Studies on the response of ‘Tifblue’ and ‘Woodard’ rabbiteye blueberries to fertilizers

A field study was conducted to investigate the effects of three fertilizer placement methods and 11 fertilizer formulations on plant survival, economics of replanting, yield, and fruit size of two rabbiteye blueberry (Vaccinium ashei Reade) cultivars Tifblue and Woodard. Fertilizer rates were either mixed with the soil under plants (before planting), sidedressed, or half-rate was placed under plants with the other half sidedressed. Fertilizers at planting caused a total of 34% Woodard and 12% Tifblue plants to die as compared to 6% for Woodard and none for Tifblue when no fertilizer was applied. Fertilizer formulas 2-1-1 and 5-10-10 oxide ratios placed under Woodard plants caused 100% mortality whereas Tifblue fertilized with oxide ratios 2-2-2 and 5-10-10 under plants reached the maximum 50% mortality. Splitting fertilizer placement under the side of the plants resulted in less Woodard plant mortality (30%) than placing all the fertilizer under plants (54%). However, plant mortality for the side/under group was not different than sidedressing all fertilizer (23%). A planted hectare in this experiment consisted of 1852 Tifblue and 926 Woodard plants, providing one Woodard plant to pollinate two Tifblue plants. Based on the results obtained, the 5-10-10 fertilizer placed under plants would be expected to cause half the Tifblue (926 plants) and all the Woodard (926 plants) to be replanted. Plant costs alone was estimated to be $2315 with additional replanting costs of $93 for Tifblue and much higher for Woodard. Sidedressing 5-10-10 fertilizer eight weeks after planting would have prevented plant mortality. Placement of various fertilizers under Woodard or Tifblue plants resulted in a significant increase in plant mortality as compared to side placement of fertilizers. Yield loss due to plant mortality increased linearly with the N level of the fertilizers (ranging from 0 to 2) for both cultivars. Woodard fruit size was not affected by fertilizer placement but placing fertilizers under Tifblue plants produced smaller yields with larger fruit than sidedressed plants. Blueberry plants in a virgin acidic soil may experience no reduction in yield if fertilization is completely eliminated.     

Chemical effects in commercial and laboratory mixtures of ‘reactive’ phosphate rock and acidulated fertilisers

The chemical analyses of different size fractions of a variety of commerical and laboratory prepared samples of partially acidulated phophate rocks and mixtures of reactive phosphate rock and single superphosphate (called LONGLIFE in New Zealand) have been studied. Whereas only minor chemical segregation effects have been observed for partially acidulated products quite a large bias has been established for LONGLIFE materials, and more especially commercial samples, where larger proportions of phosphate rock were found in the lower size fractions. This inhomogeneity was considered to arise from poor mixing of components and subsequent inconsistent granulation; more stringent rejection criteria for undersize material would greatly assist in improving the product quality. Chemical deactivation of the phosphate rock residue in LONGLIFE materials was also observed; this can be partially explained by a selective reaction of the reactive phosphate rock component with acid still present at the time of mixing with the single superphosphate component.     

Two-variable periodic perturbation of kinetic oscillations

Using one of the generic models (CO oxidation on Pt with surface-oxide formation) predicting kinetic oscillations in heterogeneous catalytic reactions, we show that the efficiency of two-variable periodic perturbations with respect to converting natural period-1 oscillations to period-l oscillations at the forcing frequency is remarkably sensitive to the kind of perturbations used. Counter-phase perturbations are much more effective compared to in-phase perturbations. The physics underlying these findings is suggestive of their applicability to many other models and/or real systems exhibiting kinetic oscillations.     

Effect of the naturally occurring salt ‘Kanwa’ as a fertilizer on the productivity ofStylosanthes in the subhumid zone of Nigeria

Soil nutrient deficiencies pose a serious limitation to higher crop and forage yields in the Nigerian subhumid zone. Some of the deficiencies may be alleviated by using as a fertilizer a salt mined locally called Kanwa which is traditionally used as a cattle lick. Yields ofStylosanthes hamata cv Verano andS. guianensis cv Cook seed and dry matter increased with Kanwa application at different locations. The effect of Kanwa was enhanced when phosphorus was adequately supplied. Improvements to soil physical properties were proportional to the yield of the legume. The implications of good quality fodder and improved soil conditions in Agro-pastoral Systems in the Nigerian SHZ are discussed.     

