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1.
Injurious self-biting is one of the most serious problems in primate colonies (Niemeyer, Gray, & Stephen, 1996). "Approximately 10% of captive, individually-housed monkeys engage in the disturbing phenomenon of self-injurious behavior (SIB). To date, no adequate explanation or effective therapy has been developed for this disorder" (Jorgensen, Novak, Kinsey, Tiefenbacher, & Meyer, 1996; cf. Novak, Kinsey, Jorgensen, & Hazen, 1998). In rhesus macaques-the predominant species found in laboratories-the incidence of self-biting may be as high as 14% (recorded in a colony of 188 single-caged males; Jorgensen, Kinsey, & Novak, 1998). Individuals affected with this "behavioral pathology" (Erwin & Deni, 1979, p. 4) repeatedly bite parts of their own bodies (see Figure 1) while intermittently showing signs of intense excitation such as threatening, trembling, head jerking, and piloerection (Reinhardt, 1999; Tinklepaugh, 1928).  相似文献   

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Maternal responsiveness in primates has long been considered emancipated from endocrine factors and entirely dependent on experience and cognition. Here we report that group-living pigtail macaque females increased their rate of interaction with infants in the last weeks of pregnancy in correspondence with an increase in plasma levels of estradiol and progesterone. Estrogen treatment increased the rate at which ovariectomized rhesus females interacted with infants. This is the first evidence that steroid hormones influence maternal responsiveness in anthropoid primates. All untreated ovariectomized females and nonpregnant females interacted with infants, indicating that although estrogen can enhance responsiveness to infants, ovarian or pregnancy hormones are not necessary for the expression of infant-directed behavior in female macaques. The findings of this study suggest fundamental similarities, rather than differences, in the endocrine modulation of maternal responsiveness in primates and other mammals.  相似文献   

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Intralocus sexual conflict and intragenomic conflict both affect sex chromosome evolution and can in extreme cases even cause the complete turnover of sex chromosomes. Additionally, established sex chromosomes often become the focus of heightened conflict. This creates a tangled relationship between sex chromosomes and conflict with respect to cause and effect. To further complicate matters, sexual and intragenomic conflict may exacerbate one another and thereby further fuel sex chromosome change. Different magnitudes and foci of conflict offer potential explanations for lineage-specific variation in sex chromosome evolution and answer long-standing questions as to why some sex chromosomes are remarkably stable, whereas others show rapid rates of evolutionary change.Compared to the autosomes, the unique inheritance pattern of the sex chromosomes is often thought to intensify evolutionary conflict (Rice 1984; Frank 1991; Jaenike 2001). Sex chromosomes are therefore hot spots for two specific types of conflict: intralocus conflict, in which an allele confers different fitness effects depending on the sex in which it is found, and intragenomic conflict, in which selfish genetic elements (SGEs) promote their own transmission at the expense of unlinked regions of the genome. These conflicts act in distinct but complementary ways. Not only do they shape sex chromosome and genome evolution, but in some cases, they also have the power to cause complete turnover of sex chromosomes.Unlike the autosomes, because the sex chromosomes are unevenly transmitted between males and females and are also unevenly distributed between the sexes (Fig. 1), the relative effect of male- and female-specific selection acting on them is unbalanced. The inherent differences in sex-specific selection on the sex chromosomes themselves, and between the sex chromosomes and the autosomes, form the basis of a large and often compelling body of evolutionary theory that predicts the ways that intralocus sexual conflict will arise, play out, and in some cases potentially be resolved. This theory predicts that, under some conditions, the sex chromosomes are hot spots of intralocus sexual conflict (Rice 1984; Albert and Otto 2005; Connallon and Clark 2010), and in some cases alleles that harm one sex more than they benefit the other can still reach high frequencies if they are sex-linked (Rice 1984; Dean et al. 2012). All this theory predicts that although the sex chromosomes generally represent a small proportion of the genome, they should play a disproportionately large role in sexual conflict, sexual dimorphism, and sexual selection. There is substantial empirical evidence supporting at least some of this theory (Dean and Mank 2014).Open in a separate windowFigure 1.Transmission of the sex chromosomes. Females are shown in red, males in blue. In male heterogamety (A), the Y chromosome is passed through the patriline and limited to males. The maternal X chromosome is passed from mother to both sons and daughters, but the paternal X can only be transmitted to daughters. Additionally, the X is present two-thirds of the time in females. In female heterogamety (B), the W chromosome is limited to females and passed solely from mother to daughter. The paternal Z chromosome can be passed from father to both daughters and sons; however, the maternal Z chromosome is only passed to sons. Converse to the X chromosome, the Z chromosome is resident in males two-thirds of the time.

