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      Upside-down fluxes Down Under: CO<sub>2</sub> net sink in winter and net source in summer in a temperate evergreen broadleaf forest

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          Abstract

          <p><strong>Abstract.</strong> Predicting the seasonal dynamics of ecosystem carbon fluxes is challenging in broadleaved evergreen forests because of their moderate climates and subtle changes in canopy phenology. We assessed the climatic and biotic drivers of the seasonality of net ecosystem–atmosphere <span class="inline-formula">CO<sub>2</sub></span> exchange (NEE) of a eucalyptus-dominated forest near Sydney, Australia, using the eddy covariance method. The climate is characterised by a mean annual precipitation of 800<span class="thinspace"></span>mm and a mean annual temperature of 18<span class="thinspace"></span><span class="inline-formula"><sup>∘</sup></span>C, hot summers and mild winters, with highly variable precipitation. In the 4-year study, the ecosystem was a sink each year (<span class="inline-formula">−</span>225<span class="thinspace"></span>g<span class="thinspace"></span>C<span class="thinspace"></span>m<span class="inline-formula"><sup>−2</sup></span><span class="thinspace"></span>yr<span class="inline-formula"><sup>−1</sup></span> on average, with a standard deviation of 108<span class="thinspace"></span>g<span class="thinspace"></span>C<span class="thinspace"></span>m<span class="inline-formula"><sup>−2</sup></span><span class="thinspace"></span>yr<span class="inline-formula"><sup>−1</sup></span>); inter-annual variations were not related to meteorological conditions. Daily net C uptake was always detected during the cooler, drier winter months (June through August), while net C loss occurred during the warmer, wetter summer months (December through February). Gross primary productivity (GPP) seasonality was low, despite longer days with higher light intensity in summer, because vapour pressure deficit (<span class="inline-formula"><i>D</i></span>) and air temperature (<span class="inline-formula"><i>T</i><sub>a</sub></span>) restricted surface conductance during summer while winter temperatures were still high enough to support photosynthesis. Maximum GPP during ideal environmental conditions was significantly correlated with remotely sensed enhanced vegetation index (EVI; <span class="inline-formula"><i>r</i><sup>2</sup></span><span class="thinspace"></span><span class="inline-formula">=</span><span class="thinspace"></span>0.46) and with canopy leaf area index (LAI; <span class="inline-formula"><i>r</i><sup>2</sup></span><span class="thinspace"></span><span class="inline-formula">=</span><span class="thinspace"></span>0.29), which increased rapidly after mid-summer rainfall events. Ecosystem respiration (ER) was highest during summer in wet soils and lowest during winter months. ER had larger seasonal amplitude compared to GPP, and therefore drove the seasonal variation of NEE. Because summer carbon uptake may become increasingly limited by atmospheric demand and high temperature, and because ecosystem respiration could be enhanced by rising temperatures, our results suggest the potential for large-scale seasonal shifts in NEE in sclerophyll vegetation under climate change.</p>

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          Carbon pools and flux of global forest ecosystems.

          Forest systems cover more than 4.1 x 10(9) hectares of the Earth's land area. Globally, forest vegetation and soils contain about 1146 petagrams of carbon, with approximately 37 percent of this carbon in low-latitude forests, 14 percent in mid-latitudes, and 49 percent at high latitudes. Over two-thirds of the carbon in forest ecosystems is contained in soils and associated peat deposits. In 1990, deforestation in the low latitudes emitted 1.6 +/- 0.4 petagrams of carbon per year, whereas forest area expansion and growth in mid- and high-latitude forest sequestered 0.7 +/- 0.2 petagrams of carbon per year, for a net flux to the atmosphere of 0.9 +/- 0.4 petagrams of carbon per year. Slowing deforestation, combined with an increase in forestation and other management measures to improve forest ecosystem productivity, could conserve or sequester significant quantities of carbon. Future forest carbon cycling trends attributable to losses and regrowth associated with global climate and land-use change are uncertain. Model projections and some results suggest that forests could be carbon sinks or sources in the future.
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            Leaf senescence.

            Leaf senescence constitutes the final stage of leaf development and is critical for plants' fitness as nutrient relocation from leaves to reproducing seeds is achieved through this process. Leaf senescence involves a coordinated action at the cellular, tissue, organ, and organism levels under the control of a highly regulated genetic program. Major breakthroughs in the molecular understanding of leaf senescence were achieved through characterization of various senescence mutants and senescence-associated genes, which revealed the nature of regulatory factors and a highly complex molecular regulatory network underlying leaf senescence. The genetically identified regulatory factors include transcription regulators, receptors and signaling components for hormones and stress responses, and regulators of metabolism. Key issues still need to be elucidated, including cellular-level analysis of senescence-associated cell death, the mechanism of coordination among cellular-, organ-, and organism-level senescence, the integration mechanism of various senescence-affecting signals, and the nature and control of leaf age.
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              Recent patterns and mechanisms of carbon exchange by terrestrial ecosystems.

              Knowledge of carbon exchange between the atmosphere, land and the oceans is important, given that the terrestrial and marine environments are currently absorbing about half of the carbon dioxide that is emitted by fossil-fuel combustion. This carbon uptake is therefore limiting the extent of atmospheric and climatic change, but its long-term nature remains uncertain. Here we provide an overview of the current state of knowledge of global and regional patterns of carbon exchange by terrestrial ecosystems. Atmospheric carbon dioxide and oxygen data confirm that the terrestrial biosphere was largely neutral with respect to net carbon exchange during the 1980s, but became a net carbon sink in the 1990s. This recent sink can be largely attributed to northern extratropical areas, and is roughly split between North America and Eurasia. Tropical land areas, however, were approximately in balance with respect to carbon exchange, implying a carbon sink that offset emissions due to tropical deforestation. The evolution of the terrestrial carbon sink is largely the result of changes in land use over time, such as regrowth on abandoned agricultural land and fire prevention, in addition to responses to environmental changes, such as longer growing seasons, and fertilization by carbon dioxide and nitrogen. Nevertheless, there remain considerable uncertainties as to the magnitude of the sink in different regions and the contribution of different processes.
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                Author and article information

                Journal
                Biogeosciences
                Biogeosciences
                Copernicus GmbH
                1726-4189
                2018
                June 19 2018
                : 15
                : 12
                : 3703-3716
                Article
                10.5194/bg-15-3703-2018
                9b5f39d4-9562-46e0-a603-00a8783754e8
                © 2018

                https://creativecommons.org/licenses/by/4.0/

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