23 research outputs found

    CO2 Flux From Tropical Land Uses on Andisol in West Java, Indonesia

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    This study measured CO2 flux by segregating effect of root respiration and organic matter decomposition by microbes. The study involved a mineral soil containing high organic matter (Andisols), in the tropic devoted to different land uses i.e. natural forest, tea plantation, and horticultural farm CO2 emission from those land uses were compared to from peatland. Observed CO2 fluxes came out in the following order: bare plot  7.32, tea plantation  10.22, horticultural farm  15.60, and natural forest  15.62 Mg C-CO2 ha-1 yr-1. While, root respiration accounted for substantial proportions: tea plantation  28%, horticultural farm  53%, and natural forest  53%. Soil temperature demonstrated a significant positive correlation with the CO2 flux, except in the natural forest. On the other hand, water-filled pore spaces displayed varying correlation with site CO2 flux: a negative relationship in both bare plot and tea plantation, appreciably positive in the horticultural farm, and weakly related in the natural forest. Soil respiration and C-organic content appeared to be strongly correlated; the rate of soil respiration increased with higher C-organic content. In field, CO2 flux from organic matter decomposition in Andisols, Latosols, and peatland ranged from 5.35-13.22 Mg C-CO2 ha-1 yr-1, with root respiration contributing most of the flux, which was, in turn, influenced by type vegetation, humidity and soil temperature.Keywords: CO2 flux; decomposition; horticultural farm; natural forest; organic matter; tea plantation [How to Cite: Jon H, Suwardi, B Sumawinata and DPT Baskoro. 2014. CO2 Flux from Tropical Land Uses on Andisol in West Java, Indonesia. J Trop Soils 19: 121-130. Doi: 10.5400/jts.2014.19.3.121]  [Permalink/DOI: www.dx.doi.org/10.5400/jts.2014.19.3.121] &nbsp

    Combined chloroquine, sulfadoxine/pyrimethamine and primaquine against Plasmodium falciparum in Central Java, Indonesia

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    BACKGROUND: Chloroquine (CQ) or sulfadoxine-pyrimethamine (SP) monotherapy for Plasmodium falciparum often leads to therapeutic failure in Indonesia. Combining CQ with other drugs, like SP, may provide an affordable, available and effective option where artemisinin-combined therapies (ACT) are not licensed or are unavailable. METHODS: This study compared CQ (n = 29 subjects) versus CQ + SP (with or without primaquine; n = 88) for clinical and parasitological cure of uncomplicated falciparum malaria in the Menoreh Hills region of southern Central Java, Indonesia. Gametocyte clearance rates were measured with (n = 56 subjects) and without (n = 61) a single 45 mg dose of primaquine (PQ). RESULTS: After 28 days, 58% of subjects receiving CQ had cleared parasitaemia and remained aparasitaemic, compared to 94% receiving CQ combined with SP (p < 0.001). Msp-2 genotyping permitted reinfection-adjusted cure rates for CQ and CQ combined with SP, 70% and 99%, respectively (p = 0.0006). CONCLUSION: Primaquine exerted no apparent affect on cure of asexual stage parasitaemia, but clearly accelerated clearance of gametocytes. CQ combined with SP was safe and well-tolerated with superior efficacy over CQ for P. falciparum parasitaemia in this study

    CO2Flux from Tropical Land Uses on Andisol in West Java, Indonesia

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    Very high risk of therapeutic failure with chloroquine for uncomplicated Plasmodium falciparum and P. vivax malaria in Indonesian Papua.

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    Chloroquine remains the first-line therapy for uncomplicated malaria in Indonesia. Among a series of trials of chloroquine for malaria on this archipelago conducted since 1990, we now report the highest risk of therapeutic failure yet observed. A clinical trial of standard chloroquine therapy for uncomplicated malaria at Arso PIR V in northeastern Indonesian Papua was conducted during 1995. We enrolled 104 non-immune subjects infected with Plasmodium falciparum (n = 55), P. vivax (n = 29), or P. falciparum plus P. vivax (n = 20) and administered supervised standard chloroquine therapy (10 + 10 + 5 mg/kg at 24-hour intervals). The 28-day cumulative incidence of therapeutic failure was 95% for P. falciparum, 84% for P. vivax, and 100% for mixed infections. Only one subject each for P. falciparum and P. vivax remained free of parasites at day 28. All recurrent parasitemias occurred with whole blood levels of chloroquine plus desethylchloroquine exceeding 100 ng/ml. These findings document almost complete failure of chloroquine against P. falciparum or P. vivax near the northeastern coast of Indonesian Papua

    Very high risk of therapeutic failure with chloroquine for uncomplicated Plasmodium falciparum and P. vivax malaria in Indonesian Papua.

    No full text
    Chloroquine remains the first-line therapy for uncomplicated malaria in Indonesia. Among a series of trials of chloroquine for malaria on this archipelago conducted since 1990, we now report the highest risk of therapeutic failure yet observed. A clinical trial of standard chloroquine therapy for uncomplicated malaria at Arso PIR V in northeastern Indonesian Papua was conducted during 1995. We enrolled 104 non-immune subjects infected with Plasmodium falciparum (n = 55), P. vivax (n = 29), or P. falciparum plus P. vivax (n = 20) and administered supervised standard chloroquine therapy (10 + 10 + 5 mg/kg at 24-hour intervals). The 28-day cumulative incidence of therapeutic failure was 95% for P. falciparum, 84% for P. vivax, and 100% for mixed infections. Only one subject each for P. falciparum and P. vivax remained free of parasites at day 28. All recurrent parasitemias occurred with whole blood levels of chloroquine plus desethylchloroquine exceeding 100 ng/ml. These findings document almost complete failure of chloroquine against P. falciparum or P. vivax near the northeastern coast of Indonesian Papua
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