繁殖季节和非繁殖季节布氏田鼠种群参数

在繁殖季节（6月份）和非繁殖季节（10月份）,采集了内蒙古自治区阿尔善宝力格地区的布氏田鼠样本,比较其种群参数与生理指标,探讨了布氏田鼠社群结构和生理特征的季节性差异,并分析了原因。结果表明,布氏田鼠的年龄组成和性比存在明显的季节差异：繁殖季节洞口系数小,种群性比接近1,主要由当年新生鼠和越冬鼠组成;非繁殖季节洞口系数大,种群性比偏雄,主要由当年新生鼠组成。繁殖器官在繁殖季节显著大于非繁殖季节,保持了更高活性。非繁殖季节个体的胴重比更高,且雄鼠高于雌鼠,表明非繁殖季节个体和雄鼠具有更好的营养状态;同时,非繁殖季节个体具有更小的肾上腺和更大的脾脏,说明非繁殖季节中的布氏田鼠表现出更低的应激状态和更强的免疫能力。这些研究结果表明,布氏田鼠的种群参数和生理特点具有明显的季节性特点,这与不同季节中布氏田鼠采取的生存策略有着紧密联系。     

粪便激素水平反映不同出生时期雄性布氏田鼠的繁殖策略

布氏田鼠是我国内蒙古草原的主要害鼠之一,具有明显的季节繁殖特征,不同季节出生个体可能具有不同的繁殖策略,但尚缺乏内分泌证据支持。本研究采用标志重捕法,连续监测大型自然围栏中不同年龄雄性布氏田鼠的繁殖状态和应激水平的季节变化,分析各年龄组雄鼠的繁殖发育策略。结果表明,越冬雄鼠可保持较高的睾丸下降率和睾酮水平至8月初;而部分5月生雄鼠的繁殖期睾酮水平较接近越冬鼠,但8月初已降至年内最低水平,而6月及以后出生雄鼠睾酮始终处于较低水平;这说明越冬鼠的繁殖状态可贯穿繁殖期始终,只有部分5月生雄鼠可能参与当年繁殖,而6月及以后出生雄鼠则不能在当年繁殖。越冬鼠皮质醇水平高于当年鼠,繁殖期高于非繁殖期,这可能是越冬鼠由于繁殖需要而保持较高应激状态,从而造成繁殖盛期后死亡率升高。这些结果说明,不同时期出生的雄性布氏田鼠具有不同的出生后性腺发育模式和繁殖策略,反映出生存与繁殖之间的权衡。     

布氏田鼠标志种群的繁殖参数

采用标志重捕和染色观测法跟踪了内蒙古典型草原区布氏田鼠野外种群,按绝对时间年龄研究其种群繁殖参数。结果3表明：4－5月份出生的雄鼠能在当年达到性成熟,性成熟发育历期约为1．5个月,6月后出生的雄鼠当年达不到性成熟。在达到性成熟的当年雄鼠中,多数个体再度转入性休止期,其平均繁殖结束时间要林越冬雄鼠早1个月,而越冬雄鼠则在整个繁殖期保持性活动状态。雌鼠性成熟发育历期约为1个月,首次产仔时间约为2月龄。雌鼠在一年中的产仔窝数与其年龄有关;越冬鼠能产3－4窝,4月份出生的雌鼠能产2－3窝,5月份出生的雌鼠当年能产1－2窝,6月份出生的雌鼠能产0－1窝,7月份之后出生雌鼠当年不参加繁殖,在自然条件下,布氏田鼠一年中最多能产4窝。     

布氏田鼠标志种群的社群等级及其季节变化

在内蒙古锡林郭勒地区,通过标志重捕、染色标记和直接观测法对布氏田鼠社群等级的季节变化进行了研究。结果表明:在繁殖季节,布氏田鼠洞群内存在明显的社群等级。越冬雄鼠在社群内社群序位最高,其次是越冬雌鼠、当年成体雌鼠、当年成体雄鼠,亚成体鼠和幼鼠的社群地位最低。在繁殖末期,越冬雄鼠的地位明显下降,而当年成体雄鼠的等级序位逐渐上升。在繁殖季节,当年雄鼠在洞群中的等级序位依然很低,很少能有机会进行有效的交配,有效交配主要由越冬雄鼠来完成,因而越冬雄鼠对种群繁殖的贡献较大。本实验倾向于支持该鼠的婚配制度为一雄多雌制的观点。     

