Geology ReportsSearch

Geology topics

Jill A. Shaffer

Publications and source records attributed to Jill A. Shaffer.

At least 55 records · Page 3Linked to original sources

The effects of management practices on grassland birds—Long-billed Curlew ( Numenius americanus )

Keys to Long-billed Curlew ( Numenius americanus ) management include providing large, open, level to gently rolling grasslands with short vegetation, and tailoring grazing regimes to local conditions. Long-billed Curlews have been reported to use habitats with 3–75 centimeters (cm) average vegetation height, less than or equal to 27 cm visual obstruction reading, 20–71 percent grass cover, 4–50 percent forb cover, 2–12 percent shrub cover, 7–40 percent bare ground, and less than 3 cm litter depth.

Professional Paper

The effects of management practices on grassland birds—Marbled Godwit ( Limosa fedoa )

Keys to Marbled Godwit ( Limosa fedoa ) management include providing large expanses of short, sparsely to moderately vegetated landscapes that include native grasslands and wetland complexes. Optimal wetland complexes should contain a diversity of wetland classes and sizes, such as ephemeral, temporary, seasonal, semipermanent, permanent, and alkali wetlands, as well as intermittent streams. Marbled Godwits use wetlands of various salinities. The species has been reported to use habitats with less than or equal to 70 centimeters (cm) average vegetation height, 4–23 cm visual obstruction reading, and 1–9 cm litter depth.

Professional Paper

The effects of management practices on grassland birds—Willet ( Tringa semipalmata inornata )

Keys to Willet ( Tringa semipalmata inornata ) management include providing large expanses of native grasslands and wetland complexes. Wetland complexes should contain a diversity of wetland sizes and classes, such as ephemeral, temporary, seasonal, semipermanent, and permanent wetlands, as well as intermittent streams. Willets use wetlands of various salinities. Willets require short, sparse upland grasslands for nesting and foraging and wetland complexes for foraging. Broods use taller, denser grass cover than do nesting adults. Willets have been reported to use habitats with less than or equal to 70 centimeters (cm) average vegetation height, 4–23 cm visual obstruction reading, 15 percent bare ground, 38 percent litter cover, and 1–9 cm litter depth.

Professional Paper

The effects of management practices on grassland birds—Wilson’s Phalarope ( Phalaropus tricolor )

The key to Wilson’s Phalarope ( Phalaropus tricolor) management is providing wetland complexes containing suitable wetland characteristics (that is, open water, emergent vegetation, and open shoreline) and upland habitat (native grassland or tame hayland) throughout the breeding season. Wilson’s Phalaropes have been reported to use habitats with 15–32 centimeters (cm) average vegetation height, 8–18 cm visual obstruction reading, 45–53 percent grass cover, 19–22 percent forb cover, and less than 3 cm litter depth.

Professional Paper

Estimating offsets for avian displacement effects of anthropogenic impacts

Biodiversity offsetting, or compensatory mitigation, is increasingly being used in temperate grassland ecosystems to compensate for unavoidable environmental damage from anthropogenic developments such as transportation infrastructure, urbanization, and energy development. Pursuit of energy independence in the United States will expand domestic energy production. Concurrent with this increased growth is increased disruption to wildlife habitats, including avian displacement from suitable breeding habitat. Recent studies at energy-extraction and -generation facilities have provided evidence for behavioral avoidance and thus reduced use of habitat by breeding waterfowl and grassland birds in the vicinity of energy infrastructure. To quantify and compensate for this loss in value of avian breeding habitat, it is necessary to determine a biologically-based currency so that the sufficiency of offsets in terms of biological equivalent value can be obtained. We describe a method for quantifying the amount of habitat needed to provide equivalent biological value for avifauna displaced by energy and transportation infrastructure, based on the ability to define five metrics: impact distance, impact area, pre-impact density, percent displacement, and offset density. We calculate percent displacement values for breeding waterfowl and grassland birds and demonstrate the applicability of our avian-impact offset method using examples for wind and oil infrastructure. We also apply our method to an example in which the biological value of the offset habitat is similar to the impacted habitat, based on similarity in habitat type (e.g., native prairie), geographical location, land use, and landscape composition, as well as to an example in which the biological value of the offset habitat is dissimilar to the impacted habitat. We provide a worksheet that informs potential users how to apply our method to their specific developments and a framework for developing decision-support tools aimed at achieving landscape-level conservation goals.

