马鹿东北亚种被毛形态结构的季节性差异

被毛作为哺乳动物特有的组织,具有保护和保温功能,一些季节性换毛动物需要通过更换被毛以适应冬季和夏季的不同环境（王泽长,1963;景松岩和张伟,1993）。因此,研究动物被毛结构与功能的季节性特征,对揭示被毛在物种生存和进化过程中的作用具有重要意义（张伟和徐艳春,2003）。对毛的结构多态性和功能多样性研究是国际毛发形态学研究中的前沿领域（Yalden,1985;Gaudette,1985;syred,1991;甘雅玲和郭中伟,2003;张伟和徐艳春,2003）。以往的毛发形态学研究多限于反映物种的特异性,并应用于分类鉴别方面（朱小曼,1987;张伟,1994;金煜,1995）。在强调毛发结构物种特异性的同时,忽略或淡化了其变异性,更缺少对结构和功能关系的研究。马鹿东北亚种（Cervus elaphus xanthopygus）为季节性换毛动物,绒毛退化,其被毛主要由上毛构成。本选择马鹿东北亚种的冬季和夏季上毛作为研究对象,初步测量了冬季和夏季其臀部、后肢上部、后肢下部及蹄部上毛的形态和微观结构数据,比较其季节性差异和部位差异。     

通河林区黄鼬背中部与爪部冬季上毛的形态结构

哺乳动物被毛携带着遗传信息,样本亦容易获取,而且在通常情况下取样不伤害动物.故长期以来,被毛的形态结构特征被用于进行物种分类(Oli,1993;张伟,1994;Sachs,1997;崔雨新等,1998;孙中武等,2003).     

黑龙江省黄鼬冬季毛被分层结构及保温功能

为了解黄鼬毛被的保温机制,选取黑龙江省通河林区黄鼬东北亚种(Mustela sibirica manchurica)冬季皮张,通过观测雄性5个部位和雌性4个部位毛被的分层结构,并结合热物性测试比对,发现了毛被的各层结构具有不同的保温隔热功能且存在部位差异。结果表明:1)毛被由外及里表现出4层结构,各层毛被厚度分别为:(12.7±3.0)mm、(6.0±1.8)mm、(5.5±2.2)mm和(1.4±0.5)mm。2)4层毛被的颜色、结构及保温机制依次为:最外层毛被棕黄色或金黄色,仅由2种类型被毛构成,耐磨损能力较强,保护下层毛被,阻挡冷空气侵入并降低毛被的热量散失;第二层毛被淡黄色,此层开始均由4种类型被毛构成,毛干细度较小,被毛间形成细小空隙,滞留大量静止空气,增强保温功能;第三层毛被灰色或灰白色,4种类型被毛的毛干更细,绒针毛和绒毛弯曲程度更大,使被毛间滞留静止空气的能力更强、更稳定,保温能力更强;最内层毛被为白色,为近毛根处,4种类型被毛均较直,便于热量传递。3)4层毛被的对整体的贡献率分别为:16.11%、27.40%、44.40%和12.09%。4)背面毛被较腹面的颜色深,厚度大,保温能力强;沿吻端至尾基的体轴方向毛被厚度增加,保温性增强。5)雄性毛被较雌性的厚度大,保温能力强。以上,反映了黄鼬冬季多部位毛被由表及里不同的空间布局及各层毛呈现的不同的形态结构,从整体上兼顾保护、保温、散热等多种功能,以适应当地的寒冷环境。     

