The upper Jejuí River is a major tributary of the Paraguay River in eastern Paraguay and is the principal drainage for the Mbaracayú Forest Biosphere Reserve. Despite the international significance of the biosphere reserve and detailed documentation of its terrestrial fauna and flora, the fish fauna in its streams remains relatively unknown, with 48 species previously recorded. We sampled 35 sites within the biosphere reserve over five years (2007–2011) to assess the richness of its ichthyofauna. These surveys yielded a new total of 105 known species for the biosphere reserve, including two newly-recorded orders, Gymnotiformes and Cyprinodontiformes, and 14 newly-recorded families. Fish community composition resembled that of previously-reported fish communities from the Paraguay River drainage, with characiforms and siluriforms comprising the majority of the species (57.1% and 31.4%, respectively). Post hoc analyses showed significantly greater ichthyofaunal diversity at sites within the Mbaracayú Forest Nature Reserve, a core protected forest area within the biosphere reserve, compared to areas outside the nature reserve, suggesting a negative impact from deforestation and land conversion on fish assemblages in these headwater streams. Broad regional deforestation places greater emphasis on important management decisions that will protect current biodiversity.

OBJECTIVE To determine plasma pharmacokinetics of penciclovir following oral and rectal administration of famciclovir to young Asian elephants (Elephas maximus). ANIMALS 6 healthy Asian elephants (5 females and 1 male), 4.5 to 9 years old and weighing 1,646 to 2,438 kg. PROCEDURES Famciclovir was administered orally or rectally in accordance with an incomplete crossover design. Three treatment groups, each comprising 4 elephants, received single doses of famciclovir (5 mg/kg, PO, or 5 or 15 mg/kg, rectally); there was a minimum 12-week washout period between subsequent famciclovir administrations. Serial blood samples were collected after each administration. Samples were analyzed for famciclovir and penciclovir with a validated liquid chromatography-mass spectroscopy assay. RESULTS Famciclovir was tolerated well for both routes of administration and underwent complete biotransformation to the active metabolite, penciclovir. Mean maximum plasma concentration of penciclovir was 1.3 μg/mL at 1.1 hours after oral administration of 5 mg/kg. Similar results were detected after rectal administration of 5 mg/kg. Mean maximum plasma concentration was 3.6 μg/mL at 0.66 hours after rectal administration of 15 mg/kg; this concentration was similar to results reported for humans receiving 7 mg/kg orally. CONCLUSIONS AND CLINICAL RELEVANCE Juvenile Asian elephants are susceptible to elephant endotheliotropic herpesvirus. Although most infections are fatal, case reports indicate administration of famciclovir has been associated with survival of 3 elephants. In Asian elephants, a dose of 8 to 15 mg of famciclovir/kg given orally or rectally at least every 8 hours may result in penciclovir concentrations that are considered therapeutic in humans.

Captive Asian elephants (Elephas maximus) are susceptible to lameness resulting from foot and joint pain, including chronic arthritis. In the past, opioid analgesics, such as butorphanol, have been used clinically for pain management. However, dosages used in treating elephants were often extrapolated from data in horses, with no pharmacokinetic information on the specific agents used in elephant species. In this pharmacokinetic study, six adult captive Asian elephants (5 female, 1 male castrate) were administered a 0.015 mg/kg dose of butorphanol by both i.v. and i.m. routes. A complete crossover design was used with a 3-wk washout period between treatments. Serial blood samples were collected immediately prior to butorphanol administration and at 5, 10, 20, and 40 min and 1, 1.5, 2, 3, 4, 5, 6, 8, 10, and 24 h after administration. The butorphanol analysis was performed using a validated liquid chromatography mass spectrophotometric assay with a limit of quantitation of 0.025 ng/ml. The mean C-max after i.m. administration was 7.9 ng/ml, with a corresponding T-max of 40 min and t(1/2) of 7.1 h. After i.v. administration, the mean Vd(ss) was 1.4 L/kg and the mean Cl-p was 0.26 L/kg/h. Mean i.m. bioavailability was 37%. The results indicate that butorphanol used at 0.015 mg/kg i.m. or i.v. could be useful in elephants when given for pain control.

