红瘰疣螈胚胎发育的初步观察

报道红瘰疣螈（Tylototmon shanjing）的胚胎发育过程。根据胚胎发育过程中的形态变化规律将胚胎发育过程分为22个时期,在室温（25±1）℃的条件下,胚胎发育历时20-22d。描述了各时期的形态特征,并讨论了发育中的一些现象。     

红瘰疣螈皮肤的显微结构观察

对我国Ⅱ级重点保护野生动物红瘰疣螈(Tylototriton shanjing)成体的皮肤结构进行了显微观察。观察结果表明,其皮肤厚薄、微血管、色素分布,以及腺体的分布和大小等方面在身体的不同部位存在差异:头和背部的皮肤厚于腹部;黑色素细胞多分布于真皮浅层,以腹部及背侧无瘰粒处多见;真皮层富含黏液腺和颗粒腺,但分布不均匀;头嵴棱部及背部瘰粒下方颗粒腺的数量多、体积大,并充满分泌物;表皮下腺体外突,其表皮细胞层数减少,形成分泌物有效通道。同时,将红瘰疣螈皮肤与其他两栖类相比可知,其以上皮肤结构特征均体现了红瘰疣螈对山区阴湿环境中陆栖生活的重要适应。     

温度对红瘰疣螈胚胎发育的影响

探讨了不同温度对红瘰疣螈Tylototriton shanjing Nussbaum,Brodie et Yang 1995胚胎发育速度、孵化率及胚长增长速度的影响,并对胚胎发育起点温度和发育有效积温等进行研究。结果表明,在试验温度范围内(10³0℃),随着温度的升高,其胚胎发育速度、胚长增长速度加快,发育时间缩短,孵化率上升。其中孵化率与孵化温度成线性关系(Y=0.0017X+0.95230),发育周期与孵化温度成线性关系(Y=-0.377X+24.154)。但红瘰疣螈有一定适宜温度范围(2030℃),随着温度的升高,其胚胎发育速度、胚长增长速度加快,发育时间缩短,孵化率上升。其中孵化率与孵化温度成线性关系(Y=0.0017X+0.95230),发育周期与孵化温度成线性关系(Y=-0.377X+24.154)。但红瘰疣螈有一定适宜温度范围(20²5℃),超过或低于该温度范围,卵的畸形率和最终死亡率明显增加。应用直线回归法和直接最优化法计算红瘰疣螈胚胎发育的发育起点温度和有效积温分别为0.58℃、68.66日度和0.46℃、69.01日度。     

红瘰疣螈的繁殖生态

红瘰疣螈(Tylototriton shanjing)为国家Ⅱ级重点保护野生动物,对其繁殖生态尚无系统的研究.2007 ～2010年在云南省新平县哀牢山对红瘰疣螈形态、繁殖栖息地、求偶和交配行为、产卵及孵化等繁殖特征进行了研究.结果表明,红瘰疣螈雌雄两性在广泛的形态学度量特征上存在着差异;繁殖栖息地主要为稻田和潮湿的沟渠;参与繁殖的雌雄成体性比随繁殖时间的推移而不断变化,繁殖前期和后期雄性比例高,中期雌性比例高.求偶和交配主要在陆地潮湿的水沟中完成,也可在静水中进行.成体产卵活动从5月初持续至6月下旬,呈现出波浪式的产卵进程,个体完成产卵平均时间为(22.2 ±2.7)h.繁殖前期雌螈产卵于稻田,中后期产于多杂草的田埂草丛和泥壁,平均产卵数( 126±18)枚(n=17).平均孵化期(17.3 ±0.1)d(n =225),孵化率59.8％ (n =79),孵化时幼体平均体长12.7mm(n =6).     

降雨决定繁殖期红瘰疣螈的活动性

有尾两栖类的繁殖活动常常受到环境因子,特别是如温度、湿度和降雨等气候因子的限制。红瘰疣螈Tylototriton shanjing是适应云南山地环境的典型有尾两栖类动物。本研究期望通过对繁殖期红瘰疣螈活动个体数量的野外调查和气候因子的分析,弄清影响红瘰疣螈繁殖行为活动的关键气候因子。研究结果显示,繁殖期红瘰疣螈活动个体数量与气温呈显著的负相关关系,与空气相对湿度和降雨量呈显著的正相关关系。然而偏相关和多元回归分析则表明,红瘰疣螈繁殖行为活动与相对湿度和降雨量关系更密切。红瘰疣螈总是在降雨后引起空气湿度增加以及气温下降时进行各种繁殖行为活动,降雨是影响红瘰疣螈繁殖行为活动关键的气候因子。红瘰疣螈的繁殖行为活动与降雨节律保持一致是对云南山地环境的重要适应。     

