Enhancements of CO and O3 from burnings in sugar cane fields

The manual harvest of sugar cane requires the burning of its foliage. This burning has strongly increased in Brazil after the National Alcohol Program was started which substituted automobile gasoline engines for alcohol engines. Presently, the source strength per unit area of this rural pollution is comparable to the well-known biomass burning source in Amazonia. The observed concentrations of CO and O₃ in the rural area of the state of São Paulo during the 1988 burning season were twice as large as those reported from an aircraft experiment of 1985 for biomass burnings of the tropical rain forest. Results are reported from airplane measurements and from three fixed ground stations. Mixing ratios of ozone and carbon monoxide in the height range below 6 km are normally less than 40 and 100 ppbv, (parts per billion by volume), respectively, in the absence of burnings. A strong O₃ and CO layer was observed during the burning period with peak concentrations of 80 ppbv of ozone and 580 ppbv of CO at about 2 km. The concentrations of CH₄ and CO₂ were also large, 1756 ppbv and 409 ppmv, respectively, at 1500 m. During the dry season period of the experiment, the ground based O₃ average diurnal variations obtained at the rural sites were practically identical to the typical urban variation observed at São José dos Campos, with daytime ozone values between 45 and 60 ppbv. A second three-day airplane excursion to the surgar cane fields in the wet season of 1989 has produces results to be contrasted with the dry (burning) season of 1988 and 1989. Carbon monoxide concentrations were below 100 ppbv at all heights and ozone concentrations were around 30–40 ppbv. The maximum daytime concentrations at the ground station Bauru was 25 ppbv of O₃, and at Jaboticabal it was 35 ppbv of O₃, only one half of what was observed in the dry season.Universidade Estadual de São Paulo.     

The control of the production process of phytoplankton by the physical structure of the aquatic environment with special reference to its optical properties

This tutorial was designed for nonbiologists requiring an introduction to the nature and general timescales of phytoplankton responses to physical forcing in aquatic environments. As such, an effort was made to highlight biological markers which might assist in identifying, measuring and/or validating physical processes controlling the variability in the distribution, abundance, composition and activity of phytoplankton communities. Given the recent advances in environmental optics and remote sensing capabilities, a special emphasis was placed on the nature and utility of phytoplankton optical properties in current bio-optical modelling efforts to predict temporal and spatial variability in phytoplankton productivity and growth.     

Validation of an annual cycle simulation with a T42-L20 GCM

An annual cycle of an atmospheric general circulation model (AGCM) is presented. The winter and summer zonal averages of the atmospheric fields are compared with an observed climatology. The main features of the observed seasonal means are well reproduced by the model. One of the main discrepancies is that the simulated atmosphere is too cold, particularly in its upper part. Some other discrepancies might be explained by the interannual variability. The AGCM surface fluxes are directly compared to climatological estimates. On the other hand, the calculation of meridional heat transport by the ocean, inferred from the simulated energy budget, can be compared to transport induced from climatologies. The main result of this double comparison is that AGCM fluxes generally are within the range of climatological estimates. The main deficiency of the model is poor partitioning between solar and non-solar heat fluxes in the tropical belt. The meridional heat transport also reveals a significant energy-loss by the Northern Hemisphere ocean north of 45° N. The possible implications of model surface flux deficiencies on coupling with an oceanic model are discussed.This paper was presented at the International Conference on Modelling of Global Climate Change and Variability, held in Hamburg 11–15 September 1989 under the auspices of the Meteorological Institute of the University of Hamburg and the Max Planck Institute for Meteorology. Guest Editor for these papers is Dr. L. Dümenil     

The Second International Conference on the Mediterranean Coastal Environment Medcoast 95

The Second International Conference on the Mediterranean Coastal Environment Medcoast 95     

Intercrystalline cation partitioning between minerals of the triplite-zwieselite-magniotriplite and the triphylite-lithiophilite series in granitic pegmatites

