Food web changes in arctic ecosystems related to climate warming

Sedimentary records from three Canadian High Arctic ponds on Ellesmere Island, spanning the last several thousand years, show major shifts in pond communities within the last ～200 years. These paleolimnological data indicate that aquatic insect (Diptera: Chironomidae) populations rapidly expanded and greatly increased in community diversity beginning in the 19th century. These invertebrate changes coincided with striking shifts in algal (diatom) populations, indicating strong food‐web effects because of climate warming and reduced ice‐cover in ponds. Predicted future warming in the Arctic may produce ecological changes that exceed the large shifts that have already occurred since the 19th century.     

Adapting a patch model to simulate the sensitivity of Central-Canadian boreal ecosystems to climate variability

Aim To investigate effects of within-season and interannual climate variability on the behaviour of boreal forest ecosystems as simulated by the FORSKA2 patch model. Location Eleven climate station locations distributed along a transect across the boreal zone of central Canada. Methods FORSKA2′s water balance submodel was modified to enable it to behave more realistically under a varying climate. Long-term actual monthly time-series of temperature and precipitation data were detrended and used to drive the modified model. Long-term monthly averages of the same detrended data were used to drive the unmodified model. Results Modifications created significant improvements when simulating species composition at sites in boreal Canada. Simulated forest biomass values were slightly higher than those obtained from the unmodified model using averaged climate records, but resembled the observed distribution of vegetation more closely. Main conclusions Modified FORSKA2 suggests that boreal forest composition and distribution may be more sensitive to changes in monthly rainfall data than to changes in temperature. Climate variability affects seasonal water balances and should be considered when using patch models to forecast vegetation dynamics during and following a period of climate transition. The modified model provided improved representation of the latitudinal trend in spatially averaged biomass density in this region.     

Changes in shallow lake functioning: response to climate change and nutrient reduction

Hydrobiologia - Nutrient, phytoplankton and zooplankton dynamics have been monitored intensively at Loch Leven for 34 years. The data collected reveal a decline in phosphorus concentrations,...     

陆地生态系统野外增温控制实验的技术与方法

由于人类活动导致的碳排放急剧增加, 工业革命以来全球地表温度显著增加约1 ℃, 未来全球气候还将持续变暖, 到21世纪末最高可升温4 ℃。这种前所未有的气候变化不仅影响陆地植被的适应策略, 也深刻影响生态系统的结构和功能。其中陆地生态系统碳收支对全球变暖的反馈, 是决定未来气候变化强度的关键因素, 因此全球已经开展了大量的生态系统尺度的野外增温控制实验, 研究生态系统碳收支对气温升高的响应, 从而提高地球系统模型的预测精度。然而由于增温技术和方法的不同, 不同研究的结果之间难以进行比较。该文系统总结了常见的野外增温技术和方法, 包括主动增温和被动增温, 阐述了其优缺点、适用对象以及相关研究成果。同时简要介绍了野外增温控制实验的前沿研究方向——新一代野外增温技术(包括全土壤剖面增温和全生态系统增温)和基于新一代增温技术开展的野外增温联网实验。     

Tissue nutrient concentrations in freshwater aquatic macrophytes: high inter-taxon differences and low phenotypic response to nutrient supply

1. The elemental composition and stoichiometry of aquatic plants has often been suggested to reflect the nutrient enrichment of aquatic habitats. However, the relationship is often weak. Moreover, uncertainties remain in the relevance of laboratory derived critical plant tissue nutrient concentrations to maximum yield or growth rates in the field.
2. Aquatic vascular plants and bryophytes, overlying water and sediment samples were collected to test whether freshwater aquatic macrophytes: (i) show tissue nutrient deficiencies when growing in oligotrophic freshwater habitats, and (ii) have strict homeostatic stoichiometry.
3. Plant nutrient concentrations were significantly related to total inorganic nitrogen (or nitrate), total dissolved phosphorus and sediment total phosphorus. However, these relationships were weak. Virtually all the variance in plant tissue nutrient concentrations, however, could be explained by species (taxon) identity.
4. Critical tissue nutrient concentrations for 95% maximum yield or 95% maximum growth rate in aquatic angiosperms, determined from laboratory bioassays, suggested that nutrients should not limit yield in wild aquatic macrophytes. However, there were a substantial number of samples where potential growth rate limitation was possible, particularly due to phosphorus.
5. Strict C : N : P stoichiometric ratios were found for both vascular plants and bryophytes, suggesting little scope for plants as indicators of nutrient enrichment, but provide robust stoichiometric data for studies on ecosystem metabolism and nutrient cycling.     

