Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Rapid population decline in migratory shorebirds relying on Yellow Sea tidal mudflats as stopover sites


Migratory animals are threatened by human-induced global change. However, little is known about how stopover habitat, essential for refuelling during migration, affects the population dynamics of migratory species. Using 20 years of continent-wide citizen science data, we assess population trends of ten shorebird taxa that refuel on Yellow Sea tidal mudflats, a threatened ecosystem that has shrunk by >65% in recent decades. Seven of the taxa declined at rates of up to 8% per year. Taxa with the greatest reliance on the Yellow Sea as a stopover site showed the greatest declines, whereas those that stop primarily in other regions had slowly declining or stable populations. Decline rate was unaffected by shared evolutionary history among taxa and was not predicted by migration distance, breeding range size, non-breeding location, generation time or body size. These results suggest that changes in stopover habitat can severely limit migratory populations.


Animal migrations are among the greatest spectacles of the natural world, yet they are increasingly imperilled by human activity1. Animals that undergo long-distance migrations spend most of their time in widely separated breeding and non-breeding habitats. As a result, research on population abundance has focused on these two phases of the annual life cycle, where demographic impacts2,3,4 and especially habitat loss5,6,7 are considered the leading cause of population declines. Migratory animals must undertake energetically demanding migrations covering thousands of kilometres between breeding and non-breeding sites, and many interrupt their journeys to rest and refuel at stopover sites along the way. Such sites have a potential importance disproportionate to their area and the amount of time they are used, and quantitative models indicate that the quantity and quality of stopover habitat can limit population abundance8,9,10. However, there are few empirical studies linking population abundance to processes, such as habitat loss, experienced during migration11,12,13.

There is growing concern that loss and degradation of stopover habitat is causing population declines of migratory shorebirds of the East Asian-Australasian Flyway (EAAF). Millions of shorebirds migrate annually through the EAAF from breeding grounds in China and the Russian and Alaskan Arctic to non-breeding habitats in Southeast Asia, Australia and New Zealand. The birds congregate at high densities on tidal mudflats in the Yellow Sea region of East Asia, using them as staging sites14 to refuel as they complete tight annual schedules of migration, reproduction and moult15. However, the Yellow Sea is increasingly being degraded and >1% of its tidal mudflats are destroyed annually for coastal development16, leading to widespread concern that collapse of this ecosystem is driving migratory species’ declines17. Indeed, shorebirds in the EAAF are undergoing severe, long-term reductions in abundance on stopover and non-breeding sites11,18,19,20,21. Although the Yellow Sea region is a migration bottleneck for many EAAF shorebirds, species vary in their reliance on migratory stopover sites in this area. At one extreme, 100% of the menzbieri subspecies of bar-tailed godwit (Limosa lapponica) refuel at stopover sites in the Yellow Sea. Conversely, grey-tailed tattler (Tringa brevipes) refuels at a wide range of sites, with only 3% of the population staging in the Yellow Sea22,23,24. This interspecific variation in the use of Yellow Sea tidal mudflats provides a unique opportunity to investigate whether deteriorating and disappearing stopover habitat can drive population declines.

Here, we measure abundance and population trends for ten EAAF shorebird taxa for which expert-defined migratory connectivity networks were available22 to test if taxa that rely heavily on Yellow Sea tidal mudflats to stage their long-distance migrations are experiencing the most rapid population declines. The migratory connectivity networks comprise nodes that identify spatially distinct populations of each taxon and edges that trace their unique migration routes through the EAAF. We also evaluate if conditions in the non-breeding grounds contribute to population trends. Our data were non-breeding season counts made between 1993 and 2012 across Australia and New Zealand at 43 sites organized into four nodes of the migratory connectivity network (Supplementary Table 1). We calculated reliance on the Yellow Sea by tallying the proportion of each taxon’s population that refuels in Yellow Sea nodes of the migratory connectivity network. Finally, we evaluated the importance of four common predictors of population decline and extinction risk25,26: migration distance, breeding range size, generation time and body size.

If threats in the Yellow Sea are driving population trends, taxon-specific changes in abundance should be correlated with Yellow Sea reliance during migration, and taxon-specific trends should vary little among non-breeding nodes. Alternatively, if environmental conditions in non-breeding areas affect population trends, taxon-specific changes in abundance should vary markedly among non-breeding nodes, and taxon-specific trends should be only weakly related to Yellow Sea reliance during migration. Under this latter scenario, taxon-specific declines might be expected to vary according to local differences in habitat change, rather than show consistency among nodes.


Predicting variation in flyway-level population trends

After accounting for the shared evolutionary history among taxa, we found that Yellow Sea reliance was the single most important predictor of variation in population trends (Fig. 1a). Population trends were strongly negatively related with Yellow Sea reliance (slope=−0.92, 95% credible interval (CRI)=−1.25, −0.59; Fig. 1b), indicating that long-term population declines were greatest for taxa that depend more heavily on refuelling stops in this region (Table 1; Fig. 2). Taxa with ≤40% of the population relying of the Yellow Sea remained stable or declined only slightly, with an average change of −1.0% year−1 (95% CRI =−3.0, 1.0). In contrast, taxa with >50% of the population relying on the Yellow Sea declined at an average of −5.2% year−1 (95% CRI: −6.5, −3.8). This group includes the EAAF endemics great knot (Calidris tenuirostris) and far eastern curlew (Numenius madagascariensis; Table 1), both of which are listed as globally threatened taxa27.

