银狐气味对根田鼠行为的影响

在实验室条件下,主要测定银狐（Vulpes vulpes)的气味对根田鼠(Microtus oeconomus）社会行为和交配行为的作用格局。结果表明,根田鼠的交配行为模式属于＃11模式既无限制,抽动,多次插入和多次射精,但有时射精前无多次插入;银狐对根田鼠的交配行为的频次具有极显抑制作用（P＜0．001）;银狐气味对根田鼠雌体 击行为以及两性的自我修饰的频次和累积时间具有显（P＜0．05）的抑制作用,而可极显提高雄体对雌体探究行为的累积时间（P＜0．01）。     

云南拉沙山黑白仰鼻猴交配行为和出生季节

灵长类的交配模式对于了解和掌握雄性的交配策略和社群的稳定机制非常重要,但是目前有关亚洲灵长类交配模式的数据较少;因此,该研究于2011年1—12月,分别采用全事件取样法和焦点动物瞬时扫描取样法收集了拉沙山黑白仰鼻猴群的交配行为和出生数据。猴群全年交配,有2个峰期,一个是繁殖交配高峰期(8一10月);另一个在出生季节,但其非繁殖交配的生物学意义尚不清楚。雌性通过俯卧/注视雄性或跳落邀配。爬跨射精比为8.8,射精交配稀少(11.4%),这说明雄性并非每次交配都射精,因而支持黑白仰鼻猴交配模式的主体为多次爬跨射精或处于从单次爬跨射精到多次爬跨射精连续谱上段的观点。雄性邀配的射精爬跨多于雌性,说明多次爬跨射精不仅是雄性的一个交配策略,而且可以决定交配模式在连续谱的位置。交配时间后延6~7个月,交配频次与婴猴出生率相关。拉沙山猴群出生模式为严格的季节性,这进一步证实了前人的观点。婴猴出生具有一定的同步性,且不同猴群婴猴出生的同步模式不同。     

建巢行为提高雄性根田鼠的个体发育和存活

为研究建巢行为对室内繁育根田鼠的可能影响,共设计两个实验:(1)选择30 对配对根田鼠分成两组,即15 对建巢根田鼠(建巢组)和15 对不建巢根田鼠(不建巢组),每对根田鼠提供5. 3 g 左右的棉花作巢材,持续30 d。记录两组有无实验动物时的巢内、巢上温度变化情况。(2)记录24 窝后代的出生时体重、断奶时体重、杀婴的数量和日龄。结果表明,建巢组巢内温度显著高于不建巢组巢内温度,相反的是,建巢组的巢上温度比不建巢组的巢上温度低。两组间后代出生时的平均体重没有显著差异但断奶时的体重存在显著差异。而且,在2 ～ 14 日龄间,建巢组和不建巢组雄性后代体重之间存在显著差异。建巢组的杀婴数量极显著低于不建巢组的杀婴数量。因此,建巢行为可以显著提高雄性后代的个体发育和后代的存活。     

根田鼠粪便皮质酮的检测效能

为验证根田鼠粪便皮质酮的可检测效能,本研究检测根田鼠粪便皮质酮含量的昼夜变化,并检测急性应激后和慢性应激期间根田鼠粪便皮质酮含量变化,及其慢性应激个体的HPA 轴负反馈功能。结果表明,根田鼠粪便皮质酮水平具有明显的似昼夜节律,粪便中皮质酮含量的最高点出现在08:00 和24:00,最低点在12:00 和16:00;在终止急性应激12 h 后,根田鼠粪便皮质酮含量显著增加,且有性别间差异;慢性应激根田鼠粪便皮质酮含量始终保持在高水平;再次急性应激,慢性应激根田鼠个体的粪便皮质酮含量较对照个体升高的时间延后。上述结果说明,根田鼠的粪便皮质酮含量能够反映机体所处的生理状态及应激水平,因此,该方法可用于野外根田鼠种群的相关研究并具有可靠性。     