Zooplankton response to climate warming: a mesocosm experiment at contrasting temperatures and nutrient levels

Zooplankton community response to the combined effects of nutrients and fish (hereafter N + F) at contrasting temperatures was studied in a long-term experiment conducted in 24 shallow lake mesocosms with low and high nutrient levels. We found a positive effect of N + F on zooplankton biomass, chlorophyll-a and turbidity. In contrast, zooplankton species and size diversity decreased with added N + F, as did submerged macrophyte plant volume inhabited (PVI). The community composition of zooplankton in high N + F mesocosms was related to chlorophyll-a and turbidity and to macrophyte PVI in the low N + F mesocosms. Macrophytes can protect zooplankton from fish predation. Compared to N + F effects, temperature appeared to have little effect on the zooplankton community. Yet analysis of community heterogeneity among treatments indicated a significant temperature effect at high N + F levels. The results indicate an indirect temperature effect at high N + F levels that can be attributed to temperature-dependent variation in fish density and/or chlorophyll-a concentration.     

Starvation effects on Escherichia coli and aquatic bacterial responses to nutrient addition and secondary warming stresses.

A gram-negative polar flagellated rod, isolated from a Colorado mountain stream and considered to be an Aeromonas sp., a mixed aquatic microbial population, and a culture of Escherichia coli were starved to determine their responses to the short-term presence of nutrients and mild warming stress (49.5 C for 2 min) in relation to starvation time. At the beginning of the starvation period, the Aeromonas isolate was extremely sensitive to the secondary warming stress. This response was markedly diminished after a 3-week starvation period. The mixed aquatic microbial population showed a similar trend in becoming less sensitive to stress with increased starvation. E coli under similar conditions, became more sensitive to the secondary stress after exposure to glucose. Respiration measurements after glucose additions also indicated that E. coli responded in a different manner to starvation stress and glucose presence than the Aeromonas isolate. The increased sensitivity of E. coli to secondary stress and short-term nutrient availability after starvation may contribute to the exclusion of this organism from aquatic environments.     

Influence of increased nutrient availability on biogenic volatile organic compound (BVOC) emissions and leaf anatomy of subarctic dwarf shrubs under climate warming and increased cloudiness

Background and AimsClimate change is subjecting subarctic ecosystems to elevated temperature, increased nutrient availability and reduced light availability (due to increasing cloud cover). This may affect subarctic vegetation by altering the emissions of biogenic volatile organic compounds (BVOCs) and leaf anatomy. We investigated the effects of increased nutrient availability on BVOC emissions and leaf anatomy of three subarctic dwarf shrub species, Empetrum hermaphroditum, Cassiope tetragona and Betula nana, and if increased nutrient availability modifies the responses to warming and shading.MethodsMeasurements of BVOCs were performed in situ in long-term field experiments in the Subarctic using a dynamic enclosure system and collection of BVOCs into adsorbent cartridges analysed by gas chromatography–mass spectrometry. Leaf anatomy was studied using light microscopy and scanning electron microscopy.Key ResultsIncreased nutrient availability increased monoterpene emission rates and altered the emission profile of B. nana, and increased sesquiterpene and oxygenated monoterpene emissions of C. tetragona. Increased nutrient availability increased leaf tissue thicknesses of B. nana and C. tetragona, while it caused thinner epidermis and the highest fraction of functional (intact) glandular trichomes for E. hermaphroditum. Increased nutrient availability and warming synergistically increased mesophyll intercellular space of B. nana and glandular trichome density of C. tetragona, while treatments combining increased nutrient availability and shading had an opposite effect in C. tetragona.ConclusionsIncreased nutrient availability may enhance the protection capacity against biotic and abiotic stresses (especially heat and drought) in subarctic shrubs under future warming conditions as opposed to increased cloudiness, which could lead to decreased resistance. The study emphasizes the importance of changes in nutrient availability in the Subarctic, which can interact with climate warming and increased cloudiness effects.     

