Isotope fractionation of neon during stepheating extraction?: a comment on ‘Re‐interpretation of the existence of a primitive plume under Australia based on neon isotope fractionation during step heating’ by Gautheron and Moreira (2003)

Using a Rayleigh distillation fractionation model, we calculate that the maximum isotope fractionation potentially achievable is less than 5% during the early stages of gas release from a sample. Our calculation corrects the erroneous conclusions of Gautheron and Moreira (2003), who re‐interpreted the plume‐like neon isotopic compositions found in metasomatic apatite from a south‐eastern Australian xenolith (Matsumoto et al., 1997) to be the result of Rayleigh‐type isotope fractionation of originally MORB‐type neon during stepheating gas extraction. We stress that the modelling of neon isotopic fractionation by Gautheron and Moreira (2003) is incorrect, and that the finding of a plume‐like neon isotopic composition in the apatite by Matsumoto et al. (1997) remains a quite valid and robust conclusion.     

The height,spectrum and mechanism of type-B red aurora and its bearing on the excitation of O(1S) in aurora

The height of the lower red border of type-B aurora has been determined by triangulation using TV cameras at two ground stations. A mean height of 91.4 ± 1.1 km was determined from a set of 12 measurements made under ideal conditions. A TV spectrograph was used simultaneously to seek possible spectral changes between 6400 and 6900 Å which would be indicative of changes in the vibrational distribution in the N₂ First Positive bands. No significant difference was found in this distribution between the spectra from 93 and 122 km. The height distribution of contributions to the OI 5577 Å emission relative to the N⁺₂ First Negative emission was modelled from 80 to 160 km. Contributions from electron impact on atomic O, O⁺₂ dissociative recombination and N₂(A)O energy transfer were included. Account was taken of recent laboratory data on O(¹S) quenching. It was concluded that these processes could explain the excitation of O(¹S) in normal aurora and the height distribution of OI 5577 Å in type-B red aurora. It was confirmed that the lifetime ofO(¹S) in type-B red auroral rapid time variations is about 0.5 s and it was found from the model that the observed time variation can be reproduced by the mechanisms considered, provided the concentration of NO in the auroral atmosphere is about 1 × 10⁹ at 95 km. Before reasonable certainty can be attained in the correctness of the interpretation it will however be necessary to have reliable simultaneous observations of neutral atmospheric composition particularly for O and NO as well as unchallengeable measurements of the yields of O(¹S) for the processes considered and for several other processes which have been suggested recently.     

Functional responses for zooplankton feeding on multiple resources: a review of assumptions and biological dynamics

Modelers often need to quantify the rates at which zooplankton consume a variety of species, size classes and trophic types. Implicit in the equations used to describe the multiple resource functional response (i.e. how nutritional intake varies with resource densities) are assumptions that are not often stated, let alone tested. This is problematic because models are sensitive to the details of these formulations. Here, we enable modelers to make more informed decisions by providing them with a new framework for considering zooplankton feeding on multiple resources. We define a new classification of multiple resource responses that is based on preference, selection and switching, and we develop a set of mathematical diagnostics that elucidate model assumptions. We use these tools to evaluate the assumptions and biological dynamics inherent in published multiple resource responses. These models are shown to simulate different resource preferences, implied single resource responses, changes in intake with changing resource densities, nutritional benefits of generalism, and nutritional costs of selection. Certain formulations are further shown to exhibit anomalous dynamics such as negative switching and sub-optimal feeding. Such varied responses can have vastly different ecological consequences for both zooplankton and their resources; inappropriate choices may incorrectly quantify biologically-mediated fluxes and predict spurious dynamics. We discuss how our classes and diagnostics can help constrain parameters, interpret behaviors, and identify limitations to a formulation's applicability for both regional (e.g. High-Nitrate-Low-Chlorophyll regions comprising large areas of the Pacific) and large-scale applications (e.g. global biogeochemical or climate change models). Strategies for assessing uncertainty and for using the mathematics to guide future experimental investigations are also discussed.     

Effects of polynuclear aromatic hydrocarbons on lysosomal membranes in molluscs

Lysosomal sequestration of polynuclear aromatic hydrocarbons (PNAHs), a major class of environmental contaminant, is a well-established phenomenon;¹ considerably less is known about their pathological effects on lysosomes. Marine molluscs contain a number of lysosome-rich tissues and PNAHs are known to induce deleterious alterations in lysosomal structure and latency of lysosomal enzymes.² The latter are presumed to involve destabilisation of the lysosomal membrane, resulting in increased permeability and reduced enzyme latency. If lysosomal injury involves derangement of membrane-lipid structure due to the interaction of PNAHs then it would be expected that membrane damage would be closely linked to the structural characteristics of the intruding molecule. Our results show that the effects of the isomeric PNAHs phenanthrene and anthracene on digestive cell lysosomal stability were markedly different in the marine mussel (Mytilus edulis) over the same range of tissue concentrations. Lysosomal membrane stability was determined using a cytochemical test for enzyme latency.³     

The influence of amphibole fractionation on the evolution of calc-alkaline andesite and dacite tephra from the central Aleutians,Alaska

