Incubation experiments to examine the production and loss of CH3I in surface seawater

In order to investigate production pathways of methyl iodide and controls on emissions from the surface ocean, a set of repeated in-vitro incubation experiments were performed over an annual cycle in the context of a time-series of in-situ measurements in Kiel Fjord (54.3 N, 10.1E). The incubation experiments revealed a diurnal variation of methyl iodide in samples exposed to natural light, with maxima during day time and losses during night hours. The amplitude of the daily accumulation varied seasonally and was not affected by filtration (0.2µm), consistent with a photochemical pathway for CH3I production. The methyl iodide loss rate during night time correlated with the concentration accumulated during daytime. Daily (24 hour) net production (Pnet) was similar in magnitude between in vitro and in situ mass balances. However, the estimated gross production (Pgross) of methyl iodide ranged from -0.07 to 2.24 pmol/day and were 5 times higher in summer than Pnet calculated from the in-situ study [Shi et al., 2014]. The large excess of Pgross over Pnet revealed by the in-vitro (incubation) experiments in summer is a consequence of large losses of CH3I by as-yet uncharacterized processes (e.g. biological degradation or chemical pathways other than Cl- substitution).

(Table 1) Granulometry, soil pH, carbonate content and color description of soil profiles obtained in Xinghai, Tibet

Large parts of the eastern half of the Tibetan Plateau are covered between (3,500) 4,000 and nearly 6,000 m a.s.l. by alpine sedge mats (key species Kobresia pygmea), which attain an extension of ca. 450,000 km**2. It is considered to be the world's largest alpine ecosystem. Moreover, there exist isolated (relic) forests in the same area up to an altitude of 4,700 m a.s.l. mainly consisting of juniper (Juniperus) and spruce (Picea). Large parts of the Kobresia ecosystem are expected to be a grazing-resistant replacement formation, replacing forests and grass-dominated plant communities due to human and/or climatic impact. Recently, a research project was launched to increase knowledge about the properties and genesis of these forests and sedge mats (Present-day dynamics and Holocene landscape history of fragmented forest biocoenoses in Tibet; headed by G. Miehe, Marburg).

Granulometry, calcium carbonate content and radiocarbon ages of soil profiles obtained in Quinghai Province, northeast Tibet

Colluvial deposits consisting of silts and loams were detected in several climatologically different areas of NE Tibet (3200-3700 m a.s.l.). Layering, distinct organic content and low content of coarse matter as well as location in the relief revealed an origin from low-energy slope erosion (hillwash). Underlying and intercalated paleosols were classified as Chernozems, Phaeozems, Regosols and Fluvisols. Fifteen radiocarbon datings predominant on charcoal from both colluvial layers and paleosols yielded ages between 8988 ± 66 and 3512 ± 56 uncal BP. Natural or anthropogenic factors could have been the triggers of the erosional processes derived. It remains unclear which reason was mainly responsible, due to controversial paleoclimatic and geomorphic records as well as insufficient archaeological knowledge from this region. Determinations of charcoal and fossil wood revealed the Holocene occurrence of tree species (spruce, juniper) for areas which nowadays have no trees or only few forest islands. Thus large areas of NE Tibet which are at present steppes and alpine pastures were forested in the past.

(Table 12-4, page 360) Percentage loss of water from manganese nodules (on a wet basis) at different temperatures

This chapter discusses the formation and distribution of some metals in ocean-floor manganese nodules in the light of the observed data in the literature and thermodynamic and kinetic considerations of the oxidation of metal ions in the oceanic environment. There are, in general, two major schools of thought on the mechanism of incorporation of the minor elements such as nickel, copper, and cobalt with the major elements such as manganese and iron. One is the lattice substitution mechanism and the other the adsorption mechanism. If the mechanism is lattice substitution, extraction of the metal ions is not possible unless the lattice of the major elements is first broken and exchanged with other ions from the bulk solution. Consequently, the leaching behavior of minor elements should display a very close relationship with that of major elements.