Mating behaviour and evidence for a female released courtship pheromone in the signal crayfish Pacifastacus leniusculus

The mating behaviour of the signal crayfish, Pacifastacus leniusculus (Dana), has been categorised into seven distinct stages:; orientation; contact; seizure; turning; mounting; spermatophore deposition; and dismounting. These categories were used in the development of a bioassay to test whether mature females release a sex pheromone during the breeding season to which males respond. Water conditioned by 1) mature females (MF water), 2) immature females (IF water) and 3) freshwater (C water), were injected through standard aquarium air-stones into tanks containing mature males. The behaviour of the male was recorded on video for 15 minutes before and after injection of each test water. The time that the males spent exhibiting the three behavioural categories of quiescent, motile and handling of the air-stone, were recorded. Handling of the air-stone included the mating behaviours of seizure, mounting, and spermatophore deposition onto the surface of the air-stone. Males exposed to MF water exhibited significantly increased levels of motile activity and handling behaviour, than males exposed to C water or IF water. These results demonstrate for the first time the presence of a sex pheromone, released during the breeding season by mature females, that stimulates courtship and mating behaviour in male P. leniusculus.     

Phosphorus efficiency of sugarcane varieties in a tropical alfisol

Varietal differences in P absorption and utilization by sugarcane were studied with the objective of selecting phosphorus efficient varieties which can perform well under conditions of low soil phosphorus availability and at low P application rates. Sugarcane varieties differed significantly in dry matter, cane and sugar yields, P-concentration and P-uptake. Based on the cane and sugar yield phosphorus efficiency indices, varieties were classified as P efficient and P-non-efficient. Phosphorus efficient varieties had low P-concentrations and produced higher dry matter per unit P absorbed.     

Effectiveness of rock phosphate, coastal superphosphate and single superphosphate for pasture on deep sandy soils

The effectiveness of coastal superphosphate and two rock phosphate fertilizers was compared with the effectiveness of single superphosphate for pasture production on deep, humic, sandy podzols in high rainfall (> 800 mm annual average) areas of south-western Australia. The pastures were subterranean clover (Trifolium subterraneum) or mixed subterraneum clover and serradella (Ornithopus compressus). Coastal superphosphate was made by adding rock phosphate and elemental sulphur to superphosphate during manufacture, as it came out of the den before granulation. One rock phosphate was a 50% mixture of apatite rock phosphate from Nauru and Christmas Islands, and which was also used to make the single and coastal superphosphate used in this study, and superphosphate made in Western Australia at the time these experiments started. The other rock phosphate was Calciphos, the fertilizer produced by heating (calcining), at about 500 °C, Christmas Island C-grade ore, a calcium iron aluminium rock phosphate. There were two types of experiments. In the three Type 1 experiments, levels of each fertilizer were applied annually. In the two Type 2 experiments, levels of fertilizer were applied once only to new plots in different years. Coastal superphosphate was the most effective fertilizer in the Type 1 experiments, with both rock phosphates and single superphosphate being equally effective. All fertilizers were equally effective in the Type 2 experiments. There were large variations in fertiliser effectiveness values between yield measurements in the same or different years. It is known that P leaches from freshly-applied superphosphate in these soils. The extent of this leaching probably varies between yield measurements affecting effectiveness values determined for all fertilizers because the effectiveness values were calculated relative to the effectiveness of single superphosphate. The humic, sandy podzols remain wet during the growing season, are acidic, and are known from laboratory studies to possess adequate hydrogen ions to cause extensive dissolution of North Carolina rock phosphate so that rock phosphates are equally or more effective than single superphosphate in these soils. When elemental sulphur in coastal superphosphate is oxidized to SO₄ hydrogen ions are produced which in previous studies has been shown to enhance dissolution of rock phosphate in biosuper, a mixture of rock phosphate and elemental sulphur.     

