Evaluation of Magnetic Coagulant (α-Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>-MO) and its Reuse in Textile Wastewater Treatment

The textile industries are characterized as one of the biggest consumers of potable water and chemical products throughout its process, being responsible for the elevated wastewater generation with intense coloration and wide polluting potential. In this context, the present study proposes the development and application of a new coagulant material for textile wastewater treatment. The proposed coagulant (α-Fe₂O₃-MO) was composed by hematite nanoparticles (α-Fe₂O₃) obtained by a simple non-pollutant methodology, associated with Moringa oleifera (MO) seeds saline extract compounds. Coagulation/flocculation (CF) efficiency was evaluated by removal of physicochemical parameters such as apparent color, turbidity, and compounds with absorption at UV_254nm (UV_254nm) through CF tests carried out on Jar test equipment and sedimentation carried out in the presence and absence of external magnetic field (600 k Am^?1). Kinetics sedimentation was from 0 to 90 min. The use of this new coagulant allowed the removal of 92.37% for apparent color, 91.43% for turbidity, and 46.09% for UV_254nm, indicating that the proposed coagulant association was efficient in the treatment of this type of wastewater under external magnetic field with only 10 min of sedimentation. In addition, the resulting sludge from CF process was tested as base material for a new coagulant synthesis, demonstrating great reuse potential. Therefore, the new proposed coagulant, composed of α-Fe₂O₃ and the compounds present in the seed extract of MO, has applicability for textile wastewater treatment demonstrating high removal rate for all evaluated parameters with cost reduction in the proposed treatment for this wastewater.     

Comparative Photocatalytic Performance on the Degradation of 2-Naphthol Under Simulated Solar Light Using α-Bi<Subscript>4</Subscript>V<Subscript>2</Subscript>O<Subscript>11</Subscript> Synthesized by Solid-State and Co-precipitation Methods

In this investigation, the photocatalytic activity of α-Bi₄V₂O₁₁ in the degradation of 2-naphthol under simulated solar light was evaluated. Bismuth vanadate α-Bi₄V₂O₁₁ was synthesized by the solid-state reaction method and by co-precipitation in aqueous media, with the aim of comparing their performance in the photodegradation of the aromatic pollutant. The latter method (co-precipitation) has not been previously reported for the synthesis of α-Bi₄V₂O₁₁. Structural evolution of the oxides precursors was determined by X-ray diffraction. Morphology and optical properties of the solids were analyzed by scanning electron microscopy (SEM) and UV-vis diffuse reflectance spectroscopy (UV-vis), respectively. The results showed that at 800 °C, only α-Bi₄V₂O₁₁ was formed in both preparations. The SEM micrographs revealed that the powders were composed of agglomerates with sizes between 0.8–2 μm for those synthesized by co-precipitation and 2–10 μm for those obtained by solid-state reaction. The optical properties indicated that α-Bi₄V₂O₁₁ was activated with visible light during the photocatalytic process. The photocatalytic degradation of 2-naphthol was largely influenced at basic pH, degrading 79% of the contaminant in 240 min, with the powder obtained by co-precipitation; meanwhile, for the solid-state preparation, the degradation reached only 55%.     

Effect of Co-Dopants in TiO<Subscript>2</Subscript>–SiO<Subscript>2</Subscript> Thin films on the Formaldehyde Degradation

Titanium dioxide (TiO₂)–silicon dioxide (SiO₂) thin films were synthesized using the peroxo titanic acid approach (PTA) combined with the sol–gel method at low temperature around 100°C. The effects of type and amount of dopants of ferric (Fe³⁺) or thiourea (N-S) and co-dopants of Fe³⁺ and N-S on the films physicochemical properties and on the photocatalytic degradation of the methylene blue and formaldehyde under UV and visible light irradiation were investigated. Physicochemical properties of photocatalysts were characterized by X-ray diffraction, transmission electron microscopy, wavelength-dispersive X-ray fluorescence spectrometry, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and UV–Vis spectroscopy. The results showed that the TiO₂ crystal phases obtained from this method were exclusively anatase and the needle-like crystals have an average diameter of 10–25 nm. Compared with the single dopant of 1.0 wt.% Fe³⁺ or 0.125 wt.% N-S that was the optimal concentration for photocatalytic degradation of methylene blue and formaldehyde, the co-dopants of 0.125 wt.% N-S + 1.0 wt.% Fe³⁺ furthermore increased the degradation efficiency. Co-dopants of 0.125 wt.% N-S + 1.0 wt.% Fe³⁺ in TiO₂–SiO₂ films were considered to play synergistic roles in narrowing TiO₂ band gap resulting in the higher methylene blue and formaldehyde degradation efficiency. Since the crystal grain size of TiO₂–SiO₂ films synthesized by the PTA method is small, in the visible light region, the high transmittance was attainable to 80% with no-doped and dropped to 50–60% with doped thin films.     

