Wild raptors brought into an ex situ environment often have poor semen quality that is further compromised by urine contamination. Generally, it is believed that in birds, artificial insemination into the cloaca or caudal vagina of females requires large doses of high-quality spermatozoa to maximize fertility. In an effort to define and overcome some of the challenges associated with reproduction in wild raptors, the objectives of this study were to 1) evaluate the frequency, impact, and remediation of urine contamination in fresh ejaculates for the purpose of maintaining sperm motility and viability in vitro, and 2) develop a deep insemination method that allows low numbers of washed sperm to be placed directly into the magnum to increase the probability of producing fertilized eggs. The species evaluated include golden eagle (Aquila chrysoetos), imperial eagle (A. adalberti), Bonelli's eagle (Hiernaetus fasciatus), and peregrine falcon (Falco peregrinus). Semen samples were collected and pooled by species, and a minimum of 25 pooled ejaculates per species were evaluated for urine contamination, pH, sperm viability, and sperm motility; the samples were either unwashed or washed in neutral (pH 7.0) or alkaline (pH 8.0) modified Lake's diluent. Female golden eagles and peregrine falcons were inseminated via transjunctional, intramagnal insemination with washed spermatozoa from urine-contaminated samples. Urine contamination occurred in 36.8 ± 12.8% (mean ± SEM) golden eagle, 43.1 ± 9.1% imperial eagle, 28.7 ± 16.1% Bonelli's eagle, and 48.2 ± 17.3% peregrine falcon ejaculates. The pH in urine-contaminated semen samples ranged from 6.48 ± 0.3 to 6.86 ± 0.2, and in noncontaminated samples it ranged from from 7.17 ± 0.1 to 7.56 ± 0.1. Sperm viability and motility were reduced (P < 0.05) in all species for unwashed vs. washed sperm after 30 min incubation at room temperature. Two peregrine falcon chicks and one golden eagle chick hatched after intramagnal insemination. This study demonstrates that urine contamination, a common and lethal acidifier in manually collected raptor ejaculates, can be circumvented by immediate, gentle seminal washing. Furthermore, these processed sperm, when deposited by transjunctional intramagnal insemination, can produce live young.

Outbreaks of morbidity and mortality in double-crested cormorants (Phalacrocorax auritus) along Florida's Gulf Coast have occurred sporadically for at least 30 yr. During these outbreaks, the Clinic for the Rehabilitation of Wildlife, located on Sanibel Island in Florida, has admitted a substantial number of cormorants with consistent presentation of primarily neurologic clinical signs. In order to investigate the association of these outbreaks in cormorants with exposure to brevetoxin, we compared the timing of admittance of cormorants with outbreak-specific clinical signs to blooms of the brevetoxin-producing marine algae, Karenia brevis (formerly Gymnodinium breve), around Sanibel Island from 1995 through 1999. The clinic admitted 360 out of 613 cormorants with the common clinical sign of severe cerebellar ataxia in six outbreaks occurring during this period. The ataxia was characterized by a broad-based stance, truncal incoordination, hypermetric gait, and intention tremors of the head. The histopathologic findings in 10 cormorants euthanized in 1997 were mild and nonspecific. An immunohistochemical staining technique for the detection of brevetoxin in cormorants documented the uptake of brevetoxin in tissues from four cormorants admitted during an outbreak in 1997, but a modified technique used on samples from 11 cormorants admitted during a K. brevis bloom in 2000 produced indeterminate results. Admittance of cormorants with outbreak-specific clinical signs was positively correlated (P < 0.05) with concurrent concentrations of K. brevis in local water. The cross-correlation coefficient was also significant when increased K. brevis levels preceded cormorant admittances by 2, 4, 6, and 8 wk. This delay in time between K. brevis blooms and cormorant admittance and our clinical finding of neurologic abnormalities in cormorants without overt histopathologic features suggest an association between K. brevis blooms and local cormorant morbidity.

