Spatial distribution and filtering efficiency of Daphnia in a deep subtropical reservoir

Studies of Daphnia distribution and function could help people manage and protect water quality. We investigated how spatial distribution and filtering efficiency of Daphnia in the transition and lacustrine zones of the Nanwan Reservoir (China). Samplings were conducted seasonally for 2 years from six sites in the reservoir. Daphnia abundance and biomass were significantly higher in the lacustrine zone than in the transition zone. Similar composition and biomass of edible phytoplankton were found in the two zones, suggesting that food quantity could not explain high Daphnia distribution in the lacustrine zone. The variations of water velocity and food quality could help explaining Daphnia patchy distribution in the reservoir. On the one hand, rapid water velocity can cause the Daphnia decrement in the transition zone. On the other hand, the ratio of particulate organic carbon (POC) to chlorophyll a (chl a) concentration was significantly higher in the transition zone, indicating more allochthonous material constituted the food source for Daphnia. The lower quality food likely suppressed Daphnia development in the transition zone. A linear regression between Daphnia abundance and Secchi depth (SD) may suggest a cause-effect relationship where increased filtering efficiency was responsible for increased water clarity to some extent.     

Modelling future conditions in the degraded semi-arid estuary of Australia's largest river using ecosystem states

Over the last ten years, there has been a major decline in the condition of the Coorong, the estuary for Australia's largest river system, the River Murray. This decline is due to prolonged drought combined with past management of the Murray-Darling Basin. In order to successfully manage the estuary in the future, predictions are needed to evaluate the effect of possible management actions on the Coorong ecosystem under a variety of climatic scenarios. The alternative stable state concept can be extended to non-equilibrium systems, allowing for modelling of condition. Rather than constraining the definition of alternative states to those that are stable, we identify a suite of ecosystem states that occur naturally, but also include those that arise during the decline of the system. Eight distinct states were defined, with thresholds between them based on a combination of environmental characteristics associated with co-occurring biota. Threshold values for environmental characteristics define the transition rules between states. Mapping these states allows us to characterise the condition of the estuary in both space and time. The distribution of these states, and the diversity of states supported can be used to create an ecosystem condition index. By calculating the value of the index over time, the trajectory of ecosystem condition merges, and predictions can be made about future condition, should the current situation continue. This trajectory modelling can then form a baseline against which to evaluate possible management actions under a variety of climatic scenarios to identify those most likely to improve the condition of the Coorong.     

Temperature independent thermal expansivities of sodium aluminosilicate melts between 713 and 1835 K

The thermal expansivities of eight sodium aluminosilicate liquids were derived from the slope of new volume data at low temperatures (713−1072 K) combined with the high temperature (1300−1835 K) volume measurements of Stein et al. (1986) on the same liquids. Melt compositions range from 47−71 wt% SiO₂, 0−31 wt% A1203, and 17−33 wt% Na₂O; the volume of albite supercooled liquid at 1092 K was also determined. The low temperature volumes were derived from measurements of the glass density of each sample at 298 K, followed by measurements of the glass thermal expansion coefficient from 298 K to the respective glass transition interval. This technique takes advantage of the fact that the volume of a glass is equal to the volume of the corresponding liquid at the limiting fictive temperature (T′_f), and that T′_f can be approximated as the onset of the rapid rise in thermal expansion at the glass transition in a heating curve (Moynihan, 1995). No assumptions were made regarding the equivalence of enthalpy and volume relaxation through the glass transition. The propagated error on the volume of each supercooled liquid at T′_f is 0.25%. Combination of these low temperature data with the high temperature measurements of Stein et al. (1986) allowed a constant thermal expansivity of each liquid to be derived over a wide temperature interval (763−1001 degrees) with a fitted 1σ error of 0.6–4.6%; in every case, no temperature dependence to dV/dT^liq could be resolved. Calibration of a linear model equation leads to fitted values ± 1σ (units of cm³/mole) for (26.91 ± .04), (37.49 ± .12), (26.48 ± .06) at 1373 K, and (7.64 ± .08 × 10^-3 cm³/mole-K). The results indicate that neither Si02 nor Al₂O₃ contribute to the thermal expansivity of the liquids, and that dV/dT^liq is independent of temperature between 713–1835 K over a wide range of liquid composition. Calculated volumes based on this model recover both low and high temperature measurements with a standard deviation <0.25%, whereas values of dV/dT^liq can be predicted within 5.6%.     