Temporal in situ dynamics of N<Subscript>2</Subscript>O reductase activity as affected by nitrogen fertilization and implications for the N<Subscript>2</Subscript>O/(N<Subscript>2</Subscript>O + N<Subscript>2</Subscript>) product ratio and N<Subscript>2</Subscript>O mitigation

In vitro, high nitrate (NO₃ ^?) concentrations significantly inhibit N₂O reductase activity. However, little information is available on the in situ temporal effects of excessive N fertilization on soil N₂O reductase activity and the regulation of the N₂O/(N₂ + N₂O) product ratio in agricultural soil. This study examined the monthly in situ dynamics of NO₃ ^? concentration, N₂O reductase activity, and N₂O/(N₂ + N₂O) product ratio for 2 years in loamy soil that had received either continuous N fertilizer at 400 kg N ha^?1 year^?1 for 15 years (N400) or no N fertilizers (CK). N₂O reductase activity was significantly lower under the N400 treatment than under the CK and correlated negatively with soil NO₃ ^? concentration. The decrease in N₂O reductase activity resulted in the N₂O/(N₂ + N₂O) product ratio increasing. These results demonstrate that excessive N fertilization has the potential to increase N₂O emissions by reducing N₂O reductase activity in soils. These results highlight the need for N₂O mitigation options to embrace the reduction of soil NO₃ ^? concentrations.     

Emission rates of N<Subscript>2</Subscript>O and CO<Subscript>2</Subscript> from soils with different organic matter content from three long-term fertilization experiments—a laboratory study

Increasing organic matter stocks in soils reduce atmospheric carbon dioxide (CO₂), but they may also promote emissions of nitrous oxide (N₂O) by providing substrates for nitrification and denitrification and by increasing microbial O₂ consumption. The objectives of this study were to determine the effects of fertilization history, which had resulted in different soil organic matter stocks on (1) the emission rates of N₂O and CO₂ at a constant soil moisture content of 60% water-holding capacity, (2) the short-term fluxes of N₂O and CO₂ following the application of different fertilizers (KNO₃ vs. farmyard manure from cattle) and (3) the response to a simulated heavy rainfall event, which increased soil moisture to field capacity. Soil samples from different treatments of three long-term fertilization experiments in Germany (Methau, Spröda and Bad Lauchstädt) were incubated in a laboratory experiment with continuous determination of N₂O and CO₂ emissions and a monitoring of soil mineral N. The long-term fertilization treatments included application of mineral N (Methau and Spröda), farmyard manure + mineral N (Methau and Spröda), farmyard manure deposition in excess (Bad Lauchstädt) and nil fertilization (Bad Lauchstädt). Long-term addition of farmyard manure increased the soil organic C (SOC) content by 55% at Methau (silt loam), by 17% at Spröda (sandy loam) and by 88% at Bad Lauchstädt (silt loam; extreme treatment which does not represent common agricultural management). Increased soil organic matter stocks induced by long-term application of farmyard manure at Methau and Spröda resulted in slightly increased N₂O emissions at a soil moisture content of 60% water-holding capacity. However, the effect of fertilization history and SOC content on N₂O emissions was small compared to the short-term effects induced by the current fertilizer application. At Bad Lauchstädt, high N₂O emissions from the treatment without fertilization for 25 years indicate the importance of a sustainable soil organic matter management to maintain soil structure and soil aeration. Emissions of N₂O following the application of nitrate and farmyard manure differed because of their specific effects on soil nitrate availability and microbial oxygen consumption. At a soil moisture content of 60% water-holding capacity, fertilizer-induced emissions were higher for farmyard manure than for nitrate. At field capacity, nitrate application induced the highest emissions. Our results indicate that feedback mechanisms of soil C sequestration on N₂O emissions have to be considered when discussing options to increase soil C stocks.     

