Last summer was a very exciting summer because we got to participate in REAL SCIEN!CE Thats right in a project funded by the State of Wisconsin we raised a biological contorl thatreduces the evasive spies of Eurasion Milfoil. The milfoil weevil is a natural plant predator of some types of milfoil and has been studied by researchers as a biological control for Eurasian watermilfoil for over two decades. Weevils are commonly found the SNC lake. However, because milfoil grows so fast, natural populations of weevils cannot typically control it. Our goal was to boost the natural weevil population to sustainable levels high enough to effectively control the milfoil over the long-term.We started with 750 weevels in our 10 tanks each of which held 50gallons. We feed the weevels Milfoil during the summer and released nearly 1500 weevels. We were hoping to relaese even more but for some reason, probably a cool summer we had less breeding weevels. We will be doing the same program again in 2012 to see if we can even increase production
Mass rearing of milfoil weevils (Euhrychiopsis lecontei)
by volunteers: Pilot Study
Phase I
AMY THORSTENSON
FEBRUARY 2012
Stevens Point, WI
715/343-6215
www.goldensandsrcd.org
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Introduction
Biological control studies are currently underway in Wisconsin to improve the
science of applied biological control of Eurasian watermilfoil (EWM). Many lake groups
are eagerly awaiting the results of those studies and are interested in applying biological
control in their lake. However, for many cash-strapped lake groups, purchasing their
weevils outright would be cost-prohibitive. As we move forward in our understanding of
the biological control of EWM, this mass rearing pilot study aims to move us forward in
making milfoil weevils a more practical option for lake groups with more sweat equity
than cash. The mass rearing method (Thorstenson 2011) is labor intensive and must
be followed to the letter in order to maximize success. Phase I of this pilot study was
the first year of evaluating the capability of volunteer groups to successfully produce
weevils on a mass scale.
Methods
Study area —Lake Holcombe (Chippewa/Rusk Co) is a 2,881-acre impoundment
of the Chippewa River, with a maximum depth of 61 ft. Large parcels of the riparian
properties belong to the State of Wisconsin or paper company holdings and remain in
natural/wooded condition. The Minong Flowage (Douglas/Washburn Co) is a 1,587-
acre impoundment of the Totagatic River, with a maximum depth of 21 feet and
surrounding natural/wooded shoreline. Goose Lake (Adams Co) is an 84-acre seepage
lake with a maximum depth of 22 ft and surrounding natural/wooded shoreline.
Study Design — Weevil rearing methods were modeled after Hanson, et al.
1995, with modifications based graduate work conducted by Amy Thorstenson at UW-
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Stevens Point (Thorstenson2011). Hanson, et al. reported that an outdoor stock tank
performed just as well their indoor, controlled 20-gal aquariums, with less management
time invested. Thorstenson’s studies found similar results, and developed a simplified
method for outdoor, mass rearing.
Each lake group set-up and maintained 10, 370-L “Freeland poly-tuf‟ stock tanks
(79cm W x 132cm L x 63cm H), stationed in an outdoor area where full sun and access
to a clean water supply was available. The sunniest location available was selected to
keep the milfoil stems (food stems) healthy, but water temperatures were monitored to
ensure they did not approach lethal temperatures (34 C / 93 F). Water temperatures
were monitored with aquarium thermometers and recorded regularly. Fresh water was
added as needed to top off the tanks. NoSeeUm (0.033 cm mesh) light duty fiberglass
screening was used to cover the tanks and pools. While the primary use of the
screening was to exclude predator/competitor insects and birds, it also functioned as
light shade to reduce peak temperatures in the tanks during sunlight hours.
EWM stems to be used for food were collected from the same lake that would be
the recipient of the weevils reared. Stems were collected from the deepest milfoil beds
available, farthest from shore, where naturally occurring weevils were less likely to be
present, in order to avoid the inadvertent introduction of unaccounted for weevils. To
minimize the introduction of predator or competitor insects, the collected food stems
were laid thinly over a mesh screen and sprayed with a hose and nozzle at a pressure
sufficient to clean the milfoil but not damage it. Cleaned stems were then be floated in a
wading pool of clean water, sorted and untangled. Because weevils lay their eggs on
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apical meristems, only stems with apical meristems were retained for use; stems that
had gone to flower or had broken tips were be discarded. Stems were trimmed to a
length sufficient to reach from the base of the rearing chamber to the surface of the
chamber’s water (62 cm). Stems were then bundled together in groups of fifteen stems,
and attached at the base to a rock with a rubber-band to weight the stems down and
achieve vertical orientation in the rearing chamber. All chambers received an initial
stocking of milfoil food bundles, with stockings repeated every 21 days to keep the
weevils supplied with actively growing milfoil (Table 1).
Table 1
Weevil feeding schedule.
# of EWM
stems to feed
per tank
Day 0
Day 21
Day 42
105
165
225
The “starter batch” of weevils were purchased from EnviroScience, Inc., Ohio.
EnviroScience Inc. provided weevil stock from northern Wisconsin, in order to ensure
weevils with winter-hardy genetics. Each tank was stocked with 0.19 weevils/L (72
weevils per 100-gal tank). The purchased weevils arrived as eggs and early instar
larvae attached to bundles of milfoil stems in sealed plastic bags. The estimated
number of weevils in each bag was written on the outside of each bag, however the
number of weevils inside were assumed to be unevenly distributed amongst the milfoil
stems within. Therefore, the stems were placed into a large tub of water and counted to
derive an estimated average of weevils per stem. Stems were then selected randomly
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to accumulate the number of weevils needed to stock each rearing chamber. Thus, the
number of weevils initially stocked to each rearing chamber was an estimated average.
