通河林区黄鼬(Mustela sibirica)冬季被毛形态结构的功能适应性

被毛在哺乳动物适应性进化过程中执行保温和保护两个重要功能,其形态结构上存在的功能适应性特征因所处的部位不同而表现出适应性分化现象,由动物体躯干至四肢末端呈显著的梯度变化。以黑龙江省通河林区黄鼬东北亚种(Mustela sibirica manchurica)冬季雌雄成体各10只完整毛皮对象,研究了背中部、腹中部和后肢下部3个部位的直针毛、披针毛、绒针毛、绒毛,以及后趾部硬毛的被毛性状因子,统计分析表明:通河林区黄鼬相同身体部位4种类型毛的长度和细度指标均为直针毛披针毛绒针毛绒毛,相同部位4种类型毛长度的相关性极显著,直针毛细度与披针毛细度相关性极显著(P0.01),绒针毛细度与绒毛细度相关性极显著(P0.01),这种特征使得被毛在整体结构上为实施保温和保护功能奠定基础;同时,黄鼬被毛各性状的保温功能从背部向后趾部呈递减趋势,而保护功能则呈现递增趋势,被毛形态结构性状上的分化与动物机体异温性充分结合,对于黄鼬适应寒冷的森林生态环境具有重要意义。     

华西蟾蜍年龄结构、体长和生长率的研究

本研究利用骨龄学方法研究了青藏高原东缘横断山脉区一个华西蟾蜍种群的年龄结构、体长、年生长率及性成熟年龄。采集的74个成体个体中(雄性47只,雌性27只),均能够在趾骨切片中观察到受抑制生长线。结果表明:两性的体长和年龄都成正相关关系(雌性:F1,26=4.87,r=0.40,P=0.04,雄性:F1,46=4.48,r=0.30,P=0.04)。雌性初始繁殖年龄为4龄,寿命至少为11龄;雄性分别为3龄和11龄。雌性和雄性的平均年龄存在显著差异(Z=2.27,P<0.01),雌性为(8.4±1.8)龄,雄性为(6.2±1.8)龄。雌性平均体长大于雄性(t=2.348,P<0.01),雌性为91.9 mm±7.2 mm,雄性为74.8 mm±5.5 mm。另外,雌性和雄性具有不同的生长模式,雌性生长率(r=2.48)大于雄性(r=2.32)。年龄和生长率对华西蟾蜍的性二型的解释有重要意义。     

洞庭湖区自然野化麋鹿种群的偏性扩散行为

大多数鹿科动物表现出偏向雄性的扩散行为。麋鹿(Elaphurus davidianus)于20世纪初在中国灭绝,1985年被重引入中国。1998年长江流域特大洪水导致部分麋鹿个体从湖北石首麋鹿国家级自然保护区围栏内外逸,最终在洞庭湖区形成自然野化种群。野化麋鹿是否也存在偏性扩散行为?1995—2012年,采用样带调查法、分区直数法、特殊个体识别法和访问调查法,按性别组成将扩散群分为雄性群、混合群和雌性群,对洞庭湖区自然野化麋鹿种群的扩散行为进行了研究,共记录到118次扩散。其中,有65次扩散可确认扩散群的类型;60次可确认扩散群准确的个体数。结果显示:(1)雄性麋鹿较雌性更倾向于扩散。雄性群的扩散频次高于雌性群和混合群;50%的雄性扩散群仅由单一成年雄体组成。(2)雄性麋鹿的扩散能力最强,雄性群、混合群和雌性群的平均扩散距离分别为(13.73±8.74)km、(11.05±4.16)km和(8.95±2.16)km,但三者之间的差异不显著(χ2=1.896,df=2,P=0.387)。雌性群和混合群的扩散距离均短于25km,而5.88%的雄性群扩散距离长于25 km。(3)雄性群的平均个体数与混合群的差异显著(F=5.324,df=24,P=0.000.05),与雌性群的差异不显著(F=9.830,df=35,P=0.813),而混合群与雌性群之间的差异显著(F=48.085,df=55,P=0.000.05)。(4)50.00%的雄性群和53.57%的混合群选择芦苇草地作为扩散目的地的生境。洞庭湖区自然野化麋鹿种群与其他野生鹿科动物一样,也存在"雄鹿较雌鹿更倾向于扩散"的现象,雄性的扩散能力比雌性强,雌性的扩散可能依赖于雄性。以上结果对麋鹿的野外放归和自然野化种群的管理与保护具有重要的意义。     

