Lexikon

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citoplasm

the cytoplasm is the part of a cell that is enclosed within the cell membrane. In eukaryotic cells, the contents of the cell nucleus are not part of the cytoplasm and are instead called the nucleoplasm. In eukaryotic cells, the cytoplasm contains organelles, such as mitochondria, Golgi, lysosomes and spherosomes. The cell organelles are filled with liquid that is kept separate from the rest of the cytoplasm by biological membranes. The cytoplasm is the site where most cellular activities occur, such as many metabolic pathways like glycolysis, and processes such as cell division. The inner, granular mass is called the endoplasm and the outer, clear and glassy layer is called the cell cortex or the ectoplasm.

The part of the cytoplasm that is not held within organelles is called the cytosol. The cytosol is a complex mixture of cytoskeleton filaments, dissolved molecules, and water that fills much of the volume of a cell. The cytosol is a gel, with a network of fibers dispersed through water. Due to this network of pores and high concentrations of dissolved macromolecules, such as proteins, an effect called macromolecular crowding occurs and the cytosol does not act as an ideal solution. This crowding effect alters how the components of the cytosol interact with each other.

(Crowding occurs since these high concentrations of macromolecules reduce the volume of solvent available for other molecules in the solution, which has the result of increasing their effective concentrations. This crowding effect can make molecules in cells behave in radically different ways than in test-tube assays. Consequently, measurements of the properties of enzymes or processes in metabolism that are made in the laboratory in dilute solutions may be different by many orders of magnitude from the true values seen in living cells. The study of biochemical processes under realistically crowded conditions is very important, since these conditions are a ubiquitous property of all cells and crowding may be essential for the efficient operation of metabolism.)

Source: Wikipedia

CMS, IT

Content Management System

coli-titre
community
Competent Authority (CA)
Mcompetent authority means the authority or authorities or bodies established by the Member States to carry out the obligations arising from REACH Regulation. (Source: REACH Glossary)
Competent Authority (CA), REACH
composite sample

composite sample is a combination of multiple individual samples taken at pre-selected times to represent the integrated composition of the wastewater being sampled. Usually all samples added to the composites are equal in size, but flow-proportional composite samples collect amounts proportional to flow.

conservation status of a natural habitat

conservation status of a natural habitat is the sum of the influences acting on a natural habitat and its typical species that may affect its long-term natural distribution, structure and functions as well as the long-term survival of its typical species within the territory referred to in Article 2. The conservative status of a natural habitat will be taken as "favourable" when its natural range and areas it covers within that range are stable or increasing, and the specific structure and functions which are necessary for its long-term maintenance exist and are likely to continue to exist for the foreseeable future, and the conservation status of its typical species is favourable as defined in 92/43.

Source: Council Directive 92/43/EEC of 21 May 1992 on the conservation of natural habitats and of wild fauna and flora.
http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=CELEX:31992L0043:EN:html

constitution

a constitution is a set of fundamental principles according to which a state or other organization is governed.

Constitution and the Environment-relationship
Constitutional Court
contaminated site
contaminated site risk
contamination limit value

treshhold concentration of chemical substances, which poses unacceptable risk in environmnetal compartment, food or cosmetics, etc. Limit values of environmental compartments depend on their use.

content of environmental toxicity test standards
control site sample

control site sample, also known as “background sample”. These are samples of the media similar to the test sample matrix and are taken near to the time and place where the analytes of interest may exist at background levels. Usually the frequency of their analysis should be equivalent to that of the reagent blank. They are used to demonstrate whether the site is contaminated or truly different from the norm. Some sort of background sample is always necessary for a valid scientific comparison of samples suspected of containing environmental contaminants. Control site samples may further be differentiated as “local control site” and “area control sites” samples.

cost-benefit assessment
cracker, IT
cracker, IT2
critical parameters of wastes, HU legislative term
critical review in LCA
D-value: site specific remedial target value of the Hungarian soil regulation

it is a risk based target concentration for contaminated sites and contaminates soils. The Hungarian low requires the calculation of this target concentration in the remedial plan. The D-value is land-use specific.

Daphnia acute toxicity test
Daphnia chronic toxicity test
Data Quality Objectives (DQO)

Data Quality Objectives (DQO) are qualitative and quantitative statements derived from the DQO process describing the decision rules and the uncertainties of the decision(s) within the context of the problem(s).

DQO process is a quality management tool that enables planners to focus their planning efforts by specifying the use of the data (the decision), the decision criteria (action level) and the decision maker’s acceptable decision error rates. The products of the DQO process are the DQOs.