Figure 1: Predictors of flyway-level population trend estimates between 1993–2012 for ten EAAF migratory shorebirds.
figure 1

(a) Bayesian variable selection identifying predictors that are important (indicator value ≥0.75; green shading), inconclusive (indicator value between 0.25 and 0.75; yellow shading) and unimportant (indicator value ≤0.25; red shading). (b) Bayesian linear regression of Yellow Sea reliance as a predictor of flyway-level population trend estimates. Grey shading shows the 95% CRI around the regression line. Points show flyway-level population trend estimates, the mean annual rate of change in total abundance estimates. Error bars represent the 95% CRI around population trends. These analyses included the menzbieri subspecies of bar-tailed godwit and excluded the baueri subspecies (see Methods).

Table 1 Flyway-level population trend estimates and 95% CRI for ten EAAF migratory shorebird taxa and their reliance on Yellow Sea tidal mudflats.
Figure 2: Total abundance between 1993 and 2012 for ten EAAF migratory shorebird taxa.
figure 2

(af) Taxa are ordered from highest to lowest Yellow Sea reliance, the proportion of the flyway population that stages on Yellow Sea tidal mudflats to refuel for long-distance migrations. (a) Menzbieri bar-tailed godwit; (b) far eastern curlew; (c) curlew sandpiper; (d) great knot; (e) red knot; (f) lesser sand plover; (g) baueri bar-tailed godwit; (h) terek sandpiper; (i) red-necked stint; and (j) grey-tailed tattler. Total abundance estimates are posterior means from Bayesian N-mixture models of counts across Australia and New Zealand, including the majority of internationally important sites. Lines show posterior mean abundance estimates for each year, with red lines indicating taxa with credibly declining populations and grey shading denoting the 95% CRI. Overall trend estimates appear in Table 1. Detection probabilities for each taxon ranged from 0.52 to 0.68 (Supplementary Fig. 1) and were reflected in modelled abundances and trend estimates. Posterior predictive checks indicated good model fit in all cases (Supplementary Fig. 2).

Geographical patterns in non-breeding population trends

We found no evidence that population trends varied markedly among non-breeding nodes in Australia and New Zealand, indicating that conditions in the non-breeding period did not account for population declines. Of the eight taxa that had sufficient data for node-level trend estimation, populations of six credibly decreased in abundance, with declines occurring in all four nodes (Fig. 3; Supplementary Table 2). Despite intervening distances of up to 5,000 km, population trends among nodes for each taxon differed by mean odds of <6% (Supplementary Table 3). None of the eight taxa credibly increased in abundance on any node (Fig. 3), suggesting that movement among nodes was unlikely to explain population declines. Decreasing habitat quality at non-breeding sites caused by urban expansion28 and river diversion for agriculture29 is unlikely to explain population trends because most resident coastal breeding shorebirds that co-occur with migrants have not declined19.

Figure 3: Abundance between 1993 and 2012 for eight EAAF migratory shorebird taxa found in four non-breeding population nodes.
figure 3

Abundance estimates are posterior means for each node from Bayesian N-mixture models of counts across Australia and New Zealand, including the majority of internationally important sites. Lines show posterior mean abundance estimates for each year, with red lines indicating credibly declining populations and grey shading denoting the 95% CRI. Map insets indicate the location of the four population nodes: (1) northwestern Australia; (2) Queensland; (3) southeastern Australia and (4) New Zealand. Lesser sand plover and the menzbieri subspecies of bar-tailed godwit were not included in analyses because they occurred on only one node.


Our analyses indicate that reliance on the Yellow Sea is a leading driver of population declines in migratory shorebirds of the EAAF. This finding is consistent with previous work showing that survival estimates across the annual cycle for three taxa that underwent some of the largest population declines are dramatically lower during the Yellow Sea staging period compared with the stationary breeding and non-breeding periods30. This result implies that population declines are driven by low survival during or soon after staging in Yellow Sea tidal mudflats, likely because birds are unable to refuel enough to meet the energetic demands of migration. Sustained reproductive failure is unlikely to explain declines because the ratio of juvenile to adult shorebirds, an indicator of breeding success, has remained relatively constant at non-breeding sites in northwestern and southeastern Australia in the six taxa for which data are available31,32. Previous research in Japan has also shown that shorebird species relying on the Yellow Sea while on migration are declining more quickly than those that do not11. However, Japan itself is a stopover site for some species and is on the periphery of the migratory connectivity networks of the taxa we found to be declining fastest, complicating interpretation of those earlier results. We have built substantially on this work by showing that Yellow Sea reliance explains variation in population trends at non-breeding destinations that support the majority of the flyway populations of ten taxa.

