SeagrassNet monitoring across the Americas: case studies of seagrass decline

Seagrasses are an important coastal habitat worldwide and are indicative of environmental health at the critical land–sea interface. In many parts of the world, seagrasses are not well known, although they provide crucial functions and values to the world's oceans and to human populations dwelling along the coast. Established in 2001, SeagrassNet, a monitoring program for seagrasses worldwide, uses a standardized protocol for detecting change in seagrass habitat to capture both seagrass parameters and environmental variables. SeagrassNet is designed to statistically detect change over a relatively short time frame (1–2 years) through quarterly monitoring of permanent plots. Currently, SeagrassNet operates in 18 countries at 48 sites; at each site, a permanent transect is established and a team of people from the area collects data which is sent to the SeagrassNet database for analysis. We present five case studies based on SeagrassNet data from across the Americas (two sites in the USA, one in Belize, and two in Brazil) which have a common theme of seagrass decline; the study represents a first latitudinal comparison across a hemisphere using a common methodology. In two cases, rapid loss of seagrass was related to eutrophication, in two cases losses related to climate change, and in one case, the loss is attributed to a complex trophic interaction resulting from the presence of a marine protected area. SeagrassNet results provide documentation of seagrass change over time and allow us to make scientifically supported statements about the status of seagrass habitat and the extent of need for management action.     

Plasma motion in umbrae and the surrounding photosphere derived from spectroscopic Doppler measurements and tracer measurements of spots

The rotational velocity of the Sun is determined by sunspot tracings and by spectroscopic measurements of the photospheric plasma using the non-Zeeman-split line Fe i 5576 and absolute iodine reference. Stationary line shifts as limb-effect and longperiodical shifts introduced by supergranulation are discussed. The dependence on solar activity as Ca⁺ emissivity and magnetic fields is investigated including line asymmetries. The results are: (a) The non active photospheric regions rotate with 1995 ± 30 m s^-1. Solar active regions yield a 60 m s^-1 higher value. (b) In quiet regions the absolute limb shift varies between 170 m s^-1 at the line core and 310 m s^-1 at I/I _cont 0.8 (C-shape); thus the limb shift is mainly due to entire line shifts. (c) In solar active regions (close to spots) asymmetries are widely reduced in line cores; this effect cannot be associated with a variation of the limb effect due to a large scatter of Doppler shifts near spots. (d) A reduced limb shift of 50 m s^-1 is found in network boundaries and is mainly due to a small scale downflow. (e) Observations with a smaller influence of stray light yield symmetric profiles in umbrae. (f) Differences between umbral rotation rates from tracer and spectroscopic measurements do not exceed 20 m s^-1, when considering straylight. The rotational velocity from umbrae exceeds that from the photosphere by 30–60 m s^-1. Some individual spots yield nearly the same rotation rate as the photosphere.     

Gaschromatographische Bestimmung von polychlorierten Biphenylen in Wasser nach Headspace-Festphasenmikroextraktion

Gas-chromatographic Determination of Polychlorinated Biphenyls in Water after Headspace Solid-phase Microextraction Headspace-analytical techniques are usually applied to the determination of easily volatile substances in water, whereas semivolatiles are generally isolated by liquid-liquid or solid-phase extraction. In the present paper, a method is presented for isolating high boiling polychlorinated biphenyls (PCB) using headspace solid-phase microextraction at elevated temperature. In spite of their low vapor pressure, the analytes are adsorbed very efficiently on a poly-dimethylsiloxane-coated fiber. Thus, in combination with GC/ECD, a very simple and sensitive solventless determination of PCB is accomplished. Using the simplest possible standard conditions, limits of determination in the lowest nanogram-per-liter range are achieved. Further increased sensitivity down to the ppq (parts per quadrillion) range is possible by stirring and increasing the sample volume and adsorption time. Moderate matrix effects have been observed in some surface and groundwaters.     

Determining the maximum degree of harmonic coefficients in geopotential models by Monte Carlo methods

Random errors for the harmonic coefficients of a geopotential model are generated from the matrix of normal equations by a parallel computer applying the Gibbs sampler. This leads to random values for the harmonic coefficients. They are transformed by nonlinear, quadratic transformations to random values for the square roots of degree variances, of mean squares of geoid undulations and gravity anomalies. The expected values of these quantities are not equal to the values of these quantities computed by the estimated harmonic coefficients, due to correlations and errors in the estimation. By hypothesis tests estimated harmonic coefficients distorted by correlations and errors are detected. Applying the tests to the geopotential model ITG-CHAMP01 of the Institute of Theoretical Geodesy in Bonn it is concluded that above the degree 62 the harmonic coefficients cannot add any information to the geopotential model.     

Incorporating Spatial Dependence in Predictive Vegetation Models: Residual Interpolation Methods*

Predictive vegetation modeling can be used statistically to relate the distribution of vegetation across a landscape as a function of important environmental variables. Often these models are developed without considering the spatial pattern that is inherent in biogeographical data, resulting from either biotic processes or missing or misspecified environmental variables. Including spatial dependence explicitly in a predictive model can be an efficient way to improve model accuracy with the available data. In this study, model residuals were interpolated and added to model predictions, and the resulting prediction accuracies were assessed. Adding kriged residuals improved model accuracy more often than adding simulated residuals, although some alliances showed no improvement or worse accuracy when residuals were added. In general, the prediction accuracies that were not increased by adding kriged residuals were either rare in the sample or had high nonspatial model accuracy. Regression interpolation methods can be an important addition to current tools used in predictive vegetation models as they allow observations that are predicted well by environmental variables to be left alone, while adjusting over‐ and underpredicted observations based on local factors.     

