Africa's elephants and rhinos: Flagships in crisis

Despite extensive conservation measures over the last two decades, populations of elephants and rhinos in Africa continue to decline. The plight of the black rhino is especially acute. Poaching for rhino horn and ivory, rather than habitat loss, remains the principal threat to these species. The only long-term hope may lie in the effective protection of small, isolated populations.     

Disruption of Rhino Demography by Poachers May Lead to Population Declines in Kruger National Park,South Africa

The onslaught on the World’s rhinoceroses continues despite numerous initiatives aimed at curbing it. When losses due to poaching exceed birth rates, declining rhino populations result. We used previously published estimates and growth rates for black rhinos (2008) and white rhinos (2010) together with known poaching trends at the time to predict population sizes and poaching rates in Kruger National Park, South Africa for 2013. Kruger is a stronghold for the south-eastern black rhino and southern white rhino. Counting rhinos on 878 blocks 3x3 km in size using helicopters, estimating availability bias and collating observer and detectability biases allowed estimates using the Jolly’s estimator. The exponential escalation in number of rhinos poached per day appears to have slowed. The black rhino estimate of 414 individuals (95% confidence interval: 343-487) was lower than the predicted 835 individuals (95% CI: 754-956). The white rhino estimate of 8,968 individuals (95% CI: 8,394-9,564) overlapped with the predicted 9,417 individuals (95% CI: 7,698-11,183). Density- and rainfall-dependent responses in birth- and death rates of white rhinos provide opportunities to offset anticipated poaching effects through removals of rhinos from high density areas to increase birth and survival rates. Biological management of rhinos, however, need complimentary management of the poaching threat as present poaching trends predict detectable declines in white rhino abundances by 2018. Strategic responses such as anti-poaching that protect supply from illegal harvesting, reducing demand, and increasing supply commonly require crime network disruption as a first step complimented by providing options for alternative economies in areas abutting protected areas.     

Anthropogenic Influences on Conservation Values of White Rhinoceros

White rhinoceros (rhinos) is a keystone conservation species and also provides revenue for protection agencies. Restoring or mimicking the outcomes of impeded ecological processes allows reconciliation of biodiversity and financial objectives. We evaluate the consequences of white rhino management removal, and in recent times, poaching, on population persistence, regional conservation outcomes and opportunities for revenue generation. In Kruger National Park, white rhinos increased from 1998 to 2008. Since then the population may vary non-directionally. In 2010, we estimated 10,621 (95% CI: 8,767–12,682) white rhinos using three different population estimation methods. The desired management effect of a varying population was detectable after 2008. Age and sex structures in sink areas (focal rhino capture areas) were different from elsewhere. This comes from relatively more sub-adults being removed by managers than what the standing age distribution defined. Poachers in turn focused on more adults in 2011. Although the effect of poaching was not detectable at the population level given the confidence intervals of estimates, managers accommodated expected poaching annually and adapted management removals. The present poaching trend predicts that 432 white rhinos may be poached in Kruger during 2012. The white rhino management model mimicking outcomes of impeded ecological processes predicts 397 rhino management removals are required. At present poachers may be doing “management removals,” but conservationists have no opportunity left to contribute to regional rhino conservation strategies or generate revenue through white rhino sales. In addition, continued trends in poaching predict detectable white rhino declines in Kruger National Park by 2016. Our results suggest that conservationists need innovative approaches that reduce financial incentives to curb the threats that poaching poses to several conservation values of natural resources such as white rhinos.     

Characteristics of black rhinoceros (Diceros bicornis) bedding sites

Black rhino numbers have decreased greatly since the early 1970s, primarily as a result of poaching. A recent strategy to protect rhinos in Kenya has been to establish fenced sanctuaries. This has increased the rhino population and that of other species, but problems have emerged because of limited dispersal and rising animal densities. Unfortunately, how rhino utilize habitat, especially areas called bedding sites, is not well understood. These areas provide shade and may be a critical component of rhino habitat. We measured habitat variables at bedding sites located in bedding plots and compared them with control plots at Sweetwaters Reserve, Kenya. Euclea divinorum was the most common tree in the bedding site comprising 64.3% of the vegetation. Elephant dung was significantly more likely to be found in bedding plots than in control plots which suggests that elephants and rhinos use overlapping habitats. Elephants may be causing damage to the tree species that are important for bedding sites. Resource competition between large herbivores in small reserves is likely to negatively affect the tree species. Black rhino habitat, particularly bedding sites, may be at risk and rhino numbers may decrease.     

