Phenological shifts and mismatch with marine productivity vary among Pacific salmon species and populations.

Global climate change is shifting the timing of life-cycle events, sometimes resulting in phenological mismatches between predators and prey. Phenological shifts and subsequent mismatches may be consistent across populations, or they could vary unpredictably across populations within the same species. For anadromous Pacific salmon (Oncorhynchus spp.), juveniles from thousands of locally adapted populations migrate from diverse freshwater habitats to the Pacific Ocean every year. Both the timing of freshwater migration and ocean arrival, relative to nearshore prey (phenological match/mismatch), can control marine survival and population dynamics. Here we examined phenological change of 66 populations across six anadromous Pacific salmon species throughout their range in western North America with the longest time series spanning 1951-2019. We show that different salmon species have different rates of phenological change but that there was substantial within-species variation that was not correlated with changing environmental conditions or geographic patterns. Moreover, outmigration phenologies have not tracked shifts in the timing of marine primary productivity, potentially increasing the frequency of future phenological mismatches. Understanding population responses to mismatches with prey are an important part of characterizing overall population-specific climate vulnerability.

Exploring the Role of the Connection Length of Screen-Printed Electrodes towards the Hydrogen and Oxygen Evolution Reactions.

Zero-emission hydrogen and oxygen production are critical for the UK to reach net-zero greenhouse gasses by 2050. Electrochemical techniques such as water splitting (electrolysis) coupled with renewables energy can provide a unique approach to achieving zero emissions. Many studies exploring electrocatalysts need to "electrically wire" to their material to measure their performance, which usually involves immobilization upon a solid electrode. We demonstrate that significant differences in the calculated onset potential for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) can be observed when using screen-printed electrodes (SPEs) of differing connection lengths which are immobilized with a range of electrocatalysts. This can lead to false improvements in the reported performance of different electrocatalysts and poor comparisons between the literature. Through the use of electrochemical impedance spectroscopy, uncompensated ohmic resistance can be overcome providing more accurate Tafel analysis.

Marine and freshwater regime changes impact a community of migratory Pacific salmonids in decline.

Marine and freshwater ecosystems are increasingly at risk of large and cascading changes from multiple human activities (termed "regime shifts"), which can impact population productivity, resilience, and ecosystem structure. Pacific salmon exhibit persistent and large fluctuations in their population dynamics driven by combinations of intrinsic (e.g., density dependence) and extrinsic factors (e.g., ecosystem changes, species interactions). In recent years, many Pacific salmon have declined due to regime shifts but clear understanding of the processes driving these changes remains elusive. Here, we unpacked the role of density dependence, ecosystem trends, and stochasticity on productivity regimes for a community of five anadromous Pacific salmonids (Steelhead, Coho Salmon, Pink Salmon, Dolly Varden, and Coastal Cutthroat Trout) across a rich 40-year time-series. We used a Bayesian multivariate state-space model to examine whether productivity shifts had similarly occurred across the community and explored marine or freshwater changes associated with those shifts. Overall, we identified three productivity regimes: an early regime (1976-1990), a compensatory regime (1991-2009), and a declining regime (since 2010) where large declines were observed for Steelhead, Dolly Varden, and Cutthroat Trout, intermediate declines in Coho and no change in Pink Salmon. These regime changes were associated with multiple cumulative effects across the salmon life cycle. For example, increased seal densities and ocean competition were associated with lower adult marine survival in Steelhead. Watershed logging also intensified over the past 40 years and was associated with (all else equal) ≥97% declines in freshwater productivity for Steelhead, Cutthroat, and Coho. For Steelhead, marine and freshwater dynamics played approximately equal roles in explaining trends in total productivity. Collectively, these changing environments limited juvenile production and lowered future adult returns. These results reveal how changes in freshwater and marine environments can jointly shape population dynamics among ecological communities, like Pacific salmon, with cascading consequences to their resilience.

Electrochemical Improvements Can Be Realized via Shortening the Length of Screen-Printed Electrochemical Platforms.

