RESUMEN
While there is currently intense effort to examine the (13)C signal of CO(2) evolved in the dark, less is known on the isotope composition of day-respired CO(2). This lack of knowledge stems from technical difficulties to measure the pure respiratory isotopic signal: day respiration is mixed up with photorespiration, and there is no obvious way to separate photosynthetic fractionation (pure c(i)/c(a) effect) from respiratory effect (production of CO(2) with a different delta(13)C value from that of net-fixed CO(2)) at the ecosystem level. Here, we took advantage of new simple equations, and applied them to sunflower canopies grown under low and high [CO(2)]. We show that whole mesocosm-respired CO(2) is slightly (13)C depleted in the light at the mesocosm level (by 0.2-0.8 per thousand), while it is slightly (13)C enriched in darkness (by 1.5-3.2 per thousand). The turnover of the respiratory carbon pool after labelling appears similar in the light and in the dark, and accordingly, a hierarchical clustering analysis shows a close correlation between the (13)C abundance in day- and night-evolved CO(2). We conclude that the carbon source for respiration is similar in the dark and in the light, but the metabolic pathways associated with CO(2) production may change, thereby explaining the different (12)C/(13)C respiratory fractionations in the light and in the dark.
Asunto(s)
Ritmo Circadiano/fisiología , Helianthus/metabolismo , Dióxido de Carbono/metabolismo , Isótopos de Carbono , Respiración de la Célula , Análisis por Conglomerados , Oscuridad , Marcaje Isotópico , Luz , Especificidad de Órganos , Fotosíntesis , Factores de TiempoRESUMEN
We studied the effects of two fertilization treatments (N and NPKCa) on wood nitrogen (N) isotope composition (delta(15)N), water-use efficiency (WUE) estimated by carbon isotope composition (delta(13)C) analyses, and ring width of trees in 80-year-old beech (Fagus sylvatica L.) stands in the forest of Fougères, western France. Four replicates were fertilized in two successive years (1973 and 1974), 20 years before core sampling. Unfertilized control trees displayed a decreasing delta(15)N trend with time. The N and NPKCa treatments both increased delta(15)N compared with the control treatment. Wood extraction by organic solvents enhanced the delta(15)N signal. Thus, N addition to the beech ecosystem, even in moderate amounts, could be traced back in tree-ring delta(15)N, suggesting that wood N isotope analysis is a promising tool for studying the long-term effects of N deposition on forests. Although WUE decreased for about 6 years after N fertilization, WUE in NPKCa-treated trees did not differ significantly from that in control trees. Results were similar whether based on cellulose or total wood delta(13)C analysis, suggesting that extraction of cellulose is not necessary when studying fertilization impacts on WUE. The NPKCa treatment had a large impact on radial growth, causing a significant long-lasting increase of 29% compared with the control treatment. Nitrogen alone did not change radial growth significantly.