维吉尼亚东部松林管理下小型哺乳动物群落的退化

J. D. Dolan, R. K. Rose
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However, after mechanical thinning of late-age stands, small mammals of forested habitats and of early successional habitats were found together. The numbers of trapped small mammals decreased progressively throughout the study. We speculate that weather events might have contributed to this pattern but the reasons are unknown. INTRODUCTION Small mammals of forests often show preferences for habitats differing in age and structure (Linzey and Linzey 1973, Kirkland and Griffin 1974, Dueser and Shugart 1978). Thus, the abundance and species of small mammals inhabiting recent clearcuts often differ greatly from those found in maturing forests. Furthermore, secondary succession sometimes is governed by attributes of the initial disturbance (Boring et al. 1981 ). For example, timber management practices such as site preparation and the use of herbicides, pesticides, fertilizers, and selective cutting can directly affect the composition of the plant community, and in tum indirectly affect small mammal communities. Much research has evaluated changes in small mammal communities in relation Present address: USATC, 1407 Washington Blvd, Fort Eustis, Virginia 23604, James.d.dolan@us.army.mil. Corresponding author: Dr. Robert K. Rose, Department of Biological Sciences, Old Dominion University, Norfolk, Virginia 23529-0266, Email : brose@odu.edu Virginia Journal of Science, Vol. 58, No. 3, 2007 http://di it commons.odu.edu/vjs/vol58/iss3 148 VIRGINIA JOURNAL OF SCIENCE to vegetation changes in hardwood forest systems in eastern North America (e.g. , Kirkland 1977, McComb and Rumsey 1982, Martell 1983, Buckner and Shure 1985). However, fewer studies have been conducted on small mammals in pine plantations in the Southeast. Atkeson and Johnson (1979) and Mengak et al. (1989) studied small mammals in pine plantations in the piedmont regions of Georgia and South Carolina, respectively, and Mitchell et al. (1995) studied small mammals in pine plantations on cleared pocosins in coastal North Carolina. In contrast, our study examined small mammal communities in managed loblolly pine plantations on upland sites in the coastal plain of Virginia, a region in which commercial stands of such pines often locally comprise a majority of the forested landscapes. To learn details of changes in the small mammal community in relation to age of pine stand, we chose pine plantations of ages 1, 8, 18, and 24 years. In eastern Virginia, most loblolly pine (Pinus taeda L.) plantations are harvested at ca. 30 years of age. Our objectives were to determine the relative abundance, biomass, and species diversity of small mammal communities in relation to the age of managed pine plantations, to examine seasonal changes in the small mammal communities of these stands, and to document the presence or disappearance of small mammal species with age of pine stand. MATERIALS AND METHODS Study sites, selected from holdings of The Union Camp Corporation, were located in Isle of Wight County, in the Southeastern Coastal Plain Region of Virginia. Pine trees had been planted at densities of 1042-1482 stems/ha using mechanical planters after stumps and debris had been pushed into windrows. We chose four age classes of pine plantations on sites in relatively close proximity (1-16 km apart) to minimize the effects of variation in local weather conditions. We had no control over the herbicide, pesticide, or thinning treatments applied to some forest stands; we sought replicate sites that were as similar as possible. We had three replicates of the 1and 24-year-old stands, and two replicates of the 8and 18-year-old stands. We trapped during five seasonal periods: (1) 12 June 26 July 1995, (2) 20 October3 December 1995, (3) 19 January3 March 1996, (4) 3 April17 May 1996, (5) 