Management Plan for the Control of
White-tailed Deer at the
The mission of Audubon Connecticut is
to further the protection of birds, other wildlife and their habitats through
science, education, advocacy and conservation, for the benefit of humanity and
the earth’s biological diversity.
The
white-tailed deer (Odocoileus virginianus)
is the most abundant and best known large mammal in the northeastern United
States. It is a beloved symbol of
wilderness to many North Americans. However,
in recent years, the white-tailed deer has become a source of controversy
throughout its range. An overabundant deer population has caused increases in
the number of car accidents and incidence of Lyme disease. Deer consume landscaping and agricultural
crops, and damage forest ecosystems by overgrazing. Connecticut has not escaped
these problems as deer population in the state increased from 12 in 1896 to
more than 76,000 and growing today.
Deer population growth in the last 25 years has been especially
concentrated around urban and suburban areas.
Fairfield County now has one of the highest deer densities in
Connecticut and overpopulation of white-tailed deer has been well documented in
Greenwich (Connecticut DEP 2002). Past
records, personal anecdotes and observations by Audubon naturalists suggest
that the overabundance of white-tailed deer is negatively impacting the forest
ecosystem on Audubon lands in Greenwich, undermining their value as biological
reserves for the protection of a diverse and balanced population of plants,
birds and animals. To sustain the
ecological health of our sanctuaries and to protect staff and visitors from the
diseases transmitted by deer ticks, implementation of a proactive deer
management plan aimed at reducing deer population to ecologically viable levels
is urgently required.
Deer
abundance in the United States during the pre-settlement period is estimated at
23-34 million, representing a mean density of 8-11 deer per square mile over
the most favorable habitat across North America (Stout 2001). Natural deer predators such as wolves,
mountain lions, bears, and bobcats, as well as hunting by the Native Americans,
kept the deer population under check.
Predation, along with winter mortality, caused 50-70% of pre-settlement
deer mortality with Native American hunting causing the remainder. Human impacts on the deer population
intensified after the arrival of the Europeans as opportunities to trade
white-tailed deer products for European goods drove the hunt for the deer. The exploitation era, from about 1850 to
1900, saw dramatic reductions in deer populations. White-tailed deer were sought after for their meat and hide, and
their habitat had been virtually eliminated in New England with deforestation
and conversion of land into pasture and agricultural fields. Also during this period, humans completely
eliminated non-human deer predators from much of New England. In the early 1900s, growing environmental
consciousness, combined with the scarcity of deer and other wildlife, led to
enactment of numerous laws to protect the dwindling deer population. These efforts coincided with the improvement
of deer habitat by abandonment of agricultural lands and a wave of timber
harvesting to support the industrial revolution. Deer found many square miles of tree seedlings and their
population quickly rebounded in the absence of natural predators. Estimated deer population for the state of
Connecticut was 12 deer in 1896, 19,000 in 1974, and 76,000 in 2000
(Connecticut Agricultural Experiment Station 2002).
The
dramatic growth of Connecticut’s deer population over the past 25 years can be
attributed to creation of edge forests by landscape fragmentation, limited hunter
access to private lands, and ability of deer to coexist with humans. Across the
entire state of Connecticut today, deer density is around 15 deer per square
mile (Connecticut DEP 2000).
In
the Town of Greenwich, a 2002 aerial survey by the Connecticut DEP revealed the
average current density of white-tailed deer to be 20 deer per square mile,
with middle and backcountry Greenwich showing higher densities of 43 and 60 deer per square mile,
respectively. In the area just north of the Audubon Center, 60 deer per square
mile were physically counted on the photographs. Experts estimate that actual
numbers are generally 50% to 100%
higher than visible in aerial photographs, so in this case a more accurate
assessment is 90-120 deer per square mile.
A conservative estimate based on this data places the deer population at
the Audubon Center’s 298 acre (0.47 sq. mile)
main sanctuary, where they are observed daily, to be 45 to 60 deer.
White-tailed deer can live up to 18 years. The mating season starts in late October and extends through early January. In Connecticut, adult females produce an average of 2 fawns annually, usually in June. Deer evolved under heavy predatory pressure. In the absence of natural predation, unmanaged deer populations can double in size in 2-3 years. Male deer can weigh up to 150 pounds while females average 110 pounds. Deer consume 5-10 pounds of forage per day, or up to 2,000 pounds per year. Their favorite foods are grasses and forbs, acorns, apples, twigs and buds from wide variety of hardwood trees, and leaves from conifers such as white pine and hemlock. Their favored habitats are edge and early successional forests with gaps and grassy openings. Clear-cut forest also provides immediate production of slash and browse, and early successional shade-intolerant tree seedlings provide good summer browse. Long-term studies show that deer are territorial and that females remain on their summer range for life. In one study conducted in New York (McNulty et al 1997), 97% of females remained on their natal range for life, whereas most males dispersed. After the deer were thinned to create a low-density area of 1.4 km2, the low density persisted for several years. No deer from adjacent home ranges moved into this area to fill the void. In urban and suburban Connecticut, deer home ranges are relatively small, at approximately 100-300 acres (Connecticut DEP 2002).
