Writing difference differently

This paper investigates the writing of situated knowledge and explores the possibilities of enacting difference by writing differently. We present a selection of research stories in which carrier bags, sounds, baskets, gardens and potatoes are interpreted less as objects of research or metaphors to aid in analysing phenomena, than as mediators of the stories. Our stories emphasise the ontological politics of engaging with and representing the relational, the messy, the spontaneous, the unpredictable, the non‐human and bodily experiences. These stories demonstrate how writing is performative and how it is integral to the production of knowledge.     

Submarine groundwater discharge is an important net source of light and middle REEs to coastal waters of the Indian River Lagoon, Florida, USA

Porewater (i.e., groundwater) samples were collected from multi-level piezometers across the freshwater-saltwater seepage face within the Indian River Lagoon subterranean estuary along Florida’s (USA) Atlantic coast for analysis of the rare earth elements (REE). Surface water samples for REE analysis were also collected from the water column of the Indian River Lagoon as well as two local rivers (Eau Gallie River, Crane Creek) that flow into the lagoon within the study area. Concentrations of REEs in porewaters from the subterranean estuary are 10-100 times higher than typical seawater values (e.g., Nd ranges from 217 to 2409 pmol kg⁻¹), with submarine groundwater discharge (SGD) at the freshwater-saltwater seepage face exhibiting the highest REE concentrations. The elevated REE concentrations for SGD at the seepage face are too high to be the result of simple, binary mixing between a seawater end-member and local terrestrial SGD. Instead, the high REE concentrations indicate that geochemical reactions occurring within the subterranean estuary contribute substantially to the REE cycle. A simple mass balance model is used to investigate the cycling of REEs in the Indian River Lagoon and its underlying subterranean estuary. Mass balance modeling reveals that the Indian River Lagoon is approximately at steady-state with respect to the REE fluxes into and out of the lagoon. However, the subterranean estuary is not at steady-state with respect to the REE fluxes. Specifically, the model suggests that the SGD Nd flux, for example, exported from the subterranean estuary to the overlying lagoon waters exceeds the combined input to the subterranean estuary from terrestrial SGD and recirculating marine SGD by, on average, ∼100 mmol day⁻¹. The mass balance model also reveals that the subterranean estuary is a net source of light REEs (LREE) and middle REEs (MREE) to the overlying lagoon waters, but acts as a sink for the heavy REEs (HREE). Geochemical modeling and statistical analysis further suggests that this fractionation occurs, in part, due to the coupling between REE cycling and iron redox cycling within the Indian River Lagoon subterranean estuary. The net SGD flux of Nd to the Indian River Lagoon is ∼7-fold larger than the local effective river flux to these coastal waters. This previously unrecognized source of Nd to the coastal ocean could conceivably be important to the global oceanic Nd budget, and help to resolve the oceanic “Nd paradox” by accounting for a substantial fraction of the hypothesized missing Nd flux to the ocean.     

Computer simulations of the interactions of the (0 1 2) and (0 0 1) surfaces of jarosite with Al, Cd, Cu and Zn

Jarosite is an important mineral on Earth, and possibly on Mars, where it controls the mobility of iron, sulfate and potentially toxic metals. Atomistic simulations have been used to study the incorporation of Al³⁺, and the M²⁺ impurities Cd, Cu and Zn, in the (0 1 2) and (0 0 1) surfaces of jarosite. The calculations show that the incorporation of Al on an Fe site is favorable on all surfaces in which terminal Fe ions are exposed, and especially on the (0 0 1) [Fe₃(OH)₃]⁶⁺ surface. Incorporation of Cd, Cu or Zn on a K site balanced by a K vacancy is predicted to stabilize the surfaces, but calculated endothermic solution energies and the high degree of distortion of the surfaces following incorporation suggest that these substitutions will be limited. The calculations also suggest that incorporation of Cd, Cu and Zn on an Fe site balanced by an OH vacancy, or by coupled substitution on both K and Fe sites, is unfavorable, although this might be compensated for by growth of a new layer of jarosite or goethite, as predicted for bulk jarosite. The results of the simulations show that surface structure will exert an influence on uptake of impurities in the order Cu > Cd > Zn, with the most favorable surfaces for incorporation being (0 1 2) [KFe(OH)₄]⁰ and (0 0 1) [Fe₃(OH)₃]⁶⁺.     

