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                  <text>COLORADO PARKS AND WILDLIFE - AVIAN RESEARCH PROGRAM
Progress Report
October 28, 2016
TITLE: Pilot study to evaluate avian response to conservation reserve program midcontract management practices in northeastern Colorado
AUTHOR: Adam C. Behney
PROJECT PERSONNEL: Trent Verquer, Ed Gorman, Jim Gammonley
Period Covered: 1 February 2016 – 30 Sep 2016
All information in this report is preliminary and subject to further evaluation.
Information MAY NOT BE PUBLISHED OR QUOTED without permission of the author.
Manipulation of these data beyond that contained in this report is discouraged.

EXTENDED ABSTRACT
The Conservation Reserve Program (CRP) is a government program in which landowners
are paid to maintain grass cover on land that was, and would otherwise be, used for row-crop
agriculture. Overall, the CRP has had many documented benefits to wildlife, specifically
grassland birds, many of which are experiencing range-wide declines due to habitat loss and
degradation. However, as CRP fields age with no disturbance, litter increases, bare ground
decreases, vegetation density increases, and plant species and structural diversity decrease, which
can reduce the value of CRP fields to certain bird species. Therefore, beginning in 2004, some
type of “mid-contract management” was required on CRP fields. In northeastern Colorado this
management typically consists of haying, disking, or disking and interseeding with forbs.
Although there is some evidence that disking and interseeding can provide benefits to ringnecked pheasants in other regions, we lack a thorough understanding of how these various
management practices affect pheasants and grassland dependent songbirds in northeastern
Colorado. In an effort to provide guidance to managers and landowners regarding grassland
management on CRP fields in northeastern Colorado, we will monitor the response of pheasants
and songbirds to the three most common CRP mid-contract management practices (haying,
disking, disking &amp; interseeding).
I will randomly assign treatments to halves of each study field so each treatment is paired
with a control. Beginning in late winter, we will capture pheasants on and around study fields
using nightlighting techniques. All captured females will be fitted with a necklace-style radio
transmitter and released at the capture site. We will locate all marked birds three times per week
and determine nest sites by locations occurring in the same spot on multiple occasions. For
successful nests, we will locate broods three times per week and flush broods at days 10 and 21
post-hatch to estimate brood survival. We will conduct vegetation samples at nest and brood
flush sites as well as paired random points to assess factors affecting nest and brood survival and
nest and brood site selection. We will conduct two rounds of songbird point counts at six points
within each study field throughout the summer.
1

�In 2016, we conducted a pre-treatment pilot study to gather baseline demographic
information on pheasants and songbirds in the study area. We captured and monitored 34 female
pheasants and surveyed songbirds on two occasions in six fields. Adult pheasant survival during
the breeding season (four months) was low 0.29 ± 0.09 and 76% of the mortality occurred during
May and June. Nest survival was influenced by whether nests were located in wheat fields (0.43
± 0.20) or CRP fields (0.33 ± 0.18). For nests in CRP fields, the amount of visual obstruction at
the nest site positively influenced nest survival (Fig 2). Pheasants selected nest sites with a
greater percentage of warm-season grasses (nest sites: 45.8 ± 8.3 %, random points: 27.3 ± 3.7
%). We was able to monitor eight pheasant broods, two of which survived to 10 days post-hatch
and one survived to 21 days post-hatch. Estimates from a constant survival model predicted
brood survival to 21 days post-hatch was 0.07 ± 0.07. Western meadowlarks were the most
common bird detected during point counts, followed by grasshopper sparrows, and mourning
doves.
INTRODUCTION
Widespread loss and alteration of grasslands in the United States has had many
consequences, most notably, increased wind erosion of soil and the loss and deterioration of
habitat for grassland-dependent wildlife (Samson and Knopf 1994). Due to these and other
concerns, conservation programs have been developed by governmental and other organizations
to maintain or increase the amount of grassland on the landscape. The Conservation Reserve
Program (CRP) is one of these programs in which landowners are paid to maintain grass cover
on land that was, and would otherwise be, used for row-crop agriculture. In 2012, over 11
million ha of land were enrolled in CRP, costing about 1.7 billion dollars (U.S. Department of
Agriculture 2012).
Overall, the CRP has had many documented benefits to wildlife, specifically grassland
birds (Patterson and Best 1996, O’Connor et al. 1999, Ryan et al. 1998). Many grassland bird
species are experiencing continental wide declines (Vickery and Herkert 1999, Peterjohn 2003,
Brennan and Kuvlesky 2005). In the western United States, this is mainly the result of habitat
fragmentation due to modern row-crop agriculture and rangeland deterioration (summarized in
Brennan and Kuvlesky 2005). In a countrywide analysis, O’Connor et al. (1999) found that the
abundance of many grassland bird species, including ring-necked pheasants (Phasianus
colchicus; hereafter ‘pheasants’), were strongly associated with CRP enrolment. Ryan et al.
(1998) found that grassland bird relative abundance was up to 10.5 times greater, nest abundance
was 13.5 times greater, and nest success was 4% greater in CRP fields than rowcrop agriculture
fields. Pheasant populations increased in Minnesota and Dixon County, Nebraska as CRP
acreage increased (summarized in Ryan et al. 1998). King and Savidge (1995) found that
pheasant counts were significantly greater in areas with high CRP enrollment. Pheasant numbers
in Iowa increased significantly in areas composed primarily of cropland as the CRP was initiated
and landowners began to enroll their lands (Riley 1995). Nielson et al. (2008) found in a nine
state analysis, that pheasant counts increased 22% with every 319 ha increase in CRP.
However, not all studies have been able to detect these positive benefits of CRP to
grassland birds. Rodgers (1999) reported that in western Kansas pheasant populations did not
respond to CRP and speculated that this was due to the simultaneous deterioration of weedy
wheat stubble fields as a result of increased herbicide use. Furthermore, the value of CRP for
various life stages (nesting, brood rearing, overwintering) may be dependent on the age of the
2

