Role of ovary-inhibiting hormone from eyestalks of marine penaeid prawns (Parapenaeopsis hardwickii) during ovarian developmental cycle

The activity of the ovary-inhibiting hormone in the eyestalks of female prawns, Parapenaeopsis hardwickii, was determined during its ovarian developmental cycle. In the inactive (stage I) and post-spawned phases of ovarian development, the ovary-inhibiting hormone activity was found to be very high. During the phase of full vitellogenesis (stage IV), the inhibiting activity is almost negligible. After spawning (stage V) it is present, but at a lower level than during inactive and post-spawned phases. Hence it is inferred that ovary-inhibiting hormone appears to be responsible for the phase of ovarian quiescence and to control the rate of vitellogenesis.     

Further studies on graft-induced off-season flowering and fruiting in mango (Mangifera indica L.)

Summary

Defoliated shoots of cvs Alphonso, Dashehari, Totapari etc. (receptors), could be induced to flower within four weeks during the off-season by veneer grafting them to leafy shoots of the off-season flowering cv. Royal Special (donor) during the non-flowering season. Experiments on defoliating the donor and receptor shoots revealed the crucial dual role of the leaves in flowering. In the ‘floral cycle’, leaves from the donor promoted flowering, whereas leaves on the receptors, in the vegative phase, were inhibitory, and prevented graft-induction of the receptors. Thus, for graft induction, leafy donors and defoliation of receptors were essential. The inhibitory effect of the leaves on the receptors was localized and did not affect flowering of the donor shoots’ The similarity between these findings and those in the herbaceous, day-length sensitive species strengthens the view that flower formation is controlled in the same way in herbaceous and in woody perennial species. A minimum threshold of the floral stimulus appeared to be another requirement for an optimum flowering response. This was concluded from an experiment in which the leafy receptors were defoliated on different dates during the off-season flowering cycle. At the end of cycle, the defoliated receptors produced small panicles, and finally only vegetative shoots, probably indicating sub-threshold levels of the stimulus. Bud activity at the apex in the receptor was also an important pre-requisite for graft-induction. Some veneer-grafted scions which remained dormant during the flowering cycle of the donor and which sprouted much later after the completion of off-season flowering, ‘escaped’ the stimulus and invariably turned out to be vegetative. It is postulated that the cyclic synthesis of the floral stimulus in the leaves in an inductive cycle, and the gap between two such cycles, mainly decides the flowering behaviour of mango cultivars—biennial, annual and multiflowering. Two other requiremets are the absence of non-induced leaves and the synchronization of meristematic activity in the bud with the inductive cycle. Juvenile shoots from one to four year old seedlings could not be graft-induced—unlike the shoots from mature, six year old seeding trees. This juvenility effect continued into the second year when defoliation of the receptor shoots had no effect and failed to induce them to flower.     

A high temperature/low oxygen pulse improves cold storage disinfestation

Short periods of elevated temperature under controlled atmospheres (CA) effectively control insect pests. Cold treatment is also an effective non-chemical disinfestation process. If synergistic effects can be found by combining treatments, these may provide opportunities for cost reduction. Tests were performed to evaluate the tolerance of Packham's Triumph pears (Pyrus communis L.) to a range of temperatures (30–40 °C) combined with low oxygen (O₂ < 1 kPa). Treatment duration was 16–48 h and was followed by 1 month storage at 0 °C under air. When held at 30 °C, pears withstood up to 30 h of hypoxia. After cold storage, pears ripened slightly faster than controls but were undamaged. A temperature of 35 °C induced slight skin browning, and 40 °C resulted in substantial skin blackening. Some treatments were also tested on survival of lightbrown apple moth (LBAM), Epiphyas postvittana (Walker). All developmental stages were subjected to either 16 h at 30 °C, or 16 h under hypoxia, or 1 month at 0 °C, or a combination of the three treatments. With all treatments combined, all eggs, larvae and adults were killed. Only 4% of the pupae produced adults and combined treatments led to an increase in pupa mortality of 38%. A combined treatment (tolerated by pears) consisting of 30 h at 30 °C under low O₂ plus 1 month cold storage under air, killed 100% of LBAM pupae, and 100% of 5th instar larvae of both codling moth, Cydia pomonella (L.), and oriental fruit moth, Grapholita molesta (Busck). Implementation of such treatments would not require substantial investments for fruit industries equipped with CA storage facilities.     

Acute cortisol responses of calves to scoop dehorning using local anaesthesia and/or cautery of the wound

Objective To measure plasma cortisol responses in calves dehorned using a scoop after administration of local anaesthesia and/or cautery of the wounds.
Design A physiological study with controls.
Procedure There were six treatments: control handling with and without local anaesthesia, dehorning, dehorning after local anaesthesia, dehorning followed by wound cautery, and dehorning after local anaesthesia followed by wound cautery. Blood samples were taken before and after dehorning.
Results Dehorning caused an increase in plasma cortisol concentrations, which decreased a little to plateau values and then declined to pretreatment values 3 to 4 h after dehorning. The peak was smaller after local anaesthesia was administered but when its effects wore off, cortisol concentrations increased and thereafter were similar to those in the dehorned animals. The combination of local anaesthesia and cautery resulted in a plasma cortisol response similar to those in control calves with or without local anaesthesia.
Conclusions If plasma cortisol concentrations reflect the distress being experienced by the calves, then local anaesthesia reduces the acute distress for about 3 h after dehorning but not during the subsequent 3 to 4 h. Combining local anaesthetic and cautery prevented the significant increase in plasma cortisol following dehorning and may eliminate the acute distress caused by scoop dehorning.     

