Pathogenic Fungi on Vascular Plants in the Arctic

2019 ◽  
pp. 44-66
Author(s):  
Shota Masumoto
2020 ◽  
pp. 75-99
Author(s):  
O. I. Sumina

One of the thermokarst relief forms is baidzharakh massif — the group of mounds separated by trenches formed as a result of the underground ice-wedge polygonal networks melting (Fig. 1). Study of baidzharakh vegetation took place on the northeast coast of the Taimyr Peninsula (the Pronchishcheva Bay area) and on the New Siberian Islands (the Kotelny Island) in 1973–1974 (Sumina, 1975, 1976, 1977a, b, 1979 et al.). The aim of this paper is to produce the classification of baidzharakh mound and trenches communities according to the Brown-Blanquet approach (Westhoff, Maarel, 1978) and to compare these data with the community types earlier established on domination principle (Sumina, 1975 et al.). The information obtained in the 1970s could be helpful in a comparative assessment of the thermokarst process dynamics over the past 4 decades, as well as for comparing these processes in other regions of the Arctic. Both studied areas are located in the northern part of the arctic tundra subzone. On the Taimyr Peninsula (and in particular in the Pronchishcheva Bay area) the plakor (zonal) communities belong to the ass. Salici polaris–Hylocomietum alaskani Matveyeva 1998. Our relevés of plakor tundra on the Kotelny Island demonstrate similarity with the zonal communities of the northeast coast of the Taimyr Peninsula (Table 2). Relevés of communities of thermokarst mounds were made within their boundaries, the size of ~ 30 m². In trenches sample plots of the same area had rectangular shape according to trench width. Relevés of plakor tundra were made on 5x6 m plots. There were marked: location in relief, moistening, stand physiognomy, nanorelief, the percent of open ground patches and degree of their overgrowing, total plant cover, that of vascular plants, mosses, and lichens (especially — crustose ons), and cover estimates for each species. The shape of thermokarst mounds depends on the stage of thermodenudation processes. Flat polygons about 0.5 m height with vegetation similar to the plakor tundra are formed at the beginning of ice melting (Fig. 3, a), after which the deformation of the mounds (from eroded flat polygon (Fig. 3, b) to eroded conical mound (Fig. 3, c). Such mounds of maximal height up to 5 m are located on the middle part of steep slopes, where thermodenudation is very active. The last stage of mound destruction is slightly convex mound with a lumpy surface and vegetation, typical to snowbed sites at slope foots (Fig. 3, d, and 5). Both on watersheds and on gentle slopes mounds are not completely destroyed; and on such elongated smooth-conical mounds dense meadow-like vegetation is developed (Fig. 6). On the Kotelny Island thermokarst mounds of all described shapes occur, while in the Pronchishcheva Bay area only flat polygons, eroded flat polygons, and elongated smooth-conical mounds are presented. Under the influence of thermodenudation the plakor (zonal) vegetation is being transformed that allows to consider the most of mound and trench communities as the variants of zonal association. On the base of 63 relevés, made in 14 baidzharakh massifs, 2 variants with 7 subvariants of the ass. Salici polaris–Hylocomietum alaskani Matveyeva 1998 were established, as well as 1 variant of the azonal ass. Poo arcticae– Dupontietum fisheri Matveyeva 1994, which combines the vegetation of wet trenches with dense herbmoss cover. A detailed description of each subvariant is done. All these syntaxa are compared with the types of mound and trenh communities established previously by the domination principle (Sumina, 1975, 1976, 1979 et al.) and with Brown-Blanquet’ syntaxa published by other authors. The Brown-Blanquet approach in compare with domination principle, clearly demonstrates the similarity between zonal and baidzharakh massifs vegetation. Diagnostic species of syntaxa of baidzharakh vegetation by other authors (Matveyeva, 1994; Zanokha, 1995; Kholod, 2007, 2014; Telyatnikov et al., 2017) differ from ours. On the one hand, this is due to the fact that all mentioned researchers worked in another areas, and on the other, with different hierarchial levels of syntaxa, which are subassociations (or vicariants) in cited works or variants and subvariants in the our. Communities of mounds as well as of trenches in different regions have unlike species composition, but similar apearance, which depends on the similarity of the life form composition and community pattern, stage of their transformation and environmental factors. This fact is a base to group communities by physiognomy in order to have an opportunity of comparative analysis of baidzharakh vegetation diversity in different regions of the Arctic. In total, 6 such groups for thermokarst mounds and trenches are proposed: “tundra-like” ― vegetation of flat polygonal mounds (or trenches) is similar to the plakor (zonal) communities; “eroded tundra-like” ― tundra-like vegetation is presented as fragments, open ground occupies the main part of flat polygonal mounds; “eroded mounds with nonassociated vegetation” ― eroded mounds of various shapes up to sharp conical with absent vegetation at the top and slopes, sparse pioneer vascular plants on a bare substrate and crustose lichens and chionophilous grasses at foots; “meadow-like” ― herb stands with a participation of tundra dwarf-shrubs, mosses, and lichens on elongated smooth-conical mounds and in moderately moist trenches; “communities in snowbeds” ― thin plant cover formed by small mosses, liverworts, crustose lichens, and sparse vascular plants in snowbed habitats on destroyed slightly convex mounds with a lumpy surface and in trenches; “communities of cotton grass” or others, depending on the dominant species ― in wet trenches where vegetation is similar to the arctic hypnum bogs with dominant hygrophyte graminoids as Eriophorum scheuchzeri, E. polystachion, Dupontia fischeri et al. This sheme according to physiognomic features of thermokarst mound and trench communities, as a simplier way to assess the current dynamic stage of the baidzharakh massifs, may be useful for monitoring the thermodenudation activity in different areas of the Arctic, particularly in connection with observed climate changes (ACIA, 2004) and a possible dramatic “cascade of their environmental consequences” (Fraser et al., 2018).