Chambers were maintained for approximately 55 days, allowing enough time for
producing two generations. Prior to releasing the weevils to their recipient lake,
subsamples were extracted to estimate total production. A 10% subsample of the
weevil-containing food stems were extracted from four of the ten tanks (selected at
random), preserved in 80% isopropyl alcohol, and refrigerated until laboratory
examination. The preserved subsample stems was examined by Thorstenson by
floating stems in water in a glass pan over a light table, with 3x magnification goggles.
Each stem was carefully examined for weevil eggs, larvae, pupae, and adults and the
total number of weevils recorded. The assistance of a higher power (30x) Carson
MagniscopeTM was used for identification of specimens when needed. Specimen
vouchers were preserved in sample vials in 80% isopropyl alcohol.
Data Analysis — For the each rearing site, average return rate and total estimated
production was estimated based on the 10% subsamples. Total estimated release (total
production – subsamples) was also calculated. Temperature records were analysed to
calculate min, max, mean, and 90% confidence intervals, to evaluate whether volunteers were
maintaining optimal water temperatures.
Results
Goose Lake – Expected return rate was 9.6 weevils out per weevil stocked, and
Goose Lake’s return rate was 0.6. (Table 2) 720 weevils were initially stocked to the10
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rearing tanks, and total production was estimated at 400 weevils. Lab examinations
observed: low occurrence of miscellaneous insects; substantial mixing of hybrid milfoil,
M. sibiricum, and M. verticillatum stems; dead or bacteria-engulfed pupa; low
occurrence of pupation sites; and low evidence of weevil damage on non-M. spicatum
stems. Due to an acute lack of available M. spicatum in Goose Lake, M. sibiricum and
hybrid milfoil were also collected as an optional food choice when it became necessary.
Water temperatures were monitored but not recorded. Tank temperatures were
moderated by adding fresh groundwater as needed.
Minong Flowage - Expected return rate was 9.6 weevils out per weevil stocked,
and Minong Flowage’s return rate was 1.8. (Table 3) 720 weevils were initially stocked
to the10 rearing tanks, and total production was estimated at 1,300 weevils. Lab
examinations observed: low occurrence of miscellaneous insects; no non-M. spicatum
mixed in; heavy weevil damage to stems in some tanks; and fused, deformed milfoil
leaflets and hardened, opaque stems (indicative of exposure to herbicides) in some
tanks. Tank temperatures were moderated by adding fresh groundwater as needed.
Water temperature ranged from 60 - 80 F, with a mean of 71 F. (Table 4) These
temperatures were similar to temperatures expected (per Thorstenson 2011), but lower
than the temperatures optimal for weevil production. (Figure 1)
Lake Holcombe - Expected return rate was 9.6 weevils out per weevil stocked,
and Lake Holcombe’s return rate was 3.1. (Table 5) 720 weevils were initially stocked
to the10 rearing tanks, and total production was estimated at 2,090 weevils. Lab
examinations observed: low occurrence of miscellaneous insects; no non-M. spicatum
species mixed in; poor stem health; heavy weevil damage to stems in some tanks;
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limited available oviposition sites; and fewer eggs than expected. Tank temperatures
were moderated by adding fresh groundwater as needed. Water temperature ranged
from 70 - 90 F, with a mean of 82 F. (Table 6) These temperatures were higher than
temperatures expected (per Thorstenson 2011), and similar to temperatures optimal for
weevil production. (Figure 1)
Discussion
Goose Lake production was substantially lower than expected, and the optional
feeding on non-M. spicatum species was likely the key problem. Temperatures were
closely monitored (although not recorded), and not believed to be a problem.
Subsample observations noted few miscellaneous insects, ruling out a predation
problem. Subsample examinations confirmed several species of milfoil were used in
feeding, including: M. sibiricum, hybrid milfoil (northern x M. spicatum), M. verticillatum.
M. heterophyllum is also present in Goose Lake and may also have been fed, although
subsample examinations did not confirm this. Subsample examinations noted problems
with pupation (bacteria-laden pupa, dead pupa, few pupal chambers observed), and
weevil damage observed on M. spicatum but not the other species that were mixed in.
Weevil developmental time is longer, and developmental performance is poorer, on M.
sibiricum than on their exotic host, M. spicatum (Newman et al. 1997). Research in the
Midwest has found that weevil performance on hybrid milfoils was intermediate between
the native hose (M. sibiricum) and the exotic host (M. spicatum) (Roley & Newman
2006). Weevil developmental time is significantly longer when reared on M.
verticillatum than on M. spicatum (37 days versus 21 days) (Solarz & Newman 2001).
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Additionally, oviposition (where they choose to lay their eggs) preference was
significantly less for M. sibiricum and nearly absent for M. verticillatum in females that
were reared on M spicatum (Solarz & Newman 2001). Weevil development on or
preference for M. heterophyllum is unknown. Therefore, the optional feeding of other
milfoils, although unpreventable due to an acute lack of M. spicatum in 2011, was likely
the main factor in low production.
Minong Flowage had lower than expected production, possibly due to a
combination of factors. One factor may have been food stem quality. The Minong site
was the shadiest of the three sites, and subsample examinations noted stems in very
poor condition, some limp, as if they did not get enough sunlight. Additionally, some
tubs had stems that were deformed (fused leaflets, tough, opaque stems) as if exposed
to herbicides. Food stem collection was in an area of the Flowage that had not been
treated with herbicides, but was within the same bay (Serenity Bay). (Appendix B) It
would be possible that residual herbicides were insufficient to kill the milfoil there, but
yet sufficient to cause growth deformities. These deformities may have negatively
affected the plant’s qualities as a host plant for successful weevil development. (Note
the dead pupa recoded in the same tub that had the deformed stems.)
