Removal of cadmium from aqueous solution by a soil containing magnesite

Removal of Cd (II) from aqueous solution by a soil containing magnesite and thermal activated soil containing magnesite was investigated. Maximum activation temperature was determined at 700°C for 2?h and maximum adsorption capacities were determined as 4.20?mg/g for natural magnesite, 38.91?mg/g for thermal activated magnesite at 25°C respectively. Equilibrium contact time of cadmium was determined for 2?h. Adsorption of Cd (II) on soil containing magnesite conforms to Langmuir's isotherm.     

The effect of zinc (Zn) application on uptake of cadmium (Cd) in some cereal species

It is widely accepted that plants absorb more Cd when they suffer from Zn deficiency, as the Zn deficiency is a critical problem in the world. The effect of increased Cadmium (Cd) application (0 and 15 mg kg^-1 Cd) on growing and Cd concentration in some cereal species was investigated at the increasing rate of Zinc (Zn) applications (0 and 15 mg kg^-1 Zn). The experiment was carried out under greenhouse conditions using a Zn deficient soil. According to the results, that increased Cd applications severely reduced dry matter production of plants. Dry matter production decreased in the following order: bread wheat > oat > maize > barley. These decreases were determined to be statistically significant (P < 0.01). Cd concentration of cereal species increased with the application of increasing rate of Cd, with a similar trend to that of the dry matter. Dry matter production of plants increased and Cd concentrations of plants decreased with the application of increasing rate of Zn. These results show that Cd accumulation of plant increase in Zn deficient soils. Cd accumulation in plants is hindered with the application of Zn.     

The influence of arbuscular mycorrhizal colonisation on key growth parameters and fruit yield of pepper plants grown at high salinity

This study investigated the effects of arbuscular mycorrhizal (AM) colonisation by Glomus clarum on growth and fruit yield of pepper (Capsicum annum cv. 11B 14) grown at high salinity. The experiment was conducted in pots containing a mixture of perlite and sand (1:1, v/v) under glasshouse conditions. Treatments were: (1) no added NaCl without arbuscular mycorrhizae (NS-AM), (2) no added NaCl with arbuscular mycorrhizae (NS + AM), (3) added 50 mM NaCl without arbuscular mycorrhizae (S1-AM) and (4) added 100 mM NaCl without arbuscular mycorrhizae (S2-AM), (5) added 50 mM NaCl with arbuscular mycorrhizae (S1 + AM) and (4) added 100 mM NaCl with arbuscular mycorrhizae (S2 + AM). The NaCl treatments reduced pepper shoot and root dry matter, and fruit yield compared with the non-saline treatments. The concentrations of N, P and K, in the leaves were significantly reduced by salinity stress, however, mycorrhizal colonisation of the salt-stressed plants restored leaf nutrient concentrations to the levels in non-stressed plants in most cases. AM inoculation improved pepper growth under salt or saltless conditions and reduced cell membrane leakage.     

Spatio‐temporal analyses of marine predator diets from data‐rich and data‐limited systems

Accounting for variation in prey mortality and predator metabolic potential arising from spatial variation in consumption is an important task in ecology and resource management. However, there is no statistical method for processing stomach content data that accounts for fine‐scale spatio‐temporal structure while expanding individual stomach samples to population‐level estimates of predation. Therefore, we developed an approach that fits a spatio‐temporal model to both prey‐biomass‐per‐predator‐biomass data (i.e. the ratio of prey biomass in stomachs to predator weight) and predator biomass survey data, to predict “predator‐expanded‐stomach‐contents” (PESCs). PESC estimates can be used to visualize either the annual landscape of PESCs (spatio‐temporal variation), or can be aggregated across space to calculate annual variation in diet proportions (variation among prey items and among years). We demonstrated our approach in two contrasting scenarios: a data‐rich situation involving eastern Bering Sea (EBS) large‐size walleye pollock (Gadus chalcogrammus, Gadidae) for 1992–2015; and a data‐limited situation involving West Florida Shelf red grouper (Epinephelus morio, Epinephelidae) for 2011–2015. Large walleye pollock PESC was predicted to be higher in very warm years on the Middle Shelf of the EBS, where food is abundant. Red grouper PESC was variable in north‐western Florida waters, presumably due to spatio‐temporal variation in harmful algal bloom severity. Our approach can be employed to parameterize or validate diverse ecosystem models, and can serve to address many fundamental ecological questions, such as providing an improved understanding of how climate‐driven changes in spatial overlap between predator and prey distributions might influence predation pressure.     

