scholarly journals DYNAMICS OF AN EXPANDING BLACK RHINOCEROS (Diceros bicornis minor) POPULATION

2015 ◽  
Author(s):  
Peter R Law ◽  
Brad Fike ◽  
Peter C Lent

Population dynamics is a central component of demography and critical for meta-population management, especially of endangered species. We employed complete individual life records to construct census data for a reintroduced black rhinoceros population over 22 years from its founding and investigated that population’s dynamics to inform black rhinoceros meta-population management practice and, more generally, megaherbivore ecology. Akaike’s information criterion applied to scalar models of population growth based on the generalized logistic unambiguously selected an exponential growth model (r = 0.102 ± 0.017), indicating a highly successful reintroduction, but yielding no evidence of density dependence. This result is consistent with, but does not confirm, the threshold model of density dependence that has influenced black rhinoceros meta-population management. Our analysis did support previous work contending that the generalized logistic is unreliable when fit to data that do not sample the entire range of possible population sizes. A stage-based matrix model of the exponential population dynamics exhibited mild transient behaviour. We found no evidence of environmental stochasticity, consistent with our previous studies of this population that found no influence of rainfall on demographic parameters. Process noise derived from demographic stochasticity, principally reflected in annual sex-specific recruitment numbers that differed from deterministic predictions of the matrix model. Demographically driven process noise should be assumed to be a component of megaherbivore population dynamics, as these populations are typically relatively small, and should be considered in managed removals and introductions. We suggest that an extended period of exponential growth is common for megaherbivore populations growing from small size and that an increase in age at first reproduction with increasing population size, manifest in the study population, may provide a warning of density feedback prior to detectable slowing of population growth rate for megaherbivores .

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Daniel Oro ◽  
Daniel F. Doak

Abstract Standard procedures for capture–mark–recapture modelling (CMR) for the study of animal demography include running goodness-of-fit tests on a general starting model. A frequent reason for poor model fit is heterogeneity in local survival among individuals captured for the first time and those already captured or seen on previous occasions. This deviation is technically termed a transience effect. In specific cases, simple, uni-state CMR modeling showing transients may allow researchers to assess the role of these transients on population dynamics. Transient individuals nearly always have a lower local survival probability, which may appear for a number of reasons. In most cases, transients arise due to permanent dispersal, higher mortality, or a combination of both. In the case of higher mortality, transients may be symptomatic of a cost of first reproduction. A few studies working at large spatial scales actually show that transients more often correspond to survival costs of first reproduction rather than to permanent dispersal, bolstering the interpretation of transience as a measure of costs of reproduction, since initial detections are often associated with first breeding attempts. Regardless of their cause, the loss of transients from a local population should lower population growth rate. We review almost 1000 papers using CMR modeling and find that almost 40% of studies fitting the searching criteria (N = 115) detected transients. Nevertheless, few researchers have considered the ecological or evolutionary meaning of the transient phenomenon. Only three studies from the reviewed papers considered transients to be a cost of first reproduction. We also analyze a long-term individual monitoring dataset (1988–2012) on a long-lived bird to quantify transients, and we use a life table response experiment (LTRE) to measure the consequences of transients at a population level. As expected, population growth rate decreased when the environment became harsher while the proportion of transients increased. LTRE analysis showed that population growth can be substantially affected by changes in traits that are variable under environmental stochasticity and deterministic perturbations, such as recruitment, fecundity of experienced individuals, and transient probabilities. This occurred even though sensitivities and elasticities of these parameters were much lower than those for adult survival. The proportion of transients also increased with the strength of density-dependence. These results have implications for ecological and evolutionary studies and may stimulate other researchers to explore the ecological processes behind the occurrence of transients in capture–recapture studies. In population models, the inclusion of a specific state for transients may help to make more reliable predictions for endangered and harvested species.


2014 ◽  
Vol 1 (2) ◽  
pp. 140075 ◽  
Author(s):  
Anna Kuparinen ◽  
Jeffrey A. Hutchings

Negative density-dependent regulation of population dynamics promotes population growth at low abundance and is therefore vital for recovery following depletion. Inversely, any process that reduces the compensatory density-dependence of population growth can negatively affect recovery. Here, we show that increased adult mortality at low abundance can reverse compensatory population dynamics into its opposite—a demographic Allee effect. Northwest Atlantic cod ( Gadus morhua ) stocks collapsed dramatically in the early 1990s and have since shown little sign of recovery. Many experienced dramatic increases in natural mortality, ostensibly attributable in some populations to increased predation by seals. Our findings show that increased natural mortality of a magnitude observed for overfished cod stocks has been more than sufficient to fundamentally alter the dynamics of density-dependent population regulation. The demographic Allee effect generated by these changes can slow down or even impede the recovery of depleted populations even in the absence of fishing.


