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At least 19 recordsLinked to original sources
USGS1985

Afrotarsius chatrathi, first tarsiiform primate (? Tarsiidae) from Africa

Tarsiiform primates have long been regarded as a Laurasian group, with an extensive fossil record in the Eocene of North America and Europe1-4 and two important but less well-known records from Asia5,6. The only living genus is Tarsius (Tarsiidae), whereas all of the fossil tarsier-like primates are usually placed in the extinct family Omomyidae3. We now report the discovery of Afrotarsius chatrathi from early Oligocene rocks of Fayum Province, Egypt. This is the first known tarsiiform primate from Africa. Compared with fossil primates, the molar tooth morphology of this diminutive prosimian is most similar to that of the European Eocene microchoerine Pseudoloris; however, the closest similarity is to the molars of Tarsius. Because the phylogenetic relationships among living Tarsius and the omomyids remain unclear7,8 and because of the fragmentary nature of the only known specimen of this new primate, allocation of Afrotarsius to either Omomyidae or Tarsiidae is necessarily provisional. As we believe that its molar teeth are more like those of Tarsius than of any omomyids (including Pseudoloris), we tentatively assign the new genus to the extant family Tarsiidae as its only known fossil representative. Recovery of a Tarsius-like primate from Africa suggests that it or its ancestors might have been immigrants from Europe, may have been derived from an unknown Asian stock related to the ancestry of Tarsius, or may have originated in Africa. ?? 1985 Nature Publishing Group.

Nature↗
USGS2010

Occurrence and distribution of Indian primates

Global and regional species conservation efforts are hindered by poor distribution data and range maps. Many Indian primates face extinction, but assessments of population status are hindered by lack of reliable distribution data. We estimated the current occurrence and distribution of 15 Indian primates by applying occupancy models to field data from a country-wide survey of local experts. We modeled species occurrence in relation to ecological and social covariates (protected areas, landscape characteristics, and human influences), which we believe are critical to determining species occurrence in India. We found evidence that protected areas positively influence occurrence of seven species and for some species are their only refuge. We found evergreen forests to be more critical for some primates along with temperate and deciduous forests. Elevation negatively influenced occurrence of three species. Lower human population density was positively associated with occurrence of five species, and higher cultural tolerance was positively associated with occurrence of three species. We find that 11 primates occupy less than 15% of the total land area of India. Vulnerable primates with restricted ranges are Golden langur, Arunachal macaque, Pig-tailed macaque, stump-tailed macaque, Phayre's leaf monkey, Nilgiri langur and Lion-tailed macaque. Only Hanuman langur and rhesus macaque are widely distributed. We find occupancy modeling to be useful in determining species ranges, and in agreement with current species ranking and IUCN status. In landscapes where monitoring efforts require optimizing cost, effort and time, we used ecological and social covariates to reliably estimate species occurrence and focus species conservation efforts. ?? Elsevier Ltd.

Biological Conservation↗
USGS2011

Birth seasonality and offspring production in threatened neotropical primates related to climate

Given the threatened status of many primate species, the impacts of global warming on primate reproduction and, consequently, population growth should be of concern. We examined relations between climatic variability and birth seasonality, offspring production, and infant sex ratios in two ateline primates, northern muriquis, and woolly monkeys. In both species, the annual birth season was delayed by dry conditions and El Niño years, and delayed birth seasons were linked to lower birth rates. Additionally, increased mean annual temperatures were associated with lower birth rates for northern muriquis. Offspring sex ratios varied with climatic conditions in both species, but in different ways: directly in woolly monkeys and indirectly in northern muriquis. Woolly monkeys displayed an increase in the proportion of males among offspring in association with El Niño events, whereas in northern muriquis, increases in the proportion of males among offspring were associated with delayed onset of the birth season, which itself was related, although weakly, to warm, dry conditions. These results illustrate that global warming, increased drought frequency, and changes in the frequency of El Niño events could limit primate reproductive output, threatening the persistence and recovery of ateline primate populations.