Biological traits and prey consumption of <Emphasis Type="Italic">Anthocoris minki</Emphasis> fed on <Emphasis Type="Italic">Agonoscena pistaciae</Emphasis> and <Emphasis Type="Italic">Brachycaudus (Thuleaphis) amygdalinus</Emphasis>

The predatory insect Anthocoris minki Dohrn (Heteroptera: Anthocoridae) is an indigenous Anthocoris species for the biological control of pests in pistachio orchards. The pistachio psylla Agonoscena pistaciae Burckhardt and Lauterer (Homoptera: Psyllidae) is an important insect pest in pistachio trees in Turkey. Similarly, Brachycaudus (Thuleaphis) amygdalinus (Schouteden) (Hemiptera: Aphididae) is a pest of almond trees that is considered as alternative prey for A. minki when pistachio psylla are not available in early spring on pistachio trees. The development time, survival percentage of immature stages, longevity, fecundity, prey consumption, and life table parameters of A. minki fed on A. pistaciae and B. amygdalinus nymphs were determined at 25 ± 1°C, 70 ± 5% r.h., and a 16 h:8 h (L:D) photoperiod under laboratory conditions. The nymphal survival rate was significantly higher when nymphs were fed on A. pistaciae (an average of 96.7%) than on B. amygdalinus (an average of 71.4%). The development time of A. minki was significantly shorter when nymphs were fed on B. amygdalinus (10.3 days) as opposed to A. pistaciae (11.0 days). No significant differences among prey species were found for longevity and fecundity. The total female longevity and fecundity of A. minki was 38.0 days and 247.2 eggs, respectively, when nymphs were fed on A. pistaciae; and 35.4 days and 233.0 eggs, respectively, when nymphs were fed on B. amygdalinus. On average, 104.4 A. pistaciae and 77.7 B. amygdalinus nymphs were consumed during the nymphal development time for A. minki. Adults of A. minki consumed significantly more psyllids than aphids throughout their life span. The greater difference did not significantly inpact the longevity and fecundity of A. minki. Females of A. minki consumed an average of 631.0 A. pistaciae and an average of 273.3 B. amygdalinus nymphs, while female predators consumed significantly more prey than males. The intrinsic rate of increase (r _m ) of A. minki fed on A. pistaciae (0.174) was significantly greater than those fed on B. amygdalinus (0.148). The successful development and reproduction of both A. pistaciae and B. amygdalinus indicates that they are suitable prey for A. minki.     

Effects of deficit irrigation on the yield and yield components of drip irrigated cotton in a mediterranean environment