Adaptive values of wild × cultivated sorghum (<Emphasis Type="Italic">Sorghum bicolor</Emphasis> (L.) Moench) hybrids in generations F<Subscript>1</Subscript>, F<Subscript>2</Subscript>, and F<Subscript>3</Subscript>

Gene flow between cultivated and their wild relatives is one of the main ecological concerns associated with the introduction genetically modified (GM) cultivars. GM sorghum cultivar has been developed and its commercial production may be possible in the near future. The rate of gene flow depends on the fitness of wild × cultivated sorghum hybrids. The study aimed at estimating adaptive values of wild × cultivated sorghum hybrids in generations F₁, F₂, and F₃ compared to their parents. Artificial crosses of four wild sorghums, five cultivated sorghums, and two male sterile lines were made to produce the F₁ generation, which were advanced to F₂ and F₃. Each hybrid generation and their respective parents were evaluated for their adaptive value at two sites in a randomised complete block design with seven replicates. The resulting progenies did not show serious fitness penalties. Some hybrids were as fit as their respective wild parents and no consistent differences exist between the three generations studied. Thus, the resultant wild × cultivated hybrids may act as avenue for introgression.     

Heterotrophic nitrification is the predominant NO<Stack><Subscript>3</Subscript><Superscript>−</Superscript></Stack> production mechanism in coniferous but not broad-leaf acid forest soil in subtropical China

A study was carried out to investigate the potential gross nitrogen (N) transformations in natural secondary coniferous and evergreen broad-leaf forest soils in subtropical China. The simultaneously occurring gross N transformations in soil were quantified by a ¹⁵N tracing study. The results showed that N dynamics were dominated by NH₄⁺ turnover in both soils. The total mineralization (from labile and recalcitrant organic N) in the broad-leaf forest was more than twice the rate in the coniferous forest soil. The total rate of mineral N production (NH₄⁺ + NO₃⁻) from the large recalcitrant organic N pool was similar in the two forest soils. However, appreciable NO₃⁻ production was only observed in the coniferous forest soil due to heterotrophic nitrification (i.e. direct oxidation of organic N to NO₃⁻), whereas nitrification in broad-leaf forest was little (or negligible). Thus, a distinct shift occurred from predominantly NH₄⁺ production in the broad-leaf forest soil to a balanced production of NH₄⁺ and NO₃⁻ in the coniferous forest soil. This may be a mechanism to ensure an adequate supply of available mineral N in the coniferous forest soil and most likely reflects differences in microbial community patterns (possibly saprophytic, fungal, activities in coniferous soils). We show for the first time that the high nitrification rate in these soils may be of heterotrophic rather than autotrophic nature. Furthermore, high NO₃⁻ production was only apparent in the coniferous but not in broad-leaf forest soil. This highlights the association of vegetation type with the size and the activity of the SOM pools that ultimately determines whether only NH₄⁺ or also a high NO₃⁻ turnover is present.     

Evaluation of organic carbon stocks and СО<Subscript>2</Subscript> fluxes in grasslands of Western Transbaikalia

The stocks of organic carbon and mean rates of the CO₂ emission during the growing season (May–September) and the entire year were estimated in a sequence of grass ecosystems along the transect encompassing chestnut and meadow-chestnut steppe soils, marsh and meadow alluvial soils, and a haloxerophytic community on a typical solonchak. The total stocks of organic carbon comprised 6.17–9.70 kg С/m² in steppe, 7.41–10.04 kg С/m² in floodplain, and 4.74 kg С/m² in haloxerophytic ecosystems. The portion of humus carbon in the upper 50-cm-thick soil layer comprised 79–92% of the total carbon stock. The mean daily CO₂ emission (С–CO₂/(m² day)) from alluvial soils was moderate (3.3–4.9) or low (1.5–2.5). The dependence of the CO₂ emission on the moistening of steppe soils, temperature of alluvial soils, and temperature and moistening of solonchak was revealed. In comparison with the CO₂ emission from the zonal chestnut soil, its mean values during the growing season and the entire year were 1.2 times higher for the meadowchestnut soil, 3.3 times higher for the marsh alluvial soil, 2.3 times higher for the meadow alluvial soil, and 1.7 times higher for the solonchak. The portion of the CO₂ emission beyond the growing season in the mean annual emission averaged 19.8–24.2% and depended on the type of grass ecosystem and on weather conditions of particular years. The sink of carbon in the grass ecosystems exceeded carbon emission, especially in the steppe ecosystems.     

