亚极地西部和北乌拉尔大斜坡落叶松林和林地的多样性

Q4 Agricultural and Biological Sciences
S. Degteva, Y. Dubrovskiy
{"title":"亚极地西部和北乌拉尔大斜坡落叶松林和林地的多样性","authors":"S. Degteva, Y. Dubrovskiy","doi":"10.31111/vegrus/2021.41.3","DOIUrl":null,"url":null,"abstract":"The study of the diversity of plant species and communities on several mountain ridges of Subpolar and Northern Urals (Fig. 1) in the basins of the rivers Kozhym, Kosyu, Bolshaya Synya, Vangyr, Schugor, and Ilych was carried out in 2007–2018 by researches of the Institute of Biology of Federal Research Centre “Komi Science Centre Ural Branch Russian Academy of Sciences”. Special attention was paid to fir (Abies sibirica) forests as well as larch (Larix sibirica) forests and woodlands due to the luck of data on their diversity. The study following both traditional (Polevaya…, 1964) and modern (Ipatov, Mirin, 2008) approaches of geobotanical and floristic researches is based on 168 original relevés (on sample plots of 400 m2 or within the community limits). The geobotanical data set which contains 184 relevés is stored in the archive (phytocoenarium) of the Institute of Biology (above). The community vertical and horizontal structure as well as the diversity and abundance of vascular plants, bryophytes, and lichens were under study. Ecological-phytocoenotical (dominant) approach was used for classification of larch forests and woodlands in the study area using both the author’s and literature data (Yudin, 1954; Gorchakovskiy, 1966; Nepomilueva, 1974; Martynenko, 1999; Neshataeva, Neshataev, 2005; Rysin, 2010; Kucherov, 2019). Larch forests and woodlands of the study area belong to the Montano-Lariceta subformation of the Lariceta sibiricae formation, which belongs to the Therhodendrosa vegetation subtype of the Aciculilignosa vegetation type (Bykov, 1960). The list of syntaxa for subformation Montano-Lariceta (M.-L.) includes 20 associations, 2 subassociations, 23 variants, and 3 community types from 5 forest types — lichen, green moss, herbaceous, hair cap moss and sphagnum ones. Three associations are transitional between various types of forest (Table 2–6, Fig. 2–10). Forest types of this subformation are allocated in different ordination areas of ecological space according to vectors of soil nitrogen content and light (Table 7, Fig. 11). Larch forests and woodlands of type M.-L. cladinosa occur in dry habitats with poor acidic soils, while phytocenoses of M.-L. polytrichosa and M.-L. sphagnosa are common on wet poor and acidic soils and those of M.-L. hylocomiosa on more fertile soils. In the study area, they do not occupy large areas. The communities of type M.-L. herbosa are common in low elevated mesophyte habitats with more fertile soils. Communities of M.-L. hylocomiosa and M.-L. herbosa types widely occur both in mountain forest and woodland altitudinal belts at the western macroslope of the Subpolar Urals northward N 64°. The use of environmental scales and statistical methods to identify classification units of lower rank did not give well-interpreted results. Analysis of the cenotic significance of species in various forest types of Montano-Lariceta revealed the stable and compact “core” of the most frequent species: trees Betula pubescens, Larix sibirica, Picea obovata, Sorbus sibirica, shrubs Betula nana and Juniperus sibirica; dwarf shrubs Vaccinium myrtillus, V. uliginosum, V. vitis-idaea; herbs Avenella flexuosa, Bistorta major, Calamagrostis purpurea, Carex arctisibirica, Empetrum hermaphroditum, Festuca ovina, Trientalis europaea; mosses Dicranum flexicaule, D. scoparium, Pleurozium schreberi, Polytrichum commune (Table 2, 8, 9). Characteristic species of forest type of M.