Molecular formulae of marine and terrigenous dissolved organic matter detected by electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry

The chemical structure of refractory marine dissolved organic matter (DOM) is still largely unknown. Electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI FT-ICR-MS) was used to resolve the complex mixtures of DOM and provide valuable information on elemental compositions on a molecular scale. We characterized and compared DOM from two sharply contrasting aquatic environments, algal-derived DOM from the Weddell Sea (Antarctica) and terrigenous DOM from pore water of a tropical mangrove area in northern Brazil. Several thousand molecular formulas in the mass range of 300-600 Da were identified and reproduced in element ratio plots. On the basis of molecular elemental composition and double-bond equivalents (DBE) we calculated an average composition for marine DOM. O/C ratios in the marine samples were lower (0.36 ± 0.01) than in the mangrove pore-water sample (0.42). A small proportion of chemical formulas with higher molecular mass in the marine samples were characterized by very low O/C and H/C ratios probably reflecting amphiphilic properties. The average number of unsaturations in the marine samples was surprisingly high (DBE = 9.9; mangrove pore water: DBE = 9.4) most likely due to a significant contribution of carbonyl carbon. There was no significant difference in elemental composition between surface and deep-water DOM in the Weddell Sea. Although there were some molecules with unique marine elemental composition, there was a conspicuous degree of similarity between the terrigenous and algal-derived end members. Approximately one third of the molecular formulas were present in all marine as well as in the mangrove samples. We infer that different forms of microbial degradation ultimately lead to similar structural features that are intrinsically refractory, independent of the source of the organic matter and the environmental conditions where degradation took place.     

Cool water geyser travertine: Crystal Geyser,Utah, USA

A sloping travertine mound, approximately 85 m across and a few metres thick is actively forming from cool temperature waters issuing out of Crystal Geyser, east‐central Utah, USA. Older travertine deposits exist at the site, the waters having used the Little Grand Wash Fault system as conduits. In contrast, the present Crystal Geyser travertine mound forms from 18°C waters which have been erupting for the last 80 years from an abandoned oil well. The present Crystal Geyser travertine accumulation forms from a ‘man‐made’ cool temperature geyser system; nevertheless, the constituents are an analogue for ancient geyser‐fed carbonate deposits. The travertine primary fabric is composed of couplets of highly porous, thin micritic laminae intercalated with thicker iron oxide rich laminae. Low Mg‐calcite is the dominant mineralogy; however, aragonite is a major constituent in deposits proximal to the vent and decreases in abundance distally. Cements exhibit a variety of fabrics, isopachous being common. Constituents include micro‐stromatolites, clasts, pisoids and the common occurrence of Frutexites‐like iron oxide precipitates. Leptothrix, a common iron‐oxidizing bacterium, is believed to be responsible for the production of the dense iron‐rich laminae. Pisoids litter the ground around the vent and rapidly decrease distally in abundance and size.     

Exploring the impact of diagenesis on (isotope) geochemical and microstructural alteration features in biogenic aragonite

For the Quaternary and Neogene, aragonitic biogenic and abiogenic carbonates are frequently exploited as archives of their environment. Conversely, pre‐Neogene aragonite is often diagenetically altered and calcite archives are studied instead. Nevertheless, the exact sequence of diagenetic processes and products is difficult to disclose from naturally altered material. Here, experiments were performed to understand biogenic aragonite alteration processes and products. Shell subsamples of the bivalve Arctica islandica were exposed to hydrothermal alteration. Thermal boundary conditions were set at 100°C, 175°C and 200°C. These comparably high temperatures were chosen to shorten experimental durations. Subsamples were exposed to different ¹⁸O‐depleted fluids for durations between two and twenty weeks. Alteration was documented using X‐ray diffraction, cathodoluminescence, fluorescence and scanning electron microscopy, as well as conventional and clumped isotope analyses. Experiments performed at 100°C show redistribution and darkening of organic matter, but lack evidence for diagenetic alteration, except in Δ₄₇ which show the effects of annealing processes. At 175°C, valves undergo significant aragonite to calcite transformation and neomorphism. The δ¹⁸O signature supports transformation via dissolution and reprecipitation, but isotopic exchange is limited by fluid migration through the subsamples. Individual growth increments in these subsamples exhibit bright orange luminescence. At 200°C, valves are fully transformed to calcite and exhibit purple‐blue luminescence with orange bands. The δ¹⁸O and Δ₄₇ signatures reveal exchange with the aqueous fluid, whereas δ¹³C remains unaltered in all experiments, indicating a carbonate‐buffered system. Clumped isotope temperatures in high‐temperature experiments show compositions in broad agreement with the measured temperature. Experimentally induced alteration patterns are comparable with individual features present in Pleistocene shells. This study represents a significant step towards sequential analysis of diagenetic features in biogenic aragonites and sheds light on reaction times and threshold limits. The limitations of a study restricted to a single test organism are acknowledged and call for refined follow‐up experiments.