Injection System for Multiwell Injection Using a Single Pump

Many hydrological and geochemical studies rely on data resulting from injection of tracers and chemicals into groundwater wells. The even distribution of liquids to multiple injection points can be challenging or expensive, especially when using multiple pumps. An injection system was designed using one chemical metering pump to evenly distribute the desired influent simultaneously to 15 individual injection points through an injection manifold. The system was constructed with only one metal part contacting the fluid due to the low pH of the injection solutions. The injection manifold system was used during a 3‐month pilot scale injection experiment at the Vineland Chemical Company Superfund site. During the two injection phases of the experiment (Phase I = 0.27 L/min total flow, Phase II = 0.56 L/min total flow), flow measurements were made 20 times over 3 months; an even distribution of flow to each injection well was maintained (RSD < 4%). This durable system is expandable to at least 16 injection points and should be adaptable to other injection experiments that require distribution of air‐stable liquids to multiple injection points with a single pump.     

Bacterial hopanoids as tracers of organic carbon sources and processing across the western Arctic continental shelf

Tracing the inputs of bacterial organic carbon to marine systems has been constrained by the lack of distinguishing geochemical tracers and limited contribution in sediments compared to other sources of organic matter. Bacteriohopanepolyols (BHPs) provide a direct means to identify bacterial inputs which also reflect potential bacterial groups and their activities in aquatic systems. We applied recent analytical approaches to identify and quantify bacterial derived carbon contributions to surface sediments from the western Arctic Ocean using BHPs. The abundance and distribution of BHPs resemble trends of water column primary production and suggest active heterotrophic recycling of in situ production with some component of long term preservation. BHPs proposed as terrestrial derived signatures (i.e. adenosylhopanes) were also abundant in western Arctic sediments and reflect offshore trends of other terrigenous lipid signatures with a fraction representing their degradative products. Analysis of BHPs in organic rich peat and surface sediments from two Arctic rivers showed the highest inputs of adenosylhopanes, implying active bacterial recycling of recalcitrant terrigenous material. BHPs observed in western Arctic surface sediments reveal significant contributions of bacteria associated with organic carbon from multiple sources.     

Taxonomic composition,paleoecology and biostratigraphy of Late Cretaceous diatoms from Devon Island,Nunavut, Canadian High Arctic

Upper Cretaceous sediments of the Kanguk Formation exposed in Eidsbotn and Viks Fiord grabens on Devon Island, Nunavut, Canadian High Arctic, yielded 91 fossil marine diatom species and varieties (including indeterminate taxa), representing 41 genera. Excellent preservation of the assemblages was aided by shallow burial, protection in downfaulted linear grabens, and the presence of abundant volcanic material. Planktonic species and resting spores comprise nearly 70% of the diatom assemblage, and provided abundant food resources for the Late Cretaceous Arctic ecosystem. Deposition of the approximately 225 m-thick stratigraphic sequence was predominantly in a shallow marine neritic setting, with an upward progression to interbedded terrestrial deposits of the Expedition Fiord Formation, reflecting a regression and eventual persistence of terrestrial facies into the Early Cenozoic. The Kanguk Formation is widespread across the Canadian Arctic, and diatom biostratigraphy indicates a Santonian–Campanian age for the sequences reported herein, based on the presence of Gladius antiquus in the lowermost strata and occurrence of Costopyxis antiqua throughout the succession. However, Amblypyrgus sp. A and Archepyrgus sp. aff. A. melosiroides, encountered in the lower part of the succession, are known exclusively from the Lower Cretaceous. This may suggest a slightly older age. New information on shallow shelf diatom assemblages from this study is compared to reports on two other Late Cretacous Arctic diatom assemblages. These three sites represent an environmental transect from shallow to distal shelf settings and into the oceanic realm.     

The ~4-ka Rungwe Pumice (South-Western Tanzania): a wind-still Plinian eruption

The ~4-ka trachytic Rungwe Pumice (RP) deposit from Rungwe Volcano in South-Western Tanzania is the first Plinian-style deposit from an African volcano to be closely documented focusing on its physical characterization. The RP is a mostly massive fall deposit with an inversely graded base. Empirical models suggest a maximum eruption column height H _T of 30.5–35 km with an associated peak mass discharge rate of 2.8–4.8 × 10⁸ kg/s. Analytical calculations result in H _T values of 33 ± 4 km (inversion of TEPHRA2 model on grain size data) corresponding to mass discharge ranging from 2.3 to 6.0 × 10⁸ kg/s. Lake-core data allow extrapolation of the deposit thinning trend far beyond onland exposures. Empirical fitting of thickness data yields volume estimates between 3.2 and 5.8 km³ (corresponding to an erupted mass of 1.1–2.0 × 10¹² kg), whereas analytical derivation yields an erupted mass of 1.1 × 10¹² kg (inversion of TEPHRA2 model). Modelling and dispersal maps are consistent with nearly no-wind conditions during the eruption. The plume corner is estimated to have been ca. 11–12 km from the vent. After an opening phase with gradually increasing intensity, a high discharge rate was maintained throughout the eruption, without fountain collapse as is evidenced by a lack of pyroclastic density current deposits.     

