ELF and VLF wave generation by HF heating: A comparison of AM and CW techniques

Antenna field 2 of the Tromsø Heating facility consists of six rows of six horizontal crossed full wave dipoles aligned with the rows running geographic east-west. In previous experiments on ELF/VLF wave generation it has been the practice to feed the rows in parallel, with HF radiation amplitude modulated at the ELF/VLF frequency it was desired to radiate (AM configuration). Here we describe how the antenna array was also configured so that it could be fed with a continuous wave (CW) input power but still carry information at an ELF/VLF frequency. To effect this the three southern most rows of the antenna array were driven with a CW signal at 4.04 MHz and the three northernmost rows with a CW signal at frequency greater than 4.04 MHz by the ELF/VLF frequency it was desired to radiate (CW configuration). Experiments were performed with modulation/difference frequencies of 565 and 2005 Hz and the signals were received at the Lycksele Geophysical Observatory, 500 km south of the heating facility. The signals were typically 11 dB greater in the AM than the CW configuration, despite the fact that the average power delivered to the ionosphere in the CW configuration was four times that in the AM configuration. Significant harmonic radiation (both odd and even) was produced in the AM configuration but no harmonic radiation was detected in the CW configuration. A simple theory has been developed to model the fields produced by HF heating using the two techniques (AM,CW). A good agreement has been obtained between the experimental observations and model computations. The model has been extended to show how the relative efficiency of generation, AM/CW, varies with the frequency of the ELF/VLF radiation and HF antenna element spacing. Radiation patterns for the ‘ionospheric ELF/VLF antenna’ have also been derived for the two generation techniques.     

Calcium carbonate dissolution in deep sea sediments: reconciling microelectrode, pore water and benthic flux chamber results

We report the benthic fluxes of O₂, titration alkalinity (TA), Ca²⁺, NO₃⁻, PO₄³⁻, and Si(OH)₄ from in situ benthic flux chamber incubations on the Ceara Rise and Cape Verde Plateau and compare them to previously published results. We find within analytical uncertainty that the TA flux is twice the calcium flux, suggesting that dissolution/precipitation of CaCO₃ is the principal mechanism controlling benthic TA and Ca²⁺ fluxes. At sites where the sediments contain significant (>35%) CaCO₃ and the overlying waters are supersaturated with respect to CaCO₃, the ratios of the total dissolution rate to the remineralization rate are significantly less than at all other study sites. We propose that these observations can be explained by precipitation of fresh CaCO₃ at the supersaturated sediment surface followed by redissolution deeper in the sediments because of metabolically-produced CO₂. A numerical simulation is presented to demonstrate the feasibility of this explanation. In addition, surface exchange reactions in high-CaCO₃ sediments coupled with high rates of particle mixing may also impact rates of metabolic dissolution and depress chamber-derived estimates of carbonate alkalinity and calcium benthic fluxes. These results suggest that at supersaturated, high CaCO₃ locations, previous models of sediment diagenesis may have overestimated the impact of metabolic dissolution on the preservation of CaCO₃ deposited on the sea floor.     

Lithium isotopes in the system Qz-Ms-fluid:An experimental study

The fractionation of lithium isotopes among quartz, muscovite, and a chloride-bearing aqueous fluid has been investigated experimentally at 400°-500°C and 50-100 MPa. Experiments were performed for 15-60 days in cold seal vessels with natural mineral specimens. Lithium was introduced primarily through the fluid, which also contained KCl and HCl. In most runs, the fluid was prepared with the L-SVEC standard (δ⁷Li = 0) and was 1 M in total chloride with K/Li/H = 100/10/1. In two experiments, a ⁶Li spike was employed. The experiments demonstrate that quartz and muscovite are susceptible to pronounced, rapid shifts in Li isotopic composition by diffusion through interaction with a Li-bearing fluid, particularly at 500°C. At 500°C, fractionation factors were determined to be Δ_{quartz-aqueous} ≅ +8 to + 12‰ and Δ_{muscovite-aqueous} ≅ +18 to + 20‰. An intermineral fractionation factor is given by Δ_{muscovite-quartz} ≈ +9‰. At 400°C, the results suggest Δ_{quartz-aqueous} ≈ +4 to + 6‰. The study provides evidence of systematic fractionation in lithium isotopes at the temperatures of some magmatic processes, such as those associated with porphyry-type ore systems and pegmatites.     

