Short-term effects of burning and disking on songbird use of floodplain conservation easements.
Since European settlement, the Midwestern United States has undergone major land-cover changes. Prairies and wetlands have been reduced to a fraction of their former extent and rowcrop agriculture has become the dominant land use in many areas (Dahl, 1990; Samson and Knopf, 1994). In Iowa, this conversion of presettlement landscapes to agriculture has resulted in the loss of >99% of native prairie and >95% of wetlands (Bishop, 1981; Smith, 1998). As interfaces between terrestrial and aquatic ecosystems, riparian areas are important landscape components that, like other natural communities, have been greatly altered. The loss of native floodplain functions, including flood-water storage, nutrient and sediment retention, and wildlife habitat, has been more widespread in the Midwest than in any other region of the United States (Brinson et al., 1981; National Research Council, 2002).
Historically, the structure and composition of Midwestern riparian plant communities were shaped by fine-scale elevation differences and the timing, duration and extent of disturbances such as flooding and fire (Brinson et al., 1981; Gregory et al., 1991; Nelson et al., 1998). Although some riparian areas were forested before European settlement, many of these areas were dominated by extensive grasslands and herbaceous wetlands (Weaver, 1968; Nelson et al., 1998; Benson et al., 2006). This diversity of habitat types and hydrologic conditions historically made riparian areas important for a diversity of plant and animal species (Fredrickson and Reid, 1986; Iowa Department of Agriculture and Land Stewardship, 1999).
In the past two decades, the implementation of Farm Bill programs such as the Conservation Reserve Program (CRP) and Wetlands Reserve Program (WRP) has led to restoration of millions of hectares of grasslands and wetlands. Authorized in 1990, WRP is a voluntary program in which landowners are compensated for taking their land out of agricultural production and restoring natural vegetation (Gray, 2005). Combined with emergency flood-mitigation programs such as the Emergency Wetlands Reserve Program (EWRP), CRP and WRP have restored thousands of hectares of riparian habitat throughout the Midwest. These programs have a variety of goals, including providing habitat for wildlife populations, especially migratory birds (Heard et al., 2000). Through these programs, restoration of riparian grasslands and wetlands may benefit many bird species, including those that have experienced widespread and consistent population declines (Peterjohn and Sauer, 1999; Benson et al., 2006).
To establish and maintain herbaceous habitats in the Midwest, managers use a range of practices including burning and disking. These practices potentially affect the habitat use of numerous bird species by altering vegetation structure or composition and availability of food resources. As a historically important source of disturbance and common management tool for grass-dominated systems in the Midwest, more is known about burning than disking. Burning alters grasslands by removing woody and residual vegetation, encouraging growth of grass species and decreasing arthropod populations (Kucera and Ehrenreich, 1962; Warren et al., 1987; Hulbert, 1988). Disking, typically used to cultivate agricultural fields, is receiving increasing attention by wildlife managers as a method to increase vegetative diversity in largely monotypic grass stands. By mechanically removing existing vegetation, decreasing grass and litter cover, and increasing bare-ground and forb cover, disking has been primarily viewed as a method for providing food-rich brood-rearing habitat for game birds (e.g., Webb and Guthery, 1983; Manley et al., 1994; Madison et al., 1995). The effects of burning on grassland birds vary regionally and among species (Reinking, 2005), and research on bird responses to disking is limited. However, disking relatively small portions of fields may, by creating concentrated patches of arthropod food resources (Benson et al., 2007), increase the density or species richness of birds in these areas.
To provide guidance for future restoration and management activities, we evaluated the effects of burning and disking on the density and species richness of birds breeding in grass-dominated riparian habitats of east-central Iowa. Because burning and disking alter vegetation structure and composition and the abundance and biomass of arthropods (Benson et al., 2007), we expected these management practices to affect bird communities. Specifically, we expected burning and disking to make habitats more suitable for species that are associated with open herbaceous habitats and less suitable for species that prefer densely vegetated herbaceous areas. Additionally, because burning causes decreases in arthropod abundance, while disking increases arthropod abundance (Benson et al., 2007), we expected decreases in bird response variables with burning but increases with disking.
MATERIALS AND METHODS
We studied grass-dominated herbaceous habitats in Tama, Benton and Iowa counties of east-central Iowa (Benson et al., 2006). Our study sites were within the >20,000 ha Iowa River Corridor Project (IRC), a cooperative project among the Natural Resources Conservation Service (NRCS), United States Fish and Wildlife Service (USFWS), and Iowa Department of Natural Resources (IDNR). This area was historically dominated by herbaceous vegetation (Benson et al., 2006). Currently, >100 riparian WRP and EWRP easements totaling about 5000 ha of former agricultural land are enrolled in NRCS conservation programs in the IRC. The watershed drains about 1.25 million ha, about 1 million ha of which were cropland prior to restoration (United States Department of Agriculture, 1976).
The plant species composition in IRC fields was dependent on hydrology, previous land use and extent of restoration efforts. We placed fields into two groups based on flood frequency; fields that flood rarely (mesic grasslands) and those that flood frequently (hydric grasslands). Mesic grasslands were generally planted to native grass species, usually switchgrass (Panicum virgatum) or big bluestem (Andropogon gerardii), and are sufficiently dry in many years to permit burning. Because of a lack of suitable seed mixes for hydric soils, managers allowed these areas to naturally revegetate and they are generally dominated by reed canarygrass (Phalaris arundinacea), an invasive perennial (Hoffman and Kearns, 1997; Merigliano and Lesica, 1998). These hydric fields are too wet to permit burning in most years and, consequently, these areas were not included in our current evaluation of management practices although results of different management evaluations for these sites are presented elsewhere (Benson, 2003; Benson et al., 2007). We collected data on 20 mesic fields in 2001 and 2002. We defined fields as separate easements or separate management units within an easement; fields ranged in size from 8.6 to 52.5 ha [[bar.x] = 18.5 ha [+ or -] 2.5 (SE)], were dominated by herbaceous vegetation, generally grasses (Benson et al., 2007), and were recognized as candidates for management by participating agencies. Fields were distributed among 15 easements, with 10 easements containing one and five easements containing two fields (these pairs of fields were an average of 558 m apart).