Sonovoltammetry at platinum electrodes: surface phenomena and mass transport processes

Application of simultaneous ultrasound to representative solution-phase reversible voltammetric couples produce a step-shaped voltammogram at platinum electrodes of both macro and micro dimensions. The limiting current increases with ultrasonic power, but is not markedly affected by ultrasonic frequency in the 20–800kHz region. In contrast the complex voltammetry of a platinized platinum electrode surface within the hydrogen adsorption regime in aqueous acid medium is very little affected by sonication. Factors affecting the reproducibility of sonoelectrochemical experiments when employing ultrasonic sources are discussed.Author to whom correspondence should be addressed     

Electroconductive membrane ‘Celec’ for application in zinc/air alkaline batteries: An impedance study of oxygen reduction at the interface Pt/Celec

Oxygen reduction was studied at a platinum electrode on a new ceramic membrane named Celec in 6m KOH with a view to application of this ceramic material in Zn/air batteries. Cyclic voltammetry and impedance measurements were carried out on the oxygen electrode to investigate the oxygen reduction mechanism in the presence of the Celec ceramic. The impedance diagrams recorded at low and high overpotentials show different characteristics, which are well interpreted by the proposed mechanisms.     

Electron-donor-acceptor interactions with cellulosic systems

Summary Using plasticizers with one or two electron donor groups at the alkyl chain end the formation of either graft-like or network-like systems with a cellulose acceptor is evidenced. The formation of thermoreversible EDA-complexes is indicated by the modification of the rheological properties of the polymeric systems in the final flow region. There is a great influence of the spacer length between the donor groups of the plasticizer but not of the bulkiness of the endgroups.Dedicated to the 60^th birthday of Prof. W. Burchard     

Development of an integrated process for electrochemical reaction and chromatographic SMB-separation

A new continuous process combining electrochemical reaction and chromatographic simulated-moving-bed (SMB) separation is presented. To demonstrate the potential of process integration, this reactor concept is applied to the direct electrochemical production of arabinose by means of simulation. Experimentally verified models of reactor and column units are combined with a model of the electrochemical SMB-reactor. These process units are characterized individually and their model parameters are discussed. The electrochemical reaction inside the microreactor can be described by a series reaction, which has an impact on the design of the integrated process: as the reaction should take place in areas of the SMB-process with maximum educt concentration, the reactors are switched on and off during operation. The integrated process shows interaction between the reaction and the separation to diminish side reactions. Case studies prove the theoretical feasibility of the integrated process. Compared to a conventional process with a reactor followed by a SMB-separation, higher yields can be obtained.     

Effects of partial acidulation on chemical and mineralogical characteristics of residual phosphate rocks

Original phosphate rocks (PR) and water insoluble residues (WIR) from mixtures of reactive PRs and single superphosphate, known commercially as longlife single superphosphate (LLSSP), and from partially acidulated PRs (PAPR), were compared in terms of their elemental content, chemical reactivity as indicated by the apatite unit cell a dimension and solubility. Phosphate rock reactivity is known to be inversely related to the a dimension. Partial acidulation (20%) with commercial grade phosphoric acid resulted in an increase in aluminium (Al), iron (Fe) and fluoride (F) concentrations in the WIRs. The apatite a dimensions of WIRs from LLSSPs were greater than those of the respective original North Carolina (NC), Khouribga (KR), Jordan (JR), Sechura (SE) and Arad (AR) PRs added to single superphosphate (SSP), made from Nauru PR (NR)) to produce the LLSSPs. This was attributed to the presence of the less reactive NR in the WIRs left-over from the SSP. Partial acidulation with phosphoric acid increased the apatite a dimensions of NC and ElHassa (EH) PRs. The increase in apatite a dimension of NC and EH was probably due to selective dissolution of a more reactive fraction of the PRs during partial acidulation. Changes in the apatite a dimension following partial acidulation with phosphoric acid were not significant for the other PRs studied, e.g. Gafsa (GF), KR and AR, although differential X-ray diffractograms (DXRD) indicated that the material dissolved during partial acidulation was more reactive than the WIRs and the original PRs. The apatite a dimension of NC PR was not affected by pretreatment with 2% or 4% citric acid (CTA). The contrasting response in a of NC PR to acidulation with phosphoric and citric acids may be related to differences in the strength of these acids, and/or to the differing environments under which the reactions took place.The 2% CTA and formic acid (FMA) solubilities of the WIRs from LLSSPs and PAPRs were markedly lower than those of the original PRs. This reduction in solubility of PRs following partial acidulation was probably related to changes in mineralogical and chemical composition of the WIRs as indicated by the increases in apatite a dimension of some residual PRs and shifts in peak positions in DXRD, to increases in the concentrations of Fe, Al and F compounds, and to coating effects of PR particles by Fe, Al and F compounds. This, in turn, may reduce the agronomic value of the residual PR component of PAPR and LLSSP fertilizers, particularly over the short-term.The solubility of residual PRs following pretreatment with 2% or 4% CTA was slightly lower than that of the original PRs. The pretreatment caused no significant change in the apatite a dimension of NC PR. The complexing effects of CTA and its lack of Fe and Al impurities may have prevented the formation of Fe, Al and F compounds. The effect of citric acid on PR reactivity is thus quite different from that of the mineral acids used to prepare LLSSPs and PAPRs.     