Relatively little information is available concerning the natural history or population ecology of the montane akodont. Akodon montensis. a sigmodontine species that harbors Jabora and Ape Aime hantaviruses On the basis of mark-recapture sampling of 3 locales during 2 years. this report provides comparative data on populational and other characteristics of the species near its distributional limit, in the Upper Parana Atlantic Forest in Paraguay We found A montensis to be almost exclusively terrestrial (nonarboreal) and to vary in population density among locales and between years. findings consistent with earlier studies. Population density was not related either to neotropical seasonality or to most precipitation variables, but sex ratio varied seasonally, which has not been reported previously We evaluated the seroprevalence of hantavirus in A montensis. in association with external. populational, and individual variables As in most previous studies of rodent hantavirus systems, seroprevalence varied among sampling locales and was higher among males However, unlike previous reports. especially those from North America. we did not find a correspondence between seroplevalence and population density. seasonal variation, or most precipitation variables Simple and direct associations between seroprevalence levels and either seasonality or precipitation may be less characteristic of humid neotropical or subtropical systems Our analyses revealed that seropositive animals exhibit several noteworthy behavioral and hie-history modifications, in particular that they have larger home ranges than do seronegatives, exhibit greater maximum distance moved, have greater home range displacement between sampling sessions. particularly those individuals that are seroconvertmg during the same period, and have greater longevity, especially among males In general. these characteristics could be postulated as favorable to the capacity of the virus to be transmitted horizontally to other hosts DOI. 10 1644/09-MAMM-A-152.1.

The anti-inflammatory agent, tepoxalin, was administered to eight healthy 6-month-old female New Zealand white rabbits once daily at an oral dose of 10 mg/kg. Blood samples were obtained immediately before and at 0.25, 0.5, 1, 2, 3, 4, 6, 8, 12, and 24 h postadministration on days 1 and 10. Tepoxalin and its active metabolite, RWJ 20142, concentrations were determined in plasma by use of high-performance liquid chromatography with mass spectrometry. C(max) of the parent compound was reached between 3 and 8 h of drug administration, with a harmonic mean t(1/2) of 3.6 h. Peak tepoxalin plasma concentrations were 207 +/- 49 ng/mL. After oral administration, the metabolite RWJ 20142 achieved C(max) in plasma 2-8 h after administration, with a t(1/2) of 1.9-4.8 h (harmonic mean 2.8 h). Peak plasma concentrations of RWJ 20142 on day 1 were 2551 +/- 1034 ng/mL.

Peroxidase-mediated oxidation has been proposed as a treatment method for naphthol-contaminated water. However, the impact of solution chemistry on naphthol polymerization and removal has not been documented. This research investigated the impact of pH and ionic strength on peroxidase-mediated removal of 1-naphthol in completely mixed batch reactors. The impact of hydrogen peroxide to 1-naphthol ratio and activity of horseradish peroxidase was also studied. Size exclusion chromatography was used to estimate the molecular weight distribution of oligomeric products, and liquid chromatography/mass spectrometry was used to estimate product structure. Naphthol transformation decreased with ionic strength, and substrate removal was lowest at neutral pHs. Solution pH influenced the size and the composition of the oligomeric products. An equimolar ratio of H(2)O(2):naphthol was sufficient for optimal naphthol removal. Polymerization products included naphthoquinones and oligomers derived from two, three, and four naphthol molecules. Our results illustrate the importance of water chemistry when considering a peroxidase-based approach for treatment of naphthol-contaminated waters.

Hantaviruses may cause serious disease when transmitted to humans by their rodent hosts. Since their emergence in the Americas in 1993, there have been extensive efforts to understand the role of environmental factors on the presence of these viruses in their host rodent populations. HPS outbreaks have been linked to precipitation, but climatic factors alone have not been sufficient to predict the spatial-temporal dynamics of the environment-reservoir-virus system. Using a series of mark-recapture sampling sites located at the Mbaracayú Biosphere Reserve, an Atlantic Forest site in eastern Paraguay, we investigated the hypothesis that microhabitat might also influence the prevalence of Jaborá hantavirus within populations of its reservoir species, Akodon montensis. Seven trapping sessions were conducted during 2005-2006 at four sites chosen to capture variable microhabitat conditions within the study site. Analysis of microhabitat preferences showed that A. montensis preferred areas with little forest overstory and denser vegetation cover on and near the ground. Moreover, there was a significant difference in the microhabitat occupied by antibody-positive vs antibody-negative rodents, indicating that microhabitats with greater overstory cover may promote transmission and maintenance of hantavirus in A. montensis.