We randomly assigned 10 of 20 mesic fields to a spring burning and disking treatment. Burning of the 10 fields took place between 19 Apr. and 11 May 2001 and was originally planned to facilitate disking. Although disking was scheduled to be completed soon after burning in spring, wet conditions delayed disking until between 27 Jun. and 20 Jul. 2001. Seven fields received a strip-disking treatment, and disking was done with a single pass of a tandem disk to a depth of about 23 cm. Strips were disked about 20 m wide spanning the length of each treated field, typically close to the center of each field (n = 5) or on the field's edge (n = 2). Although entire fields were burned, only about 1 ha of each field was disked [[bar.x] = 1.12 ha [+ or -] 0.16 (SE), range = 0.67-1.68 ha]; this corresponded to a mean of 7% of each field (SE = 2%, range = 3-15%). Only a small strip was disked to minimize disturbance to the warm-season grass plantings but provide a forb- and arthropod-rich area that could serve as a concentrated resource patch for birds throughout the field. Four burned fields were not disked because of logistical difficulties, and one unburned field was inadvertently disked. Because burned and unburned fields were similar in vegetation density and height of live vegetation at the time of disking (and therefore disking appeared equally effective in both; Benson et al., 2007), the field that was unburned and disked was included in analyses with those that had been burned and disked. Treated and untreated fields were distributed throughout the length of the IRC, and no two fields within the same easement received the same treatment.
We surveyed birds four times between 17 May and 25Jul. 2001 and again between 23 May and 30 Jul. 2002. We randomly placed four non-overlapping, 50-m-radius point-counts in each field and completed 5 min counts at these points between sunrise and 1000 h (Ralph et al., 1995). Observers were trained before initiation of field work, rotated among sites to minimize bias and did not conduct surveys on mornings with high winds (>24 km/h) or rain. We recorded all birds identified visually or by song within the survey area, the method of identification (visual, song, call) and sex of each individual when possible (based on sexual dimorphism or singing). Birds identified visually were placed into 1 of 5 distance classes, 0-10 m, 11-20 m, 21-30 m, 31-40 m or 41-50 m, and birds flying over count circles were not included in analyses. Most birds (94%) were visually detected during surveys, and we did not estimate distance for individuals identified only by sound because we considered these estimates to be less reliable. We used the same point-count locations in both years, and counts from adjacent fields were >250 m apart. Given the relatively small area disked in treated fields, point-counts were generally located outside of the treated area; however, we expected these disked areas to function as concentrated resource patches where increased arthropod abundance and biomass would lead to increased bird use of the surrounding areas and, thus, have effects at the field level. Based on published territory sizes of bird species in the study area [e.g., 7123 [m.sup.2] for dickcissel (latin names for all species are listed in Appendix), and 5261 [m.sup.2] for common yellowthroat; Schoener, 1968; Schartz and Zimmerman, 1971], we expected a response to occur within 100 m of disked areas and point-counts within treated fields were generally within this radius.
We calculated density of birds (males/ha) for common species ([greater than or equal to] 40 total observations), and all grassland and wetland species combined (males/ha; Poole et al., 1992-2002; Vickery et al., 1999) using program DISTANCE (Buckland et al., 1993). For grassland and wetland species with [greater than or equal to] 40 observations, we compared detectability models that incorporated a uniform distribution with cosine or simple polynomial adjustments, a half-normal model with cosine or hermite polynomial adjustments, and a hazard-rate model with cosine adjustments (Buckland et al., 1993). Although our results focus specifically on mesic fields within our study area, we pooled observations from mesic and hydric fields in our study area to increase our sample size and generate detection functions for both field types. Where sample sizes permitted (i.e., 40 observations per group), we examined differences in detectability functions among habitat types (mesic vs. hydric), treatments (disked, burned, untreated), years (2001 vs. 2002) and interactions of these variables. Models were ranked according to Akaike's Information Criterion for small sample sizes ([AIC.sub.c]; Burnham and Anderson, 1998). We used density estimates produced by DISTANCE for subsequent analyses. For species with <40 observations, we calculated density as average number of birds at a point divided by the area of the fixed-radius point count (males/ha; equivalent to a uniform detection function). Because we conservatively chose to use only visual detections in DISTANCE to ensure accuracy of distance estimates, for those species that required distance-related adjustments for detection probability (see RESULTS), we used the maximum of the DISTANCE and unadjusted (i.e., including sound-only detections) estimates for each sampling round.
In addition to density, we were interested in the effect of treatments on the number of species using fields as well as the overall conservation priority of the species assemblage. Therefore, we used three metrics in addition to density: total number of species observed per field, total number of grassland and wetland species observed per field, and conservation value. Grassland and wetland birds included obligate and facultative species (Poole et al., 1992-2002; Vickery et al., 1999). Conservation value was determined using the density of each grassland- or wetland-associated species and its Partners in Flight (PIF) prioritization score for the Dissected Till Plains (Carter et al., 2000; Fitzgerald and Pashley, 2000; Nuttle et al., 2003; for PIF scores see acknowledgments):
Conservation value = [S.summation over (i=1)]Z [density.sub.i] x [PIFscore.sub.i].
We used mixed-model Analysis of Variance (ANOVA) to test for effects of burning, disking, year, burn X year, disk X year, burn X disk, and burn X disk X year on density, species richness and conservation value (SAS PROC MIXED; Littell et al., 2006). In addition to these fixed effects, we treated field within treatment and field X year within treatment as random effects to account for the 2 y of data collection and four sample rounds within years. We used the Kenward-Roger approximation for denominator degrees of freedom and, to account for potential heterogeneity of variance, we modeled residual variation among treatment x year combinations (Littell et al., 2006). We used plots of the residuals from these analyses to confirm that the normal distribution was appropriate. When data did not conform to a normal distribution, usually because of a large number of occasions when zero individuals were observed, we tested for the above treatment, year and interaction effects on presence of these rare species using generalized linear mixed models using a binomial distribution and logit link function, and with the same random effects listed above (SAS PROC GLIMMIX; Littell et al., 2006).