红瘰疣螈玉龙雪山种群的两性异形

分别测量于2018年6—8月采自云南丽江玉龙雪山的32只(17♂,15♀)红瘰疣螈Tylototriton shanjing成体的全长、头体长、头长等13项形态特征指标,并检验该物种的两性异形。结果表明:雌性平均全长为160.72 mm±3.02 mm(n=15),雄性平均全长为138.58 mm±2.57 mm(n=17),雌性与雄性平均全长比为1.160,两性异形指数为0.138,属雌性大于雄性的两栖类;全长在两性间的差异有统计学意义;除了雌性的头宽、尾宽、尾高和腋至胯距外,其他形态特征与全长均有显著或极显著相关性;以全长为协变量的协方差分析结果显示,红瘰疣螈的头体长、头长、吻长、尾长和前肢长在两性间的差异有统计学意义;雌性的尾长和前肢长随全长的生长速率大于雄性,而头体长、头长和吻长随全长的生长速率小于雄性。生育力选择假说能解释红瘰疣螈玉龙雪山种群的两性异形现象。     

捕食风险对红瘰疣螈幼体生长发育的影响

捕食风险是两栖动物幼体表型和生活史进化重要的选择压力之一。红瘰疣螈Tylototriton shanjing为云南山地环境中典型的有尾两栖类,山地环境水体水量的迅速减少常导致红瘰疣螈在幼体发育阶段捕食风险增加。本研究通过实验,观察红瘰疣螈幼体的体长和体质量在不同捕食风险环境中的变化、变态时体型以及完成变态发育的时间差异,探讨捕食风险对红瘰疣螈幼体个体早期发育的影响。实验设计4个不同的捕食风险处理:无任何捕食者的无捕食组、有同种个体化学信号的同种异体组、有同种尾受伤个体化学信号的断尾组、有入侵物种——克氏原螯虾Procambarus clarkii信息的外来物种组。结果显示,红瘰疣螈幼体在不同捕食风险环境中的生长发育过程不同。在生长发育前期,所有处理组的幼体生长均相似,而在中后期,有捕食风险存在的3个处理组生长发育显著加快,最终变态时的体长和体质量要比无捕食风险组更长和更重,体型更大。幼体在有捕食风险存在的处理组完成变态的时间要比无捕食风险组显著更短。这表明,红瘰疣螈幼体在面对捕食风险增加时,通过在胚后发育后期加快生长和缩短发育时间,尽快完成变态,离开幼体发育水体来适应高捕食风险的水环境。     

云南新平哀牢山红瘰疣螈的陆地求偶交配行为模式

: 红瘰疣螈Tylototriton shanjing为云南山地环境中典型的有尾两栖类,其求偶交配行为模式尚未被系统研究。2013—2014年对云南省新平县哀牢山繁殖期红瘰疣螈在陆地环境中的求偶交配模式进行了观察。研究结果显示,红瘰疣螈的求偶交配行为是按照一定时序进行的,整个过程由定位、静止展示、劝导展示和精子转移4个阶段组成。在求偶交配中雄性个体行为包括:警戒、追逐、阻拦、蹑行、嗅探、轻推、诱导、扇尾、侧行和产精包等类型。雌性个体的行为包括离开、静止、跟随、纳精包等类型。雄性行为较雌性复杂,雄性在求偶交配行为过程中占据主动。雌雄的识别主要以视觉为主,整个求偶交配过程中无抱握行为,雄性尾部的运动也比较单一,这些行为的变化可能是对在陆地求偶交配的适应。     

氧化乐果对红瘰疣螈胚胎及蝌蚪生长发育的影响

本文研究了氧化乐果对红瘰疣螈Tylototriton shanjing胚胎及蝌蚪生长发育的影响。结果表明,氧化乐果对红瘰疣螈胚胎发育过程中的出膜期和开口期毒性较大,其余各期毒性较小。随着氧化乐果浓度的增大,红瘰疣螈的畸形率和死亡率逐渐增大。gosner22期蝌蚪的安全浓度是0.05 mg·L~(-1)。在安全浓度内,0.03 mg·L~(-1)氧化乐果溶液对蝌蚪的生长具有明显的促进作用,浓度高于0.03 mg·L~(-1)则对蝌蚪的生长发育有明显的滞育作用,对其生长的影响主要表现在10 d以后,这与处理时间延长,毒物在蝌蚪体内富集有关。氧化乐果对红瘰疣螈胚胎及蝌蚪生长发育有显著的影响和损伤,该研究为农业生产科学合理使用农药提供了依据。     

