Black-tailed deer | |
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Male Black-tailed Deer (Olympic National Park) | |
Scientific classification | |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Mammalia |
Order: | Artiodactyla |
Suborder: | Ruminantia |
Family: | Cervidae |
Subfamily: | Capreolinae |
Genus: | Odocoileus |
Species: | O. hemionus |
Subspecies: | O. h. columbianus |
Trinomial name | |
Odocoileus hemionus columbianus (Richardson, 1829) |
Two forms of black-tailed deer or blacktail deer occupying coastal temperate rainforest on North America's Pacific coast are subspecies of the mule deer. They have sometimes been treated as a species, but virtually all recent authorities maintain they are subspecies.[1][2][3][4][5][6][7] The Columbian black-tailed deer (Odocoileus hemionus columbianus) is found in western North America, from Northern California into the Pacific Northwest and coastal British Columbia.[8] The Sitka black-tailed deer (Odocoileus hemionus sitkensis) is found coastally in British Columbia, Southeast Alaska and Southcentral Alaska (as far as Kodiak Island).[9][8][10][11]
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Black-tailed deer once lived at least as far east as Wyoming. In Francis Parkman's The Oregon Trail, an eyewitness account of his 1846 trek across the early West, while within a two-days ride from Fort Laramie, Parkman writes of shooting what he believes to be an elk, only to discover that he has killed a Black-tailed Deer.[12]
The Black-tailed deer is currently common in northern California, western Oregon, Washington, in coastal and interior British Columbia, and north into the Alaskan panhandle. It is a popular game animal.
Though it has been argued that the black-tailed deer is a species, virtually all recent authorities maintain it as a subspecies of the mule deer (Odocoileus hemionus).[1][2][3][4][5][6][7] Strictly speaking the black-tailed deer group consists of two subspecies, as it also includes O. h. sitkensis (Sitka black-tailed deer).[2] The black-tailed deer group and the mule deer group (sensu stricto) hybridize, and it appears the mule deer evolved from the black-tailed deer.[6] Despite this, the mtDNA of the white-tailed deer and mule deer is similar, but differs from that of the black-tailed deer.[6] This may be the result of introgression, although hybrids between the mule deer and white-tailed deer are rare in the wild (apparently more common locally in west Texas), and the hybrid survival rate is low even in captivity.[4][6]
This species thrives on the edge of the forest, as the dark forest lacks the underbrush and grasslands that the deer prefers as food, and completely open areas lack the hiding spots and the cover it prefers for harsh weather. One of the plants that black-tailed deer browse is western poison oak, despite its allergen content.[13] This deer often is most active at dawn and dusk, and is frequently involved in collisions with automobiles.
Deer are browsers. During the winter and early spring they feed on Douglas fir, western red cedar, red huckleberry, salal, deer fern, and lichens that grow on trees. Late spring to fall they munch on grasses, blackberries, fireweed, pearly everlasting, forbs, salmonberry, salal, and maple. The mating or 'rutting' season occurs during November and early December. Bucks can be observed running back and forth across the roads in the pursuit of does. After the rut the bucks tend to hide and rest. Often they are nursing wounds. They suffer broken antlers, and have lost weight. They drop their antlers between January and March. As the antlers lie on the forest floor they provide a source of calcium and other nutrients to other forest inhabitants. Bucks regrow their antlers beginning in April through to August.
The gestation period for does is six to seven months with fawns being born late May and into June. Twins are the rule although young does often have only one. Triplets can also occur. Fawns weigh 2.7 to 4 kg and have no scent for the first week or so. This enables the mother to leave the fawn hidden while she goes off to browse and replenish her body after giving birth. She must also eat enough to produce enough milk to feed her babies. Although does are excellent mothers, fawn mortality rate is 45 to 70 percent. Does are very protective of their young and humans are viewed as predators. Stay well away from a doe with young.
Deer communicate with the aid of scent and pheromones that come from several glands located on the lower legs. The metatarsal (outside of lower leg) produces an alarm scent, the tarsal (inside of hock) serves for mutual recognition and the interdigital (between the toes) leave a scent trail when deer travel. Deer have excellent sight and smell. Their large ears can move independently of each other and pick up any unusual sounds that may signal danger.
Dawn, dusk and moonlit nights are when we see deer browsing on the roadside. Wooded areas where there are forests on both sides of the road, open grassy areas i.e. golf course attract deer. Caution when driving is prudent because often as one deer crosses another one or two follow.
In Southeast Alaska, the Sitka black-tailed deer is the primary prey of Alexander Archipelago wolf (Canis lupus ligoni), which is endemic to the region and rare.[14] In the mid-1990s the United States Fish & Wildlife Service evaluated a petition to list this wolf species as threatened, and decided in August 1997 that a listing was not warranted, largely on the basis of provisions the Forest Service had included to protect the viability of the wolf species in its Forest Plan for the Tongass National Forest, adopted three months earlier.[15] The Tongass NF is important in wolf conservation because it includes about 80% of the region's land area. The protections for the wolf included a standard and guideline intended to retain, in the face of losses logging, enough habitat carrying capacity for deer in winter to assure the viability of the Alexander Archipelago wolf and an adequate supply of deer for hunters. The need carrying capacity was originally specified as 13 deer per square mile, but was corrected in 2000 to 18. Use of a deer model is specified for determining carrying capacity, and is the only tool available for the purpose.[16][17]
However, the Forest Service's implementation of the deer provision in the Tongass wolf standard and guideline has been controversial for many years, and led to a lawsuit by Greenpeace and Cascadia Wildlands in 2008, over four logging projects.[18] Issues raised included these two. It was alleged that the dataset the Forest Service was using in the deer model was known through the agency's own study, done in 2000, to generally overestimate the carrying capacity for deer.[19] The study showed that the data set, called Vol-Strata, is uncorrelated to habitat quality, which generally causes the carrying capacity for deer to be overestimated and logging impacts to be underestimated,[20][21] Also, a conversion factor, known as the "deer multiplier" (used in calculating carrying capacity) was incorrectly applied, causing — by itself – a 30% overestimation of carrying capacity and corresponding underestimation of impacts.[19] The combined effect of the two errors is variable because Vol-Strata is uncorrelated to habitat quality. It is, for the Traitors Cove Timber Sales project the plaintiffs said in 2011 oral arguments before the 9th Circuit Court of Appeals, the difference between a claimed 21 deer per square mile in the project EIS, and 9.5 deer per square mile (about half of the Forest Plan's requirement) according to unpublished corrections made by the agency in 2008.[22]
A ruling was issued in favor of plaintiffs on August 2, 2011 by the 9th Circuit, remanding the four timber sale decisions and giving guidance for what is necessary during renanalysis of impacts to deer.[23] The ruling says in part:
In a statement to the press, a spokesman for the plaintiffs said that the errors in this lawsuit apply to every significant Tongass timber sale decision between 1996 and 2008, before the Forest Service corrected errors in the deer model when the agency issued its revised Tongass Forest Plan in 2008. But he said that despite those corrections the agency still fails to address cumulative impacts to deer, especially on Prince of Wales Island, as is being challenged in the Logjam timber sale lawsuit, by ignoring substantial logging on non-federal lands.[24]
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