Sexual Dimorphism and Mortality Bias in a Small Miocene North American Rhino, <Emphasis Type="Italic">Menoceras arikarense</Emphasis>: Insights into the Coevolution of Sexual Dimorphism and Sociality in Rhinos

Rhinos are the only modern perissodactyls that possess cranial weapons similar to the horns, antlers and ossicones of modern ruminants. Yet, unlike ruminants, there is no clear relationship between sexual dimorphism and sociality. It is possible to extend the study of the coevolution of sociality and sexual dimorphism into extinct rhinos by examining the demographic patterns in large fossil assemblages. An assemblage of the North American early Miocene (∼22 million years ago) rhino, Menoceras arikarense, from Agate Springs National Monument, Nebraska, exhibits dimorphism in incisor size and nasal bone size, but there is no detectible dimorphism in body size. The degree of dimorphism of the nasal horn is greater than the degree of sexual dimorphism of any living rhino and more like that of modern horned ruminants. The greater degree of sexual dimorphism in Menoceras horns may relate to its relatively small body size and suggests that the horn had a more sex-specific function. It could be hypothesized that Menoceras evolved a more gregarious type of sociality in which a fewer number of males were capable of monopolizing a larger number of females. Demographic patterns in the Menoceras assemblage indicate that males suffered from a localized risk of elevated mortality at an age equivalent to the years of early adulthood. This mortality pattern is typical of living rhinos and indicates that young males were susceptible to the aggressive behaviors of dominant individuals in areas conducive to fossilization (e.g., ponds, lakes, rivers). Menoceras mortality patterns do not suggest a type of sociality different from modern rhinos although a group forming type of sociality remains possible. Among both living and extinct rhinos, the severity of socially mediated mortality seems unrelated to the degree of sexual dimorphism. Thus, sexual dimorphism in rhinos is not consistent with traditional theories about the co-evolution of sexual dimorphism and sociality.     

Rhinoceros accounting in Kruger National Park,South Africa

Trends in rhinoceroses (rhinos) in Kruger National Park (Kruger) is of key concern. Poaching drives trends in the Park. Reconciling annual population estimates with yearly reports of poached carcasses fuels public critique. We account for trends in rhinos by extracting time series of estimates. Progressively modelling influences of management introductions and removals, effects of environmental variation and rhino density, direct impacts of poaching, consequences of imperfect carcass detection, and indirect impacts of deaths of dependent calves form the basis of accounting for rhinos. Models that considered all these influences explained 93% of white and 83% of black rhino population trends. In addition, the models predicted 2,515 white and 225 black rhinos, similar to estimates of 2,607 (95% CI: 2,475–2,752) and 202 (95% CI: 172–237) during 2020 respectively. The best model, however, predicts slow recovery with a white rhino population equivalent to pre-poaching achieved between 2030 and 2040. For black rhinos, recovery to pre-poaching population size would be between 2040 and 2050. The poaching onslaught in Kruger disrupted eruptive white rhino dynamics and prevented black rhinos from transitioning into eruptive dynamics. Authorities require innovative approaches within and beyond Kruger to help re-ignite rhino conservation.     

Reserve Size,Conspecific Density,and Translocation Success for Black Rhinoceros

Abstract: Fighting and accidental injury commonly cause black rhinoceros (rhino; Diceros bicornis) death after release. Smaller reserves and higher conspecific density after release (release density) might increase a rhino's encounter rate with hazards like fenced boundaries and conspecifics. We conducted a science-by-management experiment on the influence of reserve size and release density on rates of movement, association, and injury and death amongst 39 black rhinos during the first 100 days after their release into 4 Namibian and 8 South African reserves ranging in size from 670 ha to 45,000 ha. Association rates were negatively related to reserve size and positively correlated with release density. There was also a negative relationship between the proportion of the reserve traversed by individual rhinos and reserve size. In reserves ≥18,000 ha association rates were consistently zero but became elevated in reserves ≤11,500 ha and at release densities ≤9 km²/rhino. Daily displacement did not increase with increasing reserve size >8,500 ha but in smaller reserves daily displacements indicated higher encounter rates by released rhinos with fenced boundaries. Three rhinos received fight-related injuries requiring intervention and 2 of 4 deaths were fight-related. All injuries and 3 deaths occurred in reserves ≤11,500 ha. Model selection based on Akaike's second-order Information Criterion indicated that the parameter release density alone best explained mortality risk. Traditionally considered risk factors, rhino sex, age, and presence of resident conspecifics, were superseded by the risk posed by releases into smaller reserves. Reserves ≤11,500 ha and release densities ≤9 km²/rhino pose an increasing risk to rhino survivorship and so larger reserves and lower densities than these should be favored as release sites.     