-L. cladinosa are lichens Cladonia arbuscula, C. stellaris, Flavocetraria nivalis, differential species are herbs Silene acaulis, S. pauciflora, Tephroseris residifolia, and lichens Alectoria nigricans, Asahinea chrysantha, Bryocaulon divergens, Cetraria nigricans. The most abundant are dwarf shrubs Arctous alpina, Empetrum hermaphroditum, Dryas octopetala, Ledum decumbens, Vaccinium uliginosum, and herbs Carex arctisibirica and C. globilaris. The moss-lichen layer is dominated by Cetraria islandica, Cladonia arbuscula, C. rangiferina, C. stellaris, Flavocetraria nivalis, and Stereocaulon paschale; also abundant are lichens Cladonia gracilis and C. uncialis, and mosses Dicranum flexicaule and Pleurozium schreberi. Characteristic species of M.-L. hylocomiosa is Avenella flexuosa, differential species are lichens Cetrariella delisei, C. laevigata, Cladonia subfurcata, Cladonia crispata, and mosses Dicranum polysetum and Polytrichum piliferinum; constant and highly abundant species are Avenella flexuosa, Betula nana, Empetrum hermaphroditum, Vaccinium myrtillus, V. uliginosum, and moss Pleurozium schreberi; species with average constancy — Vaccinium vitis-idaea, lichens Cladonia arbuscula, C. rangiferina, and mosses Dicranum flexicaule, Hylocomium splendens, Polytrichum commune. Sometimes dwarf shrubs Ledum decumbens and Rubus arcticus, and bryophytes Barbilophozia hatcheri, B. lycopodioides, Dicranum polysetum, D. scoparium, and Sphagnum angustifolium dominate or co-dominate (Table 8). The mostly diverse is M.-L. herbosa type of larch forests and woodlands (Table 5, 6, 9). Characteristic species are Anemonastrum biarmiense, Anthoxantum alpinum, Calamagrostis purpurea, Chamaenerion angustifolium, Geranium albiflorum, Milium effusum, Rumex acetosa, Veratrum lobelianum, Viola biflora; differential species are Angelica sylvestris, Phleum alpinum, Poa pratensis, Polemonium acutiflorum, Stellaria bungeana, Tanacetum bipinnatum, Trollius europaeus, Viola palustris; mosses Plagiomnium ellipticum, Rhizomnium pseudopunctatum, Rhodobryum roseum. The most constant and abundant are Bistorta major, Calamagrostis purpurea, Geranium albiflorum, Vaccinium myrtillus; abundant but not too constant — Avenella flexuosa; mosses Dicranum flexicaule, D. scoparium, Pleurozium schreberi. Rarely, herbs Aconitum septentrionale, Athyrium distentifolium, Equisetum pretense, Hieracium hypoglaucum, and bryophytes Barbilophozia hatcheri, B. lycopodioides, Hylocomium splendens, Plagiomnium ellipticum, Polytrichum commune, P. juniperinum, P. strictum, Rhizomnium pseudopunctatum dominate or co-dominate. Constant species with low and average frequency are Chamaenerion angustifolium, Solidago virgaurea, Trientalis europaea, Veratrum lobelianum. The most abundant species in tower layers of M. L. polytrichosa communities are herbs Avenella flexuosa, Carex globilaris, and mosses Polytrichum commune, Pleurozium schreberi, Sphagnum girgensohnii (Table 2). Also common are Bistorta major, Calamagrostis purpurea, Rubus chamaemorus, Vaccinium uliginosum. There are no so far characteristic and differential species in this type, perhaps due to lack of data. Shrubs typical for M.-L. cladinosa and M.-L. hylocomiosa types of larch forests and woodlands are abundant in the communities of M.