Armillaria root disease-caused tree mortality following silvicultural treatments (shelterwood or group selection) in an Oregon mixed-conifer forest: insights from a 10-year case study.
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引用次数: 12
Abstract
however, can vary by Armillaria clone, site and soil characteristics, disturbance history, and plant association (McDonald et al.1987, Curran et al. 2007). Single genets (clones) of A. ostoyae (“the humongous fungus”) have been estimated to be 2,400 ac in size and 2,200 years old in northeast Oregon (Schmitt and Tatum 2008), and wildfires may have little effect in reducing populations of subterranean root pathogens such as A. ostoyae (Ferguson et al. 2003, Fields 2003). A name change to Armillaria solidipes has been recently proposed for A. ostoyae (Burdsall and Volk 2008). Besides tree mortality, Armillaria infections may cause crown dieback, resinous-root lesions, treegrowth reductions, lower-stem deformations, stand-structural changes, and down-wood accumulations (Bloomberg and Morrison 1989, Reaves et al. 1993, Cruickshank et al. 1997, 2009, Mallett and Volney 1999, Cruickshank 2002, Fields 2003, Omdal et al. 2004). The association between tree wounding and Armillaria infection is not well known. Severe wounding of roots or stems could exacerbate existing root infections and possibly result in tree mortality. Armillaria root disease has been associated with stressed trees resulting from soil disturbance, high stand densities, drought, or other pest attack (Wargo and Shaw 1985, Hadfield et al. 1986, Williams et al. 1986, Shaw and Kile 1991). In severely infected forests in the Pacific Northwest, tree mortality caused by A. ostoyae has been estimated at 25 ft/ac per year on 1,500 ac in south-central Washington (Shaw et al. 1976), 50 ft/ac per year on 575 ac in south-central Oregon (Filip 1977), and 30 ft/ac per year on 2,500 ac in central Oregon (Filip and Goheen 1982). Dead root systems may be completely colonized by Armillaria 1 to 5 years after tree death or harvesting, depending on Armillaria genet, tree species, size of the root system, number of infected-root lesions, and extent of root colonization by insects or other fungi. Because Armillaria can persist for millennia on infected mixedconifer sites and therefore eradication is futile, we tested the hypothesis that silvicultural treatments can reduce growth loss and mortality caused by Armillaria and reestablish Armillaria-tolerant tree species. The study was conducted in an uneven-aged mixed-conifer forest (but predominantly true fir). The objectives of our study were to determine whether significant differences occur between treated and untreated areas in the amount of 10-year leave-tree dbh-growth loss and mortality with shelterwood harvesting or group-selection harvesting, and to evaluate the frequency of mortality among six A. ostoyae“tolerant” species that were regenerated in the shelterwood and group-selection stands: ponderosa pine, lodgepole pine (Pinus contorta), sugar pine (Pinus lambertiana), coastal Douglas-fir, western larch, and incense-cedar.
然而,可能因蜜环菌无性系、地点和土壤特征、干扰历史和植物关联而异(McDonald et al.1987, Curran et al. 2007)。据估计,单基因(克隆)的A. ostoyae(“巨大的真菌”)在俄勒冈州东北部的规模为2,400 ac,已有2,200年的历史(Schmitt和Tatum 2008),野火可能对减少A. ostoyae等地下根系病原体的种群影响不大(Ferguson et al. 2003, Fields 2003)。最近有人提议将A. ostoyae的名称改为蜜环菌固化菌(Burdsall and Volk 2008)。除了树木死亡外,蜜环菌感染还可能导致树冠枯死、树脂根病变、树木生长减少、下部茎变形、林分结构变化和木材积聚(Bloomberg and Morrison 1989, Reaves et al. 1993, Cruickshank et al. 1997, 2009, Mallett and Volney 1999, Cruickshank 2002, Fields 2003, Omdal et al. 2004)。树木损伤与蜜环菌感染之间的关系尚不清楚。根或茎的严重损伤会加剧现有的根感染,并可能导致树木死亡。蜜环菌根病与土壤扰动、林分密度高、干旱或其他虫害侵袭造成的胁迫树木有关(Wargo和Shaw 1985, Hadfield等人1986,Williams等人1986,Shaw和Kile 1991)。在太平洋西北地区严重感染的森林中,据估计,在华盛顿州中南部1500ac的树木死亡率为25英尺/平方米/年(Shaw et al. 1976),在俄勒冈州中南部575ac的树木死亡率为50英尺/平方米/年(Filip 1977),在俄勒冈州中部2500 ac的树木死亡率为30英尺/平方米/年(Filip and Goheen 1982)。在树木死亡或收获后1至5年,死亡的根系可能完全被蜜环菌定殖,这取决于蜜环菌属、树种、根系大小、受感染的根系病变数量以及昆虫或其他真菌在根系定殖的程度。由于蜜环菌可以在受感染的混合针叶树上存活数千年,因此根除是徒劳的,我们测试了造林处理可以减少由蜜环菌引起的生长损失和死亡率,并重建耐蜜环菌的树种的假设。该研究是在一个年龄不均匀的混合针叶林(但主要是真冷杉)进行的。本研究的目的是确定阔叶林采伐和群选采伐在阔叶树10年生长量和死亡率方面是否存在显著差异,并评估在阔叶林和群选林分再生的6种“耐受”树种的死亡率。黄松、黑松、糖松、沿海道格拉斯冷杉、西部落叶松和香雪松。