食物季节性对野生藏酋猴家域利用的影响

食源植物的分布与食物的可获得性影响灵长类动物的家域动态。研究灵长类动物家域利用及其影响因素,对揭示野生动物的生态适应性与行为复杂性有重要意义。2020年9月—2021年8月,利用GPS技术、直接跟踪观察等方法,对黄山低海拔地区的野生藏酋猴群的家域范围进行研究。结果发现藏酋猴家域面积从春季到冬季依次递减,分别为7.16 km²、5.09 km²、3.85 km²、0.35 km²,面积与食物资源可得性呈显著正相关;猴群月平均漫游距离 (d= 1735.67 m ± 288.35 m, n = 12) 与食物可得性呈正相关,且月平均漫游距离在7月最长、1月最短。猴群偏好利用的生境类型为针阔混交林和常绿落叶阔叶混交林,春季主要偏好利用毛竹林和常绿落叶阔叶混交林,夏季和冬季为针阔混交林 (马尾松),秋季为常绿落叶阔叶混交林。结果表明,藏酋猴会根据食物资源分布、食物可得性等因素来优化家域的时空利用以适应低海拔地区。     

红耳龟在广东古田保护区的家域研究

于2010年9月至2012年6月,在广东古田保护区内利用无线电遥测技术,对保护区内21只红耳龟的家域进行研究。结果表明:红耳龟家域为5.25 hm2±8.66 hm2,核域为1.26 hm2±1.73 hm2。红耳龟的家域和核域面积在繁殖期显著大于非繁殖期,雄性的在繁殖期显著大于非繁殖期,雌性的在繁殖期和非繁殖期无显著性差异,但在繁殖期大于非繁殖期。雄性的和核域在繁殖期显著大于雌性,在非繁殖期不存在显著性差异,但雄性的都大于雌性的。家域大小与其身体大小之间没有显著相关性。     

青海省都兰县藏狐家域范围及重叠度

2006年9月21日至10月21日、2007年1月14～20日、2月6～12日和3月13日至4月8日,应用无线电追踪技术对青海省都兰县沟里乡3只藏狐(2雄,1雌)进行追踪定位,采用Kernel方法计算了3只藏狐的家域面积,确定了该物种的核域,并探讨了不同藏狐个体间家域及核域的重叠状况.结果表明,沟里乡藏狐平均家域面积为6.4±0.4 km2,平均核域面积为1.6±0.2 km2,核域约占家域总面积的1/5～1/4.3只藏狐总体家域面积相差不大,藏狐家域及核域均有一定程度的重叠,家域重叠程度约为50%～60%,核域重叠程度则远远减小,约为7%～20%.     

广西崇左白头叶猴国家级自然保护区及周边区域黑叶猴种群数量与分布

2012年10~12月采用访问法、小区蹲点数量统计方法对广西崇左白头叶猴国家级自然保护区驮逐片及周边相邻的昌平片的黑叶猴种群数量与分布进行了调查。结果显示,驮逐片黑叶猴分布面积为9714 hm2,种群数量为10群55只;昌平片黑叶猴分布面积为1073 hm2,种群数量为7群33只;两处合计为17群88只。驮逐片和昌平片黑叶猴种群数量分别占广西黑叶猴种群数量的14%和10%。驮逐片通过加强能力建设、宣传力度和保护力度,昌平片通过建立自然保护小区,加大对黑叶猴及其栖息地的保护力度。     

不同色型棕背伯劳的冬季家域对比研究

棕背伯劳Lanius schach具有典型的羽色多态现象.于2008年11月14日至12月24日,采用野外直接观察法,利用GPS存取地理坐标点信息,对广东海丰鸟类自然保护区公平保护站黑、棕两种色型棕背伯劳家域进行对比研究,所得数据利用Arcview3.2和SPSS13.0软件技术分析,以探讨不同色型间在家域行为的差异.结果表明:(1)黑、棕两种色型棕背伯劳家域的平均面积分别为11270.96 m2±1807.72 m2、13425.83 m2±3038.82 m2,两者之间无显著差异(P>0.05);(2)被调查个体的家域形状均不规则,相邻家域间的重叠幅度均<1%;(3)不同色型棕背伯劳日平均活动时间区间和时间长度无显著差异(P>0.05).据此认为,棕背伯劳两种色型在家域行为上未表现出明显的分化.     