Application of Novel Fulvic Acid-Coated Magnetite Nanoparticles for CO<Subscript>2</Subscript><Superscript>−</Superscript>-Mediated Photoreduction of Cr(VI)

We here isolate fulvic acids from vermicompost to prepare and characterize novel fulvic acid-coated magnetite nanoparticles. UV-A irradiation of suspensions of the nanoparticles under different experimental conditions led to photo-reduction of Cr(VI). In anoxic conditions in the presence of formic acid, after 60 min of irradiation ca. 100% of Cr(VI) was reduced. Under these conditions, the carbon dioxide radical anions, CO₂ ^.- , mediated the photo-reduction of Cr(VI). However, the high reduction potential of Cr(VI) and the variety of reactive species generated upon UV-A irradiation make this nanomaterial also suitable for Cr(VI) photo-reduction also under aerobic conditions in the presence of formic acid or under anoxic conditions without the addition of formic acid. The possible photodegradation routes involved are discussed in detail.     

Soil CO<Subscript>2</Subscript> sources above a subterranean cave—Pisani rov (Postojna Cave,Slovenia)

Purpose

The objective of this research is to detect abiotic sources of soil CO₂ above a subterranean cave in the Slovenian karst region.

Materials and methods

The research was performed in the forest above Pisani rov (Postojna Cave) near the town of Postojna (SW Slovenia) and also in the cave. Soil gas, atmospheric air and cave air carbon stable isotope composition (δ¹³C_CO2) and CO₂ concentration were measured. Sampling and measurements were performed bi-monthly at the test and control sites above the cave. The abiotic source of soil CO₂ was estimated using a stable isotope mass balance calculation.

Results and discussion

Similar seasonal patterns of soil CO₂ and δ¹³C_CO2 values were observed at both the test and control sites until spring, with higher levels of CO₂ observed in summer and lower in winter. The δ¹³C_CO2 showed the opposite trend, i.e. lower values (?26 to ?20 ‰) in summer and higher values (up to ?17 ‰) in winter and early spring. In spring, the soil CO₂ concentration decreases and the δ¹³C_CO2 value increases only at the control site. A time series of a modelled “isotopically light” endmember revealed large shifts in the data values, due to the presence of an abiotic CO₂ source. Results suggest that the subterranean CO₂ pool and its ventilation is the main source of soil CO₂, accounting for up to 80 % of the soil gas during cold periods.

Conclusions

Ventilation from subterranean cavities is an important source of soil CO₂ in karstic areas and should be taken into account during carbon cycling studies.

     

Low-Cost Synthesis of Organic–Inorganic Hybrid MSU-3 from Gold Mine Waste for CO<Subscript>2</Subscript> Adsorption

Amine-grafted MSU-3 mesoporous silica samples were synthesized from pure and waste silica sources and their CO₂ adsorption performances were evaluated. The obtained samples were characterized using X-ray diffraction (XRD), thermogravimetric analysis (TGA), N₂ adsorption–desorption isotherm analysis, Fourier transform infrared (FTIR), and transmission electron microscopy (TEM). CO₂ adsorption capacities of the samples at different temperatures were determined by TGA. The amine-modified MSU-3 synthesized from waste exhibited the highest CO₂ adsorption capacity of 1.32 mmol/g at 25 °C and 1 bar, depending essentially on the porous texture and the amine content of the material. The CO₂ adsorption isotherms of the synthesized samples were measured by a static volumetric method. Adsorption isotherm indicated that the amine-modified samples presented significantly higher CO₂ adsorption capacity than the pure samples. The Avrami kinetic model fitted the experimental data well and suggested that complex reaction mechanism or the appearance of multiple reaction pathway occurred in the CO₂ adsorption.