密度因素在布氏田鼠种群调节中的作用

对布氏田鼠栖息密度不同的种群同时进行取样,研究密度因素对布氏田鼠种群发展的调节作用。结果表明,在高密度区布氏田鼠种群繁殖强度受到抑制,雌鼠怀孕率、雄鼠睾丸下降率、贮精囊肥大率和睾丸长度都小于低密度种群。高密度种群繁殖季节结束时间早于低密度种群,幼鼠肥满度较小,性成熟速度较慢,种群年龄结构中,幼年鼠所占比例小于低密度种群。这些都是导致高密度种群增长速度减慢的因素。     

黑线姬鼠(Apodemus agrarius)的种群繁殖参数及其地理分异特征

黑线姬鼠（Apodemus agrarius）是我国广大地区的主要害鼠之一,是余庆县农田害鼠优势种,占总鼠数的94.81%。探讨其种群繁殖参数的变动规律及其地理分异特征,对其种群数量预测预报具有重要意义。通过对1987-2005年贵州省余庆县黑线姬鼠种群繁殖参数分析结果表明：研究期间共解剖标本5497只,其中,雌鼠2698只,雄鼠2799只,黑线姬鼠在当地1-11月份均可繁殖,主要繁殖期在3-10月份,每年4-5月份和8-9月份出现2次妊娠高峰。种群总性比（♀/♂）为0.96,多年平均怀孕率为36.91%±6.79%,平均胎仔数为5.33±1.07只,平均繁殖指数为0.81±0.17,平均睾丸下降率为59.13%±7.89%。不同年龄组种群繁殖力存在显著差异,随着种群年龄的增长繁殖力不断增加,成年Ⅰ组、成年Ⅱ组、老年组是种群繁殖的主体。种群繁殖参数不同年度之间比较稳定,不同月份、不同季节之间变化差异较大,具有明显的季节变化特征。年均种群密度与年均繁殖指数呈极显著正相关,与胎仔数显著正相关,与年均怀孕率、睾丸下降率、性比相关性不显著,繁殖指数是影响黑线姬鼠种群密度的重要因子。比较全国各地黑线姬鼠种群繁殖参数的地理分异特征认为,黑线姬鼠种群繁殖参数具有明显的地理分异现象,胎仔数、生殖强度由南向北逐渐增加,具有随纬度的升高趋向增加的特征;在高纬度地区繁殖时间较短;性比与纬度、经度的变化关系密切;各繁殖参数与海拔的变化相关性不明显,可排除海拔因素的影响。     

棕色田鼠种群繁殖特征及密度制约调节

１９９２－１９９４年在河南灵宝市郊黄土高原农作区春夏秋逐月捕获并解剖棕色田鼠１７５７只,总性比为１．２０７３。全年都有繁殖鼠出现,但怀孕率、胎仔数、性比、繁殖指数有明显的季节变化,年间也有一定的差异,不同年龄组的性比、怀孕率、胎仔数、繁殖指数、睾丸下降率不同化率较为接近种群密度对繁殖特征有明显的调节作用高密度年份的棕色田鼠的性比、怀孕率和繁殖指数低于低密度年份,高密度区种群的繁殖强度受到抑制,雌鼠     

布氏田鼠种群数量的季节动态与鼠洞的关系

布氏田鼠种群和鼠洞数量均呈单峰型季节动态,新洞口和鼠丘上洞口的季节动态与鼠的季节动态存在-种正相关关系。盗洞率随堵洞后记录时间的推延而增加,并于堵洞后3天趋于最大值。盗洞率(r″′ )春季为40～50%;夏季为8O%以上;秋季为70～80% 。但每鼠盗洞数春季最高,夏季下降到最低,秋季又有所回升。样方内鼠只数／真实盗洞率(K_3max )比较理想,鼠只数／堵洞数(K₁ )比较实用。洞口系数K₁具有显著性季节变化,春季为口0.05995,夏季为O.2336,秋季为0.141。     