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。     

关于保留球毛壳与橄榄色毛壳作为不同种的见解

球毛壳(Chaetomium globosum Kze.)系 Kunze 于1817年报道见于丹麦石竹(Dianthus carthusianorum L.)茎上的毛壳菌属(Chaetomium)的第一个种(模式种)。Cooke and Ellis 在1878年描述了见于飞蓬属(Erigeron L.)腐茎上的橄榄色毛壳(C.oliaceum C.et E.)。在 Chivers(1915)、Skolko and Groves(1953)、Udagawa(1960)、Ames(1963)和 Seth(1972)关于毛壳菌属的专著都曾指出很难划分这两个种的界限。Skolk and Groves(1953)区分此两个种时以橄榄色毛壳具有较大的子囊壳、较宽的顶附属丝和较大的子囊孢子,而 Chivers(1915)则认为橄榄色毛壳是球毛壳的异名,Udagawa(1960)区分此两个种仅根据子囊孢子的长度和宽度,他认为橄榄色毛壳的子囊孢子大于球毛壳的子囊孢子。Seth(1972)在他的专著中虽保留此两个种作为独立种,但他指出限于他镜检过的标本材料及根据 Chivers 专著中的球毛壳的特征辑要概括了橄榄色毛壳的特征,对这两个种的区分界限确实是很难划分的。最近我们在北京采集和分离了来源于不同的植物和动物材料上的毛壳菌种类,以期进行北京地区毛壳菌种类调查研究。我们分离获得许多球毛壳——橄榄色毛壳类的毛壳菌菌株。参考了不同作者对这两个种的子囊壳、顶附属丝、侧附属丝、子囊及子囊孢子的特征记载,对北京的这一类型菌株进行了细致研究,认为球毛壳与橄榄色毛壳确有形态学特征区别,表现在橄榄色毛壳的子囊壳、顶附属丝和子囊孢子较球毛壳的更为粗壮,兼之球毛壳的顶附属丝较橄榄色毛壳的为窄且有分隔和微粗糙,球毛壳的子囊孢子呈浅橄榄褐色至暗橄榄褐色,含两个折光性油滴而橄榄色毛壳的子囊孢子呈暗橄榄褐色,量度亦较大,凭依经验即可鉴别此两个不同种。     

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。     

一种快速、灵敏的血小板释放功能检测方法及其在抗血小板药物研究中的应用

本文报道了一种快速、灵敏的血小板释放功能检测方法:利用荧光素-荧光素酶在有ATP、Mg~(2+)、O_2存在时产生的生物发光素测定血小板ATP的释放量,以反映血小板的释放功能;研究了ADP、AA、胶原、凝血酶等四种诱导剂对血小板释放功能的作用,发现ADP的诱导释放能力较其他三者为弱;观察在不同剂量ADP和AA的诱导下,血小板聚集强度和释放能力之间的关系,研究了血小板数等因素对ATP释放功能测定的影响。应用该方法研究了Aspirin及活血化淤药物川芎嗪,毛冬青甲素对血小板释放功能的影响,发现Aspirin对AA诱导的释放反应有强烈的抑制作用。在以ADP诱导的释放反应中,川芎嗪的抑制作用较毛冬青甲素更为强烈。     

红色毛癣菌蛋白酶MEP和SUB的表达及临床意义

目的探讨红色毛癣菌蛋白酶MEP和SUB的表达及临床意义。方法抽提红色毛癣菌总RNA,采用半定量RTPCR法检测红色毛癣菌金属蛋白酶(Metalloproteinases,MEP)、枯草菌素蛋白酶(subtilisins,SUB)基因表达量的变化。结果不同病例的红色毛癣菌SUB的表达水平与临床症状的严重程度密切相关,而与患者的年龄、性别、病程等无明显相关性;MEP的表达水平在不同年龄、性别、病程和临床分型等方面存在一定差异,但无显著意义。结论红色毛癣菌致病力的大小可能与SUB的不同表达有关。     

灵猫科3种兽针毛显微结构比较

对灵猫科大灵猫、小灵猫、花面狸头部针毛显微结构观察与分析,结果表明：1）3种动物针毛的长度大小不同;毛髓质指数存在显著性差异;2）毛鳞片在近根部和近稍部形状存在差别,主体部分等面积鳞片个数大灵猫、小灵猫与花面狸两两差别显著,而大灵猫与小灵猫无显著性差异（P〉0．05）．这些差异有利于分辨灵猫科的3种动物．     

