Survival and site fidelity of Piping Plovers on Long Island, New York

ABSTRACT.   The threatened Atlantic Coast population of Piping Plovers ( Charadrius melodus ) has not increased in recent years and remains 332 pairs short of the recovery goal of 2000 pairs. Habitat loss to development is a major threat to the population, and there has been interest in restoring nesting and foraging habitat. However, the demographic response of coastal Piping Plovers to either habitat loss or creation has not been documented. We estimated survival rates and site fidelity of a declining Piping Plover population on Long Island, New York, from 2001 to 2005 on a beach subject to human development and recreation. The mean annual adult survival was 0.703 ± 0.032 (SE) and was similar among years. Site fidelity during the period of territory establishment averaged 0.827 ± 0.069 (SE). Given this high site fidelity, ensuring the survival of adults is important for maintaining local populations. Although the 2002–2004 average was high, site fidelity was apparently lower in 2003 than in 2002. This decrease in site fidelity may have been related to several years of habitat loss and increasing predation of nests or chicks, as reported in a partly concurrent long-term study at our site. The species-level effect of local dispersal due to anthropogenic habitat loss depends on the fitness of dispersers, and is currently unknown for Piping Plovers.     

Breeding sites and winter site fidelity of Piping Plovers wintering in The Bahamas,a previously unknown major wintering area

Most of the known wintering areas of Piping Plovers (Charadrius melodus) are along the Atlantic and Gulf coasts of the United States and into Mexico, and in the Caribbean. However, 1066 threatened/endangered Piping Plovers were recently found wintering in The Bahamas, an area not previously known to be important for the species. Although representing about 27% of the birds counted during the 2011 International Piping Plover Winter Census, the location of their breeding site(s) was unknown. Thus, our objectives were to determine the location(s) of their breeding site(s) using molecular markers and by tracking banded individuals, identify spring and fall staging sites, and examine site fidelity and survival. We captured and color‐banded 57 birds in January and February 2010 in The Bahamas. Blood samples were also collected for genetic evaluation of the likely subspecies wintering in The Bahamas. Band re‐sightings and DNA analysis revealed that at least 95% of the Piping Plovers wintering in The Bahamas originated on the Atlantic coast of the United States and Canada. Re‐sightings of birds banded in The Bahamas spanned the breeding distribution of the species along the Atlantic coast from Newfoundland to North Carolina. Site fidelity to breeding and wintering sites was high (88–100%). Spring and fall staging sites were located along the Atlantic coast of the United States, with marked birds concentrating in the Carolinas. Our estimate of true survival for the marked birds was 0.71 (95% CI: 0.61–0.80). Our results indicate that more than one third of the Piping Plover population that breeds along the Atlantic coast winters in The Bahamas. By determining the importance of The Bahamas to the Atlantic subspecies of Piping Plovers, future conservation efforts for these populations can be better focused on where they are most needed.     

Seasonal abundance of nonbreeding Piping Plovers on a Georgia barrier island

ABSTRACT.   Although breeding populations of Piping Plovers are well studied, their winter distribution is less clear. We studied the seasonal abundance of nonbreeding Piping Plovers ( Charadrius melodus ) during the winters of 2003–2004 and 2004–2005 on Little St. Simons Island (LSSI), Georgia. Our objectives were to determine the relative abundance of individuals from three breeding populations at LSSI, and identify possible differences among populations in arrival time, winter movements, or departure time. We observed up to 100 Piping Plovers during peak migration, and approximately 40 plovers wintered at LSSI. From July 2004 to May 2005, approximately 20% of the Great Lakes breeding population used LSSI. Plovers were not present at LSSI during June. All breeding populations of Piping Plovers had similar patterns of temporal occurrence on LSSI, suggesting no need for population-specific management plans at this site. Our results suggest that LSSI is among the most important wintering sites on the Atlantic coast for Piping Plovers, especially for individuals from the endangered Great Lakes population.     

