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WHOOPING CRANE NEST BUILDING IN SOUTHWEST INDIANA

Authors:
  • Indiana Department of Natural Resources

Abstract and Figures

The first documented case of whooping crane (Grus americana) nest building in Indiana is described. During spring 2015, a pair of whooping cranes did not leave their wintering grounds in Gibson County, Indiana, to return to their summering area in Wisconsin. Three nest platforms were discovered after the death of the female crane. To date, this is the only documented example of a whooping crane pair in the reintroduced Eastern Migratory Population (EMP) building nest platforms outside of Wisconsin. Although fidelity to the core nesting areas in Wisconsin is strong, and natal dispersal is usually <30 km, this example from Indiana shows that whooping cranes in the EMP may have the potential to pioneer nesting areas far outside of core reintroduction areas. PROCEEDINGS OF THE NORTH AMERICAN CRANE WORKSHOP 15:128-133
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128
WHOOPING CRANE NEST BUILDING IN SOUTHWEST INDIANA
AMY J. KEARNS,1 Indiana Division of Fish and Wildlife Mitchell Field Office, 562 DNR Road, Mitchell, IN 47446, USA
HILLARY L. THOMPSON, International Crane Foundation, E11376 Shady Lane Road, Baraboo, WI 53913, USA
ALLISYN-MARIE T. Y. GILLET, Indiana Division of Fish and Wildlife Bloomington Field Office, 5596 E State Route 46,
Bloomington, IN 47401, USA
Abstract: The rst documented case of whooping crane (Grus americana) nest building in Indiana is described. During spring
2015, a pair of whooping cranes did not leave their wintering grounds in Gibson County, Indiana, to return to their summering
area in Wisconsin. Three nest platforms were discovered after the death of the female crane. To date, this is the only documented
example of a whooping crane pair in the reintroduced Eastern Migratory Population (EMP) building nest platforms outside
of Wisconsin. Although delity to the core nesting areas in Wisconsin is strong, and natal dispersal is usually <30 km, this
example from Indiana shows that whooping cranes in the EMP may have the potential to pioneer nesting areas far outside of
core reintroduction areas.
PROCEEDINGS OF THE NORTH AMERICAN CRANE WORKSHOP 15:128-133
Key words: breeding outside core range, Eastern Migratory Population, Grus americana, Indiana, nest building,
nest platform, whooping crane.
The native range of the whooping crane (Grus
americana) includes the state of Indiana, for which a
small number of early historical records exist (Allen
1952, Austin et al. 2019). Butler (1898) was convinced
that whooping cranes nested in the Grand Kankakee
Marsh in northwestern Indiana before it was drained in
the late 1800s. Despite this, no breeding evidence from
Indiana has been described, and whooping cranes were
extirpated from the state and the eastern United States
by the early 1900s (Allen 1952, Mumford and Keller
1984). In 2001 a reintroduction eort began releasing
captive-reared whooping cranes into the wild with the
goal of establishing an Eastern Migratory Population
(EMP) of whooping cranes nesting in Wisconsin and
migrating through Indiana on their route to wintering
areas in Florida (Urbanek et al. 2014a). Beginning
in 2007, some individuals from this population
demonstrated shortstopping, or wintering north of
Florida, and as of 2021, one-third of the population
spent at least 3 months of the nonbreeding season in
Indiana (Urbanek et al. 2014a, Teitelbaum et al. 2016,
Thompson et al. 2022).
In April 2015, a pair of whooping cranes did not
migrate north to Wisconsin but stayed in their wintering
area in southwestern Indiana. These birds built 3 nest
platforms in the area prior to the death of the female
crane. We describe the rst evidence of whooping
crane nest building in Indiana and the rst record of
a whooping crane pair from the EMP building nest
platforms outside of Wisconsin.
