The fate of photosynthetically-fixed carbon in Lolium perenne grassland as modified by elevated CO2 and sward management

Prediction of the impact of climate change requires the response of carbon (C) flow in plant-soil systems to increased CO(2) to be understood. A mechanism by which grassland C sequestration might be altered was investigated by pulse-labelling Lolium perenne swards, which had been subject to CO(2) enrichment and two levels of nitrogen (N) fertilization for 10 yr, with (14)CO(2). Over a 6-d period 40-80% of the (14)C pulse was exported from mature leaves, 1-2% remained in roots, 2-7% was lost as below-ground respiration, 0.1% was recovered in soil solution, and 0.2-1.5% in soil. Swards under elevated CO(2) with the lower N supply fixed more (14)C than swards grown in ambient CO(2), exported more fixed (14)C below ground and respired less than their high-N counterparts. Sward cutting reduced root (14)C, but plants in elevated CO(2) still retained 80% more (14)C below ground than those in ambient CO(2). The potential for below-ground C sequestration in grasslands is enhanced under elevated CO(2), but any increase is likely to be small and dependent upon grassland management.     

An improved hexagon open‐top chamber system for stable diurnal and nocturnal warming and atmospheric carbon dioxide enrichment

The use of solar passive hexagonal open‐top chambers (POTCs) is a viable method for experimentally manipulating daytime air temperatures in low‐stature plant communities at high latitudes. Here we describe a new hexagon POTC‐based system that uses thermal inertia to increase overnight temperatures and variable chamber height to reduce overheating in summer. Field data collected in tall temperate grasslands show that the presence of thermal mass raised minimum and mean nighttime air temperatures by up to 1.5 °C while lowering chamber height, along with thermal mass, limited the development of extreme daytime chamber temperatures in summer. We also demonstrate that, by using a simple, inexpensive twin carbon dioxide (CO₂) injection system regulated by an infrared gas monitor, it is possible to generate targeted and stable atmospheric CO₂ enrichment within these chambers. These innovations significantly improve the conventional hexagon POTC design and represent a low‐cost method for assessing the effects of warming and CO₂ enrichment on low‐stature vegetation in low latitude environments.     

Nitrogen accumulation and distribution in Danthonia richardsonii swards in response to CO2 and nitrogen supply over four years of growth

Nitrogen‐stressed microcosms of the C3 grass Danthonia richardsonii gained nitrogen from the environment when grown under ambient or enriched (359, ‘amb’ or 719 μL L^{? 1}‘enr’, respectively) atmospheric CO₂ concentrations over a 4‐y period. This gain was apparent at all rates of supplied mineral N (2.2, 6.7 or 19.8 g N m^{? 2} y^{? 1}– low‐N, mid‐N or high‐N), although it was small at high‐N. Small losses of N occurred from the microcosm as leachate, while gaseous losses of N were estimated to be between 10% and 25% of applied mineral N. Losses of applied mineral N were slightly lower under CO₂ enrichment only at the highest rate of mineral N supply. Levels of ¹⁵N natural abundance in green leaf (δ¹⁵Ν) of ? 2‰ (amb low‐N) and of below ? 4‰ (enr low‐ & mid‐N) suggest that absorption of atmospheric NH₃ may have been a source of some of the extra N in the low and mid‐N treatments. Biological N₂ fixation, of up to 2 g m^{? 2} y^{? 1} was hypothesized to form the remainder of the environmental N source. Microcosm C:N ratio was higher under CO₂ enrichment. Nitrogen productivity of microcosm carbon gain (g C accumulated g^{? 1} leaf N day^{? 1}) was increased (up to 100%) by CO₂ enrichment at all rates of mineral N supply. Green leaf %N was reduced by CO₂ enrichment, and there was less nitrogen in the green leaf pool under CO₂ enrichment. Less, or the same amount of nitrogen was present in senesced leaf, surface litter and root under CO₂ enrichment while more nitrogen was present in the soil in organic forms, and as NH₄ + at the highest rate of mineral N supply.     

Combining limnological and palaeolimnological data to disentangle the effects of nutrient pollution and climate change on lake ecosystems: problems and potential

1. As long‐term observational lake records continue to lengthen, the historical overlap with lake sediment records grows, providing increasing opportunities for placing the contemporary ecological status of lakes in a temporal perspective. 2. Comparisons between long‐term data sets and sediment records, however, require lake sediments to be accurately dated and for sediment accumulation rates to be sufficiently rapid to allow precise matching with observational data. 3. The critical role of the sediment record in this context is its value in tracking the changing impact of human activity on a lake from a pre‐disturbance reference through to the present day. 4. Here, we use data from a range of lakes across Europe presented as case studies in this Special Section. The seven sites considered all possess both long‐term observational records and high‐quality sediment records. Our objective is to assess whether recent climate change is having an impact on their trophic status and in particular whether that impact can be disentangled from the changes associated with nutrient pollution. 5. The palaeo‐data show clear evidence for the beginning of nutrient pollution varying from the mid‐nineteenth century at Loch Leven to the early and middle twentieth century at other sites. The monitoring data show different degrees of recovery when judged against the palaeo‐reference. 6. The reason for limited recovery is attributed to continuing high nutrient concentrations related to an increase in diffuse nutrient loading or to internal P recycling, but there is some evidence that climate change may be playing a role in offsetting recovery at some sites. If this is the case, then lake ecosystems suffering from eutrophication may not necessarily return to their pre‐eutrophication reference status despite the measures that have been taken to reduce external nutrient loading. 7. The extent to which future warming might further limit such recovery can be evaluated only by continued monitoring combined with the use of palaeo‐records that set the pre‐eutrophication reference.