Holocene Monsoon Changes Inferred from Lake Sediment Pollen and Carbonate Records, Northeastern Cambodia

Major Holocene monsoon changes in continental Southeast Asia are reconstructed from analysis of ¹⁴C-dated changes in pollen and organic/inorganic carbon in sediment cores taken from permanent, closed-basin, volcanic lakes in Ratanakiri Province, northeastern Cambodia. Analysis focuses on the nature and timing of monsoon changes, inferred from changes in vegetation and lake conditions. These data provide the first well-dated palynological record, covering most of the Holocene and continuous up to the present, from a terrestrial site in mainland Southeast Asia. The record from a 15-m core retrieved from Kara Lake, representing the last 9300 years, shows that the late Glacial conditions ended about 8500 ¹⁴C yr B.P., more than 1000 years later than sites in southwest China. Summer monsoon intensity increased over the period ca. 8400–5300 ¹⁴C yr B.P., similar to most other sites in the Asian monsoon region. A subsequent expansion of secondary forests at the expense of dense semievergreen forests suggest a drier climate leading to more frequent fire disturbance. After ca. 3500 ¹⁴C yr B.P. disturbance frequency may have increased further with increasing seasonality. From ca. 2500 ¹⁴C yr B.P. to the present, dense forest has recovered in a mosaic with annually burned dry forest, but climate may not be the main control on local vegetation dynamics in the late Holocene.     

Flux between soil and atmosphere, vertical concentration profiles in soil, and turnover of nitric oxide: 2. Experiments with naturally layered soil cores

Intact soils cores were taken with a stainless steel corer from a sandy podzol and a loamy luvisol, and used to measure the flux (J) of NO between soil and atmosphere and the vertical profile of the NO mixing ratios (m) in the soil atmosphere, both as function of the NO mixing ratio (m _a) in the atmosphere of the headspace. These measurements were repeated after stepwise excavation of the soil column from the top, e.g. by removing the upper 2 cm soil layer. The gaseous diffusion coefficients of NO in the soil cores were either computed from soil porosity or were determined from experiments using SF6. The NO fluxes (J) that were actually measured at the soil surface were compared to the fluxes which were calculated either from the vertical NO profiles (J _c ) or from the NO production and uptake rates (J _m ) determined in the excavated soil samples. In the podzol, the actually measured (J) and the calculated (J _m , J_m) NO fluxes agreed within a factor of 2. In the luvisol, the measured NO fluxes (J) and those calculated from the vertical NO profiles (J _c ) also agreed well, but in the upper 6 cm soil layer the NO fluxes (J _m ) calculated from NO production and uptake rates were up to 7 times higher than the measured NO fluxes. This poor agreement was probably due to the inhomogeneous distribution of NO production and consumption processes and the change of diffusivities within the top layers of the luvisol. Indeed, the luvisol showed a pronounced maximum of the NO mixing ratios at about 6 cm depth, whereas the podzol column exhibited a steady and exponential decrease of the NO mixing ratios with depth. The inhomogeneities in the luvisol were confirmed by incubation of the soil cores under anoxic conditions. This treatment resulted in production of NO at several depths indicating a zonation of increased potential activities within the luvisol profile which may have biased the modelling of the NO surface flux from turnover measurements in soil samples. Inhomogeneities could be achieved even in homogenized soil by fertilization with nitrate solution.     

