Urban streams of the Pacific Northwest provide spawning and rearing habitat for a variety of salmon species, and food availability for developing salmon could be adversely affected by pesticide residues in these waterbodies. Sediments from Oregon and Washington streams were sampled to determine if current-use pyrethroid insecticides from residential neighborhoods were reaching aquatic habitats, and if they were at concentrations acutely toxic to sensitive invertebrates. Approximately one-third of the 35 sediment samples contained measurable pyrethroids. Bifenthrin was the pyrethroid of greatest concern with regards to aquatic life toxicity, consistent with prior studies elsewhere. Toxicity to Hyalella azteca and/or Chironomus dilutus was found in two sediment samples at standard testing temperature (23 °C), and in one additional sample at a more environmentally realistic temperature (13 °C). Given the temperature dependency of pyrethroid toxicity, low temperatures typical of northwest streams can increase the potential for toxicity above that indicated by standard testing protocols.

Critical loads (CLs) define maximum atmospheric deposition levels apparently preventative of ecosystem harm. We present first nitrogen CLs for northwestern North America’s maritime forests. Using multiple linear regression, we related epiphytic-macrolichen community composition to: 1) wet deposition from the National Atmospheric Deposition Program, 2) wet, dry, and total N deposition from the Communities Multi-Scale Air Quality model, and 3) ambient particulate N from Interagency Monitoring of Protected Visual Environments (IMPROVE). Sensitive species declines of 20-40% were associated with CLs of 1-4 and 3-9 kg N ha-1 y-1 in wet and total deposition. CLs increased with precipitation across the landscape, presumably from dilution or leaching of depositional N. Tight linear correlation between lichen and IMPROVE data suggests a simple screening tool for CL exceedance in US Class I areas. The total N model replicated several US and European lichen CLs and may therefore be helpful in estimating other temperate-forest lichen CLs. Lichen-based critical loads for N deposition in western Oregon and Washington forests ranged from 3 to 9 kg ha-1 y-1, increasing with mean annual precipitation.

Human activity is changing air quality and climate in the US Pacific Northwest. In a first application of non-metric multidimensional scaling to a large-scale, framework dataset, we modeled lichen community response to air quality and climate gradients at 1416 forested 0.4 ha plots. Model development balanced polluted plots across elevation, forest type and precipitation ranges to isolate pollution response. Air and climate scores were fitted for remaining plots, classed by lichen bioeffects, and mapped. Projected 2040 temperatures would create climate zones with no current analogue. Worst air scores occurred in urban-industrial and agricultural valleys and represented 24% of the landscape. They were correlated with: absence of sensitive lichens, enhancement of nitrophilous lichens, mean wet deposition of ammonium >0.06 mg l-1, lichen nitrogen and sulfur concentrations >0.6% and 0.07%, and SO2 levels harmful to sensitive lichens. The model can detect changes in air quality and climate by scoring re-measurements. Lichen-based air quality and climate gradients in western Oregon and Washington are responsive to regionally increasing nitrogen availability and to temperature changes predicted by climate models.

Reconstructions of 250 years historical inputs of two distinct types of black carbon (soot/graphitic black carbon (GBC) and char-BC) were conducted on sediment cores from two basins of the Puget Sound, WA. Signatures of polycyclic aromatic hydrocarbons (PAHs) were also used to support the historical reconstructions of BC to this system. Down-core maxima in GBC and combustion-derived PAHs occurred in the 1940s in the cores from the Puget Sound Main Basin, whereas in Hood Canal such peak was observed in the 1970s, showing basin-specific differences in inputs of combustion byproducts. This system showed relatively higher inputs from softwood combustion than the northeastern U.S. The historical variations in char-BC concentrations were consistent with shifts in climate indices, suggesting an influence of climate oscillations on wildfire events. Environmental loading of combustion byproducts thus appears as a complex function of urbanization, fuel usage, combustion technology, environmental policies, and climate conditions.

Pharmaceuticals and personal care products in wastewater discharge can be stressors to estuarine species. We transplanted juvenile Pacific oysters at varying distances within sites near wastewater treatment plant outfalls or oyster aquaculture control sites to assess small scale spatial variation in contaminant uptake and oyster condition. Oysters were transplanted to sites in Coos and Netarts Bays, Oregon and Grays Harbor, Washington, then collected after 9 and 12 months. Two pharmaceuticals (miconazole and virginiamycin M1) were detected in spring samples and four alkylphenols (NP1EO, NP2EO, NP and OP) were detected in summer samples, with more frequent detections at wastewater sites. Contaminant concentrations were similar across site types, indicating that even in sparsely populated coastal areas (<25,000 in the watershed), shellfish are exposed to and uptake wastewater contaminants. Additionally, oyster condition was lower at wastewater sites compared to aquaculture sites, indicating a need to better understand whether contaminant exposure affects oyster condition.