Lake Holcombe had lower than expected production, probably due to weevil
development time being shorter than expected. The rearing site was in open prairie,
with all-day sun, which allowed the tubs to warm more than expected. Volunteers
managed the temperatures frequently, adding fresh, cool groundwater twice a day if
needed to keep tanks from getting too hot during heat waves. Their temperature
records reflect that effort, with tank temperatures hovering around a mean of 81 F, and
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a tight 90% confidence interval of less than 1 degree. We were expecting tub
temperatures to average around 71 F, as in Thorstenson 2011, and for the full life cycle
to take about 21 days. Lake Holcombe’s temperatures were closer to optimal
temperatures for weevil development (84 F, Mazzei et al. 1999). At this temperature,
the full life cycle takes only 17 days (Mazzei et al. 1999), which means the weevils
should have been fed four days sooner, at each feeding cycle. Subsample
examinations found heavy feeding damage, a shortage of healthy growing buds suitable
for egg laying, and a shortage of healthy, fat stems suitable for pupation sites, all
evidence that the weevils were running out of food and habitat, which certainly led to
reduced production rates.
Although the results of this study were well below expected, the problems
encountered can be adjusted for with modifications to the methods. In future studies, it
is recommended to:
select rearing sites that have a minimum of 6 hours of sunlight to maintain
healthy food stems;
collect food stems well away from potential herbicide residue areas;
avoid the optional use of other milfoil species;
and to monitor temperatures regularly and shorten feeding cycle times at very
sunny sites where optimal temperatures are attained.
Acknowledgments
This study was funded by an Aquatic Invasive Species Grant (#AEPP-304-11)
from the Wisconsin Department of Natural Resources. This study would not have been
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possible without the dedication of team leaders at each site: David Blumer, SEH, Inc.,
Reesa Evans, Adams County Land Conservation Department, and “Doc” Dougherty,
Lake Holcombe Association; and their dedicated volunteer crews at Goose Lake
Association, Swift Nature Camp, Minong Flowage Lake Association, and Lake
Holcombe Association.
References
Hanson, T., C. Eliopoulos, and A. Walker. 1995. Field Collection, Laboratory Rearing
and In-lake Introductions of the Herbivorous Aquatic Weevil, Euhrychiopsis
lecontei, in Vermont. Vermont Department of Environmental Conservation,
Waterbury, VT.
Mazzei, K.C., R.M. Newman, A. Loos, and D.W. Ragsdale. 1999. Developmental rates
of the native milfoil weevil, Euhrychiopsis lecontei, and damage to Eurasian
watermilfoil at constant temperatures. Biological Control. 16:139-143.
Newman, R.M., M.E. Borman, and S.W. Castro. 1997. Developmental performance of
the weevil Euhrychiopsis lecontei on native and exotic watermilfoil host-plants. J.
of the North Amer. Benthological Soc. 16:627-634.
Roley, S.S., and R.M. Newman. 2006. Developmental performant of the milfoil weevil,
Euhrychiopsis lecontei (Coleoptera: Curculionidae), on northern watermilfiol,
Eurasian watermilfoil, and hybrid (northern x Eurasian) watermilfoil.
Entomological Soc. of Amer.
Solarz, S.L. and R.M. Newman. 2001. Variation in hostplant preferences and
performance by the milfoil weevil, Euhrychiopsis lecontei Dietz, exposed to native
and exotic watermilfoils. Oecologia 126:66-75.
Thorstenson, A.L. 2011. Biological control of eurasian watermilfoil (Myriophyllum
spicatum) using the native milfoil weevil (Euhrychiopsis lecontei). M.S. Thesis.
University of Wisconsin-Stevens Point, Stevens Point, WI.
As we near Earth Day 2012 it is important that
we all realize that the planting of 1 tree can make a difference.
Read more about How trees change our life
The information provided is in reference to urban forests, but these benefits and values also apply to rural forests.
Canopy, or tree canopy, is a term used to describe the leaves and branches of a tree or group of trees. In an urban forest, tree canopy is important to the potential benefits the forest may provide. In general, the more area it covers and the denser the canopy, the more benefits the trees can provide. Although one tree is better than none, 100 are better still. Whether the benefits are from one tree or many trees, they are all still real and most can be quantified in some way. Often, forest benefits are divided into three categories: social, economic, and ecologic. It is difficult to divide the benefits that the urban forest canopy provides into these categories because so many benefits fall into more than one.
Social Benefits
Just as with a rural forest, an urban forest provides many benefits. Numerous studies have been done about the social
and psychological benefits of “green” in urban environments. The findings of the studies make a strong case for the
importance of urban forests. Urban public housing residents who lived in buildings without trees and grass nearby were
asked about how they cope with major life issues. They reported more procrastination and assessed their issues as more
severe than residents with green nearby.
A study done with children with Attention Deficit Disorder (ADD) found that children with ADD were better able to focus
and concentrate after playing in natural, green settings, than in settings where concrete was predominant.
Apartment buildings with high levels of greenery have been shown to have approximately half the number of crimes
than those with little or no greenery. The results proved true for both property crimes and violent crimes. A similar study
found that residents living in areas without nearby nature reported more aggression and violence than those living with
nearby green. In addition to these specific studies, access to nature also provides humans with other social benefits.
Parks and other green spaces provide a space for people to play, walk, jog, birdwatch, or just sit quietly. These activities
are good for our physical health in a society that is increasingly sedentary. It is also good for our mental health by
providing a place to unwind. Trees also reduce noise levels.