Rangifer ◽  
1992 ◽  
Vol 12 (1) ◽  
pp. 21 ◽  
Author(s):  
David R. Klein ◽  
Tatyana J. Vlasova

Lichens are the primary winter forage for most mainland caribou and reindeer herds in North America and for the majority of domestic and wild reindeer in Siberia and northern Europe, collectively totaling in excess of 5 million animals. Lichens represent a unique forage resource throughout much of the circumpolar North that cannot effectively be replaced by vascular plants. Lichens are particularly sensitive to the effects of air pollution. The increased pace of exploitation and processing of minerals and petroleum resources throughout the circumpolar North, with associated introduction of pollution products into the atmosphere has already resulted in losses of lichens and their reduced productivity in extensive areas adjacent to large metallurgical complexes in the Taimyr of Siberia, on the Kola Peninsula, and in adjacent parts of Finland. Losses of terricolous lichens in the Taimyr from pollution generated by the Norilsk metallurgical complex have been nearly complete within a 300 000 ha area closest to the pollution source and damage and reduced growth extends over an area in excess of 600 000 ha. The Arctic also is a sink for atmospheric pollution generated in the heavily industrialized north temperate regions of the world. Assessment of the effects on lichens of this global scale increase in air pollution is difficult because of the lack of representative controls.


2020 ◽  
Vol 8 ◽  
Author(s):  
Mikhail Kozhin ◽  
Sampsa Lommi ◽  
Alexander Sennikov

The present-day demand for digital availability of distributional data in biodiversity studies requires a special effort in assembling and editing the data otherwise scattered in paper literature and herbarium collections, which can be poorly accessible or little understood to present-day users and especially automatic data processors. Although the vascular plants of Murmansk Region (northern part of European Russia) are well studied and represented in publications, the accessibility of this knowledge is highly insufficient. The most widely known source is the Flora of Murmansk Region (published in 1953–1966), which remains in use because of its high original quality, detailed elaboration and completeness. We consider digitising this source to be of primary importance in biodiversity studies in the Arctic Region because of its point occurrence maps, which were based on the comprehensive inventory of contemporary herbarium collections. We have compiled a dataset based on 554 printed point occurrence maps of species distributions published in the Flora of Murmansk Region, which includes 25,555 records of georeferenced plant occurrences that belong to 1,073 species and 5 hybrids. The occurrences are ultimately based on herbarium specimens kept at KPABG and LE, which were collected during 1837–1965. We estimate that these specimens represent ca. 60% of the current global herbarium holdings originated from Murmansk Region; this means that the dataset gives a fair representation of the regional flora.


2012 ◽  
Vol 34 (1) ◽  
pp. 101-110 ◽  
Author(s):  
Kyoo Lee ◽  
Dong-Uk Han ◽  
Jin-Oh Hyun ◽  
Young-Sim Hwang ◽  
Yoo-Kyung Lee ◽  
...  

2017 ◽  
Vol 14 (22) ◽  
pp. 5143-5169 ◽  
Author(s):  
Sarah E. Chadburn ◽  
Gerhard Krinner ◽  
Philipp Porada ◽  
Annett Bartsch ◽  
Christian Beer ◽  
...  