9 July 22 August ,1996. The interval between seasons was at least 30 days. Small Mammal Trapping Effective surveys of small mammals require two methods of trapping, one of them being removal trapping (e.g., Getz 1961; Wiener and Smith 1972). Because pine forests support low-density populations of most small mammal species (Mengak et al. 1989, Mitchell et al. 199 5) and removal trapping can locally reduce population density, we chose to use four 0.25 ha grids separated from one another by at least 50 m rather than one large hectare grid at each site. This design produces twice as much edge as one large grid, enabling small mammals living on the margins to enter the 0.25 ha grids after pitfall trapping had reduced abundances within the grids, potentially allowing populations to recover quickly. The 50 m X 50 m (0.25 ha) grids were established at each site, each with 25 trap stations 12.5 m apart. A minimum buffer zone of 50 m separated grids from both the edge of a site and from one another. One Fitch live trap (Rose 1994) and one# 10 can '","PeriodicalId":23516,"journal":{"name":"Virginia journal of science","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Depauperate Small Mammal Communities in Managed Pine Plantations in Eastern Virginia\",\"authors\":\"J. D. Dolan, R. K. 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However, after mechanical thinning of late-age stands, small mammals of forested habitats and of early successional habitats were found together. The numbers of trapped small mammals decreased progressively throughout the study. We speculate that weather events might have contributed to this pattern but the reasons are unknown. INTRODUCTION Small mammals of forests often show preferences for habitats differing in age and structure (Linzey and Linzey 1973, Kirkland and Griffin 1974, Dueser and Shugart 1978). Thus, the abundance and species of small mammals inhabiting recent clearcuts often differ greatly from those found in maturing forests. Furthermore, secondary succession sometimes is governed by attributes of the initial disturbance (Boring et al. 1981 ). For example, timber management practices such as site preparation and the use of herbicides, pesticides, fertilizers, and selective cutting can directly affect the composition of the plant community, and in tum indirectly affect small mammal communities. Much research has evaluated changes in small mammal communities in relation Present address: USATC, 1407 Washington Blvd, Fort Eustis, Virginia 23604, James.d.dolan@us.army.mil. Corresponding author: Dr. Robert K. Rose, Department of Biological Sciences, Old Dominion University, Norfolk, Virginia 23529-0266, Email : brose@odu.edu Virginia Journal of Science, Vol. 58, No. 3, 2007 http://di it commons.odu.edu/vjs/vol58/iss3 148 VIRGINIA JOURNAL OF SCIENCE to vegetation changes in hardwood forest systems in eastern North America (e.g. , Kirkland 1977, McComb and Rumsey 1982, Martell 1983, Buckner and Shure 1985). However, fewer studies have been conducted on small mammals in pine plantations in the Southeast. Atkeson and Johnson (1979) and Mengak et al. (1989) studied small mammals in pine plantations in the piedmont regions of Georgia and South Carolina, respectively, and Mitchell et al. (1995) studied small mammals in pine plantations on cleared pocosins in coastal North Carolina. In contrast, our study examined small mammal communities in managed loblolly pine plantations on upland sites in the coastal plain of Virginia, a region in which commercial stands of such pines often locally comprise a majority of the forested landscapes. To learn details of changes in the small mammal community in relation to age of pine stand, we chose pine plantations of ages 1, 8, 18, and 24 years. In eastern Virginia, most loblolly pine (Pinus taeda L.) plantations are harvested at ca. 30 years of age. 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引用次数: 2