Consistent nutrient storage and supply mediated by diverse fish communities in coral reef ecosystems

Corals thrive in low nutrient environments and the conservation of these globally imperiled ecosystems is largely dependent on mitigating the effects of anthropogenic nutrient enrichment. However, to better understand the implications of anthropogenic nutrients requires a heightened understanding of baseline nutrient dynamics within these ecosystems. Here, we provide a novel perspective on coral reef nutrient dynamics by examining the role of fish communities in the supply and storage of nitrogen (N) and phosphorus (P). We quantified fish‐mediated nutrient storage and supply for 144 species and modeled these data onto 172 fish communities (71 729 individual fish), in four types of coral reefs, as well as seagrass and mangrove ecosystems, throughout the Northern Antilles. Fish communities supplied and stored large quantities of nutrients, with rates varying among ecosystem types. The size structure and diversity of the fish communities best predicted N and P supply and storage and N : P supply, suggesting that alterations to fish communities (e.g., overfishing) will have important implications for nutrient dynamics in these systems. The stoichiometric ratio (N : P) for storage in fish mass (~8 : 1) and supply (~20 : 1) was notably consistent across the four coral reef types (but not seagrass or mangrove ecosystems). Published nutrient enrichment studies on corals show that deviations from this N : P supply ratio may be associated with poor coral fitness, providing qualitative support for the hypothesis that corals and their symbionts may be adapted to specific ratios of nutrient supply. Consumer nutrient stoichiometry provides a baseline from which to better understand nutrient dynamics in coral reef and other coastal ecosystems, information that is greatly needed if we are to implement more effective measures to ensure the future health of the world's oceans.     

Effects of solar UV radiation on aquatic ecosystems and interactions with climate change.

Recent results continue to show the general consensus that ozone-related increases in UV-B radiation can negatively influence many aquatic species and aquatic ecosystems (e.g., lakes, rivers, marshes, oceans). Solar UV radiation penetrates to ecological significant depths in aquatic systems and can affect both marine and freshwater systems from major biomass producers (phytoplankton) to consumers (e.g., zooplankton, fish, etc.) higher in the food web. Many factors influence the depth of penetration of radiation into natural waters including dissolved organic compounds whose concentration and chemical composition are likely to be influenced by future climate and UV radiation variability. There is also considerable evidence that aquatic species utilize many mechanisms for photoprotection against excessive radiation. Often, these protective mechanisms pose conflicting selection pressures on species making UV radiation an additional stressor on the organism. It is at the ecosystem level where assessments of anthropogenic climate change and UV-related effects are interrelated and where much recent research has been directed. Several studies suggest that the influence of UV-B at the ecosystem level may be more pronounced on community and trophic level structure, and hence on subsequent biogeochemical cycles, than on biomass levels per se.     

Adding climate change to the mix: responses of aquatic ectotherms to the combined effects of eutrophication and warming

The threat of excessive nutrient enrichment, or eutrophication, is intensifying across the globe as climate change progresses, presenting a major management challenge. Alterations in precipitation patterns and increases in temperature are increasing nutrient loadings in aquatic habitats and creating conditions that promote the proliferation of cyanobacterial blooms. The exacerbating effects of climate warming on eutrophication are well established, but we lack an in-depth understanding of how aquatic ectotherms respond to eutrophication and warming in tandem. Here, I provide a brief overview and critique of studies exploring the cumulative impacts of eutrophication and warming on aquatic ectotherms, and provide forward direction using mechanistically focused, multi-threat experiments to disentangle complex interactions. Evidence to date suggests that rapid warming will exacerbate the negative effects of eutrophication on aquatic ectotherms, but gradual warming will induce physiological remodelling that provides protection against nutrients and hypoxia. Moving forward, research will benefit from a greater focus on unveiling cause and effect mechanisms behind interactions and designing treatments that better mimic threat dynamics in nature. This approach will enable robust predictions of species responses to ongoing eutrophication and climate warming and enable the integration of climate warming into eutrophication management policies.     