Global Change Biology↗
USGS2005

Soils, time, and primate paleoenvironments

Soils are the skin of the earth. From both poles to the equator, wherever rocks or sediment are exposed at the surface, soils are forming through the physical and chemical action of climate and living organisms. The physical attributes (color, texture, thickness) and chemical makeup of soils vary considerably, depending on the composition of the parent material and other variables: temperature, rainfall and soil moisture, vegetation, soil fauna, and the length of time that soil–forming processes have been at work. United States soil scientists 1 have classified modern soils into ten major groups and numerous subgroups, each reflecting the composition and architecture of the soils and, to some extent, the processes that led to their formation. The physical and chemical processes of soil formation have been active throughout geologic time; the organic processes have been active at least since the Ordovician. 2 Consequently, nearly all sedimentary rocks that were deposited in nonmarine settings and exposed to the elements contain a record of ancient, buried soils or paleosols. A sequence of these rocks, such as most ancient fluvial (stream) deposits, provides a record of soil paleoenvironments through time. Paleosols are also repositories of the fossils of organisms (body fossils) and the traces of those organisms burrowing, food–seeking, and dwelling activities (ichnofossils). Indeed, most fossil primates are found in paleosols. Careful study of ancient soils gives new, valuable insights into the correct temporal reconstruction of the primate fossil record and the nature of primate paleoenvironments.

Evolutionary Anthropology↗
USGS1991

Evolutionary relationships of a new genus and three new species of Omomyid primates (Willwood Formation, Lower Eocene, Bighorn Basin, Wyoming)

Studies of new finds of omomyid primates from the lower Eocene Willwood Formation of northwest Wyoming reveal the presence of a new genus and two new species of anaptomorphines and a new species of omomyine. All were apparently short-lived immigrants into the Bighorn Basin. The new genus and speciesTatmanius szalayi is typified by a diminutive single-rooted p3 and a bilobed-rooted p4 with a crown smaller than ml. These traits were probably derived fromPseudotetonius and parallel similar conditions inTrogolemur andNannopithex. The new speciesArapahovius advena is the first occurrence ofArapahovius outside the Washakie Basin, where it appears to have also been a vagrant species.Steinius annectens, sp. nov., is larger than the olderSteinius vespertinus and strengthens the alliance between this genus and BridgerianOraorays carteri, although which species ofSteinius is closer toOmomys is not yet clear. The available evidence suggests a derivation ofOmomys (Omomyini) fromSteinius and all Washakiini from the anaptomorphineTeilhardina, which would indicate that Omomyinae were at least diphyletic. Preliminary evidence suggests that the geographic distributions of at least some Willwood omomyids correlate with paleosol distributions.

Journal of Human Evolution↗
USGS1990

New Washakiin primates (Omomyidae) from the Eocene of Wyoming and Colorado, and comments on the evolution of the Washakiini

Two new species of washakiin omomyids occur in deposits of early Bridgerian age. Shoshonius bowni , sp. nov., from the Aycross Formation, Absaroka Range, Wyoming, differs from S. cooperi in having enlarged conules on the upper molars and a second metaconule, features convergent with Washakius insignis. Washakius izetti , sp. nov., from the Green River Formation, Piceance Creek Basin, Colorado, is the most primitive known species of Washakius , showing incipient development of features present in the later W. insignis and W. woodringi. Washakius , cf. W. izetti occurs in the early Bridgerian of the Huerfano Basin. W. izetti is closely related to Utahia kayi , a. washakiin possibly related to Stockia. Hemiacodon , sometimes included in the Washakiini, is probably more closely related to the Omomyini. Stockia is distinct from Omomys and is questionably included in the Washakiini, of which Loveina is the stem taxon. More advanced washakiins form two groups between which there was significant parallel evolution in dental morphology. One group includes Washakius, Dyseolemur, Utahia , and possibly Stockia , and is characterized by development of an open talonid notch before the consistent appearance of metastylids. The other group consists of Shoshonius , where the establishment of metastylids preceded the full opening of the talonid basins.