Two sources of long-term environmental decline in the Yellow Sea are likely responsible for the negative impacts on migratory shorebird populations. First, nearly 30% of Yellow Sea tidal mudflats were lost to coastal development in the past 30 years33, a period that brackets the timing of observed population declines. Coastal China is forecast to undergo up to 14% expansion in urban development over the next 15 years, much of it concentrated on the margins of the Yellow Sea34, and tidal mudflat loss seems likely to continue or accelerate. Second, the Yellow Sea ecosystem has undergone pervasive degradation in quality35, including massive algal blooms36, discharge of heavy metals and pesticides37; and the spread of the exotic saltmarsh-grass Spartina alterniflora16. These disturbances reduce prey availability and foraging opportunities for migrating shorebirds38.

An enormous conservation intervention is needed to reverse the declines in EAAF shorebirds, and indeed an international governance framework is emerging in the region. A series of bilateral migratory bird agreements complements the EAAF Partnership (EAAFP), a collaboration among 34 countries, non-governmental organizations and multilateral arrangements. The EAAFP has thus far formally designated 136 Flyway Network Sites in response to the need for international coordination of habitat protection. Our results suggest that the most immediate priority remains preventing further tidal mudflat loss in the Yellow Sea region. Other management options include restoring lost habitat39 and modifying existing artificial coastal habitats such as salt ponds, rice paddies, wastewater treatment plants and seawalls to maximize shorebird foraging and roosting opportunities. For example, traditional salt-pans can support substantial numbers of non-breeding shorebirds40. Although artificial habitats may not provide the most specialized taxa with an adequate substitute for intact tidal mudflats, options will be increasingly limited if Yellow Sea habitat loss continues. Our findings indicate an urgent need for effective conservation actions in this flyway to prevent further population declines in the migratory shorebirds it supports.


Study species

We selected ten shorebird taxa for which detailed information on migratory connectivity was available for the EAAF. Experts with extensive flyway experience developed migratory connectivity networks that defined movements among internationally important wetland sites. Drawing on population surveys, mark-resight efforts, and daylight-level geolocator and satellite tracks from across the flyway, experts grouped individual sites into the smallest possible set for which birds were thought to follow unique migration routes through the EAAF. These relationships were depicted as a series of nodes that defined each group of sites connected by a set of edges that traced migration routes (see supplementary material in (ref. 22)). Experts reached consensus on network structure for ten taxa: bar-tailed godwit (two subspecies here analysed separately: Limosa lapponica baueri and Limosa lapponica menzbieri), far eastern curlew (Numenius madagascariensis), Terek sandpiper, (Xenus cinereus), grey-tailed tattler (Tringa brevipes), great knot (Calidris tenuirostris), red knot (two subspecies here analysed together: Calidris canutus piersmai and Calidris canutus rogersi), curlew sandpiper (Calidris ferruginea) and lesser sand plover (Charadrius mongolus). A connectivity map was unavailable for red-necked stint (Calidris ruficollis), but we included this species in analyses because it is one of the most abundant migratory shorebirds in Australia during the non-breeding period.

Data acquisition

We acquired count data for each taxon from local and national databases in Australia and New Zealand maintained by the Australasian Wader Studies Group, BirdLife Australia, BirdLife Western Australia, BirdLife Tasmania, Bird Observer’s Club of Australia, Friends of Shorebirds SE, Friends of Streaky Bay District Parks, Hunter Bird Observers Club, New South Wales Wader Study Group, Ornithological Society of New Zealand, Queensland Wader Study Group, South Australian Ornithological Association and Victorian Wader Study Group. Members of these groups conducted counts at coastal sites during the non-breeding period from October–March while the shorebirds are in the Southern Hemisphere. Movements among non-breeding sites are likely minimal during this period, so counts in these months should represent the number of birds available for detection. Each site consisted of one or more discrete roosts where shorebirds reliably congregate during high-tide cycles that inundate tidal mudflats used for foraging (Supplementary Table 2). Experienced observers timed visits to coincide with high tide and counted shorebirds at all roosts within a site. Any local movement among roosts therefore minimally affect counts.

Shorebirds were counted at the majority of sites at least twice each Austral summer. We focused our analyses on counts in January and February, but supplemented them with counts from November, December and March if necessary. Shorebirds arrive earlier from southbound migration at sites in northwestern Australia compared to other sites in Australia41, so counts there began in October–December to avoid counting during wet season rains that could have lowered detection probability42. For each taxon, we included sites with data likely to yield sufficient power to detect temporal trends in abundance, recognizing that the degree of aggregation varies among species. For example, red-necked stint is rather broadly distributed, while great knot congregates strongly, and inclusion of different sites or time series could alter resulting population trend estimates and CRIs. We included sites with overall maxima of at least 500 individuals of each taxon because sites with lower maxima had numerous years when no birds were recorded. At many sites, counts began in the early 1980s, but counts at key sites in northwestern Australia, Queensland and New Zealand began in the early 1990s (ref. 43). These criteria yielded 10–26 sites for each taxon across the non-breeding range in Australia and New Zealand with count data from 1993–2012 (Supplementary Table 2). Each site fell within a non-breeding node of at least one taxon. The location and size of nodes varied among taxon, but could be grouped into four areas: (1) northwestern Australia; (2) Queensland; (3) southeastern Australia and (4) New Zealand. For each taxon, one or two non-breeding nodes lacked count data owing to geographic isolation or absence of formal surveys. In all cases, these nodes were located in Southeast Asia and the Gulf of Carpentaria in Australia.