Economic Benefits
The economic benefits of urban forests are increasingly being documented. Economics often becomes the language
used when it comes to urban forest management. Budgets of municipalities must cover an array of services, and the
benefits of an urban ecosystem must often be proven to secure funding. In a study that considered the costs and
benefits of municipal forests in five U.S. cities, the researchers found that for every dollar spent on trees, the benefits
returned were worth from $1.37 to $3.09. A little math tells us this is clearly a good investment.
Trees save money through reduced energy costs. Cities create what is referred to as a heat island. The concrete, asphalt,
buildings, and other surfaces absorb and hold heat from the sun. During hot summer days, cities can be five to nine
degrees warmer than surrounding areas. Shading, evapotranspiration, and wind speed reduction provided by trees help
conserve energy in buildings. A study conducted in Minneapolis, Minnesota, showed that trees placed in the proper
location can reduce total heating and cooling costs by eight percent.
Homeowners not only reduce costs of heating and cooling their homes, but increase the value of their property by
planting trees. Research suggests that property value can increase three to seven percent when trees are present. Trees
also make homes and neighborhoods more desirable places to live. One economic benefit that urban trees can provide,
but often don’t, is one based on products. Municipalities and tree services across the country have come up with ways
to use the wood that is cut from an urban forest. Products range from specialty furniture, to musical instruments, to
lumber for park shelters, to artwork. The income from selling products from the wood of trees being removed could be used to defray the cost associated with the removal, making trees an even better investment.
Trees and Climate Change
The information about how trees impact climate change is taken from the National Arbor Day website
http://www.arborday.org/globalwarming/treesHelp.cfm, and the American Forest Foundation website
www.americanforests.org/resources/climatechange/
Deciduous trees, planted on the west, east and south sides, will keep your house cool in the summer and let the sun
warm your home in the winter, reducing energy use.
Just three trees, properly placed around a house, can save up to 30% of energy use.
Trees or shrubs planted to shade air conditioners help cool a building more efficiently, using less electricity. A unit
operating in the shade uses as much as 10% less electricity than the same one operating in the sun.
Neighborhoods with well-shaded streets can be up to 6–10° F cooler than neighborhoods without street trees, reducing
the heat-island effect, and reducing energy needs.
Shaded parking lots keep automobiles cooler, reducing emissions from fuel tanks and engines, and helping reduce the
heat-island effect in communities.
Trees absorb carbon dioxide (CO2), the primary gas causing global climate change. Trees retain the carbon (C) from the
CO2 molecule and release oxygen (O2) into the atmosphere. The retained carbon makes up half the dry weight of a tree.
Forests are the world's second largest carbon reservoirs (oceans are the largest). Unlike oceans, however, we can grow
new forests. One acre of forestland will sequester between 150 - 200 tons of CO2 in its first 40 years.
Mom Was Right: Go Outside
- May 25, 2012, 11:26 a.m. ET
- By JONAH LEHRER
Humans are quickly becoming an indoor species.
In part, this is a byproduct of urbanization, as most people now live in big cities. Our increasing reliance on technology is also driving the trend, with a recent study concluding that American children between the ages of 8 and 18 currently spend more than four hours a day interacting with technology.
As a result, there's no longer time for nature: From 2006 to 2010, the percentage of young children regularly engaging in outdoor recreation fell by roughly 15 percentage points.
This shift is occurring even as scientists outline the mental benefits of spending time in natural settings. According to the latest research, untamed landscapes have a restorative effect, calming our frazzled nerves and refreshing the tired cortex. After a brief exposure to the outdoors, people are more creative, happier and better able to focus. If there were a pill that delivered these same results, we'd all be popping it.
Consider a forthcoming paper by psychologist Ruth Ann Atchley and her colleagues at the University of Kansas. To collect their data, the researchers partnered with the nonprofit Outward Bound, which takes people on extended expeditions into nature. To measure the mental benefits of hiking in the middle of nowhere, Dr. Atchley gave 60 backpackers a standard test of creativity before they hit the trail. She gave the same test to a different group of hikers four days into their journey.
The results were surprising: The hikers in the midst of nature showed a nearly 50% increase in performance on the test of creativity, and the effect held across all age groups.
"There's a growing advantage over time to being in nature," says Dr. Atchley. "We think that it peaks after about three days of really getting away, turning off the cellphone. It's when you have an extended period of time surrounded by that softly fascinating environment that you start seeing all kinds of positive effects in how your mind works."
This latest study builds on a growing body of evidence demonstrating the cognitive benefits of nature. Although many of us find the outdoors alienating and uncomfortable—the bugs, the bigger critters, the lack of climate control—the brain reacts to natural settings by, essentially, sighing in relief.
In 2009, a team of psychologists led by Marc Berman at the University of Michigan outfitted undergraduates with GPS receivers. Some of the students took a stroll in an arboretum, while others walked around the busy streets of downtown Ann Arbor.
The subjects were then run through a battery of psychological tests. People who had walked through the natural setting were in a better mood and scored significantly higher on tests of attention and short-term memory, which involved repeating a series of numbers backward. In fact, just glancing at a photograph of nature led to measurable improvements, at least when compared with pictures of cities.
This also helps to explain an effect on children with attention-deficit disorder. Several studies show that, when surrounded by trees and animals, these children are less likely to have behavioral problems and are better able to focus on a particular task.
Scientists have found that even a relatively paltry patch of nature can confer cognitive benefits. In the late 1990s, Frances Kuo, director of the Landscape and Human Health Laboratory at the University of Illinois, began interviewing female residents in the Robert Taylor Homes, a massive housing project on the South Side of Chicago.