�field or level of succession that has occurred (Berthelsen and Smith 1995, King and Savidge
1995, Millenbah et al. 1996, Ryan et al. 1998, Rodgers 1999, McCoy et al. 2001, Matthews et al.
2012a,b). As CRP fields age, litter increases, bare ground decreases, vegetation density
increases, and plant species and structural diversity decrease (McCoy et al. 2001). Rodgers
(1999) suggested that this litter accumulation may restrict the movements of pheasants. In
Michigan, young (1 – 2 year) CRP fields had the greatest relative abundance and diversity of
birds whereas older (3 – 6 year) fields had greater nest density and success (Millenbah et al.
1996).
Due to this possible reduction in value to wildlife as CRP fields age, beginning in 2004
some type of disturbance was required prior to the end of year 6 for 10 year contracts and year 9
for 15 year contracts (‘mid-contract management’, U.S. Department of Agriculture 2015) and
additional management may occur except during the last three years of the contract. Disturbance
is designed to “ensure plant diversity and wildlife benefits, while ensuring protection of the soil
and water resources” and may include haying, grazing, burning, herbicide, light disking, interseeding, or light disking and interseeding (U.S. Department of Agriculture 2015:428). The
results of this mid-contract management have generally been positive for birds. In Nebraska,
overall avian abundance, avian species richness, and diversity was greater in fields that had been
disked and interseeded with legumes compared with unmanaged fields (Negus et al. 2010). Also
in Nebraska, Matthews et al. (2012b) found that ring-necked pheasant nests in CRP fields that
had been recently disked and interseeded had a greater survival rate than nests in unmanaged
grasslands and brood survival increased with the amount of time spent in disked and interseeded
fields. Hen pheasants selected disked and interseeded portions of fields for nesting and brood
rearing over unmanaged fields (Matthews et al. 2012a). However, disking and interseeding are
not the only management practice used and there has been little evaluation of alternatives.
Another practice under the CRP is management for Pollinator Habitat (CP42, hereafter
‘pollinator plots’). The purpose of pollinator plots are to “establish habitat to support a diversity
of pollinator species” (U.S. Department of Agriculture 2015:257). Under this program, plots of
at least 0.2 ha are seeded with at least 9 pollinator-friendly wildflowers, legumes, and/or shrubs,
and less than 25% grasses; native, preferably bunchgrasses (U.S. Department of Agriculture
2015). Increased forb components in fields have been shown to support greater invertebrate
biomass (Jamison et al. 2002). Pheasant chicks primarily consume invertebrates (Wiens and
Totenberry 1979) and chick survival may be directly linked to invertebrate density (Hill 1985).
Therefore, pollinator plots are thought to represent excellent bird habitat specifically for pheasant
brood rearing. However, this linkage between pheasant brood site selection and pollinator plots
has not been formally studied. Furthermore, the size at which these pollinator plots might be
beneficial is completely unknown. Currently plots must be at least 0.2 ha to qualify for the CRP.
However, if plots smaller than 0.2 ha prove beneficial, it would be a less expensive way for
landowners and managers to provide quality brood-rearing habitat. Or alternatively, if plots
must be larger than 0.2 ha to be selected, fewer, larger plots in a field may be a more worthwhile
strategy.
In northeast Colorado prairies, pheasants are an important recreational and thus economic
resource. In 2012, it was estimated that over 27,000 pheasant hunters harvested about 95,000
pheasants (Colorado Parks and Wildlife 2012). Due to the importance of pheasants in the region,
there is substantial incentive to maximize the utility of already protected grasslands (e.g., CRP)
to pheasants. Furthermore, a number of songbird species likely to use CRP fields in northeastern
Colorado are listed as species of concern in the Conservation Plan for Grassland Species
3

