DNA extraction from skins of wild (Hydrochoerus hydrochaeris and Pecari tajacu) and domestic (Sus scrofa domestica) species using a novel protocol.

Sometimes, commercial products obtained from wild animals are sold as if they were from domestic animals and vice versa. At this point of the productive chain, legal control of possible wildlife products is difficult. Common in the commerce of northern Argentina, skins of two wild species, the carpincho and the collared peccary, look very similar to each other and to those of the domestic pig; it is extremely difficult to differentiate them after they have been tanned. Because there was no an adequate methodology to discriminate between leather of these three species, we developed a new methodology of DNA extraction from skin and leather. This new method involves digesting a leather sample using proteinase K, followed by precipitation of proteins with 5 M NaCl, cleaning with absolute isopropanol and DNA precipitation with 70% ethanol. DNA is hydrated in Tris-EDTA buffer. This protocol provided good-quality DNA suitable for analysis with molecular markers. This new protocol has potential for use in identifying leather products of these species using molecular markers based on RAPDs.Fil: Ojeda, Guillermo Nicolás. Universidad Nacional del Litoral. Facultad de Humanidades y Ciencias. Departamento de Ciencias Naturales; ArgentinaFil: Amavet, Patricia Susana. Universidad Nacional del Litoral. Facultad de Humanidades y Ciencias. Departamento de Ciencias Naturales; ArgentinaFil: Rueda, Eva Carolina. Universidad Nacional del Litoral. Facultad de Humanidades y Ciencias. Departamento de Ciencias Naturales; ArgentinaFil: Siroski, Pablo Ariel. Universidad Nacional del Litoral. Facultad de Humanidades y Ciencias. Departamento de Ciencias Naturales. Laboratorio de Zoología Aplicada: Anexo Vertebrados (FHUC-UNL/MASPyMA); Argentin

The potential role of captive collared peccary (Tayassu tajacu) as a leptospirosis reservoir in the Peruvian Amazon

A serological survey was conducted in a collared peccary farm in the Peruvian Amazon to investigate variations in leptospiral seroprevalence over a period of 18 months. The first survey in 2003 revealed a prevalence of 100% of leptospirosis in the captive population (n=27) with a total of 9 different serovars (sv) identified. Leptospira spp. Varillal 010 was detected in 100% of the population reaching titers of 1:1600 and 8 other strains were detected sometimes at high titers. A second survey in 2005, confirmed a prevalence of leptospirosis in 86.4% of the sampled population (n=22) and revealed serological conversion to two new serovars in 40% of the herd. The absence of clinical symptoms and serological conversion to previously detected or to new serovars in more than 90% of the herd confirms the circulation of spirochaetes within the captive herd and the possible role the collared peccary as a potential reservoir of leptospirosis. (Résumé d'auteur

A vortex population viability analysis model for the Chacoan peccary (catagonus wagneri)

El quimilero o taguá (Catagonus wagneri) es una especie amenazada, endémica del Chaco Seco, para la cual disponemos de poca información. Para estimar cuantitativamente el riesgo de disminución y extinción de sus poblaciones silvestres generamos modelos de viabilidad poblacional. Con estos modelos matemáticos se pueden identificar factores naturales y antrópicos complejos que interactúan y que influyen en la persistencia y la salud de una población. Los modelos también se pueden utilizar para evaluar los efectos de diferentes estrategias de gestión, permitiendo identificar las acciones de conservación más efectivas para una población o especie. Además, estos modelos se pueden usar para identificar las necesidades de investigación debido a que ponen en evidencia los vacíos de información sobre la especie. Utilizando estos modelos, evaluamos la proyección poblacional en las condiciones actuales y en comparación con posibles variaciones existentes en el sistema. Para generar los parámetros ingresados en los modelos realizamos una reunión de especialistas y una revisión bibliográfica. Trabajó con valores de línea de base (base), mínimos (mín.) y máximos (máx.). Generamos diferentes modelos ante diferentes escenarios y testeamos la sensibilidad a la incertidumbre de cada modelo. Esto permitió establecer prioridades de investigación. Además, determinamos los tamaños mínimos de población viable considerando la incertidumbre y analizamos los posibles efectos de la caza en una población de esta especie.Fil: Leus, Kritin. International Union for Conservation of Nature. Species Survival Commission; DinamarcaFil: Altrichter, Mariana. International Union for Conservation of Nature. Species Survival Commission; Estados UnidosFil: Desbiez, Arnaud. International Union for Conservation of Nature. Species Survival Commission; BrasilFil: Camino, Micaela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste. Centro de Ecología Aplicada del Litoral. Universidad Nacional del Nordeste. Centro de Ecología Aplicada del Litoral; ArgentinaFil: Giordano, Anthony J.. S.P.E.C.I.E.S.; Estados UnidosFil: Campos Krauer, Juan Manuel. University of Florida. Department of Wildlife Ecology and Conservation; Estados Unidos. Centro Chaqueño para la Conservación y la Investigación; ParaguayFil: Brooks, Daniel M.. Houston Museum Of Natural Science; Estados UnidosFil: Thompson, Jeffrey. Consejo Nacional de Ciencia y Tecnología; ParaguayFil: Núñez Regueiro, Mauricio Manuel. University of Florida. Department of Wildlife Ecology and Conservation; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentin

Puberty in male collared peccary (Pecari tajacu) determined by quantitative analysis of spermatogenic cells.

Estudos biológicos são necessários para o manejo da vida silvestre em cativeiro, e o conhecimento da reprodução é um dos aspectos importantes para o aumento da produção. Esta pesquisa teve como objetivo determinar a idade da puberdade do cateto macho. Foram utilizadas amostras testiculares de 15 animais, entre 7 a 16 meses, distribuídos em cinco grupos (G1, G2, G3, G4 e G5). Os testículos aumentaram no peso, comprimento e largura consideravelmente (p < 0,05) do G1 ao G3, enquanto que, a partir deste grupo, o desenvolvimento desse órgão foi mais lento. Houve correlação positiva (p < 0,001) entre os seguintes parâmetros testiculares: peso e comprimento (r = 0,97), peso e largura (r = 0,88), comprimento e largura (r = 0,92). Com relação ao diâmetro tubular, observou-se um aumento (p < 0,05) do G1 ao G4. A quantidade total de células espermatogênicas aumentou significativamente (p < 0,05) até o G3, e se estabilizou a partir deste grupo. Houve correlação positiva entre o peso testicular e o diâmetro tubular (r = 0,99, p < 0,001), bem como o peso testicular e as células espermatogênicas (r = 0,98, p < 0,001). A quantidade de células de Sertoli reduziu significativamente (p < 0,05) do G1, onde se encontravam indiferenciadas como células de suporte, até G5, onde foram observadas juntamente com todas as células da linhagem espermática. Estes resultados demonstraram que as fases do desenvolvimento reprodutivo de catetos podem ser classificadas em: impúbere (G1, 7-8 meses), pré-púbere (G2, 9-10 meses), púbere (G3, 11-12 meses), pós-púbere 1 (G4, 13-14 meses) e pós-púbere 2 (G5, 15-16 meses). Com base na análise histológica, a puberdade dos catetos machos ocorre entre 11 e 12 meses de idade

Ovarian folliculogenesis in collared peccary, Pecari tajacu (Artiodactyla: Tayassuidae).

The sustainability and production of collared peccary (Pecari tajacu) has been studied in the last few years; however, further information on its reproduction is necessary for breeding systems success. Understanding folliculogenesis aspects will contribute to effective reproductive biotechniques, which are useful in the preservation and production of wildlife. The aim of this study was to evaluate the ovarian folliculogenesis in collared peccary. Ovaries from six adult females of collared peccary were obtained through ovariectomy and analyzed. These were fixed in aqueous Bouin’s solution and sectioned into 7µm slices, stained with hematoxilin-eosin and analyzed by light microscopy. The number of pre-antral and antral follicles per ovary was estimated using the Fractionator Method. The follicles, oocytes and oocyte nuclei were measured using an ocular micrometer. Results showed that the length, width, thickness, weight, and the gross anatomy of the right and left ovaries were not significantly different. However, the mean number of corpora lutea was different between the phases of the estrous cycle (p<0.05), with the highest mean in the luteal phase. Primordial follicles were found in the cortex; the oocytes were enveloped by a single layer of flattened follicular cells. In the primary follicles, proliferation of the follicular cells gave rise to cuboidal cells (granulosa cells). The secondary follicle was characterized by two or more concentric layers of cuboidal cells (granulosa), beginning of antrum formation, and the presence of pellucid zone and theca cells. Antral follicles were characterized by a central cavity (antrum), the presence of cumulus oophorus and theca layers (interna and externa). In the right ovary, the values of the primordial and primary follicles were similar, but significantly different from the secondary ones (p<0.05). In the left ovary, significant differences were observed between all follicles in the follicular phase (p<0.05); the mean number of primordial and primary follicles was similar in the luteal phase. The mean number of pre-antral follicles and antral follicles in the follicular phase was higher in the left ovary (p<0.05). The mean number of antral follicles in the luteal phase was similar in both ovaries. We also found significant differences in mean diameter of preantral follicles, oocyte, granulosa layer and oocyte nucleus during the estrous cycle. In the antral follicles a significant difference was observed only in follicular diameter (p<0.05). The predominance of active primordial and primary follicles was found in both phases; otherwise the secondary follicles and antral follicles showed a high degree of degeneration. The results obtained in the present work will strengthen the development of biotechnology programs to improve the productive potential and conservation of the collared peccar

