Complementary roles of European and national institutions under the Common Fisheries Policy and the Marine Strategy Framework Directive

Exploited fish and shellfish stocks in European marine waters underlie the Common Fisheries Policy (CFP). The next round of reform of the CFP is due for completion in 2012. The exploitation at maximum sustainable yield (MSY) may be confirmed as the common environmental objective for good environment status (GES) of exploited fish and shellfish stocks of the reformed CFP and the Marine Strategy Framework Directive (MSFD). The foreseen time horizon to achieve or maintain GES by 2020 appears inconsistent with the World Summit on Sustainable Development UN agreement in 2002, which stipulates that maintenance or restoring of stocks to produce MSY be realized by 2015. The MSFD requires instead that by 2015 the national programmes of measures be designed in order to become operational the following year (2016).     

Carbon in olivine single crystals analyzed by the 12C(d,p)13C method and by photoelectron spectroscopy

Carbon subsurface concentration profiles in olivine single crystals from San Carlos, Arizona, and the Sergebet Island. Red Sea, containing total carbon between 60–180 wt.-ppm, were analyzed by means of the ¹²C(d. p)¹³C nuclear reaction and by x-ray induced photoelectron spectroscopy (XPS) in combination with acid etching and with Ar⁺ ion sputtering respectively, between 200–930 K. The (d, p) analysis reveals equilibrium subsurface C profiles extending 1–2 μm or more into the bulk. Their steepness is a function of temperature. Typical mean C concentrations at 300 K in the resolvable layers, 0–0.6, 0.6–1.2, and 1.2–1.8 μm. are 1.8, and 0.6 wt.-%, corresponding to enrichment factors over the mean bulk C concentration of the order of 100, 40 and 30 respectively. In the topmost atomic layers analyzed by XPS the carbon is enriched by a factor of the order of 1000, decreasing with increasing temperature. The results suggest that the carbon is in a truly dissolved state and highly mobile, subject to a reversible subsurface segregation. Most probably local lattice strain associated with the solute C species provide the driving force for this diffusional process. The C diffusion coefficient was determined from the (d, p) data below 300 K: D= 10^?13 exp(?7.8/RT) [m²· sec^?1; KJ · mole^?1] and from XPS data between 450–925 K: D = 10^?14 exp(-6/RT) [m² · sec^?1; KJ · mole^?1] The estimated error of the preexponential factors is ± one order of magnitude, that of the activation energies ±3.5 and ±2 KJ mole^?1 respectively.     

Organic compounds in the early atmosphere formed abiotically from atomic carbon

The recent discovery that atomic carbon occurs plentiful in olivines from mantle-derived rocks opens new aspects for the chemical evolution of the early atmosphere and the origin of life. It has been shown conclusively that atomic carbon which is dissolved in the model oxide MgO is capable of reacting in an O₂-free atmosphere with the lattice oxygen to give CO₂ and with the lattice hydrogen, derived from OH^–, to give a profuse variety of hydrocarbons.The diffusional processes and low temperature gas/solid interface reactions involved in these processes are expected to introduce, purely abiotically, isotope fractionation resulting in a¹³C enrichment of the CO₂ fraction and in a¹³C depletion of the hydrocarbon fraction which may be confused with the¹²C/¹³C isotope fractionation along biological pathways.Atomic carbon dissolved in olivines and in basalts shows a similar behaviour and yields similar quantities as C in MgO: 1–2 mg/g CO₂ and 25–100g/g hydrocarbons degassing between 400 and 1000 °C. On a geological scale this means that each cubic kilometer of basaltic magma degassing in an O₂-free atmosphere has the capacity of sending off about 3–6·10⁹ kg (2·10⁹ m³) of CO₂ and about 1–3·10⁸ kg (2·10⁸ m³) of hydrocarbons. The presence of water modifies the composition to give, among others, alcohols and organic acids.On the basis of these results we are led to the conclusion that the early atmosphere of the earth may have contained a very high concentration of abiotically formed organic compounds of great chemical complexity.

---

Zusammenfassung Die Entdeckung des atomar gelösten Kohlenstoffs in Olivinen aus Mantelgesteinen führt zu neuen Vorstellungen über die Zusammensetzung der Uratmosphäre und Entwicklungsbedingungen des Lebens. Atomarer Kohlenstoff im MgO ist in der Lage, in einer O₂-freien Atmosphäre mit dem Gittersauerstoff zu CO₂ zu reagieren und mit dem aus OH^– stammenden Gitterwasserstoff eine große Vielfalt von organischen Verbindungen zu bilden.Diffusionsprozesse und Gas-Festkörper-Austauschreaktionen, die an diesen Reaktionen beteiligt sind, führen nach ersten Untersuchungen zu einer¹³C-Anreicherung im CO₂ und einer¹³C-Abreicherung bei den Kohlenwasserstoffen. Diese¹²C/¹³C-Fraktionierung ist gleichsinnig mit der biologischen¹²C/¹³C-Fraktionierung.Atomarer Kohlenstoff in Olivinen und Basalten zeigt ein sehr ähnliches Reaktionsverhalten wie im MgO und führt zu ähnlichen Reaktionsprodukten: 1–2 mg/g CO₂ und 25–100g/g Kohlenwasserstoffe zwischen 400–1000 °C. Übertragen auf geologische Verhältnisse bedeutet dies, daß jeder km³ eines entgasenden basaltischen Magmas 3–6·10⁹ kg (2·10⁹ m³) CO₂ und 1–3·10⁸ kg (2·10⁸ m³) abwüschen Kohlenwasserstoff abgeben kann. Die Anwesenheit von Wasser führt zur Bildung von Alkoholen und organischen Säuren. Diese Ergebnisse deuten darauf hin, daß die Uratmosphäre und die Ursuppe viel reicher waren als bisher angenommen an komplexen organischen Verbindungen, die rein thermisch entstanden sind.

