Mineral control of organic carbon storage in acid temperate forest soils in the Basque Country

Abstract Soil minerals are known to play a major role in soil organic carbon (SOC) stabilization. However, the exact nature of the role is still poorly understood as comparative studies are complicated by the fact that mineralogy usually varies with other important factors such as climate, land-use, texture and acidity. This study investigated naturally-occurring minerals and C storage in nine mature, second-rotation Pinus radiata D. Don forest plantations at a similar development stage and growing under similar climatic conditions, but established on soils derived from three different parent materials: sandstone, basalt and trachyte. We quantified the SOC stocks in the 0–20 cm soil layer, clay-size minerals and metal oxides. The distribution of SOC in labile and mineral-bound fractions and the chemical structure of the SOC were also determined, by CPMAS NMR spectroscopy. For similar tree biomass, mean SOC storage was 2 times higher in the soils derived from basalt and 2.5 times higher in the soils derived from trachyte which were relatively rich in chlorite/vermiculite mixed layers and short-range order aluminium and iron forms, than in the sandstone-derived soils dominated by illite and with no short-range order aluminium. The parent material also affected the major C components of the SOC. Thus, the proportion of aromatic-C forms in the total SOC was higher in the sandstone-derived soil than in the soils of volcanic origin. Furthermore, the proportion of SOC in the mineral-bound fraction was around 30% in the sandstone-derived soil and around 50% in the volcanic soils. We conclude that estimates of ecosystem SOC stocks in acid temperate forest soils should include proxies for clay mineralogy, such as phyllosilicate minerals, contents of Fe and Al (hydr-) oxides and non-crystalline compounds. In addition, we recommend the inclusion of soil parent material as a proxy in models aimed at estimating regional SOC stocks.