Modelling abundance and population trends

Our modelling goal was to estimate abundance and population trends of the 10 taxa using 20 years of count data across Australia and New Zealand. For each taxon, we first assessed population trends at each unique non-breeding node and then across all count sites to estimate flyway-level trends. Our model was an N-mixture model, formulated as a hierarchical Poisson regression that estimates parameters for the latent state of abundance by accounting for imperfect detection of individuals in spatially or temporally replicated counts44. Incorporating detection probability into abundance estimates is essential to remedy bias owing to the common failure to detect all individuals in counts (Supplementary Fig. 1)45.

Shorebird counts occurred at i (1,…, R) sites in t (1,…, K) years with j (1,…, N) monthly counts in each year. Counts cijt can therefore be considered as a binomial random variable where the local abundance of birds available for sampling Nit is observed with detection probability Pijt:

A Poisson distribution with mean λit, a standard distribution for modelling spatial or temporal variation in abundance from counts, described local abundance Nit:

We estimated parameters for the latent state of abundance λit with a log-linear model. For node-based analyses, the expected log abundance was:

where ωi is a random effect for each count site, αk is an intercept for each non-breeding node, βk is the linear trend at each node centred on mean year t* and ɛit is a random effect accounting for extra-Poisson dispersion in abundance. We assigned standard vague prior distributions to all parameters determining λit. We assumed that ωi, αk, βk and ɛit were normally distributed with mean 0 and precision τ (precision = 1/variance) and that τ was inverse gamma distributed with shape and scale 10−3. To estimate population trends across all count sites, we rephrased equation (3) without node-specific terms:

The resulting slope β is thus a single trend estimate for all sites counted across the non-breeding range in Australia and New Zealand, providing an estimate of the long-term flyway population trend for each taxon.

We modelled detection probability Pijt as:

where γt is the mean detection probability in year t and δijt is a random effect allowing detection probability to vary at site i in month j and year t. We assumed that γt was normally distributed with mean 0 and variance 103 and that δijt was uniformly distributed with range 0−100. We did not model predictors of detection probability by fitting covariates because data on weather, observer identity and similar variables were unavailable for most counts over the 20-year time series.

We fit N-mixture models in program JAGS46 through the R2jags package47 in program R (ref. 48). We ran three chains of each model for 800,000 iterations and discarded the initial 200,000 as burnin. We thinned each chain by 18, resulting in 100,000 posterior samples. Convergence was assessed with Gelman–Rubin diagnostics and was unambiguous in all cases. We judged population trends as credibly increasing or decreasing if their 95% CRIs did not overlap zero. We evaluated variation in population trends among nodes individually for each taxon. During model fitting, we derived pairwise odds ratios and 95% CRI and used them to assess differences in trends among nodes.

There are four key assumptions accompanying this model45. First, populations within each site are closed to immigration and emigration between monthly counts. Within-year movement of individually marked birds among a subset of monitored count sites was exceedingly low, suggesting that our data meet this assumption49. The second assumption is that detection probability is constant for all individuals within each taxon. Although we cannot assess this assumption directly, birds in each taxon likely were detected with equal probability because counts took place when individuals congregated at multispecies high-tide roosts. Third, abundance and detection probability are modelled with appropriate parametric distributions. We assessed this assumption through posterior predictive checks. This approach compares discrepancies in the observed data to discrepancies in replicate data simulated from the posterior distribution to diagnose model fit. Our measure of discrepancy was a chi-square goodness of fit test, a standard statistic used for posterior predictive checks45. The proportion of Markov Chain Monte Carlo (MCMC) samples where discrepancies in the observed data exceed those of the replicate data should be near 0.50 when model fit is adequate (Supplementary Fig. 2). The fourth assumption is that double counts of individuals are minimal. Violation of this assumption would overestimate abundance and bias estimates of log-linear decline rates towards zero. All counts were conducted by experienced observers, who designed surveys to minimize overlooking or double-counting shorebirds, so our data likely meet this assumption.

