Ronald G. Hodson

Bio: Ronald G. Hodson is an academic researcher from North Carolina State University. The author has contributed to research in topics: Broodstock & Bass (fish). The author has an hindex of 13, co-authored 21 publications receiving 765 citations.

Efficiency of Water Use of an Integrated Fish/Vegetable Co‐Culture System

Abstract: .– Fish and vegetable production were linked in a recirculating water system designed to achieve a high degree of efficiency of water use for food production in addition to functional and technological simplicity. Hybrid tilapia Oreochromis mossambicus×O. niloticus L. were grown in tanks associated with biofilters (sand beds) in which tomatoes Lycopersicon esculentum were grown. The effect of four biofilter volume (BFV)/fish rearing tank volume ratios (0.67/1, 1.00/1, 1.5011, 2.25/1) on water use efficiency was evaluated.‘Laura’(first experiment) or‘Kewalo’tomatoes were grown 4/m2 in biofilters of four different sizes and surface-irrigated 8 times daily with water from the associated fish tanks. Daily water consumption increased with BFV/tank ratios and with time. Fish production rates increased with biofilter volume in the first experiment, but were not significantly different in the second experiment. Total tomato fruit yield per plot increased from 13.7 to 31.7 kg (Experiment 1) and from 19.9 to 33.1 kg (Experiment 2) with increasing BFV/tank ratio. For fish plus fruit, total energy production increased from 4,950 to 8,963 kcal/ plot and from 4,804 to 7,424 kcal/plot in Experiments 1 and 2, respectively, and protein production increased from 536 to 794 and from 352 to 483 g/plot in Experiments 1 and 2, respectively, with increasing BFV/ tank ratio. Trends in water use efficiency for production of food energy (kcal/L.) and of protein (g/L) in tomatoes and fish were complex. Water use efficiency

Effects of Stocking Density, Salinity, and Light Intensity on Growth and Survival of Southern Flounder Paralichthys lethostigma Larvae

Abstract: Four separate studies were done on Southern flounder Paralichthys lethostigma larvae during first feeding and metamorphosis to determine the effects of stocking density, salinity, and light intensity on growth and survival. One study used stocking densities of 10, 20, 40, and 80 fish/L during first feeding; the second study compared the growth and survival of larvae stocked at 20 and 33 ppt; and a third experiment evaluated stocking densities of 1/L and 3/L under two different light intensities (1,600 lux vs 340 lux) during metamorphosis. The fourth experiment tested the effects of different salinities (0, 10, 20 and 30 ppt) on larval growth and survival during metamorphosis. Growth and survival (overall 6.9%) were not significantly different (P > 0.05) for stocking rates up to 80/L. Larvae placed into 20 ppt salinity had survival through first feeding similar to that of larvae raised at 33 ppt. During metamorphosis, light intensity had no effect (P > 0.05) on growth or survival, but fish stocked at 3/L had significantly lower (P 0.05) at 10, 20 and 30 ppt, but unmetamorphosed fish did not survive to day 60 at 10 ppt. Based on these results, practical larviculture of Southern flounder may require a two-step process with high stocking rates (80 fish/L) through first feeding and lower densities (1/L) through metamorphosis. Fingerling production in fertilized nursery ponds might he possible at salinity as low as 20 ppt.