香港地区毛蠓新种和新纪录(双翅目∶蠓科)

2005年11月和2006年5月,先后两次的采集中获得毛蠓1个本地新纪录,竹生毛蠓 Dasyhelea bambusaoris Yu,2005和3个新种,分别命名为何玉贤毛蠓新种 Dasyhelea heyuxiani Yu, Yuan, and Zeng sp. nov.、尖刺毛蠓新种 Dasyhelea apiculata Yu, Chen,and Yan sp. nov.和亚刺毛蠓新种 Dasyhelea subechinatus Yu,Zeng,and Yuan sp. nov..     

Morphological characteristics of the hair of Japanese monkeys (Macaca fuscata fuscata): Length,diameter and shape in cross-section,and arrangement of the medulla

A morphological study was carried out on hairs of the Japanese monkey. The shapes in cross-section were circles or ellipses. The diameters of the hairs ranged from 13.5 to 92 μ, and the mean value in each monkey was between about 30 and 40 μ. The average value of the fibre index was approximately 90 in each monkey. The arrangement of the medulla was considered to be of the narrow medulla lattice type. Medullae were developed poorly or disappeared in hairs with a diameter of less than 30 μ. A correlation was noted between the hair thickness and presence of medulla: medullated hairs were thicker than non-medullated hairs. A tendency was found for thicker hairs to be of greater length. The hairs of the Japanese monkey could be divided broadly into two types: medullated hair and non-medullated hair. The medullated hairs could be regarded as guard hair-like hairs since they were thick and long, and the non-medullated hairs as underhair-like hairs since they were thin and short.     

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。     

The effect of methyl-containing supplements during pregnancy on the phenotypic modification of offspring hair color in rats

The effect of methyl supplements to the diet of pregnant homozygous (AAHH) female rats with agouti coat color mated with homozygous (aahh) males on the phenotypic modification of the coat color of their heterozygous offspring (AaHh) has been studied. Comparative morphological analysis of the main parameters of hair that determine coat color, including the total length of hairs of different types and the length of the upper black (eumelanin) and light (pheomelanin) parts of awn hairs has been performed. The pattern of pigment granule distribution among hair layers has been analyzed. The melanin content of the hair has been determined using electron spin resonance (ESR). Although all offspring have a typical agouti coat color (alternating black and light portions of hair), 39% of them have a darker coat color than control and other experimental rats have. The main differences between the offspring with darkened and standard coat colors are accounted for by the ratio between the eumelanin and pheomelanin portions of awn hairs. In darkened offspring, this ratio is significantly higher than in control rats. The possible mechanisms of the phenotypic modification of agouti coat color in experimental animals are discussed.     

The effect of methyl supplements during pregnancy on the phenotypic modification of offspring agouti coat color in rats

The effect of methyl supplements to the diet of pregnant homozygous (AAHH) female rats with agouti coat color mated with homozygous (aahh) males on the phenotypic modification of the coat color of their heterozygous offspring (AaHh) has been studied. Comparative morphological analysis of the main parameters of hair that determine coat color, including the total length of hairs of different types and the length of the upper black (eumelanin) and light (pheomelanin) parts of awn hairs has been performed. The pattern of pigment granule distribution among hair layers has been analyzed. The melanin content of the hair has been determined using electron spin resonance (ESR). Although all offspring have a typical agouti coat color (alternating black and light portions of hair), 39% of them have a darker coat color than control and other experimental rats have. The main differences between the offspring with darkened and standard coat colors are accounted for by the ratio between the eumelanin and pheomelanin portions of awn hairs. In darkened offspring, this ratio is significantly higher than in control rats. The possible mechanisms of the phenotypic modification of agouti coat color in experimental animals are discussed.     