A study of 110mAg in aquatic and terrestrial ecosystems

Experiments on a simulated terrestrial agricultural ecosystem were carried out using the pot culture approach. The most representative plants in local vegetable gardens were selected to investigate the root uptake of (110m)Ag. The results show that carrot, kale and flowering cabbage have the largest transfer factor values among the vegetables. Flowering cabbage, as the most popular leafy vegetable in Hong Kong and the South China area, can be used as a biomonitor for radioisotope contamination in vegetables. Soil column and adsorption tests were also carried out to study the leaching ability of the silver isotope in soil and (110m)Ag was mainly adsorbed in the top 1 cm of soil regardless of the pH value. Experiments on a simulated aquatic ecosystem for freshwater fish and marine organisms were carried out in glass aquaria. The freshwater fish Cyprinus carpio, the marine fish Cuvier and some local abundant seashore molluscs were selected to investigate the kinetic metabolism of (110m)Ag in the compartmental system. The results show that molluscs absorb (110m)Ag much more than fish. Clibanarius infraspinatus has the largest concentration factor among the marine organisms selected. Fish liver, although representing a minor portion of the total body mass, shows the highest (110m)Ag concentration factor, whereas muscle, although representing a major portion of the total body mass, is characterized by an absence of (110m)Ag.     

Application of the AquaCrop model to simulate the biomass of Miscanthus x giganteus under different nutrient supply conditions

There are conflicting opinions about the need to fertilize Miscanthus and, also, the question has been raised whether Miscanthus should be irrigated, especially if water resources are limited. Crop growth modeling can help answer such questions. In this article the FAO AquaCrop water‐driven model was selected to simulate Miscanthus biomass under different nutrient and water supply conditions. The article reports the outcomes of 6‐year experiments with Miscanthus on two locations in Serbia: Zemun, where three fertilizer treatments were applied (N_l – 100 kg ha^?1, N_opt 50 kg ha^?1 and N_f nonfertilized), and Ralja, where only N_l 100 kg ha^?1 was applied. Model calibration focused on the measured data (root depth, crop phenology, and the above‐ground biomass by year of growth. Calibration results showed a very good match between measured and simulated values. The largest and only significant difference was noted in 2008, when the crop was establishing and exhibited uneven radication. The simulation results for the next 5 years showed a variance from ?4 to 5.7%, believed to be a very good match. A high coefficient of determination (R² = 0.995) and high Willmott index of agreement (0.998) were also indicative of a good match between simulated and recorded biomass yields. The measured and simulated results for validated datasets at both locations were good. The average RMSE was 2.89 Mg ha^?1; when compared to the deviations noted at the test site itself, it was apparent that they were smaller in all the years of research except the first year. The index of agreement was 0.97 and the coefficient of determination R² 0.947. The AquaCrop model can be used with a high degree of reliability in strategic planning of Miscanthus cultivation in new areas, under different nutrient and water supply and local weather and soil conditions.     

The response of peatlands to climate warming: A review

Peatlands hold a large portion of the Earth’s terrestrial organic carbon and serve as important pools in the global carbon cycle. Due to their strong feedbacks, peatlands are one of the most important ecosystems with respect to climate warming. This paper reviews the effects of climate warming on peatland ecosystems. Climate warming will shift the point in time when vascular peatland plants flower and reach maximum biomass to an earlier date. Flower production for some plants will increase, but how the phenology of peatland bryophytes will react is still unknown. Climate warming may increase productivity of peatlands, especially ombrotrophic Sphagnum bogs, but in the long run the negative effects from decreased water availability may prevail. Climate warming will change the basic characteristics of peatlands: their wetness and the related cold environment and nutrient shortage. By increased mineralization and nitrogen and phosphorus availability, climate warming will facilitate the growth of vascular plants. This will suppress endangered plant species (which usually grow in low-productive, phosphorus-limited habitats) and lead to a change in vegetation composition and a decrease in peatland biodiversity. Climate warming will change the competitive balance between bryophytes and between Sphagnum and vascular plants. Climate warming in the Late Pleistocene facilitated the initiation of peatland formation, but most current experiments show an obvious tendency for climate warming to drive many peatlands to regressive succession with a shift in dominance from Sphagnum to vascular plants. This change in vegetation will increase the flux of CH₄ and possibly also CO₂. The effect of accelerated peat decay as a result of climate warming will vary between types of peatlands. Since climate warming will generally enhance peat respiration more than net primary production, more and more peatlands will become carbon sources rather than carbon sinks, which will aggravate climate warming by positive feedback. Finally, this paper addresses some problems with current manipulative experimental studies on peatland response to climate warming and makes suggestions for further studies.     

