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Michael J. Anteau

Publications and source records attributed to Michael J. Anteau.

At least 55 records · Page 3Linked to original sources

Synergistic interaction of climate and land-use drivers alter the function of North American, Prairie-pothole Wetlands

Prairie-pothole wetlands provide the critical habitat necessary for supporting North American migratory waterfowl populations. However, climate and land-use change threaten the sustainability of these wetland ecosystems. Very few experiments and analyses have been designed to investigate the relative impacts of climate and land-use change drivers, as well as the antagonistic or synergistic interactions among these drivers on ecosystem processes. Prairie-pothole wetland water budgets are highly dependent on atmospheric inputs and especially surface runoff, which makes them especially susceptible to changes in climate and land use. Here, we present the history of prairie-pothole climate and land-use change research and address the following research questions: 1) What are the relative effects of climate and land-use change on the sustainability of prairie-pothole wetlands? and 2) Do the effects of climate and land-use change interact differently under different climatic conditions? To address these research questions, we modeled 25 wetland basins (1949–2018) and measured the response of the lowest wetland in the watershed to wetland drainage and climate variability. We found that during an extremely wet period (1993–2000) wetland drainage decreased the time at which the lowest wetland reached its spill point by four years, resulting in 10 times the amount of water spilling out of the watershed towards local stream networks. By quantifying the relative effects of both climate and land-use drivers on wetland ecosystems our findings can help managers cope with uncertainties about flooding risks and provide insight into how to manage wetlands to restore functionality

Sustainability↗

Typha (cattail) invasion in North American wetlands: Biology, regional problems, impacts, ecosystem services, and management

Typha is an iconic wetland plant found worldwide. Hybridization and anthropogenic disturbances have resulted in large increases in Typha abundance in wetland ecosystems throughout North America at a cost to native floral and faunal biodiversity. As demonstrated by three regional case studies, Typha is capable of rapidly colonizing habitats and forming monodominant vegetation stands due to traits such as robust size, rapid growth rate, and rhizomatic expansion. Increased nutrient inputs into wetlands and altered hydrologic regimes are among the principal anthropogenic drivers of Typha invasion. Typha is associated with a wide range of negative ecological impacts to wetland and agricultural systems, but also is linked with a variety of ecosystem services such as bioremediation and provisioning of biomass, as well as an assortment of traditional cultural uses. Numerous physical, chemical, and hydrologic control methods are used to manage invasive Typha, but results are inconsistent and multiple methods and repeated treatments often are required. While this review focuses on invasive Typha in North America, the literature cited comes from research on Typha and other invasive species from around the world. As such, many of the underlying concepts in this review are relevant to invasive species in other wetland ecosystems worldwide.

Wetlands↗

Demographic responses of least terns and piping plovers to the 2011 Missouri River flood—A large-scale case study

A catastrophic flood event on the Missouri River system in 2011 led to substantial changes in abundance and distribution of unvegetated sand habitat. This river system is a major component of the breeding range for interior Least terns ( Sternula antillarum ; “terns”) and piping plovers ( Charadrius melodus ; “plovers”), both of which are Federally listed ground-nesting birds that prefer open, unvegetated sand and gravel nesting substrates on sandbars and shorelines. The 2011 flood inundated essentially all tern and plover nesting habitat during 2011, but it had potential to generate post-flood habitat conditions that favored use by terns and plovers in subsequent years. We compared several tern and plover demographic parameters during the pre-flood and post-flood periods on the Garrison Reach and Lake Sakakawea, North Dakota, to determine how this event influenced these species (both species on the Garrison Reach, and plovers only on Lake Sakakawea). The principal parameters we measured (nest survival, chick survival, and breeding population) showed spatial and temporal variation typical of opportunistic species occupying highly variable habitats. There was little evidence that nest survival of least terns differed between pre- and post-flood. During 2012 when habitat was most abundant on the Garrison Reach and Lake Sakakawea, piping plover nest survival was higher than in any other year in the study, but returned to rates comparable to pre-flood years in 2013. Chick survival for terns on the Garrison Reach and plovers on Lake Sakakawea showed a similar pattern to plover nest survival, with the 2012 rate exceeding all other years of the study, and the remaining pre-flood and post-flood years being generally similar but slightly higher in post-flood years. However, plover chick survival on the Garrison Reach in 2012 was similar to pre-flood years, and increased annually thereafter to its highest rate in 2014. Although wide confidence intervals precluded firm conclusions about flood effects on breeding populations, the general pattern suggested lower populations of plovers but higher populations of least terns immediately after the flood. Despite near total absence of breeding habitat on either study area during the flood of 2011, populations of both species persisted after the flood due to their propensity to disperse and/or forgo breeding for at least a year. Tern and plover populations have similarly persisted and recovered after the flood, but their mechanisms for persistence likely differ. Data on tern dispersal is generally lacking, but they are thought to show little fidelity to their natal grounds, have a propensity to disperse potentially long distances, and routinely forgo breeding until their second year, thus a lost opportunity to breed in a given area may be easily overcome. Plovers exhibit stronger demographic ties to the general area in which they previously nested, yet they occupy much broader nesting habitat features than terns and exploit three major landforms in the Dakotas (free-flowing rivers, reservoir shorelines, and wetland shorelines). Consequently, dispersal to and from non-Missouri River habitats and potential to exploit non-traditional habitats likely sustained the Northern Great Plains population through the flood event. Terns and plovers normally occupy similar habitats on the Missouri River and both species experienced similar loss of a breeding season due to the flood. Persistence of these populations after the flood underscores the importance of understanding their unique demographic characteristics and the context within which the Missouri River operates.