Screen-printed electrodes (SPEs) are ubiquitous within the field of electrochemistry and are commonplace within the arsenal of electrochemists. Their popularity stems from their reproducibility, versatility, and extremely low-cost production, allowing their utilization as single-shot electrodes and thus removing the need for tedious electrode pretreatments. Many SPE studies have explored changing the working electrode composition and/or size to benefit the researcher's specific applications. In this paper, we explore a critical parameter of SPEs that is often overlooked; namely, we explore changing the length of the SPE connections. We provide evidence of resistance changes through altering the connection length to the working electrode through theoretical calculations, multimeter measurements, and electrochemical impedance spectroscopy (EIS). We demonstrate that changing the physical length of SPE connections gives rise to more accurate heterogeneous electrode kinetics, which cannot be overcome simply through IR compensation. Significant improvements are observed when utilized as the basis of electrochemical sensing platforms for sodium nitrite, ß-nicotinamide adenine dinucleotide (NADH), and lead (II). This work has a significant impact upon the field of SPEs and highlights the need for researchers to characterize and define their specific electrode performance. Without such fundamental characterization as the length and resistance of the SPE used, direct comparisons between two different systems for similar applications are obsolete. We therefore suggest that, when using SPEs in the future, experimentalists report the length of the working electrode connection alongside the measured resistance (multimeter or EIS) to facilitate this standardization across the field.

A novel 'bottom-up' synthesis of few- and multi-layer graphene platelets with partial oxidation via cavitation.

The transient cavitation of diaromatic components such as 1-methylnaphthalene has been used to produce graphene platelets in a 'bottom-up' synthesis via the high temperature (>5000 K) conditions that are generated inside collapsing bubbles. Acoustic cavitation produced yields of 5.7 × 10-11 kgJ-1 at a production rate of 2.2 × 10-9 kgs-1. This can be improved by generating cavitation hydrodynamically, thus making commercial scale production viable. Hydrodynamic cavitation produced platelets with larger lateral dimensions (≥2 µm) than those formed by acoustic cavitation (10-200 nm). The partially oxidised nature of the platelets enables their covalent chemical functionalisation, which was achieved by combining suitable molecules in the reaction medium to affect a one-pot formation and functionalisation of graphene.

Anodic stripping voltammetry with graphite felt electrodes for the trace analysis of silver.

Graphite felt (GF) is a mass produced porous carbon electrode material commonly used in redox flow batteries. Previous studies have suggested GF may have valuable applications in electroanalysis as a low cost disposable carbon electrode material, although most GF sensors have used flow cell arrangements. In this work, an elegant wetting technique is employed that allows GF electrodes to be used in quiescent solution to detect trace levels of silver in water via anodic stripping voltammetry. GF electrodes display good repeatability and a limit of detection of 25 nM of Ag(+) in 0.1 M HNO3, with a linear range spanning two orders of magnitude. This compares to a value of around 140 nM when using conventional carbon electrodes. Combined with their low cost and disposable nature, the results suggest GF electrodes can make a valuable contribution to electroanalysis.

Extinction risk and overfishing: reconciling conservation and fisheries perspectives on the status of marine fishes.

Anthropogenic disturbances are ubiquitous in the ocean, but their impacts on marine species are hotly debated. We evaluated marine fish statuses using conservation (Red List threatened or not) and fisheries (above or below reference points) metrics, compared their alignment, and diagnosed why discrepancies arise. Whereas only 13.5% of Red Listed marine fishes (n = 2952) are threatened, 40% and 21% of populations with stock assessments (n = 166) currently are below their more conservative and riskier reference points, respectively. Conservation and fisheries metrics aligned well (70.5% to 80.7%), despite their mathematical disconnect. Red Listings were not biased towards exaggerating threat status, and egregious errors, where populations were categorized at opposite extremes of fisheries and conservation metrics, were rare. Our analyses suggest conservation and fisheries scientists will agree on the statuses of exploited marine fishes in most cases, leaving only the question of appropriate management responses for populations of mutual concern still unresolved.