The whooping cranes described herein (male 12-
09 and female 14-09) were costume-reared in 2009 at
Patuxent Wildlife Research Center in Maryland and
trained to migrate south in fall by following an ultralight
aircraft from Necedah National Wildlife Refuge (NWR),
Wisconsin, to St. Marks NWR, Florida (Urbanek et al.
2014a). Before their release, both cranes were banded
with a unique combination of colored leg bands and a
VHF radio transmitter (Advanced Telemetry Systems,
Isanti, MN, USA) so that their movements could be
monitored. Before spring 2015, neither crane had
been conrmed nesting, although the female and her
previous mate built nest platforms in Wisconsin in the
spring of 2012 and 2013, but with no evidence of eggs.
The crane pair began associating and formed a pair
bond during fall 2014, then spent most of the winter at
Tern Bar Slough Wildlife Diversity Area (herein, Tern
Bar Slough), a remote 340-ha prairie-wetland complex
in Gibson County that is owned and managed by the
Indiana Division of Fish and Wildlife.
Whooping cranes usually depart southern Indiana
in March and begin to lay eggs in Wisconsin in late
March and early April (Urbanek et al. 2010b, Thompson
et al. 2022); however, on 30 March 2015, the pair was
observed in a remote area of Tern Bar Slough. Because
of their presence past the typical migratory window
and the availability of suitable nesting habitat, no crane
observations were made in the weeks after this date to
avoid disturbing the pair during the sensitive period
1 E-mail: akearns@dnr.IN.gov
Proc. North Am. Crane Workshop 15:2022 BRIEF COMMUNICATIONS 129
early in the nesting cycle. The whooping crane pair was
seen at Tern Bar Slough again on 16 April 2015, but
then on 20 April the male was observed there alone,
making repeated alarm calls.
On 22 and 29 April, searches on foot were
conducted for the missing female and any evidence
of nesting activity. During the rst search, the male
behaved conspicuously, ying circles around the large
wetland complex and alarm calling regularly; however,
on 29 April he was not vocalizing and his behavior
appeared normal. In the remote area where the pair
had been seen in March and April, 1 nest platform was
found on 22 April and the carcass of the female and
other 2 nest platforms were found on 29 April (Figs.
1-3). The nest platforms were spaced over a ~2.78-
ha area, in shallow water (18-23 cm), and densely
constructed from standing dead sedges (Cyperaceae).
Nest platform dimensions were measured at water
level, where the surface of the water met the main mass
of vegetation from each platform. Mean dimensions
of the nest platforms were 125×207 cm. An estimated
6-m area around each nest platform was mostly cleared
of vegetation, creating a halo-like eect. The area
beyond the rst 2 nest platforms was mostly open,
consisting of standing dead sedges and few scattered
small cottonwood (Populus deltoides) saplings (Figs.
1-2); however, the third nest platform was in a small
open area surrounded by young cottonwoods. Unlike
the rst 2 nest platforms that were at across the top,
the surface material of this third platform was clumped
and displaced (Fig. 3). No eggs or eggshell fragments
were found; however, the water surrounding the nest
platform was turbid and no underwater search by feel
was conducted. About a dozen scattered white feathers
in the water around the nest platform led to the carcass
of the female submerged in shallow water 6.4 m north
of the third platform. The head and upper two-thirds
of the neck were missing, but the rest of the skeleton
was intact and unbroken, and the remiges were still
attached. The bands and nonfunctional radio transmitter
remained on the legs.
Based on the earlier observations of the cranes and
the state of the carcass, the death was estimated to have
occurred on 17 or 18 April. A necropsy was conducted
by the U.S. Geological Survey National Wildlife
Health Center and the nal report indicated predation
or scavenging of the carcass. A more detailed analysis
could not be completed due to the poor condition of the
carcass (Lankton 2015).
