Longevity Record for a Wild Allegheny Woodrat (Neotama magister) in West Virginia

M. T. Mengak, S. Castleberry, W. Ford, Nikki L. Castleberry, Jane L. Rodrigue
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She was caught a total of 24 times in the same outcrop from 1997 through 2002. A conservative estimate of her age on 25 January 2002 was 1,734 days or 57.8 months. This extends the record longevity for a wild Allegheny woodrat by 70 days or 2.3 months. Regardless, her known time alive (from first capture to last) of 1,630 days still surpasses previous estimates of longevity for the Allegheny woodrat INTRODUCTION The Allegheny woodrat (Neotoma magister) is found throughout much of the central and southern Appalachians and adjacent portions of the Interior Highlands. It is widespread but uncommon in Virginia and West Virginia (Mengak, 1998). It is a habitat specialist closely associated with rock outcrops, cliffs, talus slopes, boulder fields and cave entrances. Allegheny woodrats are tolerant of a wide range of macrohabitats but select specific habitats based on microhabitat features (Castleberry et al., 2002b). The Allegheny woodrats' natural history and role in the local food web and in forest dynamics is unclear. Fungi and mast (hard and soft) are major components of the woodrats diet (Castleberry et al., 2002a) but it is not known what role wo.odrats play, if any, in the distribution of mycorrhizal fungi and forest regeneration. In this ecoregion, the rough and inaccessible areas inhabited by woodrats generally have not been subject to direct, large-scale disturbances from human activities such as logging, agriculture, or second-home development. The long-term effect of disturbances to Corresponding Author: (Phone) 706-583-8096, (E-mail) mmengak@smokey.forestry.uga.edu 168 VIRGINIA JOURNAL OF SCIENCE adjacent habitats on woodrat populations is unclear even as regional land use activities such as forest management and mining continue to increase in intensity. Natural history information on woodrats is needed to assess population status and recommend actions to ensure the long-term survival of this species. Allegheny woodrats have declined in the northern portions of their range and are state-listed as threatened, endangered or sensitive species of concern in every state where they occur (Beans, 1992; Laerm et al. , 2000; Castleberry et al., 2002a). Nonetheless, they still appear to be abundant in appropriate habitat ·in the central Appalachians of Kentucky, Virginia and West Virginia. Reasons for decline are unclear and are the subject of debate but likely include severe weather (Nawrot and Klimstra, 1976), increased avian and meso-mammal predation (Balcom and Yahner, 1996), reduced hard mast production brought about by the elimination of the American chestnut (Castanea dentata) and gypsy moth (Lymantria dispar) infestation in oak (Quercus spp.) forests (Hall , 1985), vegetation change from white-tailed deer (Odocoileus virginianus) herb ivory (Hassinger et al., 1996), raccoon roundworm (Baylis ascaris procyonis) parasitism (McGowan and Hicks, 1996) and habitat fragmentation (Balcom and Y ahner, 1996). Until recently, biologists have had to rely on biological data collected from the closely related eastern woodrat (N. jl.oridana) because of limited research on the Allegheny woodrat. However, numerous recent reports have addressed the ecology and natural history of the Allegheny woodrat including studies on landscape characteristics (Balcom and Yahner, 1996), population genetics (Castleberry et al., in review), effects of timber management ( Castleberry et al., 2001 ), summer microhabitat selection (Castleberry et al., 2002b), food habits (Castleberry et al., 2002a), ectoparasites (Castleberry et al. in review), reproduction and juvenile growth (Mengak, 2002), and longevity (Mengak, 1997; 2000). With this note, we extend the record for longevity in a wild Allegheny