Temperature controls temporal variation in soil CO2 efflux in a secondary beech forest in Appi Highlands, Japan

Forest soil is a huge reserve of carbon in the biosphere. Therefore to understand the carbon cycle in forest ecosystems, it is important to determine the dynamics of soil CO₂ efflux. This study was conducted to describe temporal variations in soil CO₂ efflux and identify the environmental factors that affect it. We measured soil CO₂ efflux continuously in a beech secondary forest in the Appi Highlands in Iwate Prefecture for two years (except when there was snow cover) using four dynamic closed chambers that automatically open after taking measurements. Temporal changes in soil temperature and volumetric soil water content were also measured at a depth of 5 cm. The soil CO₂ efflux ranged from 14 mg CO₂ m⁻² h⁻¹ to 2,329 mg CO₂ m⁻² h⁻¹, the peak occurring at the beginning of August. The relationship between soil temperature and soil CO₂ efflux was well represented by an exponential function. Most of temporal variation in soil CO₂ efflux was explained by soil temperature rather than volumetric soil water content. The Q ₁₀ values were 3.7 ± 0.8 and estimated annual carbon emissions were 837 ± 210 g C m⁻² year⁻¹. These results provide a foundation for further development of models for prediction of soil CO₂ efflux driven by environmental factors.     

Partial cloning of CYP2C23a genes and hepatic protein expression in eight representative avian species

Large interspecies differences in avian xenobiotic metabolism have been revealed by microsome‐based studies, but specific enzyme isoforms in different bird species have not yet been compared. We have previously shown that CYP2C23 genes are the most induced CYP isoforms in chicken liver. In this study, we collected partial CYP2C23a gene sequences from eight avian species (ostrich, blue‐eared pheasant, snowy owl, great‐horned owl, Chilean flamingo, peregrin falcon, Humboldt penguin, and black‐crowned night heron) selected to cover the whole avian lineage: Paleognathae, Galloanserae, and Neoaves. Genetic analysis showed that CYP2C23 genes of Galloanserae species (chicken and blue‐eared pheasant) had unique characteristics. We found some duplicated genes (CYP2C23a and CYP2C23b) and two missing amino acid residues in Galloanserae compared to the other two lineages. The genes have lower homology than in other avian lineages, which suggests Galloanserae‐specific rapid evolutionary changes. These genetic features suggested that the Galloanserae are not the most representative avian species, considering that the Neoaves comprise more than 95% of birds. Moreover, we succeeded in synthesizing an antipeptide polyclonal antibody against the region of CYP2C23 protein conserved in avians. However, comparative quantitation of CYP2C23 proteins in livers from six species showed that expression levels of these proteins differed no more than fourfold. Further study is needed to clarify the function of avian CYP2C23 proteins.