A field study on cotton (Gossypium hirsutum L., cv.) was carried out from 2005 to 2008 in the Çukurova Region, Eastern Mediterranean, Turkey. Treatments were designated as I₁₀₀ full irrigation; DI₇₀, DI₅₀ and DI₀₀ which received 70, 50, and 0% of the irrigation water amount applied in the I₁₀₀ treatment. The irrigation water amount to be applied to the plots was calculated using cumulative pan evaporation that occurred during the irrigation intervals. The effect of water deficit or water stress on crop yield and some plant growth parameters such as yield response, water use efficiencies, dry matter yield (DM), leaf area index (LAI) as well as on lint quality components was evaluated. The average seasonal evapotranspiration ranged from 287 ± 15 (DI₀₀) to 584 ± 80 mm (I₁₀₀). Deficit irrigation significantly affected crop yield and all yield components considered in this study. The average seed cotton yield varied from 1369 ± 197 (DI₀₀) to 3397 ± 508 kg ha⁻¹ (I₁₀₀). The average water use efficiency (WUE_ET) ranged from 6.0 ± 1.6 (I₁₀₀) to 4.8 ± 0.9 kg ha⁻¹ mm⁻¹ (DI₀₀), while average irrigation water use efficiency (WUE_I) was between 9.4 ± 3.0 (I₁₀₀) and 14.4 ± 4.8 kg ha⁻¹ mm⁻¹ (DI₅₀). Deficit irrigation increased the harvest index (HI) values from 0.26 ± 0.054 (I₁₀₀) to 0.32 ± 0.052 kg kg⁻¹ (DI₅₀). Yield response factor (Ky) was determined to be 0.98 based on four-year average. Leaf area index (LAI) and dry matter yields (DM) increased with increasing water use. This study demonstrated that the full irrigated treatment (I₁₀₀) should be used for semiarid conditions with no water shortage. However, DI₇₀ treatment needs to be considered as a viable alternative for the development of reduced irrigation strategies in semiarid regions where irrigation water supplies are limited.     

QTL analysis and regression model for estimating fruit setting in young Citrus trees based on molecular markers

This study was conducted to assess the genetic basis and develop a regression model for a QTL trait, fruit setting of a full sib population of 164 hybrids obtained between ‘Clementine’ mandarin (Citrus reticulata Blanco ‘Clementine) and ‘Orlando’ tangelo’ (Citrus paradisi Macf. ‘Duncan’ × C. reticulata Blanco ‘Dancy’). Fruit setting of a 164 full sib population field-planted in 2007 was evaluated by visual counting of fruits in 2008, 2009, and 2010. We estimated linkage groups and effects of QTLs by using MapQTL5. Based on interval mapping, seven linkage groups of the maternal and eight linkage groups of the paternal maps harboured QTLs of the fruits setting, covering a total 300 of 1744 cM Citrus map. Only three segments were associated with all three-year data (one in ‘Clementine’ and two in ‘Orlando’ map) spanning 60 cM of 1744 cM of Citrus linkage map. Twenty-seven (17%) and 13 (8%) hybrids consistently produced less than 5 fruits and the highest number of fruits (≥50) in their 2nd, 3rd, and 4th ages. Based on BACKWARD elimination procedure of PROC REG option nested in SAS program, regression models constructed for 2008, 2009, and 2010s fruit setting explained 35, 81, and 38% of the total phenotypic variation (R²) observed in the 164 full-sib hybrids, respectively (P ≤ 0.05). This study indicated that early fruit setting was a complex trait affected by many QTLs and the regression model developed in this study might be used to predict performances of hybrids with similar genetic background.     

Silicon Increases Tolerance to Boron Toxicity and Reduces Oxidative Damage in Barley

ABSTRACT

Silicon (Si) protects plants from multiple abiotic and biotic stresses The effect of exogenous Si levels (50, 75, and 100 mg kg^?1) on the growth, boron (B) and Si uptake, lipid peroxidation (MDA), lipoxygenase activity (LOX; EC 1.13.11.12), proline, and H₂O₂ accumulation, non-enzymatic antioxidant activity (AA) and the activities of major antioxidant enzymes (superoxide dismutase, SOD, EC 1.15.1.1; catalase, CAT, EC 1.11.1.6 and ascorbate peroxidase, APX, EC 1.11.1.11) of barley (Hordeum vulgare L.) were investigated under glasshouse conditions. Increasing levels of Si supplied to the soil with 20 mg kg^?1 B counteracted the deleterious effects of B on shoot growth. Application of B significantly increased the B concentration in barley plants. However, Si application decreased B concentrations. Increasing application of Si increased the Si concentration in barley plants. The concentration of H₂O₂ was increased by B toxicity but decreased by Si supply. Boron toxicity decreased proline concentrations and increased lipid peroxidation (MDA content) and LOX activity of barley. Compared with control plants, the activities of AA, SOD, CAT, and APX in B stressed plants grown without Si decreased, and application of Si increased their activities under toxic B conditions. The LOX activity was decreased by Si. Based on the present work, it can be concluded that Si alleviates B toxicity by possibly preventing oxidative membrane damage, both through lowering the uptake of B and by increasing tolerance to excess B within the tissues.     