The
evidence is overwhelming that unrestricted deer populations have a dramatic
impact on forest ecosystems.
Overabundant deer have been shown to:
The
impact of deer on vegetation can be divided into three stages. The first stage
is the selective feeding on plants for which deer have a high preference. This
stage is characterized by elimination of highly preferred plants such as
wildflowers, some other herbaceous plants and tree seedlings. The second stage
is the development of a browse line. At this stage, deer are much less
selective and eat everything within their reach, which extends 5-6 feet above
the ground. Most herbaceous and shrub species are eliminated and all tree
seedlings are susceptible to browsing. When the second stage continues for an
extended period of time, it will turn into the third stage, in which the browse
line is not apparent because there is not enough vegetation at low and
intermediate levels to show it. At this
stage, the forest composition becomes simplified and consists only of the upper
canopy and the layer of resistant vegetation of the forest floor. Understory and mid-canopy layers are
noticeably absent.
At
the Audubon Center forest, browsing damage is evident on virtually all
seedlings and saplings within deer reach.
Saplings are scarce, but where they are present, browse line is apparent
at a height of about 5 feet from the ground.
Most of the Audubon Center sanctuary, with its park-like open
understory, has apparently reached the third stage of deer impact. Its
gallery-type forests are simplified ecosystems with reduced biological
diversity and lack the resilience to bounce back from pest attacks and other
environmental stresses.
The
weight of evidence accumulated over the past decades points to specific impacts
by deer on vegetative communities. These studies do not have consistent
objectives or methodologies, but yield surprisingly consistent results. In contiguous forests, problems with tree
regeneration arise consistently at deer densities exceeding 20 deer per square
mile (Stout 2001). The impacts of browsing on shrubs, herbaceous plants and
wildlife begin at an even lower threshold. A density of no more than 10-15 deer
per square mile is recommended to ensure sustainability of wildflowers, other
palatable herbaceous and shrub species, and a full complement of the native
forest bird community (Kilpatrick 2002 and Waller et al 1997).
Endangered
and threatened plants often decline in areas with large deer populations. White-tailed
deer have been reported to browse at least 98% of endangered and threatened
plant species (The Connecticut Agricultural Experiment Station 2002). Many alien invasive plants such as the
Japanese barberry, ailanthus, oriental bittersweet, and winged euonymus, which
are resistant to deer browse, increasingly dominate the landscape due to
shifting of competitive edge.
In
an old growth forest in Pennsylvania, deer browsing has caused a dramatic
decline in tree species diversity, from 27 species to 11, and in another
Pennsylvania forest, from 41 species to 8 (Stout 2001). At both sites, deer densities were in excess
of 20 deer per square mile. A study by
Horsley et al (2003) in a Pennsylvania hardwood forest showed a negative linear
relationship between species richness and deer density.
The impact of deer browsing on forest regeneration is well demonstrated in a study conducted by the Connecticut Agricultural Experiment Station on Iron Ore Hill Forest Preserve managed by The Nature Conservancy. In 1984, approximately 82,000 seedlings per acre were observed. By 1998, deer density in the area had grown to around 60 deer per square mile, and the number of seedlings per acre had plummeted to 22,000. Sapling density in 1984 was 3,600 stems per acre. In 1998, only 1,400 stems per acre were observed. Oak and conifer regeneration was replaced by other species such as black birch and red maple. In the same study, survival rates of white pine seedlings under protected and unprotected conditions from deer browsing were compared. After 5 years, 0% of the white pine seedlings had survived under unprotected conditions, whereas 80% of protected seedlings had survived. Numerous studies conducted on replicated plots with various deer densities provide evidence that the deer strongly impact abundance, height, growth and species diversity of forest regeneration. Suppression or elimination of diverse palatable seedlings and saplings results in a slow but steady conversion of the stand to a small variety of less-palatable species.
A
description of the Audubon Center forest published in 1966 by the State
Geological and Natural History Survey of Connecticut serves as a good reference
in determining how the forest composition has changed in the last 40 years. The canopy species are unchanged, although
the beech and sugar maple which comprised the lower canopy are now the dominant
canopy trees. The most noticeable
change is in the 10 to 30-ft understory.