�(Colorado Division of Wildlife 2003): Cassin’s sparrow (Aimophila cassinii; tier 1), grasshopper
sparrow (Ammodramus savannarum; tier 2), and dickcissel (Spiza americana; tier 2), as well as
the State Wildlife Action Plan (Colorado Parks and Wildlife 2015): bobolink (Dolichonyx
oryzivorus, tier 2), grasshopper sparrow (tier 2), and Cassin’s sparrow (tier 2). In 2012, there
were over 880,000 ha of land in Colorado enrolled in CRP (U.S. Department of Agriculture
2012) which, if managed optimally, could provide additional recreation opportunity by
producing more pheasants and serve to increase grassland songbird populations, especially those
of conservation concern. Whereas evaluation of grassland management practices on songbirds
and pheasants has occurred in other regions little information exists on optimal management
strategies in northeast Colorado. Because optimal grassland management strategies may depend
on local factors such as site productivity (Spears et al. 1993), it is important to not generalize
across regions or species. In an effort to provide guidance to managers and landowners
regarding grassland management on CRP fields in northeastern Colorado, we will monitor the
response of pheasants and songbirds to the three most common CRP mid-contract management
practices (haying, disking, disking &amp; interseeding) as well as pollinator plots.
OBJECTIVES
1. Estimate pheasant adult female, nest, and brood survival in relation to CRP practices
(haying, disking, disking &amp; interseeding, pollinator plots) and general vegetation
characteristics.
2. Assess how various CRP practices influence pheasant nest and brood site selection.
3. Estimate songbird density or occupancy in CRP fields with different management
practices.
METHODS
Study area and site selection
I will conduct this study in Logan, Phillips, Sedgwick, Washington, and Yuma Counties
in northeastern Colorado. We will identify two study sites at least 20 km apart, in areas with
high densities of CRP.
Year one (2016) will serve as a pilot study to gather pre-treatment baseline demographic
information. We will select study sites where treatments are scheduled to be conducted in the
near future. During years one and two, we will work with management personnel and
landowners to create experimental treatments after the primary nesting season, which will be
used in years two and three. We will divide each field within the study site in half and randomly
assign a treatment (haying, disking, disking &amp; interseeding) to one half, while the other half will
serve as a control. We will also randomly select fields in which to plant pollinator plots. We
will randomly select 3 fields at each study site and establish two to four pollinator plots of
varying sizes (0.2, 2, 8, and 40 ha) in each field.
Field Methods
Generally, methods will follow Matthews et al. (2012a,b).

4

�Trapping
In March, we will begin trapping pheasants using baited walk-in traps and/or nightlighting techniques (Labisky 1959, Wilbur 1967, Matthews et al. 2012a,b). Walk-in traps will be
made of 14 gauge welded wire with a funnel made of welded wire or chicken wire leading into
the trap and a cloth mesh top of trap (Smith et al. 1999, Flock and Applegate 2002). We will
distribute 5 – 10 traps throughout each study site and check traps twice daily (mid-morning and
at sunset). Traps will be closed overnight because pheasants are not active at night (Giudice and
Ratti 2001). Night-lighting (Labisky 1959) is one of the most commonly used and successful
ways to capture pheasants (Whiteside and Guthery 1983, Perkins et al. 1997, Matthews et al.
2012a,b, T. Matthews personal communication). Night-lighting consists of driving through
fields with an ATV or truck and using flood and spotlights to scan the field for pheasants. When
a pheasant is detected, the light is kept on the bird while another person approaches and puts a
net over the bird. We will distribute night-lighting efforts throughout each study area with the
goal of capturing and radio-tagging 30 females (15 at each site). Year one (2016) will be treated
as a pilot study and data from this year will be used to determine sample sizes for the following
years. We will weigh and estimate age for each captured hen as well as affix a leg band and an
18 g necklace style radio transmitter (1.9% of mean adult female body mass reported in Giudice
and Ratti 2001). Marcstrom et al. (1989) showed that recovery rates of pheasants with necklace
style radio transmitters weighing 15 and 25 g were not different than pheasants with leg bands
only. Captured males will receive a leg band and be released immediately. Every effort will be
made to avoid injuring birds. However, if an injury should occur, observers will decide whether
the injury will invariably result in the bird’s death, and if so, the bird will be euthanized by rapid
cervical dislocation.
Nest and brood monitoring
Beginning in mid-April, we will locate each radio-marked pheasant three times per week
using a homing technique (White and Garrott 1990). Observers will walk toward the bird and
when they approach it, they will circle the bird at around 30 m to pinpoint an exact location. We
will then estimate the location based on the compass bearing and distance to the bird from the
observers location. Every attempt will be made to avoid flushing pheasants.
Nests sites will be determined by observing pheasant hens in the same location on
multiple, subsequent days. When a hen is deemed to be nesting, we will approach her to about
10 m and place a stake with or without flagging, 10 m to the North and South of the estimated
nest location. If visually oriented nest predators (e.g., ravens) are regularly observed around
study fields, flagging will not be used near nests. Every effort will be made to not flush hens
during this visit. Any time observers approach nests, they will take a different, circuitous route
to avoid making a path directly to the nest for predators to follow. We will continue to monitor
the locations of nesting hens ≥ 3 times per week and if the hen is found to be off the nest, we will
go to the nest location to get an exact GPS point for the nest, count the number of eggs, and note
the status of the nest (active, successful, depredated, or abandoned). If we do not have the
opportunity to visit the nest while the incubating hen happens to be off the nest, we will flush the
hen during the last week of incubation to get an exact location and count eggs. Nests will be
deemed successful if ≥ 1 egg hatches.
I will continue to locate hens from successful nests (presumably with a brood) ≥ 3 times
per week using triangulation or homing. On day 10 and 21 post-hatch, we approach hens at

