Various studies have shown that micro‐aggregated, strongly weathered tropical soils have different water retention properties than temperate‐region soils because of differences in mineralogy and weathering history. Hence, pedotransfer functions (PTFs), derived from data from temperate‐region soils (temperate PTFs) have limitations when applied to tropical soils. In the absence of PTFs specifically for tropical soils, temperate PTFs are being applied worldwide in global climate modeling exercises, regardless of their textural validity. We derived a PTF to predict the water retention parameters of the van Genuchten (1980) equation using data from more than 500 Brazilian soil horizons. A modified approach was adopted: Multiple regression was used to derive coefficients that relate the van Genuchten parameters to basic soil data, followed by re‐optimization of those coefficients by fitting the individual water content estimations to the measured data simultaneously. Pedotransfer functions were developed for four levels of availability of basic soils data and validated using independent data from 113 Brazilian soil horizons. Water retention curves were better predicted by the new PTFs than by two temperate PTFs tested: The root mean square deviation (RMSD) ranged from 3.78 to 5.84, compared with 9.08 and 10.44, respectively. The new PTFs performed better even when the comparison was restricted to the range of textural validity of the temperate PTFs. For the proposed PTF, RMSDs increased with increasing silt content, but decreased for the temperate PTFs. This reflects the differences in silt content between temperate and strongly weathered tropical soils.

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Mitoxantrone (MTX) is an antitumor agent that causes cardiotoxicity in 18 % patients. The metabolic profile of MTX was assessed after incubation of 100 lM MTX with hepatic S9 fraction isolated from rats. The presence of MTX and its metabolites was also assessed in vivo through the analysis of liver and heart extracts of MTX-treated rats. The cytotoxic effects of MTX and MTX metabolites were evaluated in the H9c2 cells after 24-h incubation with MTX alone and MTX ? metabolites. The influence of CYP450-and CYP2E1-mediated metabolism for the cytotoxicity of MTX was assessed after 96-h incubation with MTX (100 nM and 1 lM) in the presence/ absence of CYP450 or CYP2E1 inhibitors. After 4-h incubation in supplemented S9 fraction, the MTX content was 35 % lower and 5 metabolites were identified: an acetoxy ester derivative (never described before), two glutathione conjugates, a monocarboxylic acid derivative, and the naphtoquinoxaline, the later commonly related to MTX pharmacological effects. The presence of MTX and naphtoquinoxaline metabolite was evidenced in vivo in liver and heart of MTX-treated rats. The cytotoxicity caused by MTX ? metabolites was higher than that observed in the H9c2 cells incubated with non-metabolized MTX group. The co-incubation of MTX with CYP450 and CYP2E1 inhibitors partially prevented the cytotoxicity observed in the MTX groups incubated with H9c2 cells, highlighting that the metabolism of MTX is relevant for its undesirable effects. The naphtoquinoxaline metabolite is described in heart and liver in vivo, highlighting that this metabolite accumulates in these tissues. It was demonstrated that MTX P450-mediated metabolism contributed to MTX toxicity.

The potential of Global Navigation Satellite Systems-Reflectometry (GNSS-R) techniques to estimate land surface parameters such as soil moisture (SM) is experimentally studied using 2014–2017 global data from the UK TechDemoSat-1 (TDS-1) mission. The approach is based on the analysis of the sensitivity to SM of different observables extracted from the Delay Doppler Maps (DDM) computed by the Space GNSS Receiver–Remote Sensing Instrument (SGR-ReSI) instrument using the L1 (1575.42 MHz) left-hand circularly-polarized (LHCP) reflected signals emitted by the Global Positioning System (GPS) navigation satellites. The sensitivity of different GNSS-R observables to SM and its dependence on the incidence angle is analyzed. It is found that the sensitivity of the calibrated GNSS-R reflectivity to surface soil moisture is ~0.09 dB/% up to 30° incidence angle, and it decreases with increasing incidence angles, although differences are found depending on the spatial scale used for the ground-truth, and the region. The sensitivity to subsurface soil moisture has been also analyzed using a network of subsurface probes and hydrological models, apparently showing some dependence, but so far results are not conclusive.

The objective of this work was to investigate the relationship between soil water content and rainfall with rice, beans, cassava and corn yields in the semiarid region of Northeast Brazil. Precipitation and modeled soil water content were compared to yields recorded at the county levels in this region. The results were also integrated over the area of the nine States that lie within the officially recognized region of semiarid climate in Brazil. The influence of water balance components was quantified by calculating their correlation coefficient with yields of the different crop species over the municipalities of the region. It was found that rainfall had higher correlation to crop yields over most of the region, while soil water content had lower values of correlation. This result is consistent with the fact that average root depth is 40 cm, lower than the layer of soil used in the model used to estimate soil water content (100 cm). Plants respond better to the precipitation in the top layers of soil, while the water storage in the deep layer of soil might be important only in other temporal and spatial scales of the hydrological cycle.