Group dynamics, behavior, and current and historical abundance of peccaries in Costa Rica’s Caribbean lowlands

The abundances and habitat preferences of peccaries in Neotropical forests are important to understand because these keystone species influence many aspects of the ecosystem. In the Caribbean lowlands of Costa Rica, we conducted walking surveys for ~2 years to study the behavior and population trends of collared peccaries (Pecari tajacu), and found that peccaries are abundant at La Selva Biological Station and overall, detection rates were relatively constant through time. A stable estimate of detection rates was achieved only after 7–9 months of surveying. We found no habitat preferences between primary and secondary forest, yet there were some differences in group dynamics—group radius was larger and sighting distance was greater in primary forest, whereas the number of singletons was higher in secondary forest. More peccaries were seen closer to the laboratory clearing than at greater distances, for a variety of probable reasons: habituation to humans, lower predation and hunting pressure, and various environmental and habitat factors. Peccary groups had spatially clumped distributions across the landscape and were more active diurnally than nocturnally. Collared peccary densities are relatively high at La Selva compared to other Neotropical sites, with the exception of Barro Colorado Island. We combined our data with a review of the historical literature to assess changes in the populations of peccaries in the Caribbean lowlands. We found that collared peccaries have likely increased in abundance at La Selva, seemingly a few years after the extirpation of white-lipped peccaries (Tayassu pecari), which were abundant in the area 40–50 years ago. An understanding of the group dynamics, behavior, and habitat preference of collared peccaries is essential for management decisions and conservation efforts. Additionally, assessment of population changes should be carefully considered in a historical context, with a particular focus on how the populations of the 2 peccary species have changed, and how these species might differentially affect their environment. Resumen--Entender la abundancia y la preferencia de hábitat de las 2 especies de sainos en bosques neotropicales es importante porque estas especies clave afectan muchos aspectos del ecosistema. En las tierras bajas del Caribe costarricense, llevamos a cabo muestreos a pie durante ~2 años para estudiar el comportamiento y tendencias poblacionales del saino (Pecari tajacu), y encontramos que son abundantes en la Estación Biológica La Selva y las tasas de detección fueron relativamente constantes a través del tiempo. Se obtuvo una tasa estable de detección después de 7–9 meses de muestreos. Las tasas de detección fueron similares en bosque primario y secundario, sin embargo, se encontraron algunas diferencias en la dinámica de grupo (el radio de distribución del grupo era más grande y distancia de observación fue mayor en bosques primarios, mientras que el número de individuos solitarios fue mayor en bosques secundarios). Más sainos fueron vistos alrededor de las zonas abiertas rodeando el laboratorio, debido a varias posibles razones: habituación a la presencia de seres humanos, menos presión por depredación o cacería y otros factores ambientales o de hábitat. Los sainos están distribuidos de forma aglomerados y son más activos de día que de noche. Las densidades de sainos son relativamente altas en comparación con otros sitios neotropicales, con excepción de la Isla de Barro Colorado. El saino probablemente ha aumentado en abundancia en La Selva, aparentemente unos años después de la extirpación del cariblanco (Tayassu pecari), que eran abundantes en el área hace unos 40–50 años. El conocimiento de la dinámica de grupos, comportamiento y preferencias de hábitat del saino es esencial para las decisiones de manejo y los esfuerzos de conservación. Además, la evaluación de los cambios poblacionales debe considerarse cuidadosamente en un contexto histórico, con especial atención a cómo han cambiado las poblaciones del saino y cariblanco, y cómo estas especies afectan su ambiente

Measurement of cognitive bias and cortisol levels to evaluate the effects of space restriction on captive collared peccary (Mammalia, Tayassuidae)