Petrologic studies of tephra from Kanaga, Adak, and Great Sitkin Islands indicate that amphibole fractionation and magma mixing are important processes controlling the composition of calc-alkaline andesite and dacite magmas in the central Aleutians. Amphibole is ubiquitous in tephra from Kanaga and Adak Islands, whereas it is present only in a basaltic-andesite pumice from Great Sitkin. Dacitic tephra from Great Sitkin do not contain amphibole. Hornblende dacite tephra contain HB+PLAG+OX±OPX±CPX phenocrysts with simple zoning patterns, suggesting that the dacites evolved in isolated magma chambers. Andesitic tephra from Adak contain two pyroxene and hornbelende populations, and reversely zoned plagioclase, indicating a more complex history involving mixing and fractional crystallization. Mass balance calculations suggest that the andesitic tephra may represent the complements of amphibole-bearing cumulate xenoliths, both formed during the evolution of high-Al basalts. The presence of amphibole in andesitic and dacitic tephra implies that Aleutian cale-alkaline magmas evolve in the mid to lower crust under hydrous (>4 wt.% H₂O) and oxidizing (Ni–NiO) conditions. Amphibole-bearing andesites and pyroxene-bearing dacites from Great Sitkin indicates fractionation at several levels within the arc crust. Despite its absence in many calc-alkaline andesite and dacite lavas, open system behavior involving amphibole fractionation can explain the trace element characteristies of lavas found on Adak Island. Neither open nor closed system fractionation involving a pyroxene-bearing assemblage is capable of explaining the trace element concentrations or ratios found in the Adak suite. We envision a scenario where amphibole was initially a liquidus phase in many calc-alkaline magmas, but was later replaced by pyroxenes as the magmas rose to shallow levels within the crust. The mineral assemblage in these evolved lavas reflects shallow level equilibration of the magma, whereas the trace element chemistry provides evidence for a earlier, amphibole-bearing, mineral assemblage.     

Denitrification rates measured along a salinity gradient in the eutrophic Neuse River estuary, North Carolina, USA

Denitrification rates along a salinity gradient in the eutrophic Neuse River Estuary, North Carolina, were quantified using membrane inlet mass spectrometry (MIMS) within short-term batch incubations. Denitrification rates within the system were highly variable, ranging from 0 to 275 μmol N m⁻² h⁻¹. Intrasite variability increased with salinity, but no significant differences were observed across the salinity gradient. Denitrification rates were positively correlated with sediment oxygen demand at the upstream sampling site where sediment organic carbon levels were lowest. This relationship was not observed in the more saline sampling sites. Denitrification rates were highest during winter. On an annual basis, denitrification accounted for 26% of the dissolved inorganic nitrogen and 12% of the total nitrogen supplied to the system.     

Closely related thyasirid bivalves associate with multiple symbiont phylotypes

Species of thyasirid bivalves are considered to be representative of early stages of chemosymbiosis, given that bacterial symbionts occur outside gill epithelial cells, vary among species in their abundance and nutritional importance, and are environmentally acquired. For these reasons, assessing the extent of host–symbiont specificity in thyasirids could provide valuable information on the evolution of chemosymbiosis. We show that individuals of two closely related and sympatric Thyasira cf. gouldi operational taxonomic units collected from three sites in a fjord in Newfoundland, Canada, associate with one of three distinct, closely related symbiont phylotypes. While associations show some site‐specificity, there is flexibility in host–symbiont pairings within the fjord, further supporting an early and relatively unspecific stage of chemosymbiosis in this family. Morphologic differences observed both within and among symbiont phylotypes suggest physiologic variation, possibly induced by small‐scale differences in sedimentary conditions.     

Characterisation of primary and secondary carbonates in hypabyssal kimberlites: an integrated compositional and Sr-isotopic approach

Carbonates in fresh hypabyssal kimberlites worldwide have been studied to understand their origin [i.e. primary magmatic (high T) versus deuteric (‘low T’) versus hydrothermal/alteration (‘low T’)] and identify optimal strategies for petrogenetic studies of kimberlitic carbonates. The approach presented here integrates detailed textural characterisation, cathodoluminescence (CL) imaging, in situ major- and trace-element analysis, as well as in situ Sr-isotope analysis. The results reveal a wide textural diversity. Calcite occurs as fine-grained groundmass, larger laths, segregations, veins or as a late crystallising phase, replacing olivine or early carbonates. Different generations of carbonates commonly coexist in the same kimberlite, each one defined by a characteristic texture, CL response and composition (e.g., variable Sr and Ba concentrations). In situ Sr isotope analysis revealed a magmatic signature for most of the carbonates, based on comparable ⁸⁷Sr/⁸⁶Sr values between these carbonates and the coexisting perovskite, a robust magmatic phase. However, this study also shows that in situ Sr isotope analysis not always allow distinction between primary (i.e., magmatic) and texturally secondary carbonates within the same sample. Carbonates with a clear secondary origin (e.g., late-stage veins) occasionally show the same moderately depleted ⁸⁷Sr/⁸⁶Sr ratios of primary carbonates and coexisting perovskite (e.g., calcite laths-shaped crystals with ⁸⁷Sr/⁸⁶Sr values identical within uncertainty to those of vein calcite in the De Beers kimberlite). This complexity emphasises the necessity of integrating detailed petrography, geochemical and in situ Sr isotopic analyses for an accurate interpretation of carbonate petrogenesis in kimberlites. Therefore, the complex petrogenesis of carbonates demonstrated here not only highlights the compositional variability of kimberlites, but also raises concerns about the use of bulk-carbonate C-O isotope studies to characterise the parental melt compositions. Conversely, our integrated textural and in situ study successfully identifies the most appropriate (i.e. primary) carbonates for providing constraints on the isotopic parameters of parental kimberlite magmas.