{"title":"Tracing of fire-induced soil phosphorus transformations using phosphate oxygen isotope ratio","authors":"Takuya Ishida, Isao Hirota, Satoshi Yokoyama","doi":"10.1111/ejss.13591","DOIUrl":null,"url":null,"abstract":"<p>This study demonstrates that phosphate oxygen isotope (δ<sup>18</sup>O<sub>PO4</sub>) analysis effectively detects and monitors fire-induced transformation in soil phosphorus (P). Fires increase bioavailable P, potentially limiting primary production in terrestrial ecosystems. However, understanding the effects of fire on soil P dynamics in the field remains challenging due to the interaction between fire spread and soil properties with high spatial heterogeneity. Soil burning experiments were conducted using a surface soil sample collected in central Japan. The soil was burned in an electric furnace from 50 to 550°C for 3 h, and P concentrations and δ<sup>18</sup>O<sub>PO4</sub> values were determined. The results revealed that high temperatures (>350°C) depleted the soil of organic P (P<sub>o</sub>) and increased labile and stable inorganic P (P<sub>i</sub>) concentrations while significantly decreasing δ<sup>18</sup>O<sub>PO4</sub> values. By contrast, low temperatures (150°C) increased labile P<sub>i</sub> and P<sub>o</sub> concentrations without isotopic shift, indicating that low-intensity fires could increase bioavailable P while conserving soil organic matter. These findings indicate that δ<sup>18</sup>O<sub>PO4</sub> analysis can provide insight into the relationship between P transformations and fire intensity and track subsequent changes in P dynamics over time. Our research highlights the potential of δ<sup>18</sup>O<sub>PO4</sub> in predicting and managing postfire ecological and agricultural impacts.</p>","PeriodicalId":12043,"journal":{"name":"European Journal of Soil Science","volume":"75 5","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2024-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/ejss.13591","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Soil Science","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/ejss.13591","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"SOIL SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
This study demonstrates that phosphate oxygen isotope (δ18OPO4) analysis effectively detects and monitors fire-induced transformation in soil phosphorus (P). Fires increase bioavailable P, potentially limiting primary production in terrestrial ecosystems. However, understanding the effects of fire on soil P dynamics in the field remains challenging due to the interaction between fire spread and soil properties with high spatial heterogeneity. Soil burning experiments were conducted using a surface soil sample collected in central Japan. The soil was burned in an electric furnace from 50 to 550°C for 3 h, and P concentrations and δ18OPO4 values were determined. The results revealed that high temperatures (>350°C) depleted the soil of organic P (Po) and increased labile and stable inorganic P (Pi) concentrations while significantly decreasing δ18OPO4 values. By contrast, low temperatures (150°C) increased labile Pi and Po concentrations without isotopic shift, indicating that low-intensity fires could increase bioavailable P while conserving soil organic matter. These findings indicate that δ18OPO4 analysis can provide insight into the relationship between P transformations and fire intensity and track subsequent changes in P dynamics over time. Our research highlights the potential of δ18OPO4 in predicting and managing postfire ecological and agricultural impacts.
期刊介绍:
The EJSS is an international journal that publishes outstanding papers in soil science that advance the theoretical and mechanistic understanding of physical, chemical and biological processes and their interactions in soils acting from molecular to continental scales in natural and managed environments.