5

�dawn when they are still at nocturnal roost sites and visually confirm chick presence by flushing
if necessary. We will also note the UTMs of these specific brood sites.
Vegetation sampling
I will conduct a vegetation sample at each nest and each brood site (day 10 and 21 flush
site), within a week of obtaining the location. To represent available habitat, we will sample
vegetation at 4 random points within 200 m (about the daily movement of a hen pheasant,
Whiteside and Guthery 1983, Matthews et al. 2012a) of each nest or brood site. At each point
we will estimate the percentage canopy coverage of each plant species and bare ground within a
1 m2 frame centered on the point. We will also assess visual obstruction using a Robel pole
(Robel et al. 1970) and record the lowest dm visible on a 2.5 cm diameter pole, read from 4 m
away, 1 m high, in 4 directions, 90° apart.
I will digitize all study fields into a GIS to assess landcover characteristics at and around
nest and brood sites. Landcover categories will include: 1) disked, 2) disked and interseeded, 3)
hayed, 4) pollinator plot, 5) grass field: no management, and 6) active crop field (split into
specific crop type, e.g., corn, wheat). For each point, we will calculate the percentage of each
landcover type within a 200, 400, and 800 m radius circle centered on the point to evaluate the
scale at which hens select nest and brood sites. Lastly, we will calculate the size of the occupied
patch.
Songbirds
To assess songbird density in relation to management practice, we will conduct point
counts in the study fields. We will conduct point counts in three patches of each treatment type
and, in years one and two, in 3 fields scheduled for treatment the following years. These
untreated fields will serve as a control the first year they are sampled and also as a baseline for
which to compare post-treatment. We will establish 6 points spaced 250 m apart along a line in a
random direction and starting position. Point counts will follow the Integrated Monitoring in
Bird Conservation Regions protocol (Hanni et al. 2015). Counts will be six minutes in duration
and we will note the species, distance to each bird heard or seen, as well as the time that the bird
was detected. We will conduct point count surveys in early June and July in each field. The
number of points may be adjusted based on the number of detections during initial surveys
according to Buckland et al. (1993).
Statistical Analysis
Adult survival
We will use the nest survival model in Program Mark (White and Burnham 1999,
Dinsmore et al. 2002) to estimate the daily survival rate of adult female pheasants. The nest
survival model is useful for estimating survival when detections occurred at irregular intervals
(i.e., lacks some of the assumptions of the known-fate data type). To extrapolate from daily
survival rate (DSR) to breeding season survival (May – August) we will raise DSR to the power
of the number of days in May, June, July and August and calculate the standard error using the
delta method (Powell 2007). For the first year pilot study, we present estimates from a null
model (constant survival) only, but thereafter we will assess covariates related to date and
percentage of locations in habitat treatment areas and compare models using an informationtheoretic approach (Burnham and Anderson 2002).