Ecological Applications

The effects of management practices on grassland birds — An introduction to North American grasslands and the practices used to manage grasslands and grassland birds

The Great Plains of North America is defined as the land mass that encompasses the entire central portion of the North American continent that, at the time of European settlement, was an unbroken expanse of primarily herbaceous vegetation. The Great Plains extend from central Saskatchewan and Alberta to central Mexico and from Indiana to the Rocky Mountains. The expanses of herbaceous vegetation are often referred to as native prairie or native grasslands. Native grasslands share the characteristics of a general uniformity in vegetation structure, dominance by grasses and forbs, a near absence of trees and shrubs, annual precipitation ranging from 25 to 100 centimeters, extreme intra-annual fluctuations in temperature and precipitation, and a flat to rolling topography over which fires can spread. To the west of the Great Plains lie the sagebrush communities of the Great Basin, which extend from British Columbia and Saskatchewan to northern Arizona and New Mexico and from the eastern slopes of the Sierra Nevada and Cascade mountain ranges to western South Dakota. Sagebrush communities share similar characteristics to native grasslands, but their location east of the Rocky Mountains creates a more moderating influence from prevailing westerly winds that affect timing of peak precipitation and growth form of dominant vegetation. Native grasslands and sagebrush communities harbor a diverse array of grassland, wetland, and woodland plant and animal communities that are uniquely adapted to the natural forces of the Great Plains and Great Basin, namely the interactive forces of climate, fire, and grazing. The arrival of European settlers to North America brought profound change to native grassland and sagebrush communities, including the establishment of permanent towns and cities, the proliferation of cropland-based agricultural systems, and the suppression of wildfires. The near extirpation of bison by the 1860s paved the way for dramatic changes in the dominant grazers and a shift in the disturbance patterns that historically influenced vegetation structure. The greatest threat to native grasslands and sagebrush communities in modern times is their loss due to conversion to rowcrop agriculture and to urbanization. Concomitant with habitat loss is a precipitous decline in populations of bird species that evolved with, and are uniquely adapted to, the native grassland and sagebrush habitats. Avian population trends are linked strongly to agricultural land use. Besides outright loss of suitable breeding habitat, agricultural practices affect birds through factors such as pesticide exposure, habitat fragmentation, shifts in predator community composition, and occurrence of brood parasites. Bird populations face other stressors, such as loss of habitat to and behavioral avoidance of urbanized areas, roads, and infrastructure associated with energy production. Despite the many anthropogenic changes to North American grassland and sagebrush communities, some bird species are adaptable and opportunistic in their habitat selection and now utilize one or more human-created habitats. Human-created habitats include pastures, hayfields, agricultural terraces, crop buffer strips, field borders, grassed waterways, fencerows, road rights-of-way, airports, reclaimed coal mines, and planted wildlife cover. Fields of seeded grasslands enrolled in Federal long-term set-aside programs, such as the Conservation Reserve Program in the United States and the Permanent Cover Program in Canada, provide important nesting habitat for grassland bird species. The array of habitats used by birds makes habitat and avian management a complex undertaking, and the scale (for example, local, regional, international) at which management actions can be implemented are such that a universal approach to managing grasslands for the conservation of the entire suite of bird species does not exist. Experienced land managers recognize that it is impossible to manage for all bird species simultaneously, and thus, prioritization is necessary towards those habitats or bird species that the manager or management agency ranks highest for a specific region or management unit. The primary tools available for management are burning, grazing, mowing, herbicide application, and idling, but before choosing a particular practice, a manager will want to consider issues of seasonality, intensity, and frequency. Despite the thousands of studies that are cited in this compendium, much remains unknown about the effects of management practices on bird species. The series of species accounts in this compendium review the current state of knowledge regarding management of grassland and sagebrush bird species and summarize information on the effects of management practices on individual species. The accounts do not give definitive statements on the effects of management practices for any particular species, primarily because there are very few replicated studies in which identical management practices have been applied in the same geographical area with consistent results, which are elements necessary to provide concrete recommendations for the management of a particular species in a particular area. Documentation of the effects of management treatments on individual species through statistically sound methods that incorporate multiple years and locations will further scientists’ and land managers’ knowledge far more than 1–2-year studies that are limited in scope as well as time, but studies of that scope and breadth are rare.