North Dakota↗

Extreme climatic variability during migration invokes physiological and dietary plasticity among spring migrating ducks

Environmental stochasticity encountered during migration can have negative consequences for individuals and population demographics through direct reductions in survival or cross-seasonal impacts. We took advantage of substantial interannual variation in spring migration conditions over a 4 year field study to examine physiological and dietary variation among two species of migrant ducks. We collected female Lesser Scaup ( Aythya affinis (Eyton, 1838)) and Blue-winged Teal ( Spatula discors (Linnaeus, 1766)) during spring migration and measured lipid and protein reserves, an index of recent lipid metabolism based on concentrations of lipid metabolites in plasma, and diets. We documented systematic interannual variation among these metrics in both species, contrasting primarily the warmest, earliest spring and the coldest, latest spring. Lesser Scaup had reduced lipid and protein reserves and consumed less energy-rich prey during the coldest and latest spring but showed no interannual variation in the index of lipid metabolism. Blue-winged Teal similarly had reduced protein reserves in the cold, late spring but maintained constant lipid reserves among years, likely facilitated by increased consumption of energy-rich seeds reflected in diets and lipid metabolism. Our results reveal impacts of environmental stochasticity on migrants and suggest that recruitment may be impacted by variable conditions encountered during migration during extreme weather events.

South Dakota↗

Density and success of upland duck nests in native‐ and tame‐seeded conservation fields

The Conservation Reserve Program (CRP) generates substantial benefits to continental duck populations by providing grassland nesting habitat in rested cropland. Seeding mixes of CRP grasslands vary among numerous conservation practices, but one contrast of interest in the Prairie Pothole Region is the use of introduced, or “tame” versus native grass. Although the benefits of CRP to duck populations are well‐known, relative values of these planting practices to nesting ducks have received little attention. Understanding differences in benefits to ducks due to planting practices would aid in prioritizing and selecting management practices for CRP and other restoration activities. We evaluated nest survival and density of ducks nesting in tame‐ and native‐seeded CRP fields in 36 study areas in the Prairie Pothole Region of North Dakota and South Dakota, USA, during 2002–2003. We searched for duck nests in 209 fields totaling 5,386 ha and found 2,941 nests. We found no support for differences in nest survival for any upland‐nesting duck species between fields seeded to tame versus native grass based on a design and analyses that accounted for spatial and temporal variation. Additionally, nest densities, adjusted for nest survival rates, of all duck species were similar between tame‐seeded and native‐seeded fields. We conclude that benefits to nesting ducks from native‐grass seeding practices of CRP were similar to those of tame‐grass seeding practices. Although there may be other reasons to plant native seed mixes when establishing CRP tracts (e.g., native pollinators or insects, other wildlife species, etc.), our study suggests that duck nesting density and nest survival are not among those reasons.

