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.     

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.     

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.     

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.     

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.     

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.     

Synthesis of HFC-134a over CrF3/AlF3 catalysts

The effect of the structure of AlF₃ supports in CrF₃/AlF₃ catalysts and their activity were studied, and a selection of suitable reaction conditions for fluorination of trichloroethylene and HCFC-133a was made. We found that neither AlF₃ (- and -modifications) nor CrF₃/-AlF₃ exhibits significant activity for the reaction of HF with CCl₂=CHC1 or CF₃CH₂Cl. However, CrF₃/-AlF₃ exhibits high activity, which increases with increasing surface area and decreasing crystallite size of the -AlF₃ support, and that dramatically affects the fiuorination of CF₃CH₂Cl. Investigation of a series of CrF₃/-AlF₃ catalysts shows that the turnover rates per unit of the total surface area and of the free CrF₃ surface area significantly increase with increasing content of Cr³⁺ loading. Optimum temperature for the reaction of HF with CCl₂=CHCl is 260°C, while with CF₃CH₂Cl it is 350°C, with flow ratios HFTCE = 61 andHFHCFC-133a = 101.     

Selective vapor phase hydroformylation of ethylene over cluster-derived cobalt catalyst

Vapor phase hydroformylation of ethylene was studied with silica-supported metal catalysts. A cobalt metal catalyst derived from Co₂(CO)₈ gave propanal and its derivatives in as high selectivity of about 36% as Rh/SiO₂ catalyst under the reaction conditions of 1.1 MPa of a gas-mixture of ArCOC₂H₄H₂ = 1333 at 423–503 K. On the other hand, conventional cobalt catalysts derived from cobalt nitrate, chloride, or acetate, and other noble metal catalysts (Pd/SiO₂ and Ir/SiO₂) produced mainly ethane.     

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.     

Cathodic behaviour of IrO2 electrodes in alkaline solution Part I: Electrochemical surface characterization

IrO₂ electrodes prepared by thermal decomposition of IrCl₃ on a titanium support at temperatures of calcination between 300 and 500°C have been characterized by cyclic voltammetry and potential steps. Standard voltammetric curves have been recorded between –0.65 and 0.35 V vs SCE (prior to H₂ and O₂ evolution) as a fingerprint of the surface state, and the associated charge,q ^*, has been used to monitor the morphology of the active layer. The effect of hydrogen evolution has been investigated by progressively decreasing the negative potential limit, and by increasingly holding the electrode under hydrogen evolution at a constant potential. Phenomena of proton penetration beneath the outer surface into an inner surface have been quantified by potential step experiments. The effect of storing the electrodes in water rather than in the open air has also been investigated. The thermal oxides lose their typical features at calcination temperature < 350° C. Cathodic load does not appear to cause macroscopic modifications of the surface state.This paper is dedicated to Professor Brian E. Conway on the occasion of his 65th birthday, and in recognition of his outstanding contribution to electrochemistry.     

Response of two okra (Abelmoschus esculentus L. Moench) varieties to fertilizers: Yield and yield components as influenced by nitrogen and phosphorus application

The response of two okra (Abelmoschus esculentus L. Moench) varieties (White velvet and NHAE 47-4) to fertilization in northern Nigeria was examined using four rates of nitrogen (0, 25, 50 and 100 kg ha^–1) and three rates of phosphorus (0, 13 and 26 kg ha^–1). Nitrogen application significantly increased green pod yield, pod diameter, number of fruits per plant, number of seeds per pod and pod weight. Application of phosphorus also significantly increased green pod yield, pod number and number of seeds per pod. The two varieties responded to nitrogen application differentially with respect to green pod yield. For optimum green pod yield of White velvet 35 kg N ha^–1 is suggested while for variety NHAE 47-4, N fertilization can be increased to 70 kg ha^–1. There was no differential response of varieties to phosphorus fertilization for green pod yield; however, the application of 13 kg ha^–1 enhanced the performance of both varieties.     