Mitoxantrone (MTX) is a chemotherapeutic agent that emerged as an alternative to anthracycline therapy. However, MTX also causes late cardiotoxicity, being oxidative stress and mitochondrial-impaired function proposed as possible mechanisms. This work aimed to investigate the relevance of these mechanisms to the MTX toxicity in H9c2 cells, using therapeutic concentrations. The observed cytotoxicity of MTX was time and concentration dependent in both lactate dehydrogenase leakage assay and MTT reduction assay. Two therapeutic concentrations (100 nM and 1 μM) and three time points were selected (24, 48, and 96 h) for further studies. Both MTX concentrations caused a significant increase in caspase-3 activity, which was not prevented by inhibiting MTX CYP450-metabolism. Significant decreases were observed in the total and reduced glutathione levels only in MTX 100 nM at 96 h; however, neither alterations in oxidized glutathione nor increases in the malondialdehyde levels were observed at any time or concentrations tested. On the other hand, changes in the intracellular ATP levels, mitochondrial membrane potential, and intracellular calcium levels were observed in both concentrations and all time tested. Noteworthy, decreased levels of ATP-synthase expression and activity and increases in the reactive species generation were observed at 96 h in both working concentrations. However, the radical scavenger N-acetylcysteine or the mitochondrial function enhancer L-carnitine did not prevent MTX cytotoxicity. Thus, this work evidenced the early MTX-induced energetic crisis as a possible key factor in the cell injury.

Abuse of synthetic drugs is widespread among young people worldwide. In this context, piperazine derived drugs recently appeared in the recreational drug market. Clinical studies and case-reports describe sympathomimetic effects including hypertension, tachycardia, and increased heart rate. Our aim was to investigate the cytotoxicity of N-benzylpiperazine (BZP), 1-(3-trifluoromethylphenyl) piperazine (TFMPP), 1-(4-methoxyphenyl) piperazine (MeOPP), and 1-(3,4-methylenedioxybenzyl) piperazine (MDBP) in the H9c2 rat cardiac cell line. Complete cytotoxicity curves were obtained at a 0-20 mM concentration range after 24 h incubations with each drug. The EC50 values (μM) were 343.9, 59.6, 570.1, and 702.5 for BZP, TFMPP, MeOPP, and MDBP, respectively. There was no change in oxidative stress markers. However, a decrease in total GSH content was noted for MDBP, probably due to metabolic conjugation reactions. All drugs caused significant decreases in intracellular ATP, accompanied by increased intracellular calcium levels and a decrease in mitochondrial membrane potential that seems to involve the mitochondrial permeability transition pore. The cell death mode revealed early apoptotic cells and high number of cells undergoing secondary necrosis. Among the tested drugs, TFMPP seems to be the most potent cytotoxic compound. Overall, piperazine designer drugs are potentially cardiotoxic and support concerns on risks associated with the intake of these drugs.

Mitoxantrone (MTX) is a chemotherapeutic agent, which presents late irreversible cardiotoxicity. This work aims to highlight the mechanisms involved in the MTX-induced cardiotoxicity, namely the effects toward mitochondria using in vivo and in vitro studies. Male Wistar rats were treated with 3 cycles of 2.5 mg/kg MTX at day 0, 10, and 20. One treated group was euthanized on day 22 (MTX22) to evaluate the early MTX cardiac toxic effects, while the other was euthanized on day 48 (MTX48), to allow the evaluation of MTX late cardiac effects. Cardiac mitochondria isolated from 4 adult untreated rats were also used to evaluate in vitro the MTX (10 nM, 100 nM, and 1 μM) direct effects upon mitochondria functionality. Two rats of MTX48 died on day 35, and MTX treatment caused a reduction in relative body weight gain in both treated groups with no significant changes in water and food intake. Decreased levels of plasma total creatine kinase and CK-MB were detected in the MTX22 group, and increased plasma levels of lactate were seen in MTX48. Increased cardiac relative mass and microscopic changes were evident in both treated groups. Considering mitochondrial effects, for the first time, it was evidenced that MTX induced an increase in the complex IV and complex V activities in MTX22 group, while a decrease in the complex V activity was accompanied by the reduction in ATP content in the MTX48 rats. No alterations in mitochondria transmembrane potential were found in isolated mitochondria from MTX48 rats or in isolated mitochondria directly incubated with MTX. This study highlights the relevance of the cumulative MTX-induced in vivo mitochondriopathy to the MTX cardiotoxicity.