2016 ◽  
Author(s):  
Peter R Law ◽  
Wayne L. Linklater ◽  
Jay V. Gedir

AbstractGreaver et al. (2014) presented evidence for density dependence in the Ithala population of black rhinoceros. Finding that they did not place their regression-based evidence in a modelling context, we recast their result as an example of the ramp model of density dependence that underlies black rhinoceros meta-population management. Greaver et al. concluded that the Ithala population did not reach carrying capacity, a conclusion we consider unwarranted since they did not conduct any analyses of trends in demographic parameters with population density. Our interpretation implies that the Ithala population did indeed reach carrying capacity. Where relevant, we compared their results for the Ithala population with those for another southern African black-rhinoceros population in order to provide a broader basis for evaluating black rhinoceros demography. We detail inconsistent presentation of data in their paper that plagued our efforts to understand their results and also draw attention to possible errors in some analyses. In particular, we argue that the results on birth rates reported by Greaver et al. appear dubious. Greaver et al. have presented important evidence for density dependence in a population of black rhinoceros but we suggest they have underutilized their data in interpreting this density dependence while misanalysing birth data.


2017 ◽  
Vol 114 (44) ◽  
pp. 11582-11590 ◽  
Author(s):  
Russell Lande ◽  
Steinar Engen ◽  
Bernt-Erik Sæther

We analyze the stochastic demography and evolution of a density-dependent age- (or stage-) structured population in a fluctuating environment. A positive linear combination of age classes (e.g., weighted by body mass) is assumed to act as the single variable of population size, N, exerting density dependence on age-specific vital rates through an increasing function of population size. The environment fluctuates in a stationary distribution with no autocorrelation. We show by analysis and simulation of age structure, under assumptions often met by vertebrate populations, that the stochastic dynamics of population size can be accurately approximated by a univariate model governed by three key demographic parameters: the intrinsic rate of increase and carrying capacity in the average environment, r0 and K, and the environmental variance in population growth rate, σe2. Allowing these parameters to be genetically variable and to evolve, but assuming that a fourth parameter, θ, measuring the nonlinearity of density dependence, remains constant, the expected evolution maximizes E[Nθ]=[1−σe2/(2r0)]Kθ. This shows that the magnitude of environmental stochasticity governs the classical trade-off between selection for higher r0 versus higher K. However, selection also acts to decrease σe2, so the simple life-history trade-off between r- and K-selection may be obscured by additional trade-offs between them and σe2. Under the classical logistic model of population growth with linear density dependence (θ=1), life-history evolution in a fluctuating environment tends to maximize the average population size.


2015 ◽  
Vol 42 (5) ◽  
pp. 382 ◽  
Author(s):  
Holly T. Dublin ◽  
Joseph O. Ogutu

Context The processes regulating ungulate populations have been the focus of numerous studies. For the African buffalo (Syncerus caffer Sparrman) population inhabiting the Mara–Serengeti ecosystem, rinderpest was the primary regulatory factor up to the mid-1960s. Following reduction of rinderpest and buffalo population increase, interspecific competition for food, notably with cattle and wildebeest (Connochaetes taurinus Burchell), was thought to be the primary regulatory factor in the ecosystem. Aims We analysed buffalo population trends and the relationship between buffalo population growth and rainfall and density dependence in the Mara–Serengeti ecosystem and discuss the findings in the context of the key ecosystem processes governing buffalo population dynamics in African savannas, namely, food limitation, competition, predation, disease and land use changes. Methods We analysed buffalo population dynamics in the Mara–Serengeti ecosystem in relation to rainfall and density dependence feedback between 1984 and 2010. Key results Buffalo population growth was both significantly density-dependent and positively correlated with the dry season rainfall after, but not before, a severe drought in 1993. Buffalo numbers crashed by 48.6% in 1984–85 and by 76.1% in 1993–94 during severe droughts when food availability was lowest and competition with the more numerous cattle and wildebeest was highest. Conclusions Recovery of buffalo numbers to pre-drought levels took 8–9 years after the 1984–85 drought but was much slower, with buffaloes numbering merely 36% of their 1993 population (12 895 animals) 18 years after the 1993–94 drought despite intermittent periods of high rainfall, probably due to demographic and/or reproductive factors, heightened competition with livestock, land use changes in the adjoining pastoral ranches, lion predation and recurrent severe droughts. Implications Our findings demonstrate how food limitation caused by droughts associated with the hemispheric El Niño–Southern Oscillation can cause severe declines in and threaten the persistence of large ungulate populations. The findings also portray how density-dependent food limitation, competition, predation, land use changes and other factors can accentuate the effect of droughts and greatly prolong population recovery.