Methane,carbon monoxide and light non-methane hydrocarbon emissions from African savanna burnings during the FOS/DECAFE experiment

Atmospheric samples from savanna burnings were collected in the Ivory Coast during two campaigns in January 1989 and January 1991. About 30 nonmethane hydrocarbons from C₂ to C₆, carbon monoxide, carbon dioxide and methane were measured from the background and also at various distances from the burning. Concentrations in the fire plume reached ppmv levels for C₂-C₄ hydrocarbons, and 5300, 500 and 93 ppmv for CO₂, CO and CH₄ respectively. The excess in the mixing ratios of these gases above their background level is used to derive emission factors relative to CO and CO₂. For the samples collected immediately in the fire plume, a differentiation between high and low combustion efficiency conditions is made by considering the CO/CO₂ ratio. Ethene (C₂H₄), acetylene (C₂H₂), ethane (C₂H₆) and propene (C₃H₆) are the major NMHC produced in the flaming stage, whereas a different pattern with an increasing contribution of alkanes is observed in samples typical of post flaming processes. A strong correlation between methane and carbon monoxide suggests that these compounds are produced during the same stage of the combustion. In samples collected at a distance from the fire and integrated over a period of 30 minutes, the composition is very similar to that of flaming. NMHC/CO₂ is of the order of 0.7%, CH₄/CO₂ of the order of 0.4% and CO/CO₂ of the order of 6.3%. From this study, a global production by African savanna fires is derived: 65 Tg of CO-C, 4.2 Tg of CH₄-C and 6.7 Tg of NMHC-C. Whereas acetylene can be used as a conservative tracer of the fire plumes, only ethene, propene and butenes can be considered in terms of their direct photochemical impact.     

Tri- and tetraterpenoid hydrocarbons in the Messel oil shale

The high molecular weight constituents of the branched and cyclic hydrocarbon fraction of the Messel oil shale (Eocene) have been examined by high resolution gas chromatography and combined gas chromatography-mass spectrometry. The following compounds are present: perhydrolycopene (1; lycopane), together with one or more unsaturated analogues with the same skeleton; a series of 4-methylsteranes (2c) in higher abundance than their 4-desmethyl analogues; two series of pentacyclic triterpanes, one series (C₂₇-C₃₂) based on the hopane structure (3a-e), and the other (C₂₇-C₃₁) based on the 17α-H hopane structure (3a-d, 17αH); and an intact triterpene hop-17 (21)-ene [3c, Δ 17(21)]. Only two additional triterpanes were detected in minor concentrations, viz. 30-normoretane (3b, 21αH) and a C₃₁ triterpane based on the hopane/lupane-type skeleton. The presence of these compounds suggests a significant microbial contribution to the forming sediment. Comparison of the tri- and tetraterpenoid hydrocarbons with those of the Green River Shale indicates differences in the organisms contributing to the two sediments.     

Lipids of Recent sediments,Part I: Straight-chain hydrocarbons and carboxylic acids of some temperate lacustrine and sub-tropical lagoonal/tidal flat sediments

Analyses of the lipid constituents of three temperate lacustrine sediments (Rostherne Mere, Esthwaite Water and Grasmere, Great Britain) and three sub-tropical lagoonal/tidal flat sediments (U.S. Virgin Islands, Rockhampton, Qld., Australia and Port Moresby, Papua, New Guinea) indicate the presence of straight-chain components attributable to autochthonous and allochthonous sources. Despite broad similarities in carbon-number distributions, minor differences observed in the respective hydrocarbon and in the respective fatty-acid compositions of the various sediments reflect differences in the sedimentary environments. Lipid constituents obtained by organic solvent extraction following acid hydrolysis appear to include a larger bacterial contribution than that observed in the lipids extracted by solvent alone.     

Flogging a dead norm? Newspaper coverage of anthropogenic climate change in the United States and United Kingdom from 2003 to 2006

The journalistic norm of 'balanced' reporting (giving roughly equal coverage to both sides in any significant dispute) is recognised as both useful and problematic in communicating emerging scientific consensus on human attribution for global climate change. Analysis of the practice of this norm in United States (US) and United Kingdom (UK) newspaper coverage of climate science between 2003 and 2006 shows a significant divergence from scientific consensus in the US in 2003–4, followed by a decline in 2005–6, but no major divergence in UK reporting. These findings inform ongoing considerations about the spatially-differentiated media terms and conditions through which current and future climate policy is negotiated and implemented.