Archive for October, 2008

Author: dorothy smith

World Environment Day, which is commemorated each year on June 5th, is one of the most significant mode through which the United Nations stimulates the global awareness of the environment. It is by this way that the United Nations attract political attention and enhances action to shape a better global environment. Each year the World Environment Day is celebrated in recognition of unique theme. Norway was honored to host International World Environment Day 2007 celebrations in recognition of the theme — ‘Melting Ice – The Hot Topic’. Over a hundred nations across the globe celebrates the World Environment Day with highly relevant theme each year.

The slogan for World Environment Day 2008 is ‘Kick the Habit! Towards a Low Carbon Economy’. With an understanding of the fact that the change in climatic condition is gradually becoming one of the most defining issue of the age, UNEP is requesting the nations, companies and communities to put special focus on the greenhouse gas emissions and to put spare thought over how to reduce them. The World Environment Day 2008 is going to highlight resources and focuses on promoting low carbon economies with a view to shape a better and healthier future. Promoting a low carbon economy involves steps towards improved energy efficiency, alternative energy sources, forest conservation and eco-friendly consumption. The chief international celebration of the World Environment Day 2008 is going to be held in New Zealand.

The Heads of State, Prime Ministers and Ministers of Environment deliver statements and commit themselves to care for this only green planet of the universe. Serious pledges establish sound and non-transitory governmental policies related to environmental management and economic planning. bicycle parades, tree planting , recycling campaigns, clean-up campaigns, street rallies, school level essay and poster competitions etc. are organized all over the world on June 5th to celebrate the World Environment Day.

Here are some information on World Environment Day for the last ten years regarding where the WED celebration was held at and what were the respective themes each year:

Places of celebration:
World Environment Day 2007 – Tromsø, Norway
World Environment Day 2006 – Algiers, Algeria
World Environment Day 2005 – San Francisco, U.S.
World Environment Day 2004 – Barcelona, Spain
World Environment Day 2003 – Beirut, Lebanon
World Environment Day 2002 – Shenzhen, People’s Republic of China
World Environment Day 2001 – Torino, Italy and Havana, Cuba
World Environment Day 2000 – Adelaide, Australia
World Environment Day 1999 – Tokyo, Japan
World Environment Day 1998 – Moscow, Russian Federation

Themes of celebration:
World Environment Day 2007 – Melting Ice – a Hot Topic?
World Environment Day 2006 – Deserts and Desertification – Don’t Desert Drylands!
World Environment Day 2005 – Green Cities – Plan for the Planet!
World Environment Day 2004 – Wanted! Seas and Oceans – Dead or Alive?
World Environment Day 2003 – Water – Two Billion People are Dying for It!
World Environment Day 2002 – Give Earth a Chance
World Environment Day 2001 – Connect with the World Wide Web of Life
World Environment Day 2000 – The Environment Millennium – Time to Act
World Environment Day 1999 – Our Earth – Our Future – Just Save It!
World Environment Day 1998 – For Life on Earth – Save Our Seas

Article Source: http://www.articlesbase.com/environment-articles/world-environment-day-2008-kick-the-habit-towards-a-low-carbon-economy-433386.html

About the Author:

Dorothy Smith, the author of this article, writes about the events & special occasions. Want to know more about world environment day or world environment day ecards ? Celebrate world environment day 2008 by sending free ecards and check some other resources .

The programme represents a substantive development in applied science that addresses three primary environmental concerns – firstly, what harmful chemicals are in the environment, secondly, what are the effects of these harmful chemicals, and, thirdly, how can the harmful chemicals and their effects be reduced and/or mitigated?
The aim of the programme is to achieve improved capability for assessing and mitigating the impacts of contaminants in air, land, and water. The programme incorporates basic science research with applied science in relation to environmental contaminants and the development of services to end-users.
It is evident that the programme has the potential, through scientific validation and mitigation techniques, to benefit New Zealand‘s ‘clean and green’ environment status both nationally and internationally. This will affect urban and rural environments, as well as the health of people and ecosystems. It is proposed to achieve the aims of the programme through a new generation of ‘effects-based’ environmental performance indicators integrated with traditional chemical assays.

http://www.frst.govt.nz

In 1998 researchers in Sweden reported something alarming: concentrations of a class of compounds known as polybrominated diphenyl ethers (PBDEs) have been increasing exponentially in human breast milk. PBDE concentrations in breast milk have doubled every five years for the past 25 years, though their concentrations are still an order of magnitude lower than polychlorinated biphenyls (PCBs). PBDEs are widely used as fire retardants for plastics and textiles. PCBs are a now-banned toxin originally used in many electrical transformers.