不同性别和年龄的大仓鼠对黄鼬气味的反应

将雌性成体和雌雄亚成体大仓鼠 (Cricetulustriton)长期 (4周 )暴露给过量的黄鼬 (Mustelasibirica)肛腺分泌物 ,观察其行为和生理状态的变化 ,并通过与我们以前有关黄鼬气味对成年雄鼠影响的研究结果进行比较 ,表明黄鼬气味对不同性别和不同年龄大仓鼠的胁迫效应和生殖抑制存在差异。发现黄鼬气味对雌性大仓鼠的影响较雄性小 ,对亚成体的影响较成体小 ,这与雌性和未成年动物对各种胁迫因素的反应更敏感的普遍现象相反。在成年鼠中 ,雌雄鼠的攻击行为都受到黄鼬气味的抑制 ;但天敌气味使雌性的胁腺膨大 ,对胁腺标记和肾上腺大小无影响 ;成年雄鼠的肾上腺膨大 ,胁腺萎缩 ,标记减少。在亚成体中 ,除了雄性胁腺受到抑制(与成年雄鼠相同 )外 ,雌雄鼠的肾上腺和雌性的胁腺未受影响。亚成体实验鼠的体重都比对照组低 ,但成年鼠的体重未受影响。另外 ,与以往对其它鼠类的研究结果一致 ,天敌气味并不影响成年鼠的生殖器官 ,却抑制了未成年雄鼠的附睾和未成年雌鼠的子宫。这些差异可能和生理基础的性二态以及可能面临的被捕食风险大小有关     

漠河地区养殖的北极狐冬季被毛性状与保温性能的关系

被毛是哺乳动物最主要的特征之一,其保温功能对动物适应寒冷环境意义重大。为了探讨北极狐(Alopex lagopus)在被毛性状上如何适应寒冷的气候条件,对大兴安岭漠河地区人工养殖北极狐的背中部直针毛、上层绒毛、下层绒毛的长度、毛根细度、毛干细度以及毛密度、单个毛束内的毛数量、毛束密度、复合毛囊最大横切面积、1mm2内复合毛囊最大横切面总面积等14个性状因子进行测量分析。结果表明,北极狐绒毛分为上下两层,下层绒毛的长度、毛根细度和毛干细度均小于上层绒毛,上层绒毛长度与直针毛接近,直针毛长度与上层绒毛、下层绒毛长度均不存在显著相关性;毛密度与毛束密度极度正相关(P0.01),但与毛根细度、毛干细度、单个毛束内的毛数量和1mm2内复合毛囊最大横切面总面积不存在显著相关性,且与复合毛囊最大横切面积的相关性较小;复合毛囊最大横切面积受毛根细度、单个毛束内的毛数量和毛束密度的影响较小。北极狐不是通过降低毛细度的方式来增加毛密度以加强保温功能,而是通过改变被毛在皮肤内的分布格局来增加毛密度,以及将有髓质的绒毛分为上下两层来改变被毛空间结构这两种策略提高被毛内静止空气的量以加强保温功能,进而适应高纬度地区的寒冷环境。     

室内养殖雌性松鼠秋季换毛期被毛长度和保温性能变化

为了解松鼠东北亚种(Sciurus vulgaris manchuricus)秋季换毛期的被毛性状与保温性能变化的关系,选取2011年9月25日至12月15日期间采集的在哈尔滨室内人工养殖的27张雌性松鼠东北亚种生皮为材料,对背臀部毛皮样本进行传热性能测试,同时对该部位的披针毛、绒毛的长度和毛根出现无髓样本比例进行测量计算。结果表明:1)随着秋季换毛期的时间后移,新生冬毛长度不断增加,毛皮传热系数不断减小。当被毛生长结束时,保温性能达到恒定。2)披针毛长度、绒毛长度、披针毛毛根无髓段比例、绒毛毛根无髓段比例这4个被毛性状因子两两呈极显著正相关(P<0.01),且此4个性状因子皆与毛皮传热系数呈极显著负相关(P<0.01)。以上反映了在气温渐冷的秋季换毛期每时间阶段被毛的长度、生长程度、保温性能的具体变化及相互关系。     

据于矢耳石Sr/Ca值的长江日本鳗鲡迁移格局多样性分析(英文)

