Development of homeothermy in chicks of sub-Antarctic burrowing petrels

The development of homeothermy was studied in chicks of five species of sub-Antarctic burrowing petrels. Chicks of white-chinned and blue petrels were capable of maintaining body temperatures of 37° to 40°C at ambient temperatures between 5° and 30°C within one day of hatching. On average, chicks of grey petrels, great-winged petrels and Salvin’s prions attained homeothermy within five days of hatching, but some individuals exhibited well-developed homeothermy within 24 h of hatching. Chicks demonstrated a high capacity for heat production and maximum cold-induced oxygen consumptions ranged from 2,57 ml 0₂ g^-1 h^-1 in white-chinned petrel chicks to 4,94 ml 0₂ g^-1 h^-1 in the much smaller blue petrel chicks. The rapid development of homeothermy in burrowing petrel chicks is regarded as an adaptation in pelagic seabirds, in that it frees the adults both to replace energy reserves used during incubation and to forage for the chicks as soon as possible after hatching. In burrowing petrels it is reportedly facilitated by the chicks' thick down and a favourable burrow microclimate. This hypothesis was investigated by analysing cooling rates of dead chicks at wind speeds of 0,0 m s^-1 and 7,5 m s^-1, which simulated conditions within and outside burrows. Chicks exposed to windspeeds of 7,5 m s^-1 lost heat at a rate 2,5 times greater than those not exposed to wind. However, this increase was substantially less than predicted for ‘model’ chicks and this difference is attributed to the efficiency of the chicks’ down.     

Influence of Temperature on the Arginine and Methionine Requirements of Young Broiler Chicks

Two experiments were conducted with Ross × Ross broiler chicks in battery brooders from 7 to 21 d of age to determine the Arg and Met requirements of young broiler chicks at control (25°C) and warm (35°C) temperatures. In both experiments, 1-d-old broiler chicks were fed a corn and soybean meal based starter diet for 7 d. Six replications (2 replicates in each of 3 rooms per temperature) with 8 chicks each were used for each treatment. In experiment 1, the basal diet was based on corn (34.52%), whey (26.96%), corn gluten meal (16.53%), soybean meal (11.74%), and poultry fat (23% of CP and 3.20 kcal/g of ME_n). Six levels of Arg (0, 0.1, 0.2, 0.3, 0.4, and 0.5%), supplementing the basal diet containing 0.95% Arg, were the dietary treatments. A broken-line linear model was used to estimate chick Arg requirements. Based on body gain and feed conversion ratio (FCR) data, respectively, the Arg requirements of young Ross × Ross broiler chicks raised at 35°C were 1.15 ± 0.03% and 1.13 ± 0.02%, whereas those of chicks at 25°C were 1.26 ± 0.03% and 1.27 ± 0.02%. In experiment 2, the influences of temperature and dietary Arg on the Met requirements of young broiler chicks were investigated. The basal diet was based on corn (53.45%), soybean meal (37.72%), and poultry fat (23% of CP and 3.20 kcal/g of ME). Experiment 2 had a 6 × 2 factorial arrangement, with the basal diet (0.35% Met and 1.52% Arg) supplemented with 6 levels of dietary Met (0, 0.05, 0.1, 0.15, 0.2, or 0.3%) and 2 levels of dietary Arg (0 and 1.0%). When chicks were fed a corn-soybean meal basal diet containing 1.52% Arg, the Met requirements of young Ross × Ross broiler chicks raised at 35°C were 0.43 ± 0.02% and 0.43 ± 0.03%, whereas those of chicks at 25°C was 0.43 ± 0.01% and 0.48 ± 0.03%, based on body gain and FCR data, respectively. When Arg levels were increased to 2.52%, the Met requirement of young Ross × Ross broiler chicks was greater at both temperatures (P < 0.05). The requirements of chicks raised at 35°C were 0.50 ± 0.02% and 0.49 ± 0.02% and at 25°C were 0.59 ± 0.03% and 0.57 ± 0.02%, based on body gain and FCR data, respectively. Temperature and amino acid balance may both affect the amino acid requirements of broilers.     

Early heat acclimation during incubation improves Japanese quail performance under summer conditions

Effects of exposing quail eggs to high temperature on the heat tolerance ability and productivity of birds were investigated. Four groups of 600 fertile eggs were randomly selected; the first group was incubated under 37.5 °C and the hatched chicks were reared under a gradual decrease in temperature from 35 to 24 °C (Control). The second group was exposed to 39.1 °C for 2 h/day during 4–14 days of embryogenesis and the hatched chicks were reared under a gradual decrease in temperature from 35 to 24 °C. The third group was incubated under 37.5 °C and the hatched chicks were exposed to 39?±?1 °C for 2 h/day during 4–14 days of age. The fourth group was exposed to 39?±?1 °C for 2 h during 4–14 days of embryogenesis and the hatched chicks were exposed to 39?±?1 °C for 2 h/day during 4–14 days of age. The temperature applied changed (P?<?0.01) embryo weight and incubation period. Birds exposed to high temperature during brooding had superior growth performance, dressed carcass, body temperature and health traits. Birds subjected to 39?±?1 °C during brooding exhibited decreased feed consumption and body weight gain. Finally, this work suggests that thermal acclimation during embryogenesis might offer a practical method for easing heat stress.

     

Pharmacokinetics of intravenous gentamicin in healthy young‐adult compared to aged alpacas

The study objective was to evaluate the effects of age on aminoglycoside pharmacokinetics in eight young‐adult (<4 years) and eight aged (≥14 years) healthy alpacas, receiving a single 6.6 mg/kg intravenous gentamicin injection. Heparinized plasma samples were obtained at designated time points following drug administration and frozen at ?80°C until assayed by a validated immunoassay (QMS ^®). Compartmental and noncompartmental analyses of gentamicin plasma concentrations versus time were performed using WinNonlin (v6.4) software. Baseline physical and hematological parameters were not significantly different between young and old animals with the exception of sex. Data were best fitted to a two‐compartment pharmacokinetic model. The peak drug concentration at 30 min after dosing (23.8 ± 2.1 vs. 26.1 ± 2 μg/ml, p = .043 ) and area under the curve (70.4 ± 10.5 vs. 90.4 ± 17.6 μg hr/ml, p = .015 ) were significantly lower in young‐adult compared to aged alpacas. Accordingly, young alpacas had a significantly greater systemic clearance than older animals (95.5 ± 14.4 and 75.6 ± 16.1 ml hr^?1 kg^?1; p = .018 ), respectively). In conclusion, a single 6.6 mg/kg intravenous gentamicin injection achieves target blood concentrations of >10 times the MIC of gentamicin‐susceptible pathogens with MIC levels ≤2 μg/ml, in both young‐adult and geriatric alpacas. However, the observed reduction in gentamicin clearance in aged alpacas may increase their risk for gentamicin‐related adverse drug reactions.     

Effects of temperature and hypoxic stress on the oxygen consumption rates of the mudsucker fish Labeo capensis (Smith)

The specific oxygen consumption rate (VO ₂ IMb) of Labeo capensis, the freshwater mudsucker, was determined for small and large fish at winter (8°C) and summer (23°C) temperatures. VO JMb was also determined during hypoxic conditions of the experimental water. It was found that VO JMb does not differ substantially compared with other active fish. The VO 4Mb for a fish with a body mass of 250 g is 0,053 ml 0 ₂ per gram wet body mass per hour for fish acclimated at 8°C and 0,127 ml 0 ₂ per gram per hour for fish acclimated at 23°C. The calculated mass exponent, b, is 0,71 at 23°C and 0,68 at 8°C. Hypoxic conditions are relatively well tolerated especially by 23°C- adapted fish.     

Disinfection of the causative agent of contagious equine metritis by Nolvasan and Roccal II

Haemophilus equigenitalis, the proposed name for the bacterium that causes contaginous equine metritis (CEM) was tested for sensitivity to the disinfectant solutions Nolvasan® (2% chlorhexidine diacetate) and Roccal II® (10 alkyldimethylbenzylammonium chloride).Bacteria (10⁶) suspended in medium were inactivated in 10–20 min at 0°–2°C and in 2.5 min at 20°–22°C by a 3 : 128 dilution of Nolvasan. Roccal II, diluted 1 : 128, inactivated 10⁶ bacteria in 2.5 min at 0°–2°C and 20°–22°C.These dilutions of the disinfectants inactivated H. equigenitalis (titers of 0.1–11.0 × 10⁷/ml) in vaginal exudates from infected mares and pure cultures suspended in medium (titers of 1–5 × 10⁹/ml) in 10 min at 0°–2°C and 20°–22°C when the exudates and cultures were dried on metal carriers. The limit of detection of survivors was 3–32 bacteria/ml.It is recommended that contaminated instruments and other metal surfaces encountered during CEM infections should be decontaminated with either disinfectant for 10 min before rinsing.     

The effect of medetomidine and its antagonism with atipamezole on stress-related hormones, metabolites, physiologic responses, sedation, and analgesia in goats

Six 3‐year‐old goats (three males and three females) weighing 60.0 ± 18 kg (mean ± SD) were used to investigate the effect of medetomidine (MED; 20 µg kg^?1 IV) and its antagonism with atipamezole (ATI; 100 µg kg^?1 IV) on physiologic responses (heart rate (HR; beats minute^?1), respiratory rate (RR; breaths minute^?1), electrocardiogram (ECG), rectal temperature (T; °C), blood pressure (oscillometric; mm Hg), sedation (SED), posture (REC), analgesia (ALG), and stress‐related hormonal and metabolic responses (epinephrine and norepinephrine (high performance liquid chromatography with electrochemical detection), cortisol (COR; µg dL^?1; radioimmunoassay), glucose (GLU; mg mL^?1; enzymatic colorimetric assay), and free fatty acids (modified enzymatic colorimetric assay)); each goat received ATI or SAL in random order separated by 1 week. Jugular catheters were placed for drug administration and blood sampling (10–12 mL sample^?1) using a lidocaine skin block (20 mg) 2 hours prior to beginning of each trial; during this trial, goats breathed room air. Physiologic parameters were measured, SED, REC, and ALG were scored, and blood samples were collected from jugular catheters at baseline (time = ?30 minutes), 5 minutes post‐MED administration (time = ?25 minutes), 25 minute post‐MED administration and immediately prior to antagonism (time = 0 minute), and at 5, 30, 60, and 120 minutes after administering ATI or SAL. ALG was tested by clamping the withers and metacarpus with hoof testers fitted with a force transducer to measure applied isometric force (lb) (a technique used previously in goats to evaluate analgesia). Continuous variables were analyzed by Repeated Measures analysis of variance (anova ); categorical data were analyzed using a Friedman Repeated Measures anova on ranks. A p‐value of <0.05 was considered significant. If a significant difference was found, a Dunnett's pair‐wise comparison of means was conducted. Differences between ATI and SAL were examined at 5, 30, 60, and 120 minutes using a paired t‐test with a Bonferroni correction. Administration of MED resulted in a decrease in T (38.7 ± 0.3 to 34.5 ± 0.4 °C), HR (78 ± 19 to 55 ± 9), and RR (31 ± 12 to 14 ± 5) over time; an increase in mean arterial blood pressure (90 ± 19 to 132 ± 23), COR (0.254 ± 0.125 to 4.327 ± 1.233), and GLU (82.0 ± 13.2 to 255.9 ± 38.9); and changes in SED (alert to marked sedation), REC (standing to recumbent), and ALG (metacarpus = 5 ± 2 to 14 ± 0; withers = 3 ± 2 to 14 ± 0). GLU was 62–70% higher at 60 and 120 minutes and COR was 336% higher after SAL than after ATI at 120 minutes; at 30, 60, and 120 minutes, T was 4–10% higher after ATI than SAL. There were no other significant differences. REC, SED, and ALG were antagonized after ATI. ATI did not antagonize the effect of MED on HR, RR, or MAP, but stabilized T and antagonized the increase in GLU and COR.     

Intramuscular administration of alfaxalone in red‐eared sliders (Trachemys scripta elegans) – effects of dose and body temperature

ObjectiveTo characterise the effects of alfaxalone by intramuscular (IM) injection in red-eared slider turtles and the influence of body temperature on anaesthetic duration and depth.Study designProspective, randomised part-blinded experimental trial.AnimalsTen healthy adult female red-eared sliders.MethodsEach turtle was anaesthetized four times with 10 and 20 mg kg^?1 alfaxalone at 20 and 35 °C respectively. Time to maximal effect and plateau and recovery periods were recorded. Skeletal muscle tone, presence of various reflexes, response to noxious stimuli, and heart rate were assessed.ResultsResults are given for protocols 10 mg kg^?1 20 °C; 20 mg kg^?1 20 °C; 10 mg kg^?1 35 °C and 20 mg kg^?1 35 °C, respectively: mean time (±SD) to maximal effect was 16 ± 8, 19 ± 6, 5 ± 2 and 7 ± 5 minutes; duration of the plateau phase was 13 ± 12, 28 ± 13, 8 ± 5 and 8 ± 5 minutes and recovery time was 76 ± 20, 126 ± 17, 28 ± 9 and 41 ± 20 minutes. Endotracheal intubation was successful in 80%, 100%, 0% and 30% of turtles, respectively. At 35 °C, all animals retained nociceptive sensation in the front limbs, hind limbs and vent, whereas at 20 °C a few turtles lost peripheral nociceptive sensation. Corneal and tap reflexes were retained in all trials. Mean heart rates were 30 ± 2 and 66 ± 4 beats minute^?1 at 20 and 35 °C, respectively.Conclusions and clinical relevanceAlfaxalone administered IM in red-eared sliders provided smooth, rapid induction and uneventful recovery. At 35 °C either dosage provided only short (5–10 minutes) and light sedation. At 20 °C, 10 mg kg^?1 provided sedation suitable for short non-invasive procedures. About 20 mg kg^?1 provided anaesthesia of approximately 20 minutes duration, appropriate for induction of inhalational anaesthesia or for brief surgical procedures with supplemental analgesia.     

Metabolic rate and body temperature of an African sunbird,Nectarinia Chalybea: daily rhythm and the effect of ambient temperature

The oxygen consumption (VO₂) of the lesser double-collared sunbird, Nectarinia chalybea. was measured at ambient temperatures (Ta) from 7 to 35°C. The diel variation in body temperature (Tb) and wet thermal conductance (C) was also determined. The sunbirds (mean mass 8,36 g ± S.E. 0.21 g) showed a pronounced diel cycle of VO₂, with a mean reduction of 50% at night. Basal metabolic rate was estimated to be 3.23 ml O₂/g.h, which is 88% of the predicted value for a passerine bird of this size. There was a mean reduction in Tb of 3.6°C at night. Both day and night values of Tb decreased with decreasing Ta, as did individual values of C. Winter breeding in the south-west Cape is energetically stressful for lesser double-collared sunbirds, but they have the physiological capacity to reduce their energy expenditure substantially at night.     

Heat production studies on normal and oil-covered jackass penguins (Spheniscus demersus) in air and water

Heat productiorf and the importance of intact feathers for insulation were studied in jackass penguins Spheniscus demersus at various temperatures (5-25°C) by comparing their oxygen consumption in air and water with that of birds whose feather insulation was impaired when they were accidentally covered in partially weathered crude oil. Special attention was given to employing an experimental procedure that could relate oxygen consumption to level of activity. The mean ± SD metabolic rate recorded for normal inactive birds (188 ± 24 kJ kg-1 day-¹) was the same in air and water but only 80% of the mass specific rates predicted for non-passerine birds. Wetting a bird increased the inactive rate in air 1,33 times while slow swimming in water above 10°C caused a 1,76-fold increase. At low air temperatures (5°C) postural changes and feather fluffing were associated with a very low rate of 122 ± 29 kJ kg-¹ day-¹, which we interpret as behavioural control of penguins over energy expenditure. Jackass penguins in sea water at 10°C and above were within their thermal neutral range thus indicating that the water phase of their life cycle is not energetically more expensive than the terrestrial phase. Activity c level of the birds was an important influence on oxygen consumption; we suggest it is the main reason for the variations in metabolic rates within closely related species "? reported in the literature.     

Thermal and mechanical nociceptive threshold testing in pregnant sheep

ObjectiveAnalgesic regimes were compared in pregnant ewes after laparotomy by measuring thermal (TT) and mechanical (MT) nociceptive thresholds.Study designProspective randomised experimental study.AnimalsPregnant ewes at 121 days gestation underwent laparotomy as part of another research project.MethodsThermal and mechanical thresholds were measured before, and 2, 6, 24 and 48 hours after surgery. Thermal stimuli were delivered to the lateral aspect of the metatarsus via a skin-mounted probe, and mechanical stimuli to the contralateral site via a pneumatically driven 1.5 mm diameter pin. Each test was performed five times, alternating thermal and mechanical stimuli, with ten minutes between thermal stimuli. At the end of surgery ewes received either: 75 μg hour^?1 transdermal fentanyl patch (medial thigh) (group FP) (n = 8), or 3 μg kg^?1hour^?1 intra-peritoneal medetomidine via an osmotic pump (group IPM) (n = 8) inserted immediately prior to closure. Data were analysed using the Kruskal–Wallis RS Test (p < 0.05). Once a significant effect was identified, pairwise comparisons were performed using paired Wilcoxon RS tests. To compensate for multiple hypotheses testing, p < 0.005 was considered significant.ResultsPrior to surgery mean ± SD TT was 56.1 ± 5.0 °C (FP) and 55.6 ± 5.0 °C (IPM); MT was 5.3 ± 2.6 N (FP) and 8.0 ± 5.0 N (IPM). In FP there was no significant change in either TT or MT over time. In IPM there was no significant change in MT over time but TT increased at two hours to 59.2 ± 3.0 °C (p = 0.003). Skin temperature (ST) ranged from 33.0 to 34.7 °C and did not change over time. There were no significant differences between groups in TT, MT or ST.Conclusions and clinical relevanceAdministration of intra-peritoneal medetomidine (3 μg kg^?1hour^?1) by an osmotic pump increases the thermal nociceptive threshold in the immediate post operative period in pregnant sheep, suggesting that this agent may have a role in providing post-operative analgesia.     

Seasonal and age effects on energy requirements in domestic short‐hair cats (Felis catus) in a temperate environment

There is little information known about the energy requirements of cats in temperature climates. Energy requirement of domestic short‐haired cats was determined using three groups of mixed gender – old kept outside (approximately 9.9 years of age; 4.8 kg; n = 9), young kept outside (approximately 3.1 years of age; 3.9 kg; n = 8) or young kept inside (approximately 3.1 years of age; 3.9 kg; n = 8). Cats were housed individually for 5 weeks during summer (18.5 ± 0.5 °C) and winter (8.5 ± 0.4 °C) and were fed a commercially available maintenance diet ad libitum. In both periods, energy expenditure was determined from the rates of ²H and ¹⁸O elimination for blood H₂O over a 12 day period, from a doubly labelled water bolus ²H₂O (0.7 g/kg BW) and H₂¹⁸O (0.13 g/kg BW) administered intravenously. During the summer period, macronutrient digestibility was determined. Older cats had a reduction (p < 0.05) in apparent digestibility of dry matter (approximately 9%), energy (approximately 8%) and protein (6%). There was a significant effect of age and season on energy intake and energy expenditure. While lean mass was affected by age and season, there was no effect of age or season on energy expenditure when expressed as a proportion of lean mass. Possible seasonal differences in nutrient digestibility may explain these results.     

Changes in body temperature during growth and in response to fasting in growing modern meat type chickens

1. Rectal or core body temperature was determined in a study to examine the effects of fasting in modern meat type broilers at three stages of growth, namely d 19, 33 and 47.

2. There were two treatment groups: fed with feed available ad libitum and fasted. Rectal temperatures were determined at noon (1200?h). At that time, feed was removed from the fasted group. The body temperatures were then determined again after 6, 12, 18 and 24?h.

3. Core body temperatures decreased with fasting. The decrease was evident after as little as 6?h of fasting with a further decline evident by 12?h.

4. Accompanying the decrease in body temperature with fasting there were decreases in the venous concentrations of carbon dioxide in the blood and sodium in the plasma.

5. The decrease in both body temperature and carbon dioxide presumably reflects depressed metabolic rate.

6. Unexpectedly, the core body temperature increased progressively with age in the control fed group (d 19?=?41·04?±?0·02°C, d 33?=?41·65?±?0·05°C, d 47?=?42·21?±?0·12°C).

7. In the fed control group, core body temperatures were reduced at night, when feeding activity would be anticipated to be greatly reduced.     

Effect of low dose rate ketamine infusions on thermal and mechanical thresholds in conscious cats

ObjectiveTo determine the thermal and mechanical antinociceptive effects of two different subanesthetic constant rate infusions of racemic ketamine in cats.Study designProspective, randomized, blinded, experimental study.AnimalsEight healthy adult domestic shorthair cats (two intact females and six neutered males).MethodsThe thorax and the lower thoracic limbs of each cat were shaved for thermal (TT) and mechanical threshold (MT) testing and a cephalic catheter was placed. Three intravenous treatments of equivalent volume were given as loading dose (LD) followed by an infusion for 2 hours: (K5) 0.5 mg kg^?1 ketamine followed by 5 μg kg^?1 minute^?1 ketamine infusion, (K23) 0.5 mg kg^?1 ketamine followed by 23 μg kg^?1 minute^?1 ketamine infusion or (S) 0.9% saline solution. Effects on behavior, sedation scores, MT and TT were obtained prior to drug treatment and 0.25, 0.5, 0.75, 1, 1.5, 2, 2.25, 2.5 2.75, 3 hours then every 0.5 hours for 7 hours and 10, 12, 14 and 26 hours after loading dose administration.ResultsKetamine induced mild sedation for the period of the infusion, no adverse behavioral effects were observed. Thermal threshold was significantly higher than baseline (K5: 44.5 ± 0.7 °C; K23: 44.5 ± 0.5 °C) at 15 minutes in the K5 group (46.8 ± 3.5 °C) and at 45 minutes in the K23 group (47.1 ± 4.1 °C). In the K23 group TT was significantly increased compared to S and K5 at 45 minutes. In K5 at 15 minutes MT (9.6 ± 4.0 N) was different to baseline (6.1 ± 0.8 N) and to the S group (5.9 ± 2.3 N).Conclusion and clinical relevanceLow dose rate ketamine infusions minimally affect thermal and mechanical antinociception in cats. Further studies with different nociceptive testing methods are necessary to assess whether ketamine could be a useful analgesic in cats.     

Oral absorption and bioavailability of flumequine in veal calves

Summary

The oral absorption and bioavailability of flumequine was studied in 1‐, 5‐ and 18‐week‐old calves following intravenous and oral administration of different formulations of flumequine (Flumix^®, Flumix C^® and pure flumequine). Increasing age had a negative influence on the C_max after the administration of Flumix^®, based on a larger V_D in the older calves. The C_max decreased from 5.02 ± 1.46 μg/ml in the first week to 3.28 ± 0.42 μg/ml in the 18th week. Adding colistin sulfate to the flumequine formulation and administring pure flumequine mixed with milk replacer had a negative effect on the C_max of flumequine after oral administration of 5 and 10 mg/kg body weight. The bioavailability of the orally administered flumequine formulations was 100% in all cases except after the administration of Flumix C^®, for which it was 75.9 ± 18.2%. The urinary recovery of flumequine after intravenous injection of a 10% solution varied from 35.2 ± 2.3% for Group B. to 41.2 ± 6.3% for Group C.

The dosage of 5 mg/kg body weight Flumix^® twice daily in 1‐week‐old veal calves is sufficient to reach therapeutic plasma concentrations, based on a MIC value of 0.8 μg/ml of the target bacteria.

In older calves it is advisable to increase the dosage 7.5 or 10 mg/kg body weight every 12 hours. In combination with colistin sulfate it is also advisable to increase the dosage slightly because of the negative effect of the colistin sulfate on the C_max of flumequine.     

Bacteriological evaluation of composted manure solids prepared from anaerobic digested slurry for hygienic recycled bedding materials for dairy cows

Changes in mastitis‐causing pathogens, pH and water content in composted manure solids (CMS) prepared from digested slurry were evaluated during turning at 2‐day intervals for 8 days (C1–C4). The numbers of streptococci, coagulase‐negative staphylococci and coliforms were 2.6 × 10¹, 1.7 × 10² and 1.0 × 10¹ colony‐forming units (cfu)/g in CMS (C4) (summer), and these counts were markedly lower (P < 0.05) than those in CMS (C0 and C1). The bacterial counts ranged from 10¹ to 1.7 × 10² cfu/g in CMS (C4) (summer) and were within approved levels, <1 × 10⁶ cfu/g, indicating a minimal mastitis risk. The temperatures in CMS (C1–C4) increased to 63°C–74°C in summer and 67°C–70°C in winter. The mean pH values in CMS (C0–C4) were 9.2 in summer and 8.7 in winter, and water contents ranged from 61.7% to 69.6% in summer and 73.2% to 66.2% in winter. The significant decrease of pathogenic bacteria in CMS appears to be closely related to temperature >63°C for 8 days, pH 8.7–9.2, and water content 62% to 73%. This study demonstrates that prepared CMS has value as a recycled material with the potential to alleviate udder health issues in dairy cows.     

The reproductive response of female ostriches to dietary protein

1. A study was conducted with breeding ostriches over two consecutive breeding seasons to determine their response to different concentrations of a well-balanced dietary protein.

2. Five concentrations of protein were fed to both females and males at an intake of 2.5 kg/bird d. The respective diets contained 75, 91, 108, 123 and 140 g protein/kg feed with energy held constant at 9.2 MJ metabolisable energy/kg feed.

3. Egg production (mean ± SE, 39.1 ± 3.6 eggs/female/season) was unaffected by dietary protein concentration. Similarly, no significant trends were found for the number of unfertilised eggs (9.1 ± 1.8), dead-in-shell chicks (8.2 ± 1.3), the number of chicks hatched (19.5 ± 2.5) and change in the mass of females (?16.3 ± 10.2 kg). Egg weight decreased linearly as dietary protein content increased.

4. Age of the ostrich female had a highly significant effect on the number of eggs laid, the number of chicks hatched, the number of dead-in-shell and infertile eggs produced per hen, as well as the mass change of female breeding birds, but did not affect the response of any of these variables to dietary protein content.

5. It was concluded that ostriches do not benefit from dietary protein contents greater than about 75 g/kg when this is fed at a daily total feed intake rate of 2.5 kg/bird during the breeding season.

     

Different Root and Shoot Responses to Mowing and Fertility in Native and Invaded Grassland

Grassland root responses to mowing and fertility are less well known than shoot responses, even though as much as 90% of productivity in semiarid grasslands occurs belowground. Thus, understanding root responses may aid the management of invasive grassland species such as Agropyron cristatum (L.) Gaerth (crested wheatgrass). We asked whether root responses reflect shoot responses to mowing and fertility in native grassland with and without a major component of crested wheatgrass. We subjected grasslands in northern Montana to 5 yr of mowing at two nitrogen (N) levels and followed root responses with minirhizotrons. Surprisingly, the roots of both native and invaded grasslands were unaffected by mowing and N addition, despite significant changes in shoot mass across both vegetation types. Root length was significantly greater beneath areas heavily occupied by crested wheatgrass (363 m · m^-2 image ± 200, mean ± standard deviation [SD]) than areas comprising largely native grassland (168 m · m^-2 image ± 128 SD). Also, no interactions occurred between year and any other factor, indicating that there were no changes in belowground responses over the 5 yr examined. In contrast, shoot mass was significantly reduced by mowing (not mowed, 612 g · m^-2 ± 235 SD; mowed, 239 g · m^-2 ± 81 SD) and was significantly increased by N addition (no added N, 380 g · m^-2 ± 215 SD; added N, 488 g · m^-2 ± 287 SD). In conclusion, 5 yr of mowing decreased shoot mass, but not root mass. On the other hand, 5 yr of N addition increased shoot mass, but not root mass. Given that most production and competition in grasslands occurs belowground, this suggests that mowing may not be a successful tool for reducing crested wheatgrass root length, regardless of soil fertility.     

The effect of cooling to different subzero temperatures on dog sperm cryosurvival

The objective was to assess the effect of cooling to different subzero temperatures around ice formation (?5°C) on dog sperm cryosurvival and plasma membrane fluidity. Semen was centrifuged, and sperm were resuspended in a Tris‐egg yolk medium (3% glycerol). Diluted sperm were cooled from 22 to 5°C, and then, a Tris‐egg yolk medium containing 7% glycerol was added (final concentration of 5% glycerol and 200 × 10⁶ cells/ml). Sperm were packaged in 0.5‐ml plastic straws, and equilibration was done 16 hr at 5°C before freezing. I. Straws (n = 47) at 5°C were exposed to nitrogen vapours to determine the freezing point. II. Other straws (from different ejaculates) processed as mentioned, were further cooled to ?3, ?5 or ?7°C and immediately rewarmed in a water bath at 37°C. Motility, plasma membrane functionality and acrosome integrity were assessed. III. Other straws (from different ejaculates) processed as mentioned were further cooled to ?3 or ?5°C, frozen over nitrogen vapours and stored in liquid nitrogen for one month. Straws were thawed in a water bath at 38°C for 30 s. Motility, plasma membrane functionality, plasma membrane integrity, acrosome integrity, capacitation status and plasma membrane fluidity were assessed. Ice nucleation temperature was ?14.3 ± 2.05°C (mean ± SD); cooling to +5, ?3, ?5 and ?7°C, without freezing, produces no differences on sperm quality between target temperatures; cooling to +5, ?3, and ?5°C produced no differences on sperm survival and plasma membrane fluidity after freeze–thawing. In conclusion, cooling of dog spermatozoa to different subzero temperatures did not improve sperm cryosurvival and had no effect on plasma membrane fluidity after thawing.     

Pharmacokinetics of florfenicol in blunt‐snout bream (Megalobrama amblycephala) at two water temperatures with single‐dose oral administration

The pharmacokinetics and residue elimination of florfenicol (FFC) and its metabolite florfenicol amine (FFA) were studied in healthy blunt‐snout bream (Megalobrama amblycephala, 50 ± 10 g). The study was conducted with a single‐dose (25 mg/kg) oral administration at a water temperature of 18 or 28°C, while in the residue elimination study, fish were administered at 25 mg/kg daily for three consecutive days by oral gavage to determine the withdrawal period (WDT) at 28°C. The FFC and FFA levels in plasma and tissues (liver, kidneys and muscle) were analysed using high‐performance liquid chromatography (HPLC). A no‐compartment model was used to analyse the concentration versus time data of M. amblycephala. In the two groups at 18 and 28°C, the maximum plasma concentration (C_max) of FFC was 5.89 and 6.21 μg/ml, while the time to reach C_max (T_max) was 5.97 and 2.84 hr, respectively. These suggested that higher temperature absorbed more drug and more quickly at M. amblycephala. And the elimination half‐life (T_1/2kβ) of FFC was calculated as 26.75 and 16.14 hr, while the total body clearance (CL) was 0.09 and 0.15 L kg^?1 hr^?1, and the areas under the concentration–time curves (AUCs) were 265.87 and 163.31 μg hr/ml, respectively. The difference demonstrated that the elimination rate of FFC in M. amblycephala at 28°C was more quickly than that at 18°C. The results of FFA showed the same trend in tissues of M. amblycephala. After multiple oral doses (25 mg/kg daily for 3 days), the k (eliminate rate constant) of FFA in M. amblycephala muscle was 0.017, the C₀ (initial concentration) was 3.07 mg/kg, and the WDT was 10 days (water temperature 28°C).