Witch hazel and flowering dogwood were most common in this size
class, along with saplings of sugar maple, red maple, and localized colonies of
beech originating as root suckers from larger beech trees. In our forest today, saplings are largely
absent from the middle-canopy layer except for beech root suckers in our beech
stands. Maple seedlings can be observed
on the forest floor, but they do not grow past the seedling stage before being
browsed by the deer. Oak and hemlock seedlings simply cannot be found in most
areas, because they are highly preferred by the white-tailed deer and are
plucked as soon as they germinate on the forest floor. In the long-term, the striking lack of
regeneration by species destined for position in the canopy will inevitably
result in significant structural and compositional shifts in the forest canopy
as existing canopy trees die.
Most of the plant diversity within our forests exists not as trees but rather as herbaceous understory species. Two studies at the Allegheny National Forest in Pennsylvania and additional research in Wisconsin, Illinois, and Ohio show that deer can have very important impacts on diversity and health of this component of the forest community (Stout 2001). At the Allegheny National Forest, grasses and sedges represented 64% of groundcover outside a deer exclusion fence, while these species represented only 16% of the groundcover inside the fence. A study by Horsley et al (2003) showed that species avoided by deer or resilient to deer browsing increase with increasing deer density. In this study, the percent cover of ferns, grasses, and sedges displayed a positive linear trend with deer density. Herbaceous plants are important food sources for the deer, constituting up to 87% of their summer diets (Waller and Alverson 1997). An old-growth forest in northwestern Pennsylvania lost 59 to 80% percent of its ground flora species between 1929 and 1995 due to deer browsing (Waller and Alverson 1997). Lilies, orchids, species of Viburnum and Trillium, native yew, and Canada mayflower are favored food sources of deer and are the first to disappear (Rhoads 1999). Deer have a particularly high preference for and devastating impact on wildflowers. Wildflowers are able to hide underground for a few years of intensive browsing pressure. But when browsing pressure lasts for decades or longer, they are simply eliminated due to lack of seed source (Stout 2001).
The
effect of deer overgrazing on the herbaceous community is evident in the
Audubon Center forest as well. In 1966, the shrubby stratum was described as
being well developed, with relatively continuous cover of maple-leaved viburnum
reaching to a height of 2 to 3 ft.
Where there were openings in the tree canopy, the pink azalea and
low-bush blueberry were commonly associated. Together, these three shrubs
contributed up to 80% of the shrub layer coverage. Scattered woodland herbs
such as Canada mayflower, wild spikenard, wood aster, and Pennsylvania sedge
covered less than 10% of the forest floor, with belts of ferns (New York fern
and cinnamon fern) recognized in lowlands (Niering et al 1966). The picture is very different today. The understory is sparse of herbaceous
cover and is much more open.
Maple-leaved viburnum that used to dominate the shrub layer has been
entirely eliminated. There has been an increase in groundcover of ferns and
some invasive species such as the barberry. Dramatic declines in species
diversity of wildflowers have been observed.
Canada mayflower, trout lily, lady slippers, and other species of
orchids and lilies are much less common.
Trilliums have been eliminated altogether. Common spring wildflowers that numbered tens, even hundreds of
species in the 1950s can now be counted on two hands. The only species of wildflowers commonly seen today include
Jack-in-the-pulpit, blue cohosh, wild leek, mayapple, garlic mustard, and dwarf
ginseng.
Deer
exert a strong influence on other animals, both through direct competition with
animals that feed on the same foods,
and by changing the structure and composition of the forest itself. While expecting deer effects primarily on
ground-nesting birds, McShea (1997) found multiple effects on bird species
nesting at several levels in the forest, apparently reflecting complex
interactions among the forest biotic communities. DeGraaf and others (1991) studied the effects of deer browsing on
breeding birds in New England woodlots.
They found greater numbers of canopy-gleaning species and individuals in
stands with fewer deer. Rufous-sided
towhees were more abundant in low deer density stands, but hermit thrushes were
more abundant in stands with higher deer densities. The number of migratory
bird species was also greater in stands with fewer deer. In an experiment
conducted at the Allegheny National Forest, DeCalesta (1994) found that many of
the birds that are intermediate canopy nesters disappeared from the study sites
with deer densities higher than 20 deer per square mile. As shrub and
herbaceous layers disappear due to overgrazing, so do the birds that feed or
nest on the forest floor and in shrubs.
At higher deer densities, the middle canopy layer disappears over time
and songbirds lose their habitat. When the deer density reaches 64 deer per
square mile, even adaptable species like robins and phoebes are forced out
(deCalesta 1994 and McShea 1997). In
autumn, deer switch to a diet heavy in acorns, bringing them into direct
competition with many other mammals and birds, from turkeys to squirrels. In
one study, deer consumed nearly three quarters of all the fallen acorns in
Pennsylvania red oak stands, largely monopolizing the mast crop (Steiner
1995).
