Developmental exposure to vasopressin increases aggression in adult prairie voles

Although the biological roots of aggression have been the source of intense debate, the precise physiological mechanisms responsible for aggression remain poorly understood. In most species, aggression is more common in males than females; thus, gonadal hormones have been a focal point for research in this field. Although gonadal hormones have been shown to influence the expression of aggression, in many cases aggression can continue after castration, indicating that testicular steroids are not completely essential for the expression of aggression. Recently, the mammalian neuropeptide arginine vasopressin (AVP) has been implicated in aggression. AVP plays a particularly important role in social behavior in monogamous mammals, such as prairie voles (Microtus ochrogaster). In turn, the effects of social experiences may be mediated by neuropeptides, including AVP. For example, sexually naïve prairie voles are rarely aggressive. However, 24 h after the onset of mating, males of this species become significantly aggressive toward strangers. Likewise, in adult male prairie voles, central (intracerebroventricular) injections of AVP can significantly increase intermale aggression, suggesting a role for AVP in the expression of postcopulatory aggression in adult male prairie voles. In this paper, we demonstrate that early postnatal exposure to AVP can have long-lasting effects on the tendency to show aggression, producing levels of aggression in sexually naïve, adult male prairie voles that are comparable to those levels observed after mating. Females showed less aggression and were less responsive to exogenous AVP, but the capacity of an AVP V1a receptor antagonist to block female aggression also implicates AVP in the development of female aggression.

The effects of stress on social preferences are sexually dimorphic in prairie voles.

Prairie voles (Microtus ochrogaster) are monogamous rodents that form pair bonds characterized by a preference for a familiar social partner. In male prairie voles, exposure to either the stress of swimming or exogenous injections of corticosterone facilitate the development of a social preference for a female with which the male was paired after injection or swimming. Conversely, adrenalectomy inhibits partner preference formation in males and the behavioral effects of adrenalectomy are reversed by corticosterone replacement. In female prairie voles, swim stress interferes with the development of social preferences and corticosterone treatments inhibit the formation of partner preferences, while adrenalectomized females form preferences more quickly than adrenally intact controls. Because sex differences in both behavior and physiology are typically reduced in monogamous species, we initially predicted that male and female prairie voles would exhibit similar behavioral responses to corticosterone. However, our findings suggest an unanticipated sexual dimorphism in the physiological processes modulating social preferences. This dimorphic involvement of stress hormones in pair bonding provides a proximate mechanism for regulating social organization, while permitting males and females to adapt their reproductive strategies in response to environmental challenges.

Preliminary benefit analysis of Endrin use on apple orchards /

Bibliography: leaves [86]-91.

Why does social exclusion hurt? The relationship between social and physical pain

The authors forward the hypothesis that social exclusion is experienced as painful because reactions to rejection are mediated by aspects of the physical pain system. The authors begin by presenting the theory that overlap between social and physical pain was an evolutionary development to aid social animals in responding to threats to inclusion. The authors then review evidence showing that humans demonstrate convergence between the 2 types of pain in thought, emotion, and behavior, and demonstrate, primarily through nonhuman animal research, that social and physical pain share common physiological mechanisms. Finally, the authors explore the implications of social pain theory for rejection-elicited aggression and physical pain disorders.

Toxoplasma gondii seropositive rates of animals living on Svalbard

Samples (blood or tissue fluid) from 594 arctic foxes (Alopex lagopus), 390 Svalbard reindeer (Rangifer tarandus platyrhynchus), 361 sibling voles (Microtus rossiaemeridionalis), 17 walruses (Odobenus rosmarus), 149 barnacle geese (Branta leucopsis), 58 kittiwakes (Rissa tridactyla), and 27 glaucous gulls (Larus hyperboreus) from Svalbard and nearby waters were assayed for antibodies against Toxoplasma gondii using a direct agglutination test. The proportion of seropositive animals was 43% in arctic foxes, 7% in barnacle geese, and 6% (1 of 17) in walruses. There were no seropositive Svalbard reindeer, sibling voles, glaucous gulls, or kittiwakes. The prevalence in the arctic fox was relatively high compared to previous reports from canid populations. There are no wild felids in Svalbard and domestic cats are prohibited, and the absence of antibodies against T gondii among the herbivorous Svalbard reindeer and voles indicates that transmission of the parasite by oocysts is not likely to be an important mechanism in the Svalbard ecosystem. Our results suggest that migratory birds, such as the barnacle goose, may be the most important vectors bringing the parasite to Svalbard. In addition to transmission through infected prey and carrion, the age-seroprevalence profile in the fox population suggests that their infection levels are enhanced by vertical transmission.

