Background and aims Lateral tree-scale variability in plantations should be taken into account when scaling up from point samples, but appropriate methods for sampling and calculation have not been defined. Our aim was to define and evaluate such methods. Methods We evaluated several existing and new methods, using data for throughfall, root biomass and soil respiration in mature oil palm plantations with equilateral triangular spacing. Results Three ways of accounting for spatial variation within the repeating tree unit (a hexagon) were deduced. For visible patch patterns, patches can be delineated and sampled separately. For radial patterns, measurements can be made in radial transects or a triangular portion of the tree unit. For any type of pattern, including unknown patterns, a triangular sampling grid is appropriate. In the case studies examined, throughfall was 79 % of rainfall, with 95 % confidence limits being 62 and 96 % of rainfall. Root biomass and soil respiration, measured on a 35-point grid, varied by an order of magnitude. In zones with steep gradients in parameters, sampling density has a large influence on calculated mean values. Conclusions The methods defined here provide a basis for representative sampling and calculation procedures in studies requiring scaling up from point sampling, but more efficient methods are needed. (Résumé d'auteur
Impacts of palm oil industry expansion on biodiversity and greenhouse gas emissions might be mitigated if future plantings replace grassland rather than forest. However, the trajectory of soil fertility following planting of oil palm on grasslands is unknown. We assessed the changes in fertility of sandy volcanic ash soils (0–0.15 m depth) in the first 25 years following conversion of grassland to oil palm in smallholder blocks in Papua New Guinea, using a paired-site approach (nine sites). There were significant decreases in soil pH (from pH 6.1 to 5.7) and exchangeable magnesium (Mg) content following conversion to oil palm but no significant change in soil carbon (C) contents. Analyses to 1.5 m depth at three sites indicated little change in soil properties below 0.5 m. There was considerable variability between sites, despite them being in a similar landscape and having similar profile morphology. Soil Colwell phosphorus (P) and exchangeable potassium (K) contents decreased under oil palm at sites with initially high contents of C, nitrogen, Colwell P and exchangeable cations. We also assessed differences in soil fertility between soil under oil palm (established after clearing forest) and adjacent forest at two sites. At those sites, there was significantly lower soil bulk density, cation exchange capacity and exchangeable calcium, Mg and K under oil palm, but the differences may have been due to less clayey texture at the oil palm sites than the forest sites. Cultivation of oil palm maintained soil structure and fertility in the desirable range, indicating that it is a sustainable endeavour in this environment.
Soil carbon fluxes are highly variable in space and time under tree crops such as oil palm, and attempts to model such fluxes must incorporate an understanding of this variability. In this work, we measured soil CO2 emission, root biomass and pruned frond deposition rates and calculated carbon fluxes into and out of the soil in a mature (20-year-old, second planting cycle) oil palm plantation in Papua New Guinea. Tree-scale spatial variability in CO2 emission and root biomass was quantified by making measurements on a 35-point trapezoid grid covering the 38.5-m2 repeating unit of the plantation (n = 4 grids). In order to obtain an overall mean soil CO2 emission rate within 5% of the most accurate estimate, ≥24 measurement points were required. Soil CO2 emissions were spatially correlated with calculated carbon inputs (r2 = 0.605, slope 1 : 1), but not with soil water content or temperature. However, outputs were higher than inputs at all locations, with a mean overall output of 7.24 µmol m–2 s–1 and input of 3.02 µmol m–2 s–1. Inputs related to fronds, roots and groundcover constituted 60%, 36% and 4% of estimated inputs, respectively. The spatial correlation of carbon inputs and outputs indicates that mineralisation rate is controlled mostly by the amount rather than the nature or input depth of the additions. The spatially uniform net carbon emission from soil may be due to inaccuracies in calculated fluxes (especially root-related inputs) or to non-biological emissions.
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