Animated molecular dynamics simulations of hydrated caesium-smectite interlayers

Computer animation of center of mass coordinates obtained from 800 ps molecular dynamics simulations of Cs-smectite hydrates (1/3 and 2/3 water monolayers) provided information concerning the structure and dynamics of the interlayer region that could not be obtained through traditional simulation analysis methods. Cs⁺ formed inner sphere complexes with the mineral surface, and could be seen to jump from one attracting location near a layer charge site to the next, while water molecules were observed to migrate from the hydration shell of one ion to that of another. Neighboring ions maintained a partial hydration shell by sharing water molecules, such that a single water molecule hydrated two ions simultaneously for hundreds of picoseconds. Cs-montmorillonite hydrates featured the largest extent of this sharing interaction, because interlayer ions were able to inhabit positions near surface cavities as well as at their edges, close to oxygen triads. The greater positional freedom of Cs⁺ within the montmorillonite interlayer, a result of structural hydroxyl orientation and low tetrahedral charge, promoted the optimization of distances between cations and water molecules required for water sharing. Preference of Cs⁺ for locations near oxygen triads was observed within interlayer beidellite and hectorite. Water molecules also could be seen to interact directly with the mineral surface, entering its surface cavities to approach attracting charge sites and structural hydroxyls. With increasing water content, water molecules exhibited increased frequency and duration of both cavity habitation and water sharing interactions. Competition between Cs⁺ and water molecules for surface sites was evident. These important cooperative and competitive features of interlayer molecular behavior were uniquely revealed by animation of an otherwise highly complex simulation output.     

Long-Term Trends in Chesapeake Bay Seasonal Hypoxia,Stratification, and Nutrient Loading

A previously observed shift in the relationship between Chesapeake Bay hypoxia and nitrogen loading has pressing implications on the efficacy of nutrient management. Detailed temporal analyses of long-term hypoxia, nitrogen loads, and stratification were conducted to reveal different within-summer trends and understand more clearly the relative role of physical conditions. Evaluation of a 60-year record of hypoxic volumes demonstrated significant increases in early summer hypoxia, but a slight decrease in late summer hypoxia. The early summer hypoxia trend is related to an increase in Bay stratification strength during June from 1985 to 2009, while the late summer hypoxia trend matches the recently decreasing nitrogen loads. Additional results show how the duration of summertime hypoxia is significantly related to nitrogen loading, and how large-scale climatic forces may be responsible for the early summer increases. Thus, despite intra-summer differences in primary controls on hypoxia, continuing nutrient reduction remains critically important for achieving improvements in Bay water quality.     

A complete dynamical ozone budget measured in the tropical marine boundary layer during PASE

The Pacific Atmospheric Sulfur Experiment (PASE) was a field mission that took place aboard the NCAR C-130 airborne laboratory over the equatorial Pacific Ocean near Christmas Island (Kirimati, Republic of Kiribati) during August?CSeptember, 2007. Eddy covariance measurements of the ozone fluxes at various altitudes above the ocean surface, along with simultaneous mapping of the horizontal gradients provided a unique opportunity to observe all of the dynamical components of the ozone budget in this remote marine environment. The results of six daytime and two sunrise flights indicate that vertical transport into the marine boundary layer from above and horizontal advection by the tradewinds are both important source terms, while photochemical destruction consisting of 82% photolysis (leading to OH production), 11% reaction with HO₂, and 7% reaction with OH provides the main sink. The overall photochemical lifetime of ozone in the marine boundary layer was found to be 6.5 days. Ocean uptake of ozone was observed to be fairly slow (mean deposition velocity of 0.024?±?0.014 cm s^?1) accounting for a diurnally averaged loss rate that was ??30% as large as the net photochemical destruction. From the measurement of deposition velocity an ozone reactivity of ??50 s^?1 in seawater is inferred. Due to the unprecedented measurement accuracy of the dynamical budget terms, unobserved photochemistry was able to be deduced, leading to the conclusion that 3.9?±?3.0 ppt (parts per trillion by volume) of NO is present on average in the daytime tropical marine boundary layer, broadly consistent with several previous studies in similar environments. It is estimated, however, that each ppt of BrO hypothetically present would counter each ppt of NO above the requisite 3.9 ppt needed for budget closure. The long-term budget of ozone is further analyzed in the buffer layer, between the boundary layer and free troposphere, and used to derive an entrainment velocity across the trade wind inversion of 0.51 ± 0.38 cm s^?1.     