-L. sphagnosa (Table 2): Empetrum hermaphroditum, Ledum decumbens, Vaccinium uliginosum. Some times Vaccinium myrtillus, and V. vitis-idaea dominants. The most abundant but with average or low cover are herbs Bistorta major and Carex arctisibirica. The most abundant in the moss-lichen layer is Sphagnum capillifolium (characteristic species); rarely, also abundant are Sphagnum fuscum, S. girgensohnii, and S. warnstorfii; constant with average abundance is Pleurozium schreberi; Cladonia stellaris and Polytrichum commune are of average constancy. Species of taiga-forest and tundra-mire eco-coenotical groups are common in the dwarf shrub–herb layer of all types of forests under study (Table 2, 8–10). Significance of mountain tundra species is higher in M.-L. cladinosa and M.-L. hylocomiosa types compare to other types. Species of taiga meadow-forest, valley meadow-forest, valley forest and mountain meadow groups are more abundant in the communities of M.-L. herbosa type. Our research contributed to the current literature data on the species and coenotic diversity of the larch forests and woodlands of the western macroslope of the Subpolar and Northern Urals. Although it is obvious that there is a lack of data both for some associations and forest types, so further researches are necessary to clarify the status of syntaxa and to get information about the characteristic and differential species.","PeriodicalId":37606,"journal":{"name":"Rastitel''nost'' Rossii","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Diversity of larch forests and woodlands of the western macroslope of the Subpolar and Northern Urals\",\"authors\":\"S. Degteva, Y. Dubrovskiy\",\"doi\":\"10.31111/vegrus/2021.41.3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The study of the diversity of plant species and communities on several mountain ridges of Subpolar and Northern Urals (Fig. 1) in the basins of the rivers Kozhym, Kosyu, Bolshaya Synya, Vangyr, Schugor, and Ilych was carried out in 2007–2018 by researches of the Institute of Biology of Federal Research Centre “Komi Science Centre Ural Branch Russian Academy of Sciences”. Special attention was paid to fir (Abies sibirica) forests as well as larch (Larix sibirica) forests and woodlands due to the luck of data on their diversity. The study following both traditional (Polevaya…, 1964) and modern (Ipatov, Mirin, 2008) approaches of geobotanical and floristic researches is based on 168 original relevés (on sample plots of 400 m2 or within the community limits). The geobotanical data set which contains 184 relevés is stored in the archive (phytocoenarium) of the Institute of Biology (above). The community vertical and horizontal structure as well as the diversity and abundance of vascular plants, bryophytes, and lichens were under study. Ecological-phytocoenotical (dominant) approach was used for classification of larch forests and woodlands in the study area using both the author’s and literature data (Yudin, 1954; Gorchakovskiy, 1966; Nepomilueva, 1974; Martynenko, 1999; Neshataeva, Neshataev, 2005; Rysin, 2010; Kucherov, 2019). Larch forests and woodlands of the study area belong to the Montano-Lariceta subformation of the Lariceta sibiricae formation, which belongs to the Therhodendrosa vegetation subtype of the Aciculilignosa vegetation type (Bykov, 1960). The list of syntaxa for subformation Montano-Lariceta (M.