白马雪山自然保护区响古箐滇金丝猴的交配行为

灵长类交配模式是灵长类社群结构和婚配制度的重要表征之一,其研究有助于了解灵长类社群结构和两性交配策略。2013年11月至2014年10月,我们对云南白马雪山国家级自然保护区一人工辅助投食滇金丝猴群进行了观察研究,采用焦点动物取样法和全事件记录法收集了雌雄个体交配相关的行为数据,主要包括邀配对象、交配过程、持续时间和回合数,以及参与交配的雌雄对在交配结束后的相互理毛的持续时间和回合数。研究结果表明:研究群滇金丝猴全年均有交配行为,交配高峰期在7-9月,两性参与交配的积极性和对季节变化的响应不同;交配主要由雌性通过邀配发动(76%),交配高峰期也是雌性邀配的高峰期;雄性爬跨频次(年均0.43次/月,n=5)和射精爬跨比(年均19%,n=5)在全年无显著变化。交配行为发生的典型表现为:雌性通过小跑或跳跃进入雄性视线范围内,爬伏呈臀向雄性邀配;雌猴爬伏时离雄猴的远近距离不同(1 m vs.2-5 m:69%vs.31%)会影响其邀配成功率(1 m vs.2-5 m:68%vs.40%);若一次邀配失败,雌猴可能会连续爬伏邀配(最多4次),连续多次邀配的成功率显著高于单次邀配(79%vs.52%)。交配结束后雌性会主动为雄性理毛,但雌性主动理毛与交配是否射精无关。     

人工饲养下金丝猴繁殖的观察研究 Ⅰ.交配行为

金丝猴(Rhinopithecus roxellanae)是我国稀有的珍贵特产动物,笔者在多年观察金丝猴的繁殖行为的基础上,又于1986年8-9月在北京动物园,对金丝猴的交配、爬跨行为进行了专门观察,发现金丝猴发动性活动的一些特点,并在交配爬跨时,雄性金丝猴有卷尾现象。其交配行为与叶猴和猕猴有差异。     

雌性根田鼠的亲属识别与配偶选择

在Y字型选择箱中进行3种不同熟悉处理的配偶选择实验以检验动情雌性根田鼠配偶选择时的亲属识别和近交回避。（1）动情雌鼠在熟悉雄性同胞和陌生非同胞之间嗅添频次和时间、及自我修饰时间的差异非常显著（P＜0.01),所作的脊柱前凸反应时间也有显著差异（P＜0.05),这些行为均多针对于陌生非同胞雄性。结果提示动情雌性根田鼠在熟知雄性同胞身份的条件下对陌生非亲属雄性的气味更感兴趣,在择偶中与非亲属雄性交配来实现近交回避。（2）动情雌鼠对陌生雄性非同胞的嗅添频次和时间及所作的脊柱前凸反应时间显著大于陌生同胞雄性（P＜0.05),而针对陌生雄性非同胞自我修饰时间非常显著地大于针对陌生雄性同胞（P＜0.01)。这说明动情雌性根田鼠在择偶时可以识别断奶后分离不熟悉的雄性亲属,而在交配行为上偏向于非亲属雄性。（3）动情雌鼠在熟悉雄性同胞和非同胞之间跃添时间差异明显（P＜0.05),嗅添频次的差异更甚（P＜0.01);所作的脊柱前凸反应时间和社交后自我修饰时间差异也非常显著（P＜0.01),这些行为也均都偏向于非同胞雄性;结果提示断奶后继续熟悉可维持动情雌鼠对雄性亲属的嗅觉识别记忆力,在交配行为上主动回避亲属雄性。故认为：断奶后嗅觉识别持久力是发情雌性根田鼠亲属识别的机制,亲属识别是最初发情的雌性根田鼠配偶选择中近交回避的首要途径和机制,熟悉性是维持雌性根田鼠配偶选择实现近交回避的机制和特征。     

果子狸繁殖期行为的观察

描述了果子狸在繁殖期表现出的１７种子体为、１４种神群行为和交配模式。个体行为包括侧卧、叭、蹲、静立、双脚站立、食粪、理毛、抓痒、嗅闻、标记,发情叫、雄性鸣咽声、舔阴茎、咬阴部、食交配栓;社会行为包括仪式化格斗、雌性雄必与的抵抗、打斗、依偎、同性或异性之间彼此舔毛、雄性嗅闻雌性阴部及尿液、舔雌性阴部和错爬胯,交配行为主要在夜间进行,其交配模式为无锁结（可能）多次插入、插入后抽动、一次、性射精并在射精     