PBDEs are so-called persistent organic pollutants (POPs), of concern to health officials worldwide because of their toxicity, tendency to accumulate in human and animal tissue, and their long lifetime in the environment. DDT and chlorinated dioxins are two better-known examples of POPs whose toxic properties have long been recognized. In contrast little is known about PBDEs, particularly in the U.S. Based on what little research has been done, PBDE may cause thyroid disease or neurological problems in children — but these links are far from proven. As of 2000, however, Denmark and Austria have imposed strict regulation on the substance’s use, and other European nations are considering doing likewise. “PBDE may be the PCB of the future,” write Kim Hooper and Thomas McDonald, researchers at the California Environmental Protection Agency.

Cancer, neurological development of children, thyroid disease — these are the types of health effects that make headlines. That puts PBDEs and similar chemicals on the top of any list of emerging contaminants: potentially toxic substances whose effects or presence are poorly known, often because these chemicals have only begun to enter the human water or food supply.

Keeping Up with the Joneses

One of the greatest challenges of keeping U.S. water supplies clean and safe to drink is that the mix of chemicals used by society is continually changing. New compounds, or their by-products, eventually find their way into the U.S. waste stream, and ultimately in some form they become part of what we drink. How do local and national agencies keep up with perpetual change? What emerging contaminants, unknown or virtually unnoticed just a few years ago, are just cropping up today?

Ever since the 1970s, U.S. clean water regulations have been attuned to mitigating the harmful effects of new chemicals. In fact, the Clean Water Act initially required the EPA to identify, monitor, and regulate 25 new toxins every three years, a process that led to an ever-lengthening list of contaminants subject to federal controls. In 1996 Congress modified this system by amending the Safe Drinking Water Act to require a more rational approach to emerging contaminants. In addition to requiring a cost-benefit approach to new contaminant regulation, the amendments focused on developing a prioritized list of new contaminants based on scientific studies of health effects. The result has been new research on emerging contaminants and an increased emphasis on methods of analyzing health effects of contaminants.

One area in which several advances have recently been made is related to long-term health effects of chemical exposure. Humans are constantly exposed to a variety of contaminants present at low levels. These include both new chemicals, with previously unknown effects and those with well-known acute (short-term exposure) human and ecological health effects. Arsenic and radionuclides are two examples where recent long-term health studies have led to increased concern about low-level exposure. As a consequence, regulators are now looking into appropriate responses. Other studies are now examining the impacts of organic compounds that may interfere with the endocrine systems of living organisms. These so-called endocrine disruptors can also be active at very low levels. The EPA’s Endocrine Disruptor Screening Program is helping identify endocrine disruptors from the estimated 87,000 chemicals used today. The consequences of these in humans are just now being studied. In animals, endocrine disruption has been shown to hinder sexual function, complicate pregnancy, and cause thyroid problems leading to metabolic disorders.

Another active area of research is focused on how chemicals interact with each other and the natural environment. In the past, studies have focused on the effects of single chemicals because chemicals are usually regulated singly. However, chemicals are always present as complex mixtures, thus some might say the regulation approach is naïve. Thus scientists are increasingly focusing on the toxicity of mixtures of chemicals, acknowledging that the toxicity expressed may be a result of additive or multiplicative effects, depending on interactions with other chemicals present in the environment. In addition, chemicals can have indirect impacts on humans. For example, antibiotics are considered an emerging contaminant because they may influence the development of resistance in microbes. Antibiotics enter the environment through human wastes. In addition, these products are increasingly being used for veterinary purposes and thus may enter from farm and feeding operations — ranging from poultry to hog farming operations.

Finally, researchers are continuing to find new chemicals that bioaccumulate in the food chain. Such chemicals can be present in water at very low levels, yet accumulate to higher concentrations in living tissue, substantially magnifying any health effects. Methylmercury, the most toxic form of mercury, is an example of such a bioaccumulating toxin. With methylmercury, public health officials have in some cases recommended against the consumption of fish by pregnant women.

Mercury emissions from fossil fuel power plants bioaccumulate in the fatty tissue of lake and river fish; its concentrations are biomagnified yet again in fetal tissue and can lead to neurological problems in children, though these neurological studies are somewhat controversial.

DDT is another example of a chemical that bioaccumulates in aquatic organisms. In the 1960s DDT was found to be endangering the bald eagle, peregrine falcon, osprey, brown pelican, and other bird populations reliant on fish diets. DDT and its metabolites reduced the thickness of eggshells, making them more susceptible to breaking during incubation. Since the banning of DDT in 1972 populations of these birds in the U.S. have rebounded dramatically — proof that the environmental levels of the chemicals were reduced, and thus their effects were reduced.