Nest‐site selection and demography of Wilson's Plovers on a North Carolina barrier island

Despite concerns about their population status, information about the habitat preferences, population size, and vital statistics of Wilson's Plovers (Charadrius wilsonia) is currently lacking. We compared habitat characteristics of nest sites and unused sites and examined factors affecting nest success on a barrier island in North Carolina in 2010 and 2011. We monitored 83 nests with cameras and added heart‐rate monitors in artificial eggs to 36 of these nests for a concurrent study of the effects of jet overflights; predator exclosures were placed around 17 of the nests with cameras. Wilson's Plovers used interdune areas, flats, and isolated dunelets on flats more than expected based on availability, and nests were located closer to dense vegetation than unused sites. Nests in interdune areas had higher daily survival rates than nests on flats, but distance to dense vegetation did not affect nest survival. Nests without cameras, heart‐rate monitors, or exclosures had a 35% predicted probability of hatching at least one egg. Exclosed nests had higher daily survival rates than nests without exclosures, but daily survival rates were lower for nests with cameras or heart‐rate monitors and for nests initiated later in the season. Daily survival rates also declined as nests aged. The predicted probability of fledging was 74%, resulting in a reproductive output of 0.78 fledglings/pair. Apparent annual adult survival was 77%, and the apparent annual survival rate for birds banded as chicks was 42%. Additional research is needed throughout the range of Wilson's Plovers to determine if populations are stable or decreasing, and to predict the productivity rates needed to maintain current populations. However, our results suggest that in our study area, predator removal and protection of sparsely vegetated overwash habitats will likely have the greatest impact on reproductive output.     

Identification and breeding of yearling Piping Plovers

ABSTRACT Age of first breeding is an important life history trait. Many Piping Plovers (Charadrius melodus) do not breed as yearlings, but little information is available concerning the age of first breeding. From 2000 to 2006, we marked 991 chicks in three areas in Saskatchewan, Canada, and subsequently determined when 102 (49 females and 53 males) first bred. Females bred significantly earlier, on average, than males. More females (68%) bred as yearlings than did males (41%; P= 0.04), with most others first nesting when 2‐yr old (29% of females and 50% of males). As expected from differences between the sexes in age of first breeding, younger females were more likely to pair with older males than were younger males with older females. Chicks that hatched early in the breeding season did not breed at an earlier age than those that hatched late in the year. Unlike older birds, juvenile Piping Plovers do not replace flight feathers during their first winter. As a result, 18 of 27 yearlings (67%) had worn outer primaries, whereas only one of 123 (1%) older birds had worn primaries. In addition, whereas 20 of 24 yearlings (83%) retained a few buff‐tipped median coverts, none of 119 known older birds had such coverts. As a result, we were able to identify all yearlings by their worn primaries, buff‐tipped median wing coverts, or both. Wing lengths of yearling Piping Plovers were 3% shorter than those of older birds, presumably due to wear. Because there is no evidence of differences in adult survival rates between the sexes and breeding habitat is available, we speculate that fewer yearling males than females breed because primary wear may reduce the ability of yearling males to perform aerial breeding displays.     

Chick mortality leads to male‐biased sex ratios in endangered Great Lakes Piping Plovers

