Testing performance of large-scale surveys in determining trends for the critically endangered Great Indian Bustard Ardeotis nigriceps

Article metrics

Abstract

Great Indian Bustard (GIB) is listed as Critically Endangered, with less than 250 individuals surviving in three fragmented populations. The species is under tremendous threat due to various anthropogenic pressures. Effective management and conservation of GIB requires a proper monitoring protocol, which we propose using an occupancy framework approach to detect changes in the species’ population. We used occupancy estimates from various landscape level surveys and simulated scenarios to evaluate the effectiveness of the proposed protocol. Our result showed there is >70% chance of detecting 100% change in the occupancy with 100 sampling sites and 10 temporal replicates. While with double sampling sites, the same change can be detected with 4–6 temporal replicates. In absence of a robust population estimation method, we argue for the use of occupancy as a surrogate to detect change in population as it provides better insights for rare elusive species such as GIB. Our proposed methodological framework is more precise than previous methods, which will help in evaluating efficacy of management interventions proposed and the implementation of species recovery plans.

Introduction

Great Indian Bustard (GIB), India’s heaviest flying bird, was once abundant in dry grasslands of India. It is now categorized as Critically Endangered1 with less than 250 individuals surviving in three fragmented populations. The species is threatened by habitat loss, due to the conversion of grasslands into agriculture, transmission lines, wind turbines, feral dogs, livestock grazing intensification and hunting. As a result, its population has declined by 80% in 50 years from 1260 to 250 individuals2,3. This decline in GIB numbers has been recorded from all regions of its present distribution range4. Many site-specific targeted interventions, such as fencing of breeding sites, control of dog populations, and ex-situ conservation, have been planned to save the species from extinction4. In order to evaluate the efficacy of these interventions, the monitoring methods should be robust enough to detect any increase or decrease in GIB population size. The previous landscape level population estimation surveys across different monitoring years were done using a protocol developed by Dutta et al.5. This protocol has given results with a broad range of estimates which were 41–165 individuals in 20145 and 92–240 individuals in 20166. This broad range estimation interval hinders inference of population trend which impedes the process of testing the efficiency of management interventions.

Long-term conservation effort for any species relies on a sound understanding of its ecology, along with landscape-level population estimation7. Moreover, robust population estimation is fundamental as it provides an insight into the current status which helps in improving management policies8,9,10,11. Owing to the nomadic behaviour, long-life span, isolated population, rarity and long-ranging behavior12 of the GIB, it is very difficult to infer population trends using existing survey protocol and the reasons therein to serve as a rationale for conservation actions. Species with such natural history characteristics create unique challenges for both the design and implementation of population estimation surveys13.

The broad range of population estimates acquired using distance sampling from previous surveys (41–165 birds and 92–240 birds) can be made precise by increasing the sampling effort, but species behaviour like lekking may influence the detection probability in the subsequent visits. Therefore, it is logical to examine the change in habitat occupancy of the species rather than using distance sampling to infer change in numbers14,15. Occupancy modelling is based on presence and absence data and is most suited for population monitoring programs of rare and elusive species. Occupancy provides reliable information about species range, the probability of extinction16, meta-population dynamics17 and can be used as a surrogate of abundance18. Moreover, occupancy data are considered more effective for the study of rare species where abundance estimation is logistically and financially challenging14,19.

Under such circumstances, the need is to design a survey protocol which is logistically viable and able to detect change in number or occupancy within a given time frame. The statistical power to infer change in site occupancy is low with expedient number of temporal and spatial replicates20,21. In order to detect any change in GIB occupancy, we simulated different combinations of number of replicates and sites to reach the “acceptable” statistical power (typically 0.8) with a robust and feasible sampling design.

The aim of our study was to evaluate the effectiveness of the existing monitoring protocol to infer any change in the occupied area using both detection probability and occupancy estimates of previous surveys. We simulated detection histories with estimated parameters to evaluate the robustness of the surveys with 80% confidence interval. The outcome of the study will help in evaluating the implementation of target-oriented management plans to save the species from extinction threat and to guide future management interventions for conservation of endangered species.