Since burn treatments were applied to fields before the first season of data collection, we expected burn effects to appear as either a main effect (i.e., burn effect in both years) or as a burn X year interaction (i.e., burn effect in only one year). However, disking was completed either late in the first field season (i.e., after 3 or 4 survey rounds) or between the two field seasons. Consequently, vegetative responses of this treatment were not observed until the second year of our study and we expected bird responses to this treatment to appear as changes between years in disked relative to control fields (i.e., disk X year interaction). For those few cases where disking occurred before the fourth round of bird surveys, our observations and exploratory analyses confirmed that this treatment had little or no effect on the birds during that season. When significant interactions were present, we examined differences among burn X year or disk X year combinations with contrasts. The significance level was set at P <- 0.05 for all analyses. To protect against Type II error, we did not adjust for multiple comparisons (Quinn and Keough, 2002; Moran, 2003). Likewise, because the cost of making Type II errors is high, particularly when dealing with management practices that may adversely affect populations, results with 0.10 [greater than or equal to] P [greater than or equal to] 0.05 were considered marginally significant (Cousens and Marshall, 1987; Mapstone, 1995; Quinn and Keough, 2002).
In 2001 and 2002, we observed 25 bird species in mesic fields (Appendix). Five grassland or wetland species were sufficiently abundant to calculate density using DISTANCE (Appendix, Table 1). Uniform functions were best for modeling detectability of all bird species, and no adjustments to the detection function were made for red-winged blackbirds or dickcissels. The best detection model for common yellowthroats incorporated a habitat-type effect (differences in detection between mesic and hydric fields), with detection functions in both habitats incorporating one cosine adjustment. For sedge wrens, the best detection model incorporated two cosine adjustments. For American goldfinches, the best detection model incorporated a year effect with no adjustments to the uniform function in 2001 data, and one adjustment in 2002 data. For red-winged blackbirds and dickcissels, 100% of the variance associated with density estimates was related to encounter rate, whereas this value varied from 29 to 49% for the other species. Because of a low sample size for grasshopper sparrows, we did not adjust density for detectability and present density as mean number of individuals observed per ha which is equivalent to a model with a uniform detection function. Likewise, because the best detectability model for combined grassland and wetland species was uniform with no adjustments, we calculated density of this group as the sum of species-specific density estimates (both adjusted and unadjusted).
DENSITY, SPECIES RICHNESS AND CONSERVATION VALUE
The burn x disk and burn x disk X year interactions were not significant for any of the variables we evaluated (all P > 0.05). The burn x year interaction was only significant for density of common yellowthroats, and the disk x year interaction was only significant for combined density of all grassland and wetland species and conservation value (Tables 1 and 2; Figs. 1 and 2). Density of common yellowthroats was lower in burned than unburned fields in 2001 but not 2002 [difference = 0.38 males/ha [+ or -] 0.12 (SE), [F.sub.1,38] = 10.27, P = 0.003 and 0.07 [+ or -] 0.10 (SE), [F.sub.1,19] = 0.49, P = 0.491, respectively; Fig. 1]. Additionally, there was a significant decrease in density between years in unburned but not burned fields [difference = 0.28 [+ or -] 0.11 (SE), [F.sub.1,48] = 6.73, P = 0.013 and -0.04 [+ or -] 0.04 (SE), [F.sub.1,9] = 0.74, P = 0.409, respectively].
Density of all grassland and wetland species did not differ between fields that did or did not receive a disking treatment in 2001, but the difference was marginally significant in 2002 [difference = 0.30 [+ or -] 0.38 (SE), [F.sub.1,19] = 0.63, P = 0.439 and -0.70 - 0.39 (SE), [F.sub.1,20] = 3.14, P = 0.091, respectively; Fig. 2A]. The density of this group decreased between years in fields with no disking treatment but displayed a non-significant increase in those that did receive disking [difference = 0.57 [+ or -] 0.26 (SE), [F.sub.1,32] = 4.99, P = 0.027 and -0.42 [+ or -] 0.34 (SE), [F.sub.1,26] = 1.50, P = 0.224, respectively]. Conservation value did not differ between disked and undisked fields in 2001, but differed marginally in 2002 [difference = 8.18 [+ or -] 9.04 (SE), [F.sub.1,11] = 0.83, P = 0.385 and -14.62 [+ or -] 7.57, [F.sub.1,9] = 3.73, P = 0.083, respectively; Fig. 2B]. Between years, there was a marginally significant decrease in conservation value in undisked fields, but a marginal increase in disked fields [difference = 10.15 [+ or -] 5.45 (SE), [F.sub.1,17] = 3.46, P = 0.079 and -12.65 [+ or -] 7.16 (SE), [F.sub.1,16] = 3.13, P = 0.096, respectively]. There was a significant effect of burning on density of red-winged blackbirds and all grassland and wetland species combined; density was lower in burned than unburned fields [difference = 0.57 males/ha [+ or -] 0.26 (SE), and 0.72 males/ha [+ or -] 0.33 (SE), respectively; Tables 1 and 2, Fig. 3]. There were no differences between fields with and without a disking treatment for density of individual species, species richness or conservation value, nor were there differences in species richness or conservation value between burned and unburned fields. However, there were significant differences between years in density of red-winged blackbirds, occurrence of American goldfinches, and richness of grassland and wetland species (Tables 1 and 2). There was also a marginally significant difference between years in occurrence of grasshopper sparrows.
[FIGURE 1 OMITTED]
The bird species and densities found in restored grasslands of the Iowa River Corridor are similar to those found in other studies of grassland birds in Iowa and throughout the Midwest (e.g., Cink and Lowther, 1989; Johnson and Schwartz, 1993; Patterson and Best, 1996; Fletcher and Koford, 2002; Murray and Best, 2003). However, some grassland obligate species commonly observed in this region, such as bobolinks and meadowlarks, were rare in this study for unknown reasons (Appendix). Nonetheless, these restored grasslands were occupied by a number of grassland or wedand species, including eight that are considered moderate or high conservation priorities (Fitzgerald and Pashley, 2000; Nuttle et al., 2003; Benson et al., 2006).