-L.) includes 20 associations, 2 subassociations, 23 variants, and 3 community types from 5 forest types — lichen, green moss, herbaceous, hair cap moss and sphagnum ones. Three associations are transitional between various types of forest (Table 2–6, Fig. 2–10). Forest types of this subformation are allocated in different ordination areas of ecological space according to vectors of soil nitrogen content and light (Table 7, Fig. 11). Larch forests and woodlands of type M.-L. cladinosa occur in dry habitats with poor acidic soils, while phytocenoses of M.-L. polytrichosa and M.-L. sphagnosa are common on wet poor and acidic soils and those of M.-L. hylocomiosa on more fertile soils. In the study area, they do not occupy large areas. The communities of type M.-L. herbosa are common in low elevated mesophyte habitats with more fertile soils. Communities of M.-L. hylocomiosa and M.-L. herbosa types widely occur both in mountain forest and woodland altitudinal belts at the western macroslope of the Subpolar Urals northward N 64°. The use of environmental scales and statistical methods to identify classification units of lower rank did not give well-interpreted results. Analysis of the cenotic significance of species in various forest types of Montano-Lariceta revealed the stable and compact “core” of the most frequent species: trees Betula pubescens, Larix sibirica, Picea obovata, Sorbus sibirica, shrubs Betula nana and Juniperus sibirica; dwarf shrubs Vaccinium myrtillus, V. uliginosum, V. vitis-idaea; herbs Avenella flexuosa, Bistorta major, Calamagrostis purpurea, Carex arctisibirica, Empetrum hermaphroditum, Festuca ovina, Trientalis europaea; mosses Dicranum flexicaule, D. scoparium, Pleurozium schreberi, Polytrichum commune (Table 2, 8, 9). Characteristic species of forest type of M.-L. cladinosa are lichens Cladonia arbuscula, C. stellaris, Flavocetraria nivalis, differential species are herbs Silene acaulis, S. pauciflora, Tephroseris residifolia, and lichens Alectoria nigricans, Asahinea chrysantha, Bryocaulon divergens, Cetraria nigricans. The most abundant are dwarf shrubs Arctous alpina, Empetrum hermaphroditum, Dryas octopetala, Ledum decumbens, Vaccinium uliginosum, and herbs Carex arctisibirica and C. globilaris. The moss-lichen layer is dominated by Cetraria islandica, Cladonia arbuscula, C. rangiferina, C. stellaris, Flavocetraria nivalis, and Stereocaulon paschale; also abundant are lichens Cladonia gracilis and C. uncialis, and mosses Dicranum flexicaule and Pleurozium schreberi. Characteristic species of M.-L. hylocomiosa is Avenella flexuosa, differential species are lichens Cetrariella delisei, C. laevigata, Cladonia subfurcata, Cladonia crispata, and mosses Dicranum polysetum and Polytrichum piliferinum; constant and highly abundant species are Avenella flexuosa, Betula nana, Empetrum hermaphroditum, Vaccinium myrtillus, V. uliginosum, and moss Pleurozium schreberi; species with average constancy — Vaccinium vitis-idaea, lichens Cladonia arbuscula, C. rangiferina, and mosses Dicranum flexicaule, Hylocomium splendens, Polytrichum commune. Sometimes dwarf shrubs Ledum decumbens and Rubus arcticus, and bryophytes Barbilophozia hatcheri, B. lycopodioides, Dicranum polysetum, D. scoparium, and Sphagnum angustifolium dominate or co-dominate (Table 8). The mostly diverse is M.