贵州地区黑线姬鼠种群繁殖特征

黑线姬鼠(Apodemus agrarius)是贵州地区分布广泛的主要农田害鼠之一,掌握其种群繁殖特征可为种群动态的预测预报提供基础资料。1984~2014年间,采用夹夜法逐月调查了贵州省余庆县8个县(市)监测点黑线姬鼠种群动态数据,分析了其种群性比、雌鼠怀孕率和平均胎仔数、雄鼠睾丸下降率等主要繁殖生物学指标及其地理差异和季节性变动规律,明确了贵州地区黑线姬鼠种群的繁殖特征。共捕获黑线姬鼠20 113只,不同地区种群间,除平均胎仔数有显著差异外(χ~2=36.503,df=7,P0.01),其他繁殖特征值均没有差异。从时间序列看,种群中雌鼠怀孕率和雄鼠睾丸下降率的季节性变化均表现为春季(4~5月)及夏末秋初(8~9月)达到高峰的双峰型。雌鼠产仔数一般2~10只,4~7只最为常见(占93.87%)。不同季节平均胎仔数差异不大。贵州地区黑线姬鼠繁殖的总体特点为全年繁殖,春秋两季为繁殖的高峰期,冬季(12月份和翌年1、2月份)繁殖强度明显低于其他季节(F_(11,84)=61.92,P0.01),但种群密度表现为6月达到最高点的单峰型特点。     

布氏田鼠肝毛细线虫感染率与其体重的关系

2005年5月和8月,在内蒙古锡林郭勒北部典型草原调查了肝毛细线虫对布氏田鼠种群的感染特征,分析肝毛细线虫对布氏田鼠的感染率与其性别、年龄、体重及种群密度的关系。结果表明:肝毛细线虫对布氏田鼠感染率没有性别差异,雄鼠与雌鼠的感染率相当;但是与布氏田鼠体重/年龄密切相关:幼鼠的感染率较低,成鼠感染率较高,感染率和平均感染度均随着个体年龄的增长而增高。布氏田鼠达到一定的年龄(或体重)后才可感染肝毛细线虫病,其最低感染体重为24.3 g。布氏田鼠的种群密度对肝毛细线虫的感染率和平均感染度没有明显的影响,但同一样地不同季节感染率不同,本次调查显示,2005年5月份感染率高于8月份群体感染率,同一样地的春季感染率与秋季感染率之间呈现出显著的正相关。     

Excess of unpaired males in one of the World's most endangered seabirds, the Chatham Island taiko Pterodroma magentae

The Chatham Island taiko Pterodroma magentae (tchaik) is one of the World's most endangered seabirds with a population size of between 120–150 individuals that includes only 8–15 breeding pairs. Molecular techniques were used to identify the sex of taiko, which is difficult to assign morphologically. Blood samples were obtained from almost the entire known living population and from some birds now thought to be dead. We report an approximately even sex ratio in taiko chicks and adults associated with breeding burrows, but a large male-biased ratio in non-breeding adult birds caught on the ground. This finding suggests that unpaired males may be having difficulty in attracting females to burrows and that this situation may be an example of the Allee effect, that reduced density of potential mates acts to decrease population productivity. Identification of the sex of taiko using a molecular technique has important implications for the conservation management of this critically endangered species, including the future transfer of taiko chicks to a predator-excluded breeding site.     

The difference of urine between Brandt’s voleLasiopodomys brandtii in the breeding and non-breeding condition

Using animal house experiments we demonstrated that urine odor can elicit physiological changes in the maturation rate of Brandt’s vole (Radde, 1861). We showed that the urine of estrous females, anestrous females and non-breeding males had no effect on the time of sexual maturity of young voles. In contrast, the maturation rate of young female voles was accelerated, and the maturation rate of young male voles was slowed, by exposure to the urine of breeding adult males. Headspace analysis revealed significant differences in the levels of a subset of volatile constituents of urine from breeding and non-breeding males. From a total of 50 components, Propanoic acid, 2,5-Dimethylpyrazine, Dimethyldisulfide, 1-Octene, 1-Hexanol, Hexanoic acid and p-Xylene were observed only in the urine of breeding male Brandt’s voles. All other substances were present in the volatiles from urine of both breeding and non-breeding male Brandt’s vole.     