DENSITY, SPECIES RICHNESS AND CONSERVATION VALUE
Previous studies of the effects of burning on grassland birds have had variable results with species- and region-specific differences in responses to this management practice (Reinking, 2005). In this study, we found decreases in density of grassland and wetland species, and density of two species, common yellowthroats and red-winged blackbirds following burning. Past studies found little effect of burning on density of all species combined (Madden et al., 1999), or decreases in density (Zimmerman, 1992; Robel et al., 1998). Most of the observed decrease in density of all grassland and wetland species combined in our study was driven by changes in red-winged blackbird density, the most abundant species on our study area. Indeed, the estimated difference in blackbird density between unburned and burned fields accounted for 78% of the difference for combined density of all grassland and wetland species. In contrast, some past studies have found no effect (Herkert, 1994) or increases in red-winged blackbirds after burning (Zimmerman, 1992); however, others have found decreases (Robel et al., 1998). Consistent with our results from the year fields were burned (2001), past research suggests that common yellowthroats are negatively impacted by burning of their habitat (Zimmerman, 1992; Herkert, 1994; Madden et al., 1999). These differences between burned and unburned areas may have persisted into the second year, but weather-related changes in density between years, with 2002 drier than 2001 (National Oceanic and Atmospheric Administration, 2001, 2002), may have diluted any effect of burn treatments in 2002.
[FIGURE 2 OMITTED]
[FIGURE 3 OMITTED]
Density or occurrence of other species and species richness were unaffected by burning in this study. This is consistent with previous research on dickcissels (Zimmerman, 1992; Swengel, 1996; Applegate et al., 2002), and sedge wrens (Schramm et al., 1984; Zimmerman, 1992; Herkert, 1994). However, non-significant decreases in density of sedge wrens with burning have been observed in past studies (Herkert, 1994; Robel et al., 1998). Likewise, decreases in density of dickcissels and American goldfinches have been observed (Zimmerman, 1992; Robel et al., 1998; Fuhlendorf et al., 2006). Grasshopper sparrows were unaffected by burning in this study, but have been negatively affected (Huber and Steuter, 1984; Johnson, 1997) and positively affected by burning in other studies (Herkert, 1994; Swengel, 1996; Madden et al., 1999; Fuhlendorf et al., 2006). Similarly, previous studies have found both increases (e.g., Madden et al., 1999) and decreases in species richness with burning (both total and grassland-core species; Zimmerman, 1992). However, these studies evaluated well-established grasslands in more grass-dominated landscapes, in regions with more grassland species, and likely had greater vegetative diversity including cover of woody vegetation. Consequently, the total number of grassland species observed in these studies relative to ours was relatively high and there were fewer species present to respond to fire in our study.
Although two species declined with burning, the unchanged conservation value suggests there was not a shift from high- to low-conservation-priority species, or a measurable impact on density of the highest-priority species. Again, this is because burning most impacted red-winged blackbirds, a low-priority species. The mechanism of the burn-related impacts on blackbirds and common yellowthroats was likely through modification of vegetation structure rather than depression of food resources. Burning decreased the cover and height of standing dead vegetation and cover and depth of litter but had few effects on potential arthropod food resources in the burn year, and there were no significant differences in arthropod abundance or vegetation structure during the second breeding season (Benson et al., 2007). Red-winged blackbirds nest early and are dependent on residual vegetation relative to other species, and density of both blackbirds and yellowthroats was positively related to litter depth (Benson, 2003). However, the effects of burning on height and cover of residual vegetation and litter depth in 2001 were not observed in 2002 (Benson et al., 2007), so the persistence of burn effects on red-winged blackbirds and combined grassland and wetland species in 2002 is surprising but may relate to site fidelity or real but undetected differences in habitat or food resources in 2002.
Previous research on breeding bird responses to disking is limited. In Texas, abundance and diversity of nongame birds were greater on an area managed for northern bobwhites (including disking, tree cutting, grazing exclosures, brush piles and forb plantings) than a control area (Webb and Guthery, 1983). On our study area, disking led to a change in vegetation structure and composition (including decreased residual vegetation and grass cover and increased forb cover) and an increase in the abundance and biomass of arthropods (Benson et aL, 2007). Associated with this change, fields with a disking treatment held a greater density of grassland and wetland birds between 2001 and 2002, although there were no significant differences in density or occurrence of individual species or species richness. Although not significant, these fields had greater numbers of dickcissels and grasshopper sparrows than untreated fields. Because these two species are among the highest priority species for conservation, this led to increased conservation value on disked relative to undisked fields. The results of disking treatments were likely less pronounced than for burning because of the small size of treatments relative to the field size, and because of the strip configuration. Hydric fields with block-shaped disking treatments showed more pronounced increases in density, particularly for dickcissels (Benson, 2003). For both the mesic fields included in this study and the hydric fields, strip-shaped plots distributed the affected area throughout a field and may have diffused rather than concentrated any potential effects, although disking in strips likely better preserves habitat for dense-habitat specialists like common yellowthroats and sedge wrens (Benson, 2003).
The reason that disking led to increased post-treatment density was likely related to changes in habitat and food availability; disking decreased litter, shifted treated areas from grass- to forb-dominated, and increased the abundance and dry biomass of potential arthropod food resources (Benson et al., 2007). For dickcissels, the apparent positive response in mesic fields (and hydric fields; Benson, 2003) is probably related to the increase in forb cover, a habitat variable of known importance to this species (Zimmerman, 1966; Temple, 2002), and the increase in food resources (Benson, 2003). The decreased vegetation density created by disking, if done at a larger scale, would possibly also benefit other species that prefer relatively sparse herbaceous vegetation such as grasshopper sparrows, although species dependent on dense herbaceous vegetation such as common yellowthroats and sedge wrens would likely decline (Fletcher and Koford, 2002; Benson, 2003; Murray and Best, 2003).