North Dakota, South Dakota↗

Temporal variation in survival and recovery rates of lesser scaup: A response

We recently analyzed long-term (1951–2011) continental band-recovery data from lesser scaup ( Aythya affinis ) and demonstrated that harvest rates declined through time, but annual survival rates exhibited no such trends; moreover, annual harvest and survival rates were uncorrelated for all age-sex classes. We therefore concluded that declining fecundity was most likely responsible for recent population declines, rather than changes in harvest or survival. Lindberg et al. ( 2017 ) critiqued our conclusions, arguing that we did little more than fail to reject a null hypothesis of compensatory mortality, postulated ecologically unrealistic changes in fecundity, and failed to give sufficient consideration to additive harvest mortality. Herein, we re-summarize our original evidence indicating that harvest has been compensatory, or at most weakly additive, and demonstrate that our analysis had sufficient power to detect strongly additive mortality if it occurred. We further demonstrate that our conclusions were not confounded by population size, band loss, or individual heterogeneity, as suggested by Lindberg et al. ( 2017 ), and we provide additional support for our conjecture that low fecundity played a major role in declining scaup populations during 1983–2006. We therefore reiterate our original management recommendations: given low harvest rates and lack of demonstrable effect on scaup survival, harvest regulations could return to more liberal frameworks, and waterfowl biologists should work together to continue banding lesser scaup and use these data to explore alternative hypotheses to identify the true ecological causes of population change, given that it is unlikely to be excessive harvest.

Journal of Wildlife Management↗

Long-term spatial heterogeneity in mallard distribution in the Prairie pothole region

The Prairie Pothole Region (PPR) of north-central United States and south-central Canada supports greater than half of all breeding mallards ( Anas platyrhynchos ) annually counted in North America and is the focus of widespread conservation and research efforts. Allocation of conservation resources for this socioeconomically important population would benefit from an understanding of the nature of spatiotemporal variation in distribution of breeding mallards throughout the 850,000 km 2 landscape. We used mallard counts from the Waterfowl Breeding Population and Habitat Survey to test for spatial heterogeneity and identify high- and low-abundance regions of breeding mallards over a 50-year time series. We found strong annual spatial heterogeneity in all years: 90% of mallards counted annually were on an average of only 15% of surveyed segments. Using a local indicator of spatial autocorrelation, we found a relatively static distribution of low-count clusters in northern Montana, USA, and southern Alberta, Canada, and a dynamic distribution of high-count clusters throughout the study period. Distribution of high-count clusters shifted southeast from northwestern portions of the PPR in Alberta and western Saskatchewan, Canada, to North and South Dakota, USA, during the latter half of the study period. This spatial redistribution of core mallard breeding populations was likely driven by interactions between environmental variation that created favorable hydrological conditions for wetlands in the eastern PPR and dynamic land-use patterns related to upland cropping practices and government land-retirement programs. Our results highlight an opportunity for prioritizing relatively small regions within the PPR for allocation of wetland and grassland conservation for mallard populations. However, the extensive spatial heterogeneity in core distributions over our study period suggests such spatial prioritization will have to overcome challenges presented by dynamic land-use and climate patterns in the region, and thus merits additional monitoring and empirical research to anticipate future population distribution. Published 2017. This article is a U.S. Government work and is in the public domain in the USA.

Wildlife Society Bulletin↗

Prerequisites for understanding climate-change impacts on northern prairie wetlands

The Prairie Pothole Region (PPR) contains ecosystems that are typified by an extensive matrix of grasslands and depressional wetlands, which provide numerous ecosystem services. Over the past 150 years the PPR has experienced numerous landscape modifications resulting in agricultural conversion of 75–99 % of native prairie uplands and drainage of 50–90 % of wetlands. There is concern over how and where conservation dollars should be spent within the PPR to protect and restore wetland basins to support waterbird populations that will be robust to a changing climate. However, while hydrological impacts of landscape modifications appear substantial, they are still poorly understood. Previous modeling efforts addressing impacts of climate change on PPR wetlands have yet to fully incorporate interacting or potentially overshadowing impacts of landscape modification. We outlined several information needs for building more informative models to predict climate change effects on PPR wetlands. We reviewed how landscape modification influences wetland hydrology and present a conceptual model to describe how modified wetlands might respond to climate variability. We note that current climate projections do not incorporate cyclical variability in climate between wet and dry periods even though such dynamics have shaped the hydrology and ecology of PPR wetlands. We conclude that there are at least three prerequisite steps to making meaningful predictions about effects of climate change on PPR wetlands. Those evident to us are: 1) an understanding of how physical and watershed characteristics of wetland basins of similar hydroperiods vary across temperature and moisture gradients; 2) a mechanistic understanding of how wetlands respond to climate across a gradient of anthropogenic modifications; and 3) improved climate projections for the PPR that can meaningfully represent potential changes in climate variability including intensity and duration of wet and dry periods. Once these issues are addressed, we contend that modeling efforts will better inform and quantify ecosystem services provided by wetlands to meet needs of waterbird conservation and broader societal interests such as flood control and water quality.