---

Résumé La découverte du carbone atomique dans les olivines du manteau entraîne de nouvelles idées sur la composition de l'atmosphère originelle et sur les conditions du développement de la vie. Comme l'est le cas pour le MgO, le carbone atomique dans les olivines est capable de réagir, dans une atmosphère exempte de O₂, avec l'oxygène du réseau cristallin en formant du CO₂, et avec l'hydrogène provenant des groupements OH^– du réseau, pour former une grande variété de composés organiques.Les processus de diffusion et d'échange gas-solide liés à ces réactions provoquent, d'après les premiers résultats, un enrichissement en¹³C dans le CO₂ et un appauvrissement en¹³C dans les hydrocarbures formés. Ceci ressemble au fractionnement dû à des réactions biologiques.Le comportement du carbone atomique et sa réactivité se retrouvent dans les basaltes et les olivines. La gamme des produits de réaction et leur quantité ressemble à celle du MgO: 1–2 mg/g CO₂ et 25–100g/g composés organiques. A l'échelle géologique ceci implique que chaque km³ de magma basaltique dégazé en contact avec une atmosphère exempte d'oxygène pouvait émettre 3–6·10⁹ kg, soit 2·10⁹ m³ de CO₂ et 1–3·10⁸ kg, soit 2·10⁸ m³ d'hydrocarbures abiotiques. La présence d'eau entraîne la formation d'alcools et d'acides organiques.La conclusion tirée de ce travail indique que l'atmosphère originelle et la»soupe primordiale» étaient plus riches qu'on ne l'a admis jusqu'à présent en composés organiques dûs à des processus purement thermiques, et donc abiotiques.

---

. MgO , COg, -, , . , , — — ¹³ ₂ . ¹²/¹³ , . , , - : 1–2 / O₂ 25–100 / , 400–1000 . , 3–6·109 (2·10^{9 3}) ₂ 1– 3·10⁸ (2·10^{8 3}) . . , , , , .

---

---

Presented in part at the meeting Precambrian Problems, Copenhagen, March 1981.     

Gis-aided land evaluation and decision-making for regulating urban expansion: A South African case study

A computerised aid to the land use planning process is demonstrated on the urban edge of Cape Town, South Africa. Multi-criteria analysis is performed in the IDRISI GIS package to evaluate development suitability for four land use categories according to appropriately measured and weighted criteria. The four suitability images are then subjected to multi-objective land allocation to demarcate optimum locations for each land use type. The decision-making process entails execution of seven consecutive steps which are discussed in detail and applied in the case study. Technical decisions are rationalised and results displayed. The paper concludes with a call for the development of applications which can incorporate public participation in this type of decision-making process to ensure the wider acceptance of advanced GIS technology as appropriate technology.     

Intercomparison of Two Hydroxyl Radical Measurement Techniques at the Atmosphere Simulation Chamber SAPHIR

At the atmosphere simulation chamber SAPHIR in Jülich both Laser-Induced Fluorescence Spectroscopy (LIF) and Long-Path Differential Optical Laser Absorption Spectroscopy (DOAS) are operational for the detection of OH radicals at tropospheric levels. The two different spectroscopic techniques were compared within the controlled environment of SAPHIR based on all simultaneous measurements acquired in 2003 (13 days). Hydroxyl radicals were scavenged by added CO during four of these days in order to experimentally check the calculated precisions at the detection limit. LIF measurements have a higher precision (σ= 0.88×10⁶ cm^–3) and better time resolution (Δt = 60 s), but the DOAS method (σ= 1.24×10⁶ cm^–3, Δt = 135 s) is regarded as primary standard for comparisons because of its good accuracy. A high correlation coefficient of r = 0.95 was found for the whole data set highlighting the advantage of using a simulation chamber. The data set consists of two groups. The first one includes 3 days, where the LIF measurements yield (1 – 2) ×10⁶ cm^–3 higher OH concentrations than observed by the DOAS instrument. The experimental conditions during these days are characterized by increased NO_x concentration and a small dynamic range in OH. Excellent agreement is found within the other group of 6 days. The regression to the combined data of this large group yields unity slope without a significant offset.     

Historical pollution variability from abandoned mine sites,Greater Blue Mountains World Heritage Area,New South Wales,Australia

Core and surface sediments from the Tonalli River, a tributary of the artificial lake, Lake Burragorang, in the Blue Mountains National Park, New South Wales, Australia, were studied to evaluate the spatio-temporal distribution of pollutants from the Yerranderie silver-lead-zinc mine site, abandoned in the late 1920s. A sediment core was collected in the mouth of the Tonalli River, at its junction with Lake Burragorang, and surface sediment samples were collected in the Tonalli River and its tributaries. The concentrations of Pb, As, Zn, Cu, Cd, Hg and Ag in the sediments were determined by ICP-MS and ICP-AES techniques. Temporal variability of metal concentrations was established through ²¹⁰Pb dating of the core sediments and compared with published historical records, rainfall records and bushfire data. Metal concentrations in core sediments showed an overall increase around the year 1950 as well as increases coincident with heavy rainfall. Spatially, metal concentrations were up to 400 times the guideline limit around mine sites but decreased rapidly with distance downstream of the mines.