Results

In Rajasthan, a total of 118 grids (12 × 12 km) covering 16,992 km2 were surveyed along 1924 km (mean 16 ± 4 km) of transects in 20145. In 2016, a total of 120 grids covering 17,280 km2 were surveyed along 2,273 km of transects6. In Maharashtra, a total of 372 grids covering 53,568 km2 were surveyed along 6436.6 km (mean 3.03 ± 1.74 km) length of transect for GIB population estimation in 201712. The occupancy and detection probability estimates of live GIB of Rajasthan were 0.25 and 6.66% and 0.52 and 11% in 2014 and 2016, respectively5,6. The detection probability and occupancy of 30 dummy GIB in the sampling grids of Maharashtra were found to be 0.13 and 8.06% (Table 1)12.

Table 1 Details of the survey conducted in the state of Rajasthan and Maharashtra for GIB in 2014, 2016 and 2017 respectively.

Our results from cumulative detection probability suggest that a minimum of four replicates are required to reach the cumulative detection probability threshold of 0.8 (Fig. 1). Except for the Rajasthan survey of 2014, boundary estimates of the other two surveys were less than 10% with 4 sampling replicates (Table 2). The mean squared error of the occupancy and detection probability estimate with 4 replicates was also less than the usually targeted cut-off of 0.07522. The boundary estimates and mean squared error of both occupancy and detection probability decreased with an increase in sampling replicate. Mean squared error (MSE) of occupancy for the Rajasthan 2014 survey was 0.568 for 2 replicates and 0.0052 for 10 replicates; whereas, the MSE of occupancy for the Maharashtra 2017 survey decreased from 0.514 to 0.0004 for 2 to 10 replicates, respectively (Table 2, Fig. 2). In both surveys, the boundary values decreased from 60% to <1% as the replicates increased from 2 to 10 (Table 2, Fig. 2). Decline in MSE and boundary values indicate that more temporal replicates are required for robust assessment of occupancy of elusive and long ranging species like the GIB.

Figure 1
figure1

Effect of a number of replicates on the detection probability of the GIB surveys. All the surveys were carried out with one replicate though the cut-off of 0.8 is crossed with 3–4 replicates for all the surveys.

Table 2 Mean squared errors (MSE) associated with detection probability and occupancy, the percentage of boundary values associated with surveys carried out at Rajasthan and Maharashtra for GIB using the same protocol with a grid size of 12 × 12 km.
Figure 2
figure2

Distribution of the maximum likelihood estimates (MLE) from three landscape surveys dataset (Rajasthan 2014 ψ = 0.06, p = 0.25, 10000 iterations; Rajasthan 2016 ψ = 0.11, p = 0.52, 10000 iterations; Maharashtra 2017 ψ = 0.08, p = 0.13, 10000 iterations) with varying number of survey replicates [(a)2, (b)3, (c)4, (d)5, (e) 6, (f) 7, (g) 8, (h) 10 visits] keeping the number of survey grids constant.

Power analysis showed an increase in power with the number of survey replicates and sampling sites. There is >70% (78%-Rajasthan 2014, 97%-Rajasthan 2016, 73%-Maharashtra 2017) (Fig. 3) chance of detecting 100% change in occupancy with 100 sampling sites and 10 temporal replicates. The same change (76%-Rajasthan 2014, 99%-Rajasthan 2016, 70%-Maharashtra 2017) can be detected with 4–6 temporal replicates when the number of sampling sites is doubled (Fig. 3). Finally, there was insignificant change in power (mean change 0.099 ± 0.086) after 6 replicates for all surveys. The change in power was significantly more when the Type-I error was low (α = 0.05) compared to when Type-I error was 0.1 and 0.15. Also, as sampling effort (number of sites, sampling replicates) increased, there was no significant change (p 0.05,0.1 = 0.35 and p 0.1,0.15 = 0.40) in power even with different combinations of Type-I and Type-II error level.