Predicting variation in flyway-level population trends

We performed a phylogenetic comparative analysis to evaluate the ability of five different taxon-level predictors to explain the variation in flyway-level population trend estimates: Yellow Sea reliance, migration distance, breeding range size, generation time and body size. This analysis accounted for the possibility that shared evolutionary history partly could explain population declines. To develop our index of Yellow Sea reliance, we tallied the proportion of the flyway population for each taxon that stages14 on tidal mudflats within the Yellow Sea region (34°29′ N, 119°47′ E to 35°20′ N, 129°17′) based on published migratory connectivity networks22 and estimates of shorebird populations staging in the Yellow Sea23,24. Because tidal mudflats in this region are declining at >1 % annually16,33, we predicted that taxa with higher reliance on Yellow Sea staging sites would decline at a faster rate compared to those with lower reliance on this area. Ideally, this analysis would involve time series estimates of tidal mudflat loss that are contemporaneous with shorebird counts. However, the best available estimates of tidal mudflat loss are derived from only two time points33,50, and annual estimates of habitat loss cannot be determined. To estimate differences in migration distance among taxa, we used digitized distribution maps51 and a geographic information system52 to measure the degrees of latitude travelled during migration as the latitudinal difference between the centroid of breeding and non-breeding ranges. We calculated breeding range size by digitizing published distribution maps51 and acquired data on generation time and body size (measured from bill to tail) from regional handbooks53,54 and published reports55. Species with long migrations, small breeding ranges, long generation times and large body size may face a higher risk of population decline or extinction25,26. We therefore predicted that taxa with geographical and life history attributes closer to these extremes would decline at a higher rate compared to those further away from these extremes.

To incorporate uncertainty into the phylogenetic comparative analysis, we acquired 1,000 equally plausible, ultrametric trees based on the Ericson backbone56 from the BirdTree website57. Sequence data were not available for bar-tailed godwit subspecies, so trees contained a single branch for this species. We therefore performed two versions of the phylogenetic comparative analysis, one using predictors of population trends for L. l. menzbieri and another with predictors for L. l. baueri. These analyses yielded qualitatively similar results. We retained the analysis using L. l. menzbieri, the subspecies that showed the greater population decline. Simulations investigating tree samples size indicate that analyses of >1,000 trees does not yield more precise parameter estimates58. We used the ape package59 in program R (ref. 48) to convert each tree to a variance–covariance matrix under the assumption of a Brownian Motion model of character evolution. Under this assumption, the variance is the branch length from the root to tip and the covariance is the branch length from the root to the most recent common ancestor of each pair of taxa60

The phylogenetic comparative analysis was a Bayesian hierarchical linear regression that evaluated which predictors best explained the differences in flyway population trends among z (1,…, M) taxa and q (1,…, R) trees. The flyway population trend for each taxon Tdz estimated from equation (4) was drawn from a multivariate normal distribution with mean μz and variance :

where Ω is an array of dimension M × M × R in which each element Ω [ , , q] is the inverse of the scaled variance–covariance matrix for each tree q. We assumed that the variance σ2 was inverse gamma distributed with shape and scale 10−3. With Ω scaled to a branch height of 1, σ2 can be considered as residual variance and Ω as a correlation structure. Thus, larger values of Ω would to limit the ability of predictors to explain variation in population trends Tdz. The model for predicting flyway population trend differences among taxa was:

where α is an intercept, βc is a the effect of covariate c, Xzc is a vector of covariates for Yellow Sea reliance and predictors of population trends for taxon z, and ɛ is an error term to account for unexplained variability. We used Bayesian variable selection to assess which predictors were most important for explaining the differences in flyway population trends among taxa. Bayesian variable selection is one approach for choosing important predictors from a candidate set and for developing parsimonious models61,62. This method is also useful for identifying influential covariates when wide 95% CRI indicate high estimation uncertainty62. To perform Bayesian variable selection, we defined βc as the product of a binary indicator variable and a regression coefficient θc such that:

The Bernoulli prior allows the indicator variable vc to take a value of 1 if covariate c is an important predictor and a value of 0 otherwise during each MCMC iteration. A large posterior mean for a given would identify it as an important predictor, whereas a mean close to 0 would mark it as unimportant. We interpreted indicator posterior means ≥0.75 as evidence that a covariate was an important predictor, those between 0.25 and 0.75 as inconclusive, and those ≤0.25 as evidence that a covariate was unimportant62. We then repeated the analysis by fixing unimportant values of the indicator variable to 0, improving the ability of retained predictors to explain population trends62. We assumed that α, μc and ɛ were normally distributed with mean 0 and variance 103 and that was inverse gamma distributed with shape and scale 10−3. We fit the regression model in program JAGS46 through the R2JAGS package47 in program R (ref. 48). We ran three chains of the model for 120,000 iterations, discarding the initial 20,000 as burnin. We thinned each chain by three, yielding 100,000 posterior samples.

Code availability

Program JAGS code for Bayesian models that support the findings of this study is available from

Data availability

The data that support the findings of this study are available from the organizations listed in the Acknowledgements and in Supplementary Note 1, but restrictions apply to the availability of these data, which were used under agreement for the current study. The authors will work upon request with any interested parties to try to secure data sharing agreements with the aforementioned organizations.

Additional information

How to cite this article: Studds, C. E. et al. Rapid population decline in migratory shorebirds relying on Yellow Sea tidal mudflats as stopover sites. Nat. Commun. 8, 14895 doi: 10.1038/ncomms14895 (2017).

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


  1. Wilcove, D. S. & Wikelski, M. Going, going, gone: is animal migration disappearing? PLoS Biol. 6, 1361–1364 (2008).

    CAS  Article  Google Scholar 

  2. Harewood, A. & Horrocks, J. Impacts of coastal development on hawksbill hatchling survival and swimming success during the initial offshore migration. Biol. Conserv. 141, 394–401 (2008).

