Suzanne Palminteri

An ecoregion-based approach to protecting half the terrestrial realm

Abstract We assess progress toward the protection of 50% of the terrestrial biosphere to address the species-extinction crisis and conserve a global ecological heritage for future generations. Using a map of Earths 846 terrestrial ecoregions, we show that 98 ecoregions (12%) exceed Half Protected; 313 ecoregions (37%) fall short of Half Protected but have sufficient unaltered habitat remaining to reach the target; and 207 ecoregions (24%) are in peril, where an average of only 4% of natural habitat remains. We propose a Global Deal for Nature—a companion to the Paris Climate Deal—to promote increased habitat protection and restoration, national- and ecoregion-scale conservation strategies, and the empowerment of indigenous peoples to protect their sovereign lands. The goal of such an accord would be to protect half the terrestrial realm by 2050 to halt the extinction crisis while sustaining human livelihoods.

Regional-scale heterogeneity in primate community structure at multiple undisturbed forest sites across south-eastern Peru

The forests of western Amazonia support high site-level biological diversity, yet regional community heterogeneity is poorly understood. Using data from line transect surveys at 3 7 forest sites in south-eastern Peru, we assessed whether local primate assemblages are heterogeneous at the scale of a major watershed. We examined patterns of richness, abundance and community structure as a function of forest type, hunting pressure, land-management regime and geographic location. The primate assemblage composition and structure varied spatially across this relatively small region of Amazonia (≈85 000 km 2 ), resulting from large-scale species patchiness rather than species turnover. Primate species richness varied among sites by a factor of two, community similarity by a factor of four and aggregate biomass by a factor of 45. Several environmental variables exhibited influence on community heterogeneity, though none as much as geographic location. Unflooded forest sites had higher species richness than floodplain forests, although neither numerical primate abundance nor aggregate biomass varied with forest type. Non-hunted sites safeguarded higher abundance and biomass, particularly of large-bodied species, than hunted sites. Spatial differences among species assemblages of a relatively generalist taxon like primates in this largely undisturbed forest region imply that community heterogeneity may be even greater in more species-rich taxa, as well as in regions of greater forest habitat diversity.

Usefulness of species range polygons for predicting local primate occurrences in southeastern Peru

Species distribution maps are widely used in predicting areas of conservation concern, particularly where species distributions are poorly known. However, the accuracy of range maps for regional/local planning is questionable. We compared published putative geographic range polygons of ten primate species to their actual occupancy at 23 survey sites in southeastern Peru to assess the fine‐scale accuracy of these polygons for regional conservation planning. We analyzed the proportion of sites at which each species was detected, both inside and outside of its published NatureServe [Patterson et al., Digital distribution maps of the mammals of the western hemisphere. Version 1.0. Arlington, VA, 2003] and IUCN [2008; Red List, 2008] range polygons. There were mismatches between our line‐transect survey data and range polygon boundaries for nine of the ten species (from 15 to 80% cases), including both false presences and false absences. Each published dataset overestimated the presence of seven primate species and the absence of four species, though errors varied among species. Occupancy patterns of species with larger geographic ranges were no more accurately predicted than those of more narrow‐range species. Regional barriers to dispersal, such as rivers, and finer‐scale ecological specialization may limit the applicability of range map polygons to regional‐scale conservation priority setting, even for relatively well‐studied taxa. Despite the risk of errors, range polygons are still used as baseline data in conservation planning. We suggest some measures that could reduce the error risk. Am. J. Primatol. 73:53–61, 2011.

Tracking changes and preventing loss in critical tiger habitat.

Real-time forest monitoring technologies could help track changes in tiger populations. The global population of wild tigers remains dangerously low at fewer than 3500 individuals. Habitat loss, along with poaching, can undermine the international target recovery of doubling the number of wild tigers by 2022. Using a new satellite-based monitoring system, we analyzed 14 years of forest loss data within the 76 landscapes (ranging from 278 to 269,983 km2) that have been prioritized for conservation of wild tigers. Our analysis provides an update of the status of tiger habitat and describes new applications of technology to detect precisely where forest loss is occurring in order to curb future habitat loss. Across the 76 landscapes, forest loss was far less than anticipated (79,597 ± 22,629 km2, 7.7% of remaining habitat) over the 14-year study period (2001–2014). Habitat loss was unevenly distributed within a subset of 29 landscapes deemed most critical for doubling wild tiger populations: 19 showed little change (1.5%), whereas 10 accounted for more than 98% (57,392 ± 16,316 km2) of habitat loss. Habitat loss in source population sites within 76 landscapes ranged from no loss to 435 ± 124 km2 (x¯=24km2, SD = 89, total = 1676 ± 476 km2). Doubling the tiger population by 2022 requires moving beyond tracking annual changes in habitat. We highlight near–real-time forest monitoring technologies that provide alerts of forest loss at relevant spatial and temporal scales to prevent further erosion.

