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Foliar and litter needle carbon and oxygen isotope compositions relate to tree growth of an exotic pine plantation under different residue management regimes in subtropical Australia
Authors:Shane S Tutua  Zhihong Xu  Timothy J Blumfield
Institution:1. Environmental Futures Centre and Griffith School of Environment, Griffith University, Nathan, Queensland, 4111, Australia
3. Zai Na Tina Centre for Organic Systems, Kastom Gaden Road, East Honiara, Solomon Islands
2. Environmental Futures Centre and School of Biomolecular and Physical Sciences, Griffith University, Nathan, Queensland, 4111, Australia
Abstract:

Background and aim

Significant differences in tree growth were observed in an exotic pine plantation under different harvest residue management regimes at ages 2–10 years. However, the variations in tree growth between residue management treatments could not be explained by soil and foliar nutrient analyses, except by potassium (K) concentration. Therefore, this study determined the carbon isotope composition (δ13C) and oxygen isotope composition (δ18O) of current and archived foliar samples from the exotic pine plantation to establish relationships with foliar K concentration and tree growth indices as a means to determine changes in stomatal conductance (gs) and photosynthetic rate (Amax) or water use efficiency (WUE), and therefore understand the variations in tree growth across treatments.

Methods

The harvest residue treatments were: (1) residue removal, RR0; (2) single level residue retention, RR1; and (3) double level residue retention, RR2. Foliar δ13C and δ18O were determined for samples at ages 2, 4, 6 and 10 years, and the atmospheric 13C discrimination (Δ13C), intercellular CO2 concentration (Ci) and WUE were determined from the δ13C data. Litter needle δ13C and δ18O were also determined over 15 months between ages 9 and 10 years. These parameters or variables where correlated to each other as well as to the periodic mean annual increment of basal area (PAIB) and the periodic mean annual increment of tree diameter at breast height (PAID) across the treatments and over time. Foliar δ13C and δ18O were also related to published data of foliar K concentrations of the same trees.

Results

Significant variations of foliar δ13C, and therefore WUE and Δ13C, across treatments were only observed at ages 4 and 10 years old, and foliar δ18O at age 4 years old only. The results showed increasing foliar δ13C, δ18O and WUE, and decreasing Δ13C and Ci, from RR0 to RR2 treatments. However, while the WUE was positively related to the PAID and PAIB at age 4 years, it was negatively related to PAID and PAIB at age 10 years old. Litter needle δ13C, indicative of WUE, was also negatively related to the PAID at age 10 years old. . At age 4 years, foliar δ13C and δ18O were positively related with a steep slope of 7.70 ‰ across treatments, and that both isotopes were positively related to foliar K concentrations. Similarly, δ18O was negatively related to the Δ13C. No significant relationship can be determined between foliar δ13C, or Δ13C, and δ18O at age 10 years old. In addition, WUE was increasing (p?<?0.001) and Δ13C and Ci decreasing (p?<?0.001) with decreasing PAID over time.

Conclusions

The variations at age 4 years in foliar δ13C or Δ13C and δ18O and increasing WUE with increasing growth rate suggest growth induced water-stress with increasing residue-loading rate as a result of the nutritional effect of the harvest residues on tree growth. At age 10 years, the negative relationships between WUE and PAID indicate nutrient limitation has an over-riding effect on δ13C variations rather than gs. This was due to the lack of a significant relationship between foliar Δ13C and δ18O at this age, as well as over time.
Keywords:
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