Figure 3
figure3

Statistical power for different surveys with different level of type-I error(α = 0.05, 0.1, 0.15) conducted across GIB distribution range (A) Rajasthan 2014; (B) Rajasthan 2016; (C) Maharashtra 2017; with respect to number of sampling replicates (K). We computed power for all three landscapes with four different combinations with different number of sampling sites and percent change. For each combination, the solid line represents (Type-I error)α = 0.1,the dotted line represents α = 0.15 and the dashed line represents α = 0.05.

Discussion

The fragmented populations of GIBs were once distributed throughout the grasslands of northern India and the Deccan landscape in 11 states23, but are now confined to few fragmented populations4. GIBs depend on India’s semi-arid open landscape, which is rapidly being converted into agricultural lands and a significant loss in grassland habitats has been observed due to various anthropogenic factors24. In addition, farmers have been shifting to cash crop production from the traditional cultivation of pulses and oil seed25,26, which are preferred by GIB27. The rapid conversion of grasslands and shrublands into agricultural lands, excessive use of insecticides and pesticides, overgrazing in scrublands, increasing feral dog population, and power lines expansion are the major factors contributing to the decline of GIB population. The states of Rajasthan and Gujarat harbour more than 80% of the total GIB population; but according to a recent report, only one male GIB is left in the Kutch region of Gujarat28. Hence, the dwindling population of GIB needs concrete conservation measures and management policies. India has planned various site-specific management interventions such as the formation of protected areas exclusively for the species, fencing of breeding grounds to increase the success rate of breeding events, controlling free-ranging dog population, habitat improvement, as well as ex-situ conservation. In order to evaluate the effectiveness of such management interventions, it is of fundamental importance to evaluate any change in species occupancy with high accuracy.

The landscape level surveys along with blind test experiment, conducted by placing dummy GIBs, have revealed low detection of these birds which can be further confounded by low population size, nomadic movement and use of large agricultural landscape for foraging12. At least 4 temporal replicates for each grid across the landscape is required for robust estimation. Effective sampling design for species like GIB, with low occupancy estimates (6–12%) and low detection probability (0.12–0.25), needs to ensure the parameters of interest meet the design target before spending valuable time and effort in the field. We defined different thresholds for type-I error- detecting a change when there is no change (α = 0.05, 0.1, 0.15) and type-II error- not detecting a change when there is a change β = (0.7, 0.8, 0.9) for the power analysis to avoid a misleading inference about population change. Similar to other studies, we observed an increase in power with survey sites or survey replicates21,29. Sampling designs very often fail to provide sufficient statistical power for elusive and rare species, hence it becomes fundamental to increase sampling replicates for a robust assessment. Surveys carried out in Rajasthan during 2016 had the highest occupancy and detection probability hence had the highest power (0.958) compared to our other surveys (Fig. 3). The result reflects the need for higher sampling effort where occupancy and detection probability of GIB is lower particularly for states like Gujarat and Maharashtra. The outcome of power analysis concurred with the mean-squared error and cumulative detection probability results, which showed an optimum of four replicates for a threshold of 0.8.

For a species like GIB, it is imperative to include the precision of p in designing spatial and temporal replicates. For such a situation, the best protocol may require more replication than in the case where precision of the occupancy estimator is considered30. In this paper, we addressed the need for an innovative way to predict the change in population of an elusive and long-ranging species across the landscape. Our recommended modifications to the existing protocol will improve the precision to detect change in population if any. In comparison with distance sampling, occupancy sampling is more robust for analysis with low sample size, which is a pertinent issue while handling sparse datasets of such elusive species. The broad interval of population estimates resulting from distance sampling can pose a major issue to inferring trends and evaluating conservation strategies. Moreover, robust abundance estimation of such long-ranging nomadic species would be financially and logistically challenging using distance sampling. Hence, we argue using occupancy as a surrogate for population trend to monitor GIB population. For designing robust methods an in-depth understanding of species ecology and habitat-use pattern is must especially for areas where occupancy and detection probability is low and influenced by species activity pattern and space use. The effectiveness of conservation efforts can be assessed in-depth by focusing on issues derived from the tradeoff resulting from the allocation of survey efforts30. Defining the trend in species population is not only governed by statistical decisions30 but is also influenced by species ecology. We cannot buy more time to conserve such a critically endangered species as the GIB, which may reach a level where it would be impossible to bring back the species from local extirpation. The important contribution of our study is the development of a robust protocol to assess population trends of a highly endangered species.