Journal of Vertebrate Paleontology↗
USGS2015

Primative components, crustal assimilation, and magmatic degassing of the 2008 Kilauea summit eruption

Simultaneous summit and rift zone eruptions at Kīlauea starting in 2008 reflect a shallow eruptive plumbing system inundated by a bourgeoning supply of new magma from depth. Olivine-hosted melt inclusions, host glass, and bulk lava compositions of magma erupted at both the summit and east rift zone demonstrate chemical continuity at both ends of a well-worn summit-to-rift pipeline. Analysis of glass within dense-cored lapilli erupted from the summit in March – August 2008 show these are not samplings of compositionally distinct magmas stored in the shallow summit magma reservoir, but instead result from remelting and assimilation of fragments from conduit wall and vent blocks. Summit pyroclasts show the predominant and most primitive component erupted to be a homogenous, relatively trace-element-depleted melt that is a compositionally indistinguishable from east rift lava. Based on a “top-down” model for the geochemical variation in east rift zone lava over the past 30 years, we suggest that the apparent absence of a 1982 enriched component in melt inclusions, as well as the proposed summit-rift zone connectivity based on sulfur and mineral chemistry, indicate that the last of the pre-1983 magma has been flushed out of the summit reservoir during the surge of mantle-derived magma from 2003-2007.

Hawaii↗
USGS1990

Sedimentary paleoenvironments of fossil platyrrhine localities, Miocene Pinturas Formation, Santa Cruz Province, Argentina

The Pinturas Formation is a pyroclastic and epiclastic aeolian deposit of Miocene age lying discordantly upon Jurassic rocks in the elevated Andean precordillera of northwest Santa Cruz Province, Argentina. The history of development of the Pinturas Formation was significantly affected by the gradual, though sporadic, draping of this aeolian sediment across a profound, slowly filling paleotopography. The Pinturas depositional cycle consisted of: (1) minor aeolian deposition followed by soil formation, and (2) major aeolian deposition followed by intervals of regional erosion. Fluvial action seems to have been almost wholly confined to intraformational erosion, and two significant intraformational erosional unconformities divide the Pinturas Formation into three sequences. The lower sequence is dominated by pyroclastic mudrocks upon which were formed very mature, probably mollic, paleosols; the middle sequence is composed largely of epiclastic sand occurring as barchanoid paleodunes; and the upper sequence consists of massive, poorly bedded pyroclastic mudrocks. Many Pinturas lacunae were reconstructed on the basis of locally preserved strata, and a novel method of holostrome reconstruction using relative paleosol maturities places Pinturas sedimentation in a more accurate temporal light. It also indicates: (1) that the Pinturas sediment accumulation rate increased with time; (2) that regional erosive intervals are correlated directly with major influxes of pyroclastic material; and (3) that the introduction of the Pinturas platyrrhine primates occurred in the sequence:Carlocebus carmenensis, C. intermedius andSoriacebus ameghinorum. Soriacebus adrianae. Pinturas paleosols appear to have formed under moist conditions, and both mature and immature varieties yield a host of ichnofossils. These include the burrows and nests of bees, scarabeid beetles, termites, and at least two different kinds of colonial rodents, in addition to rhizoliths and the calcified boles and root systems of trees. A fossil nest of a nasutitermitine termite in the lower sequence of the formation indicates the presence of tropical forest. Climatic conditions may have been drier during deposition of the barchanoid paleodunes in early late Pinturas time, or the dunes might reflect drier source areas or have simply encroached on areas of highland forest. Fossil mammals are abundant in Pinturas sediments, and attritional concentrations of them were recognized in the upper parts of paleosols and on the floors of erosional scours. Radiometric dates indicate that the fossil mammals (including platyrrhine primates) occurring in the lower and middle parts of the formation may range in age from about 16-6 to younger than 13-3 Ma (million years ago) (Santacrucian and, almost certainly, Friasian land-mammal ages). This age range is somewhat younger than previous estimates, and suggests that the Pinturas faunas correlate broadly with those from the type Santa Cruz Formation, with the presumed position of the type Friasian, and with the base of the marine Gaiman Formation in the lower valley of the Rio Chubut.