An approach for modelling CO2 emissions from road traffic in urban areas.

An approach that incorporates three modelling components has been developed to estimate road traffic CO2 emissions for an urban area with street level resolution. The first component enables the determination of the road traffic characteristics using the SATURN (Simulation and Assignment of Traffic in Urban Road Networks) model. The output from this component is then analysed using MATrix LABoratory (MATLAB) programming to provide estimates of CO2 emissions for the urban area. Finally, ArcGIS is used to illustrate the model output. The three components are integrated using a Loose-Coupling approach in which the individual components each load the necessary data to give an independent output. The model structure is discussed in the current paper and the modelling results for a small city (Norwich, UK) are presented.

Importance of calcium in modifying the acute toxicity of sodium sulphate to Hyalella azteca and Daphnia magna.

Modification of the acute toxicity of sodium sulphate to Hyalella azteca and Daphnia magna was investigated using exposure water with different levels of water hardness (expressed as CaCO3 equivalents) and calcium-magnesium molar (Ca:Mg) ratios. The influence of Ca:Mg ratios on the toxicity of sodium and potassium chloride to D. magna also was investigated. For both species, the mean lethal concentrations that resulted in mortality of 50% of the sample population (LC50s), expressed as mg SO4(2-)/L, were increased significantly in harder water and in water with higher Ca:Mg ratios. The LC50s for H. azteca increased from 569 to 5259 mg/L with a change in water hardness from 25 to 250 mg/L. Furthermore, modifying the Ca:Mg ratio from 0.7 to 7.0 at a constant hardness of 100 mg/L significantly increased LC50s from 2101 to 2725 mg/L. The LC50s for D. magna were also significantly higher in harder water with LC50s increasing from 1194 to 3203 mg/L with a change in water hardness from 25 to 100 mg/L. In addition, modifying the Ca:Mg ratio from 0.7 to 7.0 significantly increased LC50s from 1194 to 1985 at a constant hardness of 25 mg/L, and from 3203 to 4395 mg/L at a constant hardness of 100 mg/L. No significant change in the toxicity of potassium or sodium chloride to D. magna was observed in waters with higher Ca:Mg ratios.

Sulphate toxicity to the aquatic moss, Fontinalis antipyretica.

The aquatic moss, Fontinalis antipyretica was exposed to elevated sulphate concentrations for 21-days. Gametophores were sectioned to 2 cm lengths and exposed to sulphate concentrations up to 1500 mg/l, in waters of different water hardness. Significant reductions in shoot length, dry weight, and chlorophyll a and b concentrations (per gram dry weight) were observed in soft water (19 mg/l as CaCO3); however, effects were significantly reduced in waters of increasing hardness (up to 105 mg/l as CaCO3). The substantial reduction of sulphate toxicity in waters of increasing hardness suggests water chemistry plays a significant role in affecting sulphate toxicity and should be considered when setting sulphate discharge limits.

Gold ultra-microelectrode arrays: application to the steady-state voltammetry of hydroxide ion in aqueous solution.

Gold ultra-microelectrode arrays are used to explore the electrochemical oxidation of hydroxide ions and are shown to be analytical useful. Two types of ultra-microelectrode arrays are used; the first consist of 256 individual electrodes of 5 microm in radius, 170 of which are electrochemically active in a cubic arrangement which are separated from their nearest neighbour by a distance of 100 microm. The second array compromises 2597 electrodes of 2.5 microm in radius and of which 1550 of which are electrochemically active in a hexagonal arrangement separated by the nearest neighbour by 55 microm. Well defined voltammetric waves are found with peak currents proportional to the concentration of hydroxide ions in the range 50 microM to 1 mM. Detection limits of 20 microM using the 170 ultra-microelectrode and 10 microM with the 1550 ultra-microelectrode array are shown to be possible but with a higher sensitivity of 4 mA M(-1) observed using the 1550 ultra-microelectrode array compared to 1.2 mA M(-1) with the 170 ultra-microelectrode array.