长江口是中国日本鳗鳗苗的主要产区和仅存的成鳗渔业水域。日本鳗自长江河口至上游金沙江近3000km干流及许多支流中都有分布,但其迁移行为却不为人了解。该文分析了2008年9～11月采自长江靖江段(31o30′N,120o42′E)的153尾银色鳗样本的生物学特征,测定了其中27尾标本的矢耳石Sr/Ca值。结果显示,153尾样本中有雌性85尾、雄性68尾,雌雄性比1:0.8。雌性由3～7(平均5.52)龄组成,平均体长(669±80)mm,体重(555±229)g,丰满度1.77±0.22,性腺指数(GSI)1.32±0.31。雄性由3～5(平均4.38)龄组成,平均体长(518±51)mm,体重(234±76)g,丰满度1.62±0.18,GSI0.21±0.11。雌性的这些生物学参数均显著大于雄性(P<0.05)。依据矢耳石线鳗标志轮平均Sr/Ca值(7.99±1.05)×10-3进行判断,有17尾(即62.96%个体)为"淡水型",10尾(即37.04%个体)为"河口型"。16尾雌性中有13尾(即81.25%)为"淡水型",3尾为"河口型"。11尾雄性中仅36.36%为"淡水型",63.64%为"河口型"。对每个生长层组的Sr/Ca值分析表明,雌雄间2龄时无显著差异,但3龄、4龄和洄游龄组都有显著或极显著的差异,预示着2龄时两者的栖息水域比较一致,但后来出现了明显栖息地分化。     

人工饲养条件下棕果蝠的摄食行为

2005年8～11月,对北京动物园饲养的棕果蝠(Rousettus leschenaulti)摄食行为进行了研究。每天上午和下午按时喂食,棕果蝠的摄食行为表现出一定的规律性。放置好水果约4min后,1～3只棕果蝠先在食物周围盘旋,然后返回栖息位置;再经约2min开始进食。当果篮中剩余少量水果时,部分棕果蝠到地面取食。上午喂食后,在地面取食的棕果蝠数目出现1个高峰;下午喂食后,地面取食出现4个高峰。下午取食时间显著长于上午(P<0·05)。棕果蝠进食完一块水果后,并不立即再次取食,而是存在一段时间间隔,期间雌雄棕果蝠的行为包括静止、理毛、张望、飞行、抢食、争斗、爬行、排泄、舔生殖区、舔顶棚等。雌雄的行为出现频次存在差异,其中雄性与哺乳期雌性的静止、理毛、飞行、抢食、争斗、舔生殖区行为差异显著(P<0·05);雄性与非哺乳期雌性的静止、理毛、张望、飞行、舔生殖区行为差异显著(P<0·05);哺乳期与非哺乳期雌性的静止、理毛、飞行、抢食行为差异显著(P<0·05)。     

滇金丝猴雌性个体间的理毛行为

相互理毛行为广泛存在于社会性群居灵长类动物中,通常具有清洁卫生和社会交往功能。2012 年10 月至2013 年6 月,我们在云南白马雪山国家级自然保护区对一人工辅助投食滇金丝猴群,采用全事件取样法和焦点动物取样法收集了雌性个体间相互理毛的行为数据,包括理毛的部位、理毛的姿势、理毛的时间和回合数。研究结果表明:滇金丝猴雌性个体之间每次相互理毛的平均时间为5. 7 min。相互理毛部位较多的发生在自我理毛不能进行(达到)的部位(61.1% );在不能自我理毛部位的相互理毛行为持续时间长,平均9.7 min;在个体能够进行自我理毛部位的相互理毛持续时间短,平均为3. 2 min。相互理毛的姿势以对坐为主(48. 4% ),不同理毛姿势的理毛时间差异显著。新迁入家庭单元的雌性个体为理毛的首先发起者,但其获得被理毛的时间却并不多。滇金丝猴雌性个体相互理毛部位、理毛姿势和理毛时间的差异表明,它们之间的相互理毛行为符合卫生功能假说和社会功能假说。     

刺五加花的形态学及雄蕊异长现象的观察

刺五加Eleuthercoccocus senticosus (Rupr．et Maxim．)Maxim．具有花丝长度不同的三种植株类型,本文报道了其花序和花的形态结构,开花式样,异长雄蕊现象及相应的花柱长度。结果表明：长花丝长3．96～4. 44mm ,短花丝长0．45～0．93mm,中花丝长2．16～3．08mm。伴随异长雄蕊特征的其它表现在于花药大小、花药形状和颜色、花粉大小、花粉数量、柱头宽度和雌雄蕊育性。其中,长花丝对应的花药饱满、白色、花粉量大、花柱较短、雌性败育;短花丝对应的花药小、黄褐色、无花粉、花柱较长、雌性可育;中花丝对应的花药中等、花粉粒较大、雄性半不育、雌性可育。据此,刺五加被认为是单全异株的,其长花丝类型是雄性、短花丝类型是雌性、中花丝类型是两性的。另外,对三种性别形态类型的关系进行了讨论,并认为将雌株作为变种“短蕊刺五加”var.brevistaminea 显然是不恰当的。     

The role of the adrenal glands in regulating onset of winter fur growth in mink (Mustela vison).