Nutrition most certainly affects health and may play a role in the etiology of growth and reproductive problems in captive cheetah (Acinonyx jubatus) populations. The objective of our research was to examine nutritional differences between two dietary regimens and quantify their physiologic effects on cheetahs held in captivity. Twelve cheetahs were randomly assigned to either a commercial diet (COM) or a supplemented meat diet (SMD) group. These cats were physically examined and had blood samples taken three times over the course of a year. Representative samples of COM and four separate components of the SMD treatment were analyzed over the same time frame for proximate nutrient composition, digestibility, and concentrations of taurine, fat-soluble vitamins, and selected minerals. Concentrations of fat, vitamins A and E, Se, Fe, Cu, Na, and Mn were significantly higher in COM compared with those in SMD samples, with the exception of fat content in turkey. Mg content was lower in COM than in SMD; other nutrients did not differ. Mean concentrations of vitamins A and E in COM were markedly higher than in SMD samples (408,140 vs. 29,696 IU/kg dry matter [DM] and 431 vs. 48 IU/kg DM, respectively) and varied dramatically between sampling periods. Percent crude protein and protein-to-fat ratios were high for SMD compared with either whole prey–based or commercial food preparations. Blood urea nitrogen and serum creatinine levels were above normal reference means for domestic cats. Plasma concentrations of vitamins A, D, and E were significantly higher in COM-fed than in SMD-fed cheetahs. Both plasma retinol and tocopherol levels were almost three times higher in COM-fed cats (1.26 ± 0.06 vs. 0.53 ± 0.03 μg/ml and 17.5 ± 0.7 vs. 6.4 ± 0.02 μg/ml, respectively) and exceeded the normal ranges expected for domestic felids. Significant differences between male and female cheetahs were found for plasma concentrations of vitamin E, Se, and Fe after allowing for effects of diet and time of collection. Excess fat-soluble dietary vitamins can result in direct toxicities as well as nutrient antagonisms and may be linked to reproductive and health issues in captive cheetahs. The high protein levels found in SMD may be linked to chronic renal disease, which was detected in some of these cheetahs.

Superficial and systemic mycotic infections are common among clinically ill sea turtles, which places growing importance on the establishment of pharmacokinetic-based dosage regimens for antifungal drugs. The pharmacokinetic properties of the antifungal drug fluconazole, after intravenous (i.v.) and subcutaneous (s.c.) injections, were studied in juvenile loggerhead sea turtles (Caretta caretta) housed at 23.0–26.5°C. Fluconazole pharmacokinetic properties were further assessed in a multiple-dose s.c. regimen derived from the pharmacokinetic parameters determined in the single-dose study. Pharmacokinetic parameters were calculated, using a two-compartment model, from plasma concentration–time data obtained after single i.v. and s.c. administrations of fluconazole at a dosage of 2.5 mg/kg body weight in six juvenile sea turtles. Blood samples were collected at intervals through 120 hr after each dose, and the concentration of fluconazole in plasma was measured by reverse-phase high-performance liquid chromatography. The i.v. and s.c. elimination half-lives were 139.5 ± 36.0 and 132.6 ± 48.7 hr (mean ± SD), respectively. Systemic clearance of fluconazole was 8.2 ± 4.3 ml/kg·hr, and the apparent volume of distribution at steady state was 1.38 ± 0.29 L/kg. A multiple-dose regimen was derived, which consisted of a loading dose of 21 mg/kg body weight and subsequent doses of 10 mg/kg administered through s.c. injection every 120 hr (5 days). This regimen was administered to four juvenile sea turtles for 10 days, and blood samples were taken to determine peak and trough plasma concentrations of fluconazole. The mean concentrations for the two peak concentrations were 16.9 ± 1.1 and 19.1 ± 2.8 μg/ml 4 hr after dosing, and the mean concentrations for the three trough concentrations were 7.2 ± 2.2, 10.4 ± 2.7, and 10.7 ± 2.9 μg/ml 120 hr after dosing. The terminal half-life after the last dose was calculated at 143 hr. Throughout the multiple dosing, fluconazole concentrations remained above approximately 8 μg/ml, a concentration targeted when treating mycotic infections in humans. The results of this study suggest that fluconazole can be effectively administered to sea turtles at a dosage of 10 mg/kg every 5 days after a loading dose of 21 mg/kg.

Sixteen captive and wild-caught American alligators (Alligator mississippiensis), seven juveniles (≤1 m total length [TL]; 6.75 ± 1.02 kg), and nine adults (≥2 m TL; 36.65 ± 38.85 kg), were successfully anesthetized multiple times (n = 33) with an intramuscular (i.m.) medetomidine–ketamine (MK) combination administered in either the triceps or masseter muscle. The juvenile animals required significantly larger doses of medetomidine (x̄ = 220.1 ± 76.9 μg/kg i.m.) and atipamezole (x̄ = 1,188.5 ± 328.1 μg/kg i.m.) compared with the adults (medetomidine, x̄ = 131.1 ± 19.5 μg/kg i.m.; atipamezole, x̄ = 694.0 ± 101.0 μg/kg i.m.). Juvenile alligators also required higher (statistically insignificant) doses of ketamine (x̄ = 10.0 ± 4.9 mg/kg i.m.) compared with the adult animals (x̄ = 7.5 ± 4.2 mg/kg i.m.). The differences in anesthesia induction times (juveniles, x̄ = 19.6 ± 8.5 min; adults, x̄ = 26.6 ± 17.4 min) and recovery times (juveniles, x̄ = 35.4 ± 22.1 min; adults, x̄ = 37.9 ± 20.2 min) were also not statistically significant. Anesthesia depth was judged by the loss of the righting, biting, corneal and blink, and front or rear toe-pinch withdrawal reflexes. Recovery in the animals was measured by the return of reflexes, open-mouthed hissing, and attempts to high-walk to the opposite end of the pen. Baseline heart rates (HRs) were significantly higher in the juvenile animals (x̄ = 37 ± 4 beats/min) compared with the adults (x̄ = 24 ± 5 bpm). However, RRs (juveniles, x̄ = 8 ± 2 breaths/min; adults, x̄ = 8 ± 2 breaths/min) and body temperatures (juveniles, x̄ = 24.1 ± 1.1°C; adults, x̄ = 25.2 ± 1.2°C) did not differ between the age groups. In both groups, significant HR decreases were recorded within 30–60 min after MK administration. Cardiac arrhythmias (second degree atrio-ventricular block and premature ventricular contractions) were seen in two animals but were not considered life-threatening. Total anesthesia times ranged from 61–250 min after i.m. injection. Although dosages were significantly different between the age groups, MK and atipamezole provided safe, effective, completely reversible anesthesia in alligators. Drug-dosage differences appear to be related to metabolic differences between the two size-classes, requiring more research into metabolic scaling as a method of calculating anesthetic dosages.