Burrow structure and use in the sand fiddler crab, Uca pugilator (Bosc)

Uca pugilator, the sand fiddler crab, constructs two kinds of burrows in protected, sandy upper-intertidal and supratidal substrates on the west coast of Florida. Temporary burrows are built and used as a refuge by non-breeding crabs during high tide periods and at night when crabs cease feeding in the intertidal zone. Breeding burrows are constructed and defended by courting males and are the site of mating, oviposition and the incubation of eggs by females. Up to three ovigerous females may be accommodated in a single breeding burrow, each female sequestered in a separate terminal chamber. The construction and defence of burrows specialized for breeding may be an adaptive response by males to the preferences females exhibit when selecting a breeding site.     

Reproduction and population density affect humoral immunity in bank voles under field experimental conditions

Density dependence is a common feature in the dynamics of animal populations. Availability of food resources critical to immunity is likely to be one of the mechanisms mediating the effect of population density on individual fitness. The ability to mount an immune response to an antigen is also affected by levels of immunosuppressive hormones associated with reproduction or mediating the response to ecological and social stress. We assessed variation in condition and intensity of humoral immune response to a T-cell-dependent antigen in bank voles (Clethrionomys glareolus) by experimentally altering population density before immunisation. Consistent with our prediction, males had lower humoral immunocompetence in the breeding than in the non-breeding season. Contrary to our expectation, males did not show enhanced immunocompetence and females showed depressed humoral immune response under experimentally lowered population density. Variation of immune response in relation to population density depended on sex, with females but not males showing lower immune response under experimentally reduced density. We conclude that humoral immunity of bank voles was affected by reproduction and social environment rather than by population density. Received: 2 November 1999 / Accepted: 22 March 2000     

Strong migratory connectivity and seasonally shifting isotopic niches in geographically separated populations of a long-distance migrating songbird

Whether migratory animals use similar resources during continental-scale movements that characterize their annual cycles is highly relevant to both individual performances and population dynamics. Direct knowledge of the locations and resources used by migrants during non-breeding is generally scarce. Our goal was to estimate migratory connectivity of a small Palaearctic long-distance migrant, the common nightingale Luscinia megarhynchos, and to compare resources used in non-breeding areas with resources used at the breeding grounds. We tracked individuals of three geographically separated populations and characterised their stable isotope niches during breeding and non-breeding over 2 years. Individuals spent the non-breeding period in population-specific clusters from west to central Africa, indicating strong migratory connectivity at the population level. Irrespective of origin, their isotopic niches were surprisingly similar within a particular period, although sites of residence were distant. However, niche characteristics differed markedly between breeding and non-breeding periods, indicating a consistent seasonal isotopic niche shift in the sampled populations. Although nightingales of distinct breeding populations migrated to different non-breeding areas, they chose similar foraging conditions within specific periods. However, nightingales clearly changed resource use between breeding and non-breeding periods, indicating adaptations to changes in food availability.     

Changes in population structure and reproduction during a 3-yr population cycle of voles

Cyclic changes in population growth rate are caused by changes in survival and/or reproductive rate. To find out whether cyclic changes in reproduction are an important part of the mechanism causing cyclic fluctuations in small mammal populations, we studied changes in the population structure and reproduction of field voles ( Microtus agrestis ), sibling voles ( M. rossiaemeridionalis ), bank voles ( Clethrionomys glareolus ), and common shrews ( Sorex araneus ) in western Finland during 1984–1992, in an area with 3-yr vole cycles. We also modelled the population growth of voles using parameter values from this study. The animals studied were collected by snap trapping in April, May, June, August, September, and, during 1986–1990, also in October. We found several phase-related differences in the population structure (age structure, sex ratio, proportion of mature individuals) and reproduction (litter size, length of the breeding season) of voles. In non-cyclic common shrews, the only significant phase-related difference was a lower proportion of overwintered individuals in the increase phase. According to the analyses and the vole model, phase-related changes in litter size had only a minor impact on population growth rate. The same was true for winter breeding in the increase phase. The length and intensity of the summer breeding season had an effect on yearly population growth but this impact was relatively weak compared to the effect of cyclic changes in survival. The population increase rates of Microtus were delayed dependent on density (8–12-month time lag). Our results indicate that cyclic changes in reproduction are not an important part of the mechanism driving cyclic fluctuations in vole populations. Low survival of young individuals appeared to play an important role in the shift from the peak to the decline phase in late summer and early autumn.     