野放普氏野马(Equus przewalskii)家域面积及其影响因素

采用MCP方法研究了2011年至2012年新疆卡拉麦里山有蹄类自然保护区野放普氏野马家域的变化。通过方差分析验证了年间、季节间不同群体家域及其两两重叠无差异。以家族群大小为协变量进行了野放野马家域协方差分析。利用野放野马家族大小为协变量的协方差分析分析检验了野放野马家族大小与家域关系。结果表明:(1)野马平均家域面积由2011年的(20±2)km~2/匹扩大到2012年的(30±2)km~2/匹。对部分野放群体中头马未发生更替的野马群的研究表明,随着野马群体增大,其家域面积显著增大(P0.05)。(2)单因素方差分析显示,不同野马群的家域面积在不同年份差异显著,且春季家域秋季家域夏季家域。(3)2011年不同群家域两两间相互重叠面积与群大小无显著相关(r=0.256,P=0.5800.05)。而2012年野马群家域两两之间重叠面积有显著差异(F=4.521,df=8,P0.001)。家域两两相互重叠面积与群大小显著相关(r=0.706,P=0.0330.05)。(4)不同季节间野马群家域重叠面积有显著差异(F=5.695,df=8,P0.001)。5号群、7号群和8号群的自身家域重叠面积(P0.05),3号群、6号群和9号群的家域重叠面积(P0.05)。(5)影响野放野马家域面积的生物因子有草本盖度、灌木盖度,非生物因子主要有温度、湿度、风速、最近水源地距离和最近居民点距离等。温度与草本盖度是影响野放野马家域面积大小的主要因素,两者与野放野马家域面积显著相关(P0.01)。     

海南文昌昌洒荒坡地生境中蜡皮蜥繁殖期家域

为掌握蜡皮蜥(Leiolepis reevesii)繁殖期家域大小、家域内是否存在核域,以及家域与核域的重叠程度,分别于2010年和2011年的3月至5月在海南文昌荒坡地生境中,应用无线电遥测技术对蜡皮蜥家域进行了研究,采用最小凸多边形、固定核域、线家域等方法分析了13只个体(10雄3雌)的家域、核域及其重叠度。雄性最小凸多边形(100%MCP)家域面积为(14 091.6±5 718.0)m2,显著大于雌性的(253.3±106.5)m2(t=4.064,df=11,P=0.002);雄性95%固定核域(FK)和75%FK面积为(10 707.8±2 388.5)m2和(3 282.7±1 022.8)m2,分别显著大于雌性的(379.1±74.1)m2(t=7.262,df=11,P0.001)和(172.1±37.9)m2(t=5.107,df=11,P0.001);雄性线家域为(205.8±52.5)m,显著大于雌性的(25.0±2.0)m(t=5.781,df=11,P=0.034);分析遥测个体位点利用方式,蜡皮蜥个体家域内核域明显,雄性核域为(1 380.5±429.1)m2,显著大于雌性的(80.2±18.5)m2(t=5.088,df=11,P0.001),且雄性核域占100%最小凸多边形家域面积的比例为10.9%±3.9%,显著低于雌性的33.3%±6.1%(t=﹣7.834,df=11,P0.001);雄性100%MCP面积不仅与头体长(SVL)之间线性相关显著(n=10,r=0.815,P=0.004),而且与体重(BM)之间也具有明显的线性相关(n=10,r=0.683,P=0.029);个体之间具有家域和核域重叠,雄性个体之间100%MCP家域重叠指数为0.26±0.17,显著低于雌性的0.66±0.02(t=﹣3.372,df=34,P=0.002),而雄性核域重叠面积占核域比例为2.50%±1.70%、重叠指数为0.02±0.02,雌性比例为0.34%±0.01%、重叠指数为0.01,表明蜡皮蜥具有明显的领域性,且雌性在繁殖季节其领域性明显高于雄性。     

小兴安岭南坡野猪家域分析

采用笼式活捕野猪,利用无线电遥测技术、R2V、Arcview 和SPSS 软件技术,于2004 年7 月15 日至2006年1 月19 日,对小兴安岭南坡野猪家域进行测定、计算和分析,以了解该地区野猪的家域变化规律。研究结果表明:季节变化影响野猪家域面积,在春、秋季,野猪的家域面积显著大于冬季,而春、夏季间无显著差异;不同性别及年龄野猪家域大小也不同,成体雄性秋季发情期和亚成体春季分窝期家域面积显著增加;在冬、春季家族群野猪的家域面积显著大于独体野猪家域面积,说明家族群对家域面积有影响;亚成体家域大小主要受家族群家域的影响,家族群野猪面积大,相应地家族野猪中亚成体家域面积也大。     

On the Knowledge of Coprophilus (Zonyptilus) pennifer (Motschulsky, 1845) and Coprophilus (Zonyptilus) marginalis (Reitter, 1894) (Coleoptera,Staphylinidae)

Entomological Review - The type and other extensive material of Coprophilus (Zonyptilus) pennifer (Motschulsky, 1845) and some of its synonyms was examined. Coprophilus (Zonyptilus) marginalis...     

