Does iodine gas released from seaweed contribute to dietary iodine intake?

Thyroid hormone levels sufficient for brain development and normal metabolism require a minimal supply of iodine, mainly dietary. Living near the sea may confer advantages for iodine intake. Iodine (I₂) gas released from seaweeds may, through respiration, supply a significant fraction of daily iodine requirements. Gaseous iodine released over seaweed beds was measured by a new gas chromatography–mass spectrometry (GC–MS)-based method and iodine intake assessed by measuring urinary iodine (UI) excretion. Urine samples were obtained from female schoolchildren living in coastal seaweed rich and low seaweed abundance and inland areas of Ireland. Median I₂ ranged 154–905 pg/L (daytime downwind), with higher values (~1,287 pg/L) on still nights, 1,145–3,132 pg/L (over seaweed). A rough estimate of daily gaseous iodine intake in coastal areas, based upon an arbitrary respiration of 10,000L, ranged from 1 to 20 μg/day. Despite this relatively low potential I₂ intake, UI in populations living near a seaweed hotspot were much higher than in lower abundance seaweed coastal or inland areas (158, 71 and 58 μg/L, respectively). Higher values >150 μg/L were observed in 45.6% of (seaweed rich), 3.6% (lower seaweed), 2.3% (inland)) supporting the hypothesis that iodine intake in coastal regions may be dependent on seaweed abundance rather than proximity to the sea. The findings do not exclude the possibility of a significant role for iodine inhalation in influencing iodine status. Despite lacking iodized salt, coastal communities in seaweed-rich areas can maintain an adequate iodine supply. This observation brings new meaning to the expression “Sea air is good for you!”     

Evaluation of high volume particle sampling and sample handling protocols for ambient urban air mutagenicity determinations.

An investigation of high volume particle sampling and sample handling procedures was undertaken to evaluate variations of protocols being used by the U.S. Environmental Protection Agency. These protocols are used in urban ambient air studies which collect ambient and source samples for subsequent mutagenicity analysis of the organic extracts of the aerosol fraction. Specific protocol issues investigated include: (a) duration of sampling period, (b) type of filter media used to collect air particles, (c) necessity for cryogenic field site storage and dry ice shipping of filter samples, and (d) sample handling at the receiving laboratory. Six PM10 Hi-Vol samplers were collocated at an urban site in downtown Durham, North Carolina and operated simultaneously to evaluate 12 h versus 24 h collection periods and filter media choices of glass fiber, Teflon impregnated glass fiber (TIGF), and quartz fiber. Filters from the samplers plus field blanks were collected during each of 25 sampling periods. TIGF filters from two samplers were immediately placed on dry ice in the field and transported directly to cryogenic storage. TIGF, quartz, and glass fiber filters from three samplers were transported at ambient and maintained at room temperature for three to six days prior to cryogenic storage. One TIGF sample, which was collected on a previously tared filter, was subjected to controlled environment equilibration (40 percent relative humidity, 22 degrees C) for 8 to 24 h and weighed prior to cryogenic storage. All filters were subsequently stored at -70 degrees C to -80 degrees C prior to a one-time extraction and Salmonella (Ames) mutagenicity bioassay of the entire sample set.(ABSTRACT TRUNCATED AT 250 WORDS)     

Air-to-vegetation transfer rates of natural submicron aerosols

Submicron aerosol deposition to outdoor vegetation was evaluated by measuring vegetation and air concentrations of ²¹²Pb, ²¹⁴Pb, and ⁷Be attached to atmospheric aerosols. A biomass-normalized deposition velocity (V_D), with units of m³ kg^?1 s^?1, was used to compare species and isotopes with respect to air-to-vegetation transfer rates. For ²¹²Pb ($\text{t}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 10·64 h}$), higher night-time air concebtrations dominate deposition, while for ²¹⁴Pb ($\text{t}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 26·8}\text{min}$), deposition measurements over shorter time periods relative to changing atmospheric conditions were possible. Calculated V_D values were usually higher for ²¹⁴Pb, possibly reflecting wind-enhanced deposition during the afternoon period of sampling. Evergreen species, including pines, were not appreciably different from deciduous species. Most striking was the narrow range of results (factor of 6 for 34 ²¹²Pb measurements of 20 species). Beryllium-7 ($\text{t}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 53·3 d}$) was used to evaluate time-integrated deposition by sampling vegetation in California near the end of dry summers. Similar deposition rates were found for this isotope. The results of the study indicated that naturally radioactive atmospheric aerosols can be used to understand the dynamics of submicron aerosol deposition to ecosystems.     