Professional Paper

The effects of management practices on grassland birds—Rates of Brown-headed Cowbird (Molothrus ater) parasitism in nests of North American grassland birds

The Brown-headed Cowbird ( Molothrus ater ) is an obligate brood parasite that relies entirely on host species to incubate its eggs and rear its young. The Brown-headed Cowbird is a host generalist; eggs of the cowbird have been found in nests of more than 220 species of North American birds. Although cowbirds are not considered a serious threat to their primary avian hosts, cowbird brood parasitism has been recognized as a potential threat to the survival of threatened and endangered species and has been implicated in the declines of other bird species through reduced reproductive output. In this chapter, we summarized the rates of cowbird brood parasitism for 40 grassland bird species. The reported rates of brood parasitism by Brown-headed Cowbirds varied considerably among and within grassland host species, and the factors that influence parasitism rates were described. Defenses possessed by cowbird hosts in grasslands include aggressively defending their nests against female cowbirds, egg rejection, desertion of parasitized nests, and burying cowbird eggs in the nest lining.

Professional Paper

Modeling effects of crop production, energy development and conservation-grassland loss on avian habitat

Birds are essential components of most ecosystems and provide many services valued by society. However, many populations have undergone striking declines as their habitats have been lost or degraded by human activities. Terrestrial grasslands are vital habitat for birds in the North American Prairie Pothole Region (PPR), but grassland conversion and fragmentation from agriculture and energy-production activities have destroyed or degraded millions of hectares. Conservation grasslands can provide alternate habitat. In the United States, the Conservation Reserve Program (CRP) is the largest program maintaining conservation grasslands on agricultural lands, but conservation grasslands in the PPR have declined by over 1 million ha since the program’s zenith in 2007. We used an ecosystem-services model (InVEST) parameterized for the PPR to quantify grassland-bird habitat remaining in 2014 and to assess the degradation status of the remaining grassland-bird habitat as influenced by crop and energy (i.e., oil, natural gas, and wind) production. We compared our resultant habitat-quality ratings to grassland-bird abundance data from the North American Breeding Bird Survey to confirm that ratings were related to grassland-bird abundance. Of the grassland-bird habitat remaining in 2014, about 19% was degraded by crop production that occurred within 0.1 km of grassland habitats, whereas energy production degraded an additional 16%. We further quantified the changes in availability of grassland-bird habitat under various land-cover scenarios representing incremental losses (10%, 25%, 50%, 75%, and 100%) of CRP grasslands from 2014 levels. Our model identified 1 million ha (9%) of remaining grassland-bird habitat in the PPR that would be lost or degraded if all CRP conservation grasslands were returned to crop production. Grassland regions world-wide face similar challenges in maintaining avian habitat in the face of increasing commodity and energy production to sate the food and energy needs of a growing world population. Identifying ways to model the impacts of the tradeoff between food and energy production and wildlife production is an important step in creating solutions.