Irrespective of treatment effects, there were also between-year changes in density or occurrence of red-winged blackbirds, common yellowthroats, American goldfinches, grasshopper sparrows and grassland-and-wetland-bird species richness. These changes were likely caused by weather differences between the 2 y, with 2001 being relatively wet and 2002 relatively dry (National Oceanic and Atmospheric Administration, 2001, 2002). These types
of inter-annual changes in weather and associated changes in birds are fairly common in grassland systems (e.g., Ahlering et al., 2009). At our study area, these weather differences led to decreases in vegetation height, vegetation cover and arthropod abundance (irrespective of treatment; Benson et al., 2007). Thus, in 2002 fields were less suitable for species dependent on dense vegetation, such as red-winged blackbirds and common yellowthroats but were more suitable for grasshopper sparrows.
Although necessary for controlling invasion of woody plants, frequent burning may have negative effects on bird and arthropod communities. To minimize these effects, burning in most cases should be done at >3 y intervals. However, as there is great spatial and temporal variation in susceptibility of fields to invasion of woody vegetation, managers may need to adjust burn frequencies in some situations to address these concerns. Although we did not find positive responses to burning for any species, past research suggests that fire can be used to effectively manage habitat for some species, including grasshopper sparrows (e.g., Fuhlendorf et al., 2006). Disking had short-term effects on density of all grassland and wetland bird species combined and overall conservation value but no significant effect on density of individual species or species richness. Disking may be effective for increasing habitat quality for species dependent on relatively open or forb-dominated grasslands. However, because of the effort often taken to establish native-grass plantings on mesic fields, extensive disking should be avoided and alternative methods for increasing forb and arthropod abundance should be used in conjunction with any disking treatments.
APPENDIX.--Species observed, number of detections of males of each species and total number of observations used to model detection probability and generate density estimates for point counts in mesic riparian grasslands in east-central Iowa, 2001-2002. Species are listed in order of total abundance (both sexes combined) Total observations used for Species Males DISTANCE (a) Red-winged blackbird (Agelaius phoeniceus) 404 1061 Dickcissel (b) (Spiza americana) 364 618 Common yellowthroat (b) (Geothlypis trichas) 71 96 Sedge wren (b) (Cistothmus platensis) 56 64 American goldfinch (Spinus tristis) 36 107 Grasshopper sparrow (b) (Ammodramus savannarum) 37 Savannah sparrow (Passerculus sandruichensis) 18 Song sparrow (Melospiza melodia) 12 Mourning dove (Zenaida macroura) Ring-necked pheasant (Phasianus colchicus) 7 Indigo bunting (Passerina cyanea) 10 Baltimore oriole (Icterus galbula) 4 Bobolink (b) (Dolichonyx oryzivorus) 3 Common grackle (Quiscalus quiscula) Eastern kingbird (b) (Tyrannus tyrannus) House sparrow (Passer domesticus) 2 Killdeer (Charadrius vociferous) Brown-headed cowbird (Molothrus ater) 1 Red-headed woodpecker (Melanerpes erythrocephalus) American robin (Turdus migratorius) Blue-winged teal (Anas discors) Eastern meadowlark (b) (Sturnella magna) 1 Henslow's sparrow (b) (Ammodramus henslowii) 1 Northern cardinal (Cardinalis cardinalis) Vesper sparrow (Pooecetes gramineus) (a) The observations used to model detection probability as a function of distance (Buckland et al., 1993) included visually detected males in both the mesic fields used for this study and hydric fields used in other research (Benson et al., 2006, 2007) (b) Species considered to be of moderate or high conservation priority (Fitzgerald and Pashley, 2000; Nuttle et al., 2003; Benson et al., 2006)
Acknowledgments.--We thank R. Trine, T. Smith, R. Bishop and T. Little of the Iowa Department of Natural Resources (IDNR); J. Ayen, M. Lindflott and T. Meyer of the Natural Resources Conservation Service (NRCS); S. Lewis of the U.S. Fish and Wildlife Service (USFWS); R. Koford of the Iowa Cooperative Fish and Wildlife Research Unit (ICFWRU); and T. Jurik of Iowa State University (ISU) for assistance with the design, funding or implementation of this study. We are grateful to R. Koford, T. Jurik, S. Rosenstock and anonymous reviewers for valuable comments on an earlier version of this manuscript. Funding was provided by the USDA-NRCS Wildlife Habitat Management Institute and Iowa State Office, the National Fish and Wildlife Foundation, IDNR, USFWS, ICFWRU, the Iowa Agriculture and Home Economics Experiment Station (project 3478) and the Department of Natural Resource Ecology and Management at ISU. The help of M. Ackelson of the Iowa Natural Heritage Foundation was invaluable in facilitating funding of this work. C. Bouchard, A. Carlton, K. DuBois, M. Eich, P. Gesch, G. Lawton and K. Zeltinger provided valuable laboratory or field assistance. Partners in Flight prioritization scores are available from the Rocky Mountain Bird Observatory at www.rmbo.org/pif/pifdb.html.
SUBMITTED 27 OCTOBER 2009
ACCEPTED 8 OCTOBER 2010
AHLERING, M. A., D. H. JOHNSON AND J. FAABORG. 2009. Factors associated with arrival densities of grasshopper sparrow (Ammodramus savannarum) and Baird's sparrow (A. bairdii) in the upper Great Plains. Auk, 126:799-808.
APPLEGATE, R. D., B. E. FLOCK AND G. J. HORAK. 2002. Spring burning and grassland area: effects on Henslow's sparrow [Ammodramus henslowii (Audubon)] and dickcissel [Spiza americana (Gmelin)] in eastern Kansas, USA. Nat. Area. J., 22:160-162.
BENSON, T.J. 2003. Breeding bird, plant, and arthropod responses to restoration and management of riparian conservation easements in the Iowa River Corridor, east-central Iowa. M.Sc. Thesis, Iowa State University, Ames, Iowa, USA. 119 p.
--, J. J. DINSMORE AND W. L. HOHMAN. 2006. Changes in land cover and breeding bird populations with restoration of riparian habitats in east-central Iowa. J. Iowa Acad. Sci., 113:10-16.
--, -- AND --. 2007. Responses of plants and arthropods to burning and disking of riparian habitats. J. Wildl. Manage., 71:1949-1957.
BISHOP, R. A. 1981. Iowa's wetlands. Proc. Iowa Acad. of Sci., 88:11-16.