黑龙江省圈养狼交配行为的初步观察

2005 年10 月至2006 年4 月,采用焦点动物取样法和全事件扫描取样法,对黑龙江省哈尔滨北方森林动园4 对圈养狼交配活动进行了观察,以期了解无人干扰下圈养狼的交配过程及其交配模式。观察时间共计25 d, 225 h,实际录像时间为126 h,记录到爬跨741 次,成功交配46 次,成功爬跨交配占总爬跨次数的6. 2% 。狼在交配过程中有锁结现象,雄狼通常在一次爬跨、多次抽动后出现射精。交配行为一般发生在8∶ 00 ～10∶ 00和14∶00 ～ 16∶ 00。雌性具有明显的邀配模式,一旦邀配成功,雌狼站立不动,尾巴偏向一侧,腰部微下躬,配合雄狼爬跨。对交配参数进行单因素方差分析,4 只雄狼的抽插时间没有差异(P = 0. 827),而其锁结行为的时间差异极其显著(F = 71.43,P <0.001),交配期持续5 ～ 14 d,交配平均持续时间为534 ± 402 s,最长达1 588 s,
最短只有28 s。     

白马雪山自然保护区响古箐滇金丝猴（Rhinopithecus bieti）的交配行为

灵长类交配模式是灵长类社群结构和婚配制度的重要表征之一,其研究有助于了解灵长类社群结构和两性交配策略。2013年11月至2014年10月,我们对云南白马雪山国家级自然保护区一人工辅助投食滇金丝猴群进行了观察研究,采用焦点动物取样法和全事件记录法收集了雌雄个体的交配相关的行为数据,主要包括邀配对象、交配过程、持续时间和回合数,以及参与交配的雌雄对在交配结束后的相互理毛的持续时间和回合数。研究结果表明：研究群滇金丝猴全年均有交配行为,交配高峰期在7-9月,两性参与交配的积极性和对季节变化的响应不同;交配主要由雌性通过邀配发动（76%）,交配高峰期也是雌性邀配的高峰期;雄性爬跨频次（年均0.43次/月,n=5）和射精爬跨比（年均19%,n=5）则在全年无显著变化。交配行为发生的典型表现为：雌性通过小跑或跳跃进入雄性视线范围内,爬伏呈臀向雄性邀配;雌猴爬伏时离雄猴的远近距离不同（<1m vs. 2-5m ： 69% vs. 31%）会影响其邀配成功率（<1 m vs. 2-5 m ：68% vs. 40%）;若一次邀配失败,雌猴可能会连续爬伏邀配（最多4次）,连续多次邀配的成功率显著高于单次邀配（79% vs. 52%）。交配结束后雌性会主动为雄性理毛,但雌性主动理毛与交配是否射精无关。     

Copulatory behaviour of the bank voleMyodes glareolus: matings with one and two males do not make a difference

In promiscuous species in which females mate with more than one male during oestrus, males may increase their sperm expenditure or change their copulatory behaviour in response to the risk of sperm competition. I used an experimental approach to investigate the pattern of copulatory behaviour of the bank voleMyodes glareolus Schreber, 1780 depending on whether the female mated with one or two males. The work showed that the copulatory period of the bank vole lasted about 80 minutes and consisted of 4–5 ejaculatory series, with multiple intromissions preceding ejaculation. There were no significant changes in number of intromissions across the first four ejaculatory series, but I did find a relationship between number of intromissions and first ejaculation latency; also, ejaculation latencies grew shorter as the ejaculatory series proceeded. Litter size did not differ significantly between females that mated with one male and those mating with two, nor did the reproductive success of males that mated with the same female. Mating with an oestrus female appears to be advantageous for bank vole males even if they mate as the second one, and the risk of sperm competition did not trigger changes in male copulatory behaviour. The similar durations of the copulatory period and patterns of change of ejaculation latencies during copulations with one and two males point to the role of the female in temporal copulatory behaviour of the bank vole.     

