Soil mineralogy-controlled phosphorus availability in soils mixed with phosphate fertiliser and biochar.

The biochar amendment to soil proved to be beneficial to improve soil quality and provide nutrients. However, the effect of biochar on the availability of P is still controversial. We aim to study the effect of adding phosphate fertiliser and biochar on the P bioavailability in soils of different mineralogies. Eight biochars derived from biomass (rice husk and coffee husk), soil (sandy and clayey), and phosphate fertiliser (triple superphosphate) were produced. The biochar enrichment process with superphosphate was carried out before and after pyrolysis. Thus, we tested two biochar groups: (1) enriched biochars prior to pyrolysis; (2) enriched biochars after pyrolysis. These biochars were tested as P sources in soils of three mineralogies (kaolinite/oxide, kaolinite, and smectite). Batch sorption-desorption experiments were conducted. The sorbed P was fractionated to examine the factors controlling the retention of applied P. In the three soil mineralogies the use of enriched biochars prior to pyrolysis results in lower availability of P. In contrast, the enriched biochars after pyrolysis increase the bioavailability of P. The coffee husk biochar is more suitable than rice husk biochar to protect P from soil retention reactions. The use of sandy soil rather than clayey soil in enriched biochars compositions results in higher P content availability when applied to soils. The factor that controls the retention of P is the reaction between P, organic compounds, and Fe and Al compounds. The greater the relationship between biochar and soluble P in the fertiliser, the higher the increase of P retention.

Phosphorus in soils and fluvial sediments from a Cerrado biome watershed under agricultural expansion.

Over the past decades, lands alongside Gurguéia River have witnessed rapid expansion of soybean agriculture which has increased soil degradation and affected nutrient concentration in sediment, especially phosphorus (P). The present study aimed to quantify the P concentration in soils under different land uses (i.e., croplands, grasslands, and cerrado) and fluvial sediments (suspended sediment, channel bank, and riverbed sediments), assessing pollution over the main watercourse in cerrado biome Gurguéia watershed, located in Piauí State, Brazil. In total, 136 composite soil samples at a depth of 0-5 cm, under different land uses, as well as 51 composite fluvial sediment samples were collected over the watershed. The land use change from native cerrado had resulted in an increase of total phosphorus (TP) whose concentration was higher in cropland areas, followed by suspended sediment, channel bank, and riverbed sediments. This high concentration in cropland areas resulted from phosphate fertilizer inputs. The transfer of phosphorus to water bodies was evidenced, since an increase of TP was observed in suspended sediment, channel bank and riverbed  sediments. Mineralogical signatures in sediments were identified by X-ray diffraction analysis which showed the occurrence of kaolinite, illite, smectite, iron oxides, and other minerals in lesser proportions. The presence of 1:1 minerals was higher in riverbed sediments and downstream sampling points, while 2:1 minerals were present in higher proportions in suspended sediment and channel bank sediment, as well as at the upstream and middle sampling points. This finding shows that land use change from cerrado to cropland due to soybean agriculture expansion might increase P discharges from terrestrial to aquatic environments, with sediments being the major carrier of this element.

Variation in the properties of biochars produced by mixing agricultural residues and mineral soils for agricultural application.

The research and application of biochars enriched with minerals have increased in recent years; however, the mineral fraction used consists of specific minerals, such as clay minerals and synthesized compounds. In this work, the effects of adding two specific soil types (sandy and clayey) to rice and coffee husks in order to generate biochars via pyrolysis was investigated. Chemical, physical-chemical, thermal, spectroscopic and crystallographic analyses were conducted on the produced biochars. The study confirmed that the presence of mineral soils during the pyrolysis process increases the yield, C retention ratio, and specific surface area. It also decreases the pH, cation exchange capacity (CEC), nutrient content, and carbon-to-nitrogen ratio of biochars. However, the biochars produced by mixing coffee husks and mineral soils still demonstrate a capacity to increase the pH and the CEC of tropical soils. In addition, increased C retention demonstrates an environmental benefit of this biochar production method. Biomass pyrolysis combined with clayey soil results in a biochar with a higher degree of aromaticity and higher thermal stability when compared to biomass pyrolysis alone. These characteristics give the biochar a recalcitrant character, without the necessity for steps related to the synthesis of specific mineral compounds, which reduces the economic and energy cost of the process.

Assessment of carbon storage under rainforests in Humic Hapludox along a climosequence extending from the Atlantic coast to the highlands of northeastern Brazil.

An understanding of the stock of soil organic carbon (SOC) in the umbric epipedon of Oxisols located in the tropical forests surrounded by a semi-arid region is limited but essential because of their importance in the global cycle of carbon (C). The purpose of this study was to assess the effects of climatic (temperature and rainfall), soil organic matter (SOM) composition and litter on the stability of C in surfaces and subsurfaces in five Humic Oxisols along a 475-km climosequence from 143 to 963ma.s.l. in a tropical environment in northeastern Brazil. We assessed vertical changes in SOC; soil total nitrogen (N); C from the microbial biomass; δ(13)C, δ(15)N and the humified composition of SOM; the composition of the humin (HUM) fraction by Fourier Transform Infrared (FTIR); and Thermogravimetry (TG) and Differential Scanning Calorimetry (DSC) at depth. The elemental and isotopic composition of the litter samples were analyzed in all areas studied. The results indicated that the current climate and recalcitrant organic compounds are not preponderant factors in the formation of the umbric epipedon, as suggested by the partial influence of temperature and rainfall on SOM. In addition, SOM was dominated by easily decomposable compounds, as indicated by the predominance of aliphatic C-H groups in the HUM fraction in the FTIR spectra; by the thermal oxidation through DSC-TG, which revealed that approximately 50% of the HUM was composed easily decomposable compounds; and by the high proportion of organic C present in the microbial biomass. Values of δ(13)C showed a predominance of C3 plant-C in SOM whereas δ(15)N patterns indicated that N dynamics differ among the profiles and drive the accumulation of C. These findings can help to characterize the susceptibility of these soils to changes in climate and land use and the implications for the sequestration of soil C.