2015 ◽  
Vol 112 (9) ◽  
pp. 2782-2787 ◽  
Author(s):  
Jake M. Ferguson ◽  
José M. Ponciano

Environmental stochasticity is an important concept in population dynamics, providing a quantitative model of the extrinsic fluctuations driving population abundances. It is typically formulated as a stochastic perturbation to the maximum reproductive rate, leading to a population variance that scales quadratically with abundance. However, environmental fluctuations may also drive changes in the strength of density dependence. Very few studies have examined the consequences of this alternative model formulation while even fewer have tested which model better describes fluctuations in animal populations. Here we use data from the Global Population Dynamics Database to determine the statistical support for this alternative environmental variance model in 165 animal populations and test whether these models can capture known population–environment interactions in two well-studied ungulates. Our results suggest that variation in the density dependence is common and leads to a higher-order scaling of the population variance. This scaling will often stabilize populations although dynamics may also be destabilized under certain conditions. We conclude that higher-order environmental variation is a potentially ubiquitous and consequential property of animal populations. Our results suggest that extinction risk estimates may often be overestimated when not properly taking into account how environmental fluctuations affect population parameters.


2009 ◽  
Vol 364 (1523) ◽  
pp. 1511-1518 ◽  
Author(s):  
Russell Lande ◽  
Steinar Engen ◽  
Bernt-Erik Sæther

The evolution of population dynamics in a stochastic environment is analysed under a general form of density-dependence with genetic variation in r and K , the intrinsic rate of increase and carrying capacity in the average environment, and in σ e 2 , the environmental variance of population growth rate. The continuous-time model assumes a large population size and a stationary distribution of environments with no autocorrelation. For a given population density, N , and genotype frequency, p , the expected selection gradient is always towards an increased population growth rate, and the expected fitness of a genotype is its Malthusian fitness in the average environment minus the covariance of its growth rate with that of the population. Long-term evolution maximizes the expected value of the density-dependence function, averaged over the stationary distribution of N . In the θ -logistic model, where density dependence of population growth is a function of N θ , long-term evolution maximizes E[ N θ ]=[1− σ e 2 /(2 r )] K θ . While σ e 2 is always selected to decrease, r and K are always selected to increase, implying a genetic trade-off among them. By contrast, given the other parameters, θ has an intermediate optimum between 1.781 and 2 corresponding to the limits of high or low stochasticity.


2019 ◽  
Author(s):  
Hugo Cayuela ◽  
Richard A. Griffiths ◽  
Nurul Zakaria ◽  
Jan W. Arntzen ◽  
Pauline Priol ◽  
...  

ABSTRACTIdentifying the drivers of population fluctuations in spatially distinct populations remains a significant challenge for ecologists. Whereas regional climatic factors may generate population synchrony (i.e., Moran effect), local factors including the level of density-dependence may reduce the level of synchrony. Although divergences in the scaling of population synchrony and spatial environmental variation have been observed, the regulatory factors that underlie such mismatches are poorly understood.No previous studies have investigated how density-dependent processes and population-specific responses to weather variation influence spatial synchrony at both local and continental scales. We addressed this issue in a pond-breeding amphibian, the great crested newt (Triturus cristatus). We used capture-recapture data collected through long-term surveys in five T. cristatus populations in Western Europe.We found a low level of demographic synchrony at both local and continental levels. Weather has weak and spatially variable effects on survival, recruitment and population growth rate. In contrast, density-dependence was a common phenomenon (at least for population growth) in almost all populations and subpopulations.Our findings support the idea that Moran’s effect is low in species where the population dynamics more closely depends on local factors (e.g. population density and habitat characteristics) than on large-scale environmental fluctuation (e.g. regional climatic variation). Those demographic feature likely have far-reaching consequences for the long-term viability of the spatially structured populations and their ability to response to large-scale climatic anomalies.