    Article  Google Scholar 

  3. Calles, O. et al. Size-dependent mortality of migratory silver eels at a hydropower plant, and implications for escapement to the sea. Freshwater Biol. 55, 2167–2180 (2010).

    Article  Google Scholar 

  4. Juillet, C., Choquet, R., Gauthier, G., Lefebvre, J. & Pradel, R. Carry-over effects of spring hunt and climate on recruitment to the natal colony in a migratory species. J. Appl. Ecol. 49, 1237–1246 (2012).

    Article  Google Scholar 

  5. Sutherland, W. J. et al. A horizon scanning assessment of current and potential future threats to migratory shorebirds. IBIS 154, 663–679 (2012).

    Article  Google Scholar 

  6. Robinson, S. K., Thompson, F. R., Donovan, T. M., Whitehead, D. R. & Faaborg, J. Regional forest fragmentation and the nesting success of migratory birds. Science 267, 1987–1990 (1995).

    CAS  ADS  Article  Google Scholar 

  7. Flockhart, D. T. T., Pichancourt, J. B., Norris, D. R. & Martin, T. G. Unravelling the annual cycle in a migratory animal: breeding-season habitat loss drives population declines of monarch butterflies. J. Anim. Ecol. 84, 155–165 (2015).

    Article  Google Scholar 

  8. Pettifor, R. A. et al. Spatially explicit, individual-based, behavioural models of the annual cycle of two migratory goose populations. J. Appl. Ecol. 37, 103–135 (2000).

    Article  Google Scholar 

  9. Sheehy, J., Taylor, C. M. & Norris, D. R. The importance of stopover habitat for developing effective conservation strategies for migratory animals. J. Ornithol. 152, 161–168 (2011).

    Article  Google Scholar 

  10. McLaren, J. D., Shamoun-Baranes, J. & Bouten, W. Stop early to travel fast: modelling risk-averse scheduling among nocturnally migrating birds. J. Theor. Biol. 316, 90–98 (2013).

    MathSciNet  Article  Google Scholar 

  11. Amano, T., Szekely, T., Koyama, K., Amano, H. & Sutherland, W. J. A framework for monitoring the status of populations: an example from wader populations in the East Asian-Australasian flyway. Biol. Conserv. 143, 2238–2247 (2010).

    Article  Google Scholar 

  12. Møller, A. P., Rubolini, D. & Lehikoinen, E. Populations of migratory bird species that did not show a phenological response to climate change are declining. Proc. Natl Acad. Sci. USA 105, 16195–16200 (2008).

    ADS  Article  Google Scholar 

  13. Sicurella, B., Musitelli, F., Rubolini, D., Saino, N. & Ambrosini, R. Environmental conditions at arrival to the wintering grounds and during spring migration affect population dynamics of barn swallows Hirundo rustica breeding in Northern Italy. Popul. Ecol. 58, 135–145 (2016).

    Article  Google Scholar 

  14. Warnock, N. Stopping vs. staging: the difference between a hop and a jump. J. Avian Biol. 41, 621–626 (2010).

    Article  Google Scholar 

  15. Buehler, D. M. & Piersma, T. Travelling on a budget: predictions and ecological evidence for bottlenecks in the annual cycle of long-distance migrants. Philos. Trans. R Soc. Lond. B Biol. Sci. 363, 247–266 (2008).

    Article  Google Scholar 

  16. Ma, Z. et al. Rethinking China's new great wall. Science 346, 912–914 (2014).

    CAS  ADS  Article  Google Scholar 

  17. Larson, C. Hostile shores. Science 350, 150–152 (2015).

    CAS  ADS  Article  Google Scholar 

  18. Close, D. H. Changes in wader numbers in the Gulf St Vincent, South Australia, 1979-2008. Stilt 54, 24–27 (2008).

    Google Scholar 

  19. Wilson, H. B., Kendall, B. E., Fuller, R. A., Milton, D. A. & Possingham, H. P. Analyzing variability and the rate of decline of migratory shorebirds in Moreton Bay, Australia. Conserv. Biol. 25, 758–766 (2011).

    Article  Google Scholar 

  20. Minton, C. et al. Trends of shorebirds in Corner Inlet, Victoria, 1982-2011. Stilt 61, 3–18 (2012).

    Google Scholar 

  21. Clemens, R. S. et al. Continental-scale decreases in shorebird populations in Australia. Emu. 116, 119–135 (2016).

    Article  Google Scholar 

  22. Iwamura, T. et al. Migratory connectivity magnifies the consequences of habitat loss from sea-level rise for shorebird populations. Proc. R Soc. B Biol. Sci. 280, 20130325 (2013).

    Article  Google Scholar 

  23. Barter, M. A. Shorebirds of the Yellow Sea: Importance, Threats and Conservation Status (Wetlands International-Oceana, 2002).

  24. Bamford, M., Watkins, D., Bancroft, W., Tischler, G. & Wahl, J. Migratory shorebirds of the East Asian-Austalasian Flyway: population estimates and internationally important sites Wetlands International-Oceana (2008).