Hormone induced spawning of summer flounder Paralichthys dentatus

Abstract: During their first year in captivity, summer flounder Paralicthys denratus were induced to spawn with gonadotropin releasing hormone analogue (GnRHa) implants, injected carp pituitary extract (CPE) or human chorionic gonadotropin (hCG) injections. The percentage of fertile eggs was greatest (69%) in CPE-treated females. CPE, but not GnRHa or hCG, was capable of stimulating oocyte growth (increased follicle diameter during vitellogenesis) followed by ovulation. Fish with maximum ovarian follicle diameters between 180 and 435 μm at the initiation of CPE injections produced the greatest percentage of fertile eggs. For most females, fertilization rate was greatest for the first batch of eggs ovulated. The mean fertilization rate for the first spawn of CPE-treated fish was 42% compared with 14% for the second spawn from the same fish. Fish with maximum initial follicle diameters of 585 40 μm that were implanted with GnRHa ovulated the greatest number of eggs, but fertility was low and variable. Approximately 35% of females injected with hCG ovulated a limited number of eggs, but only one hCG-treated female produced fertile eggs. Only a limited number of spermiating males were available for spawning trials. Hormone treatments used on females were ineffective for inducing or maintaining spermiation in male summer flounder.

Purification, characterization and immunoassay of striped bass (Morone saxatilis) vitellogenin.

Abstract: The egg yolk precursor, vitellogenin (VTG), was purified from blood plasma of striped bass by chromatography on hydroxylapatite or DEAE-agarose. The fish were first implanted with estradiol-17β (E2), which induced vitellogenesis. A rabbit antiserum (a-FSPP) raised against plasma from mature female striped bass, and then adsorbed with mature male plasma, was used to detect female-specific plasma protein (FSPP) in the chromatography fractions. Striped bass VTG (s-VTG) was collected from the peak fraction that was induced by E2, reacted with a-FSPP, and contained all detectable phosphoprotein. It appeared as a single band (Mr ≂ 170,000) in SDS-PAGE or Western blots using a-FSPP, and as a pair of closely-spaced phospholipoprotein bands in native gradient-PAGE, suggesting that there is more than one circulating form of s-VTG. The relationship of s-VTG to the yolk proteins was verified using a-FSPP. The antiserum reacted with the main peak from gel filtration of saline ovary extracts, and it specifically immunostained the two main bands in Western blots of the extracts and the yolk granules of mature oocytes. The amino acid composition of s-VTG was similar to that of VTG from other fish and Xenopus. A radial immunodiffusion assay for s-VTG was developed using a-FSPP and purified s-VTG as standard. The s-VTG was not detected in blood plasma of males, immature females, or regressed adult females, but plasma s-VTG levels were highly correlated with plasma E2 and testosterone levels, and oocyte growth, in maturing females. The results indicate that the maturational status of female striped bass can be identified by s-VTG immunoassay.

Age and Growth

Abstract: Flatfi shes are very accessible in the wild and hardy in the laboratory, thus many of the early studies of fi sh growth used fl atfi shes, especially plaice (Pleuronectes platessa) in the Atlantic and a number of species in the Pacifi c. As the science of fi sheries developed, so did the need to quantify the population structure and growth characteristics of the different fl atfi sh species. In fact, the importance of ageing fi shes and determining their growth rate was realised early in the last century (Allen 1916). Much of the early information on the aging and growth of fl atfi shes (primarily plaice) is referenced in Wimpenny (1953), Graham (1956) and Beverton & Holt (1957). Prior to the 1950s researchers had gained a fairly good understanding of the methods. A clear pattern of summer and winter growth was recognised in the otoliths, which were fi rst used in the late 1800s. Other bony structures such as opercular bones, the pectoral girdle and the concave faces of the vertebrae exhibited seasonal growth patterns (Cunningham 1905) but these were not as distinctive as those on the otoliths. The observation that a pair of rings may not delimit 1 year’s growth led to early verifi cation studies based on marginal increment analyses. Experimental work on plaice and fl ounder (Platichthys fl esus) showed that the seasonal pattern on both otoliths and scales was primarily driven by seasonal changes in water temperature rather than by variations in food availability. The use of otoliths for age estimation of fl atfi shes was not universal. Species differences slowly became apparent and methodological refi nements followed. Direct measurements of the growth of fl atfi shes were afforded by series of tagging and transplantation experiments, and laboratory or enclosure experiments (Johnstone et al. 1921). In all cases it was apparent that there was considerable variability in individual growth rates and that growth rates varied between areas. The widespread sexual dimorphism in growth with females growing faster and reaching larger sizes than males was also recognised (e.g. Johnstone et al. 1921; Bigelow & Schroeder 1953; Bagenal, 1955). The effects of gear selectivity and ontogenetic behavioural changes of fl atfi shes on the accurate estimation of age structure and growth rates were recognised, especially with the offshore movement of larger juvenile plaice from the nursery grounds and a general offshore movement with size and age. The possibility that fi shing pressure could make major changes to the age structure and growth of commercially exploited fl atfi sh populations was mentioned by Jones (1958), citing the prevalence of Rosa Lee’s phenomenon in plaice.