Few investigators have studied the offspring sex ratios of monomorphic shorebirds because visually determining the sex of juveniles is not possible. We investigated the ontogeny of an observed male‐biased adult sex ratio in the federally endangered Great Lakes population of Piping Plovers (Charadrius melodus). We determined sex ratios at hatching, banding ( = 9.0 d old), and fledging (23 d old) to determine if the bias arises during the pre‐fledging period and, if so, at what stage. For three consecutive years (2012–2014), we used a molecular technique to determine the sex of 307 chicks and followed individuals to a stage where survival to fledging could be inferred. Within fully‐sexed broods at hatching, the average proportions of male chicks (2012–2014) were 0.47, 0.58, and 0.54, respectively. At banding, the sex ratio remained unbiased in 2012 (0.51), but was male‐biased in 2013 (0.59) and 2014 (0.57). Overall, the sex ratio did not differ significantly from parity at fledging in 2012, but did differ during 2013 (P = 0.01) and 2014 (P = 0.03). Using logistic regression models fit using Bayesian inference, we found strong support for a sex effect on chick survival to fledging age, with higher male than female survival (μ_male = 0.83 [95% credible interval: 0.75–0.90]; μ_female = 0.71 [0.61–0.80]). These results suggest that the male‐biased adult sex ratio in Piping Plovers arises, in part, due to differential survival during the pre‐fledging period. This difference did not result from female chicks hatching later in the season or weighing less at banding than male chicks, factors that could potentially affect the likelihood of survival. Future investigations into possible behavioral‐ or weather‐related influences on sex‐specific survival are needed. Our results have important implications for (1) identifying management efforts needed to increase recruitment given female‐biased chick mortality, and (2) conducting population viability analyses, which frequently assume an unbiased fledgling sex ratio.     

Nest‐site selection by Interior Least Terns and Piping Plovers at managed,off‐channel sites along the Central Platte River in Nebraska,USA

Given the high productivity of Interior Least Terns (Sternula antillarum athalassos) and Piping Plovers (Charadrius melodus) on constructed off‐channel nesting sites along the central Platte River in Nebraska, USA, and the possibility of creating similar habitats at other locations in their breeding range, understanding how these species use off‐channel nesting habitats is important. We used data collected along the central Platte River in Nebraska, USA, over a 15‐year period (2001–2015), and a discrete‐choice modeling framework to assess the effects of physical site attributes and inter‐ and intraspecific associations on off‐channel nest‐site selection by Interior Least Terns and Piping Plovers. We found that Piping Plovers avoided nesting near each other, whereas colonial Interior Least Terns selected nest sites near those of conspecifics. In addition, the relative probability of use for both species was maximized when distance to the nearest predator perch was ≥ 150 m and elevation above the waterline was ≥ 3 m. Probability of use for nesting by Interior Least Terns increased as distance to water increased, whereas the probability of use by Piping Plovers was maximized when distance to water was ~50 m. Our results suggest that important features of constructed, off‐channel nesting sites for both species should include no potential predator perches within 150 m of nesting habitat and nesting areas at least 3 m above the waterline. Efficient site designs for Interior Least Terns would be circular, maximizing the area of nesting habitat away from the shoreline, whereas an effective site design for Piping Plovers would be more linear, maximizing the area of nesting habitat near the waterline. An efficient site design for both species would be lobate, incorporating centralized nesting habitat for Interior Least Terns and increased access to foraging areas for nesting and brood‐rearing Piping Plovers.     

State uncertainty models and mark‐resight models for understanding non‐breeding site use by Piping Plovers

Conservation of beach‐nesting medium‐distance migrants has focused on breeding areas because protection of nests is more tractable than protection of non‐breeding habitat. As breeding ground management has encountered diminishing returns, interest in understanding threats in non‐breeding areas has increased. However, robust estimates of non‐breeding demographic rates and abundance are generally lacking, hindering the study of limiting factors. Estimating such rates is made more difficult by complex population dynamics at non‐breeding sites. In South Carolina, endangered Piping Plovers Charadrius melodus start arriving in July and some depart prior to December (the autumn‐only population) while others remain through at least March (the wintering population). State uncertainty capture‐mark‐recapture models provide a means for estimating vital rates for such co‐occurring populations. We estimated the proportion of the population entering the study area per survey (entry probability) and proportion remaining per survey (persistence rate) for both populations during autumn, and abundance of the wintering population, at four sites in South Carolina in 2006/7 and 2007/8, taking advantage of birds previously colour‐ringed on the breeding grounds. We made fairly precise estimates of entry and persistence rates with small sample sizes. Cumulative entry probability was ~50% by the end of July and reached 95% for both populations by October. Estimated stopover duration for birds in the autumn‐only population was 35 days in year 1 and 42 days in year 2. We estimated a wintering super‐population size of 71 ± 16 se birds in the first year and 75 ± 16 in the second. If ringing programmes on the breeding grounds continue, standardized resighting surveys in the non‐breeding period and mark‐recapture models can provide robust estimates of entry and persistence rates and abundance. Habitat protection intended to benefit non‐breeding Piping Plovers at our coastal sites should be in effect by late summer, as many birds are resident from July to the end of winter.     