Changes
in composition and abundance of bird species as a result of the deer impact on
wildlife habitat have been observed at the Audubon Center. The following table summarizes some results
from the breeding bird census conducted in the upland beech-maple forest
(northern portion of Audubon Center) in 1971 and again in 1998.
Number
of Breeding Bird Pairs
(+): the bird was observed but breeding could
not be confirmed
Dramatic
decline in the number of ground nesting/feeding birds during the 27-year period
is apparent. Total number of species remained relatively unaffected, but the
total number of territories showed a 28% decline due to simplification of the
forest structure. In addition,
mid-canopy nesters such as the wood thrush, scarlet tanager, and eastern wood
pewee are starting to show a decline in numbers associated with the
disappearance of the middle canopy layer.
Accumulating
evidence from the Connecticut Agricultural Experiment Station scientists and
others suggests that the resurging deer population is causing an increase in incidence
of Lyme disease in humans. The
incidence of Lyme disease has doubled in the U.S. since 1991 (Center for
Disease Control and Prevention 2002). A record 3,285 cases of Lyme disease were
diagnosed in Connecticut in 2002 (http://www.ci.darien.ct.us). Fairfield
County, where the state's highest deer density is found, accounted for over 1/3
of the reported cases of Lyme disease in the state in 2000 (Center for Disease
Control and Prevention 2002).
Deer
harbor the blacklegged tick (Ixodes
scapularis), commonly referred to as the deer tick, which transmits the
Lyme disease spirochete (a type of bacterium).
The deer tick also transmits pathogens of two other diseases, human
babesiosis and human granulocytic ehrlichiosis (HGE). Abundance and distribution of the tick is correlated with deer
density. All of the Connecticut
Agricultural Experiment Station studies and those conducted elsewhere indicate
that the deer population would have to be reduced to low levels to appreciably
reduce Lyme disease occurrence.
Treating deer with a pesticide using a baited self-application system
remains an experimental approach, and it is unlikely that sufficient number of
free-ranging deer can be treated to impact the rate of tick-borne disease
(Stafford 2001).
Among
the staff at the Audubon Center, there have been 9 documented cases of Lyme
Disease and 1 confirmed case of Erlichiosis in the last 5 years. There has been
additional disease occurrence among our volunteers and visitors, and we know of
one confirmed case of Babesiosis on a
property which abuts the Audubon Center. Because one of the objectives of the
Audubon Center is to provide a safe place where people can enjoy nature, health
risks posed by the deer ticks present an immediate concern.
Deer
overabundance results in damage to ornamental plantings and agricultural crops,
especially fruit trees in orchards. Damage to landscape plantings in suburban
areas has been reported in states throughout the population range. At the
Audubon Center, we have had to erect fencing around all new apple tree
plantings, at considerable expense and labor, to protect them from deer damage.
Overabundant
deer populations in urban areas are associated with high rates of deer-vehicle
accidents. An estimated 6,000-8,000
deer are killed every year along Connecticut’s roadways, according to reports
by the Connecticut Department of Transportation. Deer-vehicle collisions are
serious public hazards. Several human fatalities have occurred from
deer-vehicle collision over the past 15 years in Connecticut (Connecticut DEP
2002). Deer roadkills in deer management zone 11, which roughly represents
Fairfield County, were 2 to 10 times greater than all other deer management
zones in the state (Kilpatrick et al. 2002). In 2000, 565 deer road kills were
reported in Fairfield County. In
Greenwich, roadkills accounted for 81 deer deaths in 2001, a high number when
compared to the 113 deer legally harvested here in the same year.
In
addressing the problem of an overabundant deer population and its harmful
effects, several management options are available: no action, fencing and use
of repellents, trapping and relocation, controlling fertility in does and
sterilizing males, supplemental feeding, and hunting. The feasibility,
advantages and disadvantages of each option are discussed in the following
paragraphs.
The
white-tailed deer evolved under heavy predatory pressure and its life history
adapted to allow for loss of individuals to predation. In the absence of natural predators and
other control methods, deer populations grow until they reach the upper limit
of their habitat's carrying capacity. High densities have adverse effects on
the deer themselves, exposing them to higher rates of disease and parasites,
injuries from car collisions, and to a greater risk of starvation in harsh
winters. Overpopulation makes it hard
for does, which seek solitude as birth approaches, to set up suitable fawning
territories. The result is fawn abandonment and increases in other forms of
infant mortality. Deer in high density
herds tend to be in relatively poor health, and are prone to cyclic population
fluctuations and catastrophic losses in response to environmental stresses. In
extreme cases, “hands off” management may even result in local herd
extinction. Because humans have greatly
altered important functions of the natural ecosystem, including natural deer
predation, allowing nature to take its course will not restore the ecosystem to
a healthy balance. In the absence of control measures, overgrazing by the
white-tailed deer will continue unabated, causing the significant destructive
consequences described earlier.