Wetlands↗

Demographics and movements of least terns and piping plovers in the Central Platte River Valley, Nebraska

The Central Platte River Valley provides breeding habitat for a variety of migratory birds, including federally endangered interior least terns ( Sternula antillarum ; least tern) and threatened piping plovers ( Charadrius melodus ). Since 2009, researchers have collected demographic data on both species that span their lifecycle (that is, from egg laying through survival of adults). Demographic data were used to estimate vital rates (for example, nest survival, chick survival, and so on) for both species and assess how these vital rates were related to type and age of nesting habitat. Nest survival of both species was unrelated to the age of the site a nest was initiated on. Piping plover chick survival to fledging age was not related to the age of the site it was hatched at, however, the probability of a least tern chick surviving to fledging was higher at older sites. In general there were fewer piping plover nests than least tern nests found at sites created through either the physical construction of a new site or new vegetation management regimes, during 2009–14. Mean daily least tern nest survival was 0.9742 (95-percent confidence interval [CI]: 0.9692–0.9783) and cumulative nest survival was 0.59 (95-percent CI: 0.53–0.65). Mean daily least tern chick survival was 0.9602 (95-percent CI: 0.9515–0.9673) and cumulative survival to fledging was 0.54 (95-percent CI = 0.48–0.61). Annual apparent survival rates were estimated at 0.42 (95-percent CI = 0.22–0.64) for adult least terns nesting in the Central Platte River Valley and an apparent survival rate of 0.14 (95-pecent CI = 0.04–0.41) for juvenile least terns. The number of least tern nests present at sites created during 2009–14 was associated with the age of the site; more least tern nests were associated with older sites. During 2009–14, there were four (less than 1 percent of all chicks marked) least tern chicks hatched from the Central Platte River Valley that were subsequently captured on nests as adults. Two of these least terns returned to nest at the same site they had hatched from. Ten instances were documented in which an adult least tern could either switch to nest at a new location or remain at the previous location with the onset of a new year. In five (50 percent) of these instances, least terns returned to nest on the site where they had nested in a previous year. For piping plovers, mean daily apparent nest survival was 0.9880 (95-pecent CI: 0.9836–0.9912) and cumulative nest survival was 0.66 (95-pecent CI: 0.57–0.74). Mean daily piping plover chick survival was 0.9621 (95-pecent CI: 0.9514–0.9706) and cumulative survival to fledging was 0.46 (95-pecent CI = 0.37– 0.56). The annual apparent survival estimate for adult piping plovers nesting in the Central Platte River Valley was 0.76 (95-pecent CI = 0.65–0.85) and was 0.20 (95-pecent CI = 0.14–0.29) for juvenile piping plovers. The number of piping plover nests present at sites created through either the physical construction of a new site or new vegetation management regimes was also associated with site age, with more piping plover nests associated with older sites; however, in general there were fewer piping plover nests found at created sites than least tern nests. Only first-year adult piping plovers were observed on sites in the first year of availability, whereas older sites had a higher proportion of after-first-year adult piping plovers than first-year adult piping plovers. Twelve piping plover chicks (approximately 3 percent of all chicks marked) hatched from the Central Platte River Valley and were subsequently documented on nests as adults. All piping plovers returned to nest on different sites from the one on which they hatched. A total of 45 instances were documented in which an adult plover could either switch to nest at a new location or remain at the previous location with the onset of a new year. In 39 instances (87 percent), the adult nested on the same site as its prior documented nesting attempt and in 6 of these instances the adult switched to a new nesting location between years. There were 13 of 75 uniquely identifiable piping plovers observed to renest (that is, initiate more than one nest in a season) during 2009–14; no renests were observed among uniquely identifiable least terns. In all but one case, piping plover renests were found at the same site as the first nest initiated that season. For birds that renested, the mean initiation date of the first nest was May 6 and the mean initiation date of the second nest was June 8. On average, renests were initiated 7.5 days plus or minus 7.3 (SD [standard deviation]) following the date the initial nesting attempt was ‘fated’ (considered either failed or hatched).