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Graphical Abstract CO₂ uptake capacities and TEM images of the amine modified samples

     

Photodegradation of 17α-Ethynylstradiol (EE2) on Nanostructured Material of Type WO<Subscript>3</Subscript>-SBA-15

The growing contamination from the use of endocrine deregulator (EDs) has made the scientific community come worrying, because of this, studies to eliminate these pollutants in the water resources have intensified. Among the processes used, ‘Advanced Oxidative Processes’ (AOP’s) stands out, by means of heterogeneous photocatalysis for the removal of these organic pollutants present in the environment. The paper’s main point is on the synthesis of photocatalysts WO₃-SBA-15 in the molar ratios Si/W (10, 25, 50, and 75) and the photocatalytic activity in the degradation process of 17α-ethynylstradiol (EE2), present in several water contaminants. The catalysts prepared were characterized by XRD, XRF, Raman, FTIR, UV-vis, adsorption, and desorption of nitrogen, and to determine the photocatalytic activity, frequency of turnover (TOF) was used. Through the characterizations, it can be observed that insertion of nanoparticles in WO₃ did not cause changes in the mesoporous structure of the SBA-15 and there is presence of monoclinic, triclinic, and orthorhombic phases of WO₃. The photocatalytic activity showed to be dependent on the calcination temperature and the molar ratio of the catalysts WO₃-SBA-15, being the sample WO₃-SBA-15(50) at 600 °C which presented the greatest degradation potential in the degradation of 17α-ethynylstradiol, with 98%, using ultraviolet radiation, for 4 h. Moreover, reuse of the catalyst did not show significant losses after 4 cycles, with 82% in EE2 degradation.     

Trends and Spatiotemporal Patterns of Tropospheric NO<Subscript>2</Subscript> over China During 2005–2014

Nitrogen dioxide (NO₂) is one of the major atmospheric pollutants, and the concentration of NO₂ is regarded as one of the indicators of air quality. In the past decades, China has experienced rapid economic growth and severe NO₂ pollution to match. We evaluate the trends and spatiotemporal patterns of tropospheric NO₂ over mainland China from 2005 to 2014 using vertical column density (VCD) datasets retrieved from the Ozone Monitoring Instrument (OMI). Results show that from 2005 to 2014, NO₂ pollution regions have enlarged at the national scale, and high NO₂ VCDs are mainly concentrated over highly populated regions in eastern China. The year 2011 is the turning point. Tropospheric NO₂ VCDs first significantly increase by 0.19?×?10¹⁵ molec cm^?2?year^?1 (R ²?=?0.94, P?=?0.002) from 2005 to 2011, and then decrease by 0.21?×?10¹⁵ molec cm^?2?year^?1 (R ²?=?0.97, P?=?0.016) from 2011 to 2014. Since 2011, tropospheric NO₂ VCDs over central-east China decrease remarkably. Tropospheric NO₂ VCDs is higher in November (3.630?×?10¹⁵ molec/cm²), December (4.758?×?10¹⁵ molec/cm²), and January (4.863?×?10¹⁵ molec/cm²), while lower in July (1.684?×?10¹⁵ molec/cm²), August (1.627?×?10¹⁵ molec/cm²), and September (1.703?×?10¹⁵ molec/cm²), indicating that winter and spring are the most polluted seasons. Due to the huge gap in population density and industry development between western and eastern China, the spatial pattern of tropospheric NO₂ VCDs shows large west-east difference.     

Are Nitric Acid (HNO<Subscript>3</Subscript>) Digestions Efficient in Isolating Microplastics from Juvenile Fish?

A standard method for the detection and isolation of microplastics is required to adequately investigate plastic ingestion by juvenile fish. Dissections of juvenile fish guts require precise handling, which can affect the processing time if sample numbers are high. To investigate the efficacy of nitric acid (HNO₃) in aiding the isolation of microplastics using whole fish, we digested juvenile glassfish, Ambassis dussumieri (Cuvier, 1828), at room temperature and at 80 °C. For a complete digestion, overnight incubation in 10 mL of 55% analytical-reagent (AR) HNO₃ was sufficient for a whole fish of 1 g at room temperature. When coupled with elevated temperature, the digestion time is shortened to a few minutes and larger fish of 3 g can be digested in 30 min. Four of the five types of plastic survived the process, with nylon being the exception. This is a shortfall to the method; however, until a better method replaces it, we still value the use of HNO₃ for its simple, inexpensive, swift and complete digestions of whole fish. Four fish species from two feeding guilds were digested using this method to validate its use. The number of plastic particles ingested did not differ between benthic and pelagic species and microplastic fibres comprised the majority of the plastic types found.     