Fencing
requires a substantial initial investment for materials and installation,
followed by regular maintenance. If properly installed, it is effective at
excluding deer from specific areas and reducing damage to plantings. Fencing
around larger landscapes will restrict the movement of other medium to large
sized wildlife species and may have a harmful effect on their natural breeding
or feeding activities. Many different types of taste and odor repellents are
available to reduce deer damage to plantings. They, too, are costly and labor
intensive, requiring repeated applications as weather erodes their
effectiveness and rapidly growing shoots outgrow protection. Noxious and unaesthetic product residues
further limit their usefulness. The effectiveness of chemical repellents is
highly variable and decreases as deer population increases. Neither fencing nor
repellents address the underlying problem of deer overpopulation.
Trapping,
netting and immobilization are used to capture and relocate deer. Studies have shown that 50 to 85% of all
trapped and relocated deer will die, mainly from capture-related stress and
from roadkills after wandering extensive distances following release (Jones and
Witham 1990, O’Bryan and McCollough 1985). Trapping and relocation has also
proven to be labor intensive and prohibitively expensive. The Connecticut DEP
estimates the costs at $400 to $3,000 per deer. Because deer are abundant
throughout most of the United States, there are no suitable places for
releasing excess deer, and relocation of deer from overpopulated ranges can
spread disease.
Fertility
control and sterilization to reduce and manage deer populations is still
experimental. Four general methods of controlling
fertility in does have been tested and may be applicable to deer management
– surgical sterilization, synthetic steroid hormones, immunocontraception, and
contragestation.
Surgical sterilization requires capture of individual does and
application of field surgery. High cost
and difficulty of treating a sufficient number of deer makes this method
unfeasible for managing free-ranging herds.
Synthetic steroid hormones alter natural reproductive cycles and
can reduce the likelihood of pregnancy.
They are administered either by treated bait or by implants. The treated bait method requires daily oral
exposure, so it is not practical. The
effectiveness of steroid hormones in preventing pregnancy has varied in
experiments, and each animal requires a new implant at least every 2
years. Currently, no synthetic steroid
hormone contraceptives have been approved by the Food and Drug Administration
for use in white-tailed deer, other than in controlled experiments.
Immunocontraception involves injecting the animal with a
vaccine to stimulate its immune system to produce antibodies against a protein
involved in reproduction. This
technique has advantages over use of synthetic hormone contraceptives, since it
can be delivered remotely using darts.
The disadvantages of this method are that each female deer requires
multiple treatments every year, and that it may prolong breeding season of the
deer. Deer are most active during the
breeding season and, as a result, deer-vehicle collisions increase dramatically
during autumn (Warren 2000). Use of
this method could increase deer-vehicle accidents.
Research
on contragestation in white-tailed
deer has focused on the commercially available drug prostaglandin F2 (PGF2).
PGF2
is approved by the FDA for use in cattle and swine intended for human
consumption. It is applied during the
winter, after females are pregnant and it is relatively easy to attract deer to
bait stations due to the scarcity of natural food sources. PGF2 can be applied remotely using darts, and
this method did achieve some level of success in reducing pregnancy rates in a
free-ranging herd in an experiment conducted in South Carolina (Warren
2000). The disadvantages of this method
are that females must be treated annually, and that abortion of fawn-like
fetuses may not be acceptable in some communities.
In
a study conducted in Groton it was demonstrated that, even with good access to
a relatively small, isolated deer population, an adequate number of female deer
could not be successfully treated for fertility control to limit population
growth. The study suggested that 70-90% of females need to be treated with any
method to effectively limit population growth. It becomes increasingly
difficult and requires greater effort to treat remaining females in the herd as
the deer become more cautious. With
continued research, there is a potential for fertility control to be applicable
in the management of deer in the future, especially smaller herds in urban
areas. However, to date, research in
this area has not proven fertility control to be effective in reducing
free-ranging deer populations.
Reducing
deer population by capturing and
sterilizing large males and retaining them in the population is still experimental. Since white-tailed deer exhibit a distinct
hierarchy in which dominant males monopolize most mating, the number of fawns
produced may be reduced (Ramakrishnan 2001).
Further investigation is being conducted in North Branford, Connecticut. However, this method is expensive and
labor-intensive, and the difficulty of treating sufficient number of large
males in a free-ranging herd will limit its application.