We chemically restrained fishers (Martes pennanti) as part of a captive-management protocol designed to facilitate veterinary evaluation and treatment, and conditioning on a high-calorie diet before reintroduction in Pennsylvania. We compared the safety and efficacy of ketamine (KET) and medetomidine–ketamine (MED–KET) by monitoring immobilization intervals (induction time, down time, alert time, and recovery time) and physiologic responses (pulse rate, respiration rate, rectal temperature, blood pressure, oxygen saturation, and mean arterial pressure) during restraint. We administered MED–KET at 0.4 mg MED combined with 20.0 mg KET to males and at 0.2 mg MED combined with 10.0 mg KET to females. The x̄ ± SD dosages were MED 0.07 ± 0.008 mg/kg KET 3.7 ± 0.5 mg/kg for males and MED 0.07 ± 0.007 mg/kg KET 3.6 ± 0.3 mg/kg for females. KET alone was administered at 100.0 mg to males and at 50.0 mg to females, resulting in x̄ ± SD dosages of 18.7 ± 1.8 mg/kg for males and 19.2 ± 2.2 mg/kg for females. Mean induction time did not differ between fishers restrained with MED–KET (4.6 min) and KET (4.5 min). However, compared with KET, MED–KET resulted in longer mean down time (36.2 vs. 142.2 min), alert time (40.8 vs. 146.8), and recovery time (81.1 vs. 199.4 min). Fishers that received MED–KET were mildly bradycardic and hypertensive compared with those that received KET. Although KET resulted in increased muscle tension and labored respiration, it would be effective for performing brief, noninvasive procedures for fishers because induction was rapid, recovery was short and calm, anesthesia was not profound, and physiologic response was generally expected on the basis of known drug pharmacology. Medetomidine–ketamine also immobilized fishers effectively, providing rapid induction, physiologic response typical to α₂ agonism, calm recovery, and possibly a plane of anesthesia adequate for invasive procedures such as tooth removal or surgery.

Nine acaricides (amitraz, carbaryl, chlorpyrifos, cyfluthrin, fipronil, lindane, permethrin, phenothrin, and pyrethrins) were studied for their efficacy in killing the African tortoise tick (Amblyomma marmoreum). Only four of the acaricides (chlorpyrifos, cyfluthrin, lindane, and permethrin) produced 100% mortality within 24 hr of application, and only two (cyfluthrin and permethrin) continued to cause 100% mortality when diluted to as low as 1:10,000. Five of the acaricides (amitraz, carbaryl, chlorpyrifos, cyfluthrin, and permethrin) were studied for toxicity to the leopard tortoise (Geochelone pardalis), the most common host of A. marmoreum. The results indicate that cyfluthrin and permethrin, which were herein found to be the two most effective acaricides for control of A. marmoreum, are also the safest acaricides for use on leopard tortoises.

Intraocular pressure (IOP) reflects a balance between aqueous humor production and outflow and is often an essential ophthalmic diagnostic procedure in animals. The objective of this study was to estimate IOP in clinically normal red-footed tortoises (Geochelone carbonaria) of various sizes by using applanation tonometry. Intraocular pressures were estimated for 25 captive red-footed tortoises (10 males, 10 females, and 5 animals of unknown sex) by using an applanation tonometer after topical anesthesia. Body length ranged from 5.1 to 54.9 cm, measured from nuchal to anal scutes. Five measurements from each eye were obtained by a single observer in an ambient temperature of approximately 30°C. Observer's reliability was good (intraclass r = 0.75), and IOP did not change over the ordered sequence of five replicate measurements. For individual tortoises the correlation for IOP between the left and right eyes was low (r = 0.20). The paired t-test did not show any statistical effect (P = 0.426) for the difference in IOP between the left and right eyes. Mean IOP determined for 10 confirmed males and 10 confirmed females did not differ between sexes (P = 0.244). The mean IOP of five small tortoises (<10 cm long) was not significantly different (P = 0.244) from that of 20 large tortoises (>10 cm long). In red-footed tortoises there does not appear to be any relation between carapace length and IOP.

An infestation by the parasitic copepod Pennella balaenopterae was found in a stranded, 8-mo-old, female northern elephant seal (Mirounga angustirostris). Diagnosis was based on the finding of the cephalothoraxes of 14 adult female copepods from three subcutaneous sites. Bacteria cultured from lesion exudate included Arcanobacterium phocae, Escherichia coli, Edwardsiella tarda, an Enterococcus sp., and Proteus mirabilis. The lesions were drained and irrigated with chlorhexidine, and the seal was treated with a subcutaneous injection of ivermectin. The seal recovered and was released after 43 days.

Atropine, an anticholinergic agent commonly used in human and veterinary medicine, is reported to cause toxicity associated with its antimuscarinic action. A juvenile pygmy sperm whale, Kogia breviceps, was treated with atropine in an attempt to relieve symptoms similar to pyloric stenosis, as has been used in humans. Two doses of 0.01 mg/kg were given i.m., 12 hr apart, followed by three doses of 0.005 mg/kg i.m. s.i.d. over the next 3 days. Symptoms associated with atropine toxicity developed gradually and included hyperexcitability, a generalized ascending paralysis of body musculature, shallow, rapid respiration, vomiting, aspiration of seawater, and pulmonary edema. Treatment with physostigmine salicylate (two doses of 2 mg i.m., 1 hr apart) was effective in counteracting the paralysis, as well as other symptoms, beginning in as little as 17 min after the first dose, and the whale was back to swimming on its own after 8 hr. All overt symptoms of atropine toxicity were gone in about 24 hr, but there were other possible sequella that lasted much longer.

Adenoviral infection was associated with hemorrhagic enteritis, serosal hemorrhages, and severe pulmonary edema in six captive moose (Alces alces) in Toronto, Ontario, Canada: an adult female moose and three calves in 1985 and two calves in 1998. Adenoviral disease was suspected based on histological findings of systemic vasculitis and widespread thrombosis associated with amphophilic intranuclear inclusions in endothelial cells. Diagnosis was confirmed by immunohistochemistry using antiserum to bovine adenovirus type 5, transmission electron microscopic identification of viral particles consistent in morphology with adenovirus within nuclei of pulmonary endothelial cells in an affected calf, and virus isolation. The restriction pattern of virus isolated from the lung of one of the calves indicated that the virus was identical to a recently characterized adenovirus in black-tailed deer (Odocoileus hemionus) in California. The moose adenovirus reported here may have been endemic in the captive moose herd, or infection may have resulted from either direct or indirect contact with other species of captive or wild cervids. This is the first report of adenoviral infection in moose and of the presence of adenoviral disease in a cervid in Canada.

Lincoln Park Zoo acquired five intact, male rock hyraxes (Procavia capensis) from three separate institutions to exhibit as a group. The animals were of varying ages at the time of acquisition. During quarantine, all five were surgically castrated via a midline laparotomy technique in an attempt to reduce expected aggression within the group. Recommendations for successful castration, based on these five procedures, include performing the procedure on sexually immature hyraxes or sexually inactive adults, the use of a second surgeon during the procedure, and the use of stainless steel surgical clips for ligation of vessels and spermatic cord. Although combinations of the castrated animals coexisted for longer periods than those documented for other nonrelated male groups, aggression was significant and resulted in the death of one individual. Ultimately, all animals were housed individually.

A high prevalence of fecal Salmonella shedding in a collection of healthy exotic felids precipitated a change to two new commercially available feline diets. One year after initiation of the new diets, 18 fecal samples from individual felines, their exhibits, and representative samples of the diets were cultured for Salmonella spp. Only one culture grew a Salmonella sp. Salmonella uganda was cultured from the feces of one snow leopard (Felis uncia). Feeding a diet with minimal to no Salmonella contamination lowered Salmonella shedding rates in this collection of captive exotic felids.

Second-generation anticoagulant rodenticides can give rise to unexpected casualties in nontarget species in zoos. The first two offspring of a pair of turkey vultures (Cathartes aura) died of brodifacoum toxicosis. The adult birds fed rodenticide-killed mice to their offspring. There are previous case reports of small carnivorous birds (Dacelo novae-guinae and Tockus deckeni) killed eating poisoned (difenacoum and brodifacoum) mice. Even a granivorous species (Rollulus roulroul) died, probably by contamination of its food by cockroaches that transported the rodenticide.