Colored plastic and metal leg bands do not affect survival of Piping Plover chicks

ABSTRACT Leg bands are commonly used to mark shorebird chicks as young as 1‐d old, but little is known about the possible impacts of bands on survival of prefledging shorebirds. We used a mark‐recapture framework to assess the impact of bands and banding‐related disturbance on prefledging survival in a federally endangered population of Piping Plovers (Charadrius melodus) breeding in the Great Lakes region from 2000 to 2008. We banded approximately 96% of all surviving chicks hatched prior to fledging, typically between 5 and 15 d of age. We used a multistate approach in program MARK whereby individuals contributed data as unbanded chicks before capture (N= 1073) and as banded chicks afterward (N= 780). The cumulative probability of surviving through 24 d of age was 0.63 and did not differ between banded and unbanded chicks. In addition, we found a positive effect of banding‐related disturbance on survival up to 3 d following banding (β= 0.60 CI: 0.17–1.02), possibly due to increased postbanding vigilance on the part of chicks and adults. Our results indicate that banding has no detrimental effect on survival of Piping Plover chicks prior to fledging and that current capture and banding methods are appropriate for this endangered species.     

Prebreeding survival of Roseate Terns Sterna dougallii varies with sex,hatching order and hatching date

Unequal sex ratios can reduce the productivity of animal populations and are especially prevalent among endangered species. A cohort of 333 Roseate Tern Sterna dougallii chicks at a site where the adult sex ratio was skewed towards females was sexed at hatching and followed through fledging and return to the breeding area, and subsequently during adulthood. The entire regional metapopulation was sampled for returning birds. Prebreeding survival (from fledging to age 3 years) was lower in males than in females, but only among B‐chicks (second in hatching order). Prebreeding survival also declined with hatching date. The proportion of females in this cohort increased from 54.6% at hatching to 56.2% at fledging and to an estimated 58.0% among survivors at age 3 years. This was more than sufficient to explain the degree of skew in the sex ratio of the adult population, but changes in this degree of skew during the study period make it difficult to identify the influence of a single cohort of recruits. Many studies of prebreeding survival in other bird species have identified effects of sex, hatching order or hatching date, but no previous study has tested for effects of all three factors simultaneously.     

Breeding ecology of Kentish Plover Charadrius alexandrinus in an extremely hot environment

Capsule Hot environments are associated with more biparental care, high nest‐site fidelity and low mate fidelity.

Aims To investigate the breeding ecology and parental behaviour of Kentish Plovers in an extremely hot environment. Kentish Plovers have an unusually diverse breeding system in which the frequencies of biparental, female‐only and male‐only care vary between populations. A common, but rarely tested, explanation for such a variation is local adaptation: birds exhibit social traits that are adaptive to their breeding environment. In particular, we investigated the effect of a hot environment on breeding success, distribution of care types, and mate and site fidelity.

Methods A breeding population of approximately 200 pairs of Kentish Plovers was investigated in 2005 and 2006 at Al Wathba Wetland near Abu Dhabi in the United Arab Emirates.

Results We found high nest‐site fidelity, low mate fidelity and more biparental care in Al Wathba than in most temperate zone populations of Kentish Plovers.