Journal of Human Evolution↗
USGS2015

Comparing spatial capture–recapture modeling and nest count methods to estimate orangutan densities in the Wehea Forest, East Kalimantan, Indonesia

Accurate information on the density and abundance of animal populations is essential for understanding species' ecology and for conservation planning, but is difficult to obtain. The endangered orangutan ( Pongo spp.) is an example; due to its elusive behavior and low densities, researchers have relied on methods that convert nest counts to orangutan densities and require substantial effort for reliable results. Camera trapping and spatial capture–recapture (SCR) models could provide an alternative but have not been used for primates. We compared density estimates calculated using the two methods for orangutans in the Wehea Forest, East Kalimantan, Indonesia. Camera trapping/SCR modeling produced a density estimate of 0.16 ± 0.09–0.29 indiv/km 2 , and nest counts produced a density estimate of 1.05 ± 0.18–6.01 indiv/km 2 . The large confidence interval of the nest count estimate is probably due to high variance in nest encounter rates, indicating the need for larger sample size and the substantial effort required to produce reliable results using this method. The SCR estimate produced a very low density estimate and had a narrower but still fairly wide confidence interval. This was likely due to unmodeled heterogeneity and small sample size, specifically a low number of individual captures and recaptures. We propose methodological fixes that could address these issues and improve precision. A comparison of the overall costs and benefits of the two methods suggests that camera trapping/SCR modeling can potentially be a useful tool for assessing the densities of orangutans and other elusive primates, and warrant further investigation to determine broad applicability and methodological adjustments needed.

East Kalimantan↗
USGS2010

Modeling the impacts of hunting on the population dynamics of red howler monkeys ( Alouatta seniculus )

Overexploitation of wildlife populations occurs across the humid tropics and is a significant threat to the long-term survival of large-bodied primates. To investigate the impacts of hunting on primates and ways to mitigate them, we developed a spatially explicit, individual-based model for a landscape that included hunted and un-hunted areas. We used the large-bodied neotropical red howler monkey ( Alouatta seniculus ) as our case study species because its life history characteristics make it vulnerable to hunting. We modeled the influence of different rates of harvest and proportions of landscape dedicated to un-hunted reserves on population persistence, population size, social dynamics, and hunting yields of red howler monkeys. In most scenarios, the un-hunted populations maintained a constant density regardless of hunting pressure elsewhere, and allowed the overall population to persist. Therefore, the overall population was quite resilient to extinction; only in scenarios without any un-hunted areas did the population go extinct. However, the total and hunted populations did experience large declines over 100 years under moderate and high hunting pressure. In addition, when reserve area decreased, population losses and losses per unit area increased disproportionately. Furthermore, hunting disrupted the social structure of troops. The number of male turnovers and infanticides increased in hunted populations, while birth rates decreased and exacerbated population losses due to hunting. Finally, our results indicated that when more than 55% of the landscape was harvested at high (30%) rates, hunting yields, as measured by kilograms of biomass, were less than those obtained from moderate harvest rates. Additionally, hunting yields, expressed as the number of individuals hunted/year/km 2 , increased in proximity to un-hunted areas, and suggested that dispersal from un-hunted areas may have contributed to hunting sustainability. These results indicate that un-hunted areas serve to enhance hunting yields, population size, and population persistence in hunted landscapes. Therefore, spatial regulation of hunting via a reserve system may be an effective management strategy for sustainable hunting, and we recommend it because it may also be more feasible to implement than harvest quotas or restrictions on season length.

Guárico↗
USGS1976

Wildlife importation into the United States, 1900-1972

Data from Bureau of Biological Survey and U.S. Fish and Wildlife Service reports show an overall increase in the number of birds and mammals imported from 1900 to 1972. The trend was interrupted by World War I, the economic depression of the 1930's, and World War II. Data are lacking for the years after World War II until 1968. Until 1942, domesticated canaries and a few species of game birds made up most of the avian imports; the shell parakeet or budgerigar was the most commonly imported parrot. Although the total number ofbirds imported 1968-72 was-not greatly different from the pre-depression years, the proportion of canaries, game species, and parakeets declined greatly and the variety and number of cage birds including other parrot species greatly increased. Until 1930 most mammals imported were for laboratory use or fur farming. After 1930 the number of imported mammals increased with the growing importance of primates, especially rhesus macaques, in research. Since 1968 the number of mammals irnported annually has been at least 5 times greater than the previous peak of 1938, and primates have made up 87% of mammalian imports. Information on reptiles and amphibians imported into the United States is available only for 1970 and 1971. Turtles were the most commonly imported reptiles, frogs and toads the most commonly imported amphibians.