woodrat and comment on reproductive strategy. Previous records for longevity by a wild Allegheny woodrat were 1,468 days and 1,502 days (Mengak, 1997). An additional record for longevity was reported as 1,664 days (Mengak, 2000). Prior to the work by Mengak (1997; 2000) reported lifespans for Allegheny woodrats were up to 48 months in captivity (Poole, 1940). Other reports for the genus include 991 days for wild eastern woodrats (Fitch and Rainey, 1956), 67 months for captive desert woodrats (N. lepida; Landstrom, 1971) and 60 months for captive white-throated woodrats (N. albigula; Landstrom, 1971 ). A juvenile woodrat (#607) was first caught on 8 August 1997 on Mead-Westvaco Corporation's Wildlife and Ecosystem Research Forest (WERF) in Randolph County, West Virginia (38° 42'N, 80°3 'W). The WERF is a 3360 ha area reserved for the study of industrial forestry impacts on ecosystems and ecological processes in an Appalachian setting (Ford and Rodrigue, 2001 ). The WERF has been described in detail in previous reports (Castleberry et al., 2001; Castleberry et al. , 2002a; Castleberry et al., 2002b). Mengak (1997; 2000) described the capture and marking methods. She was caught in a large rock outcrop in the Rocky Run drainage at an elevation of 920 m. The 2.5-3 ha site's vegetation primarily was a small sawtimber-sized northern hardwood forest with an abundant rhododendron (Rhododendron maximum) and greenbrier (Smilax spp.) shrub layer. Her weight at initial capture was 150 g. She was caught a total of 24 times in the same outcrop from 1997 through 2002. At her most recent capture on 25 January 2002, she weighed 285 g. Assuming a birth weight of 17 g (Mengak 1997; 2000) and an average weight gain of 1.26 g/d (Mengak, 2002), her estimated birth date was 25 April 1997. Therefore, a conservative estimate of her age on 25 January 2002 was 1,734 days or 57 .8 months. This extends the record longevity LONGE'1 for a wild Allegheny woodrat b) alive (from first capture to las( longevity (Mengak 1997; 2000). Because we were conducti1 individual woodrat has contribut1 She was radio-tagged for three m study (Castleberry et al., 2001). a study of population genetic st were collected from her month! habits (Castleberry et al., 2002a: occasions (Castleberry et al., in 1999 and thus is presumed to ha The Allegheny woodrat is Appalachians. Information on r controversial (Mengak, 2002). long-term trends in capture data; rate (Mengak, 2002) and long pc is functioning more like a K-sele< be attributed to most small mam1 strategies designed to protect i Allegheny woodrats . 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引用次数: 5

Abstract

The Allegheny woodrat (Neotoma magister) is found throughout much of the central and southern Appalachians and adjacent portions of the Interior Highlands. Allegheny woodrats have declined in the northern portions of their range and are state-listed as threatened, endangered or sensitive species of concern in every state where they occur. Until recently, biologists have had to rely on biological data collected from the closely related eastern woodrat (N.jloridana) because oflimited research on the Allegheny woodrat. We have been studying the ecology and natural history ofwoodrats in Virginia and West Virginia since 1990. On 8 August 1997 we caught and ear-tagged a juvenile female woodrat. She was caught a total of 24 times in the same outcrop from 1997 through 2002. A conservative estimate of her age on 25 January 2002 was 1,734 days or 57.8 months. This extends the record longevity for a wild Allegheny woodrat by 70 days or 2.3 months. Regardless, her known time alive (from first capture to last) of 1,630 days still surpasses previous estimates of longevity for the Allegheny woodrat INTRODUCTION The Allegheny woodrat (Neotoma magister) is found throughout much of the central and southern Appalachians and adjacent portions of the Interior Highlands. It