Electronic structures of collagen model polymers: (Gly-Pro)n, (Gly-Hyp)n, (Ala-Pro)n, (Ala-Hyp)n, (Gly-Pro-Gly)n, (Gly-Hyp-Gly)n, (Gly-Pro-Pro)n, and (Gly-Pro-Hyp)n

In order to investigate the relationship existing between the electronic structures of collagen and its biochemical functions in vivo, the semiempirical CNDO/2 SCF MO calculations were carried out on several model polymers of collagen, (Gly-Pro)_n, (Gly-Hyp)_n, (Ala-Pro)_n, (Ala-Hyp)_n, (Gly-Pro-Gly)_n, (Gly-Hyp-Gly)_n, (Gly-Pro-Pro)_n and (Gly-Pro-Hyp)_n. Geometries of the skeleton of these polymers were assumed to be the same as those of poly(l-proline) I (cis) and II (trans) and the calculations were performed only on infinite polymers in a single chain. The results show that the cis form is always more stable than the trans form for all the polymers treated. This energy difference between the cis and trans forms depends, for example, on the kind of amino acid residue, Gly or Ala, but this could not be seen in the Pro or Hyp residue. The flexibility or mobility of the collagen structure was explained using the energy difference between the cis and trans forms of the polymers, i.e. the cis-trans conversion of the collagen was discussed in connection with the energy difference. The reason why the collagen has the constitution of (Gly-Pro-Hyp)_n is briefly discussed.     

On the Synonymy of Coprophilus (Zonyptilus) pennifer (Motschulsky, 1845) (Coleoptera,Staphylinidae, Oxytelinae)

Entomological Review - The type material of several synonyms of Coprophilus (Zonyptilus) pennifer (Motschulsky, 1845) is revised. Both Coprophilus (Zonyptilus) striatipennis (Eppelsheim, 1894) and...     

Tachinid (Diptera, Tachinidae) parasitoids of sawflies (Hymenoptera, Symphyta)

A list of 31 genera of tachinid parasitoids of sawflies is given. Despite the ecological and habitual similarity of sawflies and Lepidoptera, utilization of sawflies by tachinids was not as successful from the evolutionary point of view as utilization of Lepidoptera. Parasitism of tachinids in sawflies is evidently secondary; it appeared repeatedly and originates from parasitism in Lepidoptera. Most genera of tachinids are polyphagous. Endoparasitic Hymenoptera are koinobionts similarly to tachinids. The direct contact of the parasitoid with active mobile host larva not only results in complication of behavior and its specialization, but also promotes formation of different morphological innovations faster than that in idiobionts.     

Spermiogenesis in Anaspides tasmaniae (Thomson) (Crustacea,Malacostraca, Syncarida)

Spermiogenesis of the syncarid Anaspides tasmaniae (subclass Eumalacostraca) was investigated by transmission electron microscopy. The spermatozoan of Anaspides is an ovoid cell with an acrosome covering the anterior pole and a lobulated nucleus and mitochondria occupying the rest of the cell. A long subacrosomal filament bypasses the nucleus and forms a spiral that supports a thin extension of the posterior cytoplasm, giving the spermatozoan a bell-shaped appearance. No flagellum is present at any stage. The immobile spermatozoans are embedded in a hard capsule, secreted by the cells of the wall of the vas deferens.     

Molecular-Mechanical studies of the mismatched base analogs of d(CGCGAATTCGCG)2:d(CGTGAATTCGCG)2, d(CGAGAATTCGCG)2, d(CGCGAATTCACG)2, d(CGCGAATTCTCG)2, and d(CGCAGAATTCGCG)·d(CGCGAATTCGCG)

Molecular-mechanical simulations have been carried out on “mismatched base” analogs of the DNA double-helical structure d(CGCGAATTCGCG)₂, in which the base pairs CG at the 3 and 10 positions have been replaced by CA, AG, TC, and TG base pairs, as well as an insertion analog in which an extra adenine has been incorporated into one strand of the above structure between bases 3 and 4. The results of these simulations (calculated relative stabilities, structures, and nmr ring-current shifts) have been compared with calorimetric and nmr data. The calculated relative stabilities of the double-helical parent dodecamer and the various “wobble” base pairs qualitatively correlate with the experimental melting temperatures. The base-pairing structure for the GT wobble pair is in agreement with that previously determined from nmr experiments. For the GA base pair, the structure with both bases anti has a slightly more favorable energy from base pairing and stacking than a structure with non-Watson-Crick H-bonding with adenine syn, in agreement with nmr experiments. The CA wobble base is calculated to favor an adenine 6NH₂ …? cytosine N3 H-bond over cytosine 4NH₂ …? adenine N1, again, in agreement with nmr experiments. There is no definitive experimental data on the TC base pair, but the existence of (somewhat long and weak) H-bonds involving cytosine 4NH₂ …? thymine 4CO and cytosine N3 …? thymine HN3 seems reasonable. We find a structure in which the extra adenine base of the insertion analogs sits “inside” the double helix.