17  
吴林  张美文 《兽类学报》1998,18(4):282-291
采用胃内容物显微组织学鉴定法,定量调查了洞庭湖区东方田鼠(Microtusfortiscalamo-rum)的食物组成。该鼠的主要食物,在苔草地是苔草和水田碎米荠,在芦荻场是碎米荠、苦草、荻和镜子苔,在稻田区是水稻和双穗雀稗,在岗地是三毛草、一年蓬、千金子和水稻。植物叶片是其主要利用对象,在绿色食物资源不足的情况下,也取食植物种子。其食物组成的变化表明,该鼠能依不同栖息地的植被结构调整摄食对象,因而能适应湖区生活环境的灾变性变化。  相似文献   

18.
The feeding ecology of the aoudad (Ammotragus lervia) was investigated for the first time in north-western Sahara, Djebel Antar (Bechar province, Algeria), from autumn 2015 to summer 2016. Microhistological analyses of faeces revealed an annual diet composed of 23 identified taxa belonging to 16 plant families. The highest species diversity was recorded in spring and summer (23 species), despite a marked consumption of two species: Vachellia tortilis (17.7%) and Avena sterilis (14.0%); diet diversity was lower in autumn and winter (16 species), including mainly Teucrium polium (14.7%, 21.0%) and Gymnocarpos decander (19.7%, 10.0%). The main plant parts consumed during these seasons were stems (77.7%, 65.3%), while leaves and inflorescences were mostly consumed during spring and summer (54.7%, 52.3%). Forbs dominated the aoudad's diet, with 46.3% average relative abundance, including mainly T. polium, Limoniastrum feei, and Chrysanthemum macrocarpum. Woody plants including mainly V. tortilis and G. decander accounted for 33.3% (50.0% in autumn), and grasses including A. sterilis and H. murinum for 20.4% (32.0% in summer). Based on this diet, A. lervia can be classified as a “generalist mixed-feeder.”  相似文献   

19.
觅食是动物最重、最常见的行为,动物通过觅食获取其生长发育、繁殖和运动所需要的营养与能量.  相似文献   

20.
Previous studies on Japanese macaque (Macaca fuscata) densities suggest that both total annual food abundance and the quality of fallback foods in the winter bottleneck period affects density. We reviewed data on the seasonal changes in home range size to explain how both factors affect density. In general, home range was large in summer or autumn and small in spring or winter, indicating that density is determined by the home range size in the seasons before winter. The main foods in these seasons are fruits and seeds. If these foods are not abundant, macaques need to range over a larger area, thus decreasing density. Macaques survive the winter by depending on the fat deposited before winter through eating these high-quality foods. If the food condition in winter is severe and the amount of required fat deposition is large, macaques need a larger home range before winter, and thus density becomes lower.  相似文献   

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