龙里瘰螈与织金瘰螈的核型

用常规涂片法对贵州产龙里瘰螈Paramesotriton longliensis与织金瘰螈P. zhijinensis的染色体核型进行了研究。结果显示,龙里瘰螈的核型为2n=24=16m+8sm,染色体臂数NF=48,其中No.7、10、11、12为亚中着丝粒染色体(sm),其余均为中着丝粒染色体(m);织金瘰螈的核型为2n=24=20m+4sm,NF=48,其中No.9、11为sm,其余均为m。2种瘰螈的核型存在差异,可为2个物种的成立提供细胞遗传学佐证。     

Validation of an individualised model of human thermoregulation for predicting responses to cold air

Most computer models of human thermoregulation are population based. Here, we individualised the Fiala model [Fiala et al. (2001) Int J Biometeorol 45:143–159] with respect to anthropometrics, body fat, and metabolic rate. The predictions of the adapted multisegmental thermoregulatory model were compared with measured skin temperatures of individuals. Data from two experiments, in which reclining subjects were suddenly exposed to mild to moderate cold environmental conditions, were used to study the effect on dynamic skin temperature responses. Body fat was measured by the three-compartment method combining underwater weighing and deuterium dilution. Metabolic rate was determined by indirect calorimetry. In experiment 1, the bias (mean difference) between predicted and measured mean skin temperature decreased from 1.8°C to −0.15°C during cold exposure. The standard deviation of the mean difference remained of the same magnitude (from 0.7°C to 0.9°C). In experiment 2 the bias of the skin temperature changed from 2.0±1.09°C using the standard model to 1.3±0.93°C using individual characteristics in the model. The inclusion of individual characteristics thus improved the predictions for an individual and led to a significantly smaller systematic error. However, a large part of the discrepancies in individual response to cold remained unexplained. Possible further improvements to the model accomplished by inclusion of more subject characteristics (i.e. body fat distribution, body shape) and model refinements on the level of (skin) blood perfusion, and control functions, are discussed.     

Torpor, thermal biology, and energetics in Australian long-eared bats (Nyctophilus)

Previous studies have suggested that Australian long-eared bats (Nyctophilus) differ from northern-hemisphere bats with respect to their thermal physiology and patterns of torpor. To determine whether this is a general trait of Australian bats, we characterised the temporal organisation of torpor and quantified metabolic rates and body temperatures of normothermic and torpid Australian bats (Nyctophilus geoffroyi, 7 g and N. gouldi, 10 g) over a range of air temperatures and in different seasons. The basal metabolic rate of normothermic bats was 1.36 ± 0.17 ml g⁻¹ h⁻¹ (N. geoffroyi) and 1.22 ± 0.13 ml g⁻¹ h⁻¹ (N. gouldi), about 65% of that predicted by allometric equations, and the corresponding body temperature was about 36 °C. Below an air temperature of about 25 °C bats usually remained normothermic for only brief periods and typically entered torpor. Arousal from torpor usually occurred shortly after the beginning of the dark phase and torpor re-entry occurred almost always during the dark phase after normothermic periods of only 111 ± 48 min (N. geoffroyi) and 115 ± 66 min (N. gouldi). At air temperatures below 10 °C, bats remained torpid for more than 1 day. Bats that were measured overnight had steady-state torpor metabolic rates representing only 2.7% (N. geoffroyi) and 4.2% (N. gouldi) of the basal metabolic rate, and their body temperatures fell to minima of 1.4 and 2.3 °C, respectively. In contrast, bats measured entirely during the day, as in previous studies, had torpor metabolic rates that were up to ten times higher than those measured overnight. The steady-state torpor metabolic rate of thermoconforming torpid bats showed an exponential relationship with body temperature (r ² = 0.94), suggesting that temperature effects are important for reduction of metabolic rate below basal levels. However, the 75% reduction of metabolic rate between basal metabolic rate and torpor metabolic rate at a body temperature of 29.3 °C suggests that metabolic inhibition also plays an important role. Torpor metabolic rate showed little or no seasonal change. Our study suggests that Australian Nyctophilus bats have a low basal metabolic rate and that their patterns of torpor are similar to those measured in bats from the northern hemisphere. The low basal metabolic rate and the high proclivity of these bats for using torpor suggest that they are constrained by limited energy availability and that heterothermy plays a key role in their natural biology. Accepted: 22 November 1999     