The role of the adrenal glands in regulating onset of winter fur growth in mink was investigated in long-term adrenalectomized animals. Bilateral adrenalectomy of adult female standard dark mink between June 23 and July 11, 1990, initiated onset of winter fur growth approximately 6 weeks earlier than controls. One month following completion of the winter fur growth in adrenalectomized mink, molting and growth of a new coat was observed. The type of pelage that grew as a result of the second growth wave was less dense than the normal summer or winter fur. However, this renewed hair growth suggests that adrenal hormones not only inhibit the onset of winter fur growth but also influence the duration of inactivity following each period of hair growth. Administration of deoxycorticosterone as a mineralocorticoid supplement had no effect on initiation of fur growth. It would appear that adrenal hormones are part of the mechanism through which photoperiod regulates fur growth in the mink. The identity of the adrenal hormones and their site of action is unknown.     

Morphological and thermal properties of mammalian insulation: the evolution of fur for aquatic living

Carnivora includes three independent evolutionary transitions to the marine environment: pinnipeds (seals, sea lions, and walruses), sea otters, and polar bears. All three lineages must contend with the thermal challenges of submersion in the marine environment. In the present study, we investigated changes in the fur associated with the transition from a terrestrial to an aquatic lifestyle, comparing fur characteristics among these lineages with those of semi‐aquatic and strictly terrestrial carnivores. Characteristics included gross morphology (hair cuticle shape, circularity, length, and density) and thermal conductivity. We found consistent trends in hair morphology associated with aquatic living, such that marine carnivores have significantly flatter (P < 0.001), shorter (P < 0.001), and denser hairs (P < 0.001) than terrestrial carnivores. However, sea lions, phocids, and walrus, which have thicker blubber layers than fur seals, have lower fur densities than fur seals (P < 0.001). Species utilizing fur for insulation in water also showed an elongation of hair cuticle scales compared to terrestrial species and marine species relying on blubber for insulation (P < 0.001). By testing pelts under hydrostatic pressure, we determined that flattening of the hairs, cuticular scale elongation, and increased fur density are critical characteristics for maintaining an insulating air layer within the fur during submersion. Overall, these results indicate consistent evolutionary modifications to the fur associated with the transition to aquatic living, as well as a decrease in fur function associated with a greater reliance on blubber in some groups. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ?? , ??–??.     

Supravital Methylene Blue Staining of Piloneural Complexes of Common Fur Hair Follicles in the Rat

Light microscopic observations employing supravital methylene blue staining are presented for piloneural complexes of common fur hairs in the mystacial pad of the rat snout. The investigation revealed anatomical details of piloneural complexes belonging to follicles of both vellus and guard hairs. In the methylene blue stained preparations, different types of palisade-like lanceolate nerve fiber endings could be discriminated. The thicker vellus and thinner guard hairs (hair diameter: 15-25 μm) exhibited a different innervation pattern compared to the thicker guard hairs, and two subtypes of piloneural complexes could be distinguished. Both subtypes were characterized by slightly stained lanceolate endings and the absence of a circular nerve fiber plexus. One subtype, however, showed strongly stained spines originating from the lanceolate endings. A few spines of adjacent lanceolate endings appeared in contact with each other. In the second subtype, these spines were replaced by anastomoses suggesting a delicate terminal nerve fiber network. The moderately stained lanceolate endings located primarily at the follicles of thicker guard hairs (hair diameter: 30-40 μm) showed smooth outlines, but were characterized by the occurrence of an intensely stained additional circular nerve fiber plexus. The differences in the morphology of piloneural complexes associated with the follicles of common fur hairs suggest differences regarding their mechanoreceptive tasks.     