A single injection of 17 beta-estradiol facilitates sexual behavior in castrated male mice

Sexual behavior was assessed in castrated adult CD-1 male mice given exogenous steroids under various treatment regimens. Castrated mice maintained on 20 μg testosterone (T) daily for 1 week, but given 250 μg testosterone propionate (TP) on the day of testing showed higher levels of copulatory activity than intact mice or the males receiving an additional dose of 20 μg T on the test day, although plasma testosterone levels were not different at the time of behavioral testing. Castrated males given 50, 125, or 250 μg TP for 1 week including the day of testing showed higher levels of sexual behavior than males receiving the same doses of TP only once, on the test day. A single injection of 17β-estradiol (E₂) completely restored the male copulatory pattern, including ejaculation, in castrated mice under every condition examined. Testosterone and dihydrotestosterone (DHT) were less effective than E₂, as was the combination of E₂ and DHT. The relative efficacy of a single dose of T, DHT, and E₂ plus DHT was dependent upon factors such as the delay between steroid administration and testing, as well as whether or not the castrated mice received androgen replacement prior to testing. Estradiol benzoate (E₂B) was not capable of restoring sexual behavior in castrated mice in this study. The comparison of results obtained with TP, T, E₂, and E₂B suggests that an appreciable, but not necessarily sustained, elevation of E₂ levels in the brain may be critical in the facilitation of male copulatory behavior in mice.     

A single injection of 17β-estradiol facilitates sexual behavior in castrated male mice

Sexual behavior was assessed in castrated adult CD-1 male mice given exogenous steroids under various treatment regimens. Castrated mice maintained on 20 μg testosterone (T) daily for 1 week, but given 250 μg testosterone propionate (TP) on the day of testing showed higher levels of copulatory activity than intact mice or the males receiving an additional dose of 20 μg T on the test day, although plasma testosterone levels were not different at the time of behavioral testing. Castrated males given 50, 125, or 250 μg TP for 1 week including the day of testing showed higher levels of sexual behavior than males receiving the same doses of TP only once, on the test day. A single injection of 17β-estradiol (E₂) completely restored the male copulatory pattern, including ejaculation, in castrated mice under every condition examined. Testosterone and dihydrotestosterone (DHT) were less effective than E₂, as was the combination of E₂ and DHT. The relative efficacy of a single dose of T, DHT, and E₂ plus DHT was dependent upon factors such as the delay between steroid administration and testing, as well as whether or not the castrated mice received androgen replacement prior to testing. Estradiol benzoate (E₂B) was not capable of restoring sexual behavior in castrated mice in this study. The comparison of results obtained with TP, T, E₂, and E₂B suggests that an appreciable, but not necessarily sustained, elevation of E₂ levels in the brain may be critical in the facilitation of male copulatory behavior in mice.     

Sexual behavior in developing male rats

During normal development, the onset of reproductive behavior in male rats was not preceded by any change in plasma testosterone (T) levels. Implantation of Silastic capsules containing T in 14-day-old male rats advanced the onset of all parameters of sexual behavior by 20 days. Implantation of Silastic capsules containing estradiol in 14-day-old male rats stimulated precocious mounting and intromitting, but not ejaculation. Implantation of dihydrotestosterone-filled Silastic capsules in 14-day-old male rats completely inhibited the development of sexual behavior. All hormones suppressed plasma LH levels. These findings in immature male rats are similar to previous findings in adult males. Immature male rats were behaviorally less responsive to T than adult males, and it was suggested that, during development, male rats become progressively more sensitive to the behavior-stimulating effects of circulating T. No effects of copulatory experience on plasma concentration of T or on the weights of testes, penes, or accessory sexual glands were detected.     

Changes in masculine sexual behavior, corticosterone and testosterone in response to acute and chronic stress in male rats

Chronic exposure to stressors increases HPA axis activity and concomitantly reduces HPG axis activity. This antagonistic relationship between both these axes has been proposed to underlie the inhibition of reproductive function due to stress. Sexual behavior in males may be the most vulnerable aspect of male reproduction to acute and chronic stress and it has been suggested that alterations in sexual behavior during stress are due to the antagonistic relationship between testosterone and corticosteroids. However, only in a few studies has a correlation between the levels of testosterone and corticosterone, and sexual behavior been made. In this study, we evaluated the effects of different stressors, applied both acute and chronically, on masculine sexual behavior and whether or not these effects on sexual behavior are accompanied by changes in plasma levels of corticosterone and testosterone. Additionally, we evaluated the effect of testosterone treatment on the effects of stress on sexual behavior. Sexually experienced male rats were exposed to one of the following stressors: immobilization (IMB), electric foot shocks (EFS) or immersion in cold water (ICW). Sexual behavior and plasma levels of testosterone and corticosterone were assessed on days 1, 5, 10, 15, and 20 of stress. In a second experiment, males were castrated, treated with 3 different doses of testosterone propionate (TP) and exposed to ICW for 20 consecutive days. Sexual behavior was assessed on days 1, 5, 10, 15, and 20 and steroids were evaluated on day 20. Parameters of masculine sexual behavior were modified depending on the characteristics of each stressor. Mount, intromission and ejaculation latencies increased significantly, the number of mounts increased, and ejaculations decreased significantly in males exposed to EFS and to ICW but not in males exposed to IMB. Associated with these effects, testosterone decreased in the EFS and ICW groups on days 1, 15, and 20. However, corticosterone increased only in males exposed to ICW. In castrated males, TP treatment failed to block the effects of stress by ICW on sexual behavior and corticosterone. These results indicate that the effects of stress on sexual behavior depend on the characteristics of each stressor, and these effects, as well as the decrease in testosterone are not necessarily associated with the increase in corticosterone. The fact that testosterone treatment did not prevent the effects of stress on sexual behavior suggests that other mediators could be involved in the alterations of sexual behavior caused by stress.     

