Community forest management in Indonesia: Avoided deforestation in the context of anthropogenic and climate complexities

Community forest management has been identified as a win-win option for reducing deforestation while improving the welfare of rural communities in developing countries. Despite considerable investment in community forestry globally, systematic evaluations of the impact of these policies at appropriate scales are lacking. We assessed the extent to which deforestation has been avoided as a result of the Indonesian government’s community forestry scheme, Hutan Desa (Village Forest). We used annual data on deforestation rates between 2012 and 2016 from two rapidly developing islands: Sumatra and Kalimantan. The total area of Hutan Desa increased from 750 km2 in 2012 to 2500 km2 in 2016. We applied a spatial matching approach to account for biophysical variables affecting deforestation and Hutan Desa selection criteria. Performance was assessed relative to a counterfactual likelihood of deforestation in the absence of Hutan Desa tenure. We found that Hutan Desa management has successfully achieved avoided deforestation overall, but performance has been increasingly variable through time. Hutan Desa performance was influenced by anthropogenic and climatic factors, as well as land use history. Hutan Desa allocated on watershed protection forest or limited production forest typically led to a less avoided deforestation regardless of location. Conversely, Hutan Desa granted on permanent or convertible production forest had variable performance across different years and locations. The amount of rainfall during the dry season in any given year was an important climatic factor influencing performance. Extremely dry conditions during drought years pose additional challenges to Hutan Desa management, particularly on peatland, due to increased vulnerability to fire outbreaks. This study demonstrates how the performance of Hutan Desa in avoiding deforestation is fundamentally affected by biophysical and anthropogenic circumstances over time and space. Our study improves understanding on where and when the policy is most effective with respect to deforestation, and helps identify opportunities to improve policy implementation. This provides an important first step towards evaluating the overall effectiveness of this policy in achieving both social and environmental goals

State of the world’s plants and fungi 2020

Kew’s State of the World’s Plants and Fungi project provides assessments of our current knowledge of the diversity of plants and fungi on Earth, the global threats that they face, and the policies to safeguard them. Produced in conjunction with an international scientific symposium, Kew’s State of the World’s Plants and Fungi sets an important international standard from which we can annually track trends in the global status of plant and fungal diversity

Kinetics and thermodynamic analysis in one-pot pyrolysis of rice hull using renewable calcium oxide based catalysts

Thermodynamic and kinetic parameters of catalytic pyrolysis of rice hull (RH) pyrolysis using two different types of renewable catalysts namely natural limestone (LS) and eggshells (ES) using thermogravimetric analysis (TG) approach at different heating rates of 10–100 K min-1in temperature range of 323–1173 K are investigated. Catalytic pyrolysis mechanism of both catalysts had shown significant effect on the degradation of RH. Model free kinetic of iso-conversional method (Flynn-Wall-Ozawa) and multi-step reaction model (Distributed Activation Energy Model) were employed into present study. The average activation energy was found in the range of 175.4–177.7 kJ mol-1(RH), 123.3–132.5 kJ mol-1(RH-LS), and 96.1–100.4 kJ mol-1(RH-ES) respectively. The syngas composition had increased from 60.05 wt% to 63.1 wt% (RH-LS) and 63.4 wt% (RH-ES). However, the CO2content had decreased from 24.1 wt% (RH) to 20.8 wt% (RH-LS) and 19.9 wt% (RH-ES)

Thermogravimetric kinetic modelling of in-situ catalytic pyrolytic conversion of rice husk to bioenergy using rice hull ash catalyst

The thermal degradation behaviour and kinetic parameter of non-catalytic and catalytic pyrolysis of rice husk (RH) using rice hull ash (RHA) as catalyst were investigated using thermogravimetric analysis at four different heating rates of 10, 20, 50 and 100 K/min. Four different iso conversional kinetic models such as Kissinger, Friedman, Kissinger-Akahira-Sunose (KAS) and Ozawa-Flynn-Wall (OFW) were applied in this study to calculate the activation energy (EA) and pre-exponential value (A) of the system. The EAof non-catalytic and catalytic pyrolysis was found to be in the range of 152–190 kJ/mol and 146–153 kJ/mol, respectively. The results showed that the catalytic pyrolysis of RH had resulted in a lower EAas compared to non-catalytic pyrolysis of RH and other biomass in literature. Furthermore, the high Gibb's free energy obtained in RH implied that it has the potential to serve as a source of bioenergy production

An In-Situ Thermogravimetric Study of Pyrolysis of Rice Hull with Alkali Catalyst of CaCO<inf>3</inf>

© Published under licence by IOP Publishing Ltd. Pyrolysis of rice hull (RH) with the presence of CaCO3 catalyst was carried out in this study to understand the effect of alkali catalyst in the thermal degradation behaviour and evaluate the kinetic parameter of rice hull for bio-oil or syngas production. Five different heating rates of the pyrolysis experiments at 10, 20, 30, 50, and 100 Kmin-1 were carried out in thermogravimetric analysis (TGA) equipment. Model fitting kinetic Coats Redfern integral method was applied in this study to estimate the activation energy (EA) and pre-exponential (A) value of catalytic pyrolysis in RH. The results showed that the maximum degradation increased from 6.69 to 52.67 wt% min-1 as heating rates increases from 10 to 100 Kmin-1. Besides that, the EA of the catalytic pyrolysis for RH using CaCO3 catalyst 60.86 kJmol-1 which is lower than other similar pyrolysis reaction reported in literature i.e. 77.4 kJ/mol. Meanwhile, the A value for the catalytic pyrolysis for RH using CaCO3 catalyst was 4.68×1010 min-1 which is significantly higher than 1.1×106 min-1 as reported in literature for non-catalytic pyrolysis of rice husk

Dispersive liquid-liquid microextraction coupled with dispersive μ-solid-phase extraction for the fast determination of polycyclic aromatic hydrocarbons in environmental water samples

10.1021/ac9023632Analytical Chemistry8241540-1545ANCH