  25. Thomas, G. H., Lanctot, R. B. & Szekely, T. Can intrinsic factors explain population declines in North American breeding shorebirds? A comparative analysis. Anim. Conserv. 9, 252–258 (2006).

    Article  Google Scholar 

  26. Murray, K. A., Arregoitia, L. D. V., Davidson, A., Di Marco, M. & Di Fonzo, M. M. I. Threat to the point: improving the value of comparative extinction risk analysis for conservation action. Global Change Biol. 20, 483–494 (2014).

    ADS  Article  Google Scholar 

  27. IUCN. IUCN Red List of Threatened Species. Version 2014.1, Available at: Accessed on 1 July 2014.

  28. Milton, D. A. & Harding, S. B. Death by a thousand cuts – the incremental loss of coastal high tide roosts for Shorebirds in Australia: Sandfly Creek Environmental Reserve, Central Queensland. Stilt 60, 22–33 (2011).

    Google Scholar 

  29. Nebel, S., Porter, J. L. & Kingsford, R. T. Long-term trends of shorebird populations in eastern Australia and impacts of freshwater extraction. Biol. Conserv. 141, 971–980 (2008).

    Article  Google Scholar 

  30. Piersma, T. et al. Simultaneous declines in summer survival of three shorebird species signals a flyway at risk. J. Appl. Ecol. 53, 479–490 (2016).

    Article  Google Scholar 

  31. Minton, C., Jessop, R., Collins, P. & Gosbell, K. in Status and Conservation of Shorebirds in the East Asian–Australasian Flyway. Proceedings of the Australasian Shorebirds Conference 13–15 December 2003, Canberra, Australia Wetlands International Global Series 18, International Wader Studies 17 (ed Straw, P.) 73–85 (2006).

  32. Rogers, K. G. & Gosbell, K. Demographic models for Red-necked Stint and Curlew Sandpiper. Stilt 50, 205–214 (2006).

    Google Scholar 

  33. Murray, N. J., Clemens, R. S., Phinn, S. R., Possingham, H. P. & Fuller, R. A. Tracking the rapid loss of tidal wetlands in the Yellow Sea. Front. Ecol. Environ. 12, 267–272 (2014).

    Article  Google Scholar 

  34. Seto, K. C., Guneralp, B. & Hutyra, L. R. Global forecasts of urban expansion to 2030 and direct impacts on biodiversity and carbon pools. Proc. Natl Acad. Sci. USA 109, 16083–16088 (2012).

    CAS  ADS  Article  Google Scholar 

  35. He, Q. et al. Economic development and coastal ecosystem change in China. Sci. Rep. 4, 5995 (2014).

    CAS  Article  Google Scholar 

  36. Strokal, M. et al. Increasing eutrophication in the coastal seas of China from 1970 to 2050. Mar. Pollut. Bull. 85, 123–140 (2014).

    CAS  Article  Google Scholar 

  37. Hu, L. et al. Occurrence and distribution of organochlorine pesticides (OCPs) in surface sediments of the Bohai Sea, China. Chemosphere 77, 663–672 (2009).

    CAS  ADS  Article  Google Scholar 

  38. Diaz, R. J. & Rosenberg, R. Spreading dead zones and consequences for marine ecosystems. Science 321, 926–929 (2008).

    CAS  ADS  Article  Google Scholar 

  39. McIntyre, A. F. & Heath, J. A. Evaluating the effects of foraging habitat restoration on shorebird reproduction: the importance of performance criteria and comparative design. J. Coastal Conserv. 15, 151–157 (2011).

    Article  Google Scholar 

  40. Sripanomyom, S., Round, P. D., Savini, T., Trisurat, Y. & Gale, G. A. Traditional salt-pans hold major concentrations of overwintering shorebirds in Southeast Asia. Biol. Conserv. 144, 526–537 (2011).

    Article  Google Scholar 

  41. Choi, C.-Y. et al. Phenology of southward migration of shorebirds in the East Asian–Australasian Flyway and inferences about stop-over strategies. Emu. 116, 178–189 (2016).

    Article  Google Scholar 

  42. Rogers, D. I., Rogers, K. G., Gosbell, K. B. & hassell, C. J. Causes of variation in population monitoring surveys: insights from non-breeding counts in north-western Australia, 2004–2005. Stilt 50, 176–193 (2006).

    Google Scholar 

  43. Clemens, R. S., Kendall, B. E., Guillet, J. & Fuller, R. A. Review of Australian shorebird survey data, with notes on their suitability for comprehensive population trend analysis. Stilt 62, 3–17 (2012).

    Google Scholar 

  44. Royle, J. A. N-mixture models for estimating population size from spatially replicated counts. Biometrics 60, 108–115 (2004).

    MathSciNet  Article  Google Scholar 

  45. Kery, & Schaub, M. Bayesian Population Analysis Using WinBUGS Academic Press (2012).

  46. Plummer, M. JAGS: A Program for Analysis of Bayesian Graphical Models Using Gibbs Sampling Proceedings of the 3rd International Workshop on Distributed Statistical Computing, March 20–22, Vienna, Austria. ISSN 1609-395X (2003).