Prairie Pothole Region

Model parameters for representative wetland plant functional groups

Wetlands provide a wide variety of ecosystem services including water quality remediation, biodiversity refugia, groundwater recharge, and floodwater storage. Realistic estimation of ecosystem service benefits associated with wetlands requires reasonable simulation of the hydrology of each site and realistic simulation of the upland and wetland plant growth cycles. Objectives of this study were to quantify leaf area index (LAI), light extinction coefficient ( k ), and plant nitrogen (N), phosphorus (P), and potassium (K) concentrations in natural stands of representative plant species for some major plant functional groups in the United States. Functional groups in this study were based on these parameters and plant growth types to enable process-based modeling. We collected data at four locations representing some of the main wetland regions of the United States. At each site, we collected on-the-ground measurements of fraction of light intercepted, LAI, and dry matter within the 2013–2015 growing seasons. Maximum LAI and k variables showed noticeable variations among sites and years, while overall averages and functional group averages give useful estimates for multisite simulation modeling. Variation within each species gives an indication of what can be expected in such natural ecosystems. For P and K, the concentrations from highest to lowest were spikerush ( Eleocharis macrostachya ), reed canary grass ( Phalaris arundinacea ), smartweed ( Polygonum spp.), cattail ( Typha spp.), and hardstem bulrush ( Schoenoplectus acutus ). Spikerush had the highest N concentration, followed by smartweed, bulrush, reed canary grass, and then cattail. These parameters will be useful for the actual wetland species measured and for the wetland plant functional groups they represent. These parameters and the associated process-based models offer promise as valuable tools for evaluating environmental benefits of wetlands and for evaluating impacts of various agronomic practices in adjacent areas as they affect wetlands.

Ecosphere

The influence of local- and landscape-level factors on wetland breeding birds in the Prairie Pothole Region of North and South Dakota

We examined the relationship between local- (wetland) and landscape-level factors and breeding bird abundances on 1,190 depressional wetlands in the Prairie Pothole Region of North and South Dakota during the breeding seasons in 1995–97. The surveyed wetlands were selected from five wetland classes (alkali, permanent, semipermanent, seasonal, or temporary), two wetland types (natural or restored), and two landowner groups (private or Federal). We recorded 133 species of birds in the surveyed wetlands during the 3 years. We analyzed the nine most common (or focal) species (that is, species that were present in 25 percent or more of the 1,190 wetlands): the Red-winged Blackbird ( Agelaius phoeniceus ), Blue-winged Teal ( Anas discors ), Mallard (Anas platyrhynchos ), American Coot ( Fulica americana ), Gadwall ( Anas strepera ), Common Yellowthroat ( Geothlypis trichas ), Yellow-headed Blackbird ( Xanthocephalus xanthocephalus ), Northern Shoveler ( Anas clypeata ), and Savannah Sparrow ( Passerculus sandwichensis ). Our results emphasize the ecological value of all wetland classes, natural and restored wetlands, and publicly and privately owned wetlands in this region, including wetlands that are generally smaller and shallower (that is, temporary and seasonal wetlands) and thus most vulnerable to drainage. Blue-winged Teal, Northern Shoveler, Gadwall, Common Yellowthroat, and Red-winged Blackbird had higher abundances on Federal than on private wetlands. Abundances differed among wetland classes for seven of the nine focal species: Blue-winged Teal, Northern Shoveler, Mallard, American Coot, Common Yellowthroat, Yellow-headed Blackbird, Red-winged Blackbird. American Coot had higher abundances on restored wetlands than on natural wetlands overall, and Gadwall and Common Yellowthroat had higher abundances on private restored wetlands than on private natural wetlands. The Common Yellowthroat was the only species that had higher abundances on restored private wetlands than on restored Federal wetlands. After adjusting for wetland size and the date and location of the surveys, our results demonstrated that incorporating wetland- and landscape-level factors in models can improve our ability to predict abundances of wetland birds in this region. The top model for eight of the nine focal species included wetland- and landscape-level factors, whereas the best model for Blue-winged Teal included only wetland-level attributes. Although local factors (for example, percent open water or emergent vegetation) in individual wetlands are important factors for some wetland breeding birds, it is important that natural resource managers consider landscape-level factors beyond the local factors in their conservation plans for wetland birds.