The response of peatlands to climate warming: A review

Peatlands hold a large portion of the Earth’s terrestrial organic carbon and serve as important pools in the global carbon cycle. Due to their strong feedbacks, peatlands are one of the most important ecosystems with respect to climate warming. This paper reviews the effects of climate warming on peatland ecosystems. Climate warming will shift the point in time when vascular peatland plants flower and reach maximum biomass to an earlier date. Flower production for some plants will increase, but how the phenology of peatland bryophytes will react is still unknown. Climate warming may increase productivity of peatlands, especially ombrotrophic Sphagnum bogs, but in the long run the negative effects from decreased water availability may prevail. Climate warming will change the basic characteristics of peatlands: their wetness and the related cold environment and nutrient shortage. By increased mineralization and nitrogen and phosphorus availability, climate warming will facilitate the growth of vascular plants. This will suppress endangered plant species (which usually grow in low-productive, phosphorus-limited habitats) and lead to a change in vegetation composition and a decrease in peatland biodiversity. Climate warming will change the competitive balance between bryophytes and between Sphagnum and vascular plants. Climate warming in the Late Pleistocene facilitated the initiation of peatland formation, but most current experiments show an obvious tendency for climate warming to drive many peatlands to regressive succession with a shift in dominance from Sphagnum to vascular plants. This change in vegetation will increase the flux of CH₄ and possibly also CO₂. The effect of accelerated peat decay as a result of climate warming will vary between types of peatlands. Since climate warming will generally enhance peat respiration more than net primary production, more and more peatlands will become carbon sources rather than carbon sinks, which will aggravate climate warming by positive feedback. Finally, this paper addresses some problems with current manipulative experimental studies on peatland response to climate warming and makes suggestions for further studies.     

Light and heavy fractions of soil organic matter in response to climate warming and increased precipitation in a temperate steppe

Soil is one of the most important carbon (C) and nitrogen (N) pools and plays a crucial role in ecosystem C and N cycling. Climate change profoundly affects soil C and N storage via changing C and N inputs and outputs. However, the influences of climate warming and changing precipitation regime on labile and recalcitrant fractions of soil organic C and N remain unclear. Here, we investigated soil labile and recalcitrant C and N under 6 years' treatments of experimental warming and increased precipitation in a temperate steppe in Northern China. We measured soil light fraction C (LFC) and N (LFN), microbial biomass C (MBC) and N (MBN), dissolved organic C (DOC) and heavy fraction C (HFC) and N (HFN). The results showed that increased precipitation significantly stimulated soil LFC and LFN by 16.1% and 18.5%, respectively, and increased LFC:HFC ratio and LFN:HFN ratio, suggesting that increased precipitation transferred more soil organic carbon into the quick-decayed carbon pool. Experimental warming reduced soil labile C (LFC, MBC, and DOC). In contrast, soil heavy fraction C and N, and total C and N were not significantly impacted by increased precipitation or warming. Soil labile C significantly correlated with gross ecosystem productivity, ecosystem respiration and soil respiration, but not with soil moisture and temperature, suggesting that biotic processes rather than abiotic factors determine variations in soil labile C. Our results indicate that certain soil carbon fraction is sensitive to climate change in the temperate steppe, which may in turn impact ecosystem carbon fluxes in response and feedback to climate change.     

Energy feedbacks of northern high-latitude ecosystems to the climate system due to reduced snow cover during 20th century warming

The warming associated with changes in snow cover in northern high-latitude terrestrial regions represents an important energy feedback to the climate system. Here, we simulate snow cover-climate feedbacks (i.e. changes in snow cover on atmospheric heating) across the Pan-arctic over two distinct warming periods during the 20th century, 1910–1940 and 1970–2000. We offer evidence that increases in snow cover–climate feedbacks during 1970–2000 were nearly three times larger than during 1910–1940 because the recent snow-cover change occurred in spring, when radiation load is highest, rather than in autumn. Based on linear regression analysis, we also detected a greater sensitivity of snow cover–climate feedbacks to temperature trends during the more recent time period. Pan-arctic vegetation types differed substantially in snow cover–climate feedbacks. Those with a high seasonal contrast in albedo, such as tundra, showed much larger changes in atmospheric heating than did those with a low seasonal contrast in albedo, such as forests, even if the changes in snow-cover duration were similar across the vegetation types. These changes in energy exchange warrant careful consideration in studies of climate change, particularly with respect to associated shifts in vegetation between forests, grasslands, and tundra.