Abstract. It is important that climate models can accurately simulate the terrestrial carbon cycle in the Arctic due to the large and potentially labile carbon stocks found in permafrost-affected environments, which can lead to a positive climate feedback, along with the possibility of future carbon sinks from northward expansion of vegetation under climate warming. Here we evaluate the simulation of tundra carbon stocks and fluxes in three land surface schemes that each form part of major Earth system models (JSBACH, Germany; JULES, UK; ORCHIDEE, France). We use a site-level approach in which comprehensive, high-frequency datasets allow us to disentangle the importance of different processes. The models have improved physical permafrost processes and there is a reasonable correspondence between the simulated and measured physical variables, including soil temperature, soil moisture and snow. We show that if the models simulate the correct leaf area index (LAI), the standard C3 photosynthesis schemes produce the correct order of magnitude of carbon fluxes. Therefore, simulating the correct LAI is one of the first priorities. LAI depends quite strongly on climatic variables alone, as we see by the fact that the dynamic vegetation model can simulate most of the differences in LAI between sites, based almost entirely on climate inputs. However, we also identify an influence from nutrient limitation as the LAI becomes too large at some of the more nutrient-limited sites. We conclude that including moss as well as vascular plants is of primary importance to the carbon budget, as moss contributes a large fraction to the seasonal CO2 flux in nutrient-limited conditions. Moss photosynthetic activity can be strongly influenced by the moisture content of moss, and the carbon uptake can be significantly different from vascular plants with a similar LAI. The soil carbon stocks depend strongly on the rate of input of carbon from the vegetation to the soil, and our analysis suggests that an improved simulation of photosynthesis would also lead to an improved simulation of soil carbon stocks. However, the stocks are also influenced by soil carbon burial (e.g. through cryoturbation) and the rate of heterotrophic respiration, which depends on the soil physical state. More detailed below-ground measurements are needed to fully evaluate biological and physical soil processes. Furthermore, even if these processes are well modelled, the soil carbon profiles cannot resemble peat layers as peat accumulation processes are not represented in the models. Thus, we identify three priority areas for model development: (1) dynamic vegetation including (a) climate and (b) nutrient limitation effects; (2) adding moss as a plant functional type; and an (3) improved vertical profile of soil carbon including peat processes.


2017 ◽  
Vol 10 (12) ◽  
pp. 4693-4722 ◽  
Author(s):  
Arsène Druel ◽  
Philippe Peylin ◽  
Gerhard Krinner ◽  
Philippe Ciais ◽  
Nicolas Viovy ◽  
...  

Abstract. Simulation of vegetation–climate feedbacks in high latitudes in the ORCHIDEE land surface model was improved by the addition of three new circumpolar plant functional types (PFTs), namely non-vascular plants representing bryophytes and lichens, Arctic shrubs and Arctic C3 grasses. Non-vascular plants are assigned no stomatal conductance, very shallow roots, and can desiccate during dry episodes and become active again during wet periods, which gives them a larger phenological plasticity (i.e. adaptability and resilience to severe climatic constraints) compared to grasses and shrubs. Shrubs have a specific carbon allocation scheme, and differ from trees by their larger survival rates in winter, due to protection by snow. Arctic C3 grasses have the same equations as in the original ORCHIDEE version, but different parameter values, optimised from in situ observations of biomass and net primary productivity (NPP) in Siberia. In situ observations of living biomass and productivity from Siberia were used to calibrate the parameters of the new PFTs using a Bayesian optimisation procedure. With the new PFTs, we obtain a lower NPP by 31 % (from 55° N), as well as a lower roughness length (−41 %), transpiration (−33 %) and a higher winter albedo (by +3.6 %) due to increased snow cover. A simulation of the water balance and runoff and drainage in the high northern latitudes using the new PFTs results in an increase of fresh water discharge in the Arctic ocean by 11 % (+140 km3 yr−1), owing to less evapotranspiration. Future developments should focus on the competition between these three PFTs and boreal tree PFTs, in order to simulate their area changes in response to climate change, and the effect of carbon–nitrogen interactions.