6

�Nest and brood survival
We will use the nest survival model in program Mark (White and Burnham 1999,
Dinsmore et al. 2002) to estimate nest and brood survival. We will group the predictor variables
into a vegetation group (% coverage of bare ground, forb, warm-season grass, cool-season grass,
etc. and visual obstruction), a landcover group (landcover of site, % landcover at various scales),
and date. We will find the most parsimonious model within the vegetation and landcover groups
and then compare those models to each other and combined. Lastly, we will add date and date2
to account for temporal effects, if it increases model parsimony. We will also include a null
model for comparison. We will evaluate candidate models using an information-theoretic
approach (Burnham and Anderson 2002), using ΔAICc and model weights (wi).
Nest and brood site selection
We will use discrete choice models (Cooper and Millspaugh 1999) in the mlogit package
(Croissant 2013) in program R (R Core Team 2015) to evaluate nest and brood site selection.
The choice set for each nest or brood site will consist of five alternatives (the chosen point and
four random points). We will use the same modeling strategy and variables as described above.
Songbirds
We will use distance sampling and/or time removal to estimate detection probability and
density of each species in each field and treatment type according to Buckland et al. (1993),
Farnsworth et al. (2002), and Amundson et al. (2014). If low sample sizes preclude estimating
density for some species, we will attempt to estimate occupancy (MacKenzie et al. 2006). We
will test for differences in density or occupancy among treatment types by comparing a null
model with a model including field landcover type as a predictor variable.
RESULTS AND DISCUSSION FROM YEAR ONE PILOT STUDY
Pheasants
Capture and adult female survival
We captured and affixed radio transmitters on 34 female pheasants and we had four
collars slip off soon after capture. Overall, we had 23 mortalities. Of the collars we were able to
recover and assess cause of mortality, we estimated that one mortality was due to hail, one ran
into a powerline, one was avian predation, and 10 were mammalian predation. Most mortalities
occurred early in the summer with 76% occurring during May and June. Based on initial
analysis, a model estimating constant survival over the breeding season predicted a daily survival
rate of 0.990 ± 0.002. Extrapolating over the entire four month breeding season (May – August),
the estimated overall breeding season survival was 0.291 ± 0.087. These estimates are lower
than that reported in the literature (Leif 1994, Schmitz and Clark 1999). In northeastern
Colorado, Snyder (1985) found six month breeding season survival was 0.56 with greatest
mortality occurring in April. My results of low adult female breeding season survival are
interesting and counter to field observations of abundant pheasants in the area. It is possible that
radio packages negatively influenced survival although previous research has shown that similar
weight transmitters did not affect recovery rates (Marcstrom et al. 1989). Furthermore, we never
deployed transmitters on birds where the mass of the transmitter would make up more than 3%
of body mass.

7

�Nest site selection
The most parsimonious model of nest microhabitat selection indicated that percent warmseason grass within the 1 m2 sampling frame was the most influential factor determining nest site
selection (Table 1) and this relationship was positive (Fig. 1). Nest sites had 45.8 ± 8.3 % and
random points had 27.3 ± 3.7 % warm-season grasses in the sampling frame. These results are
consistent with Matthews et al. (2012a) in Nebraska who found a weak positive selection for
warm-season grasses and noted the majority of hens nesting in CRP nested in areas dominated
by warm-season grasses.
Nest survival
We monitored 23 pheasant nests. Of these, 17 were first nest attempts, four were second
nest attempts, and two were third nest attempts. Two nests were abandoned after observers
accidentally flushed the hen off their nest early in incubation. Two nests were abandoned
unrelated to observers and one nest was in a wheat field that was harvested. Overall, seven nests
were in wheat and 16 were in CRP. The most parsimonious model of pheasant nest survival
included an interaction between visual obstruction and field type (CRP vs. Wheat; Table 2).
Wheat fields had very little variation in visual obstruction readings and the model predicted
values show no effect of visual obstruction on nest survival in wheat fields (Fig. 2). However, in
CRP fields, visual obstruction had a positive effect on nest survival (Fig. 2). In other words,
when the CRP field vegetation was taller and denser, nests had greater survival rates. Holding
visual obstruction values at their mean for wheat field nests, daily survival rate of nests in wheat
were 0.964 ± 0.020 giving a 23 day nest survival estimate of 0.428 ± 0.203. Holding visual
obstruction values at their mean for CRP nests, daily nest survival rate was 0.952 ± 0.023, giving
a 23 day nest survival estimate of 0.326 ± 0.181. Our CRP estimate is similar to that reported in
Matthews et al. (2012b) of 0.31 for unmanaged CRP fields in Nebraska, however for disced and
interseeded fields, they report much greater nests success (0.70). The fields we used in the year
one pilot study had not had any management action recently and were probably similar to
Matthews et al. (2012b) unmanaged fields.
Brood survival
We monitored 8 pheasant broods. Two broods survived (at least one chick) to the 10 day
brood flush and one brood survived to the 21 day brood flush (two chicks) giving apparent brood
survival to 21 days of 0.125. Based on a constant survival model, daily survival rate of broods ±
SE was 0.879 ± 0.045. Extrapolating to the 21 day period gives a model estimated 21 day brood
survival of 0.066 ± 0.071. This is much lower than Matthews et al. (2012b) who reported brood
survival to 21 days was 0.71 in Nebraska. However, our low sample size precludes any
meaningful comparison.
Brood habitat selection
Due to time constraints we did not sample vegetation with regard to pheasant broods in
2016. However, we plan to examine patterns in brood site selection in relation to field type (i.e.,
CRP vs. crops).
Songbirds
We conducted point counts at six points within six fields, twice during the summer. The
first round of point counts occurred 8-11 June and the second, 13-20 July. Western meadowlarks
8