-L. herbosa type of larch forests and woodlands (Table 5, 6, 9). Characteristic species are Anemonastrum biarmiense, Anthoxantum alpinum, Calamagrostis purpurea, Chamaenerion angustifolium, Geranium albiflorum, Milium effusum, Rumex acetosa, Veratrum lobelianum, Viola biflora; differential species are Angelica sylvestris, Phleum alpinum, Poa pratensis, Polemonium acutiflorum, Stellaria bungeana, Tanacetum bipinnatum, Trollius europaeus, Viola palustris; mosses Plagiomnium ellipticum, Rhizomnium pseudopunctatum, Rhodobryum roseum. The most constant and abundant are Bistorta major, Calamagrostis purpurea, Geranium albiflorum, Vaccinium myrtillus; abundant but not too constant — Avenella flexuosa; mosses Dicranum flexicaule, D. scoparium, Pleurozium schreberi. Rarely, herbs Aconitum septentrionale, Athyrium distentifolium, Equisetum pretense, Hieracium hypoglaucum, and bryophytes Barbilophozia hatcheri, B. lycopodioides, Hylocomium splendens, Plagiomnium ellipticum, Polytrichum commune, P. juniperinum, P. strictum, Rhizomnium pseudopunctatum dominate or co-dominate. Constant species with low and average frequency are Chamaenerion angustifolium, Solidago virgaurea, Trientalis europaea, Veratrum lobelianum. The most abundant species in tower layers of M. L. polytrichosa communities are herbs Avenella flexuosa, Carex globilaris, and mosses Polytrichum commune, Pleurozium schreberi, Sphagnum girgensohnii (Table 2). Also common are Bistorta major, Calamagrostis purpurea, Rubus chamaemorus, Vaccinium uliginosum. There are no so far characteristic and differential species in this type, perhaps due to lack of data. Shrubs typical for M.-L. cladinosa and M.-L. hylocomiosa types of larch forests and woodlands are abundant in the communities of M.-L. sphagnosa (Table 2): Empetrum hermaphroditum, Ledum decumbens, Vaccinium uliginosum. Some times Vaccinium myrtillus, and V. vitis-idaea dominants. The most abundant but with average or low cover are herbs Bistorta major and Carex arctisibirica. The most abundant in the moss-lichen layer is Sphagnum capillifolium (characteristic species); rarely, also abundant are Sphagnum fuscum, S. girgensohnii, and S. warnstorfii; constant with average abundance is Pleurozium schreberi; Cladonia stellaris and Polytrichum commune are of average constancy. Species of taiga-forest and tundra-mire eco-coenotical groups are common in the dwarf shrub–herb layer of all types of forests under study (Table 2, 8–10). Significance of mountain tundra species is higher in M.-L. cladinosa and M.-L. hylocomiosa types compare to other types. Species of taiga meadow-forest, valley meadow-forest, valley forest and mountain meadow groups are more abundant in the communities of M.-L. herbosa type. Our research contributed to the current literature data on the species and coenotic diversity of the larch forests and woodlands of the western macroslope of the Subpolar and Northern Urals. 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引用次数: 0

摘要

联邦研究中心生物研究所“科米科学中心-俄罗斯科学院乌拉尔分院”于2007-2008年对Kozhym河、Kosyu河、Bolshaya Synya河、Vangyr河、Schugor河和Ilych河流域的亚极地和北乌拉尔山脉(图1)的植物物种和群落多样性进行了研究。由于其多样性数据的运气,人们特别关注冷杉林、落叶松林和林地。这项研究遵循了传统(Polevaya…,1964)和现代(Ipatov,Mirin,2008)的地植物学和区系研究方法,基于168 原始相关(在400平方米的样地上或在社区范围内)。地球植物学数据集包含184个相关信息,存储在生物研究所的档案(植物群落)中(上图)。群落的垂直和水平结构以及维管植物、苔藓植物和地衣的多样性和丰度正在进行研究。利用作者和文献数据,采用生态植物群落(优势)方法对研究区域的落叶松森林和林地进行分类(Yudin,1954;Gorchakovskiy,1966;Nepomileuva,1974;Martynenko,1999;Neshataeva,Neshataev,2005;Rysin,2010;Kucherov,2019)。研究区的落叶松森林和林地属于西伯利亚落叶松组的Montano落叶松亚组,属于Aciculinsa植被类型的Theropendrosa植被亚型(Bykov,1960)。Montano Lariceta(M.-L.)亚组的句法结构列表包括20个组合、2个亚组合、23个变体和3个群落类型,它们来自5种森林类型——地衣、绿苔藓、草本、毛帽苔藓和泥炭藓。三种关联是不同类型森林之间的过渡(表2-6,图2-10)。根据土壤含氮量和光照的载体,该亚组的森林类型被分配在生态空间的不同排序区域(表7,图11)。M.-L.枝状落叶松的落叶松林和林地分布在酸性土壤较差的干燥栖息地,而多毛M.-L.和球形M.-L.