Changes in CO<Subscript>2</Subscript>, <Superscript>13</Superscript>C abundance,inorganic nitrogen, β-glucosidase,and oxidative enzyme activities of soil during the decomposition of switchgrass root carbon as affected by inorganic nitrogen additions

This study was conducted to investigate the effect of inorganic nitrogen (N) and root carbon (C) addition on decomposition of organic matter (OM). Soil was incubated for 200 days with nine treatments (three levels of N (no addition (N0) = 0, low N (NL) = 0.021, high N (NH) = 0.083 mg N g⁻¹ soil) × three levels of C (no addition (C0) = 0, low C (CL) = 5, high C (CH) = 10 mg root g⁻¹ soil)). The carbon dioxide (CO₂) efflux rates, inorganic N concentration, pH, and potential activities of β-glucosidase and oxidative enzyme were measured during incubation. At the beginning and the end of incubation, the native soil organic carbon (SOC) and root-derived SOC were quantified by using a natural labeling technique based on the differences in δ ¹³C between C3 and C4 plants. Overall, the interaction between C and N was not significant. The decomposition of OM in the NH treatment decreased. This could be attributed to the formation of recalcitrant OM by N because the potentially mineralizable C pool was significantly lower in the NH treatment (3.1 mg C g⁻¹) than in the N0 treatment (3.6 mg C  g⁻¹). In root C addition treatments, the CO₂ efflux rate was generally in order of CH > CL > C0 over the incubation period. Despite no differences in the total SOC concentration among C treatments, the native SOC in the CH treatment (18.29 mg C g⁻¹) was significantly lower than that in the C0 treatment (19.16 mg C g⁻¹).     

Quantifying Local Creation and Regional Transport Using a Hierarchical Space–Time Model of Ozone as a Function of Observed NO<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>, a Latent Space–Time VOC Process,Emissions, and Meteorology

We explore the ability of a process-based space–time model to decompose 8-hour ozone on a given day and site into parts attributable to local emissions and regional transport, to provide space–time predictions, and to assess the efficacy of past and future emission controls. We model ozone as created plus transported plus an error with seasonally varying spatial covariance parameters. Created ozone is a function of the observed NO _x concentration, the latent VOC concentration, and solar radiation surrogates. Transported ozone is a weighted average of the ozone observed at all sites on the previous day, where the weights are a function of wind speed and direction. The latent VOC process mean includes emissions, temperature, and a workday indicator, and the error has seasonally varying spatial covariance parameters. Using likelihood methods, we fit the model and obtain one set of predictions appropriate for prediction backward in time, and another appropriate for predicting under hypothetical emission scenarios. The first set of predictions has a lower root-mean-squared error (RMSE) when compared to point observations than do the 36 km gridcell averages from the Community Mesoscale Air Quality Model (CMAQ) used by the EPA; the second set has the same RMSE as CMAQ, but under-predicts high ozone values.     

For how long does the quality and quantity of residues in the soil affect the carbon compartments and CO<Subscript>2</Subscript>-C emissions?

Purpose

The mineralization/immobilization of nutrients from the crop residues is correlated with the quality of the plant material and carbon compartments in the recalcitrant and labile soil fractions. The objective of this study was to correlate the quality and quantity of crop residues incubated in the soil with carbon compartments and CO₂-C emission, using multivariate analysis.

Materials and methods

The experiment was conducted in factorial 4?+?2?+?5 with three replicates, referring to three types of residues (control, sugarcane, Brachiaria, and soybean), and two contributions of the crop residues in constant rate, CR (10 Mg ha^?1 residue), and agronomic rate, AR (20, 8, and 5 Mg ha^?1 residue, respectively, for sugarcane, soybean, and Brachiaria), evaluated five times (1, 3, 6, 12, and 48 days after incubation). At each time, we determined the CO₂-C emission, nitrogen and organic carbon in the soil, and the residues. In addition, the microbial biomass and water-soluble, labile, and humic substance carbons fractionated into fulvic acids, humic acids and humin were quantified.

Results and discussion

Higher CO₂-C emissions occurred in the soil with added residue ranging from 0.5 to 1.1 g CO₂-C m^?2 h^?1 in the first 6 days of incubation, and there was a positive correlation with the less labile organic soil fractions as well as residue type. In the final period, after 12 days of soil incubation, there was a higher relation of CO₂-C emission with carbon humin. The sugarcane and soybean residue (20 Mg ha^?1) promoted higher CO₂-C emission and the reduction of carbon residue. The addition of residue contributed to an 82.32 % increase in the emission of CO₂-C, being more significant in the residue with higher nitrogen availability.