Does a reduction in the price of rhino horn prevent poaching?

Rhino poaching around the world has increased inordinately, to the extent that concerns exist over the possible survival of the species. An open access rhino poaching model is developed for South African rhino. The model is a hybrid dynamical model, as both a system dynamics model as well as a Bayesian network model are developed. The system dynamics model is used to estimate the unknown parameter values (through optimisation) and also to determine the intervals for the parameters. These intervals are then used in the Bayesian Belief Network model to assess uncertainty. Hybrid approaches improve the ability to validate models compared with conventional modelling. The resultant model indicates that reducing the price of rhino horn would not be effective at curbing poaching, unless poacher costs are also increased. However, increasing poacher costs is not a realistic policy option since these costs are largely beyond the control of decision-makers. The insensitivity of price to poaching effort has implications for methods proposed to reduce the value of rhinos, such as introducing synthetic rhino horn and the de-horning of rhinos.     

Assessing and managing the rising rhino population in Kaziranga (India)

The greater one-horned rhinoceros (Rhinoceros unicornis) is a flagship species, and yet is poorly known unlike its African cousin. The species future is now under a growing threat, judging by the prospect of a legalization of the horn trade that has been the subject of recent debate, coupled with the fragmentation of the animal's habitat. In this study, we analyze the rhino habitat and assess its dynamics in the Kaziranga National Park (KNP), Assam, India. To compensate for the limited size of the data available, we use some numerical models and propose some original spatial analyses and indicators.Our findings point to a healthy and increasing rhino population in a density-dependent scenario. An increase of at least 30% in the rhino population is expected in the coming twelve years, mainly as a result of the effective implementation of wildlife protection laws in the country. Kaziranga's grasslands have been quite stable in the past (7% between years, in average, and less than 19% at most), and are expected to remain so in the near future, especially in the core area of the KNP. In the absence of a detailed suitability map and known carrying-capacity values, we identified the areas most favoured by the rhinos, and developed a so-called “preference map”. We conclude by stressing the need to realistically combine the existing conservation strategies while increasing the monitoring effort on the species distribution.     

Behavioural ecology of the Greater one-horned rhinoceros (Rhinoceros unicornis)

In the Chitawan Valley of Nepal there were estimated to be between 270 and 310 Greater one-horned or Indian rhinoceroses (Rhinoceros unicornis L.). Population densities reached 4.85 rhinos/km² in the favoured areas of high diversity of early successional vegetation types on the valley floor. The overall population composition was 32.3% adult females, 19.9% adult males, 21.2% sub-adults and 26.6% calves. Females first calved at a mean age of 7.1 years and the median intercalving interval was 2.8 years. Causes of death included poaching, tiger predation on calves and fighting among males. The population was increasing.
Rhinos fed from 183 species of plants belonging to 57 botanical families but grass (50 species) made up between 70 and 89% of their diet according to the season. Considerable seasonal variations in food availability resulted in movements of rhinos between vegetation types. Rhinos' ranges were smallest in the areas of greatest vegetational diversity.
Rhinos rarely formed groups. The most common type consisted of sub-adults–mainly males. Ten auditory displays were distinguished and visual displays, although less striking, included baring the lower incisor tusks. Scents were carried in the dung, the urine and the pedal scent glands. Squirt urination and foot-dragging displays were performed by breeding males only.
There was some degree of range exclusivity among breeding males but no true territoriality. Poor visibility and the relatively unpredictable distribution of resources in time and space have perhaps selected against a territorial mating system. Relationships between ecology and social organization are discussed with reference to other rhino species.
Threats to the continued survival of the Indian rhino include poaching, agricultural encroachment and erosion. In order to spread the risk of a catastrophe, reintroductions of rhinos to other protected areas are proposed.     

A study on the postrelease behaviour and habitat preferences of black rhinos (Diceros bicornis) reintroduced into a fenced reserve in Namibia

Translocations and reintroductions are key elements for the population management of the critically endangered black rhino (Diceros bicornis, Linnaeus, 1758). In this study, we investigated the postrelease behaviour and habitat preferences of a black rhino starter group (n = 4) on the individual level. The animals were reintroduced to a fenced game reserve (87 km²) in North‐Central Namibia 1 year prior to our study. We used camera traps and very high frequency (VHF) radiotelemetry to examine the animals' temporal and spatial behaviour over a period of 4 months at transition between wet and dry seasons. Our results underline a peak in drinking activity and waterhole visits occurring between 7 p.m. and 8 p.m. We found a shift in intensity in drinking activity during the period of the study. Satellite‐based woody cover estimations only suggest positive correlations between the density of woody cover and favoured black rhino habitat types. Although the area seems suitable to facilitate breeding success of this starter group, it does not support a self‐sustaining population. However, black rhinos were already successfully reintroduced to several additional fenced reserves in this region. The selective opening of fences in the future could help to enable genetic exchange between currently isolated groups of rhinos.     

