Mechanisms generating modification of benthos following tidal flat invasion by a Spartina hybrid.

Many coastal habitats are being substantially altered by introduced plants. In San Francisco Bay, California, USA, a hybrid form of the eastern cordgrass Spartina alterniflora is rapidly invading open mudflats in southern and central sections of the Bay, altering habitat, reducing macrofaunal densities, and shifting species composition. The invasion has resulted in significant losses of surface-feeding amphipods, bivalves, and cirratulid polychaetes, while subsurface feeding groups such as tubificid oligochaetes and capitellid polychaetes have been unaffected. In the present paper, we document the causes and mechanisms underlying the changes observed. Through a series of in situ manipulative experiments we examined the influence of hybrid Spartina canopy on a range of physical, chemical, and biological properties. The hybrid Spartina canopy exerted a strong influence on the hydrodynamic regime, triggering a series of physical, chemical, and biological changes in the benthic system. Relative to tidal flats, water velocity was reduced in hybrid patches, promoting deposition of fine-grained, organic-rich particles. The resulting changes in the sediment environment included increased porewater sulfide concentrations and anoxia, which led to poor survivorship of surface feeders such as bivalves, amphipods, and polychaetes. These are key taxa that support higher trophic levels including migratory shorebirds that feed on tidal flats. Altered flow in the Spartina canopy further contributed to changes in barnacle recruitment and resuspension of adult benthic invertebrates. Increased crab-induced predation pressure associated with Spartina invasion also contributed to changes in benthic invertebrate communities. Our results suggest that multiple physical, chemical, biotic, and trophic impacts of the Spartina invasion have resulted in substantial changes in benthic communities that are likely to have important effects on the entire ecosystem.     

Emerging conservation challenges and prospects in an era of offshore hydrocarbon exploration and exploitation

Globally, extensive marine areas important for biodiversity conservation and ecosystem functioning are undergoing exploration and extraction of oil and natural gas resources. Such operations are expanding to previously inaccessible deep waters and other frontier regions, while conservation‐related legislation and planning is often lacking. Conservation challenges arising from offshore hydrocarbon development are wide‐ranging. These challenges include threats to ecosystems and marine species from oil spills, negative impacts on native biodiversity from invasive species colonizing drilling infrastructure, and increased political conflicts that can delay conservation actions. With mounting offshore operations, conservationists need to urgently consider some possible opportunities that could be leveraged for conservation. Leveraging options, as part of multi‐billion dollar marine hydrocarbon operations, include the use of facilities and costly equipment of the deep and ultra‐deep hydrocarbon industry for deep‐sea conservation research and monitoring and establishing new conservation research, practice, and monitoring funds and environmental offsetting schemes. The conservation community, including conservation scientists, should become more involved in the earliest planning and exploration phases and remain involved throughout the operations so as to influence decision making and promote continuous monitoring of biodiversity and ecosystems. A prompt response by conservation professionals to offshore oil and gas developments can mitigate impacts of future decisions and actions of the industry and governments. New environmental decision support tools can be used to explicitly incorporate the impacts of hydrocarbon operations on biodiversity into marine spatial and conservation plans and thus allow for optimum trade‐offs among multiple objectives, costs, and risks.     

The ecology of cirratulid mudballs on the Oman margin, northwest Arabian Sea

Mudball-building cirratulid polychaetes have been described previously only from the southern California margin. During a study of oxygen minimum-zone benthos in fall 1994, we observed dense aggregations of agglutinated mudballs at 840 to 875 m on the Oman margin in the northwest Arabian Sea. These were inhabited, and probably constructed, by a cirratulid polychaete species in the genus Monticellina. The mudballs were cigar-shaped, 4.5 to 25 mm long, and positioned vertically so as to protrude several millimeters above the sediment–water interface. Total mudball densities were ∼16 000 m⁻². Occupied mudballs occurred at densities of 2 112 m⁻²; 89% were in the uppermost 2 cm of sediment, and no occupied mudballs were found below 10 cm. Organisms other than the cirratulid were present on 1.7% of the mudballs examined, and included epizoic polychaetes, agglutinated and calcareous Foraminifera. Various polychaetes, a nemertean and nematodes were found inside tests. Mudball abundance exhibited positive associations with densities of several paraonid polychaete species, and with densities of burrowing and subsurface-deposit-feeding polychaetes. Negative associations were observed between mudballs and three tube-building taxa (two polychaetes and an amphipod). Mudball-inhabiting cirratulids are abundant in at least two low-oxygen, margin settings. We expect further sampling of bathyal environments to yield additional systems in which cirratulid mudballs are common. Such observations are valuable because mudballs appear to represent a significant source of heterogeneity that can influence macrofaunal community structure in deep-sea sediments. Received: 15 January 1997 / Accepted: 30 January 1997     

Sampling of ethylene glycol and ethylene glycol derivatives in work-room air using Amberlite XAD resins

The porous polymers Amberlite XAD-2 and XAD-7 were evaluated for the sampling of ethylene glycol, 2-methoxyethanol, 2-ethoxyethanol, 2-butoxyethanol and 2-ethoxyethyl acetate in work-room air. Using diethyl ether desorption, these adsorbents were found excellent for the compounds studied.     