Materials and Methods

Monitoring protocol

Potential GIB habitat across the distribution range was divided into 12*12 km grids. Each grid was monitored simultaneously by trained survey teams to avoid detection of the same individual twice (Fig. 4). A total distance of 20 km was traversed along the trails and roads by the survey team in a slow-moving vehicle (10–20 km/hr.). For each sighting of GIB, distance from the trail, angle, GPS coordinates and number of individuals were recorded13.

Figure 4
figure4

Map showing the former and present distribution of GIB in India along with the survey sites across the country (Distribution map source: BirdLife International; IUCN RedData List3).

Blind Test to estimate detection probability

Owing to their low population density, nomadic behaviour and large range, the chances of sighting a GIB during the survey period was very low. This influences detection probability and affects occupancy estimates. In order to overcome this shortcoming, we designed a blind test using life-sized dummies of GIB to predict the probability of missing a GIB in its presence. A total of 30 GIB dummies were deployed across the survey area. These dummy GIBs were placed in areas known to be sampled by the survey team without their knowledge.

Evaluating the effectiveness of the existing protocol

We used the detection probability from surveys conducted in the states of Rajasthan and Maharashtra to calculate the cumulative detection probability. The cumulative detection probability is p* = 1 − (1 − p)^k, where k is the number of sampling replicates and p is the sampling-replicate-specific detection probability (i.e., the probability of detecting an animal during a single replicate). We estimated the optimum k required to surpass the threshold of 0.8, which is the probability of detecting the species at least once with 80% confidence interval31, in the conducted surveys.

In order to assess the effectiveness of the current protocol, we calculated the mean-squared error for both the occupancy estimate and detection probability with 10,000 simulations of the parameter estimates. We simulated capture histories with the occupancy and detection probability estimates following binomial distribution and estimated occupancy and detection probability based on the capture histories. We also evaluated boundary estimates (\(\hat{\psi }=1\))30, which can be used to evaluate the performance of various sampling strategies to identify the optimal sampling design. Boundary values are a major issue when the number of replicates is small and the probability values are low30. Both of the conditions were of major concern in our case. Simulation and analysis were carried out in R 3.4 (R Core Team 2017)32.

Power of a statistical test given by 1 − β (Type II error) represents the probability of correctly rejecting a false hypothesis and the levels of significance indicate the relative seriousness of committing Type I and II errors22,33. We used power analysis to investigate robustness using detection probability and occupancy estimates of the previous surveys22. We considered effect size as a function of both occupancy and detection probability to calculate power. The precision of estimates usually improves with the increasing temporal replicates. However, when this is performed reducing the number of sampling sites, it creates a trade-off leading to an optimal number of repeated visits which depends on the characteristics of the species22.

Considering our monitoring goal with a large landscape, we assumed that making a Type II error (β) would be highly costly and chose three different levels (0.7, 0.8, 0.9) for β (i.e., not detecting a change in occupancy and detection probability when there is a change) and used three different levels (0.05, 0.1, 0.15) for α (Type I error). In this scenario, committing Type-I error (i.e. detecting a change when there is no change) would be very less feasible as the species is known for their site-fidelity. Moreover, the spatial extent of the survey encompassed all available suitable habitats of the species reducing the chances of Type I error. We tested the effectiveness by varying number of sites (100–400) and replicates (2, 4, 6, 8, 10) to investigate the power of different surveys. We constructed a power curve from the analysis keeping the estimated occupancy parameters and daily detection probability constant.