Studies concerning charged nickel hydroxide electrodes IV. Reversible potentials in LiOH,NaOH, RbOH and CsOH

The variation of reversible potential E_r with log a_moh and has been studied for several nickel hydroxide/oxyhydroxide couples in various alkali hydroxides. Both activated and deactivated -phase couples show only a small dependence ofE _r with log_moh (or where known) in LiOH, NaOH, RbOH and CsOH electrolytes. The change in MOH content on oxidation/reduction is found to be about 0.1 mol MOH per two-electron transfer and is the same as found previously in KOH. These results confirm that the bulk oxidized -phase lattice is devoid of alkali cation although a small quantity may be adsorbed by the surface. On the other hand both activated and deactivated /-phase couples show a marked dependence of 0.45 mol MOH per two-electron transfer in LiOH, NaOH and RbOH (at concentrations > 0.5 m), also in good agreement with earlier data for KOH. On the basis of these results a general stoichiometry can be inferred for the -phase, namely M_0.32NiO₂ · 0.7H₂O where M=Li⁺, Na⁺, K⁺ or Rb⁺. Measurements imply that the Cs⁺ ion or the Rb⁺ ion at low concentration (<0.5 m) do not enter the interlayer structure of the -phase. This behaviour is thought to be related to the low Rb-O and Cs-O bond strengths afforded by the -phase structure.     

Improvement of Catalytic Performance in Isobutane Oxidation to Methacrylic Acid of Keggin-Type Phosphomolybdates by Preparation via Lacunary Precursors: Nature of the Active Sites

A solvent-free method of preparation of a vanadium(V) phosphate is described and discussed. Reaction of V₂O₅ with H₃PO₄ in the absence of water at 150°C leads to the formation of a new catalytic material that is designated as anhydrous VOPO₄. The material readily hydrates to form VOPO₄2H₂O and has been characterised using powder X-ray diffraction, in situ Raman spectroscopy and ³¹P MAS NMR spectrometry. On activation in dry N₂ followed by reaction with butane/air another novel material is formed that has an intrinsic activity for maleic anhydride that is similar to catalysts derived from VOHPO₄0.5H₂O under comparable conditions. Activation of VOPO₄2H₂O under comparable conditions leads to the formation of _I-VOPO₄ which exhibits no partial oxidation activity. Reaction of anhydrous VOPO₄ with alcohols leads to the exclusive formation of VO(H₂PO₄)₂ in further contrast to VOPO₄2H₂O which under similar conditions leads to the synthesis of VOHPO₄0.5H₂O.     

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.     

Heterogeneous asymmetric reactions. 23. Enantioselective hydrogenation of ethyl pyruvate over cinchonine- and α-isocinchonine-modified platinum catalysts

The enantioselective hydrogenation of ethyl pyruvate to (S)-ethyl lactate over cinchonine- and -isocinchonine-modified Pt/Al₂O₃ catalysts was studied as a function of modifier concentration and reaction temperature. The maximum enantioselectivities obtained under the applied mild conditions were 89% ee using cinchonine (0.014 mmoldm^–3, 1 bar H₂, 23°C, 6% AcOH in toluene), and 76% ee in the case of -isocinchonine (0.14 mmoldm^–3, 1 bar H₂, –10°C, 6% AcOH in toluene). Since -isocinchonine of rigid structure exists only in anti-open conformation these data provide additional experimental evidence to support the former suggestion concerning the dominating role of anti-open conformation in these cinchona-modified enantioselective hydrogenations.     

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.     

Yield response and iron status of Japanese mint as influenced by soil and foliar applied iron

Japanese mint (Mentha arvensis L.) often suffers from Fe-chlorosis during the regeneration phase after first harvest when grown on alkaline/calcareous soils. Field studies were conducted during 1987 and 1988 seasons on an alkaline sandy loam soil (pH = 8.0; 4.6% CaCO₃) to investigate the influence of soil and foliar applied Fe on yield and Fe status of MAS-1 and Hybrid-77 Japanese mint. Significant oil yield increases were obtained with two applications of Fe-EDTA, and FeSO₄ in mixtures with ammonium sulphate and mint compost (mint distillation waste) and four split applications of FeSO₄ (total Fe of 12 kg ha^–1) between sprouting and 30 days after first harvest compared to the control. The highest oil yields from two harvests (180 kg ha^–1) were consistently obtained with the Fe-EDTA treatment. Soil application of FeSO₄ at sprouting and first harvest were ineffective compared to Fe-EDTA application. Foliar application of 30 kg ha^–1 of Fe-EDTA resulted in oil yields equal to the yields obtained with soil application of 140 kg ha^–1 of Fe-EDTA. Fe applications increased the concentration and the total uptake of Fe by the crop. Foliar application of Fe-EDTA at two weeks interval alleviates Fe-chlorosis in Japanese mint.     

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.     

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