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Woodland caribou persistence and extirpation in relic populations on Lake Superior

机译:苏必利尔湖文物种群的林地驯鹿持久性和灭绝

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Extended: The hypothesis was proposed that woodland caribou (Rangifer tarandus caribou) in North America had declined due to wolf predation and over-hunting rather than from a shortage of winter lichens (Bergerud, 1974). In 1974, two study areas were selected for testing: for the lichen hypothesis, we selected the Slate Islands in Lake Superior (36 km2), a closed canopy forest without terrestrial lichens, wolves, bears, or moose; for the predation hypothesis, we selected the nearby Pukaskwa National Park (PNP) where terrestrial lichens, wolves, bears, and moose were present. Both areas were monitored from 1974 to 2003 (30 years). The living and dead caribou on the Slates were estimated by the ‘King census’ strip transect (mean length 108±9.3 km, extremes 22-190, total 3026 km) and the Lincoln Index (mean tagged 45±3.6, extremes 15-78). The mean annual population on the Slate Islands based on the strip transects was 262±22 animals (extremes 104-606), or 7.3/km2 (29 years) and from the Lincoln Index 303±64 (extremes 181-482), or 8.4/km2 (23 years). These are the highest densities in North America and have persisted at least since 1949 (56 years). Mountain maple (Acer spicatum) interacted with caribou density creating a record in its age structure which corroborates persistence at relatively high density from c. 1930. The mean percentage of calves was 14.8±0.34% (20 years) in the fall and 14.1±1.95% (19 years) in late winter. The Slate Islands herd was regulated by the density dependent abundance of summer green foods and fall physical condition rather than density independent arboreal lichen availability and snow depths. Two wolves (1 wolf/150 caribou) crossed to the islands in 1993-94 and reduced two calf cohorts (3 and 4.9 per cent calves) while female adult survival declined from a mean of 82% to 71% and the population declined ≈100 animals. In PNP, caribou/moose/wolf populations were estimated by aerial surveys (in some years assisted by telemetry). The caribou population estimates ranged from 31 in 1979 to 9 in 2003 (Y=1267 - 0.628X, r=-0.783, n=21, P<0.01) and extirpation is forecast in 2018. Animals lived within 3 km of Lake Superior (Bergerud, 1985) with an original density of 0.06/km2, similar to many other woodland herds coexisting with wolves (Bergerud, 1992), and 100 times less than the density found on the Slate Islands. The mean moose population was 0.25±0.016/km2 and the wolf population averaged 8.5±0.65/1000 km2. Late winter calf percentages in PNP averaged 16.2±1.89 (25 years); the population was gradually reduced by winter wolf predation (Bergerud, 1989; 1996). The refuge habitat available is apparently insufficient for persistence in an area where the continuous distribution of woodland caribou is fragmented due to moose exceeding 0.10/km2 and thereby supporting wolf densities ≥6.5/1000 km2. A second experimental study was to introduce Slate Island caribou to areas with and without wolves. A release to Bowman Island, where wolves and moose were present, failed due to predation. Bowman Island is adjacent to St. Ignace Island where caribou had persisted into the late 1940s. A second release in 1989 to the mainland in Lake Superior Provincial Park of 39 animals has persisted (<10 animals) because the animals utilize off-shore islands but numbers are also declining. A third release to Montréal Island in 1984 doubled in numbers (up to 20 animals) until Lake Superior froze in 1994 and wolves reached the island. A fourth release was to Michipicoten Island (188 km2) in 1982 where wolves were absent and few lichens were available. This herd increased at λ= 1.18 (8 to ±200, 160 seen 2001) in 19 years. This was the island envisioned for the crucial test of the lichen/predation hypotheses (Bergerud, 1974: p.769). These studies strongly support the idea that ecosystems without predators are limited bottom–up by food and those with wolves top-down by predation; however the proposed crucial test which has been initiated on M
机译:扩展:提出了一个假设,即北美的林地驯鹿(Rangifer tarandus驯鹿)的减少是由于狼的捕食和过度捕猎,而不是由于冬季地衣的短缺(Bergerud,1974)。 1974年,选择了两个研究区域进行测试:对于地衣假说,我们选择了苏必利尔湖(36公里2)中的石板群岛,这是一个没有陆地地衣,狼,熊或驼鹿的封闭冠层森林。对于捕食假设,我们选择了附近的普卡斯夸国家公园(PNP),那里有陆生地衣,狼,熊和驼鹿。从1974年到2003年(30年)对这两个区域进行了监测。通过“国王普查”地带样带(平均长度108±9.3 km,极限22-190,总计3026 km)和林肯指数(平均标记45±3.6,极限15-78)估计了斯拉特斯上生死的驯鹿。 )。根据带状横断面,板岩群岛的年平均人口为262±22只动物(极端104-606),或7.3 / km2(29岁),林肯指数303±64(极端181-482),或8.4 / km2(23年)。这些是北美最高的密度,至少自1949年(56年)以来一直持续。山枫(Acer spicatum)与驯鹿密度相互作用,在其年龄结构上创造了一个记录,证实了c相对较高密度下的持久性。 1930年。小牛的平均百分比在秋季为14.8±0.34%(20岁),在冬季末为14.1±1.95%(19岁)。板岩群岛的羊群受夏季绿色食品的密度依赖性丰富和秋天的自然状况所调节,而不是由密度无关的树栖地衣的可利用性和降雪深度来调节。在1993-94年,两只狼(1头狼/ 150北美驯鹿)越过了岛屿,减少了两只小牛群(分别是3和4.9%的小牛),而成年女性的平均存活率则从82%下降到71%,人口减少了≈100动物。在PNP中,驯鹿/驼鹿/狼的数量是通过航测(在某些遥测技术的协助下)估算的。北美驯鹿种群的估计范围从1979年的31只到2003年的9只(Y = 1267-0.628X,r = -0.783,n = 21,P <0.01),并预计在2018年灭绝。动物生活在苏必利尔湖3公里以内( Bergerud,1985年)的原始密度为0.06 / km2,与狼共存的许多其他林地畜群相似(Bergerud,1992年),比石板群岛的密度低100倍。平均驼鹿种群数量为0.25±0.016 / km2,而狼种群平均为8.5±0.65 / 1000 km2。 PNP的冬末小牛百分比平均为16.2±1.89(25年);冬季狼的捕食使人口逐渐减少(Bergerud,1989; 1996)。在由于驼鹿超过0.10 / km2从而使狼密度≥6.5/ 1000 km2导致林地驯鹿的连续分布不连续的地区,可用的避难所栖息地显然不足以维持生存。第二项实验研究是将石板岛驯鹿引入有或没有狼的地区。由于捕食,释放到有狼和麋的鲍曼岛(Bowman Island)失败了。鲍曼岛(Bowman Island)与圣伊格纳斯岛(St. Ignace Island)相邻,驯鹿一直持续到1940年代后期。 1989年,在苏必利尔湖省立公园向大陆的第二次放牧持续了39只动物(<10只),因为这些动物利用了离岸岛屿,但数量也在下降。 1984年第三次投放蒙特利尔岛的数量翻了一番(最多20头动物),直到1994年苏必利尔湖冻结,狼才到达该岛。第四版发布于1982年的Michipicoten岛(188平方公里),那里没有狼,几乎没有地衣。该牧群在19年中以λ= 1.18(8到±200,160见2001)增长。这是对地衣/捕食假说的关键检验的设想(Bergerud,1974:p.769)。这些研究强烈支持以下观点:没有捕食者的生态系统受食物限制自下而上,而有捕食者则由捕食者自上而下。但是,已提议的针对M的关键测试

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