Sex differences and effects of neonatal aromatase inhibition on masculine and feminine copulatory potentials in prairie voles

Copulatory behaviors in most rodents are highly sexually dimorphic, even when circulating hormones are equated between the sexes. Prairie voles (Microtus ochrogaster) are monomorphic in their display of some social behaviors, including partner preferences and parenting, but differences between the sexes in their masculine and feminine copulatory behavior potentials have not been studied in detail. Furthermore, the role of neonatal aromatization of testosterone to estradiol on the development of prairie vole sexual behavior potentials or their brain is unknown. To address these issues, prairie vole pups were injected daily for the first week after birth with 0.5 mg of the aromatase inhibitor 1,4,6-androstatriene-3,17-dione (ATD) or oil. Masculine and feminine copulatory behaviors in response to testosterone or estradiol were later examined in both sexes. Males and females showed high mounting and thrusting in response to testosterone, but only males reliably showed ejaculatory behavior. Conversely, males never showed feminine copulatory behaviors in response to estradiol. Sex differences in these behaviors were not affected by neonatal ATD, but ATD-treated females received fewer mounts and thrusts than controls, possibly indicating reduced attractiveness to males. In other groups of subjects, neonatal ATD demasculinized males' tyrosine hydroxylase expression in the anteroventral periventricular preoptic area, and estrogen receptor alpha expression in the medial preoptic area. Thus, although sexual behavior in both sexes of prairie voles is highly masculinized, aromatase during neonatal life is necessary only for females' femininity. Furthermore, copulatory behavior potentials and at least some aspects of brain development in male prairie voles are dissociable by their requirement for neonatal aromatase.     

Sperm competition roles and ejaculate investment in a promiscuous mammal

Theoretical models of sperm competition predict how males should allocate sperm and seminal fluid components to ejaculates according to their mating role (dominant vs. subordinate). Here, we present a detailed analysis of ejaculate expenditure according to male roles in the bank vole (Myodes glareolus). Sperm competition occurs regularly in this species, and dominant males typically achieve higher fertilization success than subordinates. Contrary to theoretical predictions, we found that dominant male bank voles invest more sperm per ejaculate than subordinates, both absolutely and relative to body and testes mass. The testes of dominant males were also absolutely (although not relatively) larger than those of subordinates. However, we found no evidence that subordinate males compensate for lower sperm numbers per ejaculate by increasing ejaculation frequency or sperm velocity. Similarly, we found no evidence for differential investment in copulatory plug size according to male roles in sperm competition, although dominant males had significantly larger seminal vesicles (both absolutely and relative to body mass) compared with subordinates. We conclude that sperm competition roles can have significant but unexpected influences on ejaculate investment in mammals with clearly defined differences in male social status.     

Copulatory behavior of sexually inexperienced male voles paired with proestrous females

The copulatory behavior in sexually inexperienced male voles aged 9-13 weeks old was observed under dim red illumination. Proestrous females were used as stimulus voles in copulatory behavior tests. A 30-min test session was recorded. All males showed at least one ejaculation within 30 min. In addition, the pattern of copulatory behavior in male voles was compared to that reported previously in male hamsters. The frequencies of mount, intromission and ejaculation in male voles were similar to that in male hamsters but there were significant differences in the latencies of mounting, intromission, ejaculation and post-ejaculation between the two species.     