Analysis of gaseous diisocyanates in air using chemosorption sampling

A sampling procedure for 2,4- and 2,6-toluenediisocyanate (TDI) and 4,4′-diphenylmethane diisocyanate (MDI) in the range 0.007-0.7 mg/m³ in a 15 L air sample is described. The sampling is performed with 9-(N-methylaminomethyl)-anthracene (MAMA) adsorbed on a solid sorbent, Amberlite XAD-2. The recoveries are 80–100% in this chemosorption reaction. The urea derivatives are desorbed with N,N-dimethylformamide and analysed by high performance liquid chromatography (HPLC). Samples and prepared chemosorption tubes are stable for at least two weeks if stored in the dark. To complete the investigation, field measurements of TDI were performed in an industrial atmosphere.     

Performance of the Button Personal Inhalable Sampler for the measurement of outdoor aeroallergens

No personal aerosol sampler has been evaluated for monitoring aeroallergens in outdoor field conditions and compared to conventional stationary aerobiological samplers. Recently developed Button Personal Inhalable Aerosol Sampler has demonstrated high sampling efficiency for non-biological particles and low sensitivity to the wind direction and velocity. The aim of the present study was to evaluate the Button Sampler for the measurement of outdoor pollen grains and fungal spores side-by-side with the widely used Rotorod Sampler. The sampling was performed for 8 months (spring, summer and fall) at a monitoring station on the roof of a two-storied office building located in the center of the city of Cincinnati. Two identical Button Samplers, one oriented towards the most prevalent wind and the other towards the opposite wind and a Rotorod Sampler were placed side-by-side. The total fungal spore concentration ranged from 129 to 12,980 spores m(-3) (number per cubic meter of air) and the total pollen concentration from 4 to 4536 pollen m(-3). The fungal spore concentrations obtained with the two Button Samplers correlated well (r = 0.95; p<0.0001). The pollen data also showed positive correlation. These findings strongly support the results of earlier studies conducted with non-biological aerosol particles, which demonstrated a low wind dependence of the performance of the Button Sampler compared to other samplers. The Button Sampler's inlet efficiency was found to be more dependent on wind direction when sampling larger sized Pinaceae pollen grains (aerodynamic diameter approximately 65 mum). Compared to Rotorod, both Button Samplers measured significantly higher total fungal spore concentrations. For total pollen count, the Button Sampler facing the prevalent wind showed concentrations levels comparable to that of the Rotorod, but the Button Sampler oriented opposite to the prevalent wind demonstrated lower concentration levels. Overall, it was concluded that the Button Sampler is efficient for the personal sampling of outdoor aeroallergens, and is especially beneficial for aeroallergens of small particle size.     

Influence of air humidity on sampling efficiency of some solid adsorbents used for sampling organics from work-room air

The influence of air humidity on the sampling efficiency of Amberlite XAD porous polymers and activated charcoal was studied by determining the recovery of various organics at 20% and 85% relative humidity. The sampling efficiency of XAD-7 was found to decrease with increasing relative humidity, while the sampling efficiency of XAD-2 and activated charcoal was relatively unaffected for the compounds studied. Activated charcoal had a greater capacity than Amberlite XAD for several types of compounds, however.     

The sensitivity of PM2.5 source-receptor relationships to atmospheric chemistry and transport in a three-dimensional air quality model

Air quality model simulations constitute an effective approach to developing source-receptor relationships (so-called transfer coefficients in the risk analysis framework) because a significant fraction of particulate matter (particularly PM2.5) is secondary (i.e., formed in the atmosphere) and, therefore, depends on the atmospheric chemistry of the airshed. In this study, we have used a comprehensive three-dimensional air quality model for PM2.5 (SAQM-AERO) to compare three approaches to generating episodic transfer coefficients for several source regions in the Los Angeles Basin. First, transfer coefficients were developed by conducting PM2.5 SAQM-AERO simulations with reduced emissions of one of four precursors (i.e., primary PM, sulfur dioxide (SO2), oxides of nitrogen (NOx), and volatile organic compounds) from each source region. Next, we calculated transfer coefficients using two other methods: (1) a simplified chemistry for PM2.5 formation, and (2) simplifying assumptions on transport using information limited to basin-wide emission reductions. Transfer coefficients obtained with the simplified chemistry were similar to those obtained with the comprehensive model for VOC emission changes but differed for NOx and SOz emission changes. The differences were due to the parameterization of the rates of secondary PM formation in the simplified chemistry. In 90% of the cases, transfer coefficients estimated using only basin-wide information were within a factor of two of those obtained with the explicit source-receptor simulations conducted with the comprehensive model. The best agreement was obtained for VOC emission changes; poor agreement was obtained for primary PM2.5.     

Spatial distribution of copper in relation to recreational boating in a California shallow-water basin

The overall effect of the number of boats on the copper (Cu) levels in the water column and sediment, along with their spatial variability within Shelter Island Yacht Basin (SIYB), San Diego Bay, California was examined. We identified a horizontal gradient of increasing dissolved Cu and Cu in sediment from outside to the head of SIYB which was coincident with the increasing number of boats. Spatial models of Cu distribution in water and sediment indicated the presence of ‘hotspots’ of Cu concentration. From outside to the head of SIYB, dissolved Cu ranged from 1.3 μ g L^?1 to 14.6 μ g L^?1 in surface water, and 2.0 μ g L^?1 to 10.2 μ g L^?1 in bottom water. Cu in sediment exceeded the Effect Range Low of 34 mg kg^?1 (i.e. where adverse effects to fauna may occur), with a peak concentration of 442 mg kg^?1 at the head of the basin. Free Cu⁺⁺ in surface water was several orders of magnitude higher than in sediment porewater. High-resolution data of Cu species together with probability maps presented in this paper will allow managers to easily visualise and localise areas of impaired quality and to prioritise which areas should be targeted to improve Cu-related conditions.