Dr. Kuo and her colleagues compared women who were randomly assigned to various apartments. Some had a view of nothing but concrete sprawl, the blacktop of parking lots and basketball courts. Others looked out on grassy courtyards filled with trees and flower beds. Dr. Kuo then measured the two groups on a variety of tasks, from basic tests of attention to surveys that looked at how the women were handling major life challenges. She found that living in an apartment with a view of greenery led to significant improvements in every category.
Cities are here to stay; so are smartphones. What this research suggests, however, is that we need to make time to escape from everyone else, to explore those parts of the world that weren't designed for us. It's when we are lost in the wild that the mind is finally at home.
Gray wolf factsheet
- Legal status in U.S.: Federally delisted since January 27, 2012. Currently a "Protected Wild Animal" in Wisconsin.
- 2011 Numbers in Wisconsin: ~800
- Length: 5.0-5.5 feet long (including 15-19 inch tail)
- Height: 2.5 feet high
- Weight: 50-100 pounds/average for adult males is 75 pounds, average for adult females is 60 pounds.
Description
Gray wolves, also referred to as timber wolves, are the largest wild members of the dog family. Males are usually bigger than females. Wolves have many color variations but tend to be buff-colored tans grizzled with gray and black (although they can also be black or white). In winter, their fur becomes darker on the neck, shoulders and rump. Their ears are rounded and relatively short, and the muzzle is large and blocky. Wolves generally hold their tail straight out from the body or down. The tail is black tipped and longer than 18 inches.
Wolves can be distinguished by tracks and various physical features. A wolf, along other wild canids, usually places its hind foot in the track left by the front foot, whereas a dog's front and hind foot tracks usually do not overlap each other. See the wolf identification page for more details.
Thumbnails link to larger images.
Habits
A wolf pack's territory may cover 20-120 square miles, about one tenth the size of an average Wisconsin county. Thus, wolves require a lot of space in which to live, a fact that often invites conflict with humans.
While neighboring wolf packs might share a common border, their territories seldom overlap by more than a mile. A wolf that trespasses in another pack's territory risks being killed by that pack. It knows where its territory ends and another begins by smelling scent messages - urine and feces - left by other wolves. In addition, wolves announce their territory by howling. Howling also helps identify and reunite individuals that are scattered over their large territory.
How does a non-breeding wolf attain dominant, or breeding status? It can stay with its natal pack, bide its time and work its way up the dominance hierarchy. Or it can disperse, leaving the pack to find a mate and a vacant area in which to start its own pack. Both strategies involve risk. A bider may be out-competed by another wolf and never achieve dominance. Dispersers usually leave the pack in autumn or winter, during hunting and trapping season.
Dispersers must be alert to entering other wolf packs' territories, and they must keep a constant vigil to avoid encounters with people, their major enemy. Dispersers have been known to travel great distances in a short time. One radio-collared Wisconsin wolf traveled 23 miles in one day. In ten months, one Minnesota wolf traveled 550 miles to Saskatchewan, Canada. A female wolf pup trapped in the eastern part of the Upper Peninsula of Michigan, died from a vehicle collision near Johnson Creek in Jefferson County, Wisconsin in March 2001, about 300 miles from her home territory.
Nobody knows why some wolves disperse and others don't. Even siblings behave differently, as in the case of Carol and Big Al, radio-collared yearling sisters in one Wisconsin pack. Carol left the pack one December, returned in February, then dispersed 40 miles away. Big Al remained with the pack and probably became the pack's dominant female when her mother was illegally shot.
In another case, two siblings dispersed from their pack, but did so at different times and in different directions. One left in September and moved 45 miles east and the other went 85 miles west in November.
Food
Timber wolves are carnivores feeding on other animals. A study in the early 1980s showed that the diet of Wisconsin wolves was comprised of 55 percent white-tailed deer, 16 percent beavers, 10 percent snowshoe hares and 19 percent mice, squirrels, muskrats and other small mammals. Deer comprise over 80 percent of the diet much of the year, but beaver become important in spring and fall. Beavers spend a lot of time on shore in the fall and spring, cutting trees for their food supply. Since beavers are easy to catch on land, wolves eat more of them in the fall and spring than during the rest of the year. In the winter, when beavers are in their lodges or moving safely beneath the ice, wolves rely on deer and hares. Wolves' summer diet is more diverse, including a greater variety of small mammals.
Breeding biology
Wolves are sexually mature when two years old, but seldom breed until they are older. In each pack, the dominant male and female are usually the only ones to breed. They prevent subordinate adults from mating by physically harassing them. Thus, a pack generally produces only one litter each year, averaging five to six pups.
In Wisconsin, wolves breed in late winter (late January and February). The female delivers the pups two months later in the back chamber of a den that she digs. The den's entrance tunnel is 6-12 feet long and 15-25 inches in diameter. Sometimes the female selects a hollow log, cave or abandoned beaver lodge instead of making a den.
At birth, wolf pups are deaf and blind, have dark fuzzy fur and weigh about 1 pound. They grow rapidly during the first three months, gaining about 3 pounds each week. Pups begin to see when two weeks old and can hear after three weeks. At this time, they become very active and playful.
When about six weeks old, the pups are weaned and the adults begin to bring them meat. Adults eat the meat at a kill site often miles away from the pups, then return and regurgitate the food for the pups to eat. The hungry pups jump and nip at the adults' muzzles to stimulate regurgitation.
The pack abandons the den when the pups are six to eight weeks old. The female carries the pups in her mouth to the first of a series of rendezvous sites or nursery areas. These sites are the focus of the pack's social activities for the summer months and are usually near water.