Minerals of the triphylite-lithiophilite, Li(Fe, Mn)PO₄, and the triplite-zwieselite-magniotriplite series, (Mn, Fe, Mg)₂PO₄F, occur in the late stage period of pegmatite evolution. Unfortunately, neither are the genetic relationships between these phosphates fully understood nor are thermodynamic data known. Consequently, phosphate associations and assemblages from 8 granitic pegmatites — Clementine II, Rubicon II and III, and Tsaobismund (Namibia); Hagendorf-Süd and Rabenstein (Germany); Valmy (France); Viitaniemi (Finland) — have been tested for compositional zoning and intercrystalline partitioning of main elements by electron microprobe techniques. Although the selected pegmatites display varying degrees of fractionation, and the intergrowth textures indicate different genetic relationships between the phosphates, the plots of mole fractions X _Fe=Fe/(Fe+Mn+Mg+Ca), X _Mn=Mn/(Fe+Mn+Mg+Ca), and X _Mg=Mg/(Fe+Mn+Mg+Ca) can be fitted relatively well with smooth curves in Roozeboom diagrams. Their deviations from symmetrical distribution curves are mainly dependent upon X _Mg or X _Ca, and upon non-ideal solutions. Surprisingly small differences between the partition coefficients were detected for intergrowths of different origin. However, the partitioning of shared components among coexisting phases is clearly dependent upon the conditions of formation. Compositional zoning is observed only when both Fe–Mn phosphates are intergrown mutually or with other Fe–Mn–Mg mineral solid-solutios. Thus, the zoning does not seem to be due to continuous crystallization, but to later diffusion processes. The triplite structure has preference for Mn, Mg, and Ca, while Fe prefers minerals of the triphylite series. A quantification of main element fractionation between minerals of the triphylite and the triplite series is possible in the cases where diffusion can be excluded. For the Fe/(Fe+Mn) ratios of core compositions an equation with a high correlation coefficient (R=0.988) was determined: Fe/(Fe+Mn)_Tr=[Fe/(Fe+Mn)_Li]/{2.737-(1.737)[Fe/(Fe+Mn)_Li]} (Tr=triplite series, Li=triphylite series). Consequently, the Fe/(Fe+Mn) ratio of the triplite series can now also be used in the interpretation of pegmatite evolution, just like that of the triphylite series which has been successfully applied in the past.     

Magma mixing,the petrogenetic link between anorthositic suites and rapakivi granites, Åland,SW Finland

Summary The Åland, rapakivi batholith consists of several granites that differ texturally and mineralogically from quartz-porphyritic varieties to rapakivi varieties with K-feldspar ovoids (wiborgites and pyterlites) and aplitic granites. Closely associated with the batholith there is a mafc magmatic series of dolerite dykes, norites, anorthosites and monzodiorites.The earliest major intrusive phase of the Åland, rapakivi batholith consists of quartzporphyritic hornblende rapakivi. This rock contains small amoeboidal mafc enclaves, labradorite megacrysts, quartz ocelli, amphibole-mantled xenoliths and irregular clots of granophyric granite. These disequilibrium features are products of mixing between basaltic and granitic magmas. Geochemical modelling indicates that the quartzporphyritic hornblende rapakivi is a mixture of 15% hi-Fe monzodiorite (mafic endmember) and 85% quartz-feldspar porphyry (felsic end-member). The monzodiorite is derived from a norite-anorthosite-monzodiorite series. The quartz-feldspar porphyry is produced by partial melting of the country rock caused by intrusions of hot basic magma.Structural, textural and geochemical features suggest that magma mixing was an important petrogenetic process in the formation of the earliest rapakivi granite intrusions in the Åland, rapakivi batholith. Petrographic evidence of magma mixing can also be found in the major intrusion of the batholith, the wiborgite rapakivi granites. Chemically the mixing is difficult to specify in these rocks because of a high proportion of felsic component. Zircon and apatite fractionation trends, however, indicate that the wiborgite rapakivis also contain components from a mixed source.

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Magmamixing, die petrogenetische Verbindung zwischen Anorthositen und RapakiviGraniten, Åland, SW Finnland