摘要

以4个不同林龄的火炬松人工林为研究对象,探讨了植被群落变化与小型哺乳动物群落的关系。采用两种诱捕方法对5个季节的小型兽类进行了评估。活捕器捕获的种类占捕获总数的65%,9种中有7种,而陷阱捕获的种类为8种,其中2种不是用活捕器捕获的。对于这两种捕集器,每100个捕集器夜平均捕获率不到2个,即使在松林中也很低。小兽类的丰度和生物量随林龄的增加而下降,而物种多样性随林龄的增加而增加。冠合后各营养类群的相对比例由以花岗动物和杂食动物为主转变为以食虫动物为主。然而,经过后期林分的机械间伐后,森林生境和早期演替生境的小型哺乳动物同时出现。在整个研究过程中,被困小型哺乳动物的数量逐渐减少。我们推测天气事件可能促成了这种模式,但原因尚不清楚。森林中的小型哺乳动物往往表现出对不同年龄和结构的栖息地的偏好(Linzey and Linzey 1973, Kirkland and Griffin 1974, Dueser and Shugart 1978)。因此,居住在最近砍伐地区的小型哺乳动物的数量和种类往往与在成熟森林中发现的大不相同。此外,次生演替有时是由初始扰动的属性控制的(Boring et al. 1981)。例如,木材管理实践,如场地准备和使用除草剂、杀虫剂、肥料和选择性砍伐,可以直接影响植物群落的组成,反过来间接影响小型哺乳动物群落。许多研究已经评估了与之相关的小型哺乳动物群落的变化。现在的地址:USATC, 1407 Washington Blvd, Fort Eustis, Virginia 23604, James.d.dolan@us.army.mil。通讯作者:Robert K. Rose博士,Old Dominion University生物科学系,Norfolk, Virginia 23529-0266, Email: brose@odu.edu Virginia Journal of Science, Vol. 58, No. 3, 2007 http://di it commons.odu.edu/vjs/vol58/iss3 148 Virginia Journal of Science对北美东部阔叶林系统植被变化的研究(例如,Kirkland 1977, McComb and Rumsey 1982, Martell 1983, Buckner and Shure 1985)。然而,对东南部松林中的小型哺乳动物进行的研究较少。Atkeson and Johnson(1979)和Mengak et al.(1989)分别研究了佐治亚州和南卡罗来纳州山前地区松树林中的小型哺乳动物,Mitchell et al.(1995)研究了北卡罗来纳州沿海砍伐后的松林林中的小型哺乳动物。相比之下,我们的研究调查了弗吉尼亚沿海平原高地上有管理的火炬松人工林中的小型哺乳动物群落,在该地区,这种松树的商业林分通常占当地森林景观的大部分。为了了解小型哺乳动物群落与林龄的关系,我们选择了林龄为1、8、18和24年的松林。在弗吉尼亚州东部,大多数火炬松(Pinus taeda L.)种植园在大约30岁时收获。我们的目标是确定小型哺乳动物群落的相对丰度、生物量和物种多样性与管理松林林龄的关系,研究这些林分的小型哺乳动物群落的季节变化,并记录小型哺乳动物物种的存在或消失与松林林龄的关系。材料和方法研究地点选自联合营公司,位于弗吉尼亚州东南沿海平原地区的怀特岛县。在树桩和碎片被推入窗户后,使用机械播种机以1042-1482根/公顷的密度种植松树。我们在相对较近的地点(相距1-16公里)选择了四个年龄等级的松树种植园,以尽量减少当地天气条件变化的影响。我们无法控制对某些林分使用的除草剂、杀虫剂或间伐处理;我们寻找尽可能相似的复制站点。1岁和24岁林分有3个重复,8岁和18岁林分有2个重复。我们在五个季节期间捕获:(1)1995年6月12日7月26日,(2)1995年10月20日12月3日,(3)1996年1月19日3月3日,(4)1996年4月3日5月17日,(5)1996年7月9日8月22日。季节之间的间隔至少为30天。小型哺乳动物的有效调查需要两种诱捕方法,其中一种是清除诱捕(例如,Getz 1961;Wiener and Smith 1972)。因为松林支持大多数小型哺乳动物物种的低密度种群(Mengak et al. 1989; Mitchell et al. 1989)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Depauperate Small Mammal Communities in Managed Pine Plantations in Eastern Virginia
Loblolly pine (Pinus taeda L.) plantations of four different ages were examined to identify changes in the small mammal community in relation to changes in the vegetational community. Small mammals were evaluated during five seasons using two methods of trapping. Live traps accounted for 65% of captures and seven of nine species, whereas pitfall traps yielded eight species, of which two were not taken with live traps. For both trap types, catch rates averaged less than two per 100 trap-nights, very low even for pine forests. Both abundance and biomass of small mammals declined with increasing stand age, whereas species diversity increased with increasing stand age. The relative proportions of trophic groups changed after crown closure from mostly granivores and omnivores to mostly insectivores. However, after mechanical thinning of late-age stands, small mammals of forested habitats and of early successional habitats were found together. The numbers of trapped small mammals decreased progressively throughout the study. We speculate that weather events might have contributed to this pattern but the reasons are unknown. INTRODUCTION Small mammals of forests often show preferences for habitats differing in age and structure (Linzey and Linzey 1973, Kirkland and Griffin 1974, Dueser and Shugart 1978). Thus, the abundance and species of small mammals inhabiting recent clearcuts often differ greatly from those found in maturing forests. Furthermore, secondary succession sometimes is governed by attributes of the initial disturbance (Boring et al. 1981 ). For example, timber management practices such as site preparation and the use of herbicides, pesticides, fertilizers, and selective cutting can directly affect the composition of the plant community, and in tum indirectly affect small mammal