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1.
Sci Total Environ ; 800: 149312, 2021 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-34392206

RESUMO

The prediction of soil organic carbon (SOC) changes in response to environmental change is often limited by a scarcity of revisited temporal data, which constrains scientific understanding and realistic predictions of soil carbon change. The present study improved the potential of nonrevisited temporal data in the prediction of SOC stocks (SOCS) variations. We proposed a method to develop predictions of SOCS change using two independent temporal data sets (pertaining to the 1980s and 2010s) in China based on the digital soil mapping technique. Changes in SOCS over time at the site level were analyzed via the interpolation of missing SOCS values in each data set. Quantitative SOCS change predictions were generated by modeling the relationship between SOCS change and variables that represent changes in climate, vegetation indices, and land cover. The scale-dependent response of SOCS change to these environmental dynamics was assessed. On average, a slight increase was observed from 3.70 kg m-2 in the 1980s to 4.53 kg m-2 in the 2010s. The proposed approach attained moderate accuracy with an R2 value of 0.32 and a root mean squared error (RMSE) of 1.73 kg m-2. We found that changes in climate factors were dominant controls of SOCS change over time at the country scale. At the regional scale, the controlling factors of SOCS change were distinct and variable. Our case study may be of value in the application of independent temporal data sets to analyze soil carbon change on multiple scales. The method may be used to resolve questions of soil carbon change projections and provide an alternative solution to predict likely changes in soil carbon in response to future environmental change when no temporal data are available.


Assuntos
Carbono , Solo , Carbono/análise , China , Clima
2.
Behav Pharmacol ; 17(1): 51-9, 2006 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16377963

RESUMO

We recently found that rats' ability to discriminate durations of exteroceptive stimuli is disrupted by the non-selective 5-HT receptor agonist quipazine. Ketanserin reversed this effect, suggesting that the effect may be mediated by 5-HT2A receptors. Here, we report that the 5-HT2A/2C receptor agonist 2,5-dimethoxy-4-iodoamphetamine (DOI) also disrupts temporal discrimination, and that this effect can be reversed by ketanserin and the highly selective 5-HT2A receptor antagonist (+/-)2,3-dimethoxyphenyl-1-[2-(4-piperidine)-methanol] (MDL-100907). Twenty rats were trained to discriminate durations in a discrete-trials psychophysical procedure. In each 50-s trial, a light was presented for t seconds, following which two levers (A and B) were presented. A response on A was reinforced if t < 25 s, and a response on B if t > 25 s. Logistic psychometric curves were fitted to the proportional choice of B (%B) for derivation of timing indices [T50: time corresponding to %B = 50; Weber fraction: (T75-T25)/2T50, where T75 and T25 are times corresponding to %B = 75 and 25, respectively]. DOI 0.25 mg kg (subcutaneous) significantly increased the Weber fraction and tended to increase T50. Ketanserin 2 mg kg (subcutaneous) did not alter either parameter, but completely antagonized the effects of DOI. Similarly, MDL-100907 0.5 and 1 mg kg (intraperitoneal) did not affect performance, but completely antagonized the effects of DOI. The results indicate that the mixed 5-HT2A/2C receptor agonist DOI disrupts temporal discrimination via stimulation of 5-HT2A receptors.


Assuntos
Anfetaminas/farmacologia , Aprendizagem por Discriminação/efeitos dos fármacos , Fluorbenzenos/farmacologia , Ketanserina/farmacologia , Piperidinas/farmacologia , Receptor 5-HT2A de Serotonina/efeitos dos fármacos , Antagonistas da Serotonina/farmacologia , Agonistas do Receptor de Serotonina/farmacologia , Percepção do Tempo/efeitos dos fármacos , Anfetaminas/antagonistas & inibidores , Animais , Aprendizagem por Associação/efeitos dos fármacos , Encéfalo/efeitos dos fármacos , Feminino , Injeções Intraperitoneais , Injeções Subcutâneas , Psicofísica , Ratos , Ratos Wistar , Receptor 5-HT2C de Serotonina/efeitos dos fármacos
3.
Pharmacol Biochem Behav ; 72(1-2): 39-43, 2002 May.
Artigo em Inglês | MEDLINE | ID: mdl-11900767

RESUMO

The present study observed the antidepressant-like action of the medicinal plant Morinda officinalis in the differential reinforcement of low rate 72-s (DRL 72-s) schedule, a behavioral screen selective and sensitive to antidepressant drugs, and the forced swimming test, a well-known animal model of depression. In the DRL 72-s schedule in rats, the plant extract (25-50 mg/kg), similar to clinically effective antidepressant drug desipramine (5-10 mg/kg), significantly reduced response rate and efficiency ratio while at the same time increasing reinforcement rate. In the forced swimming test in mice, the plant extract (50 mg/kg), like the effect of desipramine (20 mg/kg), also elicited a significant reduction in the duration of immobility. A tendency to this phenomenon could be seen at the dose of 100 mg/kg. Meanwhile, the plant extract, in the effective doses for the forced swimming test, had no effects on spontaneous motor activity in mice. These findings provide further support for the conclusion that M. officinalis extract possesses the antidepressant effect.


Assuntos
Antidepressivos/farmacologia , Medicamentos de Ervas Chinesas/farmacologia , Morinda , Esquema de Reforço , Animais , Antidepressivos/isolamento & purificação , Antidepressivos/uso terapêutico , Relação Dose-Resposta a Droga , Medicamentos de Ervas Chinesas/isolamento & purificação , Medicamentos de Ervas Chinesas/uso terapêutico , Imobilização/fisiologia , Masculino , Camundongos , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/farmacologia , Extratos Vegetais/uso terapêutico , Raízes de Plantas , Plantas Medicinais , Ratos , Ratos Wistar , Natação/fisiologia
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