Providing
supplemental food for deer herds in order to control their overgrazing effect
has been shown to be counterproductive, because it encourages additional
population growth. In fact, additional
food sources for the deer, such as bird feeders within their reach, should be
eliminated in high deer population areas to avoid compounding future population
growth.
Regulated
hunting has been proven as a practical deer population management tool with
high rates of success (Connecticut DEP 2002).
It is cost effective, and results in immediate removal of excess animals
from the population. It is the principal
management tool used by state wildlife agencies throughout the United States.
A
common perception is that hunting is unsafe. However, hunting is one of the
safest sporting activities in Connecticut (Connecticut DEP 2002). All hunters, both firearms and archery, are
required to take a Conservation Education/Firearms Safety (CE/FS) course
administered by the state before they can purchase a hunting license. No
hunting accidents and no reports of wounded deer have occurred in special deer
hunts implemented to reduce deer populations in residential areas (Connecticut
DEP 2002).
Numerous examples of successful management of deer populations by hunting have been documented in Connecticut. At the 7,700-acre Yale Forest in the towns of Eastford, Ashford and Woodstock, a controlled deer hunt was implemented in 1984. The forest managers indicated that forest regeneration has improved considerably since. At the Bluff Point Coastal Reserve in Groton, CT DEP's Wildlife Division annually documented severe deer browsing of vegetation and stripping of bark from trees from 1984 to 1996. Controlled deer hunts there in 1996 and 1997 reduced deer population from 284 to 35 deer. Hunting took place again in 2000 and 2001, reducing the deer population to 19, a level compatible with ecological diversity for the first time in 20 years. The removal of excess deer from the reserve has positively affected the overall condition of the deer herd as indicated by improved body weights and fat measurements. Browse surveys conducted before and after the deer removal indicated a 36-45% reduction in browse rates of shrubs and tree seedlings. The presence of oak regeneration was noted for the first time in 1997. Amount of bark stripping on apple trees was reduced from 77% in 1994 to only 4% in 1997. In Groton Long Point, Mumford Cove, and the Town of New Canaan, archery and shotgun/archery hunts successfully reduced white-tailed deer populations. A 3-day hunt removed 82% of the deer population in Mumford Cove, and a 6-day hunt removed 92% in the joint Mumford/Groton Long Beach hunt (Kilpatrick et al 2002).
A
multitude of practices for population control and behavior modification have
surfaced, but the bottom line remains that removal of animals from the population,
specifically adult females, is the only effective way to impact deer numbers.
Hunting is the most practical and economic way to accomplish that. It is the
method chosen to manage the deer population at the Audubon Center in Greenwich.
Controlled
deer hunts have two phases: the initial reduction phase when hunting intensity
and deer harvests are high, and the maintenance phase when hunting intensity is
lower (McDonald 1998). It is important
that an adequate number of antler-less deer – both females and male fawns - be
harvested to reduce both the current deer density and the potential for future
growth. Typically, the removal of one
adult doe during the hunting season results in 3 fewer deer the following
spring (Kilpatrick 2002). As deer
numbers decrease, the number of deer necessary to be removed also
decreases. During the maintenance
phase, the number and ecological impact of the remaining deer are regularly
assessed, and, depending on the assessment findings, the deer are periodically
culled.
Hunting
can be controlled by establishing restrictions on: 1) number of hunters; 2)
selection of hunters; 3) hunting implements used (shotgun, rifle, bow and
arrow); 4) timing of the hunt; 5) duration of hunt; 6) number and sex of deer
harvested; and 7) areas open to hunting.
These restrictions can be tailored to meet the specific circumstance and
objectives of the landowner. In 2001, a total of 11,950 deer were harvested in
Connecticut, reducing deer populations via tag limits and season length.
According to data published by the Connecticut DEP, success rates among the
various hunting methods used in these hunts were: shotgun/rifle hunters
(24.7%), followed by archers (19.1%), and muzzleloader (5.3%).
Deer hunting is strictly regulated in Connecticut. Hunting with firearms is usually allowed only from mid-November to late December. Bowhunting is permitted in 2003-2004 from September 15 to January 31. Deer hunting is permitted from one hour before sunrise to sunset, and is not allowed on Sundays. For safety, firearm hunting is prohibited within 500 feet of occupied dwellings. In bowhunting, in which the archers shoot downward on the deer from scaffolds in trees, there are no minimum distance restrictions. Bowhunters with state permits are allocated four tags for deer harvest each year. Two can be used for either a male or a female deer, and two are used only for females. Unlimited numbers of replacement tags are issued by the state for any does harvested. Use of sharpshooters is prohibited.