A framework for evaluation of on-farm mastitis diagnostics in Australia

Numerous culture-based diagnostics are available on the Australian and international markets for on-farm detection of bacterial pathogens in milk. Use of such diagnostics may provide an opportunity to improve the prudent use of antimicrobials in udder health management. Farms are low-resource settings in terms of diagnostic microbiology capacity. The World Health Organisation has identified criteria for the evaluation of diagnostic tests in low resource settings based on Accuracy, Sensitivity, Specificity, User-friendliness, being Rapid or Robust, Equipment-free and being Deliverable (ASSURED). Here, we review how those criteria can be interpreted in the context of microbiological diagnosis of mastitis pathogens, and how on-farm diagnostics that are currently available in Australia perform relative to ASSURED criteria. This evaluation identifies multiple trade-offs, both with regard to scientific criteria and with regards to convenience criteria. More importantly, the purpose of testing may differ between farms, and test performance should be evaluated relative to its intended use. The ability of on-farm mastitis diagnostics to inform mastitis treatment decision-making in a timely and cost-effective manner depends not just on test characteristics but also on farm-specific pathogen prevalence, and on the farm enterprise's priorities and the farm manager's potential courses of action. With most assay evaluations to date conducted in professional laboratories, there is a surprising dearth of information on how well any of the diagnostic tests perform on-farm and, indeed, of the on-farm decision-making processes that they aim to inform.     

Elevating glucose and insulin secretion by carbohydrate formulation diets in late lactation to improve post‐weaning fertility in primiparous sows

Primiparous (P1) sows commonly lose excessive body reserves to meet energy requirements for maintenance and milk production during lactation, and consequently, post‐weaning reproductive performance may be compromised. The present studies determined whether ad libitum feeding a glucogenic carbohydrate diet (CHO) during late lactation could stimulate insulin and glucose secretion (experiment 1) and improve subsequent litter size (experiment 2). For experiment 1, 15 P1 sows, and for experiment 2, 99 P1 sows (198.5 ± 2.7 kg) were allocated randomly according to suckled litter size (≥10 piglets), either to a CHO diet (14.3 MJ DE/kg, 19.8% crude protein) or a standard lactation diet (control; 14.2 DE MJ/kg, 19.5% crude protein) at 8 days before weaning. The CHO diet aimed to provide glucogenic content (extruded wheat, dextrose and sugar) as energy sources instead of fat sources without changing total dietary energy. Pre‐prandial plasma glucose and insulin concentrations were not influenced by treatments. However, post‐prandial plasma glucose and insulin concentrations and their peaks were both higher (p < .05) compared to the control treatment. Body weight loss during lactation was relatively low at 3%–4% for both treatments and did not differ between control and CHO treatments (?7.6 ± 1.6 vs ?5.4 ± 1.2 kg; p > .05). Second litter size was not influenced by diet (p > .05), but the weaning‐to‐mating interval was shorter in CHO sows (p < .05). This study demonstrates that providing an enriched CHO diet in late lactation did influence post‐weaning follicle growth but did not improve subsequent litter size. This may be due to the primiparous sows in this study not experiencing severe negative energy balance and there was no second litter syndrome in this farm which limited the ability of diet to improve sow fertility.     

Leaf anatomical characteristics and physiological responses to short-term drought in Ziziphusmauritiana (Lamk.)

The aim of this work was to study the association between leaf anatomical characteristics and response to short-term drought stress in Ziziphusmauritiana Lamk. Six Z. mauritiana cultivars (Seb, Gola, Umran, Keitly, Q-29 and B-5/4) under field conditions in Israel's Negev desert were studied. Width of palisade mesophyll, spongy mesophyll and epidermis, xylem number and diameter in mid-vein were investigated with light microscopy. Short-term (3 weeks) drought stress tolerance was evaluated by monitoring plant response (leaf transpiration, diffusive resistance, chlorophyll fluorescence, leaf water potential and leaf relative water content). Greater epidermis and mesophyll widths and xylem diameters and densities were associated with increased tolerance to short-term water deficit expressed by preliminary wilting symptoms and proportional differences between initial and final physiological parameters. Significantly larger differences were found in Keitly, Umran and B-5/4 than in Seb, Gola and Q-29, indicating that the former cultivars are more sensitive to drought stress. Our results indicate that tolerance in descending order was Seb, Q-29, Gola, B-5/4, Keitly and finally Umran. The existence of an association between anatomical characteristics and short-term drought stress tolerance based on physiological responses is suggested.     

In vitro studies on the binding, antioxidant, and cytotoxic actions of punicalagin

The protective bioactivity of punicalagin, a high molecular weight polyphenol isolated from pomegranate fruit pith and carpellary membrane, against oxidative damages to lipids, amino acids constituting the proteins, and guanosine as a model for DNA has been investigated. The ABTS*-, guanosine, and tryptophan radical generated pulse radiolytically were repaired by punicalagin, k = (0.9-15) x 10(7) dm3 mol-1 s-1. The results are rationalized on the basis of the scavenging activity of punicalagin against various one-electron oxidizing radicals, namely, .OH, N3., and NO2. . The formation of the transient species in these reactions and the rate constants of the scavenging reactions have been probed using a time-resolved kinetic spectrophotometric technique. The antioxidant action of punicalagin is expressed not only through its scavenging reactions but also by its ability to form metal chelates. Binding of punicalagin with bovine serum albumin and metal ions such as iron and copper revealed different binding affinities, whereas its binding with DNA was very weak and nonspecific. In vitro cytotoxic studies against three cell lines, namely, Vero (normal African green monkey kidney cell line), Hep-2 (human larynx epithelial cancer cell line), and A-549 (human small cell lung carcinoma cell line) showed that this polyphenol is toxic only at higher concentration.