DDR SDRAM, IT

Double Data Rate Synchronous Dynamic Random Access Memory

DDR2, IT
demolition waste
dermal irritation

is the production of reversible damage of the skin following the application of a test substance for up to 4 hours.

detection limit

the lowest concentration of a chemical that can reliably be distinguished from a zero concentration.

detection limit in chemical analysis

in analytical chemistry, the detection limit is the lower limit of detection, or LOD (limit of detection), is the lowest quantity of a substance that can be distinguished from the absence of that substance (a blank value) within a stated confidence limit (generally 1%). The detection limit is estimated from the mean of the blank, the standard deviation of the blank and some confidence factor. Another consideration that affects the detection limit is the accuracy of the model used to predict concentration from the raw analytical signal.

There are a number of different "detection limits" that are commonly used. These include the instrument detection limit (IDL), the method detection limit (MDL), the practical quantification limit (PQL), and the limit of quantification (LOQ). Even when the same terminology is used, there can be differences in the LOD according to nuances of what definition is used and what type of noise contributes to the measurement and calibration.

Source: http://en.wikipedia.org/wiki/Detection_limit

device with mixed firing
digital
direct contact toxicity tests
diversity
diversity index
DMU, Digital MockUp, IT

DMU is a concept that allows the description of a product, usually in 3D, for its entire life cycle. Digital Mockup is enriched by all the activities that contribute to describing the product. The product design engineers, the manufacturing engineers, and the support engineers work together to create and manage the DMU. One of the objectives is to have an important knowledge of the future or the supported product to replace any physical prototypes with virtual ones, using 3D computer graphics techniques. As an extension it is also frequently referred to as Digital Prototyping or Virtual Prototyping. These two specific definitions refer to the production of a physical prototype, but they are part of the DMU concept. DMU allows engineers to design and configure complex products and validate their designs without ever needing to build a physical model.

Source: http://en.wikipedia.org/wiki/Digital_mockup

Among the techniques and technologies that make this possible are:

the use of light-weight 3D models with multiple levels of detail using lightweight data structures such as JT XVL and PDF allow engineers to visualize, analyze, and interact with large amounts of product data in real-time on standard desktop computers.

direct interface to between Digital Mockups and PDM systems.

active digital mockup technology that unites the ability to visualize the assembly mockup with the ability to measure, analyze, simulate, design and redesign.

Drupal, IT

Drupal is an open-source platform and content management system for building dynamic web sites. It offers a broad range of features and services including user administration, publishing workflow, discussion capabilities, news aggregation, metadata functionalities using controlled vocabularies and XML publishing for content sharing purposes. Equipped with a powerful blend of features and configurability, Drupal can support a diverse range of web projects ranging from personal weblogs to large community-driven sites.

Forrás: http://drupal.org/project/drupal

ecotoxicity
ecotoxicity tests, REACH

ECOTOXICITY TESTING METHODS TO BE USED BY THE REACH REGULATION are enlisted in the COUNCIL REGULATION (EC) No 440/2008 of 30 May 2008 laying down test methods pursuant to Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)

(1) Pursuant to Regulation (EC) No 1907/2006, test methods are to be adopted at Community level for the purposes of tests on substances where such tests are required to generate information on intrinsic properties of substances.

(2) Council Directive 67/548/EEC of 27 June 1967 on the approximation of the laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances laid down, in Annex V, methods for the determination of the physico-chemical properties, toxicity and ecotoxicity of substances and preparations. Annex V to Directive 67/548/EEC has been deleted by Directive 2006/121/EC of the European Parliament and of the Council with effect from 1 June 2008.

(3) The test methods contained in Annex V to Directive 67/ 548/EEC should be incorporated into this Regulation.

(4) This Regulation does not exclude the use of other test methods, provided that their use is in accordance with Article 13(3) of Regulation 1907/2006.

(5) The principles of replacement, reduction and refinement of the use of animals in procedures should be fully taken into account in the design of the test methods, in particular when appropriate validated methods become available to replace, reduce or refine animal testing.

(6) The provisions of this Regulation are in accordance with the opinion of the Committee established under Article 133 of Regulation (EC) No 1907/2006

Article 1: The test methods to be applied for the purposes of Regulation 1907/2006/EC are set out in the Annex to this Regulation.

Article 2: The Commission shall review, where appropriate, the test methods contained in this Regulation with a view to replacing, reducing or refining testing on vertebrate animals.

Article 3: All references to Annex V to Directive 67/548/EEC shall be construed as references to this Regulation.

Article 4: This Regulation shall enter into force on the day following its publication in the Official Journal of the European Union.