Intercalibration of Mg Isotope Delta Scales and Realisation of SI Traceability for Mg Isotope Amount Ratios and Isotope Delta Values

The continuous improvement of analytical procedures using multi‐collector technologies in ICP‐mass spectrometry has led to an increased demand for isotope standards with improved homogeneity and reduced measurement uncertainty. For magnesium, this has led to a variety of available standards with different quality levels ranging from artefact standards to isotope reference materials certified for absolute isotope ratios. This required an intercalibration of all standards and reference materials, which we present in this interlaboratory comparison study. The materials Cambridge1, DSM3, ERM‐AE143, ERM‐AE144, ERM‐AE145, IRMM‐009 and NIST SRM 980 were cross‐calibrated with expanded measurement uncertainties (95% confidence level) of less than 0.030‰ for the δ^25/24Mg values and less than 0.037‰ for the δ^26/24Mg values. Thus, comparability of all magnesium isotope delta (δ) measurements based on these standards and reference materials is established. Further, ERM‐AE143 anchors all magnesium δ‐scales to absolute isotope ratios and therefore establishes SI traceability, here traceability to the SI base unit mole. This applies especially to the DSM3 scale, which is proposed to be maintained. With ERM‐AE144 and ERM‐AE145, which are product and educt of a sublimation–condensation process, for the first time a set of isotope reference materials is available with a published value for the apparent triple isotope fractionation exponent θ_app, the fractionation relationship ln α(^25/24Mg)/ln α(^26/24Mg).     

Dynamic stream network intermittence explains emergent dissolved organic carbon chemostasis in headwaters

Dissolved organic carbon (DOC) concentrations vary among headwaters, with variation typically decreasing with watershed area. We hypothesized that streamflow intermittence could be an important source of variation in DOC concentrations across a small watershed, through (a) temporal legacies of drying on organic matter accumulation and biotic communities and (b) spatial patterns of connectivity with DOC sources. To test these hypotheses, we conducted three synoptic water chemistry sampling campaigns across a 25.5‐km² watershed in south‐eastern Idaho during early spring, late summer, and late fall. Using changepoint analysis, we found that DOC variability collapsed at a consistent location (watershed areas ~1.3 to ~1.8 km²) across seasons, which coincided with the watershed area where variability in streamflow intermittence collapsed (~1.5 km²). To test hypothesized mechanisms through which intermittence may affect DOC, we developed temporal, spatial, and spatio‐temporal metrics of streamflow intermittence and related these to DOC concentrations. Streamflow intermittence was a strong predictor of DOC across seasons, but different metrics predicted DOC depending on season. Seasonal changes in the effects of intermittence on DOC reflected seasonal changes from instream to flowpath controls. A metric that captured spatial connectivity to sources significantly predicted DOC during high flows, when DOC is typically controlled by transport. In contrast, a reach‐scale temporal metric of intermittence predicted DOC during the late growing season, when DOC is typically controlled by instream processes and when legacy effects of drying (e.g., diminished biological communities) would likely affect DOC. The effects of intermittence on DOC extend beyond temporal legacies at a point. Our results suggest that legacy effects of intermittence do not propagate downstream in this system. Instead, snapshots of spatial patterns of intermittence upstream of a reach are critical for understanding spatial patterns of DOC through connectivity to DOC sources, and these processes drive patterns of DOC even in perennial reaches.     

Supernova kicks and misaligned Be star binaries

Be stars are rapidly spinning B stars surrounded by an outflowing disc of gas in Keplerian rotation. Be star/X-ray binary systems contain a Be star and a neutron star. They are found to have non-zero eccentricities and there is evidence that some systems have a misalignment between the spin axis of the star and the spin axis of the binary orbit. The eccentricities in these systems are caused by a kick to the neutron star during the supernova that formed it. Such kicks would also give rise to misalignments. In this paper, we investigate the extent to which the same kick distribution can give rise to both the observed eccentricity distribution and the observed misalignments. We find that a Maxwellian distribution of velocity kicks with a low velocity dispersion,  σ_k≈ 15 km s⁻¹  , is consistent with the observed eccentricity distribution but is hard to reconcile with the observed misalignments, typically   i ≥ 25°  . Alternatively, a higher velocity kick distribution,  σ_k= 265 km s⁻¹  , is consistent with the observed misalignments but not with the observed eccentricities, unless post-supernova circularization of the binary orbits has taken place. We discuss briefly how this might be achieved.