�were the most common bird detected, followed by grasshopper sparrow, and mourning dove
(Table 3). Initial attempts to estimate songbird density revealed a major assumptions of distance
sampling was violated (detection probability at the point = 1). Therefore, we are currently
exploring other ways to estimate density, namely removal models (Farnsworth et al. 2002) or
fixed-area methods which assume constant detection probability (Hutto 2016).
CURRENT PROGRESS
We are currently finishing up analyses from the 2016 pilot study and planning for the
2017 field season.
LITERATURE CITED
Amundson, C. L., J. A. Royle, and C. M. Handel. 2014. A hierarchical model combining
distance sampling and time removal to estimate detection probability during avian point
counts. Auk 131:476-494.
Berthelsen, P. S. and L. M. Smith. 1995. Nongame bird nesting on CRP lands in the Texas
southern high plains. Journal of Soil and Water Conservation 50:672-675.
Brennan, L. A. and W. P. Kuvlesky Jr. 2005. North American grassland birds: an unfolding
conservation crisis? Journal of Wildlife Management 69:1-13.
Buckland, S. T., D. R. Anderson, K. P. Burnham, and J. L. Laake. 1993. Distance sampling:
estimating abundance of biological populations. Chapman and Hall, New York, USA.
Burnham, K. P. and D. R. Anderson. 2002. Model selection and multi-model inference: a
practical information-theoretic approach. Springer-Verlag, New York, USA.
Colorado Division of Wildlife. 2003. Conservation plan for grassland species in Colorado. 205
pp.
Colorado Parks and Wildlife. 2012. 2011/2012 Small game harvest report.
Colorado Parks and Wildlife. 2015. State Wildlife Action Plan: a strategy for conserving wildlife
in Colorado.
Cooper, A. B. and J. J. Millspaugh. 1999. The application of discrete choice models to wildlife
resource selection studies. Ecology 80:566-575.
Croissant, Y. 2013. mlogit: multinomial logit model. R package version 0.2-4.
Dinsmore, S. J., G. C. White, and F. L. Knopf. 2002. Advanced techniques for modeling avian
nest survival. Ecology 83:3476-3488.
Farnsworth, G. L., K. H. Pollock, J. D. Nichols, T. R. Simons, J. E. Hines, and J. R. Sauer. 2002.
A removal model for estimating detection probabilities from point-count surveys. Auk
119:414-425.
Flock, B. E. and R. D. Applegate. 2002. Comparison of trapping methods for ring-necked
pheasants in North-Central Kansas. North American Bird Bander 27:4-8.
Giudice, J. H. and J. T. Ratti. 2001. Ring-necked pheasant (Phasianus colchicus). The Birds of
North America Online (A. Poole, Ed.). Ithaca: Cornell Lab of Ornithology.
Hanni, D. J., C. M. White, N. J. Van Lanen, J. J. Birek, J. M. Berven, and M. F. McLaren. 2015.
Integrated Monitoring in Bird conservation Regions (IMBCR): Field protocol for
spatially-balanced sampling of landbird populations. Unpublished report. Rocky
Mountain Bird Observatory, Brighton, USA.