On 4 May 2015, the male crane was observed
at Necedah NWR, Wisconsin, on traditional EMP
whooping crane breeding grounds; however, by 26
May he had returned to the area around Tern Bar
Slough where he remained for 11 months until at least
4 April 2016. In 2016 and subsequent years, the male
summered in Juneau County, Wisconsin, and continued
to spend much of the winter around Tern Bar Slough.
Annually since 2012, one-third of the EMP has
spent 3 or more months of the nonbreeding season
in Indiana (Urbanek et al. 2014a, Teitelbaum et al.
2016, Thompson et al. 2022). Important wintering
habitat for whooping cranes in Indiana includes private
agricultural elds and protected wetlands, including
Jasper-Pulaski Fish and Wildlife Area (FWA), Goose
Pond FWA, Muscatatuck NWR, the Cane Ridge
Wildlife Management Area (WMA) of Patoka River
NWR, and Tern Bar Slough (Thompson 2018; WCEP,
unpublished data). Cane Ridge WMA and Tern Bar
Slough are adjacent properties in a remote area just
east of the Wabash River. This area seasonally oods
and is surrounded by approximately 7,500 ha of
agricultural lands, restored wetlands, borrow pits, and
an aboveground freshwater reservoir. Although sandhill
cranes (Grus canadensis) are sporadically found in this
area in winter, they typically depart for their northern
breeding grounds by the end of March, and there are
no known nesting records within 80 km (Castrale et
al. 1998, Castrale and Gillet 2022, eBird 2022, A. J.
Kearns, personal observation).
The habitat surrounding the Indiana whooping
crane nest platforms is congruent with that of historic
nest records described in Allen (1952), as well as
nests observed in the EMP and other whooping crane
populations in modern times (Timoney 1999, Strobel
and Giorgi 2017, Barzen 2019). These 3 nest platforms
were found in the remote interior of a 528-ha shallow
water emergent wetland complex that is closed to public
access; therefore, human disturbance at this site is rare.
The nearest road is infrequently traveled and 565-770 m
from the nest platform locations, and the interior of the
wetland where the platforms were located is obscured
by vegetation and topography and not visible from the
road.
The 3 nest platforms found at Tern Bar Slough
(Figs.1-3) are comparable to whooping crane nests
observed elsewhere, including on the breeding grounds
of the EMP in Wisconsin. Water depth at the nest
platforms was shallow with a mean depth of 20.33 cm,
130 BRIEF COMMUNICATIONS Proc. North Am. Crane Workshop 15:2022
Figure 1. One of 3 nest platforms built by whooping cranes in southwestern Indiana. This nest was in 23 cm of shallow water and
measured 124 × 236 cm at water level.
Figure 2. One of 3 nest platforms built by whooping cranes in southwestern Indiana. This nest was in 20 cm of shallow water and
measured 150 × 142 cm at water level. The remains of an American coot (Fulica americana) were on the nest.
Proc. North Am. Crane Workshop 15:2022 BRIEF COMMUNICATIONS 131
which is somewhat shallower than mean water depth
around nests observed at Necedah NWR (33 cm; Strobel
and Giorgi 2017), in Florida (29.11 cm; Dellinger 2019),
and at Wood Bualo National Park (25.4 cm; Kuyt
1981). The size and shape of the Tern Bar Slough nest
platforms resemble those described in other accounts of
whooping crane nests in Wood Bualo National Park
(Walkinshaw 1973) and Wisconsin (H. L. Thompson,
unpublished data). Like nest platforms described in
other accounts, surrounding vegetation was broken or
pulled up at the roots, leaving a narrow halo (5-7 m) of
cleared space around each nest platform (Allen 1952,
Walkinshaw 1973). Furthermore, the pair built 3 nest
platforms, which is not unusual for whooping cranes,
which occasionally build more than 1 nest platform
before egg laying (Folk et al. 2005, Urbanek and Lewis
2020).
Although no eggs or eggshells were recovered
at Tern Bar Slough, it is possible that the female had
laid eggs. The approximate date of the female’s death
was 17 or 18 April, by which most of the whooping
crane pairs in the EMP have laid eggs (Urbanek et al.
