Climate Change and Plant Communities on Unusual Soils

Author(s):  
Ellen I. Damschen ◽  
Susan Harrison ◽  
Barbara M. Going ◽  
Brian L. Anacker
Author(s):  
George P Malanson ◽  
Michelle L Talal ◽  
Elizabeth R Pansing ◽  
Scott B Franklin

Current research on vegetation makes a difference in people’s lives. Plant community classification is a backbone of land management, plant communities are changing in response to anthropogenic drivers, and the processes of change have impacts on ecosystem services. In the following progress report, we summarize the status of classification and recent research on vegetation responses to pollution, especially nitrogen deposition, invasive species, climate change, and land use and direct exploitation. Two areas with human feedbacks are underscored: fire ecology and urban ecology. Prominent questions at the current research frontier are highlighted with attention to new perspectives.


Solid Earth ◽  
2015 ◽  
Vol 6 (2) ◽  
pp. 583-594 ◽  
Author(s):  
E. L. Poelking ◽  
C. E. R. Schaefer ◽  
E. I. Fernandes Filho ◽  
A. M. de Andrade ◽  
A. A. Spielmann

Abstract. Integrated studies on the interplay between soils, periglacial geomorphology and plant communities are crucial for the understanding of climate change effects on terrestrial ecosystems of maritime Antarctica, one of the most sensitive areas to global warming. Knowledge on physical environmental factors that influence plant communities can greatly benefit studies on the monitoring of climate change in maritime Antarctica, where new ice-free areas are being constantly exposed, allowing plant growth and organic carbon inputs. The relationship between topography, plant communities and soils was investigated on Potter Peninsula, King George Island, maritime Antarctica. We mapped the occurrence and distribution of plant communities and identified soil–landform–vegetation relationships. The vegetation map was obtained by classification of a QuickBird image, coupled with detailed landform and characterization of 18 soil profiles. The sub-formations were identified and classified, and we also determined the total elemental composition of lichens, mosses and grasses. Plant communities on Potter Peninsula occupy 23% of the ice-free area, at different landscape positions, showing decreasing diversity and biomass from the coastal zone to inland areas where sub-desert conditions prevail. There is a clear dependency between landform and vegetated soils. Soils that have greater moisture or are poorly drained, and with acid to neutral pH, are favourable for moss sub-formations. Saline, organic-matter-rich ornithogenic soils of former penguin rookeries have greater biomass and diversity, with mixed associations of mosses and grasses, while stable felsenmeers and flat rocky cryoplanation surfaces are the preferred sites for Usnea and Himantormia lugubris lichens at the highest surface. Lichens sub-formations cover the largest vegetated area, showing varying associations with mosses.


2021 ◽  
Author(s):  
Meng Na ◽  
Mingyue Yuan ◽  
Lettice Hicks ◽  
Johannes Rousk

<p>Soil organic matter (SOM) stabilization plays an important role in the long-term storage of carbon (C). However, many ecosystems are undergoing climate change, which will change the soil C balance via altered plant communities and productivity that change C inputs, and altered C losses via changes in SOM decomposition. The ongoing change of aboveground plant communities in the Subarctic (“greening”) will increase rhizosphere inputs containing low molecular weight organic substances (LMWOS), which will likely affect C-starved microbial decomposers and their subsequent contribution to SOM mineralization (priming effect).In the present study, we simulated the effects of climate change with N fertilization (simulating warming enhanced nutrient cycling) and litter additions (simulating arctic greening) in Abisko, Sweden. The 6 sampled field-treatments included a full factorial combination of 3-years of chronic N addition and litter additions, as well as, a single year of extreme climate change (3x N fertilizer or litter additions in one growth season). We found that N treatments changed plant community composition and productivityand that the associated shift in belowground LMWOS induced shifts in the soil microbial community. In the chronic N fertilization treatments, plant productivity, and therefore belowground LMWOS input, increased. This coincided with a tendency for more bacterial dominated decomposition (lower fungi/bacterial growth ratio). However, N treatments had no effect on soil C mineralization, but increased gross N mineralization.</p><p>These responses in belowground communities and processes driven by rhizosphere input prompted the next question: how does simulated climate change affect the susceptibility of SOM to priming by LMWOS? To assess this question and determine the microbial mechanisms underpinning priming of SOM mineralization, we added a factorial set of additions including <sup>13</sup>C-glucose with and without mineral N, and <sup>13</sup>C-alanine semi-continuously (every 48 hours) to simulate the effect of rhizosphere LMWOS on SOM mineralization and microbial activity. We incubated these samples for 2 weeks and assessed the priming of soil C and gross N mineralization, bacterial and fungal growth rates, PLFAs, enzyme activities, and microbial C use efficiency (CUE). We found that alanine addition primed soil C mineralization by 34%, which was higher than soil C priming induced by glucose and glucose with N. Furthermore, glucose primed fungal growth, whereas the alanine primed bacterial growth, but microbial PLFAs did not respond to either treatment. The C enzyme acquisition activity was higher than N enzyme acquisition activity in all the treatments, while P enzyme acquisition activity was higher than C for all the treatments. Surprisingly, this suggested a chronic microbial limitation by P, which was unaffected by field and lab treatments. LMWOS additions generally reduced microbial CUE. Responses of microbial mineralization of N from SOM to LMWOS suggested a directed microbial effort towards targeting resources that limited bacterial or fungal growth, suggesting that microbial SOM-use shifted to N-rich components (selective microbial “N-mining”), in contrast with enzyme results. Surprisingly, alanine primed the highest N mineralization compared other additions indicating that there was strong N-mining even if N was sufficient.</p>