communities. Much research has evaluated changes in small mammal communities in relation Present address: USATC, 1407 Washington Blvd, Fort Eustis, Virginia 23604, James.d.dolan@us.army.mil. Corresponding author: Dr. Robert K. Rose, Department of Biological Sciences, Old Dominion University, Norfolk, Virginia 23529-0266, Email : brose@odu.edu Virginia Journal of Science, Vol. 58, No. 3, 2007 http://di it commons.odu.edu/vjs/vol58/iss3 148 VIRGINIA JOURNAL OF SCIENCE to vegetation changes in hardwood forest systems in eastern North America (e.g. , Kirkland 1977, McComb and Rumsey 1982, Martell 1983, Buckner and Shure 1985). However, fewer studies have been conducted on small mammals in pine plantations in the Southeast. Atkeson and Johnson (1979) and Mengak et al. (1989) studied small mammals in pine plantations in the piedmont regions of Georgia and South Carolina, respectively, and Mitchell et al. (1995) studied small mammals in pine plantations on cleared pocosins in coastal North Carolina. In contrast, our study examined small mammal communities in managed loblolly pine plantations on upland sites in the coastal plain of Virginia, a region in which commercial stands of such pines often locally comprise a majority of the forested landscapes. To learn details of changes in the small mammal community in relation to age of pine stand, we chose pine plantations of ages 1, 8, 18, and 24 years. In eastern Virginia, most loblolly pine (Pinus taeda L.) plantations are harvested at ca. 30 years of age. Our objectives were to determine the relative abundance, biomass, and species diversity of small mammal communities in relation to the age of managed pine plantations, to examine seasonal changes in the small mammal communities of these stands, and to document the presence or disappearance of small mammal species with age of pine stand. MATERIALS AND METHODS Study sites, selected from holdings of The Union Camp Corporation, were located in Isle of Wight County, in the Southeastern Coastal Plain Region of Virginia. Pine trees had been planted at densities of 1042-1482 stems/ha using mechanical planters after stumps and debris had been pushed into windrows. We chose four age classes of pine plantations on sites in relatively close proximity (1-16 km apart) to minimize the effects of variation in local weather conditions. We had no control over the herbicide, pesticide, or thinning treatments applied to some forest stands; we sought replicate sites that were as similar as possible. We had three replicates of the 1and 24-year-old stands, and two replicates of the 8and 18-year-old stands. We trapped during five seasonal periods: (1) 12 June 26 July 1995, (2) 20 October3 December 1995, (3) 19 January3 March 1996, (4) 3 April17 May 1996, (5) 9 July 22 August ,1996. The interval between seasons was at least 30 days. Small Mammal Trapping Effective surveys of small mammals require two methods of trapping, one of them being removal trapping (e.g., Getz 1961; Wiener and Smith 1972). Because pine forests support low-density populations of most small mammal species (Mengak et al. 1989, Mitchell et al. 199 5) and removal trapping can locally reduce population density, we chose to use four 0.25 ha grids separated from one another by at least 50 m rather than one large hectare grid at each site. This design produces twice as much edge as one large grid, enabling small mammals living on the margins to enter the 0.25 ha grids after pitfall trapping had reduced abundances within the grids, potentially allowing populations to recover quickly. The 50 m X 50 m (0.25 ha) grids were established at each site, each with 25 trap stations 12.5 m apart. A minimum buffer zone of 50 m separated grids from both the edge of a site and from one another. One Fitch live trap (Rose 1994) and one# 10 can '
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