Eficiência de fontes, dinâmica do magnésio no solo sob a cultura do café no Brasil e comparação da análise de K, Ca e Mg em solos do Arkansas-EUA seco em estufa e úmido de campo

A cultura do café no Brasil tem apresentado frequente deficiência de magnésio (Mg) limitando sua produtividade, portanto faz-se necessário o estudo de fontes que contenham Mg para essa cultura. Por outro lado, o estudo das metodologias de análise de K, Ca e Mg no solo é um outro ponto que precisa ser estudado para melhor manejo da fertilidade do solo e recomendação de adubações. Objetivou-se com o primeiro experimento avaliar a eficiência de fontes de magnésio para a cultura do café e a dinâmica deste nutriente no perfil do solo. E com o experimento desenvolvido em Arkansas-EUA, avaliar as correlações entre as concentrações de nutrientes do solo seco em estufa e úmido de campo extraídos com Mehlich-3 e 1 mol L-1 NH4OAc. Observou-se que o óxido e oxissulfato de Mg elevaram os valores de pH e CTC e diminuíram a concentração de H + Al do solo. As fontes diminuíram a disponibilidade de K e Ca, e aumentaram o Mg no solo. Na planta, óxido e sulfato de Mg proporcionaram maior concentração de Mg foliar. Apenas no segundo ano de avaliação houve aumento de produtividade do café. Os fertilizantes óxido e oxissulfato de Mg obtiveram o maior índice de eficiência agronômica em relação ao carbonato de Mg. No segundo experimento, K, Ca e Mg extraíveis com Mehlich-3 e NH4OAc foram altamente correlacionados (r2> 0,95) tanto para solo úmido de campo quanto para o seco em estufa. A relação entre as concentrações de K no solo seco em estufa e úmido de campo para Mehlich-3 e NH4OAc foram muito semelhantes e altamente correlacionados (r2 = 0,92). A secagem do solo em estufa teve efeito mínimo sobre as concentrações de Ca e reduziu a concentração de Mg tanto para Mehlich-3 quanto para NH4OAc. Entre os nutrientes estudados, a concentração de K foi a mais afetada pela secagem em estufa, necessitando de pesquisas de campo para correlacionar e calibrar novas recomendações agronômicas.

Summary of boron isotope and Mg/Ca data

Biological productivity and carbon export in the equatorial Atlantic are thought to have been dramatically higher during the last glacial period than during the Holocene. Here we reconstruct the pH and CO2 content of surface waters from the eastern equatorial Atlantic Ocean over the past ~30 k.y. using the boron isotope composition of Globigerinoides ruber (a mixed-layer-dwelling planktic foraminifera). Our new record, combined with previously published data, indicates that during the last glacial, in contrast to today, a strong west to east gradient existed in the extent of air:sea equilibrium with respect to pCO2 (DeltapCO2), with the eastern equatorial Atlantic acting as a significant source of CO2 (+100 µatm) while the western Atlantic remained close to equilibrium (+25 µatm). This pattern suggests that a fivefold increase in the upwelling rate of deeper waters drove increased Atlantic productivity and large-scale regional cooling during the last glacial, but the higher than modern DeltapCO2 in the east indicates that export production did not keep up with enhanced upwelling of nutrients. However, the downstream decline of DeltapCO2 provides evidence that the unused nutrients from the east were eventually used for biologic carbon export, thereby effectively negating the impact of changes in upwelling on atmospheric CO2 levels. Our findings indicate that the equatorial Atlantic exerted a minimal role in contributing to lower glacial-age atmospheric CO2.

Stable isotope and Mg/Ca ratio of sediment core GeoB12610-2

To reconstruct the still poorly understood thermocline fluctuations in the western tropical Indian Ocean, a sediment core located off Tanzania (GeoB12610-2; 04°49.00'S, 39°25.42'E, 399?m water depth) covering the last 35 ka was analysed. Mg/Ca-derived temperatures from the planktonic foraminifera Globigerinoides ruber (white) and Neogloboquadrina dutertrei indicate that the last glacial was ~2.5 °C colder in the surface waters and ~3.5 °C colder in the thermocline compared with the present day. The depth of the thermocline and thus the stratification of the water column were shallower during glacial periods and deepened during the deglaciation and Holocene. The increased inflow of Southern Ocean Intermediate Waters via 'ocean tunnels' appears to cool the thermocline from below, leading to a similarity between the thermocline record of GeoB12610-2 with the Antarctic EDML temperature curve during the glacial. With rising sea level and the corresponding greater inflow of Red Sea Waters and Indonesian Intermediate Waters, the proportion of Southern Ocean Intermediate Water within the South Equatorial Current is reduced and, by Holocene time, the correlation to Antarctica is barely traceable. Comparison with the eastern Indian Ocean reveals that the thermocline depth reverses from the last glacial to present.