is widespread but uncommon in Virginia and West Virginia (Mengak, 1998). It is a habitat specialist closely associated with rock outcrops, cliffs, talus slopes, boulder fields and cave entrances. Allegheny woodrats are tolerant of a wide range of macrohabitats but select specific habitats based on microhabitat features (Castleberry et al., 2002b). The Allegheny woodrats' natural history and role in the local food web and in forest dynamics is unclear. Fungi and mast (hard and soft) are major components of the woodrats diet (Castleberry et al., 2002a) but it is not known what role wo.odrats play, if any, in the distribution of mycorrhizal fungi and forest regeneration. In this ecoregion, the rough and inaccessible areas inhabited by woodrats generally have not been subject to direct, large-scale disturbances from human activities such as logging, agriculture, or second-home development. The long-term effect of disturbances to Corresponding Author: (Phone) 706-583-8096, (E-mail) mmengak@smokey.forestry.uga.edu 168 VIRGINIA JOURNAL OF SCIENCE adjacent habitats on woodrat populations is unclear even as regional land use activities such as forest management and mining continue to increase in intensity. Natural history information on woodrats is needed to assess population status and recommend actions to ensure the long-term survival of this species. Allegheny woodrats have declined in the northern portions of their range and are state-listed as threatened, endangered or sensitive species of concern in every state where they occur (Beans, 1992; Laerm et al. , 2000; Castleberry et al., 2002a). Nonetheless, they still appear to be abundant in appropriate habitat ·in the central Appalachians of Kentucky, Virginia and West Virginia. Reasons for decline are unclear and are the subject of debate but likely include severe weather (Nawrot and Klimstra, 1976), increased avian and meso-mammal predation (Balcom and Yahner, 1996), reduced hard mast production brought about by the elimination of the American chestnut (Castanea dentata) and gypsy moth (Lymantria dispar) infestation in oak (Quercus spp.) forests (Hall , 1985), vegetation change from white-tailed deer (Odocoileus virginianus) herb ivory (Hassinger et al., 1996), raccoon roundworm (Baylis ascaris procyonis) parasitism (McGowan and Hicks, 1996) and habitat fragmentation (Balcom and Y ahner, 1996). Until recently, biologists have had to rely on biological data collected from the closely related eastern woodrat (N. jl.oridana) because of limited research on the Allegheny woodrat. However, numerous recent reports have addressed the ecology and natural history of the Allegheny woodrat including studies on landscape characteristics (Balcom and Yahner, 1996), population genetics (Castleberry et al., in review), effects of timber management ( Castleberry et al., 2001 ), summer microhabitat selection (Castleberry et al., 2002b), food habits (Castleberry et al., 2002a), ectoparasites (Castleberry et al. in review), reproduction and juvenile growth (Mengak, 2002), and longevity (Mengak, 1997; 2000). With this note, we extend the record for longevity in a wild Allegheny woodrat and comment on reproductive strategy. Previous records for longevity by a wild Allegheny woodrat were 1,468 days and 1,502 days (Mengak, 1997). An additional record for longevity was reported as 1,664 days (Mengak, 2000). Prior to the work by Mengak (1997; 2000) reported lifespans for Allegheny woodrats were up to 48 months in captivity (Poole, 1940). Other reports for the genus include 991 days for wild eastern woodrats (Fitch and Rainey, 1956), 67 months for captive desert woodrats (N. lepida; Landstrom, 1971) and 60 months for captive white-throated woodrats (N. albigula; Landstrom, 1971 ). A juvenile woodrat (#607) was first caught on 8 August 1997 on Mead-Westvaco Corporation's Wildlife and Ecosystem Research Forest (WERF) in Randolph County, West Virginia (38° 42'N, 80°3 'W). The WERF is a 3360 ha area reserved for the study of industrial forestry impacts on ecosystems and ecological processes in an Appalachian setting (Ford and Rodrigue, 2001 ). The WERF has been described in detail in previous reports (Castleberry et al., 2001; Castleberry et al. , 2002a; Castleberry et al., 2002b). Mengak (1997; 2000) described the capture and marking methods. She was caught in a large rock outcrop in the Rocky Run drainage at an elevation of 920 m. The 2.5-3 ha site's vegetation primarily was a small sawtimber-sized northern hardwood forest with an abundant rhododendron (Rhododendron maximum) and greenbrier (Smilax spp.) shrub layer. Her weight at initial capture was 150 g. She was caught a total of 24 times in the same outcrop from 1997 through 2002. At her most recent capture on 25 January 2002, she weighed 285 g. Assuming a birth weight of 17 g (Mengak 1997; 2000) and an average weight gain of 1.26 g/d (Mengak, 2002), her estimated birth date was 25 April 1997. Therefore, a conservative estimate of her age on 25 January 2002 was 1,734 days or 57 .8 months. This extends the record longevity LONGE'1 for a wild Allegheny woodrat b) alive (from first capture to las( longevity (Mengak 1997; 2000). Because we were conducti1 individual woodrat has contribut1 She was radio-tagged for three m study (Castleberry et al., 2001). a study of population genetic st were collected from her month! habits (Castleberry et al., 2002a: occasions (Castleberry et al., in 1999 and thus is presumed to ha The Allegheny woodrat is Appalachians. Information on r controversial (Mengak, 2002). long-term trends in capture data; rate (Mengak, 2002) and long pc is functioning more like a K-sele< be attributed to most small mam1 strategies designed to protect i Allegheny woodrats . We sugges rat population demographics w critical for formulating future m;
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西弗吉尼亚州一只野生阿勒格尼伍德拉特(新州州长)的长寿记录
阿勒格尼木鼠(Neotoma magister)遍布阿巴拉契亚山脉中部和南部的大部分地区以及内陆高地的邻近地区。阿勒格尼森林鼠在其活动范围的北部地区已经减少,在它们生长的每个州都被列为受威胁、濒危或敏感物种。直到最近,由于对阿勒格尼木鼠的研究有限,生物学家不得不依靠从密切相关的东部木鼠(N.jloridana)收集的生物数据。自1990年以来,我们一直在研究弗吉尼亚州和西弗吉尼亚州的木鼠生态和自然历史。1997年8月8日,我们捕获了一只年轻的雌性木鼠,并给它贴上了耳标。从1997年到2002年,她在同一露头共被捕获了24次。保守估计她在2002年1月25日的年龄为1734天或57.8个月。这使得野生阿勒格尼木鼠的寿命延长了70天,也就是2.3个月。无论如何,她已知的存活时间(从第一次捕获到最后一次捕获)为1630天,仍然超过了之前对阿勒格尼木鼠寿命的估计。阿勒格尼木鼠(Neotoma magister)分布在阿巴拉契亚山脉中部和南部以及内陆高地邻近地区的大部分地区。它在弗吉尼亚州和西弗吉尼亚州很普遍,但并不常见(Mengak, 1998)。它是一个与岩石露头、悬崖、talus斜坡、巨石场和洞穴入口密切相关的栖息地专家。阿勒格尼木鼠对各种大生境都有耐受性,但会根据微生境特征选择特定的生境(Castleberry et al., 2002b)。阿勒格尼森林鼠的自然历史和在当地食物网和森林动态中的作用尚不清楚。真菌和桅杆(硬的和软的)是木鼠饮食的主要成分(Castleberry et al., 2002a),但它们的作用尚不清楚。如果有的话,蛇在菌根真菌的分布和森林再生中起着作用。在这一生态区域中,木鼠居住的粗糙和难以到达的地区通常不会受到人类活动(如伐木、农业或第二家园开发)的直接、大规模干扰。干扰对通讯作者:(电话)706-583-8096,(电子邮件)mmengak@smokey.forestry.uga.edu 168弗吉尼亚科学杂志邻近栖息地对木鼠种群的长期影响尚不清楚,即使区域土地利用活动(如森林管理和采矿)的强度继续增加。需要关于木鼠的自然历史信息来评估种群状况,并建议采取行动以确保该物种的长期生存。阿勒格尼木鼠在其活动范围的北部地区已经减少,在它们出现的每个州都被列为受威胁、濒危或敏感物种(Beans, 1992;Laerm et al., 2000;Castleberry et al., 2002a)。尽管如此,在肯塔基州、弗吉尼亚州和西弗吉尼亚州的阿巴拉契亚中部的适当栖息地,它们似乎仍然大量存在。下降的原因尚不清楚,是争论的主题,但可能包括恶劣的天气(Nawrot和Klimstra, 1976),鸟类和中哺乳动物捕食增加(Balcom和Yahner, 1996),消除美洲板栗(Castanea dentata)和毒蛾(Lymantria dispar)在栎林(Quercus spp.)中的侵害所带来的硬杆产量减少(Hall, 1985),白尾鹿(Odocoileus virginianus)草本象牙的植被变化(Hassinger等,1996),浣熊蛔虫(Baylis ascaris procyonis)寄生(McGowan and Hicks, 1996)和栖息地破碎化(Balcom and Y ahner, 1996)。直到最近,由于对阿勒格尼木鼠的研究有限,生物学家不得不依靠从密切相关的东部木鼠(N. jl.oridana)收集的生物学数据。然而,最近的许多报告都涉及了阿勒格尼木鼠的生态和自然历史,包括景观特征(Balcom和Yahner, 1996)、种群遗传学(Castleberry等人,回顾)、木材管理的影响(Castleberry等人,2001)、夏季微生境选择(Castleberry等人,2002b)、饮食习惯(Castleberry等人,2002a)、外寄生(Castleberry等人,2002)、繁殖和幼树生长(Mengak, 2002)、和长寿(Mengak, 1997;2000)。通过这篇笔记,我们延长了野生阿勒格尼木鼠的寿命记录,并对繁殖策略进行了评论。此前,野生阿勒格尼森林鼠的寿命纪录分别为1468天和1502天(Mengak, 1997)。另一项长寿记录是1664天(Mengak, 2000)。在Mengak (1997;2000年)报道,圈养的阿勒格尼木鼠的寿命可达48个月(Poole, 1940)。其他关于该属的报道包括野生东部木鼠991天(Fitch and Rainey, 1956),圈养沙漠木鼠67个月(N。
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