ABSTRACT
To better assess greenhouse gas (GHG) emissions from livestock folds in semi-arid steppe zones and reduce uncertainties in regional and national GHG emission inventories, we measured the fluxes of carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O) from sheepfolds under contrasting management regimes (i.e., summer sheepfolds under continuous and rotational grazing strategies and the winter sheepfold) for 3 consecutive years. Our results showed that these GHG fluxes had high intra-annual and interannual variations, emphasizing the importance of multi-year measurement for achieving temporally representative annual budgets. Sheep presence and temperature appeared to be the key factors driving CH4, CO2 and N2O fluxes from sheepfolds, e.g., higher GHG emissions usually occurred in seasons with sheep presence. However, the sheepfold type exerted a distinct influence on the temperature sensitivity of GHG fluxes, i.e., the Q10 values for GHG fluxes were generally higher in summer sheepfolds than in winter sheepfold. The annual CH4, CO2 and N2O emissions for the 3 sheepfolds were estimated to be 1.5-16.5 kg C ha-1 yr-1 (or 1.9-2.6 g C yr-1sheep-1), 8.6-16.0 t C ha-1 yr-1 (or 5.1-6.6 kg C yr-1sheep-1) and 28.3-41.9 kg N ha-1 yr-1 (or 19.0-26.8 g N yr-1sheep-1), respectively. Averaging across the 3 years, the annual net GHG emissions (CH4 + CO2 + N2O) for all sheepfolds ranged from 47 to 71 t CO2-eq ha-1 yr-1 (or 27-36 kg CO2-eq yr-1 sheep-1), of which CO2 and N2O emissions contributed the most; moreover, the annual net GHG emissions had no significant differences between sheepfold types or grazing strategies. Given that local steppe soils have a lower magnitude of soil respiration (CO2) and N2O emissions and are also net sink for atmospheric CH4, the sheepfold sites in this region are undoubtedly one of the significant hotspots for GHG emissions and could be key areas to focus mitigation action.
ABSTRACT
Alternative splicing (AS) is a gene regulatory mechanism that generates multiple transcripts of the same gene precursor by the spliceosome complex, promoting messenger RNA complexity, and proteome diversity. Although AS is extensively studied in response to environmental stresses, whether it mediates age-dependent development and how it is adjusted by growth transitions are largely unknown. Here, we comprehensively explored the AS landscape at different developmental stages in the grass model plant Brachypodium (Brachypodium distachyon). We identified abundant coding genes and noncoding transcripts subject to dynamic AS regulation during juvenile, adult, and reproductive transitions. Moreover, we revealed that SC35-LIKE SPLICING FACTOR 33 (SCL33), a serine/arginine-rich splicing factor in spliceosomes, plays a redundant and antagonistic role with its putative paralog, SCL33L, in regulating intron assembly across distinct developmental stages. In addition, we determined global AS variations in microRNA156 (miR156)-overproducing plants, in which growth transitions are delayed, and found that SPLs were regulated by miR156 in intron retention alteration in addition to mRNA clearance and translation inhibition manners. Finally, we demonstrated a complex regulatory process of age-dependent AS events in B. distachyon that was coincidently or separately regulated by miR156 and SCL33/SCL33L. These results illustrate a substantial machinery of AS that mediates phase transitions in plants.