Zusammenfassung Der Rapakivi Batholit von Åland besteht aus verschiedenen Graniten, die in ihrer Textur und Zusammensetzung das Feld von quarzporphyritischen über Rapakivigranite mit K-Feldspat-Ovoiden (Wiborgite und Pyterlite) und aplitischen Graniten abdecken. Eine mafische magmatische Serie von Dolerit-Gängen, Noriten, Anorthositen und Monzodioriten ist mit diesen Batholiten eng verbunden.Die erste größere Intrusivphase des Åland, Rapakivi Batholiten besteht aus quarzporphyritischem Hornblende Rapakivi. Dieses Gestein enhält kleine Amöboide, mafische Enklaven, Labradorit Megakristalle, Quarzocelli, Xenolithe mit Amphibolrändern und unregelmäßige Aggregate von granophyrischem Granit. Diese Produkte von Ungleichgewichts-Bedingungen gehen auf die Mischung zwischen basaltischen und granitischen Magmen zurück. Geochemische Modelle zeigen, daß der quarzporphyritische Hornblende-Rapakivi eine Mischung von 15%. eisenreichen Monzodiorit (mafisches Endglied) und 85% Quarz-Feldspatporphyr (felsisches Endglied) ist. Der Monzodiorit stammt von einer Norit-Anorthosit-Monzodiorit Serie. Der QuarzFeldspat-Porphyr entstand durch teilweise Aufschmelzung des Nebengesteines, die durch Intrusionen heißen basischen Magmas verursacht wurden.Strukturelle, texturelle und geochemische Daten zeigen, daß Magmamischung ein wichtiger petrogenetischer Prozeß der Bildung der frühesten Rapakivi-Granit-Intrusionen im Åland, Batholith waren. Petrographische Hinweise auf Magmamischung können auch in der größten Intrusion des Batholiths, dem Wiborg Rapakivi Granit, gefunden werden. Wegen des hohen Anteils felsischer Komponenten ist es schwierig, das Magmamixing in diesen Gesteinen chemisch zu quantifizieren. Zirkon- und Apatitfraktionierungs-Trends weisen jedoch darauf hin, daß auch die WiborgitRapakivis Komponenten aus einer gemischten Quelle enthalten.

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With 5 figures     

Paleomagnetism of Lower Devonian volcanics and Devonian dykes from northcentral New Brunswick,Canada

Some 50 oriented samples (120 specimens) have been collected on eight sites of volcanic rocks from the Lower Devonian Dalhousie Group of northern New Brunswick and Devonian andesitic to basic dykes from central New Brunswick. Univectorial and occasional multivectorial components were extracted from the various samples. Results after AF and thermal demagnetization compare relatively well. In the volcanics and tuffs, two components of magnetization have been isolated: A (D = 33°, I = ?58°, α₉₅ = 7.3°, K = 236) for four sites and B (D = 66°, I = +53°) for three sites. The grouping of component A is improved after tilt correction but the fold test is not significantly positive at the 95% confidence level. Component A is interpreted as being primary while component B is unresolved and appears to be the resultant magnetization of a Late Paleozoic and a recent component. The pole position obtained for tilt corrected component A is 268°E, 1°S, d_p = 6.5°, d_m = 8.8°. The paleolatitude calculated for component A is 39°S. The paleopole of in situ component A is located close to those of the Early-Middle Devonian formations from Quebec, New Brunswick and New England states while the paleopole of tilt-corrected component A is similar to Lower Devonian poles of rock units from the Canadian Arctic Archipelago. If component A is primary (as we believe it to be), then the western half of the northern Appalachians had already docked onto the North American Craton by Early Devonian time. Alternatively, if component A is secondary the same conclusion applies but the juxtaposition took place in Middle Devonian time.     

Crystal structure refinement of hendricksite,A Zn- and Mn-rich trioctahedral potassium mica: A contribution to the crystal chemistry of zinc-bearing minerals

Summary The crystal structure of hendricksite, a trioctahedral mica of biotite type, characterized by high Zn²⁺ and Mn²⁺ contents has been refined by least square methods. The structural formula is: (K_0.89Na_0.10Ba_0.04)(Mg_1.57Zn_0.54Mn _0.40 ²⁺ Fe _0.25 ²⁺ Al_0.07Ti_0.07Cr_0.01)(Si_2.92Al_1.08)O₁₀ (OH)₂. The space group isC2/m and the cell parameters are:a=5.340(2) Å,b=9.524(2) Å,c=10.235(3) Å, =100.07(2)^o, the cell volume isV=497.98 ų. The final unweightedR=0.072. Average cation-anion distances in polyhedra are: T–O=1.659 Å, M(1)–O=2.093 Å, M(2)–O=2.088 Å, A–O_long=3.316 Å and A–O_short=3.004 Å; A is the alkaline cation. The rotation angle of tetrahedra is =6.7°. The analysis of electron densities, of the dimensions and distorsions of polyhedra shows that Zn²⁺ is exclusively in octahedral sites; there is no order between six-fold coordinated cations. A comparison between the structural features of hendricksite and those of the two main end-members of biotites, phlogopite and annite, is presented.The effect of the strong covalence of Zn–O bonds is particularly visible on the dimensions and orientations of the thermal ellipsoids of octahedral sites M(1) and M(2) which contain zinc. In all the published structures of trioctahedral micas, the ellipsoids of cationic sites are uniaxial positive, elongated parallel toc ^*. In hendricksite, this is observed only for the two zinc-free sites (T and A; in the octahedra M(1) and M(2), which contain zinc, the ellipsoids are approximately uniaxial negative, flattened parallel toa, which is a unique situation.Zinc which habitually favours the tetrahedral coordinations with oxygen, enters the octahedra only, i.e. the chemically anisotropic sites, in hendricksite. The strong polarizability of Zn²⁺ is proposed to explain this behaviour.An examination of the behaviour of Zn²⁺ in other compounds shows that this situation is general, zinc favours chemically anisotropic sites and specially those adjacent to OH or H₂O.