Terrestrial Activity in Pitheciins (Cacajao, Chiropotes, and Pithecia)

Neotropical monkeys of the genera Cacajao, Chiropotes, and Pithecia (Pitheciidae) are considered to be highly arboreal, spending most of their time feeding and traveling in the upper canopy. Until now, the use of terrestrial substrates has not been analyzed in detail in this group. Here, we review the frequency of terrestrial use among pitheciin taxa to determine the ecological and social conditions that might lead to such behavior. We collated published and unpublished data from 14 taxa in the three genera. Data were gleaned from 53 published studies (including five on multiple pitheciin genera) and personal communications of unpublished data distributed across 31 localities. Terrestrial activity was reported in 61% of Pithecia field studies (11 of 18), in 34% of Chiropotes studies (10 of 29), and 36% of Cacajao studies (4 of 11). Within Pithecia, terrestrial behavior was more frequently reported in smaller species (e.g. P. pithecia) that are vertical clingers and leapers and make extensive use of the understory than in in the larger bodied canopy dwellers of the western Amazon (e.g. P. irrorata). Terrestrial behavior in Pithecia also occurred more frequently and lasted longer than in Cacajao or Chiropotes. An apparent association was found between flooded habitats and terrestrial activity and there is evidence of the development of a “local pattern” of terrestrial use in some populations. Seasonal fruit availability also may stimulate terrestrial behavior. Individuals also descended to the ground when visiting mineral licks, escaping predators, and responding to accidents such as a dropped infant. Overall, the results of this review emphasize that terrestrial use is rare among the pitheciins in general and is usually associated with the exploitation of specific resources or habitat types. Am. J. Primatol. 74:1106‐1127, 2012.

Determinants of spatial behavior of a tropical forest seed predator: The roles of optimal foraging, dietary diversification, and home range defense

Specialized seed predators in tropical forests may avoid seasonal food scarcity and interspecific feeding competition but may need to diversify their daily diet to limit ingestion of any given toxin. Seed predators may, therefore, adopt foraging strategies that favor dietary diversity and resource monitoring, rather than efficient energy intake, as suggested by optimal foraging theory. We tested whether fine‐scale space use by a small‐group‐living seed predator—the bald‐faced saki monkey (Pithecia irrorata)—reflected optimization of short‐term foraging efficiency, maximization of daily dietary diversity, and/or responses to the threat of territorial encroachment by neighboring groups. Food patches across home ranges of five adjacent saki groups were widely spread, but areas with higher densities of stems or food species were not allocated greater feeding time. Foraging patterns—specifically, relatively long daily travel paths that bypassed available fruiting trees and relatively short feeding bouts in undepleted food patches—suggest a strategy that maximizes dietary diversification, rather than “optimal” foraging. Travel distance was unrelated to the proportion of seeds in the diet. Moreover, while taxonomically diverse, the daily diets of our study groups were no more species‐rich than randomly derived diets based on co‐occurring available food species. Sakis preferentially used overlapping areas of their HRs, within which adjacent groups shared many food trees, yet the density of food plants or food species in these areas was no greater than in other HR areas. The high likelihood of depletion by neighboring groups of otherwise enduring food sources may encourage monitoring of peripheral food patches in overlap areas, even if at the expense of immediate energy intake, suggesting that between‐group competition is a key driver of fine‐scale home range use in sakis. Am. J. Primatol. 78:523–533, 2016.

Geographic comparison of plant genera used in frugivory among the pitheciids Cacajao, Callicebus, Chiropotes, and Pithecia.

Pitheciids are known for their frugivorous diets, but there has been no broad‐scale comparison of fruit genera used by these primates that range across five geographic regions in South America. We compiled 31 fruit lists from data collected from 18 species (three Cacajao, six Callicebus, five Chiropotes, and four Pithecia) at 26 study sites in six countries. Together, these lists contained 455 plant genera from 96 families. We predicted that 1) closely related Chiropotes and Cacajao would demonstrate the greatest similarity in fruit lists; 2) pitheciids living in closer geographic proximity would have greater similarities in fruit lists; and 3) fruit genus richness would be lower in lists from forest fragments than continuous forests. Fruit genus richness was greatest for the composite Chiropotes list, even though Pithecia had the greatest overall sampling effort. We also found that the Callicebus composite fruit list had lower similarity scores in comparison with the composite food lists of the other three genera (both within and between geographic areas). Chiropotes and Pithecia showed strongest similarities in fruit lists, followed by sister taxa Chiropotes and Cacajao. Overall, pitheciids in closer proximity had more similarities in their fruit list, and this pattern was evident in the fruit lists for both Callicebus and Chiropotes. There was no difference in the number of fruit genera used by pitheciids in habitat fragments and continuous forest. Our findings demonstrate that pitheciids use a variety of fruit genera, but phylogenetic and geographic patterns in fruit use are not consistent across all pitheciid genera. This study represents the most extensive examination of pitheciid fruit consumption to date, but future research is needed to investigate the extent to which the trends in fruit genus richness noted here are attributable to habitat differences among study sites, differences in feeding ecology, or a combination of both. Am. J. Primatol. 78:493–506, 2016.

Unmanned aerial vehicles mitigate human–elephant conflict on the borders of Tanzanian Parks: a case study

Protected areas across the range of the African savannah elephant Loxodonta africana are increasingly being surrounded and isolated by agriculture and human settlements. Conflicts between people and crop-raiding elephants regularly lead to direct reprisals and diminish community support for conservation. We report on field trials in northern Tanzania that employed a new, humane way for wildlife managers to move elephants away from conflict zones, from distances of > 100 m, thereby enhancing the safety of wildlife managers, farmers and elephants. We deployed 10 unmanned aerial vehicles (drones) piloted by five trained teams of wildlife managers in the Tarangire–Manyara and Serengeti ecosystems. Game Scouts deployed the drones opportunistically during crop-raiding events at the peak of the maize ripening period in 2015 and 2016. In 100% of trials (n = 51) elephants responded to the presence of a drone by departing rapidly from crop fields (n = 38) and settlements (n = 13). The cost of five teams responsible for 617 km 2 in Tarangire–Manyara was estimated to be USD 15,520 for 1 year, and all drones remained operational for the duration of the study. The initial success of this tool warrants further testing of the utility of small unmanned aerial vehicles as part of the toolbox for wildlife managers and communities dealing with high levels of conflict with wildlife.