在潮湿的贫瘠和酸性土壤上常见,而hylocomiosa在较肥沃的土壤上常见。在研究区域,它们并不占据很大的面积。草本M.-L.群落常见于土壤肥沃的低海拔中生植物栖息地。M.-L.hylocomiosa和M.-L.herbosa类型的群落广泛分布在北纬64°以北的亚极地乌拉尔山脉西部宏观斜坡的山林和林地海拔带。使用环境尺度和统计方法来识别较低级别的分类单元并没有得到很好的解释结果。对Montano Lariceta不同森林类型中物种的群落意义的分析揭示了最常见物种的稳定和紧凑的“核心”:乔木Betula pubescens、Larix sibirica、Picea obovata、Sorbus sibirica,灌木Betula nana和Juniperus sibirica;矮生灌木越橘属(Vaccinium myrtillus)、紫丁香属(V.uliginosum)、葡萄属(V.vitis idaea);草本Avenella flexuosa,Bistorta major,Calamagrostis purpurea,Carex arctisibrica,Empetrum hermachroditum,Festuca ovina,Trientalis europaea;苔藓Dicranum flexicaule、D.scoparium、Pleurozium schreberi、Polytrichum community(表2、8、9)。分枝杆菌森林类型的特征种是地衣Cladonia arbuscula、C.stellaris、Flavocetraria nivalis,差异种是草本Silene acaulis、S.pauciflora、Tephroseris residifolia和地衣Alectoria nigricans、Ashinea chrysantha、Bryocoulon diversions、Cetraria nigricans。最丰富的是矮灌木Arctous alpina、Empetrum hermachroditum、Dryas octopala、Ledum decumbens、Vaccinium uliginosum,以及草本植物Carex arctisibrica和C.globilaris。苔藓地衣层主要为岛状Cetraria islandica、丛枝Cladonia arbuscula、兰枝C.rangiferina、星状C.stellaris、雪花Flavocetraria nivalis和Stereocaulon paschale;同样丰富的还有地衣Cladonia gracilis和C.uncialis,以及苔藓Dicranum flexicaule和Pleurozium schreberi。M.-L.hylocomiosa的特征种是Avenella flexuosa,差异种是地衣Cetrariella delisei、C.laevigata、Cladonia subfurcata、Cladona crispata以及苔藓Dicranum polystum和Polytrichum piliferinum;恒定且高度丰富的物种有弯曲Avenella flexuosa、南桦Betula nana、两性Empetrum hermachroditum、越橘Vaccinium myrtillus、V.uliginosum和苔藓Pleurozium schreberi;具有平均恒常性的物种——越橘属、地衣Cladonia arbuscula、C.rangiferina和苔藓Dicranum flexicaule、Hylocomeum splines、Polytrichum community。有时矮生灌木Ledum decumbens和Rubus arcticus,以及苔藓植物Barbilophozia hatcheri、B.lycopdioides、Dicranum polysitem、D.scoparium和Sphagnum angustifolium占主导地位或共同占主导地位(表8)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diversity of larch forests and woodlands of the western macroslope of the Subpolar and Northern Urals
The study of the diversity of plant species and communities on several mountain ridges of Subpolar and Northern Urals (Fig. 1) in the basins of the rivers Kozhym, Kosyu, Bolshaya Synya, Vangyr, Schugor, and Ilych was carried out in 2007–2018 by researches of the Institute of Biology of Federal Research Centre “Komi Science Centre Ural Branch Russian Academy of Sciences”. Special attention was paid to fir (Abies sibirica) forests as well as larch (Larix sibirica) forests and woodlands due to the luck of data on their diversity. The study following both traditional (Polevaya…, 1964) and modern (Ipatov, Mirin, 2008) approaches of geobotanical and floristic researches is based on 168 original relevés (on sample plots of 400 m2 or within the community limits). The geobotanical data set which contains 184 relevés is stored in the archive (phytocoenarium) of the Institute of Biology (above). The community vertical and horizontal structure as well as the diversity and abundance of vascular plants, bryophytes, and lichens were under study. Ecological-phytocoenotical (dominant) approach was used for classification of larch forests and woodlands in the study area using both the author’s and literature data (Yudin, 1954; Gorchakovskiy, 1966; Nepomilueva, 1974; Martynenko, 1999; Neshataeva, Neshataev, 2005; Rysin, 2010; Kucherov, 2019). Larch forests and woodlands of the study area belong to the Montano-Lariceta subformation of the Lariceta sibiricae formation, which belongs to the Therhodendrosa vegetation subtype of the Aciculilignosa vegetation type (Bykov, 1960). The list of syntaxa for subformation Montano-Lariceta (M.