Seasonal patterns of carbon dioxide and water fluxes in three representative tundra ecosystems in northern Alaska

© The Author(s), 2012. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Ecosphere 3, no 1 (2012): art4, doi:10.1890/ES11-00202.1.Understanding the carbon dioxide and water fluxes in the Arctic is essential for accurate assessment and prediction of the responses of these ecosystems to climate change. In the Arctic, there have been relatively few studies of net CO2, water, and energy exchange using micrometeorological methods due to the difficulty of performing these measurements in cold, remote regions. When these measurements are performed, they are usually collected only during the short summer growing season. We established eddy covariance flux towers in three representative Alaska tundra ecosystems (heath tundra, tussock tundra, and wet sedge tundra), and have collected CO2, water, and energy flux data continuously for over three years (September 2007–May 2011). In all ecosystems, peak CO2 uptake occurred during July, with accumulations of 51–95 g C/m2 during June–August. The timing of the switch from CO2 source to sink in the spring appears to be regulated by the number of growing degree days early in the season, indicating that warmer springs may promote increased net CO2 uptake. However, this increased uptake in the spring may be lost through warmer temperatures in the late growing season that promote respiration, if this respiration is not impeded by large amounts of precipitation or cooler temperatures. Net CO2 accumulation during the growing season was generally lost through respiration during the snow covered months of September–May, turning the ecosystems into net sources of CO2 over measurement period. The water balance from June to August at the three ecosystems was variable, with the most variability observed in the heath tundra, and the least in the tussock tundra. These findings underline the importance of collecting data over the full annual cycle and across multiple types of tundra ecosystems in order to come to a more complete understanding of CO2 and water fluxes in the Arctic.This research was funded by the National Science Foundation Office of Polar Programs (OPP 0632264), with a grant during the International Polar Year, ‘Collaborative Research on Carbon, Water, and Energy Balance of the Arctic Landscape at Flagship Observatories and in a PanArctic Network’. Trac

Nitrogen dynamics in a small arctic watershed: retention and downhill movement of 15N

Author Posting. © The Author(s), 2009. This is the author's version of the work. It is posted here by permission of Ecological Society of America for personal use, not for redistribution. The definitive version was published in Ecological Monographs 80 (2010): 331-351, doi:10.1890/08-0773.1.We examined short- and long-term nitrogen (N) dynamics and availability along an arctic hillslope in Alaska, USA, using stable isotope of nitrogen (15N), as a tracer. Tracer levels of 15NH4+ were sprayed once onto the tundra at six sites in four tundra types; heath (crest), tussock with high and low water flux (mid- and foot-slope), and wet sedge (riparian). 15N in vegetation and soil was monitored to estimate retention and loss over a 3-yr period. Nearly all 15NH4+ was immediately retained in the surface moss-detritus-plant layer and > 57 % of the 15N added remained in this layer at the end of the second year. Organic soil was the second largest 15N sink. By the end of the third growing season, the moss-detritus-plant layer and organic soil combined retained ≥ 87 % of the 15N added except at the mid-slope site with high water flux, where recovery declined to 68 %. At all sites, non-extractable and non-labile-N pools were the principal sinks for added 15N in the organic soil. Hydrology played an important role in downslope movement of dissolved 15N. Crest and mid-slope with high water flux sites were most susceptible to 15N losses via leaching perhaps because of deep permeable mineral soil (crest) and high water flow (mid-slope with high water flux). Late spring melt-season also resulted in downslope dissolved-15N losses, perhaps because of an asynchrony between N release into melt water and soil immobilization capacity. We conclude that separation of the rooting zone from the strong sink for incoming N in the moss detritus-plant layer, rapid incorporation of new N into relatively recalcitrant soil-N pools within the rooting zone, and leaching loss from the upper hillslope would all contribute to the strong N limitation of this ecosystem. An extended snow-free season and deeper depth of thaw under warmer climate may significantly alter current N dynamics in this arctic ecosystem.Funding was provided by NSF grant #0444592. Additional support was provided by Toolik Field Station Long Term Ecological Research program, funded by National Science Foundation, Office of Polar Programs

Contrasting effects of long term versus short-term nitrogen addition on photosynthesis and respiration in the Arctic

We examined the effects of short (<1–4 years) and long-term (22 years) nitrogen (N) and/or phosphorus (P) addition on the foliar CO2 exchange parameters of the Arctic species Betula nana and Eriophorum vaginatum in northern Alaska. Measured variables included: the carboxylation efficiency of Rubisco (Vcmax), electron transport capacity (Jmax), dark respiration (Rd), chlorophyll a and b content (Chl), and total foliar N (N). For both B. nana and E. vaginatum, foliar N increased by 20–50 % as a consequence of 1–22 years of fertilisation, respectively, and for B. nana foliar N increase was consistent throughout the whole canopy. However, despite this large increase in foliar N, no significant changes in Vcmax and Jmax were observed. In contrast, Rd was significantly higher (>25 %) in both species after 22 years of N addition, but not in the shorter-term treatments. Surprisingly, Chl only increased in both species the first year of fertilisation (i.e. the first season of nutrients applied), but not in the longer-term treatments. These results imply that: (1) under current (low) N availability, these Arctic species either already optimize their photosynthetic capacity per leaf area, or are limited by other nutrients; (2) observed increases in Arctic NEE and GPP with increased nutrient availability are caused by structural changes like increased leaf area index, rather than increased foliar photosynthetic capacity and (3) short-term effects (1–4 years) of nutrient addition cannot always be extrapolated to a larger time scale, which emphasizes the importance of long-term ecological experiments