Supravital Methylene Blue Staining of Piloneural Complexes of Common Fur Hair Follicles in the Rat

Light microscopic observations employing supravital methylene blue staining are presented for piloneural complexes of common fur hairs in the mystacial pad of the rat snout. The investigation revealed anatomical details of piloneural complexes belonging to follicles of both vellus and guard hairs. In the methylene blue stained preparations, different types of palisade-like lanceolate nerve fiber endings could be discriminated. The thicker vellus and thinner guard hairs (hair diameter: 15-25 μm) exhibited a different innervation pattern compared to the thicker guard hairs, and two subtypes of piloneural complexes could be distinguished. Both subtypes were characterized by slightly stained lanceolate endings and the absence of a circular nerve fiber plexus. One subtype, however, showed strongly stained spines originating from the lanceolate endings. A few spines of adjacent lanceolate endings appeared in contact with each other. In the second subtype, these spines were replaced by anastomoses suggesting a delicate terminal nerve fiber network. The moderately stained lanceolate endings located primarily at the follicles of thicker guard hairs (hair diameter: 30-40 μm) showed smooth outlines, but were characterized by the occurrence of an intensely stained additional circular nerve fiber plexus. The differences in the morphology of piloneural complexes associated with the follicles of common fur hairs suggest differences regarding their mechanoreceptive tasks.     

紫貂和水貂被毛比较形态学研究

研究表明紫貂和水貂被毛的形态高度分化,可分为针毛,中间针毛和绒毛3类。针毛笔直,远端(大约3/4处)皮质高度发育,有良好的耐磨性。中间针毛比针毛短、细,大约有3个弯曲,且髓质含量最高。绒毛最短、细,大约有5个弯曲,髓质也较发达。 扫描电镜下的毛小皮形态可归纳为波纹形,披针形,菱形和倒三角形4种。光镜下的髓质形态可归纳为单柱组型,多柱组型和网型3种。比较分析的结果表明:毛小皮和髓质形态在这两种动物间的差别较明显,具有种的特异性、可作为哺乳动物分类的参考指标。     

The mutant gene "wal" is active in cells of mouse hair follicles

In order to determine the place of action of the mutant gene waved alopecia (wal), we have obtained chimeric wal/wal c/c Gpi-1aa<-->+/+ C/C Gpi-1bb animals by aggregation of eight-cellular embryos of BALB/c-wal/wal mice and CBA (+/+) mice. The presence or absence of the chimeric structure was determined from the mosaic nature of fur color and hair structure, as well as on the basis of the presence of electrophoretically distinct variants of glucosephosphate isomerase in blood. Chimeras had alternating transverse patches of different lengths and widths consisting of curly (genotype wal/wal) or straight (genotype +/+) hairs. The percentage of cells with wal/wal mutant genotype in chimeras established on the basis of glucosephosphate isomerase isozymes varied from 10 to 80%. A higher percentage of the parental wal/wal component in chimeras correlated with the number of patches having wavy hairs. Analysis of the fur pattern represented by the alternation of transverse patches of wavy or straight hairs in chimeric wal/wal (+/+ mice has shown that mutant gene wal acts in ectodermal cells of hair follicles.     

Seasonal hair follicle activity and fibre growth in some New Zealand Cashmere-bearing goats (Caprus hircus)

Hair follicle activity and fibre growth were studied using histological sections from the skin of five adult feral does sampled every four weeks for 18 months. The main period of guard hair growth in primary follicles was from November to April. Secondary follicles grew fine, long, nonmedullated fibres (cashmere) from December to June. Shedding of these fibres from secondary follicles had commenced by July and cashmere was absent from the fleece by November. From September to December a subsidiary hair cycle occurred in many secondary follicles which produced minute (vellus) fibres, less than 2.4 mm in length. Some secondary follicles probably shed their cashmere fibres and remain quiescent over spring. Annual pelage changes were therefore achieved with one main growth period, although many secondary follicles underwent another brief hair cycle in spring.     

Simulation of sensible and latent heat losses from wet-skin surface and fur layer

A simulation model that simultaneously calculates heat and mass transfer from a wetted skin surface and fur layer of a cow is presented. The model predicts evaporative, convective and radiant heat losses for different levels of skin and fur wetness, air velocity, air temperature and relative humidity. In the model, fur layer (hair coat) properties such as fur thickness and hair density assumed are that of summer conditions. Evaporative cooling from wet-skin surface and hair coat is the dominant mode of heat mitigation mechanism in stressful hot environments and is further enhanced by increased air velocity. Evaporative cooling is, however, depressed by increased relative humidity because of deficit of water-vapor concentration between the skin surface and ambient air.