AVMA Guidelines for the Euthanasia of Animals: 2013 Edition

Abstract: 1. Clarification: The 2013 Guidelines make a distinction between euthanasia, humane killing, and slaughter, and state that neither slaughter nor humane killing is covered in the document P.68, S6.1.1. Not included among the definitions of these terms are ending the lives of healthy animals or scientific collection of animals. For clarification, whatever the term used, classification of the method, or reason given for killing animals: euthanasia, humane killing, slaughter, harvest, depopulation, scientific collection, or research-related, the Council on Accreditation’s foremost concern, in all situations, is with humane technique. The goal of humane technique is to minimize pain, distress, and the negative effect to the animal. The technique employed should result in rapid loss of consciousness followed by cardiac or respiratory arrest and, ultimately, a loss of brain function. Although complete absence of pain and distress is preferred, it is understood that it cannot always be achieved P7.13.2.

Egg quality in fish: what makes a good egg?

Abstract: Factors affecting egg quality are determined by the intrinsic properties of the egg itself and the environment in which the egg is fertilized and subsequently incubated. Egg quality in fish is very variable. Some of the factors affecting egg quality in fish are known, but many (probably most) are unknown. Components that do affect egg quality include the endocrine status of the female during the growth of the oocyte in the ovary, the diet of the broodfish, the complement of nutrients deposited into the oocyte, and the physiochemical conditions of the water in which the eggs are subsequently incubated. In captive broodfish, the husbandry practices to which fish are subjected are probably a major contributory factor affecting egg quality. Our knowledge of the genetic influences on egg quality is very limited indeed. We know that parental genes strongly influence both fecundity and egg quality, but almost nothing is known about gene expression and/or mRNA translation in fish oocytes/embryos. This is surprising because the products synthesized in ovoand the mechanisms controlling their expression are likely to play a central role in determining egg quality. The genetic mechanisms underpinning oocyte and embryo growth and development are a priority for research

Current issues in fish welfare

Abstract: Human beings may affect the welfare of fish through fisheries, aquaculture and a number of other activities. There is no agreement on just how to we igh the concern for welfare of fish against the hum an interests involved, but ethical frameworks exist th at suggest how this might be approached. Different definitions of animal welfare focus on an animal's condition, on its subjective experience o f that condition and/or on whether it can lead a natu ral life. These provide different, legitimate, pers pectives, but the approach taken in this paper is to focus on welfare as the absence of suffering. An unresolved and controversial issue in discussion s about animal welfare is whether non-human animals exposed to adverse experiences such as physical injury or confinement experience what humans would call suffering. The neocortex, which in huma ns is an important part of the neural mechanism tha t generates the subjective experience of suffering, i s lacking in fish and non-mammalian animals, and it has been argued that its absence in fish indicates that fish cannot suffer. However, a strong alternative view is that complex animals with sophisticated behaviour, such as fish, probably have the capacity for suffer ing, though this may be different in degree and kind fro m the human experience of this state. Recent empirical studies support this view and show that painful stimuli are, at least, strongly avers ive to fish. Consequently, injury or experience of othe r harmful conditions is a cause for concern in term s of welfare of individual fish. There is also growing e vidence that fish can experience fear-like states a nd that they avoid situations in which they have experience d adverse conditions.