Conclusions Our results are consistent with the argument that a harsh environment can select for biparental care. However, further studies are warranted to distinguish between alternative hypotheses for the different distribution of social behaviours of breeding populations.     

Arrival times,laying dates,and reproductive success of Snowy Plovers in two habitats in coastal northern California

ABSTRACT Habitat quality, as indexed by the reproductive success of individuals, can greatly influence population growth, especially for rare species near the limits of their range. Along the Pacific coast, the Snowy Plover (Charadrius alexandrinus nivosus) is a threatened species that, in recent years, has been breeding on both riverine gravel bars and ocean beaches in northern California. From 2001 to 2009, we compared the habitat characteristics, breeding phenology, reproductive success, and abundance of Western Snowy Plovers occupying these two habitats. Similar percentages of yearling and adult plovers returned to gravel bars and beaches, but plovers breeding on gravel bars arrived and initiated first clutches 2–3 weeks later than those breeding on beaches. Despite this delay, however, the mean annual fledging success of plovers on gravel bars (1.4 ± 0.4 [SD]) was double that on beaches (0.7 ± 0.3). Differences in cumulative reproductive success produced a stronger pattern. By their sixth year, males on gravel bars had fledged 14.5 ± 2.1 chicks, more than four times the number of young fledged by males on beaches (3.3 ± 3.1). Over 9 years, local population size decreased by about 75%, coincident with a shift in breeding distribution away from high‐quality gravel bars to ocean beaches. This unexpected population decline and shift to poorer quality beaches may have been related to occasional low survival of plovers that over‐winter exclusively on beaches in our study area. Consistently low productivity of plovers breeding on ocean beaches suggests the need for intensified management to ameliorate the negative impacts of predation and human activity on the recovery of this population.     

Mountain Plovers in Oklahoma: distribution, abundance, and habitat use

ABSTRACT.   Mountain Plover ( Charadrius montanus ) populations are inefficiently sampled by Breeding Bird Surveys. As a result, targeted sampling of select populations of this species (with an estimated global population of 11,000–14,000 birds) can be valuable. Our objectives were to determine the breeding distribution and estimate the size of the Mountain Plover population in Oklahoma. We conducted a randomized point count survey in an area where Mountain Plovers were previously known to breed and conducted additional surveys over a larger area to better delimit the distribution. We used a removal model to estimate detection probability for raw counts obtained from 1104 point counts in 2004 and 2005, and derived a state-level population estimate using the detection-adjusted counts. Mountain Plovers used flat, bare, cultivated fields for nesting, and their distribution was closely tied to the presence of clay loam soils. We estimated that at least 68–91 Mountain Plovers bred in Oklahoma in 2004–2005. The low breeding density we observed may be due to the location of our study area near the southeastern edge of the breeding range of these plovers, the low-quality habitat provided by cultivated landscapes, or a combination of factors. Because the number of birds is small, the status of the Oklahoma population is not likely to have a large effect on the global population. However, additional information is needed to help determine if cultivated landscapes represented population sources or sinks.     

Estimating survival of precocial chicks during the prefledging period using a catch-curve analysis and count-based age-class data

ABSTRACT.   Estimating reproductive success for birds with precocial young can be difficult because chicks leave nests soon after hatching and individuals or broods can be difficult to track. Researchers often turn to estimating survival during the prefledging period and, though effective, mark-recapture based approaches are not always feasible due to cost, time, and animal welfare concerns. Using a threatened population of Piping Plovers ( Charadrius melodus ) that breeds along the Missouri River, we present an approach for estimating chick survival during the prefledging period using long-term (1993–2005), count-based, age-class data. We used a modified catch-curve analysis, and data collected during three 5-day sampling periods near the middle of the breeding season. The approach has several ecological and statistical assumptions and our analyses were designed to minimize the probability of violating those assumptions. For example, limiting the sampling periods to only 5 days gave reasonable assurance that population size was stable during the sampling period. Annual daily survival estimates ranged from 0.825 (SD = 0.03) to 0.931 (0.02) depending on year and sampling period, with these estimates assuming constant survival during the prefledging period and no change in the age structure of the population. The average probability of survival to fledging ranged from 0.126 to 0.188. Our results are similar to other published estimates for this species in similar habitats. This method of estimating chick survival may be useful for a variety of precocial bird species when mark-recapture methods are not feasible and only count-based age class data are available.     