Neuroendocrine regulation of sexually dimorphic brain structure and associated sexual behavior in male rats is genetically controlled

Steroid hormones, particularly 17beta-estradiol (E2), regulate the development and expression of neural structures and sexual behavior. Recently, we demonstrated that E2-regulated responses are controlled by quantitative trait loci. In this study, we quantified 1) volume of the sexually dimorphic nucleus (SDN) of the preoptic area (POA); 2) medial basal hypothalamic (MBH)-POA aromatase and 5alpha-reductase enzyme activities during prenatal development and in adults; 3) serum LH, testosterone, FSH, E2, prolactin (PRL), and corticosterone levels; 4) reproductive organ (i.e., testis and ventral prostate) weights; and 5) male mating behavior in Noble (NB/Cr) and Wistar-Furth (WF/NCr) rat strains to determine the genetic influence on the measured parameters. Maximal phenotypic divergence in male SDN-POA volumes was seen between NB/Cr versus WF/NCr and BDIX/Cr rats (among nine rat strains initially examined), with the average SDN-POA volume of NB/Cr male rats being significantly greater ( approximately 30%) than that of either WF/NCr or BDIX/Cr males. Subsequent experiments investigated WF/NCr versus NB/Cr male rats in further detail. Significantly higher MBH-POA aromatase activity was seen in adult WF/NCr versus NB/Cr males, while MBH-POA 5alpha-reductase rates were not significantly different (within or between sex) for the two rat strains assayed. Serum LH levels were significantly higher (by greater than sixfold) in WF/NCr versus NB/Cr males, whereas testis organ:body weight and ventral prostate:body weight ratios in WF/NCr versus NB/Cr males were significantly smaller (by approximately 6-fold for testis and approximately 1.5-fold for prostate values). Serum FSH levels were significantly higher (by twofold) in WF/NCr versus NB/Cr males. However, serum testosterone levels were not significantly different, whereas E2 levels were approximately twofold higher (but not significantly different) in WF/NCr versus NB/Cr animals. No significant differences were found in basal (i.e., nonstress) serum PRL or corticosterone levels between the WF/NCr and NB/Cr males. In male copulatory tests, NB/Cr males exhibited significantly more aggressive sexual behavior (e.g., in mounting, intromission, and ejaculation parameters) compared with WF/NCr males. Taken together, these findings indicate that WF/NCr males are, in general, low responders, whereas NB/Cr males are high responders to hormonal signals. The obtained data suggest that the correlative, phenotypic variation in SDN-POA volume (i.e., structure) and reproductive hormone patterns and mating behavior (i.e., function) of WF/NCr versus NB/Cr males is regulated by potentially E2-mediated mechanisms that are genetically controlled.     

Effects of corticosterone on territorial behavior of free-living male song sparrows Melospiza melodia

A group of 10 territorial male song sparrows, Melospiza melodia, were given subcutaneous implants of corticosterone in Silastic tubing. A second group of 10 territorial males were given empty implants as controls. After 18-24 hr all males were then subjected to a simulated territorial intrusion (STI) by placing a caged male song sparrow in the center of the subject's territory, and playing tape recorded songs through a speaker placed alongside. Significantly fewer males with corticosterone implants responded to STI than to controls, and the latency to respond was longer. Of the 3 experimental males that did respond to STI, all had a lower frequency of songs and did not approach the simulated intruder as closely as controls. Many males were captured 2-7 days after implantation and blood samples collected for measurement of circulating hormone levels. As expected, plasma levels of corticosterone were high in the group given corticosterone implants. However, plasma levels of luteinizing hormone (LH) were not affected by treatment with corticosterone, and although circulating levels of testosterone were depressed slightly compared with controls, they were within the normal range for territorial and breeding males. There were no differences in body mass despite greatly increased fat depots in males treated with corticosterone. These data suggest that high levels of corticosterone, similar to those measured during stressful episodes both in the laboratory and field, may suppress territorial behavior independently of the adenohypophysial-gonad axis. Since plasma levels of LH and testosterone are not depressed markedly, thus maintaining the gonads in a near functional state, renesting can begin as soon as environmental conditions ameliorate. Such mechanisms could potentially increase the probability of raising viable young after unpredictable, severe weather resulted in failure of the previous breeding attempt.