Special Scientific Report - Wildlife↗
USGS2013

Variation in hair δ 13 C and δ 15 N values in long-tailed macaques (Macaca fascicularis) from Singapore

Much of the primatology literature on stable isotope ratios of carbon (δ 13 C) and nitrogen (δ 15 N) has focused on African and New World species, with comparatively little research published on Asian primates. Here we present hair δ 13 C and δ 15 N isotope values for a sample of 33 long-tailed macaques from Singapore. We evaluate the suggestion by a previous researcher that forest degradation and biodiversity loss in Singapore have led to a decline in macaque trophic level. The results of our analysis indicated significant spatial variability in δ 13 C but not δ 15 N. The range of variation in δ 13 C was consistent with a diet based on C 3 resources, with one group exhibiting low values consistent with a closed canopy environment. Relative to other macaque species from Europe and Asia, the macaques from Singapore exhibited a low mean δ 13 C value but mid-range mean δ 15 N value. Previous research suggesting a decline in macaque trophic level is not supported by the results of our study.

Primates↗
USGS1999

Environmental enrichment of brown capuchins (Cebus apella): Behavioral and plasma and fecal cortisol measures of effectiveness

No consensus exists about the quantity and variety of environmental enrichment needed to achieve an acceptable level of psychological well-being among singly housed primates. Behavioral and plasma and fecal cortisol measures were used to evaluate the effectiveness of four levels of toy and foraging enrichment provided to eight wild-caught, singly housed adult male brown capuchins (Cebus apella). The 16-week-long study comprised six conditions and began with a 4-week-long preexperimental and ended with a 4-week-long postexperimental period during which the subjects were maintained at baseline enrichment levels. During the intervening 8 weeks, the subjects were randomly assigned to a sequence of four 2-week-long experimental conditions: control (baseline conditions), toy (the addition of two plastic toys to each cage), box (access to a foraging box with food treats hidden within crushed alfalfa), and box and toy (the addition of two plastic toys and access to a foraging box). Behavioral responses to changes in enrichment were rapid and extensive. Within-subject repeated-measure ANOVAs with planned post hoc contrasts identified highly significant reductions in abnormal and undesirable behaviors (and increases in normal behaviors) as the level of enrichment increased from control to toy to box to box and toy. No significant behavioral differences were found between the control and pre- and postexperimental conditions. Plasma and fecal cortisol measures revealed a different response to changing enrichment levels. Repeated-measure ANOVA models found significant changes in both these measures across the six conditions. The planned post hoc analyses, however, while finding dramatic increases in cortisol titers in both the pre- and postexperimental conditions relative to the control condition, did not distinguish cortisol responses among the four enrichment levels. Linear regressions among weekly group means in behavioral and cortisol measures (n = 16) found that plasma cortisol was significantly predicted by the proportions of both normal and abnormal behaviors; as the proportion of normal behaviors increased, the plasma cortisol measures decreased. Plasma cortisol weekly group means were also significantly and positively predicted by fecal cortisol weekly group means, but no behavioral measure significantly predicted fecal cortisol weekly group means. In sum, these findings argue strongly that access to a variety of toy and foraging enrichment positively affects behavioral and physiological responses to stress and enhances psychological well-being in singly housed brown capuchins.

