Influence of a dispersant on the bioaccumulation of phenanthrene by topsmelt (Atherinops affinis).

Chemical dispersants enhance oil spill dispersion by forming water-accommodated micelles with oil droplets. However, how dispersants alter bioavailability and subsequent bioaccumulation of hydrocarbons is not well understood. Thus, the goal was to investigate the influence of a chemical dispersant on the disposition (uptake, biotransformation, and depuration) of a model hydrocarbon, [14C]-phenanthrene ([14C]PHN), by larval topsmelt (Atherinops affinis). Exposure was via aqueous-only or combined dietary and aqueous routes from a water-accommodated fraction (WAF) of Prudhoe Bay Crude Oil (PBCO) or a WAF of Corexit 9527-dispersed PBCO (DO). Trophic transfer was measured by incorporating into exposure media both a rotifer (Brachionus plicatilis) as food for the fish and a phytoplankton (Isochrysis galbana) as food for the rotifers. Short-term (4 h) bioconcentration of PHN was significantly decreased in topsmelt when oil was treated with dispersant (P < 0.05), but differences diminished after 12 h. When trophic transfer was incorporated, PHN accumulation was initially delayed but after 12 h attained similar levels. Dispersant use also significantly decreased the proportion of biotransformed PHN (as 9-phenanthrylsulfate) produced by topsmelt (P < 0.05). However, overall PHN depuration was not affected by dispersant use. Thus, chemical dispersant use in oil spill response may reduce short-term uptake but not long-term accumulation of hydrocarbons such as PHN in pelagic fish.

Effect of nutritional state on Hsp60 levels in the rotifer Brachionus plicatilis following toxicant exposure.

The nutritional state of an organism can affect the results of toxicity testing. Here we exemplified this fact by examining the effect of nutritional deprivation on heat shock protein 60 (hsp60) production in the rotifer Brachionus plicatilis following exposure to two proven inducers of hsp60, a water-accommodated fraction of crude oil (WAF) and a dispersed oil preparation (DO). Both DO and WAF exposures of unfed rotifers resulted in significantly greater hsp60 levels than that of fed DO and WAF exposed rotifers at 8 h: 870 and 3100% of control, respectively. Results clearly demonstrate that a poor nutritional state potentiates stress protein induction upon exposure to water-soluble petroleum products. It is therefore critical to define the organismal nutritional status when reporting toxic responses.

Influence of dispersants on the bioavailability and trophic transfer of petroleum hydrocarbons to larval topsmelt (Atherinops affinis).

Use of chemical dispersants as oil spill clean-up agents may alter the normal behavior of petroleum hydrocarbons (PH) by increasing their functional water solubility, resulting in increased bioavailability and altered interactions between dispersant, oil, and biological membranes. The objective of this research was to determine the impact of dispersing agents on PH bioavailability and trophic transfer to larval fish from primary levels of a marine food chain. Uptake, bioaccumulation, depuration, and metabolic transformation of a model PH, [14C]naphthalene, were measured and compared for Prudhoe Bay crude oil (PBCO) dispersed with Corexit 9527(R) (DO) and undispersed preparations of the water-accommodated fraction (WAF) of PBCO. The model food chain consisted of a primary producer, Isochrysis galbana; and a primary consumer, the rotifer, Brachionus plicatilis; and larval topsmelt, Atherinops affinis. Direct aqueous (AQ) exposure was compared with combined aqueous and dietary (AQ&D) exposure. Dispersants altered the uptake and depuration processes of naphthalene, independent of aqueous concentrations, in primary trophic species of a marine food chain. The amount of naphthalene taken up by topsmelt was initially significantly (P < or = 0.05) enhanced in the presence of dispersant, reaching a maximum more quickly than undispersed samples. Dispersion treatment significantly increased naphthalene dispension in topsmelt (P < or = 0.05) from both AQ and AQ&D exposures. No significant change in naphthalene uptake by fish was observed with the addition of contaminated food for either WAF or DO medium; however, both uptake and depuration rate constants varied significantly with route of exposure consistent with greater naphthalene turnover. The majority (> or = 72%) of naphthalene-derived radioactivity from fish tissue following all exposures was in the parent form, with smaller quantities of alpha- and beta-naphthols, alpha- and beta-naphthyl sulfates, and an unidentified derivative.

Hsp60-induced tolerance in the rotifer Brachionus plicatilis exposed to multiple environmental contaminants.

Hsp60 induction was selected as a sublethal endpoint of toxicity for Brachionus plicatilis exposed to a water accommodated fraction (WAF) of Prudhoe Bay crude oil (PBCO), a PBCO/dispersant (Corexit 9527(R)) fraction and Corexit 9527(R) alone. To examine the effect of multiple stressors, exposures modeled San Francisco Bay, where copper levels are approximately 5 microgram/L, salinity is 22 per thousand, significant oil transport and refining occurs, and petroleum releases have occurred historically. Rotifers were exposed to copper at 5 microgram/L for 24 h, followed by one of the oil/dispersant preparations for 24 h. Batch-cultured rotifers were used in this study to model wild populations instead of cysts. SDS-PAGE with Western Blotting using hsp60-specific antibodies and chemiluminescent detection were used to isolate, identify, and measure induced hsp60 as a percentage of control values. Both PBCO/dispersant and dispersant alone preparations induced significant levels of hsp60. However, hsp60 expression was reduced to that of controls at high WAF concentrations, suggesting interference with protein synthesis. Rotifers that had been preexposed to copper maintained elevated levels of hsp60 upon treatment with WAF at all concentrations. Results suggest that induction of hsp60 by chronic low-level exposure may serve as a protective mechanism against subsequent or multiple stressors and that hsp60 levels are not additive for the toxicants tested in this study, giving no dose-response relationship. The methods employed in this study could be useful for quantifying hsp60 levels in wild rotifer populations.

Environmental activation of pesticides.

Spray drift from application sites, runoff from agricultural fields, leftover products from home use, and accidental spills have made pesticide contamination ubiquitous in the environment. As a pesticide moves through the environment, it may react through chemical and biotic processes such as hydrolysis, oxidation, or reduction, or be metabolized in microorganisms, animals, plants, and humans. Most reactions will be inactivations, forming degradation products less toxic or persistent than the parent compound. However, some reactions are activations, creating breakdown products equally or more toxic, persistent, or mobile than the parent and posing a greater threat to nontarget organisms and the environment. Examples are drawn from the major classes of pesticides including organochlorine compounds (DDT and aldrin), organophosphorus pesticides (malathion), carbamate pesticides (aldicarb), and fungicides to illustrate the various activation routes.

A method for the trace analysis of naptalam (N-1-naphthylphthalamic acid) in water.

A method for the trace analysis of naptalam, N-1-naphthylphthalamic acid, in water is presented. Naptalam, a pre-emergent, broad-leaf, and grassy herbicide, is used with soybean, peanut, and vine crops. Tap and well water samples are extracted on a cyclohexyl solid phase extraction cartridge, eluted from the cartridge with methanol, and evaporated to dryness. The sample is esterified with diazoethane, evaporated to dryness, reconstituted with methanol, and converted to the stable N-1-naphthyl phthalimide in the gas chromatograph (GC) injector port for detection and quantitation using a nitrogen-phosphorus detector. Sample injection technique and injector port temperature are critical to high derivatization yields. Confirmation of conversion to N-1-naphthyl phthalimide was made by gas chromatograph/mass spectrometer (GC/MS). Spiking tests at levels of 3 to 100 micrograms/L showed good recovery.