2014b, Thompson et al. 2022). At 6 years old, this pair
of whooping cranes was sexually mature and capable
of producing eggs. In the EMP of whooping cranes,
a female usually lays her rst egg at age 3 or 4 years
(mean 3.92 years, Urbanek et al. 2010a; 3.7 ± 0.2 years,
Thompson et al. 2021).
In this example from Indiana, a pair of whooping
cranes built 3 nest platforms more than 650 km south
of their reintroduction area at Necedah NWR. Although
the habitat at Tern Bar Slough closely resembles nest
site descriptions found in Allen (1952), there are
no other records of whooping crane pairs with nest
platforms, eggs, or chicks in Indiana or the neighboring
states of Illinois, Ohio, and Michigan (Allen 1952,
Austin et al. 2019). This is likely due to strong natal
philopatry to breeding areas caused by innate homing,
low population sizes, and abundant available nesting
habitat in core areas (Johns et al. 2005, Urbanek et al.
2014b). However, despite these inherent barriers, this
example provides evidence that young pioneering pairs
from the EMP could establish breeding sites in suitable
habitat far outside of their known historic nesting range
or areas of reintroduction, particularly if the population
grows.
Figure 3: One of 3 nest platforms built by whooping cranes in southwestern Indiana. This nest was in 18 cm of shallow water and
measured 109 × 234 cm at water level. The carcass of the female whooping crane was submerged beneath shallow water 6.4 m
north of this nest (circled area).
132 BRIEF COMMUNICATIONS Proc. North Am. Crane Workshop 15:2022
Other species of birds have successfully expanded
their nesting range through the initial eorts of
pioneering individuals (Johnson 1994, Winkler et
al. 2017), including the related greater sandhill crane
(Grus canadensis tabida), which has recolonized
much of its historic nesting range in the Midwest
(Meine and Archibald 1996). Furthermore, there are
recent examples of long-distance natal dispersal in
reintroduced populations of whooping cranes. During
springs 2016-2021 a breeding pair from the EMP
nested in far northwestern Wisconsin, 306 and 358 km
from the male’s and female’s respective natal areas
(Thompson et al. 2021). In addition, in springs 2020-
2021, a male whooping crane nested with a sandhill
crane in southern Michigan, 414 km from his natal site
(Thompson et al. 2022). Lastly, in spring 2021 2 pairs
of whooping cranes from the Louisiana Non-migratory
Population nested in Texas, 152 and 173 km from their
respective natal site in Louisiana (U.S. Fish and Wildlife
Service 2021; E. K. Szyszkoski, Louisiana Department
of Wildlife and Fisheries, personal communication). All
of these whooping cranes were successful at hatching
chicks despite the long distance between their natal and
nesting areas. Although the occurrence would be rare,
it seems likely that another young pair of whooping
cranes from the EMP will attempt to nest outside of
Wisconsin.
Wetlands are essential habitat for whooping cranes
and many other imperiled species. Within the historic
range of the whooping crane, wetlands have been
destroyed on a massive scale. For example, over 85% of
Indiana’s wetlands have been lost in the last 200 years
(Indiana Department of Environmental Management
2021). In the face of current threats such as climate
change, land development, and human population
growth, more wetlands on public and private land
should be restored and protected.
If whooping cranes are not limited to nesting in
historical or reintroduction areas, then there are nesting
opportunities available to this imperiled species where
large blocks of productive emergent marsh remain within
their range. Conservationists and property managers
in areas like these, especially when the areas host
whooping cranes for extended periods during summer,
winter, and migration, should consider the possibility
that whooping cranes could nest and should prioritize
these sites, so they are protected from development and
disturbance.