(Table 2) Mg/Ca and Sr/Ca composition of planktonic foraminifera from ODP Hole 143-865B

To understand the climate dynamics of hypothesized past greenhouse intervals, it is essential to constrain tropical sea-surface temperatures (SST), yet existing proxy records give conflicting results. Here we present the first Mg/Ca-based study of pre-Quaternary SST and investigate early Paleogene (late Paleocene through late middle Eocene; 58.6-39.8 Ma) tropical temperatures, using planktonic foraminifera belonging to the genus Morozovella from Ocean Drilling Program Site 865 on Allison Guyot (western central equatorial Pacific Ocean). Calcification temperatures similar to or warmer than modern tropical SST are calculated using a range of assumptions regarding diagenesis, temperature calibration, and seawater Mg/Ca. Long-term warming is observed into the early Eocene (54.8-49.0 Ma), with peak SST between 51 and 48 Ma and rapid cooling of 4°C beginning at 48 Ma. These findings are inconsistent with the d18O-based SST previously estimated for this site.

Mg/Ca ratio, Sr/Ca ratio and stable isotopes of the foraminifera Oridorsalis umbonatus in surface sediment samples

We investigate the influence of carbonate system parameters (carbonate ion concentration, [CO3**2-]; carbonate ion saturation, Delta [CO3**2-]) on the trace element and stable isotope ratios in the endobenthic foraminifera Oridorsalis umbonatus. Data from modern core top samples from the Namibian continental slope suggest that the shell composition of this species is influenced by the chemistry of the pore-water. For these organic-rich sediments, the impact of ocean bottom water properties on both pore-water and shell chemistry is surprisingly small. Sr/Ca correlates positively with [CO3**2-] and to a lesser extent with Delta [CO3**2-], which is opposed to previous results. A [CO3**2-] decrease of 10 µmol/kg leads to an increase of 0.05 mmol/mol in Sr/Ca. We observe a correlation between shell d18O (corrected for temperature and d18O seawater) and [CO3**2-], however, the variability of the corrected d18O is close to the analytical limit. No clear dependences were observed for d13C and Mg/Ca.

Mg/Ca ratio of Globorotalia tumida and subsurface temperature reconstruction for ODP Site 130-806

The tropical Pacific thermocline strength, depth, and tilt are critical to tropical mean state and variability. During the early Pliocene (~3.5 to 4.5 Ma), the Eastern Equatorial Pacific (EEP) thermocline was deeper and the cold tongue was warmer than today, which resulted in an mean state with a reduced zonal sea surface temperature gradient, or El Padre. However, it is unclear whether the deep thermocline was a local feature of the EEP or a basin-wide condition with global implications. Our measurements of Mg/Ca of Globorotalia tumida in a western equatorial Pacific site indicate Pliocene subsurface temperatures warmer than today; thus, El Padre included a basin-wide thermocline that was relatively warm, deep, and weakly tilted. At ~4 Ma, thermocline steepening was coupled to cooling of the cold tongue. Since ~4 Ma, the basin-wide thermocline cooled/shoaled gradually, with implications for thermocline feedbacks in tropical dynamics and the interpretation of TEX86-derived temperatures.

Vapour composition and activities in Mg-Zn liquid alloy at 923 K

Vapour species effusing from a magnesia Knudsen cell containing Mg-Zn alloy at 923 K were condensed on a water cooled copper plate. The equilibrium composition of the vapour phase over the alloy was determined from chemical analysis of the condensate. The activity coefficients of both components in the alloy have been derived from the data using a modified Gibbs-Duhem relation. The ratio of saturation vapour pressures of pure Zn and Mg obtained from the analysis of alloy data agree well with values from the literature, providing an internal check on the accuracy of data obtained in this study. Both components of the alloy exhibit negative deviations from Raoult's law. The concentration-concentration structure factor of Bhatia and Thomton at zero wave vector, evaluated from the measurements, indicate the presence of MgZn2 type complex in the liquid state. The associated regular solution model has been used for the thermodynamic description of liquid Mg-Zn alloys.

Gibbs energies of formation of intermetallic phases in the systems Pt Mg, Pt Ca and Pt Ba and some applications

The standard Gibbs energies of formation of platinum-rich intermetallic compounds in the systems Pt-Mg, Pt-Ca, and Pt-Ba have been measured in the temperature range of 950 to 1200 K using solid-state galvanic cells based on MgF2, CaF2, and BaF2 as solid electrolytes. The results are summarized by the following equations: ΔG° (MgPt7) = −256,100 + 16.5T (±2000) J/mol ΔG° (MgPt3) = −217,400 + 10.7T (±2000) J/mol ΔG° (CaPt5) = −297,500 + 13.0T (±5000) J/mol ΔG° (Ca2Pt7) = −551,800 + 22.3T (±5000) J/mol ΔG° (CaPt2) = −245,400 + 9.3T (±5000) J/mol ΔG° (BaPt5) = −238,700 + 8.1T (±4000) J/mol ΔG° (BaPt2) = −197,300 + 4.0T (±4000) J/mol where solid platinum and liquid alkaline earth metals are selected as the standard states. The relatively large error estimates reflect the uncertainties in the auxiliary thermodynamic data used in the calculation. Because of the strong interaction between platinum and alkaline earth metals, it is possible to reduce oxides of Group ILA metals by hydrogen at high temperature in the presence of platinum. The alkaline earth metals can be recovered from the resulting intermetallic compounds by distillation, regenerating platinum for recycling. The platinum-slag-gas equilibration technique for the study of the activities of FeO, MnO, or Cr2O3 in slags containing MgO, CaO, or BaO is feasible provided oxygen partial pressure in the gas is maintained above that corresponding to the coexistence of Fe and “FeO.”