A test of functional convergence in carbon fluxes from coupled C and N cycles in Arctic tundra

2018 ◽  
Vol 383 ◽  
pp. 31-40 ◽  
Author(s):  
Kelseyann S. Wright ◽  
Adrian V. Rocha
2015 ◽  
Vol 120 (4) ◽  
pp. 788-808 ◽  
Author(s):  
Haruko M. Wainwright ◽  
Baptiste Dafflon ◽  
Lydia J. Smith ◽  
Melanie S. Hahn ◽  
John B. Curtis ◽  
...  

2020 ◽  
Vol 15 (1) ◽  
Author(s):  
João Paulo Gonsiorkiewicz Rigon ◽  
Juliano Carlos Calonego

Abstract Background A field study with the same crop rotations was conducted to test the hypothesis that the soil Carbon fluxes and balances could vary according to the crop species and also mitigate carbon dioxide (CO2) emission. This study aimed to assess the CO2 emission from crop rotations according to C and N inputs from crop residue, the influences on soil organic carbon (SOC) and total soil nitrogen (TN) stocks, identifying the soybean production systems with positive C balance. Triticale (x Triticosecale) or sunflower (Helianthus annuus) are grown in the fall/winter; sunn hemp (Crotalaria juncea), forage sorghum (Sorghum bicolor), pearl millet (Pennisetum glaucum), or fallow are the spring treatments, and soybean as a main crop in summer. Results We found that high C inputs from crop residues modify the C dynamics in crop rotations by reducing the C output (CO2) and increasing C sequestration in the soil. In general, the higher SOC, C stocks, and TN in soil surface were due to higher C and N inputs from sunn hemp or forage sorghum crop residues in spring. These crops also produced lower accumulated CO2 emissions and, when rotating with triticale in the fall-winter season resulted in a positive C balance, making these soybean crop rotations more efficient. Conclusion Our study suggests the ideal crop species choice in a rotation can mitigate the CO2 emissions by increasing C and N input from crop residues and consequently SOC and C stocks. In particular, crop rotation comprises an important tool to achieve a positive C balance, mitigate CO2 emissions and provide an additional ecosystem service to soybean cultivation option.


2021 ◽  
Author(s):  
Jessica Plein ◽  
Rulon W. Clark ◽  
Kyle A. Arndt ◽  
Walter C. Oechel ◽  
Douglas Stow ◽  
...  

Abstract. The Arctic is warming at double the average global rate, affecting the carbon cycle of tundra ecosystems. Most research on carbon fluxes from Arctic tundra ecosystems has focused on abiotic environmental controls (e.g. temperature, rainfall, or radiation). However, Arctic tundra vegetation, and therefore the carbon balance of these ecosystems, can be substantially impacted by herbivory. In this study we tested how vegetation consumption by brown lemmings (Lemmus trimucronatus) can impact carbon exchange of a wet-sedge tundra ecosystem near Utqiaġvik, Alaska during the summer, and the recovery of vegetation during a following summer. We placed brown lemmings in individual enclosure plots and tested the impact of lemmings’ herbivory on carbon dioxide (CO2) and methane (CH4) fluxes and the normalized difference vegetation index (NDVI) immediately after lemming removal and during the following growing season. During the first summer of the experiment, lemmings’ herbivory reduced plant biomass (as shown by the decrease in the NDVI) and decreased CO2 uptake, while not significantly impacting CH4 emissions. Methane emissions were likely not significantly affected due to CH4 being produced deeper in the soil and escaping from the stem bases of the vascular plants. The summer following the lemming treatments, NDVI and CO2 fluxes returned to magnitudes similar to those observed before the start of the experiment, suggesting recovery of the vegetation, and a transitory nature of the impact of lemming herbivory. Overall, lemming herbivory has short-term but substantial effects on carbon sequestration by vegetation and might contribute to the considerable interannual variability in CO2 fluxes from tundra ecosystems.


2020 ◽  
Author(s):  
Mariasilvia Giamberini ◽  
Ilaria Baneschi ◽  
Matteo Lelli ◽  
Marta Magnani ◽  
Brunella Raco ◽  
...  

<p>Arctic tundra is currently undergoing significant changes induced by the effects of a rapid temperature rise, that in the Arctic is about twice as fast as in the rest of the world. The response of the system composed by the permafrost active layer, soil and vegetation is especially relevant. In fact, it is still unclear whether the system will turn from a carbon sink to a carbon source, owing to the interplay of two opposite phenomena: the increasing time span of the growing season, favouring Net Ecosystem Production (NEP), and the increasing soil temperatures, favouring degradation of organic matter through heterotrophic respiration (HR) and then creating a positive climate feedback. In this work, we analyse soil-vegetation-atmosphere CO<sub>2</sub> flux data of a field campaign conducted in the Bayelva river basin, Spitzbergen, in the Svalbard Archipelago (NO) during summer 2019, measured by a portable accumulation chamber. We use a “Critical Zone” perspective, considering the multiple interactions between biotic and abiotic components. We measured the Net Ecosystem Exchange (NEE) and Ecosystem Respiration (ER) along a slope gradient at different degrees of soil humidity and active layer depths, relating flux data to climate and environmental parameters, soil physical-chemical parameters and vegetation type. The statistical empirical relationships between variables are analysed to identify the main drivers of carbon exchanges. An empirical data-driven model is built to describe the coupled dynamics of soil, vegetation, water and atmosphere that contributes to budgeting the carbon cycle in the Arctic Critical Zone. A comparison of the carbon fluxes obtained with the accumulation chamber method and an Eddy Covariance tower located in the same area is also addressed.</p>


2020 ◽  
Vol 54 (2) ◽  
pp. 497-513 ◽  
Author(s):  
L. N. Beldiman ◽  
I. N. Urbanavichene ◽  
V. E. Fedosov ◽  
E. Yu. Kuzmina

We studied in detail a moss-lichen component of Shokalsky Island vegetation for the first time and identified 79 species of mosses and 54 species and 2 subspecies of lichens and lichenicolous fungi. All species of mosses and 23 species and 2 subspecies of lichens and lichenicolous fungi are recorded for the first time for the island. The study is based on collections made in South West part of the island, in arctic tundra. We also explored the participation of the mosses and lichens in the main types of plant communities and the species distribution in 10 ecotopes. The paper describes the noteworthy findings (Abrothallus parmeliarum, Aongstroemia longipes, Arthonia peltigerea, Caloplaca caesiorufella, Catillaria stereocaulorum, Ceratodon heterophyllus, Lecanora leptacinella, Sphagnum concinnum, S. olafii) and features of bryo- and lichenoflora of Shokalsky Island.


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).


Tellus B ◽  
2011 ◽  
Vol 63 (2) ◽  
Author(s):  
Margaret S. Torn ◽  
Sebastien C. Biraud ◽  
Christopher J. Still ◽  
William J. Riley ◽  
Joe A. Berry

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