Brood provisioning rates and fledgling behavior of Cordilleran Flycatchers in southwestern Colorado

The behavior of young songbirds after fledging is one of the least understood phases of the breeding cycle, although parental provisioning rates and movement of fledglings are key to understanding life history evolution. We studied Cordilleran Flycatchers (Empidonax occidentalis) at two sites in southwestern Colorado, USA, from 2012 to 2017. We banded and sexed breeding adults to determine the relative contributions of males and females to nestling and fledgling care, and attached radio‐transmitters to nestlings to facilitate observations of brood behavior after fledging. Females made 60% and 78% of total observed feedings of nestlings and fledglings, respectively. Parental provisioning rates increased with nestling age, and per‐nestling provisioning rates increased with brood size. Parental provisioning rates declined just before fledging, then increased just after fledging. Fledging times of individuals in broods were asynchronous and concentrated during the late afternoon and early evening. Males stopped caring for fledglings before females even though this species is single‐brooded, with some late‐season broods being abandoned by males. Broods spent the first three weeks after fledging within 400 m of nests, after which they began to disperse. Most aspects of the breeding biology of Cordilleran Flycatchers in our study, including the duration of nestling and fledging periods, female‐dominated provisioning, and movement patterns of fledglings, were similar to those of other Empidonax species. However, the times when young fledged were not concentrated in the morning as reported in most other songbirds, and this result warrants additional study of the timing of fledging in ecologically and taxonomically similar species. The increased per‐nestling provisioning rate with increasing brood size was unexpected, and additional study is needed to determine if this increase results from a trade‐off between adult annual survival and productivity favoring increased provisioning of young in larger broods, or from the existence of high‐quality individuals where larger clutches and higher provisioning rates are linked.     

Behaviour of young Ringed Plovers Charadrius hiaticula and its relationship to growth and survival to reproductive age

The behaviour, growth and survival of Ringed Plover chicks were studied in 1974 at Mestersvig, northeast Greenland, and from 1973 to 1976 at Lindisfarne, northeast England. Post-fledging survival, dispersal and recruitment were also investigated for the Lindisfarne population. Growth rates were similar in both study areas, and to those reported from other sites. A diurnal rhythm in feeding activity was more evident in the Arctic than at temperate latitudes, despite continuous daylight in the former area. This was correlated with low nocturnal temperatures and prey availability. It is concluded that food supply did not limit growth or chick survival in either study area. Brooding decreased progressively during the pre-fledging period; the relationship of brooding period to age, environmental conditions and area was investigated. The adaptations of feeding and brooding behaviour for arctic and temperate breeding Ringed Plovers are discussed. Survival from hatching to fledging varied between 40% and 60% in different areas and years, and at least 59% of birds survived from fledging to about one year old. Minimum survival from one to two years old was only 57%. but year-to-year survival of older birds was higher, that of breeding adults being at least so?;. Most birds returned to the breeding area and attempted to breed when one year old. The extent of dispersal from Lindisfarne and the wintering areas of the Lindisfarne-breeding birds are investigated.     

Golden Plover Pluvialis apricaria breeding success on a moor managed for shooting Red Grouse Lagopus lagopus

Capsule The best estimate of breeding success was a mean of 0.57 fledglings per pair, which when combined with adult survival rates, successfully explained the observed population trend.

Aims To quantify Golden Plover breeding success on a moor managed for shooting Red Grouse Lagopus lagopus.