Regular arrays of microdisc electrodes: simulation quantifies the fraction of 'dead' electrodes.

Arrays of microdisc electrodes have found widespread use in electroanalysis. These are commonly produced lithographically and practical arrays may contain up to hundreds of individual disc electrodes (e.g. of gold, platinum, indium,...) to maximise sensitivity and minimise limits of detection. Typically, however, the lithographic fabrication process is imperfect resulting in a significant fraction (often tens of percent) of electrochemically inactive electrodes. We demonstrate that a 2-dimensional simulation based on the diffusion domain approximation in conjugation with simple experiments on the ferrocyanide redox couple in aqueous solutions can be used to rigorously 'count' the number of active electrodes in a non-destructive fashion. The agreement with an independent count in which active electrodes are identified via electro-plating with copper followed by ex situ microscopic examination is quantitatively excellent.

Insights into the role of the liquid-liquid interface in biphasic reactions: the reaction of vitamin B12s(aq) with vicinal dibromides(oil).

Electrocatalytic processes can take place either homogeneously in a single liquid phase or heterogeneously at the liquid-liquid interface formed in emulsions. This Article addresses the question as to whether a change in rate and/or mechanism can occur between the two possibilities. Specifically, cyclic voltammetry and electrosynthetic experiments are used to demonstrate that for the vitamin B12 mediated reduction of vicinal dibromides producing olefins, electric field effects likely operate at the liquid-liquid interface which can change the populations of different conformers relative to the single homogeneous-phase experiment, leading to significant changes in rate.

Boron-doped diamond microdisc arrays: electrochemical characterisation and their use as a substrate for the production of microelectrode arrays of diverse metals (Ag, Au, Cu)via electrodeposition.

A novel boron-doped diamond (BDD) microelectrode array is characterised with electrochemical and atomic force microscopic techniques. The array consists of 40 micron-diameter sized BDD discs which are separated by 250 microns from their nearest neighbour in a hexagonal arrangement. The conducting discs can be electroplated to produce arrays of copper, silver or gold for analytical purposes in addition to operating as an array of BDD-microelectrodes. Proof-of-concept is shown for four separate examples; a gold plated array for arsenic detection, a copper plated array for nitrate analysis, a silver plated array for hydrogen peroxide monitoring and last, cathodic stripping voltammetry for lead at the bare BDD-array.

Voltammetric sizing of inert particles.

The average size of inert particles is determined using a simple electrochemical procedure. Alumina particles are deposited on an edge-plane graphite electrode, and a cyclic voltammogram is recorded. The scan rate employed varies between 0.2 and 2 V s(-1). At these scan rates the diffusion layer thickness is greater than the size of the alumina particles, minimizing the influence of the particles' height on the observed voltammetry. The average size of the particles is determined via comparison of the experimental voltammograms with simulations.

Electrochemical cell for surface analysis.

We present a simple cost-effective design for an HOPG electrode that is well suited to voltammetric experiments accompanied by surface analysis. The utility of the electrode is demonstrated by an AFM study on the morphology of electrodeposited MoO2 nanowires. The design can be applied to a wide range of electrode materials.

Electrocatalysis at graphite and carbon nanotube modified electrodes: edge-plane sites and tube ends are the reactive sites.

Carbon, and particularly graphite in its various forms, is an attractive electrode material. Two areas of particular interest are modified carbon electrodes and carbon nanotube electrodes. In this article we focus on the relationship between surface structure and electrochemical and chemical reactivity of electrodes based on these materials. We overview recent work in this area which has led us to believe that much of the catalytic activity, electron transfer and chemical reactivity of graphitic carbon electrodes is at surface defect sites, and in particular edge-plane-like defect sites. We also question the claimed special "catalytic" properties of carbon nanotube modified electrodes.