Another challenge faced by researchers is uncovering how widespread emerging contaminants are in the environment. After all, many of the contaminants being examined today are not released in easily measured quantities, like those initially targeted by environmental regulations. For example, pesticides are intentionally released in easily measured quantities. In contrast, household chemicals, drugs, animal feed, viruses, and parasites in fecal matter are all released into the environment after passing through municipal water treatment or solid waste systems, and they can also be released directly. The multiplicity of paths of entry complicates the study of such substances.

To help with this problem, the U.S. Geological Survey, in cooperation with the EPA, has launched the National Emerging Contaminants Reconnaissance, a project targeted at finding and monitoring locations where certain suspect chemicals are highly concentrated. USGS is focusing on four groups of compounds: veterinary and human antibiotics, human drugs, industrial and household products (examples include insecticides, detergents, fire retardants, and fuels), and sex and steroidal hormones. Many of the substances under study are familiar to everyday life: caffeine and ibuprofen, for example.

An Evolving Problem

Contamination of water supplies is an evolving problem and will remain an issue as long as technological change continues. Some of the contaminants now being targeted by researchers may come out with a clean slate, while others will require additional scrutiny. One of the hopes of today’s researchers is that more sophisticated science will help speed the process of identifying and remedying the problems, before damage to either human health or the environment can occur. In any case, science and regulation must continue to evolve and change, as it has in the past few years, to respond to new needs presented by chemicals and our increasing knowledge of them.

[Source: http://www.rand.org]

Recent advances in laboratory methodologies made by USGS Toxics Hydrology Program scientists are providing improved capabilities for detecting large numbers of new and potentially harmful contaminants in our water resources at very low levels. There are many thousands of chemicals (including pesticides, human and veterinary medicines, personal care products, and other organic compounds) that enter our water resources by accidental spills, runoff from land applications, conventional waste-management practices and other mechanisms. Many of these compounds are known or suspected to have ecological or human health effects at very low concentrations. Development of capabilities to detect low concentrations in aquatic environments is important for several reasons: 1) many compounds are used in relatively small quantities and therefore concentrations in the environment are low; 2) many degrade or are transformed to other compounds, thereby reducing environmental concentrations; 3) compounds can partition among various environmental media such as soil or sediment particles; 4) the complex mix of natural and manufactured chemicals found in environmental waters can mask the detection of contaminants of concern, and 5) some classes of contaminants may have ecological health effects at low levels.

These new methods provide crucial tools that are enabling scientists to determine:

  • The levels and mixtures of compounds that occur in the environment,
  • The mechanisms by which these compounds enter the environment (source pathways), and
  • The processes that affect the transport, persistence, and fate of the compounds in the environment.

Toxics Program scientists have developed eight new methods during the past year that provide improved measurement capability for many tens of contaminants, including methyl mercury, surfactants, pesticides, and pharmaceuticals. Analytical method development is a continuing research topic for Toxics Program scientists.