By August, the pups wander up to two to three miles from the rendezvous sites and use them less often. The pack abandons the sites in September or October and the pups, now almost full-grown, follow the adults.
Photos of wolf pups at a den site
Thumbnails link to larger images.
Distribution
Before Europeans settled North America, gray wolves inhabited areas from the southern swamps to the northern tundra, from coast to coast. They existed wherever there was an adequate food supply. However, people overharvested wolf prey species (e.g., elk, bison and deer), transformed wolf habitat into farms and towns and persistently killed wolves. As the continent was settled, wolves declined in numbers and became more restricted in range. Today, the majority of wolves in North America live in remote regions of Canada and Alaska. In the lower 48 states, wolves exist in forests and mountainous regions in Minnesota, Michigan, Wisconsin, Montana, Idaho, Wyoming, Washington, Arizona, New Mexico, North Dakota, and possibly in Oregon, Utah and South Dakota.
Map showing wolf distribution
History in Wisconsin
Before Wisconsin was settled in the 1830s, wolves lived throughout the state. Nobody knows how many wolves there were, but best estimates would be 3,000-5,000 animals. Explorers, trappers and settlers transformed Wisconsin's native habitat into farmland, hunted elk and bison to extirpation, and reduced deer populations. As their prey species declined, wolves began to feed on easy-to-capture livestock. As might be expected, this was unpopular among farmers. In response to pressure from farmers, the Wisconsin Legislature passed a state bounty in 1865, offering $5 for every wolf killed. By 1900, no timber wolves existed in the southern two-thirds of the state.
At that time, sport hunting of deer was becoming an economic boost to Wisconsin. To help preserve the dwindling deer population for this purpose, the state supported the elimination of predators like wolves. The wolf bounty was increased to $20 for adults and $10 for pups. The state bounty on wolves persisted until 1957. By the time bounties were lifted, millions of taxpayers' dollars had been spent to kill Wisconsin's wolves, and few wolves were left. By 1960, wolves were declared extirpated from Wisconsin. Ironically, studies have shown that wolves have minimal negative impact on deer populations, since they feed primarily on weak, sick, or disabled individuals.
The story was similar throughout the United States. By 1960, few wolves remained in the lower 48 states (only 350-500 in Minnesota and about 20 on Isle Royale in Michigan). In 1974, however, the value of timber wolves was recognized on the federal level and they were given protection under the Endangered Species Act [exit DNR]. With protection, the Minnesota wolf population in-creased and several individuals dispersed into northern Wisconsin in the mid-1970s. In 1975, the Wisconsin Department of Natural Resources declared timber wolves endangered.
Intense monitoring of wolves in Wisconsin by the DNR began in 1979. Attempts were made to capture, attach radio collars and radio-track wolves from most packs in the state. Additional surveys were done by snow-tracking wolf packs in the winter and by howl surveys in the summer. In 1980, 25 wolves in 5 packs occurred in the state, but dropped to 14 in 1985 when parvovirus reduced pup survival and killed adults. Wisconsin DNR completed a wolf recovery plan in 1989. The recovery plan set a state goal for reclassifying wolves as threatened once the population remained at or above 80 for three years. Recovery efforts were based on education, legal protection, habitat protection, and providing compensation for problem wolves.
In the 1990s the wolf population grew rapidly, despite an outbreak of mange between 1992 -1995. The DNR completed a new management plan in 1999. This management plan set a delisting goal of 250 wolves in late winter outside of Indian reservations, and a management goal of 350 wolves outside of Indian reservations. In 1999, wolves were reclassified to state threatened status with 205 wolves in the state. In 2004 wolves were removed from the state threatened species list and were reclassified as a protected wild animal with 373 wolves in the state.
Current status (as of April 2012)
The wolf is a "Protected Wild Animal" in Wisconsin. After five years of delisting attempts and subsequent court challenges, a new federal delisting process began on May 5, 2011 and wolves were officially delisted on January 27, 2012. The count in winter 2011 was about 782-824 wolves with 202-203 packs, 19-plus loners, and 31 wolves on Indian reservations in the state.
Misconceptions and controversies
Wolves are the "bad guys" of fable, myth and folklore. The "big bad wolf" fears portrayed in "Little Red Riding Hood," "Peter and the Wolf" and other tales have their roots in the experiences and stories of medieval Europe. Wolves were portrayed as vile, demented, immoral beasts. These powerful negative attitudes and misconceptions about wolves have persisted through time, perpetuated by stories, films and word-of-mouth, even when few Americans will ever have the opportunity to encounter a wolf.
Wolves are controversial because they are large predators. Farmers are concerned about wolves preying on their livestock. In northern Wisconsin, about 50-60 cases of wolf depredation occur per year, about half are on livestock and half on dogs. As the population continues to increase, slight increases in depredation are likely to occur. In Minnesota, with about 3,000 wolves, there are usually 60 to 100 cases per year.
A few hunters continue to illegally kill wolves, believing that such actions will help the deer herd. It is important to place in perspective the impact of wolves preying on deer. Each wolf kills about 20 deer per year. Multiply this by the number of wolves found in Wisconsin in recent years (800), and approximately 16,000 deer may be consumed by wolves annually. This compares to about 27,000 deer hit by cars each year, and about 340,000 deer shot annually by hunters statewide. Within the northern and central forests where most wolves live, wolves kill similar numbers of deer as are killed by vehicles (about 8,000), and about 1/10 of those killed by hunters (8,000 in 2010). Wolves are a factor in the deer herd, but only one of many factors that affects the total number of deer on the landscape.