Comparison of different methods to detect genetic barriers in a small mammal population

Habitat fragmentation and the consequently the loss of connectivity between populations can reduce the individuals interchange and gene flow, increasing the chances of inbreeding, and the increase the risk of local extinction. Landscape genetics is providing more and better tools to identify genetic barriers.. To our knowledge, no comparison of methods in terms of consistency has been made with observed data and species with low dispersal ability. The aim of this study is to examine the consistency of the results of five methods to detect barriers to gene flow in a Mediterranean pine vole population Microtus duodecimcostatus: F-statistics estimations, Non-Bayesian clustering, Bayesian clustering, Boundary detection and Simple/Partial Mantel tests. All methods were consistent in detecting the stream as a non-genetic barrier. However, no consistency in results among the methods were found regarding the role of the highway as a genetic barrier. Fst, Bayesian clustering assignment test and Partial Mantel test identifyed the highway as a filter to individual interchange. The Mantel tests were the most sensitive method. Boundary detection method (Monmonier’s Algorithm) and Non-Bayesian approaches did not detect any genetic differentiation of the pine vole due to the highway. Based on our findings we recommend that the genetic barrier detection in low dispersal ability populations should be analyzed with multiple methods such as Mantel tests, Bayesian clustering approaches because they show more sensibility in those scenarios and with boundary detection methods by having the aim of detect drastic changes in a variable of interest between the closest individuals. Although simulation studies highlight the weaknesses and the strengths of each method and the factors that promote some results, tests with real data are needed to increase the effectiveness of genetic barrier detection.

Distribución y taxonomía de mamíferos (clase mammalia) en el Cerro El Potosí Galeana, Nuevo León, México

El Cerro El Potosí es un área prioritaria para la Comisión Nacional para la Biodiversidad (CONABIO) y un Área Natural Protegida por el estado (Anónimo, 2000), debido a la existencia de una gran diversidad de tipos de vegetación y de especies de importancia fitogeografica o su orografía y altitud (3715 msnm) se considera un área promotora de procesos de especiación, registrándose especies endémicas y relictuales como el caso del Pinus culminicola y Nucifraga columbiana , es una de las montañas más altas del noroeste del país, está enclavada en la Sierra Madre Oriental. Con base en la información previa disponible, se presume que esta área ostente una mayor diversidad de flora y fauna. El objetivo principal fue el análisis de la diversidad y distribución de los mamíferos en los diferentes estratos vegetativos y altitudes dentro de los límites del Cerro El Potosí. Con el propósito de realizar las comparaciones de las diversidades de las especies en forma altitudinal, por vegetación, estacional; Se seleccionó la prueba de Chi-cuadrada para determinar dependencia entre especies y la altitud, tipo de muestreo o tipo de vegetación. Se efectuaron 24 salidas (mensuales) de campo, de noviembre del 2006 a octubre del 2008, de 3 a 4 días por salida. Se registraron 27 especies (14 Familias, 24 géneros, 27 especies, y 14 especies no reportadas previamente). De acuerdo al tipo de vegetación la riqueza se concentro en el bosque de pino seguido por el bosque de encino, las especies se distribuyeron en uno, en dos o más estratos de vegetación (patrones), para los diferentes tipos de vegetación se distribuyeron las especies de Silvilagus floridanus, Thomomys bottae, Peromyscus melanotis, Peromyscus levipes ambiguus, Canis latrans y Lynx rufus. Las especies que sólo se encontraron en un solo tipo de vegetación fueron Bassariscus astutus, Conepatus mesoleucus, Corynorhinus townsendii, Didelphis virginiana, Eptesicus fuscus, Puma yagouaroundi, Lasiurus cinereus, Lasiurus ega, Leptonycteris nivalis, Mustela frenata y Sorex milleri, por lo que se aprecia la diversidad encontrada en el sitio, esto en gran medida por la asociación de la vegetación y la altura marcado por la temperatura reportada para el sitio. Las especies que se localizaron en dos o más estratos o patrones de vegetación fueron Myotis thysanodes, Sciurus alleni, Otospermophilus variegatus, Microtus mexicanus, Urocyon cinereoargenteus, Procyon lotor, Puma concolor, Pecari tajacu y Odocoileus virginianus.