BRINSON, M. M., B. L. SWIFT, R. C. PLANTICO AND J. S. BARCLAY. 1981. Riparian ecosystems: their ecology and status. United States Fish and Wildlife Service, Kearneysville, West Virginia, USA. 155 p.
BUCKLAND, S. T., D. R. ANDERSON, K. P. BURNHAM AND J. L. LAAKE. 1993. Distance sampling: estimating abundance of biological populations. Chapman & Hall, London, United Kingdom. 446 p.
BURNHAM, K. P. AND D. R. ANDERSON. 1998. Model selection and inference: a practical information-theoretic approach. Springer-Verlag, New York, USA. 353 p.
CARTER, M. F., W. C. HUNTER, D. N. PASHLEVANI AND K. V. ROSENBERG. 2000. Setting conservation priorities for landbirds in the United States: the Partners in Flight Approach. Auk, 117:541-548.
CINK, C. L. AND P. E. LOWTHER. 1989. Breeding bird populations of a floodplain tallgrass prairie in Kansas. Proc. North Amer. Prairie Conf., 11:259-262.
COUSENS, R. AND C. MARSHALL. 1987. Dangers in testing statistical hypotheses. Ann. Appl. Biol., 111:469-476.
DAHL, T. E. 1990. Wetlands: losses in the United States 1780s to 1980s. United States Fish and Wildlife Service, Washington, D.C., USA. 22 p.
FITZGERALD. A. AND D. N. PASHLEY. 2000. Partners in Flight bird conservation plan for the Dissected Till Plains (physiographic area 32). <http://www.partnersinflight.org/bcps/plan/p1-32-10.pdf> Accessed 21 Oct. 2009. 60 p.
FLETCHER, R.J.,JR. AND R. R. KOFORD. 2002. Habitat and landscape associations of breeding birds in native and restored grasslands. J. Wildl. Manage., 66:1011-1022.
FREDRICKSON, SON, L. H. AND F. A. REID. 1986. Wetland and riparian habitats: a nongame management overview, p. 59-96. In: J. B. Hale, L. B. Best and R. L. Clawson (eds.). Management of nongame wildlife in the Midwest: a developing art. North Central Section of the Wildlife Society, Grand Rapids, Michigan, USA.
FUHLENDORF, S. D., W. C. HARRELL, D. M. ENGLE, R. G. HAMILTON, C. A. DAVIS AND D. M. LESLIE, JR. 2006. Should heterogeneity be the basis for conservation? Grassland bird response to fire and grazing. Ecol. Appl., 16:1706-1716.
GRAY, R. L. 2005. Wetlands Reserve Program: a partnership to restore wetlands and associated habitat, p. 1189. In: C. J. Ralph and T. D. Rich (eds.). Bird Conservation Implementation and Integration in the Americas: Proceedings of the Third International Partners in Flight Conference, Volume 2. USDA Forest Service General Technical Report PSW-GTR-191.
GREGORY, S. V.,J. F. SWANSON, W. A. MCKEE AND K. W. CUMMINS. 1991. An ecosystem perspective of riparian zones. BioScience, 41:540-551.
HEARD, L. P., A. W. ALLEN, L. B. BEST, S.J. BRADY, W. BURGER, A.J. ESSER, E. HACKETT, D. H. JOHNSON, R. L.
PEDERSON, R. E. REYNOLDS, C. REWA, M. R. RYAN, R. T. MOLLEUR AND P. BUCK. 2000. A comprehensive review of Farm Bill contributions to wildlife conservation, 1985-2000. In: W. L. Hohman and D. J. Halloum (eds.). United States Department of Agriculture, Natural Resources Conservation Service, Wildlife Habitat Management Institute, Technical Report, USDA/NRCS/WHMI-2000.
HERKERT, J. R. 1994. Breeding bird communities of Midwestern prairie fragments: the effects of prescribed burning and habitat-area. Nat. Area. J., 14:128-135.
HOFFMAN, R. AND K. KEARNS. 1997. Wisconsin manual of control recommendations for ecologically invasive plants. Wisconsin Department of Natural Resources, Madison, Wisconsin, USA. 102 p.
HUBER, G. E. AND A. A. STEUTER. 1984. Vegetation profile and grassland bird response to spring burning. Prairie Nat., 16:55-61.
HULBERT, L. C. 1988. Causes of fire effects in tallgrass prairie. Ecology, 69:46-58.
IOWA DEPARTMENT OF AGRICULTURE AND LAND STEWARDSHIP. 1999. Iowa wetlands and riparian areas conservation plan. Division of Soil Conservation, Des Moines, Iowa, USA. 100 p.
JOHNSON, D. H. 1997. Effects of fire on bird populations in mixed-grass prairie, p. 181-206. In: F. L. Knopf and F. B. Samson (eds.). Ecology and conservation of Great Plains vertebrates. Springer-Verlag, New York, New York, USA.
-- AND M. D. SCHWARTZ. 1993. The Conservation Reserve Program and grassland birds. Conserv. Biol., 7:934-937.
KUCERA, C. L. AND J. H. EHRENREICH. 1962. Some effects of annual burning on central Missouri prairie. Ecology, 43:334-336.
LITTELL, R. C., G. A. MILLIKEN, W. W. STROUP, R. D. WOLFINGER AND O. SCHANENBERGER. 2006. SAS for mixed models. SAS Institute, Cary, North Carolina, USA. 813 p.
MADDEN, E. M., A.J. HANSEN AND R. K. MURPHY. 1999. Influence of prescribed fire history on habitat and abundance of passerine birds in northern mixed-grass prairie. Can. Field Nat., 113:627-640.
MADISON, L. A., T. G. BARNES ANDJ. D. SOLE. 1995. Improving northern bobwhite brood rearing habitat in tall fescue dominated fields. Proc. Annu. Conf. Southeast. Assoc. Fish and Wildl. Agencies, 49:525-536.
MANLEV, S. W., R. S. FULLER, J. M. LEE AND L. A. BRENNAN. 1994. Arthropod response to strip disking in old fields managed for northern bobwhite. Proc. Annu. Conf. Southeast. Assoc. Fish and Wildl. Agencies, 48:227-235.
MAPSTONE, B. D. 1995. Scalable decision rules for environmental impact studies: effect size, type I, and type II errors. Ecol. Appl., 5:401-410.