More Information

Related Headlines

Recent Publications

  • Babiarz, C.L., Hurley, J.P., Krabbenhoft, D.P., Gilmour, C., and Branfireun, B.A., 2003, Application of ultrafiltration and stable isotopic amendments to field studies of mercury partitioning to filterable carbon in lake water and overland runoff :The Science of the Total Environment, v. 304, p. 295-303.
  • DeWild, J.F., Olson, M.L., and Olund , S.D. , 2002, Determination of methyl mercury by aqueous phase ethylation, followed by gas chromatographic separation with cold vapor atomic fluorescence detection : U.S. Geological Survey Open-File Report 01-445, 14 p.
  • Ferrer, I., Schroeder, H.F., and Furlong, E.T., 2003, LC/MS analyses of cationic surfactants–Methods and applications, in: Knepper, T.P., Barcelo, D., and de Voogt, P., eds., Analysis and fate of surfactants in the aquatic environment: Amsterdam, Elsevier, Comprehensive Analytical Chemistry Series, v. XL, p. 353-383.
  • Ferrer, Imma, Furlong, E.T., and Thurman, E.M., 2003, Identification of Homologue Unknowns in Wastewater by Ion Trap MS: in Liquid Chromatography/Mass Spectrometry, MS/MS and Time-of-Flight MS: Analysis of Emerging Contaminants. American Chemical Society Symposium 850, p. 376-393.
  • Ferrer, Imma and Thurman, E.M., 2003, Analysis of Emerging Contaminants: in Liquid Chromatography/Mass Spectrometry, MS/MS and Time-of-Flight MS: Analysis of Emerging Contaminants. American Chemical Society Symposium 850, Ferrer and Thurman, eds, Chapter 1, p. 2-13.
  • Furlong, E.T., Ferrer, I. , Gates, P.M., Cahill, J.D., and Thurman, E.M., 2003, Identification of Labile Polar Organic Contaminants by Atmospheric-Pressure Ionization Tandem Mass Spectrometry, in: LC/MS/MS and TOF/MS: Analysis of Emerging Contaminants (eds. I Ferrer and E.M. Thurman) American Chemical Society Symposium Series Number 850 p. 175-187.
  • Lee, E.A., Strahan, A.P., and Thurman, E.M., 2002, Methods of analysis by the U.S. Geological Survey Organic Geochemistry Research Group – Determination of glyphosate, aminomethylphosphonic acid, and glufosinate in water using online solid-phase extraction and high-performance liquid chromatography/mass spectrometry: U.S. Geological Survey Open-File Report 01-454, 13 p.
  • Lee, E.A., Zimmerman, L.R., Bhullar, B.S., and Thurman, E.M., 2002, Linker-assisted immunoassay and liquid chromatography/mass spectrometry for the analysis of glyphosate : Analytical Chemistry, v. 74, no. 19, p. 4937-4943.
  • Lee, E.A., Kish , J.L., Zimmerman, L.R., and Thurman, E.M., 2001,Methods of analysis by the U.S. Geological Survey Organic Geochemistry Research Group–Update and additions to the determination of chloroacetanilide herbicide degradation compounds in water using high-performance liquid chromatography/mass spectrometry: U.S. Geological Survey Open-File Report 01-10, 17 p.
  • Leenheer, J.A., Furlong, E.T., Ferrer, I. , and Rostad C.E., 2003, Charge Characteristics and Fragmentation of Polycarboxylic Acids by Electrospray Ionization/Multistage Tandem Mass Spectrometry (ESI/MS/MS), in: LC/MS/MS and TOF/MS: Analysis of Emerging Contaminants (eds. I Ferrer and E.M. Thurman) American Chemical Society Symposium Series Number 850; p. 312-324.
  • Lindsey , M.E. , Meyer, M.T., and Thurman, E.M., 2001, Analysis of trace levels of sulfonamide and tetracycline antimicrobials in groundwater and surface water using solid-phase extraction and liquid chromatography/mass spectrometry : Analytical Chemistry, v. 73, no. 19, p. 4640-4646.
  • Thurman, E.M., and Ferrer, Imma, 2003, Comparison of Quadrupole-Time-of-Flight, Triple Quadrupole, and Ion-Trap Mass Spectrometry/Mass Spectrometry for the Analysis of Emerging Contaminants, ACS Symposium, volume 850.
  • Thurman, E.M. and Ferrer, Imma, 2003, Comparison of Quadrupole Time-of-Flight, Triple Quadrupole, and Ion-Trap Mass Spectrometry/Mass Spectrometry for the Analysis of Emerging Contaminants: in Liquid Chromatography/Mass Spectrometry, MS/MS and Time-of-Flight MS: Analysis of Emerging Contaminants. American Chemical Society Symposium 850, p. 14-31.
  • Thurman, E.M., Ferrer, I. , and Furlong E.T., 2003, TOF/MS and Quadrupole Ion Trap MS/MS for the Discovery of Herbicide Degradates in Groundwater, in: LC/MS/MS and TOF/MS: Analysis of Emerging Contaminants (eds. I Ferrer and E.M. Thurman) American Chemical Society Symposium Series Number 850 p. 128-144.
  • Zimmerman, L.R., Schneider, R.J., and Thurman, E.M., 2002, Analysis and detection of the herbicides dimethanamid and flufenacet and their sulfonic and oxanilic acid degradates in natural water: Journal of Agricultural and Food Chemistry, v. 50, no. 5, p. 1045-1052.
  • Zimmerman, L.R., Ziegler, A.C., and Thurman, E.M., 2002, Method of analysis and quality-assurance practices by U.S. Geological Survey Organic Geochemistry Research Group–Determination of geosmin and methylisoborneol in water using solid-phase microextraction and gas chromatography/mass spectrometry: U.S. Geological Survey Open-File Report 02-337, 12 p.
  • Zimmerman, L.R., Schneider, R.J., and Thurman, E.M., 2002, Analysis and detection of the herbicides dimethanamid and flufenacet and their sulfonic and oxanilic acid degradates in natural water : Journal of Agricultural and Food Chemistry, v. 50, no. 5, p. 1045-1052.

[Source: http://toxics.usgs.gov]