Methods An intensive study recorded the fate of individual Golden Plover nests and, using radiotelemetry, chicks. The factors associated with mortality were examined, allowing the construction of a model of breeding success. Adult survival was estimated from return rates of colour-ringed birds.

Results Estimated rates of daily nest survival during laying (0.8636) were significantly lower than during incubation (0.9913). The daily survival rate of chicks less than nine days (0.8868) was significantly lower than for older chicks (0.9792). A population model based on these parameters overestimated the rate of nest losses, but accurately described brood survival and fledging success. Although predation rates were low, poor survival of young chicks through starvation or exposure suggest other factors were limiting breeding success at the study site.

Conclusions Predation rates of Golden Plover nests and chicks can be low on moorlands managed for shooting Red Grouse. However, in the absence of predation, other factors may still reduce chick survival and limit breeding success.     

Abundance of Snowy and Wilson's Plovers in the lower Laguna Madre region of Texas

ABSTRACT.   Snowy Plovers ( Charadrius alexandrinus ) and Wilson's Plovers ( C. wilsonia ) are shorebird species of increasing conservation concern, with populations apparently declining in North America. However, estimates of current populations are needed before initiating long-term monitoring or planning. In 2004, we estimated abundance of breeding Snowy and Wilson's plovers in the lower Laguna Madre region of Texas using occupancy abundance estimation. We made repeated visits to survey plots from April to June, recording the number of adults of both species observed and the amount of suitable breeding habitat within each plot. We considered Bayesian occupancy abundance models with and without habitat covariates to explain the abundance of both species. For both Snowy and Wilson's plovers, the number of birds counted in each plot was influenced by the amount of suitable breeding habitat within the plot (Snowy Plover α_habitat= 0.52, SD = 0.10, 95% CI = 0.33–0.71; Wilson's Plover α_habitat= 0.48, SD = 0.12, 95% CI = 0.24–0.71). Using the habitat covariate models for each species, we estimated that 416 adult Snowy Plovers (95% CI = 394–438) and 279 adult Wilson's Plovers (95% CI = 262–296) were present in our study area. Our results illustrate the use of a relatively new method for abundance estimation, and indicate that the lower Laguna Madre region of Texas is an important breeding area for both Snowy and Wilson's plovers. Given the documented and suspected population declines for Snowy and Wilson's plovers, we recommend protection of their breeding habitats along the coast of Texas from development and degradation resulting from unregulated use.     

Space use by Great Lakes Piping Plovers during the breeding season

ABSTRACT.   Identifying and protecting breeding habitat for imperiled species requires an understanding of the spatial and temporal movements of breeding individuals. During the 2003 and 2004 breeding seasons, we examined space use by Piping Plovers ( Charadrius melodus ) in the federally endangered Great Lakes population. We used coordinate geometry to estimate home range sizes of individual birds and examined relationships between home range size and breeding stage (incubation versus chick rearing), year, sex, number of locations, minimum plover age, distance to the nearest nest, and human beach use (high, medium, or low). The mean size of home ranges of Piping Plovers that fledged at least one chick was 2.9 ± 0.5 (SE) ha (range = 0.4–11.2 ha), and the mean linear beach distance traversed was 475 ± 53 m (range = 130–1435 m). Individuals used 3 times more beach area and 1.5 times more shoreline distance in 2003 than in 2004. Females used smaller areas than males overall and during chick rearing. Home ranges were smallest on beaches with low public use, suggesting that human disturbance may cause greater movement by individual plovers and that larger protected areas may be warranted on beaches frequented by the public to minimize disturbance to breeding birds. Our results demonstrate that nesting Great Lakes Piping Plovers occupy relatively small ranges and, therefore, that even relatively small areas of suitable habitat can have a high conservation value for this endangered population. However, the total area of habitat used varied substantially among individuals, and this should be considered when protecting habitat for the species.