2019 ◽  
Vol 9 (2) ◽  
pp. 182-199
Author(s):  
Liudmila Konoreva ◽  
Mikhail Kozhin ◽  
Sergey Chesnokov ◽  
Soon Gyu Hong

Floristic check-lists were compiled for the first time for Duvefjorden Bay on Nordaustlandet, Svalbard, based on field work in July 2012 and on data from literature and herbaria. The check-lists include 172 species of lichens and 51 species of vascular plants. Several species rare in Svalbard and in the Arctic were discovered: Candelariella borealis was new to Svalbard. 51 lichen species were newly recorded on Nordaustlandet and 131 lichen species were observed in the Duvefjorden area for the first time. Among lichen species rare in Svalbard and in the Arctic the following can be mentioned: Caloplaca magni-filii, C. nivalis, Lecidea silacea, Phaeophyscia nigricans, Polyblastia gothica, Protothelenella sphinctrinoidella, Rinodina conradii, Stenia geophana, and Tetramelas pulverulentus. Two species of vascular plants, Saxifraga svalbardensis and S. hyperborea, were found new to the Duvefjorden area. The investigated flora is represented mostly by species widespread in Svalbard and in the Arctic. Although Duvefjorden area is situated in the northernmost part of Svalbard, its flora is characterized by relatively high diversity of vascular plants and lichens. Apparently this is due to the influence of the warm North Atlantic Current.


Nature ◽  
1954 ◽  
Vol 173 (4409) ◽  
pp. 816-817
Author(s):  
NICHOLAS POLUNIN

2017 ◽  
Author(s):  
Sarah Chadburn ◽  
Gerhard Krinner ◽  
Philipp Porada ◽  
Annett Bartsch ◽  
Christian Beer ◽  
...  

Abstract. It is important that climate models can accurately simulate the terrestrial carbon cycle in the Arctic, due to the large and potentially labile carbon stocks found in permafrost-affected environments, which can lead to a positive climate feedback, along with the possibility of future carbon sinks from northward expansion of vegetation under climate warming. Here we evaluate the simulation of tundra carbon stocks and fluxes in three land surface schemes that each form part of major Earth System Models (JSBACH, Germany; JULES, UK and ORCHIDEE, France). We use a site-level approach where comprehensive, high-frequency datasets allow us to disentangle the importance of different processes. The models have improved physical permafrost processes and there is a reasonable correspondence between the simulated and measured physical variables, including soil temperature, soil moisture and snow. We show that if the models simulate the correct leaf area index (LAI), the standard C3 photosynthesis schemes produce the correct order of magnitude of carbon fluxes. Therefore, simulating the correct LAI is one of the first priorities. LAI depends quite strongly on climatic variables alone, as we see by the fact that the dynamic vegetation model can simulate most of the differences in LAI between sites, based almost entirely on climate inputs. However, we also identify an influence from nutrient limitation as the LAI becomes too large at some of the more nutrient-limited sites. We conclude that including moss as well as vascular plants is of primary importance to the carbon budget, as moss contributes a large fraction to the seasonal CO2 flux in nutrient-limited conditions. Moss photosynthetic activity can be strongly influenced by the moisture content of moss, and the carbon uptake can be significantly different from vascular plants with similar LAI. The soil carbon stocks depend strongly on the rate of input of carbon from the vegetation to the soil, and our analysis suggests that an improved simulation of photosynthesis would also lead to an improved simulation of soil carbon stocks. However, the stocks are also influenced by soil carbon burial (e.g. through cryoturbation) and the rate of heterotrophic respiration, which depends on the soil physical state. More detailed below-ground measurements are needed to fully evaluate soil biological and physical processes. Furthermore, even if these processes are well modelled, the soil carbon profiles cannot resemble peat layers as peat accumulation processes are not represented in the models. Thus we identify three priority areas for model development: 1. Dynamic vegetation including a. climate and b. nutrient limitation effects. 2. Adding moss as a plant functional type. 3. Improved vertical profile of soil carbon including peat processes.


1966 ◽  
Vol 98 (11) ◽  
pp. 1135-1144 ◽  
Author(s):  
J. A. Downes

AbstractFrom the revised list of the Lepidoptera of Greenland and from recent work in Ellesmere Island it is shown that almost all the species found in high arctic Canada occur also in Greenland, predominantly in the north, and that this high arctic element constitutes a large fraction of the fauna of Greenland as a whole. It is suggested that this part of the fauna originated entirely from the nearctic by the little-interrupted land route across the arctic islands. The poverty of southerly Lepidoptera in Greenland stands in sharp contrast. It is illustrated by a comparison with the vascular plants and by other comparisons with the Lepidoptera found in the corresponding life zones in North America, and this section of the paper includes the first published list of the Lepidoptera of Baffin Island. It is suggested that this southerly fauna is of adventitious origin, by casual dispersal from overseas (Labrador, Iceland) or perhaps in a few cases by introduction by man. Thus Greenland, in respect of its fauna of southerly type, is an oceanic island of post-glacial age. Similar evidence suggests that Iceland also has been populated mainly in the same way. The conclusions derived from the Lepidoptera apply to several other groups of insects and also to the mammals, including man.


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