An outbreak of Type C botulism in waterbirds was investigated at Lake Lalbert in northwestern Victoria, Australia. Total losses were estimated at 1,500 birds, with 80% of affected birds being grey teal (Anas gibberifrons). The outbreak was associated with a falling water level, and extensive decomposition of plant material.

Published reports of Brucella abortus infections in wild North American ungulates and domestic cattle herds were reviewed to determine if infection in these species was related. Bison (Bison bison) were frequently found infected, but are probably a minor threat to livestock due to their current limited distribution. Most elk (Cervus elaphus) were free of infection except where their range was shared with infected bison or livestock. Deer (Odocoileus spp.), pronghorns (Antilocapra americana), moose (Alces alces), and bighorn sheep (Ovis canadensis) appeared to be insignificant hosts of Brucella abortus. The lack of significant wild ungulate hosts and the distribution of infected livestock herds in the United States suggests that wild ungulates are of little importance in the epidemiology of infections by B. abortus in cattle.

A Lactobacillus sp. was consistently isolated from dead and moribund postspawning brood stock rainbow trout. Pathology was characterized by massive chronic inflammation throughout the abdominal cavity and formation of pseudomembranes. The bacteria were most abundant in spent testes. Repeated handling was considered to be the major stressor leading to this infection and subsequent high mortality.

A new species of coccidium, Eimeria lettyae sp. n. (Protozoa: Eimeriidae) was recovered from feces of the northern bobwhite, Colinus virginianus (L.), from Pennsylvania and Florida. Oocysts measured 21.1 μm(16.4 to 25.8) by 17.2 μm (14.1 to 21.2); index (L/W ratio) = 1.22. Oocysts lacked a micropyle, residuum, and polar granules. Sporozoites penetrated the upper ½ of the villi, then moved to the lamina propria at the base of the villi. There were five asexual generations, all of which developed above the nucleus of the host cell. Meronts measured 9.4 × 7.0 μm, 18.6 × 11.2 μm, 11.8 × 10.1 μm, 7.1 × 6.2 μm, and 20.2 × 12.8 μm, respectively. These matured at 32, 40, 48, 56, and 72 hr postinoculation (PI) and contained 12, 50 , 24 to 36, 12 to 24, and 50 merozoites, respectively. Infection was most intense in the duodenum although some gamonts were found in the ileum and ceca. The prepatent period was 88 to 91 hr PI. Sporulation time was 18 hr at 25 C. The peak of oocyst production was broad and extended from 4 days PI through 14 days PI. Oocysts were passed for at least 67 to 76 days PI. Eimeria lettyae sp. n. did not infect chickens (Gallus domesticus), domestic turkeys (Meleagris gallopavo), ring-necked pheasants (Phasianus cochicus), chukar partridge (Alectoris graeca), or Japanese quail (Coturnix coturnix). Immunizing bobwhite with E. lettyae sp. n. did not protect against challenge with E. dispersa. Immunizing bobwhites 25 times with 10² or 10³ sporulated oocysts of E. lettyae did not entirely eliminate oocyst production following challenge with the same species.

Six species of parasites were recovered 4 mo after walleye fry were stocked in Heming Lake, Manitoba. The species of parasites acquired most rapidly were those that were non-host-specific and common to the indigenous populations of both walleye and yellow perch (Perca flavescens). Parasite species overlap (Jaccard's indices) was greatest within age groups of walleye and yellow perch, but was also high between older walleye and yellow perch. The higher numbers of parasites recruited by stocked walleye, particularly ones known to induce pathology, raises questions on the success of walleye introductions to aquatic systems with a diverse indigenous parasite fauna and a fish population with a large proportion of yellow perch.

Thirty-five swamp wallabies from Victoria, New South Wales and Queensland, Australia were examined for parasites. Thirty-nine species of nematodes, five species of cestodes and eight species of arthropods were found. Wallabies from Queensland and northern New South Wales had a less diverse helminth fauna (23 species) than did wallabies from southern New South Wales and Victoria (32 species). Rugopharynx spp. and Cloacina spp. occurred in large numbers in the stomach but provoked no pathological changes. Known pathogenic species (Globocephaloides trifidospicularis and Hypodontus macropi) were encountered in small numbers only and did not produce any lesions. Pathological changes associated with parasites were: gastric nodules associated with Labiostrongylus clelandi and Parazoniolaimus collaris, bronchopneumonia due to Marsupostrongylus spp., biliary fibrosis associated with Progamotaenia festiva and fibrous peritonitis, pleuritis, pericarditis and eosinophilic splenitis due to Breinlia mundayi. Echinococcus granulosus was the only parasite found which also occurs in domestic animals.

Diagnostic findings are presented on 139 sick or dead wild turkeys examined during the period 1972 through 1984. Turkeys originated from eight southeastern states (Alabama, Arkansas, Florida, Georgia, South Carolina, Tennessee, Virginia, West Virginia) and included 31 turkeys categorized as capture-related mortalities and 108 turkeys categorized as natural mortalities. Frequent diagnoses (≥10% of case accessions) in the natural mortality group were trauma, avian pox, and histomoniasis. Less frequent diagnoses (≤4% of case accessions) included malnutrition/environmental stress syndrome, coligranuloma-like condition, crop impaction, bumblefoot, organophosphate toxicosis, infectious sinusitis, a lympho-proliferative disease, salmonellosis, aspergillosis, toxoplasmosis, crop trichomoniasis, and melorheostosis.