MERIGLIANO, M. F. AND P. LESICA. 1998. The native status of reed canarygrass (Phalaris arundinacea L.) in the inland northwest, USA. Nat. Area. J., 18:223-230.
MORAN, M. D. 2003. Arguments for rejecting the sequential Bonferroni in ecological studies. Oikos, 100:403-405.
MURRAY, L. D. AND L. B. BEST. 2003. Short-term bird response to harvesting switchgrass for biomass in Iowa. J. Wildl. Manage., 67:611-621.
NATIONAL OCEANIC AND ATMOSPHERIC ADMINISTRATION. 2001. Climatological data annual summary, Iowa. Volume 112. National Climatic Center Data, Asheville, North Carolina, USA.
--. 2002. Climatological data annual summary, Iowa. Volume 113. National Climatic Center Data, Asheville, North Carolina, USA.
NATIONAL RESEARCH COUNCIL. 2002. Riparian areas: functions and strategies for management. National Academy Press, Washington, D.C., USA. 428 p.
NELSON, J. C., L. DEHAAN, R. E. SPARKS AND L. ROBINSON. 1998. Presettlement and contemporary vegetation patterns along two navigational reaches of the Upper Mississippi River, p. 51-60. In: T. D. Sisk (ed.). Perspectives on land use history of North America: a context for understanding our changing environment. United States Geological Survey, Reston, Virginia, USA.
NUTTLE, T., A. LEIDOLF AND L. W. BURGER, JR. 2003. Assessing conservation value of bird communities with Partners in Flight-based ranks. Auk, 120:541-549.
PATTERSON, M. P. AND L. B. BEST. 1996. Bird abundance and nesting success in Iowa CRP fields: the importance of vegetation structure and composition. Am. Midl. Nat., 135:153-167.
PETERJOHN, B. G. AND J. R. SAUER. 1999. Population status of North American grassland birds from the North American Breeding Bird Survey, 1966-1996. Stud. Avian Biol., 19:27-44.
POOLE, A., P. STETTENHEIM and F. GILL (eds.). 1992-2002. The birds of North America: life histories for the 21st century. The Academy of Natural Sciences, Philadelphia, Pennsylvania, USA, and the American Ornithologists' Union, Washington, D.C., USA.
QUINN, G. P. AND M. J. KEOUGH. 2002. Experimental design and data analysis for biologists. Cambridge University Press, Cambridge, United Kingdom. 537 p.
RALPH, C. J., J. R. SAUER and S. DROGE (eds.). 1995. Monitoring bird populations by point counts. U.S. Forest Service General Technical Report PSW-GTR-149.
REINKING, D. L. 2005. Fire regimes and avian responses in the central tallgrass prairie. Stud. Avian Biol., 30:11 6-126.
ROBEL, R.J.,J. P. HUGHES, S. D. HULL, K. E. KEMP AND D. S. KLUTE. 1998. Spring burning: resulting avian abundance and nesting in Kansas CRP. J. Range Manage., 51:132-138.
SAMSON, F. AND F. KNOPr. 1994. Prairie conservation in North America. BioScience, 44:418-421.
SCHARTZ, R. L. AND J. L. ZIMMERMAN. 1971. The time and energy budget of the male dickcissel (Spiza americana). Condor, 73:65-76.
SCHOENER, T. W. 1968. Sizes of feeding territories among birds. Ecology, 49:123-141.
SCHRAMM, P., D. S. SCHRAMM AND S. G. JOHNSON. 1984. Seasonal phenology and habitat selection of the sedge wren Cistothorus platensis in a restored tallgrass prairie. Proc. North Amer. Prairie Conf, 9:95-99.
SMITH, D. D. 1998. Iowa prairie: original extent and loss, preservation and recovery attempts. J. Iowa Acad. Sci., 105:94-108.
SWENGEL, S. R. 1996. Management responses of three species of declining sparrows in tallgrass prairie. Bird Conser. Int., 6:241-253.
TEMPLE, S. A. 2002. Dickcissel, p. 1-24. In: A. Poole and F. Gill (eds.). The birds of North America, number 703. The Academy of Natural Sciences, Philadelphia, Pennsylvania, USA, and the American Ornithologists' Union, Washington, D.C., USA.
UNITED STATES DEPARTMENT OF AGRICULTURE. 1976. Iowa-Cedar rivers basin study. Des Moines, Iowa, USA. 250 p.
VICKERY, P. D., P. L. TUBARO, J. M. CARDOSO DA SILVA, B. G. PETERJOHN, J. R. HERKERT AND R. B. CAVALCANTI. 1999. Conservation of grassland birds in the western hemisphere. Stud. Avian Biol., 19:2-26.
WARREN, S. D., C.J. SCIFERS AND P. D. TEEL. 1987. Response of grassland arthropods to burning: a review. Agr. Ecosyst. Environ., 19:105-130.
WEAVER, J. E. 1968. Prairie plants and their environment. University of Nebraska Press, Lincoln, Nebraska, USA. 276 p.
WEBB, W. M. AND F. S. GUTHERY. 1983. Avian response to habitat management for northern bobwhites in northwest Texas. J. Wildl. Manage., 47:220-222.
ZIMMERMAN, J. L. 1966. Polygyny in the dickcissel. Auk, 83:534-546.
--. 1992. Density-independent factors affecting the avian diversity of the tallgrass prairie community. Wilson Bull., 104:85-94.