Nebraska↗

Temporal variation in survival and recovery rates of lesser scaup

Management of lesser scaup (Aythya affinis) has been hindered by access to reliable data on population trajectories and vital rates. We conducted a Bayesian analysis of historical (1951–2011) band-recovery data throughout North America to estimate annual survival and recovery rates for juvenile and adult male and female lesser scaup to determine if increasing harvest or declining survival rates have contributed to population changes and to determine if harvest has been primarily additive or compensatory. Annual recovery rates were low, ranging from 1% to 4% for adults and 2% to 10% for juveniles during most years, with trend models indicating that recovery rates have declined through time for all age–sex classes. Annual survival (mid-Aug to mid-Aug) averaged 0.402 (σ ̂ 0.043) for juvenile males, 0.416 (σ ̂ 0.067) for juvenile females, 0.689 (σ ̂ 0.109) for adult males, and 0.602 (σ ̂ 0.115) for adult females, where σ ̂ represents an estimate of annual process variation in each survival rate. Annual survival rates exhibited no evidence of long-term declines or negative correlations with annual recovery rates (i.e., an index of harvest intensity) for any age–sex class, suggesting that declining fecundity was the most likely explanation for population declines during 1975–2005. We conclude that hunting mortality played a minor role in affecting population dynamics of lesser scaup and waterfowl managers could take a less cautious approach in managing harvest, especially if recruiting or maintaining waterfowl hunters are viewed as important management objectives.

Journal of Wildlife Management↗

A Bayesian approach for temporally scaling climate for modeling ecological systems

With climate change becoming more of concern, many ecologists are including climate variables in their system and statistical models. The Standardized Precipitation Evapotranspiration Index (SPEI) is a drought index that has potential advantages in modeling ecological response variables, including a flexible computation of the index over different timescales. However, little development has been made in terms of the choice of timescale for SPEI. We developed a Bayesian modeling approach for estimating the timescale for SPEI and demonstrated its use in modeling wetland hydrologic dynamics in two different eras (i.e., historical [pre-1970] and contemporary [post-2003]). Our goal was to determine whether differences in climate between the two eras could explain changes in the amount of water in wetlands. Our results showed that wetland water surface areas tended to be larger in wetter conditions, but also changed less in response to climate fluctuations in the contemporary era. We also found that the average timescale parameter was greater in the historical period, compared with the contemporary period. We were not able to determine whether this shift in timescale was due to a change in the timing of wet–dry periods or whether it was due to changes in the way wetlands responded to climate. Our results suggest that perhaps some interaction between climate and hydrologic response may be at work, and further analysis is needed to determine which has a stronger influence. Despite this, we suggest that our modeling approach enabled us to estimate the relevant timescale for SPEI and make inferences from those estimates. Likewise, our approach provides a mechanism for using prior information with future data to assess whether these patterns may continue over time. We suggest that ecologists consider using temporally scalable climate indices in conjunction with Bayesian analysis for assessing the role of climate in ecological systems.

Ecology and Evolution↗

Is consolidation drainage an indirect mechanism for increased abundance of cattail in northern prairie wetlands?

In the Prairie Pothole Region of North America, disturbances to wetlands that disrupt water-level fluctuations in response to wet–dry climatic conditions have the potential to alter natural vegetative communities in favor of species that proliferate in stable environments, such as cattail ( Typha spp.). We evaluated the effect of water-level dynamics during a recent fluctuation in wet–dry conditions on cattail coverage within semipermanently and permanently ponded wetlands situated in watersheds with different land use and amounts of wetland drainage. We found that ponded water depth increase was significantly greater in wetlands where water levels were not near the spill point of the topographic basin, where banks were steeper, and in larger wetlands where past dry conditions had less influence on change in pond area. Proportion of the wetland covered by cattail was negatively correlated with increased water depth, bank slope and pond area. Our observations provide evidence that cattail coverage in prairie wetlands is regulated by water-level fluctuations and that land use surrounding the wetland might have an indirect effect on cattail coverage by altering water-level response to wet–dry climate conditions. For example, drainage of smaller wetlands into larger wetlands that are characterized by more permanent hydroperiods, leads to stabilized water levels near their spill point and is therefore a potential mechanism for increased cattail abundance in the northern prairie region.