2020 ◽  
Author(s):  
Pablo Raguet ◽  
Pierre Barré ◽  
François Baudin ◽  
Norine Khedim ◽  
Jérôme Poulenard ◽  
...  

<p><span>Soil organic carbon (SOC) stocks play a significant role in global climate regulation. CO</span><sub><span>2</span></sub><span> fluxes between soils and atmosphere partly depend on soil organic matter (SOM) biogeochemical stability. Cold ecosystems are generally characterized by a high SOC stock, a large part of it being stabilized by environmental conditions (</span><span><em>e.g.</em></span><span> low pH and temperature). SOC stocks of cold ecosystems are also supposed to be highly vulnerable to climate change that is cancelling the stabilizing effect of low temperature on SOM.</span></p><p> </p><p><span>The aim of this study was to investigate the biogeochemical characteristics of SOM in mountain meadows at the European scale. Our goal was also to determine how environmental factors, including climate, elevation and plant functional traits could drive SOM stability and chemistry. To do so, we used the soil sample set of the ODYSSEE project (</span><span></span><span>), collected in 65 sites located in the main European’s mountains range (Alps, Pyrenees, Carpathians, Balkans). Topsoils (0–10 cm) from two plant communities (when both were present) were sampled in acidic meadows: </span><span><em>Nardetum strictae</em></span><span> and </span><span><em>Caricetum curvulae</em></span><span>. To assess SOM chemistry and biogeochemical stability, we used several indices based on Rock-Eval® 6 thermal analysis.</span></p><p> </p><p><span>The topsoil samples showed a high concentration of organic carbon (114 ± 54 gC/kg of soil), and a weakly decomposed SOM as indicated by a relatively high C:N ratio (15 ± 2.5), hydrogen content (Rock-Eval® hydrogen index = 358 ± 44 mgHC/gC) and a relatively low oxygen content (Rock-Eval® OI</span><sub><span>RE6</span></sub><span> = 151 ± 10 mgO</span><sub><span>2</span></sub><span>/gC). The decomposition state of SOM increased with mean air temperature in winter. The size of the thermally labile SOC pool was high for all samples (pyrolysable SOC = 27 to 44% of total SOC), and it strongly increased with elevation. The size of the labile SOC pool (pyrolysable SOC) was also negatively correlated to a plant functional trait: the mean height of the plant community. </span></p><p> </p><p><span>The topsoils of European mountains meadows have a high SOC content characterized by a globally high lability that further increases with elevation. The high lability of SOM revealed by Rock-Eval® 6 thermal analysis indicates a generally high vulnerability of SOC to climate change throughout European mountain meadows ecosystems.</span></p><p><span>The grass adaptative strategy developed under a cold climate induces lower plant height and higher carbon allocation to the root system. Higher carbon input to soil and/or allelopathic mechanisms protecting SOM from decomposition could possibly explain that lower plant communities of European acidic alpine meadows are characterized by a more labile SOM.</span></p>


2018 ◽  
Vol 85 ◽  
pp. 525-536 ◽  
Author(s):  
Mariusz Gałka ◽  
Graeme T. Swindles ◽  
Marta Szal ◽  
Randy Fulweber ◽  
Angelica Feurdean

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