ACKNOWLEDGMENTS
Thanks to E. Szyszkoski, S. Giord, J. Pohl, and
H. Ray for sharing their observations and information
about the whooping cranes (12-09 and 14-09). Thank
you to N. Gordon, the editors, and an anonymous
reviewer for their feedback on an earlier version of
this manuscript. The observations gathered in the eld
and time writing this manuscript were funded by the
federal State Wildlife Grant Program and the Indiana
Nongame Wildlife Fund. Thank you to all who donate
to the Indiana Nongame Wildlife Fund to help make
this essential work possible.
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... There have been 2 documented third nesting attempts in a season (in 2010 and 2019), both of which hatched, and 1 nest produced a wild-fledged chick. The nest platforms built farthest from the core reintroduction area were in Gibson County, Indiana, during 2015; however, eggs were never confirmed (Kearns et al. 2022). The first nest in the Eastern Rectangle was in 2014 by male no. ...
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Since the 10-year status update in 2011, the first parent-reared whooping cranes (Grus americana) were released in the Eastern Migratory Population, the ultralight program (UL) ended, and cranes were released at new sites in eastern Wisconsin. During 2011-2020, 117 captive-reared whooping cranes were released; 75 costume-reared (35 in UL and 40 in the Direct Autumn Release program) and 42 parent-reared. There were no significant differences in 1-or 3-year survival rates based on rearing technique or release site. The population size remained at about 100 cranes during 2010-2018 but then decreased during 2018-2020 due to a reduced number of releases of captive-reared cranes and low recruitment. Predation remained the leading cause of death (54.1% of confirmed cases) for cases in which the cause of death could be determined, followed by impact trauma (18.8%), gunshot (10.5%), and disease (9.0%). The winter distribution shifted northward into more agricultural landscapes, with the majority of the population wintering in southern Indiana or northern Alabama. The summer distribution remained concentrated in Wisconsin, and breeding areas expanded into eastern Wisconsin. As a management response to nest abandonments caused by avian-feeding black flies (Simulium spp.), the first clutch of eggs was removed from nests at Necedah National Wildlife Refuge (i.e., forced renesting), which increased renesting rates from 42% to 79%. In total, 152 cranes were confirmed to have hatched in the wild, 27 of which survived to fledging. Two male whooping cranes nested with female sandhill cranes (Grus canadensis) and produced hybrid chicks. Three cranes were removed from the population due to using an active air strip on an Air National Guard base. As of April 2021, the estimated population size was 76 individuals (38 females, 36 males, and 2 of unknown sex), 16 of which were wild-hatched. PROCEEDINGS OF THE NORTH AMERICAN CRANE WORKSHOP 15:34-52
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Natal dispersal is a key demographic process for evaluating the population rate of change, especially for long‐lived, highly mobile species. This process is largely unknown for reintroduced populations of endangered avian species. We evaluated natal dispersal distances (NDD) for male and female Whooping Cranes (Grus americana) introduced into two locations in central Wisconsin (Necedah National Wildlife Refuge, or NNWR, and the Eastern Rectangle, or ER) using a series of demographic, spatial, and life history‐related covariates. Data were analyzed using gamma regression models with a log‐link function and compared using Akaike information criterion corrected for small sample sizes (AICc). Whooping Cranes released in the ER dispersed 261% further than those released into NNWR, dispersal distance increased 4% for each additional nesting pair, decreased about 24% for males as compared to females, increased by 21% for inexperienced pairs, and decreased by 3% for each additional year of age. Natal philopatry, habitat availability or suitability, and competition for breeding territories may be influencing observed patterns of NDD. Whooping Cranes released in the ER may exhibit longer NDD due to fragmented habitat or conspecific attraction to established breeding pairs at NNWR. Additionally, sex‐biased dispersal may be increasing in this population as there are more individuals from different natal sites forming breeding pairs. As the population grows and continues to disperse, the drivers of NDD patterns may change based on individual or population behavior.