Physiological effects of hypercapnia in the deep-sea bivalve Acesta excavata (Fabricius, 1779) (Bivalvia; Limidae)

The option of storing CO₂ in subsea rock formations to mitigate future increases in atmospheric CO₂ may induce problems for animals in the deep sea. In the present study the deep-sea bivalve Acesta excavata was subjected to environmental hypercapnia (pHSW 6.35, PCO₂ = 33,000 μatm) corresponding to conditions reported from natural CO₂ seeps. Effects on acid–base status and metabolic rate were related to time of exposure and subsequent recovery. During exposure there was an uncompensated drop in both hemolymph and intracellular pH. Intracellular pH returned to control values, while extracellular pH remained significantly lower during recovery. Intracellular non-bicarbonate buffering capacity of the posterior adductor muscle of hypercapnic animals was significantly lower than control values, but this was not the case for the remaining tissues analyzed. Oxygen consumption initially dropped by 60%, but then increased during the final stages of exposure, which may suggest a higher tolerance to hypercapnia than expected for a deep-living species.     

Dissolved and particulate organic carbon in hydrothermal plumes from the East Pacific Rise, 9°50′N

Chemoautotrophic production in seafloor hydrothermal systems has the potential to provide an important source of organic carbon that is exported to the surrounding deep-ocean. While hydrothermal plumes may export carbon, entrained from chimney walls and biologically rich diffuse flow areas, away from sites of venting they also have the potential to provide an environment for in-situ carbon fixation. In this study, we have followed the fate of dissolved and particulate organic carbon (DOC and POC) as it is dispersed through and settles beneath a hydrothermal plume system at 9°50′N on the East Pacific Rise. Concentrations of both DOC and POC are elevated in buoyant plume samples that were collected directly above sites of active venting using both DSV Alvin and a CTD-rosette. Similar levels of POC enrichment are also observed in the dispersing non-buoyant plume, ∼500 m downstream from the vent-site. Further, sediment-trap samples collected beneath the same dispersing plume system, show evidence for a close coupling between organic carbon and Fe oxyhydroxide fluxes. We propose, therefore, a process that concentrates POC into hydrothermal plumes as they disperse through the deep-ocean. This is most probably the result of some combination of preferential adsorption of organic carbon onto Fe-oxyhydroxides and/or microbial activity that preferentially concentrates organic carbon in association with Fe-oxyhydroxides (e.g. through the microbial oxidation of Fe(II) and Fe sulfides). This potential for biological production and consumption within hydrothermal plumes highlights the importance of a multidisciplinary approach to understanding the role of the carbon cycle in deep-sea hydrothermal systems as well as the role that hydrothermal systems may play in regulating global deep-ocean carbon budgets.     

Development and deployment of a precision underwater positioning system for in situ laser Raman spectroscopy in the deep ocean

The field of ocean geochemistry has recently been expanded to include in situ laser Raman spectroscopic measurements in the deep ocean. While this technique has proved to be successful for transparent targets, such as fluids and gases, difficulty exists in using deep submergence vehicle manipulators to position and control the very small laser spot with respect to opaque samples of interest, such as many rocks, minerals, bacterial mats, and seafloor gas hydrates. We have developed, tested, and successfully deployed by remotely operated vehicle (ROV) a precision underwater positioner (PUP) which provides the stability and precision movement required to perform spectroscopic measurements using the Deep Ocean Raman In situ Spectrometer (DORISS) instrument on opaque targets in the deep ocean for geochemical research. The positioner is also adaptable to other sensors, such as electrodes, which require precise control and positioning on the seafloor. PUP is capable of translating the DORISS optical head with a precision of 0.1 mm in three dimensions over a range of at least 15 cm, at depths up to 4000 m, and under the normal range of oceanic conditions (T, P, current velocity). The positioner is controlled, and spectra are obtained, in real time via Ethernet by scientists aboard the surface vessel. This capability has allowed us to acquire high quality Raman spectra of targets such as rocks, shells, and gas hydrates on the seafloor, including the ability to scan the laser spot across a rock surface in sub-millimeter increments to identify the constituent mineral grains. These developments have greatly enhanced the ability to obtain in situ Raman spectra on the seafloor from an enormous range of specimens.