Conclusions

This study shows that the quality and quantity of residue added to soil affects the carbon sequestration and CO₂-C emission. In the first 6 days of incubation, there was a higher CO₂-C emission ratio which correlates with the less stable soil carbon compartments as well as residue. In the final period of incubation, there is no effect of quality and quantity of residue added to soil on the CO₂-C emission.

     

Chromosome and genome composition of a <Emphasis Type="Italic">Triticum</Emphasis> × <Emphasis Type="Italic">Thinopyrum</Emphasis> hybrid by classical and molecular cytogenetic techniques

Triticum–Thinopyrum amphiploids arose from the need to obtain forage grasses highly resistant to pest, drought, soil salinity and frost and they can be used as efficient bridges to transfer desired genes from wheatgrass species to wheat. One of them is trigopiro SH16 INTA, it was introduced in Argentina in 1947 but its genomic composition was unknown. The aim of this work was to determine the chromosome number and genomic and chromosome composition of trigopiro SH16 INTA in order to use it in breeding programs. The simultaneous use of the in situ hybridization technique with different probes (genomic DNA of Th. ponticum (Podp.) Barkworth et D.R. Dewey, pSc119.2 and pAs1) allowed us to conclude that the chromosome number of trigopiro SH16 is 2n = 42 and the genome composition would be: 14 chromosomes of the B genome, the 2D and 4D chromosome pairs of wheat, 14 chromosomes of the J genome of Thinopyrum and the remaining chromosomes probably belong to the A genome of wheat.     

Comparative genetic diversity of <Emphasis Type="Italic">Triticum aestivum–Triticum polonicum</Emphasis> introgression lines with long glume and <Emphasis Type="Italic">Triticum petropavlovskyi</Emphasis> by AFLP-based assessment

Genetic diversity of a set of introgression lines of Triticum aestivum L./T. polonicum L. with long glume and T. petropavlovskyi Udacz. et Migusch. were analyzed by Amplified Fragments Length Polymorphism (AFLP). Small-scale bulk breeding method was applied throughout until F₆ generation to develop the introgression lines. Thirty-eight hexapolid F₇ plants with long glume phenotype and their parents were subjected to AFLP analysis by four primer combinations. A total of 47 polymorphic loci were detected between the parents, 15 of them were introgressed across the 38 lines. It was hypothesized that approximately 50% of A or B genomes associated polymorphic loci were introgressed. The variation of introgression lines was limited within the diversity between their parents, T. aestivum L. cv. Novosibirskaya 67 (N67) and T. polonicum L. cv. IC12196. N67 was closer to 38 introgression lines than that of IC12196. The UPGMA cluster and principal coordinate analysis (PCO) grouping showed 0.84 to 0.98 similarity values between N67 and the introgression lines. Eleven T. petropavlovskyi accessions were distinguished from introgression lines with UPGMA clusters and PCO groupings, and T. petropavlovskyi was located between the introgressions lines and IC12196. Several introgression lines resembled with T. petropavlovskyi for awning and glume length. The genetic variation among 38 introgression lines was much wider than that of T. petropavlovskyi. We concluded that T. petropavlovskyi was established by intensive selection of hybrid between T. aestivum/T. polonicum.     

The introgression of 2× 1EBN <Emphasis Type="Italic">Solanum</Emphasis> species into the cultivated potato using <Emphasis Type="Italic">Solanum verrucosum</Emphasis> as a bridge

Wild diploid Solanum species with an endosperm balance number (EBN) of one are a rich source of disease resistance, pest resistance, and tuber quality traits. They are not sexually compatible with 4× 4EBN or 2× 2EBN forms of the cultivated potato. In this study, the wild 2× 2EBN Mexican species S. verrucosum (ver) was used as a bridge species to access 2× 1EBN germplasm. Hybrids (V1) were created between ver as a female parent and the 1EBN species S. cardiophyllum, S. chancayense, S. commersonii, and S. trifidum. Most of the V1 hybrids were successfully crossed as females to cultivated 2× 2EBN clones. However, due to stylar barriers, reciprocal crosses were unsuccessful. Additional studies are underway to determine the effectiveness of ver as a bridge to introgress specific traits from 2× 1EBN germplasm into the cultivated potato.