Isotopic constraints on Columbia River flood basalt genesis and the nature of the subcontinental mantle

Pb, O, Nd, and Sr isotopic data for the Columbia River basalts paint a complex picture for the origin of this flood basalt province. At least 3 distinct mantle sources appear to have been involved, superimposed upon which are the effects of crystal fractionation and mass exchange with evolved crustal wallrocks. To a large degree, the initiation of Columbia River volcanism and the geochemical characteristics of the basalts appear to have been influenced by subduction of the Juan de Fuca plate beneath the North American plate in a manner analogous to the origin of back-arc basins. The physical structure of the crust appears to have influenced the late stage evolution of the magmas by directing the locus of eruption to the border between the ancient continental interior and much younger crust to the south and west. This proximity to the continental interior also allowed old enriched subcontinental mantle to become involved in the very late stages of Columbia River volcanism. An important consequence of the existence of enriched mantle regions beneath continents is that the combination, crust plus enriched mantle, requires more incompatible elements to have been extracted from the remainder of the mantle than would be the case if no enriched mantle existed.     

pp′-DDT adsorption to suspended particulate matter in sea water

A procedure was devised to study pp′-DDT [2,2-bis($\text{p-}\text{chlorophenyl}$)-1,1,1-trichloroethane] adsorption and desorption to suspended particulates in aqueous solutions. DDT adsorption to a marine sediment, sediment fractions, clay and humic acid suspended in sea water was investigated and the humic fraction was found to have a greater adsorbing capacity than the clay or sediment. Removal of the humic fraction from sediment reduced the adsorption capacity to less than 60 per cent of the original sediment sample. It was concluded that suspended humic particulates may be important agents for transporting chlorinated hydrocarbons through the water column and for concentrating them in sediments and in detritus-feeding organisms.     

The effect of annealing on the luminescence decay-time of synthetic calcite:Mn

Calcite was synthesized by four methods, and the luminescence decay-time was measured for nine samples before and after heating hydrothermally in the temperature range 200–400°C. Decay-time data were collected between room temperature and approximately 15 K. The decay time at room temperature is approximately 50 ms, with little difference between a given calcite before and after hydrothermal treatment. The decay time at 15 K is always greater than at room temperature as the effect of thermal quenching diminishes. Differences in decay time before and after heating are more apparent at low temperature owing to this reduction in thermal quenching. The decay time decreased significantly in two samples, and an increase in decay time was observed in the remaining seven samples following heating. Among the latter group, the change in decay time was insignificant in three samples. The results are compared with previous data in which it was shown that the effect of heating is to increase the intensity of luminescence.     

An Anatomy of Adaptation to Climate Change and Variability

Adaptation to climate variability and change is important both for impact assessment (to estimate adaptations which are likely to occur) and for policy development (to advise on or prescribe adaptations). This paper proposes an "anatomy of adaptation" to systematically specify and differentiate adaptations, based upon three questions: (i) adapt to what? (ii) who or what adapts? and (iii) how does adaptation occur? Climatic stimuli include changes in long-term mean conditions and variability about means, both current and future, and including extremes. Adaptation depends fundamentally on the characteristics of the system of interest, including its sensitivities and vulnerabilities. The nature of adaptation processes and forms can be distinguished by numerous attributes including timing, purposefulness, and effect. The paper notes the contribution of conceptual and numerical models and empirical studies to the understanding of adaptation, and outlines approaches to the normative evaluation of adaptation measures and strategies.