-L.) includes 20 associations, 2 subassociations, 23 variants, and 3 community types from 5 forest types — lichen, green moss, herbaceous, hair cap moss and sphagnum ones. Three associations are transitional between various types of forest (Table 2–6, Fig. 2–10). Forest types of this subformation are allocated in different ordination areas of ecological space according to vectors of soil nitrogen content and light (Table 7, Fig. 11). Larch forests and woodlands of type M.-L. cladinosa occur in dry habitats with poor acidic soils, while phytocenoses of M.-L. polytrichosa and M.-L. sphagnosa are common on wet poor and acidic soils and those of M.-L. hylocomiosa on more fertile soils. In the study area, they do not occupy large areas. The communities of type M.-L. herbosa are common in low elevated mesophyte habitats with more fertile soils. Communities of M.-L. hylocomiosa and M.-L. herbosa types widely occur both in mountain forest and woodland altitudinal belts at the western macroslope of the Subpolar Urals northward N 64°. The use of environmental scales and statistical methods to identify classification units of lower rank did not give well-interpreted results. Analysis of the cenotic significance of species in various forest types of Montano-Lariceta revealed the stable and compact “core” of the most frequent species: trees Betula pubescens, Larix sibirica, Picea obovata, Sorbus sibirica, shrubs Betula nana and Juniperus sibirica; dwarf shrubs Vaccinium myrtillus, V. uliginosum, V. vitis-idaea; herbs Avenella flexuosa, Bistorta major, Calamagrostis purpurea, Carex arctisibirica, Empetrum hermaphroditum, Festuca ovina, Trientalis europaea; mosses Dicranum flexicaule, D. scoparium, Pleurozium schreberi, Polytrichum commune (Table 2, 8, 9). Characteristic species of forest type of M.-L. cladinosa are lichens Cladonia arbuscula, C. stellaris, Flavocetraria nivalis, differential species are herbs Silene acaulis, S. pauciflora, Tephroseris residifolia, and lichens Alectoria nigricans, Asahinea chrysantha, Bryocaulon divergens, Cetraria nigricans. The most abundant are dwarf shrubs Arctous alpina, Empetrum hermaphroditum, Dryas octopetala, Ledum decumbens, Vaccinium uliginosum, and herbs Carex arctisibirica and C. globilaris. The moss-lichen layer is dominated by Cetraria islandica, Cladonia arbuscula, C. rangiferina, C. stellaris, Flavocetraria nivalis, and Stereocaulon paschale; also abundant are lichens Cladonia gracilis and C. uncialis, and mosses Dicranum flexicaule and Pleurozium schreberi. Characteristic species of M.-L. hylocomiosa is Avenella flexuosa, differential species are lichens Cetrariella delisei, C. laevigata, Cladonia subfurcata, Cladonia crispata, and mosses Dicranum polysetum and Polytrichum piliferinum; constant and highly abundant species are Avenella flexuosa, Betula nana, Empetrum hermaphroditum, Vaccinium myrtillus, V. uliginosum, and moss Pleurozium schreberi; species with average constancy — Vaccinium vitis-idaea, lichens Cladonia arbuscula, C. rangiferina, and mosses Dicranum flexicaule, Hylocomium splendens, Polytrichum commune. Sometimes dwarf shrubs Ledum decumbens and Rubus arcticus, and bryophytes Barbilophozia hatcheri, B. lycopodioides, Dicranum polysetum, D. scoparium, and Sphagnum angustifolium dominate or co-dominate (Table 8). The mostly diverse is M.