A moribund, emaciated California quail (Callipepla californica) that was found in an orchard in the state of Washington had an impacted crop and gizzard. Pellets containing the anticoagulant chlorophacinone (Rozol^®, RO) were in the crop; the gizzard contents consisted of a pink mass of paraffin that was selectively accumulated from the paraffinized pellets. The plasma prothrombin time of 28 sec was near that determined for control quail. The signs of RO intoxication seen in the moribund wild quail were duplicated in captive quail given ad libitum diets of either RO or another paraffinized chlorophacinone pellet (Mr. Rat Guard II^®, MRG). This left little doubt that paraffin impaction of the gizzard was the primary problem. All captive quail fed RO or MRG pellets showed no increases in prothrombin times compared to control values, died in an emaciated condition, and had gizzards impacted with paraffin.

Yohimbine hydrochloride (YH) effectively reversed the immobilizing effects of ketamine hydrochloride (KH) combined with xylazine hydrochloride (XH) in 48 wild polar bears (Ursus maritimus) handled in the summer. Single intravenous doses of YH ranging between 0.029 and 0.198 mg/kg resulted in a median time of 10 min (range: 1–123 min) to post-injection recovery from KH-XH immobilization. Convulsions and muscle twitching were observed in some bears after YH was administered and one death occurred. Median respiratory rate and heartbeat rate increased from 5 br/min to 12 br/min and 51 BPM to 79 BPM, respectively, soon after yohimbine was administered. The median time to recovery after KH-XH administration, including processing and handling time, was 113 min for bears administered yohimbine and 202 min for bears not administered YH. After YH-induced recovery, polar bears showed signs of reduced awareness and many remained recumbent for undetermined periods although they could coordinate movements, stand, and walk or run if disturbed. YH proved to be a useful antagonist to immobilization induced by KH-XH in a field situation.

The combination of 55 mg/ml xylazine hydrochloride and 200 mg/ml ketamine hydrochloride was effective for immobilizing African lions in Tanzania. Nineteen adult females were given between 55 and 110 mg xylazine hydrochloride in the first dart. Initial doses of 110 mg xylazine hydrochloride and 450 mg ketamine hydrochloride equivalent to >0.9 mg/kg xylazine hydrochloride were most effective in achieving rapid immobilization. Lower doses of xylazine hydrochloride required supplementation with ketamine hydrochloride. These doses could be delivered easily in 3-ml darts. The use of lightweight darts and a blowgun was found to be useful as a supplement to longer range dart projector systems since many animals could be approached at short range.

Thirteen captive and one free-ranging white-tailed deer (Odocoileus virginianus) were immobilized one to six times each with ketamine hydrochloride and xylazine hydrochloride during winter and spring in northern Minnesota. Administration of 0.09 to 0.53 mg of yohimbine hydrochloride per kg IV after each trial reversed the immobilization. The deer raised their heads within a median time of 2.0 min, stood in 6.0 min and walked away in 9.5 min. No adverse side effects were observed for several weeks following the immobilization.

Combinations of etorphine hydrochloride and xylazine hydrochloride in different dosages were tested for their efficacy as immobilizing agents on 16 recently captured feral mares in corrals. The results of these trials led to the utilization of a standard combination of 5.5 mg of etorphine hydrochloride, 150 mg of xylazine hydrochloride, and 3 mg of atropine sulfate in a 7-ml dart syringe for field capture. This combination was used, administered by dart gun from helicopters, to capture 87 free-ranging feral horses from about 80 bands. Five mares died at the time of capture and the remains of three other mares were found near the site of capture 4 mo later. Blood samples collected from each animal and analyzed for hematologic variables, concentrations of urea, and glucose yielded values comparable to domestic “hot-blooded horses.” Serum cortisol concentrations (4.7 ±0.4 µg/d1) were comparable to values from undisturbed captive animals. Approximately 48 min of helicopter time were required per horse captured. The cost per animal captured was $159 for helicopter time and $66.70 for drugs and darts.

Serial physiological responses were examined for 150 min from captive collared peccaries during immobilization with ketamine hydrochloride. Rectal temperatures decreased significantly (P < 0.01) during anesthesia. Serum concentrations of total proteins, albumin, cholesterol, alanine aminotransferase, and calcium declined significantly (P < 0.05) during the first 45 min post-immobilization before stabilizing. Concentrations of lactate dehydrogenase and alkaline phosphatase in sera showed similar but nonsignificant (P > 0.05) trends. Inorganic phosphorus and aspartate aminotransferase concentrations increased significantly (P < 0.05) throughout the trial. Concentrations of serum glucose and glucocorticoid during the immobilization period were highly variable between individuals. Serum electrolytes, urea nitrogen, creatinine, gammaglutamyl transferase and progesterone were not significantly (P > 0.05) affected by immobilization. Elevations in serum testosterone were noted. Results indicated appropriate sampling times relative to immobilization for assay of particular serum biochemicals and steroid hormones during investigations of the physiology of the collared peccary.