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In 2001, a reintroduced population of Whooping Cranes, known as the Eastern Migratory Population (EMP), was established in the eastern United States. The breeding range for the EMP was in central Wisconsin and the populated originally migrated to the Florida Gulf coast during the nonbreeding season. Beginning in approximately 2004-05, the wintering range for cranes shifted from the Florida Gulf coast to inland marshes in Florida. Between 2007-08 and 2017-18 the winter distribution of this population expanded north to include areas as distant as southern Indiana. To date, there has been no assessment of habitat use of the EMP across the current winter distribution. The objectives of this study were to identify factors influencing daily home range sizes of wintering Whooping Cranes in the EMP, describe habitat characteristics of areas used by cranes within their daily home range, identify the water depths and vegetation heights of used areas, and assess behavior associations with habitat. During two winters (2014- 15 and 2015-16), we used radio-telemetry to track 20 and 23 groups of wintering Whooping Cranes, respectively, each for one full day. We recorded their location, behavior, and the habitat characteristics of their locations. Based on natural clustering of winter areas of Whooping Cranes, we grouped winter sites into three regions: North (Illinois, Indiana, Kentucky), Central (Tennessee, Alabama), and South (Georgia, Florida, Louisiana). We calculated home range sizes using a 95% kernel density estimate, and home ranges decreased in size from north (4.9 ± 2.8 km2) to central (3.1 ± 1.0 km2) to south (2.3 ± 0.5 km2). Home ranges in the south were also comprised of the greatest proportion of wetlands compared to other regions (south = 37%, central = 7%, north = 1%). To identify habitat characteristics of winter sites, we compared used locations to randomly generated locations within a crane’s home range separately by region. In the north region, cranes used agricultural areas more often than forests, and used areas with hydric soil that were potentially seasonally inundated during winter. In the central region, cranes selected for both agriculture and wetlands compared to forests. Cranes wintering in the south did not select habitat characteristics out of proportion to their availability within their home ranges. We also measured water depths and vegetation heights of used areas, respective to a crane. In all regions, cranes used areas with water or vegetation below the tibiotarsal joint more often than areas with deep water or tall vegetation. Lastly, we compared foraging and loafing behavior in three habitat types (agriculture, grasslands, and wetlands), both pooled and separately by region. Whooping Cranes in the north foraged more often in agriculture than in grasslands or wetlands. However, in the central region, cranes foraged equally in all three habitats, and cranes in the south foraged in either grasslands or wetlands. Loafing behavior was associated with wetlands compared to agriculture or grasslands in all three regions. The findings of this study are the first description of habitat characteristics of areas used by cranes wintering throughout the current and entire winter range of the EMP. Results from this study will inform land managers of wintering habitat use and can benefit conservation planning with respect to future reintroduction efforts of this endangered species.
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Though Whooping Cranes historically nested in varied biomes they also needed specific habitat components located within each biome. The goal here is to compare current Whooping Crane habitat use to historical records and inform predictions related to recovery and management in today’s changing world. Among 4 populations (Aransas Wood Buffalo, AWBP; Eastern Migratory, EMP; Florida Non-migratory; and Louisiana Non-migratory, LNMP) Whooping Cranes used open wetlands dominated by emergent vegetation and open water for foraging and roosting throughout the year but the amount of wetland use varied among populations and seasons. Summer territories in the AWBP and EMP averaged 4 km2 while home ranges of non-territorial cranes were 10 – 100 times larger, making habitat availability between the two groups substantially different. Average natal dispersal distance was < 28 km, making only habitats close to natal areas available for territory establishment. Though not an annual occurrence, cranes used wetlands 92% of the time during the flightless molt and home range was the smallest home range measured, suggesting this period may be the most sensitive of the annual cycle. In winter cranes in the AWBP used mostly natural salt marshes, both day and night, in a narrow band of the Texas Coast whereas the EMP was distributed throughout the eastern US and utilized agricultural areas. Cranes in the LNMP used man-made wetlands all year. The breadth of habitats used by other populations during winter suggests that the AWBP could utilize alternative habitats if needed. Strong territorial behavior in winter by the AWBP may reduce the rate at which dispersal outside of the Texas Coast can occur. In fall migration, AWBP cranes staged before moving rapidly to winter areas but no staging occurred in the EMP during either migration. If energetic or nutritional needs are unmet on winter or summer areas, spring and fall staging areas could serve as alternate habitats. Future research should address the role of territoriality in cranes and the degree to which use of agricultural fields may be beneficial.