We use the judgement-bias paradigm to evaluate whether space restriction in metabolism pens affects the emotional state of collared peccary (Pecari tajacu) during a nutritional experiment. We trained individual adult males to ‘go’ to a specific location within 30 s when a positive auditory cue (whistle; CS+) was given in order to receive cassava root pieces as a reward, and to ‘no-go’ when a negative cue (caxixi percussion instrument; CS−) was sounded to avoid punishment (jet of water) and no reward. An ‘ambiguous’ auditory cue (a drumstick hitting an aluminum plate; CSA) was presented to probe decision-making under ambiguity. Individuals were subjected to five 8-day housing conditions in the order: H1 (control-no space restriction-metabolism pen and additional area), H2 space restriction without environmental enrichment (metabolism pen only), H3 (control-no space restriction), H4 (space restriction with environmental enrichment), and H5 (control-no space restriction). On the eighth day of each housing condition, each animal was exposed to 10 judgement bias trials of each of the three cue types: CS+, CS−, and CSA. We recorded whether animals showed the ‘go’ or ‘no-go’ response after each type of cue and collected fecal samples to assess fecal glucocorticoid metabolite concentrations. Peccaries learnt to discriminate CS+ and CS− and maintained this discrimination during the five housing conditions tested. The response to the ambiguous cue (CSA) varied according to the housing condition. During H1, the peccaries made a similar proportion of ‘go’ responses to all three types of cue (Ps > 0.07). During H2 and H3, ‘go’ responses to CSA and CS− cues occurred in similar proportions (Ps > 0.70), but peccaries showed more go responses to CS+ (Ps < 0.03) indicating that they were responding to CSA as if it were more likely to predict the waterjet than food. During H4 and H5, peccaries again made a similar proportion of ‘go’ responses to all three types of cue, as in H1. During H2 and H3, fecal glucocorticoid metabolite concentrations were higher than during the other tests (208.0 ± 16.4 vs. 141.6 ± 25.9 ngg−1 dry feces, Ps < 0.03). Our results suggest that space restriction may induce physiological stress and influence judgement bias and affective state in peccaries, and that these effects may be offset by environmental enrichment. However, the possibility of a general habituation to the housing conditions across time cannot be ruled out

Social, Spacing, and Cooperative Behavior of the Collared Peccary, Tayassu tajacu

Social behavior of the collared peccary was studied on the lower, eastern slopes of the Mazatzal Mountains, Arizona. The social unit in this species is a cohesive herd, in which small inter-individual distances are maintained. Two conspicuous acts, one olfactory and one auditory, functioned to maintain close spacing. Social interactions were brief but tended to synchronize the activities of animals and also to bring them closer together. Amicable and neutral actions occurred far more frequently than agonistic interactions. Most agonistic behavior did not involve physical contact. Cooperative nursing, predator defense, and feeding occurred; all adults were tolerant of young, and males showed little overt competition over estrous females. The absence of sexual dimorphism, the 1:1 sex ratio within social groups, and the small, precocial litters in this species suggest an evolutionary history of pronounced sociality. Kin selection possibly was important in the evolution of social behavior in peccaries

Landscape composition influences abundance patterns and habitat use of three ungulate species in fragmented secondary deciduous tropical forests, Mexico

AbstractSecondary forests are extensive in the tropics. Currently, these plant communities are the available habitats for wildlife and in the future they will possibly be some of the most wide-spread ecosystems world-wide. To understand the potential role of secondary forests for wildlife conservation, three ungulate species were studied: Mazama temama, Odocoileus virginianus and Pecari tajacu. We analyzed their relative abundance and habitat use at two spatial scales: (1) Local, where three different successional stages of tropical deciduous forest were compared, and (2) Landscape, where available habitats were compared in terms of landscape composition (proportion of forests, pastures and croplands within 113 ha). To determine the most important habitat-related environmental factors influencing the Sign Encounter Rate (SER) of the three ungulate species, 11 physical, anthropogenic and vegetation variables were simultaneously analyzed through model selection using Akaike’s Information Criterion. We found, that P. tajacu and O. virginianus mainly used early successional stages, while M. temama used all successional stages in similar proportions. The latter species, however, used early vegetation stages only when they were located in landscapes mainly covered by forest (97%). P. tajacu and O. virginianus also selected landscapes covered essentially by forests, although they required smaller percentages of forest (86%). All ungulate species avoided landscape fragments covered by pastures. For all three species, landscape composition and human activities were the variables that best explained SER. We concluded that landscape is the fundamental scale for ungulate management, and that secondary forests are potentially important landscape elements for ungulate conservation