  47. Su, Y. & Yajima, M. R2jags: A package for running JAGS from R. R package version 0.03-11 (2013).

  48. R Foundation for Statistical Computing. R: A Language and Environment for Statistical Computing (R Foundation for Statistical Computing, 2014). Available at:

  49. Clemens, R. S., Herrod, A. & Weston, M. A. Lines in the mud; revisiting the boundaries of important shorebird areas. J. Nat. Conserv. 22, 59–67 (2014).

    Article  Google Scholar 

  50. Murray, N. J., Phinn, S. R., Clemens, R. S., Roelfsema, C. M. & Fuller, R. A. Continental scale mapping of tidal flats across East Asia using the Landsat archive. Remote Sens. 4, 3417–3426 (2012).

    ADS  Article  Google Scholar 

  51. NatureServe, B. I. a. Bird species distribution maps of the world. Version 5.0 BirdLife International (2015).

  52. ESRI. ArcGIS Desktop: Release 10.4.1. Redlands, California Environmental Systems Research Institute (2016).

  53. Marchant, S. & Higgins, P. J. Raptors to Lapwings, Vol 2 (Oxford University Press, 1993).

  54. Higgins, P. J. & Davies, S. J. J. F. Snipe to Pigeons, Vol 3 (Oxford University Press, 1996).

  55. Garnett, S. T., Szabo, J. K. & Dutson, G. The Action Plan for Australian Birds 2010, Vol 456 (CSIRO Publishing, 2011).

  56. Ericson, P. G. P. et al. Diversification of Neoaves: integration of molecular sequence data and fossils. Biol. Lett. 2, 543–U541 (2006).

    Article  Google Scholar 

  57. Jetz, W., Thomas, G. H., Joy, J. B., Hartmann, K. & Mooers, A. O. The global diversity of birds in space and time. Nature 491, 444–448 (2012).

    CAS  ADS  Article  Google Scholar 

  58. Rubolini, D., Liker, A., Garamszegi, L. Z., Moller, A. P. & Saino, N. Using the website to obtain robust phylogenies for avian comparative studies: a primer. Curr. Zoo. 61, 959–965 (2015).

    Article  Google Scholar 

  59. Paradis, E., Claude, J. & Strimmer, K. APE: analyses of phylogenetics and evolution in R language. Bioinformatics 20, 289–290 (2004).

    CAS  Article  Google Scholar 

  60. de Villemereuil, P., Wells, J. A., Edwards, R. D. & Blomberg, S. P. Bayesian models for comparative analysis integrating phylogenetic uncertainty. BMC Evol. Biol. 12, 102 (2012).

    Article  Google Scholar 

  61. Hooten, M. B. & Hobbs, N. T. A guide to Bayesian model selection for ecologists. Ecol. Monogr. 85, 3–28 (2015).

    Article  Google Scholar 

  62. Mutshinda, C. M., Finkel, Z. V. & Irwin, A. J. Which environmental factors control phytoplankton populations? A Bayesian variable selection approach. Ecol. Modell. 269, 1–8 (2013).

    Article  Google Scholar 

Download references


This work is only possible because of the efforts of hundreds of people who have counted shorebirds across Australia and New Zealand, and those who have collated and curated those data; we list these in Supplementary Note 1 with grateful thanks to additional people who do not appear on this list. For data contributions we are grateful to: Australasian Wader Studies Group, Bird Observers Club of Australia, BirdLife Australia and their Shorebirds 2020 team, BirdLife Western Australia, BirdLife South Australia, BirdLife Tasmania, Hunter Bird Observers Club, Monitoring Yellow Sea Migrants in Australia, Ornithological Society of New Zealand, Queensland Wader Study Group, Victorian Wader Study Group and Wetlands International. Financial support was provided by Australian Research Council Linkage grant LP100200418, a Future Fellowship to R.A.F., a Federation Fellowship to H.P.P., the Queensland Wader Study Group, the Department of Environment Heritage and Protection (Queensland), the Department of the Environment and the Port of Brisbane. C.J.H. was supported by the major funders of the Global Flyway Network, including BirdLife Netherlands (2007–2012), WWF Netherlands (2010–2014, 2016) and the Spinoza Premium of Netherlands Organization Prize for Scientific Research to Theunis Piersma (2014–2016).

Author information

Authors and Affiliations



C.E.S. and R.A.F. wrote the manuscript, with contribution from all authors. C.E.S. and N.J.M. conducted the statistical analyses. R.S.C., K.G., C.J.H., D.S.M., D.A.M., C.D.T.M., A.C.R., D.I.R., E.J.W. and R.J. contributed to data collation and interpretation. R.A.F., B.E.K., H.B.W. and H.P.P. conceived of and funded the research.

Corresponding author

Correspondence to Colin E. Studds.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Supplementary Information

Supplementary Figures, Supplementary Tables and Supplementary Note (PDF 643 kb)

Peer review file (PDF 285 kb)

Rights and permissions

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Studds, C., Kendall, B., Murray, N. et al. Rapid population decline in migratory shorebirds relying on Yellow Sea tidal mudflats as stopover sites. Nat Commun 8, 14895 (2017).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:

Further reading


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.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing