Review of morphological and behavioural differences between reared and wild individuals: Implications for sea-ranching of Atlantic salmon, Salmo salar L., Atlantic cod, Gadus morhua L., and European lobster, Homarus gammarus L.

Abstract The main question which must be raised when planning to enhance natural populations through sea ranching is whether reared organisms are fit for a life in the wild, or more specifically, whether there are differences between reared and naturally resident individuals. The causes and effects of these differences are reviewed, and results from the Norwegian enhancement programme, which compared reared and wild individuals of Atlantic salmon, Salmo salar L., Atlantic cod, Gadus morhua L., and European lobster, Homarus gammarus L., are discussed with emphasis on morphological and behavioural differences. It was concluded that exposure to an artificial rearing environment during ontogeny can affect both the phenotype and the behaviour of the reared individuals, and thereby, their potential for survival after release into the wild as well. Suggestions are made as to how to diminish observed differences, and thereby, improve the survival potential.     

Assessment of impact of the introduction of exotic fish species in north-east Thailand

Abstract. Within the framework of a fisheries project in north-east Thailand, project MK/FSPC/069 entitled ‘The Fish Seed Production Centre, North East Thailand’, an assessment was carried out of the ecological impact of introducing exotic fish species (common carp, Cyprinus carpio L., Nile tilapia, Oreochromis niloticus (L.), and Chinese and Indian carps). For the assessment, the protocol of Kohler & Stanley (1984) was followed, covering feasibility of introduction, acclimatization potential, potential impact, and control potentials. Regarding the (ongoing) use of the proposed exotic species in aquaculture, it was concluded that so far no clear ecological impact has been reported from escapes to open water; the use of the exotic species has shown to be highly beneficial from a 9 socio-economic point of view. Regarding the proposed introduction of the exotic species into public waters (natural lakes and man-made reservoirs), it was concluded that earlier releases of these species in north-east Thailand did not provoke severe ecological impact in terms of deterioration of aquatic ecosystems. Incidental cases of minor ecological impact were reported for common carp and nile tilapia. Indications were obtained for niche competition between Chinese and Indian carps and indigenous carps, while similar niche competition was concluded for bighead carp, Aristichthys nobilis (Richardson), and indigenous pelagic zooplankton feeders. Observing the prolific development of the Nile tilapia in a number of reported cases, it was recommended not to include this species in stocking programmes for public water bodies, until more risk assessments are available.     

Antipyrine disposition in the dehydrated camel

In the present study the effects of water deprivation in the camel ( Camelus dromedarius ) on the pharmacokinetic profile of antipyrine were assessed. A crossover design was used. The pharmacokinetics of antipyrine in adult and young camels were compared. Antipyrine was administered intravenously to young and adult female camels when water was available ad libitum and to the adult camels after 14 days of dehydration. The elimination half-life of antipyrine in watered adult camels was 136.5 ± 16.7 min. The half-life of elimination and the mean residence time of antipyrine were significantly prolonged following dehydration. The observed effects of water deprivation were not a function of age, as the pharmacokinetic profile of antipyrine in young camels was similar to that of the adults, but more likely due to the changes in oxidative metabolic capacity of the liver as a result of a reduced general metabolism. The results of the present study also show that the intrinsic clearance of antipyrine is proportional to the camel's body weight, as previously shown for other mammalian species.     

Some pharmacokinetic data of aditoprim and trimethoprim in healthy and tick-borne fever infected dwarf goats

Aditoprim (AP) is a new dihydrofolate reductase inhibitor, which is structurally related to trimethoprim (TMP). The pharmacokinetics of AP (10 mg/kg) and TMP (20 mg/kg) were assessed in healthy dwarf goats. Therapeutic efficacy against rickettsial infections was tested in tick-borne fever (TBF) infected goats. The animals were given TMP (n = 5) or AP (n = 5) by i.v. injection, and subsequently the drugs were administered orally (same groups, similar doses). Finally, both groups were infected with TBF and the i.v. experiment was repeated. Plasma concentration-time curves for both drugs followed first-order two-compartment decay. For TMP, mean t1/2 beta +/- SEM (h) was 0.84 +/- 0.06 (i.v. control) and 0.90 +/- 0.06 (i.v. infected), respectively, whereas for AP values of 8.00 +/- 0.31 (i.v. control) and 10.28 +/- 0.67 (i.v. infected) were obtained (P less than 0.05). Mean Vd beta +/- SEM values (l/kg) were 3.84 +/- 0.27 (i.v. control) and 4.07 +/- 0.85 (i.v. infected) for TMP (NS) and 7.02 +/- 0.63 vs 9.29 +/- 0.21 (P less than 0.05) for AP. After i.v. injection, rumen fluid concentrations of AP were significantly (P less than 0.05) higher and more persistent than those of TMP. For AP, the plasma and rumen fluid concentrations at 3 h were 1.20 +/- 0.06 micrograms/ml and 0.85 +/- 0.17 microgram/ml, respectively. After oral administration of TMP, Cmax in plasma was 0.12 +/- 0.01 microgram/ml and the maximum was reached after 1.2 +/- 0.16 h; systemic bioavailability (F) was 10.3% (relative to AUC i.v.). Oral treatment with AP resulted in a Cmax value of 0.21 +/- 0.02 microgram/ml with Tmax of 22.5 +/- 1.65 h and a F value of 71%. Based on WBC, serum ALP and rectal temperature responses, it was concluded that both TMP and AP were inactive against Ehrlichia phagocytophila.     

Sulphadimidine metabolism in vitro: I. sex differences in acetylation and hydroxylation in cultured rat hepatocytes

The hydroxylation and acetylation of 0.5 mM sulphadimidine (SDD) was studied in primary cultures of hepatocytes from male and female rats, and from castrated male and sham operated male rats. In addition, SDD metabolism was investigated in hepatocytes from castrated male rats treated with testosterone, prior to liver cell isolation. In male rat hepatocytes a significantly higher hydroxylation activity was observed than in hepatocytes from female and castrated male rats. Acetylation activity was higher in females. Testosterone induced hydroxylation but did not affect acetylation. These results correlate well with data from previous in vivo studies, showing the relevance of this in vitro model.     

The pharmacokinetics and tissue levels of polymyxin B, colistin and gentamicin in calves

Following a single intravenous injection of polymyxin B, colistin (5 mg/kg, each) and gentamicin (3 mg/kg) to calves, the decline in serum antibiotic concentration generally suggested a three-compartment (open system) pharmacokinetic model. Tissue binding is a dominant factor in the distribution and elimination kinetics of the drugs. Less than 65% of the dose of polymyxin B and colistin was recovered in the urine during 48 h after treatment. Concentrations of nonbound polymyxin B and colistin in the kidney, liver, lung, heart, and skeletal muscles were similar to total (free and bound) serum drug levels, but considerably higher concentrations were found, in bound form, in chloroform-ethanol extracts of these organs.
At 24 h after treatment, more than 50% of the doses of polymyxin B and colistin were present bound to the tissues; the largest amount was in the skeletal muscles. Gentamicin was concentrated in the kidney, predominantly in the free form. At 48 h after treatment the amount of gentamicin in the kidney was 6.3% of the administered dose, being more than five times greater than the corresponding amounts of polymyxin B and colistin.
The extent of tissue uptake of polymyxin B and colistin limits the usefulness of kinetic values, which are derived from the analysis of serum drug levels, for the purpose of designing dosage schedules. The strong affinity of the polymyxins to the muscle tissue, and gentamicin to the kidney, can result in drug residues persisting in the body for several weeks.     

Oral treatment with ketoconazole of plantar candidosis in a mute swan

Candida albicans infection of the plantar region of the digit was diagnosed in a mute swan (Cygnus olor). Diagnosis was based on histological examination and on cultures. The pathogenicity of the C. albicans isolate was proven by inoculation in laboratory animals. Oral treatment with ketoconazole resulted in complete clinical recovery; no relapse occurred during a sixteen-month follow-up period.     

Validation of a new dental plaque quantification method in dogs

Current methods for the quantification of plaque accumulation in cats and dogs are well-accepted adaptations of traditional human models, but have required substantial modifications in order to compensate for the inherent differences in compliance, cooperation, and temperament between animals and humans. While these modifications have sought to maintain or improve upon the accuracy and reproducibility of the original methods, they also have increased the complexity of the technique and have required additional scorer time and animal cooperation, which leads to increased cost of trials. Therefore, research was directed toward the development and validation of a new substrate scoring system that reduces resources while maintaining or increasing the reproducibility attributed to the more traditional methods. This new gingival contour plaque index was shown to be accurate and reproducible, but used fewer animals, required less time, and eliminated the need for many of the specialized procedures required by traditional methods.     

Mechanical Properties of Four Suture Patterns for Transected Equine Tendon Repair

Thirty-six superficial digital flexor tendons from nine fresh equine cadavers were transected and sutured with size 2 monofilament nylon. Nine tendons were repaired with each of four suture patterns: single-locking loop, double-locking loop, triple-locking loop, or three-loop pulley. The times required for application, tensile strengths, resistance to distraction (gap), and modes of failure were analyzed. The mean times required were: single-locking loop, 3 mins, 15 secs; double-locking loop, 4 mins, 15 secs; triple-locking loop, 10 mins, 50 secs; and three-loop pulley, 4 mins. The double-locking loop, triple-locking loop, and three-loop pulley suture patterns were stronger than the single-locking loop. The triple-locking loop and three-loop pulley patterns were close in strength and only the triple-locking loop was stronger than the double-locking loop. The three-loop pulley had the greatest resistance to gap formation and its mode of failure was different from the others. The three-locking loop suture patterns failed by suture breakage but the three-loop pulley failed first by suture pull-out and then by suture breakage.