Table 1.

Studies showing a disproportionate role of the sex chromosomes in sexual dimorphism, fitness, or fertility
Male heterogametyFemale heterogamety
X chromosomeY chromosomeZ chromosomeW chromosome
Associations with sexually dimorphic phenotypic traitsSize dimorphism in red deer (Foerster et al. 2007)
Sexually antagonistic fitness variation in Drosophila (Gibson et al. 2002; Innocenti and Morrow 2010)
Variation in stalk-eyed fly eye span (Wolfenbarger and Wilkinson 2001)
Male coloration in guppies (Winge 1927; Postma et al. 2011)
Male mating behavior in sticklebacks (Kitano et al. 2009; although see Natri et al. 2013)
Female mating preference in moths (Iyengar et al. 2002)
Female mate choice in flycatchers (Saether et al. 2007)
Male plumage traits in flycatchers (Saetre et al. 2003)
Female benefit coloration in cichlids (Roberts et al. 2009)
Associations with reproduction and fertilityMale reproductive genes in mice (Mueller et al. 2008)Male fertility genes in mammals (Lange et al. 2009)
Male fitness in Drosophila (Lemos et al. 2010; Sackton et al. 2011)
Genes related to male reproductive function in silk moth (Arunkumar et al. 2009)Genes related to female fecundity and fertility in chickens (Moghadam et al. 2012)
Open in a separate windowIn addition to their role in sexual conflict, the sex chromosomes also experience high levels of intragenomic conflict resulting from SGEs that promote their own transmission at the expense of the rest of the genome (Burt and Trivers 2006). Of particular importance are sex-linked segregation distorters, as these generate strong selection favoring genes that suppress their action. Theory predicts that intragenomic conflict should be particularly intense when involving the sex chromosomes (Hurst and Pomiankowski 1991). This is because sex chromosomes can generate antagonistic coevolution between sex-linked segregation distorters and their suppressors (Partridge and Hurst 1998).In addition to shaping the evolutionary properties of existing sex chromosomes, in some situations sexual and intragenomic conflict may also actually catalyze the formation of sex chromosomes (Fisher 1931; Charlesworth and Charlesworth 1980; Rice 1987; Werren and Beukeboom 1998). Conflict may also explain the rate of degradation of the sex-limited Y and W chromosomes (Bachtrog et al. 2011) and turnover of sex chromosomes (Hall 2004; van Doorn and Kirkpatrick 2007, 2010), suggesting that conflict plays a causal role in sex chromosome evolution.There is also growing evidence of a direct relationship between SGEs and sexual conflict involving the sex chromosomes. Many SGEs increase their transmission advantage by targeting sperm, which can reduce male fertility owing to reduced overall sperm production. Lower sperm production can in turn result in reduced siring success during sperm competition (Price and Wedell 2008) and potentially favor polyandry as a female strategy to bias paternity against SGE-carrying males (Wedell 2013). As a consequence, SGEs may also influence the potential for sexual conflict as they can favor increased female mating rates, which increases the potential for conflict between the sexes.Sexual and intragenomic conflict are therefore critical for sex chromosome evolution and, once sex chromosomes are established, can further shape their evolutionary and genomic properties. Disentangling cause and effect is difficult but crucial to understanding the role of sex chromosomes in sexual and intragenomic conflict and vice versa.  相似文献   

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The effects of caffeine on the activity of central and peripheral catecholaminergic structures have been studied in rats ingesting high doses of caffeine. The activities of the enzymes tyrosine hydroxylase and dopamine-beta-hydroxylase were measured as well as 3,4-dihydroxyphenylethylamine (dopamine), adrenaline, and noradrenaline concentrations, in brain (striatum and hypothalamus), heart, and adrenal gland. At the peripheral level, we observed a significant increase in the dopamine and adrenaline plus noradrenaline content in the heart, but an increase in dopamine content only was found in the adrenal gland. Dopamine-beta-hydroxylase activity in serum was increased, but the only significant enzymic change in brain was an increase in the dopamine-beta-hydroxylase activity of the hypothalamus. However, an increase in catecholamine content was observed in both structures of the brain. These data suggest that the mechanisms involved in caffeine-induced self-biting in rats are not limited to the dopaminergic system, because we have also observed an increase in noradrenaline turnover.  相似文献   