The goal of this study was to document if lakes in National Parks in Washington have exceeded critical levels of nitrogen (N) deposition, as observed in other Western States. We measured atmospheric N deposition, lake water quality, and sediment diatoms at our study lakes. Water chemistry showed that our study lakes were ultra-oligotrophic with ammonia and nitrate concentrations often at or below detection limits with low specific conductance (<100 μS/cm), and acid neutralizing capacities (<400 μeq/L). Rates of summer bulk inorganic N deposition at all our sites ranged from 0.6 to 2.4 kg N ha⁻¹ year⁻¹and were variable both within and across the parks. Diatom assemblages in a single sediment core from Hoh Lake (Olympic National Park) displayed a shift to increased relative abundances of Asterionella formosa and Fragilaria tenera beginning in the 1969–1975 timeframe, whereas these species were not found at the remaining (nine) sites. These diatom species are known to be indicative of N enrichment and were used to determine an empirical critical load of N deposition, or threshold level, where changes in diatom communities were observed at Hoh Lake. However, N deposition at the remaining nine lakes does not seem to exceed a critical load at this time. At Milk Lake, also in Olympic National Park, there was some evidence that climate change might be altering diatom communities, but more research is needed to confirm this. We used modeled precipitation for Hoh Lake and annual inorganic N concentrations from a nearby National Atmospheric Deposition Program station, to calculate elevation-corrected N deposition for 1980–2009 at Hoh Lake. An exponential fit to this data was hindcasted to the 1969–1975 time period, and we estimate a critical load of 1.0 to 1.2 kg N ha⁻¹ year⁻¹for wet deposition for this lake.

Mercury concentrations in largemouth bass and mercury accumulation rates in age-dated sediment cores were examined at Lake Ozette and Lake Dickey in Washington State. Goals of the study were to compare concentrations in fish tissues at the two lakes with a larger statewide dataset and examine mercury pathways to the lakes. After accounting for fish length, tissue concentrations at the lakes were significantly higher than other Washington State lakes. Wet deposition and historical atmospheric monitoring from the area show no indication of enhanced local or regional deposition. Sediment core records from the lakes indicate rising sedimentation rates coinciding with logging in the lakes' drainages has greatly increased the net flux of mercury to the waterbodies.

Concentrations of mercury (Hg) were measured in six dated cores from four lakes in western Whatcom County, Washington, USA, that were at various bearings from a chlor-alkali plant, two municipal waste incinerators and a municipal sewage sludge incinerator. The importance of atmospheric emissions of Hg from these local municipal and industrial sources was evaluating by comparing the temporal trends in sedimentation of the lake cores with the emission history of each Hg species and by examining the geographical distribution of Hg sedimentation in relation to the region's primary wind pattern. Local municipal and industrial sources of atmospheric Hg were not responsible for the majority of the Hg in the upper layer of sediments of Whatcom County lakes because of (1) the significant enrichment of Hg in lake sediments prior to emissions of local industrial and municipal sources in 1964, (2) smaller increases in Hg concentrations occurred after 1964, (3) the similarity of maximum enrichments found in Whatcom County lakes to those in rural lakes around the world, (4) the inconsistency of the temporal trends in Hg sedimentation with the local emission history, and (5) the inconsistency of the geographic trends in Hg sedimentation with estimated deposition. Maximum enrichment ratios of Hg in lake sediments between 2 and 3 that are similar to rural areas in Alaska, Minnesota, and New England suggest that global sources of Hg were primarily responsible for increases of Hg in Whatcom County lakes beginning about 1900.

The odor emissions from three types of biosolidsfrom King County, WA, were measured usingdilution-to-threshold olfactometry and mass spectralanalyses. This article describes thermal desorption andcryogenic GC/MS methods developed to characterizeodorant emissions from biosolids application to forestsoil. The major odorous compounds volatilized from twoanaerobically digested biosolids were ammonia anddimethyl disulfide, with lesser quantities of carbondisulfide, dimethyl sulfide, trimethyl amine, acetoneand methyl ethyl ketone. A third type of biosolidswas formed by centrifuge and drying one of the otherbiosolids at 190 °C. This dry biosolids producedmore odor and volatilized a more complex array ofvolatile compounds including: dimethyl disulfide,dimethyl sulfide, carbon disulfide, methylethyldisulfide, methane thiol, trimethyl amine, aceticacid, propionic acid, and butyric acid. Odor unitemissions were not found to correlate with microbialactivity, initial biosolids ammonium, organicnitrogen, and total sulfur. Variability in odoremission were explained by the number of odorouscompounds volatilized from each material, surface areaof biosolids and drying of the biosolids.