EQUIPMENT REVIEW

ABSTRACT

The Northern White Rhinoceros Ceratotherium simum cottoni is a subspecies of the White Rhino that is almost extinct in the wild. We studied the last reproducing herd kept in Zoo Dvur Kralove to describe its vocal repertoire. The calls produced by eight individuals were recorded and analysed as concerned both sound properties and behavioural contexts in which they were emitted. We distinguished 11 calls belonging to four categories: (1) tonal harmonic sounds, (2) puffing sounds, (3) growling sounds, and (4) repetitive sounds. We found an apparent similarity between acoustic parameters of homologous calls recorded in both white rhino subspecies. We further confirmed that the repertoire of white rhino calls is much larger than that reported in other rhino species. We tentatively interpret this finding as an adaptation to increased sociality. Four calls reach the infrasound range; nevertheless, they are probably not used for communication over distance. This is obvious in the case of the grouch call, which contains the highest infrasound component. There are, however, other candidates for such a communication function: the repetitive pant sound, which is not known in other rhino species. We hypothesise that the repetitions may enhance their audibility in the typical open habitats of white rhinos.     

Patterns of depletion in a black rhinoceros population in Luangwa Valley, Zambia

Black rhinos in Luangwa Valley, Zambia have been subjected to heavy illegal hunting since the late 1970s. A study population monitored by individual recognition decreased at an instantaneous rate of - 0.29 yr^-1 between 1981 and 1985. Two-thirds of skulls found throughout Luangwa Valley between 1979 and 1985 were axed, indicating death from poaching. All age- and sex-classes of rhino were equally susceptible to being shot, presumably due to the high market-price of rhino horn.     

Impact of the black rhinoceros (Diceros bicornis minor) on a local population of Euphorbia bothae in the Great Fish River Reserve,South Africa

In the Great Fish River Reserve, South Africa, black rhinoceros (Diceros bicornis minor) feed extensively on a local population of Euphorbia bothae. Maintaining the endangered black rhinoceros and the protected E. bothae population are both conservation priorities of the reserve. Therefore, the sustainability of this plant–animal interaction was investigated by comparing population characteristics, browsing incidence and intensity within the reserve and in an adjacent exclosure without access to rhino. Fixed‐point photographs showed that over a 2‐month period 36.6% of 213 monitored plants were browsed, with an average biomass loss of 13%, and 1% were destroyed. Of 26 plants re‐photographed after approximately 3 years, 70% showed a decrease in biomass, averaging 37.8% over this period. In this time span, 19% of the monitored plants died. Small plants (<45 cm) were over‐represented in the rhino‐browsed area, whereas the fraction of reproductively active plants and overall plant density were found to be lower than in the adjacent exclosure. No evidence of short‐term compensatory growth in response to browsing was found for E. bothae. This study indicates that, with the current population size, rhinos are overexploiting the E. bothae population and special measures should be taken to prevent local extinction.     

Standardising Home Range Studies for Improved Management of the Critically Endangered Black Rhinoceros

Comparisons of recent estimations of home range sizes for the critically endangered black rhinoceros in Hluhluwe-iMfolozi Park (HiP), South Africa, with historical estimates led reports of a substantial (54%) increase, attributed to over-stocking and habitat deterioration that has far-reaching implications for rhino conservation. Other reports, however, suggest the increase is more likely an artefact caused by applying various home range estimators to non-standardised datasets. We collected 1939 locations of 25 black rhino over six years (2004–2009) to estimate annual home ranges and evaluate the hypothesis that they have increased in size. A minimum of 30 and 25 locations were required for accurate 95% MCP estimation of home range of adult rhinos, during the dry and wet seasons respectively. Forty and 55 locations were required for adult female and male annual MCP home ranges, respectively, and 30 locations were necessary for estimating 90% bivariate kernel home ranges accurately. Average annual 95% bivariate kernel home ranges were 20.4 ± 1.2 km², 53 ±1.9% larger than 95% MCP ranges (9.8 km² ± 0.9). When home range techniques used during the late-1960s in HiP were applied to our dataset, estimates were similar, indicating that ranges have not changed substantially in 50 years. Inaccurate, non-standardised, home range estimates and their comparison have the potential to mislead black rhino population management. We recommend that more care be taken to collect adequate numbers of rhino locations within standardized time periods (i.e., season or year) and that the comparison of home ranges estimated using dissimilar procedures be avoided. Home range studies of black rhino have been data deficient and procedurally inconsistent. Standardisation of methods is required.     