环境温度对爪鲵体温及能量代谢的影响

应用封闭式小动物能量代谢仪测定了爪鲵在6℃、10℃、15℃、20℃和25℃环境条件下的体温和能量代谢以及在极端环境中的耐受性,探讨环境温度对爪鲵体温及能量代谢的影响.结果表明:爪鲵体温与环境温度呈正相关,其直线回归方程为:Tb=0.6966 0.9518Ta,相关非常显著.爪鲵对极端环境温度的耐受力较弱,在32℃-35℃高温和-2℃到-6℃低温 环境中的致死体温(TbL50)分别为27.7℃±0.9165℃和2.85℃±0.1539℃.在环 境温度为6℃-25℃的范围内,爪鲵的能量代谢与环境温度呈指数回归相关,指数方程为MR=0 .7495e0.0408x,相关显著.其代谢水平随环境温度的升高而升高,不同于内热源动物的代谢特征,爪鲵的体温调节和能量代谢显示出外热源动物的特点     

The origin of allometric scaling laws in biology

The empirical rules relating metabolic rate and body size are described in terms of (i) a scaling exponent, which refers to the ratio of the fractional change in metabolic rate to a change in body size, (ii) a proportionality constant, which describes the rate of energy expenditure in an organism of unit mass. This article integrates the chemiosmotic theory of energy transduction with the methods of quantum statistics to propose a molecular mechanism which, in sharp contrast to competing models, explains both the variation in scaling exponents and the taxon-specific differences in proportionality constants. The new model is universal in the sense that it applies to unicellular organisms, plants and animals.     

从线粒体Cyt b基因探讨红瘰疣螈物种地位的有效性

疣螈属的红瘰疣螈(Tylototriton shanjing)和棕黑疣螈(T.verrucosus)的物种界限一直不清楚。测定了来自中国西南地区14个地点的T.shanjing和T.verrucosus共40只标本的线粒体DNACytb基因(753bp)。结果表明:(1)用邻接法、最大简约法和贝叶斯法等3种系统发育分析法分别重建棕黑疣螈种组系统发育树的拓扑结构不支持T.shanjing是单系群;(2)T.shanjing与T.verrucsus的mtDNA Cytb序列差异平均值仅为1.2%,未达到种级水平。因此,全部T.shanjing样品都属于同一个物种,即T.verrucosus,不支持T.shanjing的物种地位,T.shanjing为T.verrucosus的同物异名,并建议恢复T.verrucosus的中文名红瘰疣螈。根据基于40个样品Cyt b基因序列的系统发育树和遗传变异以及地理分布,这些红瘰疣螈(T.verrucosus)样品聚为3支,即中国西南地区的红瘰疣螈可分为片马、滇中滇西和滇东南3个地理居群。     

Seasonal effects on thermoregulatory abilities of the Wahlberg's epauletted fruit bat (Epomophorus wahlbergi) in KwaZulu-Natal,South Africa

Seasonal variations in ambient temperature (T_a) require changes in thermoregulatory responses of endotherms. These responses vary according to several factors including taxon and energy constraints. Despite a plethora of studies on chiropteran variations in thermoregulation, few have examined African species. In this study, we used the Wahlberg's epauletted fruit bat (Epomophorus wahlbergi, body mass≈115 g) to determine how the thermoregulatory abilities of an Afrotropical chiropteran respond to seasonal changes in T_a. Mass specific Resting Metabolic Rates (RMR_Ta) and basal metabolic rate (BMR) were significantly higher in winter than in summer. Furthermore, winter body mass was significantly higher than summer body mass. A broad thermoneutral zone (TNZ) was observed in winter (15–35 °C) compared with summer (25–30 °C). This species exhibited heterothermy (rectal and core body temperature) during the photophase (bats' rest-phase) particularly at lower T_as and had a low tolerance of high T_as. Overall, there was a significant seasonal variation in the thermoregulatory abilities of E. wahlbergi. The relative paucity of data relating to the seasonal thermoregulatory abilities of Afrotropical bats suggest further work is needed for comparison and possible effects of climate change, particularly extreme hot days.     

Thermosensitivity changes in cold-adapted rats

Cold-adapted rats (unlike non-adapted animals) respond to an acute exposure to external cold by an overshoot increase in metabolic rate and a paradoxical increase in body core temperature. In contrast to external cooling, internal cooling with the aid of a chronically implanted intravenous heat exchanger elicited comparable increase in metabolic rate, coupled with a large fall in core temperature. It is concluded that cold adaptation alters peripheral thermosensitivity (enhances cold sensitivity), while the thermosensitivity of the core is not affected by the adaptation process.