Nutrient addition prompts rapid destabilization of organic matter in an arctic tundra ecosystem

Nutrient availability in the arctic is expected to increase in the next century due to accelerated decomposition associated with warming and, to a lesser extent, increased nitrogen deposition. To explore how changes in nutrient availability affect ecosystem carbon (C) cycling, we used radiocarbon to quantify changes in belowground C dynamics associated with long-term fertilization of graminoid-dominated tussock tundra at Toolik Lake, Alaska. Since 1981, yearly fertilization with nitrogen (N) and phosphorus (P) has resulted in a shift to shrub-dominated vegetation. These combined changes have altered the quantity and quality of litter inputs, the vertical distribution and dynamics of fine roots, and the decomposition rate of soil organic C. The loss of C from the deep organic and mineral soil has more than offset the C accumulation in the litter and upper organic soil horizons. In the litter and upper organic horizons, radiocarbon measurements show that increased inputs resulted in overall C accumulation, despite being offset by increased decomposition in some soil pools. To reconcile radiocarbon observations in the deeper organic and mineral soil layers, where most of the ecosystem C loss occurred, both a decrease in input of new root material and a dramatic increase of decomposition rates in centuries-old soil C pools were required. Therefore, with future increases in nutrient availability, we may expect substantial losses of C which took centuries to accumulate. Key words: nitrogen; phosphorus; radiocarbon; carbon dynamics; tundra; decomposition

The effect of experimental warming and precipitation change on proteolytic enzyme activity : positive feedbacks to nitrogen availability are not universal

Nitrogen regulates the Earth's climate system by constraining the terrestrial sink for atmospheric CO2. Proteolytic enzymes are a principal driver of the within-system cycle of soil nitrogen, yet there is little to no understanding of their response to climate change. Here, we use a single methodology to investigate potential proteolytic enzyme activity in soils from 16 global change experiments. We show that regardless of geographical location or experimental manipulation (i.e., temperature, precipitation, or both), all sites plotted along a single line relating the response ratio of potential proteolytic activity to soil moisture deficit, the difference between precipitation and evapotranspiration. In particular, warming and reductions in precipitation stimulated potential proteolytic activity in mesic sites – temperate and boreal forests, arctic tundra – whereas these manipulations suppressed potential activity in dry grasslands. This study provides a foundation for a simple representation of the impacts of climate change on a central component of the nitrogen cycle

Global assessment of experimental climate warming on tundra vegetation: heterogeneity over space and time

Understanding the sensitivity of tundra vegetation to climate warming is critical to forecasting future biodiversity and vegetation feedbacks to climate. In situ warming experiments accelerate climate change on a small scale to forecast responses of local plant communities. Limitations of this approach include the apparent site-specificity of results and uncertainty about the power of short-term studies to anticipate longer term change. We address these issues with a synthesis of 61 experimental warming studies, of up to 20 years duration, in tundra sites worldwide. The response of plant groups to warming often differed with ambient summer temperature, soil moisture and experimental duration. Shrubs increased with warming only where ambient temperature was high, whereas graminoids increased primarily in the coldest study sites. Linear increases in effect size over time were frequently observed. There was little indication of saturating or accelerating effects, as would be predicted if negative or positive vegetation feedbacks were common. These results indicate that tundra vegetation exhibits strong regional variation in response to warming, and that in vulnerable regions, cumulative effects of long-term warming on tundra vegetation – and associated ecosystem consequences – have the potential to be much greater than we have observed to date

BioTIME:a database of biodiversity time series for the Anthropocene

Abstract Motivation: The BioTIME database contains raw data on species identities and abundances in ecological assemblages through time. These data enable users to calculate temporal trends in biodiversity within and amongst assemblages using a broad range of metrics. BioTIME is being developed as a community‐led open‐source database of biodiversity time series. Our goal is to accelerate and facilitate quantitative analysis of temporal patterns of biodiversity in the Anthropocene. Main types of variables included: The database contains 8,777,413 species abundance records, from assemblages consistently sampled for a minimum of 2 years, which need not necessarily be consecutive. In addition, the database contains metadata relating to sampling methodology and contextual information about each record. Spatial location and grain: BioTIME is a global database of 547,161 unique sampling locations spanning the marine, freshwater and terrestrial realms. Grain size varies across datasets from 0.0000000158 km² (158 cm²) to 100 km² (1,000,000,000,000 cm²). Time period and grain: BioTIME records span from 1874 to 2016. The minimal temporal grain across all datasets in BioTIME is a year. Major taxa and level of measurement: BioTIME includes data from 44,440 species across the plant and animal kingdoms, ranging from plants, plankton and terrestrial invertebrates to small and large vertebrates. Software format: .csv and .SQL