Social and spatial relationships in captive southern white rhinoceros (Ceratotherium simum simum)

Although critical to the conservation of white rhinoceros, captive breeding has proven challenging because of the poor and irregular reproductive health of many captive rhinos, and social interactions may play a significant role. This research investigated the social and spatial relationships of two captive groups of southern white rhinoceros (Ceratotherium simum simum) by examining the frequency of companion changes, the number of space maintenance vocalizations made per hour by each reproductively mature female, and dominant/subordinate interactions. The observed captive rhinos did not change their companionships during the study. They exhibited space maintenance vocalizations and display greater than once per hour, particularly when feeding. Females housed with four calves on 0.033 km² exhibited space maintenance vocalizations more frequently (X±SE = 6.19±0.199/hr) than females housed with one calf and more space (0.06 km², X±SE = 0.55±0.182/hr) and females housed without calves and more space (0.65 km², X±SE = 1.90±0.086/hr). Wider separation of food piles and of females with young calves is suggested to reduce the interpreted spatial stress. The presence of a large number of rhinos in restricted captive space resulted in the formation of herds with dominance hierarchies that were enforced during competition for food and shade. The most subordinate rhino in each of the herds exhibited unusual behaviors such as dung‐kicking and nonestrus urine squirting, and neither has ever reproduced. Suppression of subordinate rhinos might lead to social stress that could negatively impact reproductive success. Zoo Biol 26:487–502, 2007. © 2007 Wiley‐Liss, Inc.     

Social and reproductive behaviour of critically endangered northern white rhinoceros in a zoological garden

Northern and southern white rhinos have poor reproduction in captivity and social interactions between them, especially increased agonistic behaviour, are believed to be one of the possible reasons. Northern white rhino is currently on the brink of extinction with less than ten animals surviving. We studied the social behaviour of northern white rhinos in zoological garden and investigated the effects of separation of the oldest, wild-born female from the herd on the social behaviour of other group members. After the separation, the numbers of agonistic and the play interactions between the animals significantly increased, no change was found in cohesive behaviour. Our results suggest that a composition of white rhino groups has a significant influence on social interactions between the animals and that better knowledge of proper composition of their groups in captivity in terms of age, sex and wild or zoo origin might improve animals’ well-being and also increase a chance for reproduction.     

Genetic and plastic responses of a northern mammal to climate change

Climate change is predicted to be most severe in northern regions and there has been much interest in to what extent organisms can cope with these changes through phenotypic plasticity or microevolutionary processes. A red squirrel population in the southwest Yukon, Canada, faced with increasing spring temperatures and food supply has advanced the timing of breeding by 18 days over the last 10 years (6 days per generation). Longitudinal analysis of females breeding in multiple years suggests that much of this change in parturition date can be explained by a plastic response to increased food abundance (3.7 days per generation). Significant changes in breeding values (0.8 days per generation), were in concordance with predictions from the breeder's equation (0.6 days per generation), and indicated that an evolutionary response to strong selection favouring earlier breeders also contributed to the observed advancement of this heritable trait. The timing of breeding in this population of squirrels, therefore, has advanced as a result of both phenotypic changes within generations, and genetic changes among generations in response to a rapidly changing environment.     

Alarming decline and range reduction of the highly threatened Great Bustard Otis tarda in Morocco

A Great Bustard Otis tarda survey carried out in spring 2015 in Morocco confirmed the decline of this highly endangered population. Bustards were only seen at two of the seven leks occupied ten years ago. The total number of birds counted was 40-44, which represents a 40% decline over the last decade. The sex-ratio was still strongly female-biased (1 male: 3 females), but less than in previous surveys, which suggests that trophy hunting has not been the major mortality cause in recent times. The productivity was 0.29-0.33 juveniles per female, the highest ever recorded in this population, suggesting that breeding success doesn’t represent the main problem for the survival of this population. Based on the recent development of the power line network at some areas, the main threat today is probably collision with power lines. Reducing this mortality cause should be considered a high conservation priority.