It shall apply from 1 June 2008.

LIST OF METHODS FOR THE DETERMINATION OF ECOTOXICITY

C.1. Acute toxicity for fish
C.2. Daphnia sp. Acute immobilisation test
C.3. Algal inhibition test
C.4. Determination of ‘ready’ biodegradability
Part i. General considerations
Part ii. Doc die-away test (method C.4-a)
Part iii. Modified oecd screening test (method C.4-b)
Part iv. Co2 evolution test (method C.4-c)
Part v. Manometric respirometry test (method C.4-d)
Part vi. Closed bottle test (method C.4-e)
Part vii. M.I.T.I. Test (method C.4-f)
C.5. Degradation — biochemical oxygen demand
C.6. Degradation — chemical oxygen demand
C.7. Degradation — abiotic degradation: hydrolysis as a function of ph
C.8. Toxicity for earthworms
C.9. Biodegradation — Zahn-Wellens test
C.10. Biodegradation — activated sludge simulation tests
C.11. Biodegradation — activated sludge respiration inhibition
C.12. Biodegradation — modified SCAS test
C.13. Bioconcentration: flow-through fish test
C.14. Fish juvenile growth test
C.15. Fish, short-term toxicity test on embryo and sac-fry stages
C.16. Honeybees — acute oral toxicity test
C.17. Honeybees — acute contact toxicity test
C.18. Adsorption/desorption using a batch equilibrium method
C.19. Estimation of the adsorption coefficient (koc) on soil and on sewage sludge using high performance liquid chromatography (HPLC)
C.20. Daphnia magna reproduction test
C.21. Soil microorganisms: nitrogen transformation test
C.22. Soil microorganisms: carbon transformation test
C.23. Aerobic and anaerobic transformation in soil
C.24. Aerobic and anaerobic transformation in aquatic sediment systems

effective chimney altitude
emission limit value

a maximum permitted emission into the environment, fixed by any of the legislations. These values are determined based on scientific knowledge and represent a limit value, which beyond the emitted substance may cause unacceptable risk on the ecosystem or human.

emission limit value, WFD

the definition of the Water Framework Directive (FWD) says, that emission limit value is the mass, expressed in terms of certain specific parameters, concentration and/or level of an emission, which may not be exceeded during any one or more periods of time. Emission limit values may also be laid down for certain groups, families or categories of substances.

The emission limit values for substances shall normally apply at the point where the emissions leave the installation, dilution being disregarded when determining them. With regard to indirect releases into water, the effect of a waste-water treatment plant may be taken into account when determining the emission limit values of the installations involved, provided that an equivalent level is guaranteed for protection of the environment as a whole and provided that this does not lead to higher levels of pollution in the environment.

emission unit in the air protection
endpoints of environmental toxicity testing
entrance velocity
environmental accreditation system

it is a system for the accreditation and supervision of environmental verifiers operated by an impartial institution or organisation designated or created by the Member State (accreditation body), with sufficient resources and competency and having appropriate procedures for performing the functions defined by the Regulation of 761/2001 for such a system.

Regulation (EC) No 761/2001 of the European Parliament and of the Council of 19 March 2001 allowing voluntary participation by organisations in a Community eco-management and audit scheme (EMAS).

For the purposes of Article 9 of Regulation (EC) No 761/2001, the Commission recognises the following standards and accreditation requirements for the certification bodies:

1. in Austrian legislation: Environmental Management Law (UMG BGBl.I Nr.96/2001) in the relevant version applicable to environmental verifier organisations and individual environmental verifiers;

2. in German legislation: guidelines for accreditation of certification bodies for environmental management systems (EMS) and certification procedures for EMS — issued September 1996 by the German Federal Ministries of Environment, Nature Conservation and Nuclear Safety and for Economics and approved by the Environmental Verification Committee pursuant to Article 21 of the German EMAS Act (Umweltauditgesetz);

3. accreditation requirements, based on the corresponding Guidelines endorsed and made publicly available by the European cooperation for Accreditation (EA), for ISO 14001:2004 certification bodies accredited according to either of the following:

(a) ISO/IEC 17021:2006 (Conformity assessment — Requirements for bodies providing audit and certification of management systems);

(b) ISO/IEC Guide 66:1999 (General Requirements for bodies operating assessment and certification/registration of environmental management systems EMS) until 15 September 2008.

environmental effects of management activities
environmental monitoring

the observation of environmental conditions. Periodic or continuous surveillance or testing to determine the level of compliance with statutory requirements and/or pollutant levels in groundwater, water, soils or fauna and flora. Source: EUGRIS

environmental quality standards