Author(s):  
I. M. Grod ◽  
I. V. Zagorodniuk ◽  
L. O. Shevchyk ◽  
N. Ya. Kravets

Monitoring and predicting the dynamics of abundance of species living in natural habitats is an important component stability analysis of ecosystem as well as dynamics and direction of change of biotic communities under global climate change and pressure of the alien species. The aim of the work was to build a matrix model and study the state of stabilisation of the dynamics of the bank vole population within the Leslie model. The object of the study was the population dynamics of Myodes glareolus Schreber, 1780 = Clethrionomys glareolus auct. The study is based on materials obtained during 2017–2019. This period covered one phase of the long-term population dynamics of the bank vole, named “population growth”. The research was carried out according to generally accepted methods. A total of 6400 trap-days were processed, and 358 forest fistulas were collected and studied. The intensity of harmful activity of rodents is due to the variability of the number of animals in the population. The quantitative population changes are the result of three factors: births, deaths, and migrations. The main condition for the existence of the species is the stability of the population, which is determined by the action of thecompensatory mechanisms. The growth phase of the bank vole lasted all three years of the research, the quantitative indicators were respectively: 2017 – 1.8 individuals per 100 trap-days; 2018 – 2.0 individuals per 100 trap-days; 2019 – 2.7 individuals per 100 trap-days. Low levels of the abundance in the spring of each year of the study, namely at the beginning of the breeding season (3.7 – 2.6 – 8.9 individuals per 100 trap-days). Favourable for the abundance growth was the sex ratio of the population (approximately 1:1), with some rise in the share of females, which decreases on the period of spring 2018 to autumn 2019). Some decrease in the share of immature individuals (4.5 – 3.9 – 3.1 %) is an indirect confirmation of the stability of puberty of animals with subsequent replenishment of the "stock", which led to accelerated reproduction and, consequently, provided prerequisites for further population growth. The causal mechanisms of population control established by us, without a doubt, can serve as a basis for further prognosis, of the number of pests in natural habitats. To predict population changes, the Leslie model, which is widely used in mathematical analyses of the abundance of both plant and animal groups, was chosen. The algorithm for building a matrix model, detailed in the article, has five following steps. The exponential nature of the actual and projected growth of the bank vole population during the five-year cycle (2017–2019 with a prognosis until 2023) revealed in the analysis can be explained not so much by the power of the species' reproductive potential as by the lack of the significant changes in habitat, caused by constant weather conditions, low individual mortality from predators and non-communicable diseases or other accidents. The application of the matrix model allowed to confirm the key role of the main compensatory mechanisms of population dynamics, as they contribute to the stabilisation of the population and, as a consequence, are an important condition for the existence of the species.


2009 ◽  
Vol 364 (1520) ◽  
pp. 1049-1058 ◽  
Author(s):  
S.J Plaistow ◽  
T.G Benton

Parental effects arise when either the maternal or paternal phenotype influences the phenotypes of subsequent generations. Simple analytical models assume maternal effects are a mechanism creating delayed density dependence. Such models predict that maternal effects can very easily lead to population cycles. Despite this, unambiguous maternal-effect mediated cycles have not been demonstrated in any system. Additionally, much evidence has arisen to invalidate the underlying assumption that there is a simple positive correlation between maternal performance and offspring performance. A key issue in understanding how maternal effects may affect population dynamics is determining how the expression of parental effects changes in different environments. In this study, we tested the hypothesis that maternal effects influence population dynamics in a context-dependent way. Populations of the soil mite, Sancassania berlesei , were set up at high density (500 eggs) or low density (50 eggs), with eggs that were either laid by young mothers or old mothers (a previously documented maternal effect in this system). The influence of maternal age on both population and egg and body-size dynamics was only observed in the populations initiated under low density rather than high density. This difference was attributable to the context-dependence of maternal effects at the individual level. In low-density (high food) conditions, maternal effects have an impact on offspring reproductive performance, creating an impact on the population growth rate. In high density (low food), maternal effects impact more on juvenile survival (not adult size or reproduction), creating a smaller impact on the population growth rate. This context dependence of effects at the population level means that, in fluctuating populations, maternal effects cause intermittent delayed density dependence that does not lead to persistent cycles.


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