THOMAS J. BENSON (1)
Department of Natural Resource Ecology and Management, Iowa State University, 339 Science Hall II, Ames 50011
JAMES J. DINSMORE
Department of Natural Resource Ecology and Management, Iowa State University, 339 Science Hall II, Ames 50011
WILLIAM L. HOHMAN (2)
United States Department of Agriculture/Natural Resources Conservation Service, Wildlife Habitat Management Institute, Department of Natural Resource Ecology and Management, Iowa State University, 339 Science Hall II, Ames 50011
(1) Present address: Illinois Natural History Survey, 1816 South Oak Street, Champaign 61820; e-mail: email@example.com
(2) Present address: United States Department of Agriculture/Natural Resources Conservation Service, Central National Technology Support Center, CNTSC, Fort Worth, Texas 76115
TABLE 1.--Density (mean and standard error; males-ha) of common bird species, species richness (species-field) and conservation value in mesic riparian grasslands in east-central Iowa, USA, 2001-2002 2001 Unburned Burned (n = 10) (n = 10) Variable [bar.x] SE (a) [bar.x] SE (a) Density Red-winged blackbird 1.19 0.24 0.64 0.13 Dickcissel 0.70 0.15 0.68 0.17 Common yellowthroat (b) 0.43 0.11 0.06 0.02 Sedge wren (b) 0.28 0.16 0.25 0.11 American goldfinch (b) 0.10 0.03 0.10 0.03 Grasshopper sparrow 0.00 0.00 0.06 0.06 Grassland/wetland species (c),(d) 2.76 0.31 1.90 0.18 Species richness Grassland/wetland species (c) 5.00 0.39 5.00 0.33 All species 5.80 0.39 5.70 0.33 Conservation value (e) 52.33 5.96 38.07 4.60 2002 Disked Unburned Burned (n = 1) (n = 6) Variable [bar.x] SE (a) [bar.x] SE (a) Density Red-winged blackbird 0.87 -- 0.62 0.24 Dickcissel 0.56 -- 0.93 0.22 Common yellowthroat (b) 0.00 -- 0.15 0.09 Sedge wren (b) 0.26 -- 0.09 0.09 American goldfinch (b) 0.00 -- 0.07 0.04 Grasshopper sparrow 0.00 -- 0.32 0.21 Grassland/wetland species (c),(d) 1.77 -- 2.25 0.13 Species richness Grassland/wetland species (c) 4.00 -- 4.50 0.43 All species 4.00 -- 5.67 0.76 Conservation value (e) 34.25 -- 46.95 2.89 2002 Undisked Unburned Burned (n = 9) (n = 4) Variable [bar.x] SE (a) [bar.x] SE (a) Density Red-winged blackbird 0.92 0.21 0.24 0.06 Dickcissel 0.75 0.17 0.58 0.12 Common yellowthroat (b) 0.15 0.07 0.03 0.03 Sedge wren (b) 0.43 0.23 0.45 0.30 American goldfinch (b) 0.07 0.04 0.03 0.03 Grasshopper sparrow 0.02 0.01 0.06 0.04 Grassland/wetland species (c),(d) 2.36 0.36 1.41 0.40 Species richness Grassland/wetland species (c) 4.11 0.51 4.00 0.82 All species 5.00 0.67 4.00 0.41 Conservation value (e) 46.85 7.33 30.76 8.43 (a) Standard error estimates are based on variation within point estimates and do not explicitly account for detection probability (b) Density corrected for detectability using program DISTANCE (Buckland et al., 1993) (c) Obligate and facultative grassland and wetland bird species (Poole et al., 1992-2002; Vickery et aL,1999) (d) Includes estimates corrected for detectability and uncorrected estimates (e) Conservation value = [[summation].sup.S.sub.i=1] [density.sub.i] x [PIFscore.sub.i] TABLE 2.--Statistics for effects of burning, disking, and year on bird density (males-ha) or presence, species richness (species/field) and conservation value in mesic riparian grasslands in east-central Iowa, USA, 2001-2002 Burn Disk Variable F P F P Density/presence Red-winged blackbird (a) 4.66 0.047 0.37 0.555 Dickcissel (a) 0.01 0.909 0.01 0.927 Common yellowthroat (a) 6.17 0.024 0.32 0.582 Sedge wren (b) 0.01 0.920 0.69 0.416 American goldfinch (b) 0.54 0.472 0.34 0.567 Grasshopper sparrow (b) 1.59 0.224 0.00 0.962 Grassland/wetland species (a),(c) 4.85 0.043 0.38 0.120 Species richness (a) Grassland/wetland species (a),(c) 0.17 0.681 0.17 0.684 All species (a) 0.10 0.760 0.18 0.679 Conservation value (a),(d) 2.44 0.136 0.20 0.662 Year Burn X Year Variable F P F P Density/presence Red-winged blackbird (a) 4.68 0.033 0.02 0.890 Dickcissel (a) 1.62 0.220 0.32 0.579 Common yellowthroat (a) 4.42 0.040 7.10 0.011 Sedge wren (b) 0.06 0.813 1.32 0.253 American goldfinch (b) 7.51 0.007 0.34 0.562 Grasshopper sparrow (b) 3.89 0.063 0.00 0.995 Grassland/wetland species (a),(c) 0.12 0.729 0.00 0.959 Species richness (a) Grassland/wetland species (a),(c) 4.18 0.049 0.31 0.586 All species (a) 2.79 0.112 0.13 0.727 Conservation value (a),(d) 0.07 0.795 0.05 0.825 Disk X Year Variable F P Density/presence Red-winged blackbird (a) 1.69 0.198 Dickcissel (a) 2.99 0.103 Common yellowthroat (a) 0.35 0.568 Sedge wren (b) 0.01 0.908 American goldfinch (b) 0.16 0.688 Grasshopper sparrow (b) 0.48 0.496 Grassland/wetland species (a),(c) 5.67 0.019 Species richness (a) Grassland/wetland species (a),(c) 2.69 0.131 All species (a) 1.03 0.327 Conservation value (a),(d) 7.25 0.023 (a) Effects of bum, disk, year, burn X year, and disk X year were tested with repeated-measures ANOVA (SAS PROC MIXED; Littell et al., 2006; 1, 10 124 df) (b) Effects of bum, disk, year, burn X year and disk X year were tested with generalized linear mixed models using a binomial distribution and logit link function (SAS PROC GLIMMIX; Littell et al., 2006; 1, 16-154 df) (c) Obligate and facultative grassland and wetland bird species (Poole et al., 1992-2002; Vickery et al., 1999) (d) Conservation value = [[summation].sup.S.sub.i=e] [density.sub.i] x [PIFscore.sub.i]
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|Author:||Benson, Thomas J.; Dinsmore, James J.; Hohman, William L.|
|Publication:||The American Midland Naturalist|
|Date:||Apr 1, 2011|
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