Potassium fertilization in relation to plant water potential of wheat

The water potential of wheat plants increased during the mid-day noon, probably as an adaptation; the rise was greater with less frequent irrigation and was increased by KCl application.     

Available nitrogen in soils and its determination by the ‘Nmin-method’ and by electroultrafiltration (EUF)

Excess nitrogen fertilizer rates are an environmental hazard. To avoid excess rates, the level of available nitrogen in the soil must be known and considered for assessing the nitrogen fertilizer rate. In arable soils nitrate and exchangeable ammonium in the rooting depth of a crop are directly available to plant roots. These two nitrogen forms are recovered with the Nmin method and they are considered in assessing the nitrogen fertilizer rate for arable crops.Besides nitrate and ammonium recovered by the Nmin method from soil samples taken in early spring, a considerable amount of organic soil nitrogen may be mineralized during the growth period and contribute to crop nutrition. The nitrogen mineralization potential can be determined in incubation tests. The absolute quantities of mineralized nitrogen thus obtained, however, are much higher than the mineralization rates under field conditions. It is for this reason that incubation tests have not obtained a major importance for assessing nitrogen fertilizer rates.With the electro-ultrafiltration (EUF) method nitrate, ammonium, and a minor portion of organic soil nitrogen are extracted from a soil suspension. There is experimental evidence that this organic nitrogen (=Norg) is easily mineralizable. Based on field experiments with cereals and maize formulae were established by which the nitrogen fertilizer rate can be calculated. In these formulae nitrate, ammonium and organic nitrogen extracted by EUF are considered.Advantages and drawbacks of the Nmin method and EUF method are discussed.     

Net nitrogen mineralisation in a drained mollic gleysol under variable soil moisture conditions

Mineralisation of organic matter can substantially add to the risk of nitrogen leaching from drained humus-rich soils under intensive agricultural use. The objective of this study was to investigate net nitrogen mineralisation (NNM) in a drained Mollic Gleysol over the course of a year and to separate contributions from the decomposition of fresh organic residues (litter) and stabilised soil organic matter (humus). Using NNM rates measured under different moisture conditions in two undisturbed subsoil monoliths and a moisture response function determined by incubation experiments with small soil cores from a humus-rich subsoil layer, a first-order rate model was calibrated to describe NNM of the humus pool. Standardised to the same moisture conditions by means of this response function, NNM rate constants were independent of depth and also did not differ between monoliths and small soil cores. The model predicted NNM rates determined in situ at a depth of 20–40 cm well. For the topsoil (0–20 cm) it was necessary to extend the model by a second pool of organic matter with a higher turnover rate (litter pool). Assuming the same moisture and temperature dependence of NNM in the two pools, the basic NNM rate constant of the litter pool was determined by data fitting. With this calibration, the two-pool model predicted a net mineralisation of 322 kg N ha^–1 during the experimental year in the upper 40 cm of the soil of which 55% occurred in the litter pool. While overall NNM predictions relating to the entire study period agreed well with the field data, predictions for individual incubation periods (3–6 weeks) and soil layers were much less reliable.     

Performance of zinc molybdenum phosphate in anticorrosive paints by accelerated and electrochemical tests

This work studied the anticorrosive behaviour of micronized zinc molybdenum phosphate (zinc phosphate modified with zinc molybdate). It was proposed to evaluate its efficiency in solvent borne paints with 30 and 15% of the pigment by volume and a pigment volume concentration/critical pigment volume concentration ratio (PVC/CPVC) of 0.8. The behaviour of paints formulated with different binders such as epoxy, chlorinated rubber, vinyl and alkyd resins, was assessed by accelerated (salt spray cabinet and accelerated weathering) and electrochemical tests. Epoxy and chlorinated rubber paints showed the best anticorrosive performance. The inhibitive action of zinc molybdenum phosphate was confirmed. Good correlation was obtained between salt spray and electrochemical tests.     