9

�Hill, D. A. 1985. The feeding ecology and survival of pheasant chicks on arable farmland.
Journal of Applied Ecology 22:645-654.
Hutto, R. L. 2016. Should scientists be required to use a model-based solution to adjust for
possible distance-based detectability bias? Ecological Applications 26:1287-1294.
Jamison, B. E., R. J. Robel, J. S. Pontius, and R. D. Applegate. 2002. Invertebrate biomass:
associations with lesser prairie-chicken habitat use and sand sagebrush density in
southwestern Kansas. Wildlife Society Bulletin 30:517-526.
King, J. W. and J. A. Savidge. 1995. Effects of the Conservation Reserve Program on wildlife in
southeast Nebraska. Wildlife Society Bulletin 23:377-385.
Labisky, R. F. 1959. Night-lighting: a technique for capturing birds and mammals. Illinois
Natural History Survey Biology Notes No. 49, Urbana, USA.
Leif, A. P. 1994. Survival and reproduction of wild and pen-reared ring-necked pheasant hens.
Journal of Wildlife Management 58:501-506.
MacKenzie, D. I., J. D. Nichols, J. A. Royle, K. H. Pollock, J. E. Hines, and L. L. Bailey. 2006.
Occupancy estimation and modeling: inferring patterns and dynamics of species
occurrence. Academic Press, San Diego, USA.
Marcstrom, V., R. E. Kenward, and M. Karlbom. 1989. Survival of ring-necked pheasants with
backpacks, necklaces, and leg bands. Journal of Wildlife Management 53:808-810.
Matthews, T. W., J. S. Taylor, and L. A. Powell. 2012a. Ring-necked pheasant hens select
managed Conservation Reserve Program grasslands for nesting and brood-rearing.
Journal of Wildlife Management 76:1653-1660.
Matthews, T. W., J. S. Taylor, and L. A. Powell. 2012b. Mid-contract management of
Conservation Reserve Program grasslands provides benefits for ring-necked pheasant
nest and brood survival. Journal of Wildlife Management 76:1543-1652.
McCoy, T. D., E. W. Kurzejeski, L. W. Burger Jr., and M. R. Ryan. 2001. Effects of
conservation practice, mowing, and temporal changes on vegetation structure on CRP
fields in northern Missouri. Wildlife Society Bulletin 29:979-987.
Millenbah, K. F., S. R. Winterstein, H. Campa III, L. T. Furrow, and R. B. Minnis. 1996. Effects
of Conservation Reserve Program field age on avian relative abundance, diversity, and
productivity. Wilson Bulletin 108:760-770.
Negus, L. P., C. A. Davis, and S. E. Wessel. 2010. Avian response to mid-contract management
of Conservation Reserve Program fields. American Midland Naturalist 164:296-310.
Nielson, R. M., et al. 2008. Estimating the response of ring-necked pheasants (Phasianus
colchicus) to the Conservation Reserve Program. Auk 125:434-444.
O’Connor, R. J., M. T. Jones, R. B. Boone, and T. B. Lauber. 1999. Linking continental climate
and land use patterns with grassland bird distribution across the conterminous United
States. Studies in Avian Biology 19:35-59.
Patterson, M. P. and L. B. Best. 1996. Bird abundance and nesting success in Iowa CRP fields:
the importance of vegetation structure and composition. American Midland Naturalist
135:153-167.
Perkins, A. L., W. R. Clark, T. Z. Riley, and P. A. Vohs. 1997. Effects of landscape and weather
on winter survival of ring-necked pheasant hens. Journal of Wildlife Management
61:634-644.
Peterjohn, B. G. 2003. Agricultural landscapes: can they support healthy bird populations and
agricultural products? Auk 120:14-27.

10

�Powell, L. A. 2007. Approximating variance of demographic parameters using the delta method:
a reference for avian biologists. Condor 109:949-954.
R Core Team. 2015. R: a language and environment for statistical computing. R Foundation for
Statistical Computing, Vienna, Austria.
Riley, T. Z. 1995. Association of the Conservation Reserve Program with ring-necked pheasant
survey counts in Iowa. Wildlife Society Bulletin 23:386-390.
Robel, R. J., J. N. Briggs, A. D. Dayton, and L. C. Hurlbert. 1970. Relationship between visual
obstruction measurements and weight of grassland vegetation. Journal of Range
Management 23:295-297.
Rodgers, R. D. 1999. Why haven’t pheasant populations in western Kansas increased with CRP?
Wildlife Society Bulletin 27:654-665.
Ryan, M. R., L. W. Burger, and E. W. Kurzejeski. 1998. The impact of CRP on avian wildlife: a
review. Journal of Production Agriculture 11:61-66.
Samson, F. and F. Knopf. 1994. Prairie conservation in North America. BioScience 44:418-421.
Schmitz, R. A. and W. R. Clark. 1999. Survival of ring-necked pheasant hens during spring in
relation to landscape features. Journal of Wildlife Management 63:147-154.
Smith, S. A., N. J. Stewart, and J. E. Gates. 1999. Home ranges, habitat selection and mortality
of ring-necked pheasants (Phasianus colchicus) in North-central Maryland. American
Midland Naturalist 141:185-197.
Snyder, W. D. 1985. Survival of radio-marked hen ring-necked pheasants in Colorado. Journal of
Wildlife Management 49:1044-1050.
Spears, G. S., F. S. Guthery, S. M. Rice, S. J. DeMaso, and B. Zaiglin. 1993. Optimum seral
stage for Northern bobwhites as influenced by site productivity. Journal of Wildlife
Management 57:805-811.
U.S. Department of Agriculture. 2012. Conservation Reserve Program: annual summary and
enrollment statistics FY 2012. U. S. Department of Agriculture, Washington, D.C., USA.
U.S. Department of Agriculture. 2015. FSA Handbook: Agricultural Resource Conservation
Program. U. S. Department of Agriculture, Washington, D.C., USA.
Vickery, P. D. and J. R. Herkert. 1999. Ecology and conservation of grassland birds of the
western hemisphere. Studies in Avian Biology 19:1-199.
White, G. C. and K. P. Burnham. 1999. Program Mark: Survival estimation from populations of
marked animals. Bird Study 46:120-138.
White, G. C. and R. A. Garrott. 1990. Analysis of wildlife radio-tracking data. Academic Press,
Inc. San Diego, California, USA.
Whiteside, R. W. and F. S. Guthery. 1983. Ring-necked pheasant movements, home ranges, and
habitat use in West Texas. Journal of Wildlife Management 47:1097-1104.
Wilbur, S. R. 1967. Live-trapping North American upland game birds. U.S. Bureau of Sport
Fisheries and Wildlife Special Scientific Report Wildlife 106, Washington, D.C., USA.
Wiens, J. A. and J. T. Rotenberry. 1979. Diet niche relationships among North American
grassland and shrubsteppe birds. Oecologia 42:252-292.