American Journal of Primatology↗
USGS2017

Vectors, hosts, and control measures for Zika virus in the Americas

We examine Zika virus (ZIKV) from an ecological perspective and with a focus on the Americas. We assess (1) the role of wildlife in ZIKV disease ecology, (2) how mosquito behavior and biology influence disease dynamics, and (3) how nontarget species and ecosystems may be impacted by vector control programs. Our review suggests that free-ranging, non-human primates may be involved in ZIKV transmission in the Old World; however, other wildlife species likely play a limited role in maintaining or transmitting ZIKV. In the Americas, a zoonotic cycle has not yet been definitively established. Understanding behaviors and habitat tolerances of Aedes aegypti and Aedes albopictus , two ZIKV competent vectors in the Americas, will allow more accurate modeling of disease spread and facilitate targeted and effective control efforts. Vector control efforts may have direct and indirect impacts to wildlife, particularly invertebrate feeding species; however, strategies could be implemented to limit detrimental ecological effects.

EcoHealth↗
USGS2026

Resilience thinking for human-wildlife coexistence: Bridging dynamic systems, archetypes, and transformations

As human activities and wildlife increasingly overlap in the Anthropocene, conventional conservation paradigms focused on land-sparing are shifting toward strategies that support human–wildlife coexistence. However, achieving sustainable coexistence is often hindered by a limited understanding of the dynamic social–ecological processes that drive integrated human–wildlife systems. This Special Issue explores “resilience thinking” as a scientific framework to address these knowledge gaps. By bridging sustainability and wildlife sciences, we examine how concepts such as adaptive capacity, feedback loops, system archetypes, and tipping points can illuminate the conditions that facilitate stable coexistence or lead to persistent conflict. Through diverse global case studies ranging from carnivore management in Europe to primate interactions in Indonesia, contributions highlight how societal perceptions, governance, and co-adaptation shape system trajectories. Ultimately, we argue that fostering durable coexistence requires moving beyond incremental adaptation toward transformative governance that centers on equity, relationality, and proactive management.

Ambio↗
USGS2017

Turtles: Freshwater

With their iconic shells, turtles are morphologically distinct in being the only extant or extinct vertebrate animals to have their shoulders and hips inside their rib cages. By the time an asteroid hit the earth 65.5 million years ago, causing the extinction of dinosaurs, turtles were already an ancient lineage that was 70% through their evolutionary history to date. The remarkable evolutionary success of turtles over 220 million years is due to a combination of both conservative and effective life history traits and an essentially unchanging morphology that withstood the test of time. However, the life history traits of many species make them particularly susceptible to overharvest and habitat destruction in the modern world, and a majority of the world’s species face serious conservation challenges with several extinctions documented in modern times. The global plight of turtles is underscored by the fact that the percentage of imperiled species exceeds that of even the critically endangered primates. Freshwater turtles, with over 260 recognized species, have become a focus on a worldwide scale for many conservation issues. This article is a synthesis of a diverse body of information on the general biology of freshwater turtles, with particular emphasis on the extensive research on ecology, life history, and behavior that has been accomplished in the last half century. Much of the research has been applicable to the aforementioned conservation challenges. The studies presented include a combination of laboratory and field experiments and observational studies on this intriguing group of animals.

Book chapter↗
USGS2005

Disentangling association patterns in fission-fusion societies using African buffalo as an example

A description of the social network of a population aids us in understanding dispersal, the spread of disease, and genetic structure in that population. Many animal populations can be classified as fission–fusion societies, whereby groups form and separate over time. Examples discussed in the literature include ungulates, primates and cetaceans (Lott and Minta, 1983, Whitehead et al., 1991, Henzi et al., 1997, Christal et al., 1998 and Chilvers and Corkeron, 2002). In this study, we use a heuristic simulation model to illustrate potential problems in applying traditional techniques of association analysis to fission–fusion societies and propose a new index of association: the fission decision index (FDI). We compare the conclusions resulting from traditional methods with those of the FDI using data from African buffalo, Syncerus caffer , in the Kruger National Park. The traditional approach suggested that the buffalo population was spatially and temporally structured into four different ‘herds’ with adult males only peripherally associated with mixed herds. Our FDI method indicated that association decisions of adult males appeared random, but those of other sex and age categories were nonrandom, particularly when we included the fission events associated with adult males. Furthermore, the amount of time that individuals spent together was only weakly correlated with their propensity to remain together during fission events. We conclude with a discussion of the applicability of the FDI to other studies.

Kruger National Park↗