The site of the action of the angora-Y gene and its interaction with the fuzzy-Y gene in the mouse

The site of action of the goY mutant gene was determined in the aggregation chimaeras C57BL-goY/goY----DBA (+/+). Chimerism was detected by mosaicism of coat pigmentation and electrophoretic pattern of glucose phosphate isomerase. In 28-day-old chimaeras the regions of light-brown coat alternated black coat, stripes of short hairs alternated those of long hairs. These stripes of different length and width extended from spine in lateral-ventral direction. The hairs plucked from long hairs stripes had a similar length that those of goY/goY mice of same age, but the hairs plucked from short hair stripes corresponded to the hair length of +/+ mice. These data show that the goY gene acts in epidermal cells of hair follicles and its expression is autonomous. It has been established that in double homozygotes goY/goYfzY/fzY both mutant genes are expressed: the considerable increase of hair length as compared to norm--the effect of the goY gene and curly coat--the effect of the fzY gene. In goY/goYfzY/fzY mice during the formation of G1 guard hairs the incomplete expression of the goY gene is observed that is due to the suppression of hair growth by the fzY mutant gene. The fzY gene does not suppress the growth of G2 hairs and therefore the full expression of the goY gene occurs in goY/goYfzY/fzY adult mice.     

A preliminary study on hair length in the Japanese monkey (Macaca fuscata fuscata)

The hair length of Japanese monkeys was investigated. The hair of the Japanese monkey is long on the back and the lateral side of the upper arm and short on the back of the hand. There was variation in the length of hairs in the same region of the body. The distribution of hair length approximated to a normal curve and did not display any marked bias or skewness. The increase in length of hairs was remarkable from 0 to 1 year of age, and then continued at a constant rate. Sex differences in hair length were not so remarkable at any age.     

The failure behavior of the anchorage of hairs during slow extraction

Treatment of excessive hair growth is an important issue in both dermatological and cosmetic practice. In contrast to treatments with medication, most physical methods are treatments that focus on the hair follicle. To obtain insight in the failure behavior of the anchorage of hairs, hairs were extracted (in vitro) from pig skin at a speed of 0.1mm/s, one at a time. The pulling force and tweezers displacement were recorded. The extracted hairs were classified with respect to the phase in the growing cycle: anagen (growing phase), telogen (resting phase) or other (catagen phase or unable to determine). The anagen hairs showed a different relation between the tweezers displacement and the pulling force than the telogen hairs. Moreover, the maximum force that could be applied before a hair was extracted proved to be lower for anagen hairs than for telogen hairs (0.36N, 1.8N, respectively). The extracted hair length, defined as the part of the hair that had been embedded in the skin which was extracted, was higher for anagen hairs than for telogen hairs (4.8mm, 3.0mm, respectively). Removing proximal skin tissue and the embedded parts of the anagen hair (root) resulted in a change of the extraction curves. The results indicate that two phenomena play a role in the anchorage of anagen hairs. We have proposed a model for the extraction of an anagen hair that has been based on these results: first the interface between hair and skin that is located around the inner root sheath (IRS) starts to fail, followed by failing of the hair itself in the region where the hair keratinizes.     

Annual changes in hair length of the Japanese monkey (Macaca fuscata fuscata)

The hair length of Japanese monkeys was investigated for a period of one year and the molting phenomenon was clarified. Nine monkeys were employed in the study. The molting of the Japanese monkey was found to be of a seasonal type and occurred once during the year. The molting continued for one to four months in each monkey. The hair of the Japanese monkeys was wholly replaced during the period from April to August. The hair length was thus short in summer, and long in winter. Hair replacement in pregnant females began after parturition and was generally later than that in other individuals. During molting, both new and old hairs could be observed simultaneously in the same region of the body. The hair replacement ended around summer when the hair became the shortest. The new hairs continued to grow after molting and became the longest towards autumn or winter. Thus, the summer coat and the winter coat were essentially the same in the Japanese monkey. Such annual changes in the hair of the Japanese monkey were considered to be suitable for the climate of Japan.