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We examined the question of whether the occurrence of menopause in rhesus macaque (Macaca mulatta) females approximates that found in women from a life history standpoint. We used data from two provisioned free-ranging populations of rhesus macaques to estimate the probability that a juvenile female not only will survive to the potentially postmenopausal age of 25 years but also will cease to experience menstrual cycles between 25 and 27 years. We used the same data to assess whether an age-related deterioration in body condition can predict whether females 25 years old will be acyclic. Our analyses indicate that, within our study populations, (1) 1 in every 10 juvenile females can be expected eventually to undergo the climacteric, and (2) being in poor condition is strongly associated with being acyclic in old age. Current theory regarding the evolution of senescence in species that do not reproduce by binary fission posits that aging is a consequence of the force of natural selection declining with age. Inasmuch as the proportion of female rhesus macaque juveniles that ultimately experience menopause is small, and inasmuch as reproductive senescence does not appear to outpace organismal aging in general (as indexed by an age-related decline in body condition), we conclude that the occurrence of menopause in rhesus females is parsimoniously explained by the general evolutionary theory of aging and that the invocation of a special adaptive explanation, such as the grandmother hypothesis or a variant thereof, is unnecessary.  相似文献   

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A critical reexamination of the empirical data on male-infantinteractions among baboons and macaques reveals a number ofsignificant contrasts between them. On an absolute and relativescale, the frequency of occurrence among baboons is rare. Whenmale baboons do interact with infants, only a small proportionof all available male actors do so, and even fewer still (lessthan one-quarter) account for any substantial percentage ofall interactions. In contrast, macaque males are very frequentlyand commonly involved with infants; all males of the group interactwith infants to some degree, and a greater proportion of allthe group's males can be characterized as "heavily involved"with infants. The rejection of the role of kinship in interpretingthis phenomenon, especially as it occurs among baboons, hasrested almost exclusively on the pattern of estimated paternitybetween male and infant from behavioral (consort) criteria.These behavioralbased data are incomplete at best, possiblyincorrect in some instances, and in fact, in many studies kinshipappears to be a predominant factor. Until patrilineal data arederived from independent cytogenetic studies, these evolutionaryinterpretations must be viewed with extreme skepticism.  相似文献   

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Summary. Caged probes offer a novel approach to study plant cell-to-cell communication. Instead of introducing fluorescent molecules into cells by microinjection, their caged counterparts can be preloaded into the tissue by diffusion. Following spatially controlled photoactivation, movement of the uncaged fluorochrome can be followed in time and direction by confocal laser scanning microscopy. In the onion bulb scale epidermis used as a model system, symplasmic transport of the tracer out of a target cell was followed. Transport via the symplasmic pathway was challenged by plasmolysing the tissue. The experiments confirmed the symplasmic nature of tracer transport.Correspondence and reprints: Department of Plant Biology, Royal Veterinary and Agricultural University, Thorvaldsensvej 40, 1871 Frederiksberg C. Denmark. E-mail: hjm@kvl.dk  相似文献   