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Anthropogenic changes in climate and land use are driving changes in migration patterns of birds worldwide. Spatial changes in migration have been related to long-term temperature trends, but the intrinsic mechanisms by which migratory species adapt to environmental change remain largely unexplored. We show that, for a long-lived social species, older birds with more experience are critical for innovating new migration behaviours. Groups containing older, more experienced individuals establish new overwintering sites closer to the breeding grounds, leading to a rapid population-level shift in migration patterns. Furthermore, these new overwintering sites are in areas where changes in climate have increased temperatures and where food availability from agriculture is high, creating favourable conditions for overwintering. Our results reveal that the age structure of populations is critical for the behavioural mechanisms that allow species to adapt to global change, particularly for long-lived animals, where changes in behaviour can occur faster than evolution.
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Understanding the historic range and habitats of an endangered species can assist in conservation and reintroduction efforts for that species. Individuals reintroduced into a species’ historic core range have a higher survival rate compared to individuals introduced near the periphery or outside the historic range (Falk and Olwell, 1992; Griffith et al., 1989). Individuals on the periphery of a species’ range tend to occupy less favorable habitats and have lower and more variable densities than those near the core of their range (Brown, 1984; Brown et al., 1995, 1996). Such conclusions, however, presume that historic habitats have not changed since a species was extirpated from core areas – a difficult assumption for many areas, and particularly for wetland habitat (Prince, 1997). Many endangered species persist only on the periphery of their historic range because of habitat loss or modification in their core range (Channell and Lomolino, 2000), which can bias our understanding of the species’ habitat preferences. Further, habitat models based on locations where species persist necessarily emphasize local conditions rather than historical conditions (Kuemmerle et al., 2011). For example, habitat models for the European bison (Bison bonasus) suggested it was a woodland species, but assessment of the bison’s historic range indicated it preferred mosaictype landscapes and had a more eastern and northern distribution than previously reported (Kuemmerle et al., 2011, 2012). Hence, accurate determination of the historic range and habitat conditions for endangered species can improve our understanding of their ecology and assist in conservation and reintroduction efforts. Examining the historic range from an ecological perspective can also help identify where appropriate habitat still exists that could sustain a population.
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From 1993 through 2006, 289 subadult Whooping Cranes were released in central Florida. Within 3 years of the initial release, a pair of Whooping Cranes hatched eggs, the first time in 60 years that Whooping Cranes had been hatched in the wild in the United States. In this chapter, we discuss research and management efforts that were aimed at increasing survival and productivity in this population. We describe challenges to survival related to release methods, drought, and powerline strikes. We also give details of the breeding biology of Florida nonmigratory Whooping Cranes. Specifically from 1999 through 2012, 90 nests were monitored in the Florida nonmigratory population, from which 37 young hatched and 11 fledged. Observations of incubation behavior gathered via video surveillance showed that adults incubate in bouts that average 30 min and nest exchanges occurred about every 2 h. Video surveillance also recorded nighttime incubation exchanges, a behavior never before documented with this species. Research on this experimental population has increased our knowledge about Whooping Cranes in the wild, and this knowledge may increase prospects for the success of future reintroduction efforts. Ultimately, this reintroduction effort was discontinued in 2006 due to the birds’ poor survival and low productivity and the complications of drought, habitat loss, scarcity of release birds, and cost.
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