Mitigation Effects of Silicon on Maize Plants Grown at High Zinc

The effects of exogenous silicon (Si) on key growth parameters and mineral nutrients were investigated in maize grown at high zinc (Zn). Four treatments with three replicates were investigated consisting of a control (basal nutrients with 0.05 mM Zn with or without 1.0 mM Si added), 0.5 mM Zn, and 0.5 mM Zn plus 1.0 mM Si. Plants growing with high Zn alone had a lower chlorophyll (Chl.) content, leaf relative water content (RWC) and produced less biomass than the control plants. Proline content and membrane permeability was higher in zinc-treated plants than in untreated controls. Compared with the plants treated with high Zn alone, added Si significantly increased plant growth, chlorophyll content, and RWC and significantly reduced the membrane permeability and proline content. As expected, added high Zn increased leaf and root Zn, but reduced leaf phosphorus (P) and iron (Fe). Added Si reduced Zn concentration and increased Fe in leaves of maize. It can be concluded that improvement in the key growth parameters tested and mineral nutrition status in maize plants grown at high Zn induced by Si addition may protect membrane permeability under high zinc, thus mitigating Zn toxicity and improving the growth of maize plants. The results of the present experiment support the conclusion that Si may be involved in physiological and nutritional changes in plants grown at high Zn.     

RESPONSES OF SOME ENZYMES AND KEY GROWTH PARAMETERS OF SALT-STRESSED MAIZE PLANTS TO FOLIAR AND SEED APPLICATIONS OF KINETIN AND INDOLE ACETIC ACID

The study examined the effects of kinetin (KIN) and indoleacetic acid (IAA) applied as seed treatment or sprayed on leaves of salinity stressed plants. Five -week old maize (Zea mays L. cv. ‘DK 647 F1’) plants were grown in pots containing peat and perlite in 1:1 (v/v) mixture. Different treatments used were: 1) control (nutrient solution alone), 2) salt stress [100 mM sodium chloride (NaCl)], 3) 100 mM NaCl and 1 mM kinetin (KIN), 4) 100 mM NaCl and 2 mM KIN, 5) 100 mM NaCl and 1 mM indole acetic acid (IAA), 6) 100 mM NaCl and 2 mM IAA, 7) 100 mM NaCl and 25 mg L^?1 KIN and 8) 100 mM NaCl and 25 mg L^?1 IAA. In treatments 7 and 8 application was to the seeds, for treatments 3-6 it was applied to foliage. The seeds were soaked in KIN or IAA solution for 12 h. Salt stress reduced the total dry matter, chlorophyll content, and relative water content (RWC), but increased proline accumulation, activities of superoxide dismutase (SOD; EC 1.15.1.1), peroxidase (POD; EC. 1.11.1.7), catalase (CAT; EC. 1.11.1.6) and polyphenol oxidase (PPO; 1.10.3.1) and electrolyte leakage. Both foliar applications of KIN and IAA treatments overcame to variable extents the adverse effects of NaCl stress on the above mentioned physiological parameters. However, seed treatments with KIN or IAA did not improve salinity tolerance in maize plants. Furthermore, foliar application or seed treatments with KIN and IAA reduced the activities of antioxidant enzymes in the salt stressed-plants. Salt stress lowered some macronutrient concentrations [calcium (Ca) and potassium (K) in leaves and roots, phosphorus (P) in roots] but foliar application of both KIN and IAA increased Ca in both leaves and roots and P in leaves. Foliar application of IAA increased K concentrations in leaves of the salt-stressed plants. Foliar application of KIN and IAA, especially at 2 mM concentration, counteracted some of the adverse effects of NaCl salinity by causing the accumulation of proline and essential inorganic nutrients as well as by maintaining membrane permeability.