Research and management
The Wisconsin DNR has been studying wolves since 1979 by live capturing, attaching radio collars and monitoring movements. Much has been learned about wolf ecology in northern Wisconsin. In 1992, the department began a research project to determine the impact of highway development in northwest Wisconsin on wolves. A Geographic Information System, (computer mapping system) was used to determine that northern Wisconsin has about 6,000 square miles of habitat that could support 300-500 wolves. Recent studies suggest the state can perhaps support 700 to 1,000 wolves (in late winter), but this level may not be socially tolerated and recent federal delisting of wolves will allow the department to manage the wolf population toward sustainable but acceptable population levels.
The DNR recognizes wolves as native wildlife species that are of value to natural ecosystems and benefit biological diversity of Wisconsin. The department approved a Wolf Recovery Plan in 1989. The plan's goal of 80 wolves was first achieved in 1995 mainly through protection and public education programs, and did not require any active reintroductions into the state. In 1999, wolves were reclassified to threatened in Wisconsin, and a new wolf management plan was approved that set a state delisting goal at 250 and management goal at 350 wolves in late winter outside of Indian reservations. The wolf management goal represents a threshold level that allows the Department to use a full range of lethal controls, including public harvest, to manage the wolf population. Wolves were state delisted in 2004 and federally in 2012, returning management back to the state and Indian tribes. Landowners will be able to control some problem wolves on their land and government trappers will remove problem wolves from depredation sites.
The 2016 Centennial of the National Park Service is fast approaching and provides the national parks community with an opportunity to draw attention to the needs and opportunities of the park system and inspire the American public to become engaged on behalf of our nearly 400 national park units and park programs ranging from Yosemite National Park to the Rivers, Trails, and Conservation Assistance Program.
Live Long and take care of your Health.... Make good choices
Saturday, September 29, 2012 12 p.m. - 3 p.m.
(Please note: You must arrive between 12 p.m. - 1 p.m.)
Forest Preserve District of Cook County Bemis Woods Picnic Grove #7 * 11500 Ogden Avenue Western Springs, IL 60558
*To get to Grove # 7 follow the preserve road north to the most northern grove off of Ogden. Number 7 is where the parking lot loops around and where the hiking trails begin.
//illinois.hometownlocator.com/maps/distance-directions2.cfm?bemis%20woods%This email address is being protected from spambots. You need JavaScript enabled to view it.,-87.9097828" style="color: rgb(0, 89, 0);">Driving directions and park information
Please Note: Registration fees cannot be transferred and are non-refundable.
Event Updates
AT BASE CAMP
Northern Illinois Raptor Rehab
- Learn about the rehabilitation of injured, sick and orphaned birds of prey during this live wildlife display. You’re sure to create lasting memories as you and your children interact with these amazing creatures!
Midewin National Tallgrass Prairie
- At Base camp, you will have the opportunity to build “nature sculptures” with the Midewin National Tallgrass Prairie of the US Forest Service. During this activity, kids will utilize local, natural materials that surround them to create artistic “habitats”.
Cook County Forest Preserve
- This year, the Cook County Forest Preserve will be joined by their very own snake and turtle for an up-close and personal encounter.
Promotional Partner, REI
- REI will have a presentation on PEAK, a hands-on, interactive program where children are taught to have fun outside while practicing responsible outdoor recreation. Children will also learn the 7 Leave No Trace principles: know before you go; choose the right path; pack your trash; leave what you find; be careful with fire; respect wildlife; and be kind to other visitors. REI will also be handing out some cool goodies as well.
ON THE TRAIL
Plant Station
Insect Station
Bird Station
Reptiles Station
Mammals Station
Wisconsin Summer Campsare the perfect place to expose kids to camp. Picking. a Wisconsin summer camp offers a child the chance to be away from daily civilization. No place in the midwest will give a child an amazing experience in the country. At Camp Nature Swift child gets to play, make new friends and learn new outdoor activities, this takes place in the fun sun of the northwoods of Wisconsin.
A Wonderful Summer Camp. (Summary)
The children have such a diverse selection of activities at this Wisconsin summer camp that they can barely fit it all in during their stay! From horseback riding and swimming to archery and craft making the time is action packed with fun filled adventure that your child won’t stop talking about.
Swift Camp is dedicated to the spirit of Naturalist Ernie Swift. The camps goal is to provide a traditional summer camp while encouraging children to respect nature and to understand it in a more profound way, This ACA accredited camp has been helping children have a great summer for over 40 years.
The Discovery Program is a unique camp program only for the first time camper. This special session is unlike any other sleepaway camp because it is designed to give additional attention to those children a little reluctant to leave home for their first overnight summer camp experience. Regardless if your child is a first time campers or is experienced at overnight backpacking and canoeing trips your child can attend this camp.
To learn more about picking the best summer camp for your child visit SummerCampAdvice.com
Recently I read this very complicated study and found the results not all the surprising...We all do better in nature.
Introduction
Attention Restoration Theory (ART) [5] suggests that nature has specific restorative effects on the prefrontal cortex-mediated executive attentional system, which can become depleted with overuse. High levels of engagement with technology and multitasking place demands on executive attention to switch amongst tasks, maintain task goals, and inhibit irrelevant actions or cognitions. ART suggests that interactions with nature are particularly effective in replenishing depleted attentional resources. Our modern society is filled with sudden events (sirens, horns, ringing phones, alarms, television, etc.) that hijack attention. By contrast, natural environments are associated with a gentle, soft fascination, allowing the executive attentional system to replenish. In fact, early studies have found that interacting with nature (e.g., a wilderness hike) led to improvements in proof reading [6], control of Necker Cube pattern reversals [7],[8], and performance on the backwards digit span task [9]. Laboratory-based studies have also reported that viewing slides of nature improved sustained attention [10] and the suppression of distracting information [9]. However, the impact of more sustained exposure to natural environments on higher-level cognitive function such as creative problem solving has not been explored.