North Dakota, South Dakota

Effects of wind-energy facilities on grassland bird distributions

The contribution of renewable energy to meet worldwide demand continues to grow. Wind energy is one of the fastest growing renewable sectors, but new wind facilities are often placed in prime wildlife habitat. Long-term studies that incorporate a rigorous statistical design to evaluate the effects of wind facilities on wildlife are rare. We conducted a before-after-control-impact (BACI) assessment to determine if wind facilities placed in native mixed-grass prairies displaced breeding grassland birds. During 2003–2012, we monitored changes in bird density in 3 study areas in North Dakota and South Dakota (U.S.A.). We examined whether displacement or attraction occurred 1 year after construction (immediate effect) and the average displacement or attraction 2–5 years after construction (delayed effect). We tested for these effects overall and within distance bands of 100, 200, 300, and >300 m from turbines. We observed displacement for 7 of 9 species. One species was unaffected by wind facilities and one species exhibited attraction. Displacement and attraction generally occurred within 100 m and often extended up to 300 m. In a few instances, displacement extended beyond 300 m. Displacement and attraction occurred 1 year after construction and persisted at least 5 years. Our research provides a framework for applying a BACI design to displacement studies and highlights the erroneous conclusions that can be made without the benefit of adopting such a design. More broadly, species-specific behaviors can be used to inform management decisions about turbine placement and the potential impact to individual species. Additionally, the avoidance distance metrics we estimated can facilitate future development of models evaluating impacts of wind facilities under differing land-use scenarios.

North Dakota, South Dakota

Distribution of burrowing owls in east-central South Dakota

Western burrowing owl (Athene cunicularia hypugaea) populations have declined across much of western North America, particularly at the northern and eastern edges of the species’ breeding range (Martell et al. 2001, Murphy et al. 2001, Shyry et al. 2001, Skeel et al. 2001, Klute et al. 2003). In South Dakota, the burrowing owl is a summer resident that historically was relatively common throughout the state, but its range has decreased in recent decades, especially in the eastern half of the state (Whitney et al. 1978, South Dakota Ornithologists’ Union [SDOU] 1991, Peterson 1995). Tallman et al. (2002) described the species as uncommon to locally common in western South Dakota, uncommon in the north-central part of the state, and casual (i.e., not within the species’ normal range, but with 3–10 records in the past 10 years) elsewhere in the eastern half. The burrowing owl is a Species of Greatest Conservation Need (South Dakota Department of Game, Fish and Parks [SDGFP] 2006) and a Level I Priority Species in South Dakota (Bakker 2005).

South Dakota

Influence of trees in the landscape on parasitism rates of grassland passerine nests in Southeastern North Dakota

Woody vegetation has been linked to increased rates of Brown-headed Cowbird ( Molothrus ater ) parasitism for some grassland hosts. In northern North Dakota, however, studies reported that parasitism of grassland passerine nests was lower in landscapes with trees than in those without trees. We looked for evidence of this pattern elsewhere, using data from two studies conducted on the Sheyenne National Grassland in southeastern North Dakota. Specifically, we examined the probability of parasitism relative to percent tree cover within 2 km of a nest. We found a negative relationship for grassland passerine nests of all species tested. Our results support the suggestion that cowbirds are less likely to parasitize nests of grassland passerines where tree cover on the landscape is greater. This pattern could be explained by cowbirds switching to alternative hosts in woodlands, but this hypothesis needs further testing.

Condor

Pattern and potential causes of White-faced Ibis, Plegadis chihi, establishment in the northern prairie and parkland region of North America

The Northern Prairie and Parkland Waterbird Conservation Plan calls for renewed attention to determining the current status of waterbird populations, their distributions, and conservation needs. It highlights the need for baseline information on the White-faced Ibis (Plegadis chihi). In response, we examined the historical and current distribution of the ibis in North Dakota and summarized first sightings and nest records for the provinces and other states composing the northern prairie and parkland region. The establishment of breeding colonies of White-faced Ibis here may be due to climate and precipitation patterns, invasion and spread of Narrowleaf Cattail (Typha angustifolia), changes in agricultural practices, habitat loss and range expansion in the southern and western portions of the species' range, and increases in ibis populations in the Intermountain West. We placed special emphasis on North Dakota, a state for which there is scant published information concerning the current status of this species. In recent decades, the ibis has become a regular breeding-season resident in North Dakota and in other areas of the northern prairie and parkland region. From 1882 to 2002, there were 145 reports of one or more White-faced Ibis in North Dakota, including 93 reports during the breeding season (15 May to 31 August), 49 during the non-breeding season (1 September to 14 May), and three for which the season of occurrence was not reported. Prior to the 1960s, there were only three records of the species in North Dakota. Observations of White-faced Ibises in North Dakota increased dramatically between the 1960s and the early 21st century, and the species has been observed nearly annually since 1971. The first White-faced Ibis nesting activity in the state was recorded in 1978, and to date, there have been 21 known records of nesting activity in the state. The species nested in large (>300 ha) semipermanent or permanent wetlands within mixed-species colonies ranging in areal extent from small (0.1 ha) to fairly large (27 ha), and colonies were located in patches of emergent vegetation dominated by cattails (Typha) and bulrushes (Scirpus). We classify the White-faced Ibis as a fairly common migrant and a locally uncommon breeder east of the Missouri River and a casual migrant west of the Missouri River.