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Affinement de la structure cristalline de la hendricksite, mica trioctaédrique potassique riche en Zn et Mn; une contribution à la connaissance cristallochimique des minéraux zincifères

Résumé On a affiné par moindres carrés la structure de la hendricksite, mica trioctaédrique de type biotite, caractérisé par une teneur élevée en Zn²⁺ et Mn²⁺. La formule structurale de ce mica est: (K_0m89Na_0,10Ba_0,04)(Mg_1,57Zn_0,54Mn _0,40 ²⁺ Fe _0,25 ²⁺ Al_0,07Ti_0,07Cr_0,01)(Si_2,92Al_1,08)O₁₀(OH)₂. Le groupe spatial estC2/m et les paramètres de la maille:a=5,340(2) Å,b=9,254(2) Å,c=10,235(3) Å, =100,07(2)°; le volume de la maille estV=497,98 ų. Le résidu final non-pondéré estR=0,072. Les distances cation-anion moyennes dans les polyèdres sont les suivantes: T–O=1,659 Å, M(1)–O=2,093 Å, M(2)–O=2,088 Å, A–O_long=3,316 Å et A–O_court=3,004 Å où A désigne le cation alcalin. L'angle de rotation tétraédrique, =6,7°, est très semblable à celui de la phlogopite. L'analyse des densités électroniques, des dimensions et distorsions des polyèdres montre que Zn²⁺ est exclusivement en coordinance octaédrique et qu'il n'y a pas d'ordre entre les cations hexacoordonnés. On présente une comparaison des caractères structuraux de la hendricksite avec ceux des deux principaux pôles des biotites, la phlogopite et l'annite.L'effet de la forte covalence de la liaison Zn–O est particulièrement visible sur les dimensions et orientations des ellipsoides d'agitation thermique des deux sites octaédriques, sites zincifères. Dans toutes les structures de micas trioctaédriques publiées, les ellipsoides des sites cationiques sont uniaxes positifs, allongés parallèlement àc ^*, ce qui s' observe effectivement dans les deux sites non-zincifères (T et A) de la hendricksite, par contre, dans les octaèdres M(1) et M(2), qui contiennent le zinc, les ellipsoides sont approximativement uniaxes négatifs, applatis parallèlement àa, ce qui est une situation unique.Le zinc, qui se fixe généralement en sites tétraédriques dans les structures de type oxyde, occupe les sites octaédriques, c'est-à-dire les sites chimiquement anisotropes dans la hendricksite. La forte polarisabilité de Zn²⁺ est proposée pour expliquer ce comportement.Un examen du comportement de Zn²⁺ dans d'autres phases montre que cette situation est tout à fait générale, le zinc privilégiant les sites chimiquement anisotropes et en particulier ceux adjacents à OH où H₂O.

     

Isotope and trace element geochemistry of sediments from the Barbados Ridge-Demerara Plain region,Atlantic Ocean

Twenty-four piston core sediment samples and 13 sediments and 3 basalts from DSDP Leg 78 Site 543 were analyzed for Sr, Nd and Pb isotopic compositions. The results show sediment with highly radiogenic Pb${}^{206}\text{Pb}{}^{204}\text{Pb}$ up to 19.8) and rather radiogenic Sr and unradiogenic Nd has been deposited in the region since the Cretaceous. The source of this sediment is probably the Archean Guiana Highland, which is drained by the Orinoco River. Pb and Sr isotopic compositions and sediment thickness decrease and${}^{143}\text{Nd}{}^{144}\text{Nd}$ increases northward due to a decrease in turbiditic component. This decrease is partly due to the damming action of basement ridges. Rare earth concentrations in the sediments are somewhat low, due to the abundance of detrital and biogenic components in the sediment and rapid sedimentation rates. Both positive and negative Ce anomalies occur in the surface sediments, but only positive Ce anomalies occur in the Site 543 sediments. It is unlikely that sediment subducted to the source region of Lesser Antilles arc magmas could be the cause of negative Ce anomalies in those magmas.Isotopic compositions of Site 543 basalts show some effect of contamination by seawater-basalt reaction products and sediments. Beyond this, however, they are typical of “normal” depleted MORB.