Bowhunting
is the preferred hunting method in suburban areas due to its quiet nature and
safety concerns. In the Town of Greenwich, of the 113 deer harvested in 2000,
112 were taken by bowhunters. Chances of bowhunters wounding, but not killing,
the animal are low. A wounding rate of 7% has been reported by the Greenwich
Sportsmen and Landowner’s Association. It is even less likely that a deer will
walk away with an arrow in its body. Controlled archery hunts conducted elsewhere
in the state did not result in the sighting of any wounded deer.
The goal of Audubon's deer management program is not to eliminate the deer population, but to maintain it at a level where deer and their habitat are in balance. Successful implementation of our management plan will result in a healthier deer herd, reduction of health risks from deer tick borne diseases, decrease in number of deer/vehicle accidents, and in the maintenance of a healthy ecosystem.
Our
research and consideration of our circumstance has led us to a conclusion that
bowhunting is the most feasible method of deer removal. In the initial two
years of the plan, hunting will be implemented only on the 300-acre parcel at the
Audubon Center. Our goal is to reduce
the deer population within the Center Sanctuary to 5 to 7 deer. This number
represents an ecologically sustainable deer density of 10-15 per square mile. As noted earlier, based on the 2002 DEP
aerial survey of the surrounding neighborhood, the deer population at the
Audubon Center is currently estimated to be 45 to 60 deer, so a minimum of 40
deer will need to be removed during the initial reduction stage.
We
will be working with a bowhunter group in Greenwich, the Greenwich Sportsmen
and Landowner’s Association (GSLA),
which will implement the deer hunt on the Audubon Center grounds without
charge. The mission of the GSLA is to promote and protect bowhunting as a means
of deer population control. Its 12 members all reside in Greenwich. Two are
close neighbors to the Audubon Center property. The GSLA emphasizes training
and ethical methods in all of its hunts and requires the 12-hour National
Bowhunter Education Foundation course and proficiency testing of all its
members, as well as a formal application and interview.
Due
to the nature of bowhunting, it is not feasible to reduce the deer population
to our target level in a concentrated hunting effort that spans only a few
days. GSLA's expert opinion is that a harvest
of 25 or more deer in one season is reasonable, and a harvest of up to 40 deer
is possible. We expect to meet our reduction target within the first two years
of the hunting program. Once it has been achieved, we will establish a
monitoring program, with periodic hunting implemented as necessary to maintain
the deer herd at a sustainable level. Hunting by GSLA members will be initially
conducted between October 13 and December 6, 2003, with periodic reviews to
determine if the season should be extended or abbreviated.
Aerial
photos of the Center grounds will be used to divide the property into numbered
sections, and scouting for tree stand locations will occur in August and
September. The stands will not damage
the trees, as no nails or screws are used on the trees. All stands will be
located away from hiking trails. When a deer is hit, the bowhunter will descend
from the stand and locate the deer, which may walk up to 100 yards before
dropping.
Bowhunters need 2.5 hours of sunlight either after sunrise or before sunset to hunt effectively. Audubon will allow the GLSA bowhunters access to the sanctuary at dawn on three weekday mornings each week during the program, and the Center will remain closed to the public until 9:30 am on the scheduled hunting days, by which time the hunters will have cleared from the sanctuary. The GSLA will inform the Center Manager which sections of the property will be hunted and which of their members will participate each day. The hunt leader for the day will confirm with staff that all hunters have checked out by 9:30 each morning, and report on any deer harvested. The protocol will be monitored continually and adjustments made as necessary to reduce safety risks or increase its effectiveness.
Parking
and site access for hunters will not be through the main entrance to the
Center. Hunted deer will be gutted on site. Any blood trail will be covered
with leaves to conceal it, and the gut will be buried at least 50 yards from
any hiking trail. Raccoons and coyotes
often consume the buried deer entrails within days. The deer will be taken out on a hand cart, transported to the DEP
check station in Greenwich, then butchered by a licensed processor. The cost of
butchering is $40 per deer. Audubon will raise money for this cost. All meat
will be donated to the Food Bank of Lower Fairfield County.
The
safety of our visitors and neighbors is of utmost concern. Every effort will be
made to clearly communicate our management plan to the public and to restrict
access to the site during hunting hours. To avoid unduly prolonged public
debate on implementation of the deer management plan, public notice will be
given two weeks in advance of the first hunt. All adjoining landowners will be
notified of the hunt by letters. Local media and our own mailing list and
website will be used to communicate the plan to potential visitors in the
broader community. Most landowners near the Audubon Center understand the
problem of an overabundant deer population and many have tried to reduce deer
population by hunting their own properties.
Explanation on details of our deer management plan, its goals, rationale
and timetable will be conveyed to the media to promote understanding of the
issue and inform the community of our slightly reduced hours.