North Dakota↗

Synchrony of Piping Plover breeding populations in the U.S. Northern Great Plains

Local populations that fluctuate synchronously are at a greater risk of extinction than those that do not. The closer the geographic proximity of populations, the more prone they are to synchronizing. Shorebird species select habitat broadly, and many breed across regions with diverse nesting habitat types. Under these conditions, nearby populations may experience conditions sufficiently different to prevent population synchrony, despite dispersal. In the U.S. Northern Great Plains, the Piping Plover ( Charadrius melodus ), federally listed as Threatened, is a migratory shorebird species that nests on the shorelines of rivers, reservoirs, and alkaline lakes. We assessed the degree to which local plover breeding population abundances were correlated (population synchrony), changed over time (population stability), and were influenced by environmental factors such as available habitat, precipitation, and within-season reservoir level rise. We found that the abundances of breeding populations nesting in riverine and reservoir habitats were the most synchronous, while populations nesting in alkaline lake habitats exhibited the greatest stability. Changes in local breeding population abundances were not explained by a single factor across habitat types. However, the abundances of local populations nesting in alkaline lake and river shoreline habitats were positively correlated with changes in nesting habitat availability. Our results suggest that dispersal among populations nesting in either river or reservoir and alkaline lake shoreline habitat may have an overall stabilizing effect on the persistence of the Great Plains Piping Plover metapopulation.

Condor↗

Consolidation drainage and climate change may reduce Piping Plover habitat in the Great Plains

Many waterbird species utilize a diversity of aquatic habitats; however, with increasing anthropogenic needs to manage water regimes there is global concern over impacts to waterbird populations. The federally threatened Piping Plover (Charadrius melodus; hereafter plovers) is a shorebird that breeds in three habitat types in the Prairie Pothole Region of North Dakota, South Dakota, and Canada: riverine sandbars; reservoir shorelines; and prairie wetlands. Water surface areas of these habitats fluctuate in response to wet-dry periods; decreasing water surface areas expose shorelines that plovers utilize for nesting. Climate varies across the region so when other habitats are unavailable for plover nesting because of flooding, prairie wetlands may periodically provide habitat. Over the last century, many of the wetlands used by plovers in the Prairie Pothole Region have been modified to receive water from consolidation drainage (drainage of smaller wetlands into another wetland), which could eliminate shoreline nesting habitat. We evaluated whether consolidation drainage and fuller wetlands have decreased plover presence in 32 wetlands historically used by plovers. We found that wetlands with more consolidation drainage in their catchment and wetlands that were fuller had a lower probability of plover presence. These results suggest that plovers could have historically used prairie wetlands during the breeding season but consolidation drainage and/or climate change have reduced available shoreline habitat for plovers through increased water levels. Prairie wetlands, outside of some alkali wetlands in the western portion of the region, are less studied as habitat for plovers when compared to river and reservoir shorelines. Our study suggests that these wetlands may have played a larger role in plover ecology than previously thought. Wetland restoration and conservation, through the restoration of natural hydrology, may be required to ensure that adequate habitat exists among the three habitat types in the face of existing or changing climate and to ensure long-term conservation.

North Dakota↗

Habitat selection and movements of Piping Plover broods suggest a tradeoff between breeding stages

In precocial birds, adults select breeding areas using cues associated with habitat characteristics that are favorable for nesting success and chick survival, but there may be tradeoffs in habitat selection between these breeding stages. Here we describe habitat selection and intra-territory movements of 53 Piping Plover ( Charadrius melodus ) broods (320 observations) during the 2007–2008 breeding seasons on mainland- and island-shoreline habitats at Lake Sakakawea, North Dakota, USA. We used remotely sensed habitat characteristics to separately examine habitat selection and movements at two spatiotemporal scales to account for potential confounding effects of nest-site selection on brood-rearing habitat used. The scales used were (1) the entire brood-rearing period within available brood-rearing areas and (2) 2-day observation intervals within age-specific discrete habitat selection choice sets. Analyses at both scales indicated that broods selected areas which were non-vegetated, moderately level, and nearer to the shoreline. Rate of brood movement increased with age up to 5 days, then stabilized; broods that hatched >50 m away from the shoreline moved toward the shoreline. Brood movements were greater when they were in vegetated areas, when the brood-rearing area was of greater topographic complexity, and when broods aged 6–25 days were further away from the shoreline. Using inferences from our results and those of previously published work, we postulate how a potential tradeoff in habitat selection between nesting and brood-rearing can contribute to an ecological trap in a novel habitat. This work, in the context of published works, suggests that plover breeding habitat is a complex of both nesting and brood-rearing habitats and provides a basis for making remotely sensed abundance estimates of suitable breeding habitat for Piping Plovers.