AQUATIC IMPACTS OF DEICING SALTS IN THE CENTRAL SIERRA NEVADA MOUNTAINS,CALIFORNIA1

ABSTRACT: The fate and effect of sodium chloride applied to Californian highways in the Lake Tahoe, Truckee River, and Yuba River watersheds were studied over a period of 14 months in 1974–75. Chloride levels in streams below major freeways were found to be elevated during the winter. The high chloride levels occurred after the application of salt to roads, decreasing as the time from application increases. Small lakes receiving runoff from major highways were also enriched with chloride. Several of these lakes displayed a temporary chemocline, which was sufficiently strong to stabilize a temperature inversion in one lake.     

A COLORIMETRIC METHOD FOR THE DETERMINATION OF TRACE COPPER CONCENTRATIONS IN WATER1

Trace quantities of copper (II) ion can be found in natural water as waste products from industrial, mining, and agricultural operations. Because low concentrations of copper can be toxic to plant life, many workers have devised methods of analysis for this metal in water. These methods require expensive equipment and skilled technicians. The described study illustrates a simple method in which copper (II) ion is concentrated by a batch ion exchange technique and estimated colorimetrically after formation of the blue triethylenetetramine complex. Using the visible absorption peak of the complex at 600 nm it was possible to obtain accurate estimations of original copper concentrations in the range 0.5-3 ppm. Using the complex absorption peak at 260 nm in the ultra-violet region of the spectrum increased the sensitivity by a factor of twenty. Because of the dependence of the complex formation reaction on solution acidity it is possible to optimize conditions for the detection of copper (II) in the presence of other metal ions. This type of method, which could be extended to the analysis of other metal ions, could be performed by a relatively unskilled technician under field conditions.     

Application of in-situ bioremediation to a gasoline spill in fractured bedrock

After achieving remediation goals during only thirty-two months of operation, the first full-scale in-situ bioremediation (ISB) system in the state of Missouri was shut down in 1990. In addition to ISB, the system included a combination of soil venting and air stripping to remediate subsurface gasoline contamination at a large manufacturing facility. More than 84,000 pounds of gasoline were degraded or removed from the fractured limestone bedrock aquifer and overburden materials. The successful application of ISB in this complex geologic environment and the fact that this was the first such system to complete remediation in Missouri make this system unique.     

Environmental justice along product life cycles: importance,renewable energy examples and policy complexities

Environmental justice is critical to our efforts to preserve the human habitat from the degradation of pollution and climate change because of the need for cooperation and due to our ignorance of how the intertwined effects of our actions in one locality affect the quality of life in other localities across the world. While environmental justice questions are often focused on the location choices for specific activities that pollute, another important perspective is environmental justice over the life cycle of the production of products. Upon close examination renewable energies, critical alternatives to the fossil fuels which induce climate change, have environmental justice issues over their life cycles. Formal, statutory national law is not sufficient to address environmental justice problems along product life cycles in a world in which production is globalised and environmental effects pass beyond political borders. The responses to this challenge must draw on an interacting combination of information, custom, soft law, such as international standards and certification, and formal national laws. Through an interesting complex of intertwined effects, this system has already advanced our capacity to address environmental justice problems along product life cycles. The magnitude of the challenge and the complexity of the system demand ongoing effort and further innovation. Also, the system is not well configured to address our burgeoning consumption which continues to expand the burdens of future generations.     

Mapping Grazing-Induced Degradation in a Semi-Arid Environment: A Rapid and Cost Effective Approach for Assessment and Monitoring

Improved techniques for measuring and monitoring the state of biodiversity are required for reporting on national obligations to international and regional conservation institutions. Measuring the extent of grazing-related degradation in semi-arid ecosystems has proved difficult. Here we present an accurate and cost-effective method for doing this, and apply it in a South African semi-arid region that forms part of a globally significant biodiversity hotspot. We grouped structurally and functionally similar vegetation units, which were expert-mapped at the 1:50,000 scale, into four habitat types, and developed habitat-specific degradation models. We quantified degradation into three categories, using differences between dry and wet season values of the Normalized Difference Vegetation Index (NDVI) for the three succulent karoo habitats, and the difference between maximum and mean NDVI values for the subtropical thicket habitat. Field evaluation revealed an accuracy of 86%. Overall, degradation was high: 24% of the study area was modeled as severely degraded, and only 9% as intact. Levels of degradation were highest for bottomland habitats that were most exposed to grazing impacts. In sharp contrast to our methods, a widely used, broad-scale and snapshot assessment of land cover in South Africa was only 33% accurate, and it considerably underestimated the extent of severely degraded habitat in the study area. While our approach requires a multidisciplinary team, and in particular expert knowledge on the characteristics and spatial delimitation of vegetation types, it is repeatable, rapid, and relatively inexpensive. Consequently, it holds great promise for monitoring and evaluation programs in semi-arid ecosystems, in Africa, and beyond.