The
only impact on our typical use of the site is that the hiking trails will
remain closed an extra half hour three mornings per week during the hunting
period. There will be a clear posting at the main entrance of our property as
well as all other potential entry points to inform visitors of the hours the
Center will be closed for hunting.
Access to the Kimberlin Nature Education Center, offices, staff housing,
and hawkwatch site need not be restricted. If protesters are expected on the
first days of the deer hunt, we will hire police officers and/or other security
personnel to ensure safety of the demonstrators, our staff, and the hunters. To
gain the support and understanding of our members and the local community,
every effort will be made to clearly explain the scientific basis for reducing
deer population and the rationale for the chosen method. We will also
communicate our plan and its progress to local and state government agencies to
engage their support.
Forest
ecosystems are not static but are constantly changing in successional stages
and in response to disturbances and environmental conditions. Some of the changes in the vegetative
patterns and in the abundance of bird species on Audubon lands can be
attributed to forest maturation. However, evidence from numerous studies on
ecological impacts of overabundant deer population and observations made at the
Audubon Center suggest that the current deer population level may be
incompatible with full renewal of the forest community – its trees,
wildflowers, shrubs and wildlife, its biodiversity, and its ecological
integrity.
Recovery
of plant species composition and structure in overpopulated areas after the
reduction of deer has been demonstrated through a variety of thoughtful and
replicated studies. Deer have a devastating impact on tree seedlings as we have
examined earlier. Evidence shows that
the abundance and diversity of tree seedlings respond fairly quickly to a
reduction of deer population. The successful comeback at the Bluff Point
Coastal Reserve is noted above. In research conducted at the Huntington
Wildlife Forest Station in New York, a controlled deer hunt was conducted to
discern the impact of deer grazing on tree seedlings. When deer density was
reduced from 27 per square mile to 12 per square mile, the number of white ash,
yellow birch and sugar maple seedlings greater than three feet tall increased
from 200 per acre to more than 10,000 over a 3-year period. There are numerous
other examples of recovery of tree regeneration following removal or reduction
of deer population.
Data
suggest that the herbaceous community recovers more slowly than woody species
from deer browsing because herbaceous cover and frequency are more closely tied
to historic deer densities. Groundstory
plants cannot grow past the browse line and remain susceptible to browsing
throughout their life cycles. Heavy
grazing by an overabundant deer population will tend to transform a naturally
diverse herbaceous community into one dominated by ferns, grasses and sedges
which may interfere with the re-establishment of native herbaceous plants and
tree seedlings. In these areas,
physical removal and site treatment may be necessary to promote recruitment of
the native plant community.
Perhaps
the most devastating effect of an overabundant deer population is on the spring
wildflowers. As noted above, when browsing pressure lasts for a decade or
longer, they are simply eliminated due to lack of seed source (Stout
2001). Relieving grazing pressure by
the reduction of deer may not restore the wildflower community, in which case
active restoration efforts will be necessary to re-establish the representative
native wildflower species.
Studies
have shown that tick density and the incidence of Lyme disease decrease with
reduction of deer population. Tick densities were monitored in Bridgeport and
Groton, Connecticut, both areas with deer density of around 200 deer per square
mile. When deer populations at these
sites were reduced over the past decade to 44 and 27 per square mile, the
number of blacklegged ticks collected per 100 m2 declined by 68-93%. Reduction in population of deer ticks can
naturally be expected to reduce the risks of human contraction of tick-borne
diseases such as the Lyme disease, Erlichiosis and Babesiosis.
The
deer management program will need continuous monitoring and adjustment. Besides monitoring the status of the
white-tailed deer population, we will develop accurate and convenient
indicators of its direct and indirect impacts on components of the ecosystem
that are sensitive to high deer density.
Vegetation monitoring plots in each representative forest type on
our property will be established for measuring and recording herbaceous plant
abundance and diversity, the number, growth and species of tree seedlings and
saplings, and browse damage. As noted earlier, the herbaceous community is
expected to recover more slowly than woody species. Because intensive grazing by deer has persisted for at least the
past two decades, any seed bank remaining in the soil may have been
extirpated. If viable seed source is no
longer present, then wildflowers and other herbaceous species heavily grazed by
deer may not come back. In such a case,
the abundance and diversity of tree seedlings would serve as a more appropriate
indicator. The annual breeding bird census
can be used to help detect any shifts in abundance and species diversity of the
bird community.
Long
and short-term monitoring of ecological effects of deer will provide a gauge of
appropriate population levels, contribute to a better understanding of the
ecological connections between deer and other ecosystem components, demonstrate
the benefits of sound conservation measures, and help establish the Audubon
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