North Dakota↗

Is income breeding an appropriate construct for waterfowl?

Breeding birds use a range of nutrient accumulation and allocation strategies to meet the nutritional demands of clutch formation and incubation. On one end of the spectrum, capital breeders use stored nutrients acquired prior to clutch formation and incubation to sustain metabolism during reproduction, while on the opposite end, income breeders derive nutrients solely from exogenous sources on the breeding grounds. Blue-winged Teal ( Anas discors ) are an ideal candidate to test for adoption of an income strategy among migratory waterfowl because of their small body size, temperate breeding range, and timing of reproduction relative to pulses in nutrient availability within breeding habitats. We collected migrating and pre-breeding Blue-winged Teal ( n = 110) during the warmest spring in over a century in the southern edge of the species’ breeding range, which produced ideal conditions to test for adoption of an income breeding strategy among migratory waterfowl. Regression analyses revealed that females accumulated protein and fat reserves early in follicle development and appeared to mobilize at least some reserves coincident with the onset of clutch formation. Accumulation and subsequent mobilization of nutrient reserves was inconsistent with adherence to an income breeding strategy and suggested breeding Blue-winged Teal used capital (albeit locally acquired) for reproduction. Our results add to existing knowledge on the ubiquity of endogenous nutrient reserve accumulation prior to and during reproduction by waterfowl, perhaps suggesting endogenous nutrient reserves are universally used for clutch formation or incubation to some degree. If indeed Blue-winged Teal and other waterfowl universally use capital for breeding, research and conservation efforts should shift from evaluating whether an income breeding strategy is used and focus on when and where necessary capital is acquired prior to clutch formation.

Journal of Ornithology↗

Generating nested wetland catchments with readily-available digital elevation data may improve evaluations of land-use change on wetlands

The important ecosystem functions wetlands perform are influenced by land-use changes in their surrounding uplands and thus, identifying the upland area that flows into a wetland is important. We provide a method to define wetland catchments as the portion of the landscape that flows into a wetland; we allowed catchments to be nested and include other wetlands and their catchments, forming a hydrologic wetland complex. We generated catchments using multiple sources and resolutions of digital elevation data to evaluate whether catchment sizes generated from those data were similar. While non-contributing areas, or sinks, differed between elevation data sets, catchment areas were similar among high-resolution LiDAR- and IfSAR-derived data and readily available lower resolution data from the National Elevation Dataset. Accordingly, the higher-resolution DEM data, which may be expensive or not available, will not likely yield more accurate wetland catchment boundaries in flat or glaciated landscapes. We contend that this method to generate wetland catchments can be used to improve wetland studies where the location of a wetland within a catchment is important. Furthermore, the size of the catchment is important for understanding how wetlands respond to climate, land-use practices, and contamination.

North Dakota↗

Landscape selection by piping plovers has implications for measuring habitat and population size

How breeding birds distribute in relation to landscape-scale habitat features has important implications for conservation because those features may constrain habitat suitability. Furthermore, knowledge of these associations can help build models to improve area-wide demographic estimates or to develop a sampling stratification for research and monitoring. This is particularly important for rare species that have uneven distributions across vast areas, such as the federally listed piping plover (Charadrius melodus; hereafter plover). We examined how remotely-sensed landscape features influenced the distribution of breeding plover pairs among 2-km shoreline segments during 2006–2009 at Lake Sakakawea in North Dakota, USA. We found strong associations between remotely-sensed landscape features and plover abundance and distribution (R 2 = 0.65). Plovers were nearly absent from segments with bluffs (>25 m elevation increase within 250 m of shoreline). Relative plover density (pairs/ha) was markedly greater on islands (4.84 ± 1.22 SE) than on mainlands (0.85 ± 0.17 SE). Pair numbers increased with abundance of nesting habitat (unvegetated-flat areas β^=0.28±0.08SE ). On islands, pair numbers also increased with the relative proportion of the total area that was habitat ( β^=3.27±0.46SE ). Our model could be adapted to estimate the breeding population of plovers or to make predictions that provide a basis for stratification and design of future surveys. Knowledge of landscape features, such as bluffs, that exclude use by birds refines habitat suitability and facilitates more accurate estimates of habitat and population abundance, by decreasing the size of the sampling universe. Furthermore, techniques demonstrated here are applicable to other vast areas where birds breed in sparse or uneven densities.

North Dakota↗