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Simian varicella virus (SVV; Cercopithecine herpesvirus 9) is a naturally occurring herpesvirus of nonhuman primates. Here we present the clinical, pathologic, and virologic findings from 2 cases of SVV in adult female pigtailed macaques (Macaca nemestrina). The initial case presented with hyperthermia and a diffuse inguinal rash which spread centripetally, progressing to vesiculoulcerative dermatitis of the trunk, face, and extremities. At 96 h after presentation, the animal was anorexic and lethargic and had oral and glossal ulcerations. Euthanasia was elected in light of the macaque''s failure to respond to clinical treatment. Seven days after the first case was identified, a second macaque presented with a vesicular rash and was euthanized. Gross necropsy lesions for both cases included vesicular, ulcerative dermatitis with mucocutaneous extension and hepatic necrosis; the initial case also demonstrated necrohemorrhagic gastroenterocolitis and multifocal splenic necrosis. Histology confirmed herpetic viral infection with abundant intranuclear inclusion bodies. Immunofluorescence assays detected antibodies specific for SVV. PCR assays of vesicular fluid, tissue, and blood confirmed SVV and excluded varicella–zoster virus (Human herpesvirus 3). Serology for Macacine herpesvirus 1 (formerly Cercopithecine herpesvirus 1), poxvirus (monkeypox), and rubella was negative. Banked serum samples confirmed SVV exposure and seroconversion. Investigation into the epidemiology of the seroconversion demonstrated a SVV colony prevalence of 20%. The described cases occurred in animals with reconstituted immune systems (after total-body irradiation) and demonstrate the clinical effects of infection with an endemic infectious agent in animals with a questionable immune status.Abbreviations: IFA, immunofluorescence assay; SVV, simian varicella virus; TBI, total body irradiation; WaNPRC, Washington National Primate Research Center; VZV, varicella–zoster virus; McHv1, Macacine herpesvuris 1; SRV-2, Simian retrovirus 2 (type D)Simian varicella virus (SVV; Cercopithecine herpesvirus 9) is a naturally occurring herpesvirus of Old World primates responsible for sporadic epizootics in biomedical research facilities.2 Signs of infection include fever, vesicular skin lesions, hemorrhagic ulceration throughout the gastrointestinal tract, and multifocal hemorrhagic necrosis of the liver, spleen, lymph nodes, and endocrine organs.6,7,8 Other names for SVV include Delta herpesvirus, Liverpool vervet virus, patas herpesvirus, and Medical Lake macaque virus.16, 20-23 Like many other herpesviruses, SVV establishes persistent lifelong infections, with viral DNA detectable in neural ganglia.12 Infection with SVV does not necessarily lead to lifelong latency, and periodic reactivation of SVV may occur.3 SVV is genetically and antigenically similar to Human herpesvirus 3,2 commonly known as varicela–zoster virus (VZV), the etiologic agent of chickenpox and shingles in humans. SVV in macaques and VZV in man present with similar clinical signs; SVV has been proposed as an animal model of VZV disease in man.24 Rarely, VZV may occur in higher primates (Gorilla).18 The 2 viruses must be distinguished from one another through molecular techniques.1,410,11 Both viral infections are usually mild and self-limiting in immunocompetent hosts,4,8 reactivation and viral shedding may occur during times of stress or immunosupression.80,21,22A recent review of SVV in Old World Monkeys8 focused on SVV as a disease of nonhuman primates. This case report expands on the 2 most recent cases of SVV mentioned in that review.8 The animals described were housed in accordance with the regulations of the Animal Welfare Act and the recommendations of the Guide for the Care and Use of Laboratory Animals11 at the Washington National Primate Research Center (WaNPRC) facility in Seattle. The Institutional Animal Care and Use Committee of the University of Washington approved all aspects of the study to which the animals were assigned. The 2 clinical cases described in this report originated at the WaNPR–Seattle facility; contact animals described originated at the WaNPR–Tulane facility. When animals are relocated between the 2 facilities, they are processed through a domestic quarantine consisting of isolation for 30 d, during which time 3 tuberculin skin tests, 2 physical examinations, and 1 complete blood count and serological panel are performed. The WaNPRC–Tulane facility houses a breeding colony founded by animals relocated to Louisiana from the WaNPRC–Medical Lake facility in 1996.  相似文献   

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Agonistic support is generally considered a classical example of altruistic behaviour. It plays a critical role in the process of rank acquisition. This study investigates agonistic coalitions involving juvenile Japanese macaques (Macaca fuscata) living in a large captive group. Kinship was a good predictor of agonistic support received by juvenile macaques. Kinship also had a significant, though weaker, influence on agonistic support given by juvenile macaques. The latter was strongly influenced by the prospective rank of the individual against which the coalition was directed, i.e. by the rank relationship between the target of the coalition and the juvenile’s mother. Juvenile macaques intervened aggressively more against prospectively subordinate individuals than against prospectively dominant individuals. These results imply agonistic support is not necessarily altruistic, and support the hypothesis that primates may understand the rank relationship that exist among their group mates, i.e. that they are aware of third‐party social relationships. They also suggest that selective pressures associated with the process of rank acquisition may have favoured the evolution of higher cognitive abilities.  相似文献   

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野生太行山猕猴血液生理生化指标测定与分析   总被引:1,自引:0,他引:1  
猕猴华北亚种Macaca mulatta tcheliensis为中国特有亚种,目前主要分布于河南、山西两省交界的太行山南端,常被称为太行山猕猴.2009年11月~2010年1月,在太行山猕猴国家级自然保护区济源管理局所辖范围内对野生太行山猕猴进行生存状况调查的同时,对18只雌体、8只雄体的血液生理与生化指标进行了测定,结果表明:1)雌性的淋巴细胞数(P=0.019)、中间细胞数(P=0.017)均显著地高于雄性;而雌性的平均血小板体积则显著低于雄性(P=0.046);2)雌性的血糖(GLU)、总胆固醇(CH)、甘油三酯(TG)、高密度胆固醇(HDL)、低密度胆固醇(LDL)的测定值均略高于雄性,但其差异未达到显著性水平.并与相关研究作了比较分析.  相似文献   

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2004年8月,成都大熊猫繁育研究基地1只雌性大熊猫发生难产,临床表现以阵缩及努责匮乏为主要特征,经过B超检查、药物辅助治疗等一系列保守措施后,胎儿于4天后排出。鉴于大熊猫难产病例在国内外至今未见报道,现将该病的临床特点、诊断和处治情况介绍如下。  相似文献   

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