Canadian Field-Naturalist

Does body size affect a bird's sensitivity to patch size and landscape structure?

Larger birds are generally more strongly affected by habitat loss and fragmentation than are smaller ones because they require more resources and thus larger habitat patches. Consequently, conservation actions often favor the creation or protection of larger over smaller patches. However, in grassland systems the boundaries between a patch and the surrounding landscape, and thus the perceived size of a patch, can be indistinct. We investigated whether eight grassland bird species with different body sizes perceived variation in patch size and landscape structure in a consistent manner. Data were collected from surveys conducted in 44 patches of northern tallgrass prairie during 1998–2001. The response to patch size was very similar among species regardless of body size (density was little affected by patch size), except in the Greater Prairie-Chicken ( Tympanuchus cupido ), which showed a threshold effect and was not found in patches smaller than 140 ha. In landscapes containing 0%–30% woody vegetation, smaller species responded more negatively to increases in the percentage of woody vegetation than larger species, but above an apparent threshold of 30%, larger species were not detected. Further analyses revealed that the observed variation in responses to patch size and landscape structure among species was not solely due to body size per se, but to other differences among species. These results indicate that a stringent application of concepts requiring larger habitat patches for larger species appears to limit the number of grassland habitats that can be protected and may not always be the most effective conservation strategy.

Condor

Patch size and landscape effects on density and nesting success of grassland birds

Current management recommendations for grassland birds in North America emphasize providing large patches of grassland habitat within landscapes that have few forest or shrubland areas. These Bird Conservation Areas are being proposed under the assumption that large patches of habitat in treeless landscapes will maintain viable populations of grassland birds. This assumption requires that patch size and landscape features affect density and nesting success of grassland birds, and that these effects are consistent among years and regions and across focal species. However, these assumptions have not yet been validated for grassland birds, and the relative importance of local vegetation structure, patch size, and landscape composition on grassland bird populations is not well known. In addition, factors influencing grassland bird nesting success have been investigated mostly in small-scale and short-duration studies. To develop management guidelines for grassland birds, we tested the spatial and temporal repeatability of the influence of patch size and landscape composition on density and nesting success of 3 grassland passerines, after controlling for local-scale vegetation structure, climate, and—when analyzing nest success—bird density. We conducted our study during 4 years (1998–2001) in 44 study plots that were set up in 3 regions of the northern tallgrass prairie in Minnesota and North Dakota, USA. In these study plots we measured density and nesting success of clay-colored sparrows ( Spizella pallida ), Savannah sparrows ( Passerculus sandwichensis ), and bobolinks ( Dolichonyx oryzivorus ). Statistical models indicated that density was influenced by patch size, landscape, region, and local vegetation structure more so than by local vegetation structure alone. Both magnitude and direction of the response of density to patch size varied among regions, years, and species. In contrast, the direction of landscape effects was consistent among regions, years, and between Savannah sparrows and bobolinks. In each species, this landscape effect was independent of patch size. Nesting success was not clearly influenced by patch size or landscape composition, and none of the factors that influenced avian density also influenced nesting success in any of the 3 species. General statements on “optimal habitat” for grassland birds should therefore be viewed cautiously. Instead, long-term studies in different regions as well as a deeper understanding of the local system are needed to determine which factors are most important for grassland birds in a particular area.

Journal of Wildlife Management