Electrochemical and thermal behaviour of LiNi0.8Co0.2O2 cathode in sealed 18650 Li-ion cells

The electrochemical performance of LiNi_0.8Co_0.2O₂ cathodes in Li ion cells was investigated under static and dynamic load conditions, which prevail in electric and hybrid vehicles using constant current constant voltage and hybrid pulse power characteristic procedures.The thermal properties of this cathode were investigated using the differential scanning calorimetric and accelerated rate calorimetric techniques. The cell fabricated with a LiNi_0.8Co_0.2O₂ cathode showed excellent power performance. The specific energy produced by the 18650 cell was 90 Wh kg^–1 at 100 W kg^–1 power level.     

Electrochemistry of anodic F2 evolution at carbon electrodes: Bubble adherence effects in the kinetics at rotating cone electrodes

Fluorine-evolving carbon anodes exhibit unusually high overvoltages characterized also by remarkably large Tafel slopes having values 0.4–0.8 V per decade of current density change. Also, at high current densities, a so-called anode effect associated with a type of passivation sets in. Experiments are described which aim to distinguish high polarization arising from an intrinsically large Tafel slope, generated by a non-ohmic charge transfer barrier layer effect due to CF film formation, from effects due to difficulties of F₂ bubble detechment and F₂ gas film formation at the CF film. Steady state polarization measurements have been made at a rotating carbon cone electrode from which F₂ bubbles, which otherwise remain attached to the electrode and block access to the electrolyte, can be spun away. At the rotated electrode, at low and intermediate current densities, linear Tafel behaviour is still observed but with high slopes associated with the barrier layer film effect. At higher current densities an anode effect, associated with the F₂ gas film, is developed, leading to a type of passivation of the electrode. The two sources of unusually high polarization in the F₂ evolution reaction at carbon are not independent as it is also the formation of the CF film that causes difficulties in gas bubble detachment owing to the lyophobic properties of the fluorinated C/F₂/KF·2HF interface. Polishing effects confirm this conclusion.     

Ultra-high strength polyethylene by hot drawing of surface growth fibers

Summary Hot drawing at 150°C has been applied to high molecular weight polyethylene fibers produced by flow induced crystallization in a Couette apparatus, referred to as the surface growth technique. A distinct improvement of the tensile properties of the fibers was noticed upon drawing. A tensile strength at break of 4.7 GPa was reached. Drawability is discussed in relation to fiber morphology. The shish-kebab like structure of the surface growth fiber was transformed into a morphology consisting of smooth fibrils upon drawing.     

Studies concerning charged nickel hydroxide electrodes I. Measurement of reversible potentials

Reversible potentials (E _R) have been measured for nickel hydroxide/oxyhydroxide couples over a range of KOH concentrations from 0·01–10 M. It is shown that the couples derived from the parent- and-Ni(OH)₂ systems can be distinguished by the relative change in KOH level on oxidation and reduction. In the case of couples derived from the-class of materials a dependence of 0·470 moles of KOH per 2e change is found compared with 0·102 moles of KOH per 2e change for the-class of materials. Couples derived from the- and-Ni(OH)₂ systems can be encountered in a series of activated and de-activated forms having a range of formal potentialsE ₀ . Activated. and de-activated-Ni(OH)₂/-NiOOH couples are found to lie in the range 0·443–0·470 V whilst-Ni(OH)₂/-NiOOH couples lie in the range 0·392–0·440 V w.r.t. Hg/HgO/KOH. It is demonstrated for de-activated,-Ni(OH)₂/-NiOOH couples thatE _R is independent of the degree of oxidation of the nickel cation between states of charge of 25% and 70%. SimilarlyE _R is constant for states of charge between 12% and 60% for activated-Ni(OH)₂/-NiOOH couples. The constant potential regions are considered to be derived from heterogeneous equilibria between pairs of co-existing phases both containing nickel in upper and lower states of oxidation. Differences inE ₀ between the activated and de-activated couples are considered to be related to the degree of order/disorder in the crystal lattice.