References

  1. 1.

    IUCN Red List version 2016-2″. The IUCN Red List of Threatened Species. International Union for Conservation of Nature and Natural Resources (IUCN) (2016).

  2. 2.

    Dharmakumarsinhji, R. S. Study of the Great Indian Bustard. Final report. WWF, Morges (1971).

  3. 3.

    BirdLife International. Ardeotis nigriceps. The IUCN Red List of Threatened Species 2017: e.T22691932A118025435, 10.2305/IUCN.UK.2017-3.RLTS.T22691932A118025435.en. (2018).

  4. 4.

    Dutta, S., Rahmani, A. R. & Jhala, Y. V. Running out of time? The Great Indian Bustard Ardeotis nigriceps—status, viability, and conservation strategies. European Journal of Wildlife Research 57, 615–625 (2010).

  5. 5.

    Dutta, S., Bhardwaj, G. S., Bhardwaj, D. K. & Jhala, Y. V. Status of Great Indian Bustard and Associated Wildlife in Thar. Wildlife Institute of India, Dehradun and Rajasthan Forest Department, Jaipur (2014).

  6. 6.

    Dutta, S., Bipin C. M., Bhardwaj, G. S., Anoop, K. R. & Jhala, Y. V. Status of Great Indian Bustard and Associated Wildlife in Thar. Wildlife Institute of India, Dehradun and Rajasthan Forest Department, Jaipur (2016).

  7. 7.

    Apps, C. D., McLellan, B. N., Woods, J. G. & Proctor, M. F. Estimating grizzly bear distribution and abundance relative to habitat and human influence. The Journal of Wildlife Management 68, 138–152 (2004).

  8. 8.

    Cook, L. M., Brower, L. P. & Croze, H. J. The accuracy of a population estimation from multiple recapture data. Journal of Animal Ecology, 57–60 (1967).

  9. 9.

    Burnham, K. P., Anderson, D. R. & Laake, J. L. Estimation of density from line transect sampling of biological populations. Wildlife Monographs 72, 3–202 (1980).

  10. 10.

    Lancia, R. A., William L. K., Pollock, K. H. & Nichols, J. D. Estimating the number of animals in wildlife populations. 106–153 (2005).

  11. 11.

    Thogmartin et al. A review of the population estimation approach of the North American Landbird Conservation Plan. The Auk. 123, 892–904 (2006).

  12. 12.

    Habib, B., Khan, S., Talukdar, G., & Kumar, R. S. Status of Great Indian Bustard and associated species in the State of Maharashtra, India – 2017. Status Survey Report. Wildlife Institute of India and Maharashtra Forest Department; TR No. 2018/14 42 (2018).

  13. 13.

    Thompson, W. L. Estimating Abundance of Rare or Elusive Species. Sampling rare or elusive species: concepts, designs, and techniques for estimating population parameters, 389 (2004).

  14. 14.

    Hames, R. S., Rosenberg, K. V., Lowe, J. D. & Dhondt, A. A. Site reoccupation in fragmented landscapes: testing predictions of metapopulation theory. Journal of Animal Ecology. 70, 182–190 (2001).

  15. 15.

    Barbraud, C., Nichols, J. D., Hines, J. E. & Hafner, H. Estimating rates of extinction and colonization in colonial species and an extension to the metapopulation and community levels. Oikos. 101, 113–126 (2003).

  16. 16.

    Lande, R. Demographic models of the Northern Spotted Owl (Strix occidentalis caurina). Oecologia. 75, 601–607 (1988).

  17. 17.

    Hanski, I. Metapopulation ecology. Oxford University Press, Oxford, UK (1999).

  18. 18.

    MacKenzie, D. I. et al. Improving inferences in population studies of rare species that are detected imperfectly. Ecology. 86, 1101–1113 (2005).