To empirically test the intriguing hypotheses that complex cognition is facilitated by prolonged exposure to natural settings and the parallel release from technology immersion, the current research utilized a simple and ecologically valid paradigm of measuring higher order cognitive production in a pre-post design looking at the cognitive facilitative effects of immersion in nature. To the best of our knowledge, this is the first attempt to examine changes in higher-order cognitive production after sustained exposure to nature, while participants are still in the natural environment. The higher order cognitive task used was the Remote Associates Test (RAT) developed by Mednick [11], [12], which has been widely used as a measure of creative thinking and insight problem-solving. Utilizing insight, problem solving, and convergent creative reasoning to effectively connect the cues provided through a mediated relationship (for example: SAME/TENNIS/HEAD = MATCH) is thought to draw on the same pre-frontal cortical structures that are hypothesized to be overtaxed by the constant demands on our selective attention and threat detection systems from our modern, technology-intensive environment.
Methods
The pre-hike participant sample was composed of twenty-four participants (11 Female, average age = 34) and the in-hike group was made up of 32 participants (15 Female, average age = 24). Because age has an effect on the task, age was run as a covariate in subsequent analyses. The pre-hike group completed the RAT measure on the morning before they began their backpacking trip. The in-hike group completed the RAT measure in the morning of the fourth day or their trip. All participants were given an unlimited amount of time to complete 10 Remote Associate Items [13] and the primary dependent variable was the number of correct items provided out of 10 possible. All RAT tasks were completed independently and both analysis of the responses provided and Outward Bound councilors indicated that no collaboration happened between participants.
Results
Discussion
There are multiple candidates for potential mechanisms underlying the effects observed here and in other studies. It is likely that the cognitive benefits of nature are due to a range of these mechanisms and it will require a sustained program of research to fully understand this phenomenon. One suggestion is that natural environments, like the environment that we evolved in, are associated with exposure to stimuli that elicit a kind of gentle, soft fascination, and are both emotionally positive and low-arousing [9]. It is also worth noting that with exposure to nature in decline, there is a reciprocal increase in the adoption of, use, and dependency upon technology [14]. Thus, the effects observed here could represent either removal of the costs associated with over-connection or a benefit associated with a return to a more positive/low-arousing restorative environment.
Exposure to nature may also engage what has been termed the “default mode” networks of the brain, which an emerging literature suggests may be important for peak psychosocial health [15]. The default mode network is a set of brain areas that are active during restful introspection and that have been implicated in efficient performance on tasks requiring frontal lobe function such as the divergent thinking task used here [16]. On a hike or during exposure to natural stimuli which produce soft-fascination, the mind may be more able to enter a state of introspection and mind wandering which can engage the default mode. Interestingly, engaging the default mode has been shown to be disrupted by multimedia use, which requires an external attentional focus, again pointing to the possibility that natural environments such as those experienced by the current participants may have both removed a cost (technology) and added a benefit (activation of brain systems that aid divergent thinking).
This study is the first to document systematic changes in higher-level cognitive function associated with immersion in nature. There is clearly much more research to be done in this area, but the current work shows that effects are measurable, even in completely disconnected natural environments, laying the groundwork for further studies. Much about our cognitive and social experience has changed in our current technology-rich society and it is challenging to fully assess the health costs associated with these changes. Nevertheless, the current research establishes that there are cognitive costs associated with constant exposure to a technology-rich, suburban or urban environment, as contrasted with exposure to the natural environment that we experience when we are immersed in nature. When our research participants spent four days in a natural setting, absent all the tools of technology, the surrounding natural setting allowed them to bring a wide range of cognitive resources to bear when asked to engage in a task that requires creativity and complex convergent problem solving.
A limitation to the current research is the inability to determine if the effects are due to an increased exposure to nature, to a decreased exposure to technology, or to other factors associated with spending three days immersed in nature. In the majority of real-world multi-day hiking experiences, the exposure to nature and technology are inversely related and we cannot determine if one factor has more influence than another. From a scientific perspective, it may prove theoretically important to understand the unique influences of nature and technology on creative problem solving; however, from a pragmatic perspective these two factors are often so strongly interrelated that they may be considered to be different sides of the same coin. We suggest that attempts to meaningfully dissociate the highly correlated real-world effects of nature and technology may be like asking Gestalt psychologists whether figure or ground is more important in perceptual grouping.
In principle, a 2×2 factorial study with high or low levels of nature (N+ or N−, respectively) and high or low levels of technology (T+ or T−, respectively) could shed light on the issue of dissociating the effects of nature and technology on complex problem solving. In the majority of real-world urban environments, T+N− is the norm whereas T−N+ is more common in the outdoor settings. Our research demonstrates that interacting for three days in T−N+ environments (i.e., the in-hike group) results in significant improvements in creative problem solving compared to T+N− environments (i.e., the pre-hike group). The T+N+ condition reflects an interesting situation where the interloper brings technology with them on the hike (assuming there is service and power) and, based on ART, we predict that interacting in this sort of environment would not benefit creative problem solving. The T−N− condition reflects a different scenario in which people interact in urban settings without the use of technology – a condition that is becoming increasingly rare in the modern world. Based upon ART, which places an emphasis on natural environments for maximal restoration, we predict that T−N+ condition would result in superior creative problem solving compared to T−N−condition (assuming that we could convince people to part with their digital technology for three full days). Future research will be required to evaluate these latter predictions.