-L. herbosa type of larch forests and woodlands (Table 5, 6, 9). Characteristic species are Anemonastrum biarmiense, Anthoxantum alpinum, Calamagrostis purpurea, Chamaenerion angustifolium, Geranium albiflorum, Milium effusum, Rumex acetosa, Veratrum lobelianum, Viola biflora; differential species are Angelica sylvestris, Phleum alpinum, Poa pratensis, Polemonium acutiflorum, Stellaria bungeana, Tanacetum bipinnatum, Trollius europaeus, Viola palustris; mosses Plagiomnium ellipticum, Rhizomnium pseudopunctatum, Rhodobryum roseum. The most constant and abundant are Bistorta major, Calamagrostis purpurea, Geranium albiflorum, Vaccinium myrtillus; abundant but not too constant — Avenella flexuosa; mosses Dicranum flexicaule, D. scoparium, Pleurozium schreberi. Rarely, herbs Aconitum septentrionale, Athyrium distentifolium, Equisetum pretense, Hieracium hypoglaucum, and bryophytes Barbilophozia hatcheri, B. lycopodioides, Hylocomium splendens, Plagiomnium ellipticum, Polytrichum commune, P. juniperinum, P. strictum, Rhizomnium pseudopunctatum dominate or co-dominate. Constant species with low and average frequency are Chamaenerion angustifolium, Solidago virgaurea, Trientalis europaea, Veratrum lobelianum. The most abundant species in tower layers of M. L. polytrichosa communities are herbs Avenella flexuosa, Carex globilaris, and mosses Polytrichum commune, Pleurozium schreberi, Sphagnum girgensohnii (Table 2). Also common are Bistorta major, Calamagrostis purpurea, Rubus chamaemorus, Vaccinium uliginosum. There are no so far characteristic and differential species in this type, perhaps due to lack of data. Shrubs typical for M.-L. cladinosa and M.-L. hylocomiosa types of larch forests and woodlands are abundant in the communities of M.-L. sphagnosa (Table 2): Empetrum hermaphroditum, Ledum decumbens, Vaccinium uliginosum. Some times Vaccinium myrtillus, and V. vitis-idaea dominants. The most abundant but with average or low cover are herbs Bistorta major and Carex arctisibirica. The most abundant in the moss-lichen layer is Sphagnum capillifolium (characteristic species); rarely, also abundant are Sphagnum fuscum, S. girgensohnii, and S. warnstorfii; constant with average abundance is Pleurozium schreberi; Cladonia stellaris and Polytrichum commune are of average constancy. Species of taiga-forest and tundra-mire eco-coenotical groups are common in the dwarf shrub–herb layer of all types of forests under study (Table 2, 8–10). Significance of mountain tundra species is higher in M.-L. cladinosa and M.-L. hylocomiosa types compare to other types. Species of taiga meadow-forest, valley meadow-forest, valley forest and mountain meadow groups are more abundant in the communities of M.-L. herbosa type. Our research contributed to the current literature data on the species and coenotic diversity of the larch forests and woodlands of the western macroslope of the Subpolar and Northern Urals. Although it is obvious that there is a lack of data both for some associations and forest types, so further researches are necessary to clarify the status of syntaxa and to get information about the characteristic and differential species.
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来源期刊
Rastitel''nost'' Rossii
Rastitel''nost'' Rossii Agricultural and Biological Sciences-Plant Science
CiteScore
1.20
自引率
0.00%
发文量
5
期刊介绍: The scientific journal Rastitel''nost'' Rossii is included in the Scopus database. Publisher country is Russia. The main subject areas of published articles are Ecology, Evolution, Behavior and Systematics, Plant Science, Общая биология.
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