  19. 19.

    Diefenbach, D. R. et al. A test of the scent-station survey technique for bobcats. Journal of Wildlife Management. 58, 10–17 (1994).

  20. 20.

    Rhodes, J. R. et al. Optimizing presence–absence surveys for detecting population trends. Journal of Wildlife Management. 70, 8–18 (2006).

  21. 21.

    Woods, C. M. et al. Detecting small changes in populations at landscape scales: a bioacoustics site-occupancy framework. Ecological Indicators. 98, 492–507 (2019).

  22. 22.

    Barata, I. M., Griffiths, R. A. & Ridout, M. S. The power of monitoring: optimizing survey designs to detect occupancy changes in a rare amphibian population. Scientific Reports. 7(16491) (2017).

  23. 23.

    Rahmani A. R. The Great Indian Bustard. Final report in the study of ecology of certain endangered species of wildlife and their habitats. Final Report, Bombay Natural History Society, Mumbai (1989).

  24. 24.

    Tian, H., Banger, K., Tao, B. & Dadhwal, V. K. History of land use in India during 1880–2010: Large-scale land transformations reconstructed from satellite data and historical archives. Global and Planetary Change. 121, 78–88 (2014).

  25. 25.

    Nalawade, D. B., Chavan, S. M. & Pawar, C. T. Spatio Temporal Changes in Cropping Pattern of South Konkan of Maharashtra: A Geographical Analysis, Cyber Literature. The International Online Journal. 3, 76–83 (2010).

  26. 26.

    Seethalakshmi, P. Shifting land use pattern in Andhra Pradesh: Implications for agricultural and food security. Final Report. Center for sustainable agricultural (CSA) Hyderabad, Andhra Pradesh, 78 (2010).

  27. 27.

    Habib, B., et al Tracking of Great Indian Bustard in Maharashtra India. Technical Report, Wildlife Institute of India and Maharashtra Forest Department, 22 (2016).

  28. 28.

    Down to Earth. Only one male Great Indian Bustard left in Gujarat. Down to Earth Magzine https://www.downtoearth.org.in/news/wildlife-biodiversity (2018).

  29. 29.

    Loos, J. et al. Developing robust field survey protocols in landscape ecology: a case study on birds, plants and butterflies. Biodivers. Conserv. 24, 33–46 (2014).

  30. 30.

    Guillera-Arroita, G., Ridout, M. S. & Morgan, B. J. Design of occupancy studies with imperfect detection. Methods in Ecology and Evolution. 1, 131–139 (2010).

  31. 31.

    Long, R. A. et al. Designing effective non-invasive carnivore surveys. Non-invasive survey methods for carnivores. 8–44 (2008).

  32. 32.

    R Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. https://www.R-project.org/ (2017).

  33. 33.

    Guillera-Arroita, G. & Lahoz-Monfort, J. J. Designing studies to detect differences in species occupancy: power analysis under imperfect detection. Methods in Ecology and Evolution. 3, 860–869 (2012).

Download references

Acknowledgements

We would like to thank Forest Department of Maharashtra for the financial and logistic support during the survey and for permits to conduct research on GIB in the State. The fellowship of SK was provided by GIB Species Recovery Project funded by CAMPA. We acknowledge all the volunteers and forest staff for their support during the survey in Maharashtra.

Author information

B.H. conceived the idea of the manuscript, S.K. collected the data, N.C. and S.K. analyzed the data, S.K., N.C. and B.H. wrote the manuscript; all the authors read and approved the final version of this manuscript.

Correspondence to Bilal Habib.

Ethics declarations

Competing Interests

The authors declare no competing interests.

Additional information

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Khan, S., Chatterjee, N. & Habib, B. Testing performance of large-scale surveys in determining trends for the critically endangered Great Indian Bustard Ardeotis nigriceps. Sci Rep 9, 11627 (2019) doi:10.1038/s41598-019-48193-2

Download citation

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.