To breed or not to breed: causes and implications of non-breeding habit in the willow tit Parus montanus

Causes and consequences of non-breeding in willow tits were studied in northern Finland during 1986–1992. The breeding status was sex and age biased; males and yearling birds were in excess among the non-reproducers. Due to sex bias in the population it appeared detrimental for males to lose a mate, especially shortly before breeding. Lack of a mate was a important factor for males not reproducing (37% of non-breeding males) than for females (14%). Most of the non-breeding birds maintained a pair bond which only rarely broke up for the next breeding season (divorce rate 5.5%). This implies that parental incompatibility is not a possible explanation for pairs not reproducing. Males that did not breed tended to survive better than reproducing ones, whereas such a relationship was not found for females. It is possible that this sex-related difference in survival cost is attributable to quality differences among non-breeding individuals. It was especially low-quality yearling females, with low survival prospects, that were responsible for the discrepancy. The proportion of non-breeding females in the population correlated highly with clutch size and subsequent juvenile survival. It is therefore suggested that for most of these females non-breeding is a phenotypic response to low offspring value in the prevailing circumstances (inter-generational tradeoff). However, it is uncertain whether willow tits in a northern population can use breeding density as an indicator of changing survival prospects of their descendants, as suggested by Ekman and Askenmo (1986) for southern Sweden.     

Seasonal changes in the seminiferous epithelium of rhesus and bonnet monkeys

With a view to elucidate seasonal variations in testicular spermatogenesis, quantitative analysis of spermatogenic cells was carried out in non-human primate species viz. rhesus (Macaca mulatta) and bonnet (M. radiata) monkeys during breeding (October-December) and non-breeding (May-June) seasons. The results revealed significant inhibition of testicular germ cell population during non-breeding compared with the breeding period in both the species. Quantitative determination of Sertoli cell-germ cell ratio showed a marked decrease in the number of type A-spermatogonia, spermatocytes (non-pachytene and pachytene) and spermatids (in steps 1-12 of spermiogenesis) in rhesus monkey during the non-breeding period. Bonnet monkeys exhibited the significant decline in the number of primary spermatocytes and spermatids during the non-breeding phase. In addition, average diameter of round seminiferous tubules and nuclear diameter of Leydig cells also decreased significantly in rhesus monkeys. However, bonnet monkeys did not show any significant change in nuclear diameter/morphology of Leydig cells, testicular tubular diameter and number of type A-spermatogoniae. Sertoli cell number did not show any significant change during both breeding and non-breeding periods in both the species. The results of this study indicate a prominent seasonal variation in testicular spermatogenic/Leydig cells in rhesus monkeys than those observed in bonnet monkeys.     

Adult philopatry and dispersal in the field vol Microtus agrestis

Summary Using mark-recapture data, we related the movements of adult field voles to population density, sex ratio and population growth. Dispersal movements (defined as distances larger than 1 home range diameter) were few in both sexes; 4 out of 197 (2.0%) in males and 8 of 316 (2.5%) in females. The distance moved between sequential trapping periods was similar for males and females; the mean being 10.2 m and 9.0 m respectively. Both males and females moved larger distances during the breeding season than during the nonbreeding period. The distance moved between sequential trapping periods showed a strong negative relation to density, i.e. both sexes moved shorter distances at higher densities, but there were no differences between periods of increasing and declining population densities. These results contradict the dispersal predictions of all major hypotheses proposed to explain population fluctuations in small mammals. The dispersal patterns fit a geometric distribution, suggesting that competition is the primary factor determining the dispersal characteristics of this population.