11

�Table 1. Nest site selection models for ring-necked pheasants in northeastern Colorado.
Model
Ka
ΔAICc wib
Percent warm-grass
1
0.0
0.9
Percent bare ground
1
6.0
0.0
Visual obstruction
1
7.4
0.0
Tallest vegetation
1
7.6
0.0
Percent cool-grass
1
7.8
0.0
Percent grass
1
8.0
0.0
Percent forb
1
9.5
0.0
a
Number of parameters in the model
b
Model weight

Table 2. Nest survival models for ring-necked pheasants in northeastern Colorado.
Model
Ka
ΔAICc
wib
Field * VO
4
0.0
0.18
Field + VO
3
0.3
0.15
Tallest
2
0.9
0.11
VO
2
1.9
0.07
Field + tallest
3
2.9
0.04
Null
1
4.0
0.02
Field * tallest
4
5.0
0.01
Forb
2
5.1
0.01
Cool-season
2
5.3
0.01
Grass
2
5.5
0.01
Bare ground
2
5.8
0.01
Warm-season
2
5.8
0.01
Field
2
5.9
0.01
a
Number of parameters in the model
b
Model weight

12

�Table 3. Grassland bird detection during point counts.
Species
Num. of detections
Western meadowlark
108
Grasshopper sparrow
78
Mourning dove
69
Brewer's blackbird
20
Lark bunting
20
Common grackle
17
Ring-necked pheasant
16
Dickcissel
12
Red-winged blackbird
9
Barn swallow
6
Western kingbird
5
Killdeer
3
Brown-headed cowbird
2
Eastern kingbird
2
Mallard
2
Red-tailed hawk
2
Turkey vulture
2
Unknown
2
American robin
1
European starling
1
Great-horned owl
1
Horned lark
1
House sparrow
1
Unknown sparrow
1

13

�Figure 1. Standardized coefficients ± SE from discrete choice models predicting nest site
selection of ring-necked pheasants in northeastern Colorado. Positive values indicate selection
for a variable and negative values indicate selection against a variable. All coefficients are taken
from single variable models.

14

�Figure 2. Model predicted values and 95% confidence interval of nest daily survival rate in
relation to visual obstruction reading for nests in wheat (top) and Conservation Reserve Program
(bottom) fields.

15

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              <text>The Conservation Reserve Program (CRP) is a government program in which landowners are paid to maintain grass cover on land that was, and would otherwise be, used for row-crop agriculture. Overall, the CRP has had many documented benefits to wildlife, specifically grassland birds, many of which are experiencing range-wide declines due to habitat loss and degradation. However, as CRP fields age with no disturbance, litter increases, bare ground decreases, vegetation density increases, and plant species and structural diversity decrease, which can reduce the value of CRP fields to certain bird species. Therefore, beginning in 2004, some type of “mid-contract management” was required on CRP fields. In northeastern Colorado this management typically consists of haying, disking, or disking and interseeding with forbs. Although there is some evidence that disking and interseeding can provide benefits to ring-necked pheasants in other regions, we lack a thorough understanding of how these various management practices affect pheasants and grassland dependent songbirds in northeastern Colorado. In an effort to provide guidance to managers and landowners regarding grassland management on CRP fields in northeastern Colorado, we will monitor the response of pheasants and songbirds to the three most common CRP mid-contract management practices (haying, disking, disking &amp; interseeding).</text>
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