OBJECTIVE-To determine the pharmacokinetics of marbofloxacin after oral administration every 24 hours to rabbits during a 10-day period. ANIMALS-8 healthy 9-month-old female New Zealand White rabbits. PROCEDURES-Marbofloxacin (5 mg/kg) was administered orally every 24 hours to 8 rabbits for 10 days. The first day of administration was designated as day 1. Blood samples were obtained at 0, 0.17, 0.33, 0.5, 0.75, 1, 1.5, 2, 3, 4, 5, 6, 8, 12, and 24 hours on days 1 and 10 of marbofloxacin administration. Plasma marbofloxacin concentrations were quantitated by use of a validated liquid chromatography-mass spectrometry assay. Pharmacokinetic analysis of marbofloxacin was analyzed via noncompartmental methods. RESULTS-After oral administration, mean +/- SD area under the curve was 10.50 +/- 2.00 microg.h/mL and 10.90 +/- 2.45 microg.h/mL, maximum plasma concentration was 1.73 +/- 0.35 microg/mL and 2.56 +/- 0.71 microg/mL, and harmonic mean terminal half-life was 8.0 hours and 3.9 hours for days 0 and 10, respectively. CONCLUSIONS AND CLINICAL RELEVANCE-Marbofloxacin administered orally every 24 hours for 10 days appeared to be absorbed well and tolerated by rabbits. Administration of marbofloxacin at a dosage of 5 mg/kg, PO, every 24 hours is recommended for rabbits to control infections attributable to susceptible bacteria.

The occurrence of ciprofloxacin (CIP), sulfamethoxazole (SMX), and azithromycin (AZI) was evaluated in various aqueous streams of four municipal wastewater treatment plants (WWTPs) in the Midwestern United States. Aqueous phase grab samples were collected from different locations in the WWTPs at four different times of the year. The target compounds were extracted using solid phase extraction, separated with high-performance liquid chromatography, and identified/quantified using ultraviolet and fluorescence spectroscopy (CIP and SMX) or mass spectrometry (AZI). Aqueous phase concentrations for CIP and AZI were similar to literature values while SMX concentrations were generally higher than those reported in the literature. The average aqueous phase concentrations for CIP, AZI, and SMX in the raw wastewater were 1.44, 1.11, and 18.3μg∕L, respectively, while the concentrations in the WWTP effluent were 0.59, 1.23, and 3.25μg∕L, respectively. AZI concentration was consistently lower in the winter. While some CIP and SMX removal from the aqueous phase was observed in the WWTP, such reductions were not seen for AZI. Composite sampling data indicated that CIP and SMX concentrations were significantly higher in summer than in winter.

Landscape epidemiology has made significant strides recently, driven in part by increasing availability of land cover data derived from remotely-sensed imagery. Using an example from a study of land cover effects on hantavirus dynamics at an Atlantic Forest site in eastern Paraguay, we demonstrate how automated classification methods can be used to stratify remotely-sensed land cover for studies of infectious disease dynamics. For this application, it was necessary to develop a scheme that could yield both land cover and land use data from the same classification. Hypothesizing that automated discrimination between classes would be more accurate using an object-based method compared to a per-pixel method, we used a single Landsat Enhanced Thematic Mapper+ (ETM+) image to classify land cover into eight classes using both per-pixel and object-based classification algorithms. Our results show that the object-based method achieves 84% overall accuracy, compared to only 43% using the per-pixel method. Producer's and user's accuracies for the object-based map were higher for every class compared to the per-pixel classification. The Kappa statistic was also significantly higher for the object-based classification. These results show the importance of using image information from domains beyond the spectral domain, and also illustrate the importance of object-based techniques for remote sensing applications in epidemiological studies.

The pharmacokinetic parameters of carfentanil and naltrexone were determined in the common eland (Taurotragus oryx). Six adult females were immobilized with xylazine (0.23 +/- 0.03 mg/kg i.m.) and carfentanil (0.0169 +/- 0.0005 mg/kg i.m.) for a 45-min period, during which time routine health care procedures were performed. Heart and respiration rates and body temperatures were monitored throughout the immobilization period. A single intramuscular injection of naltrexone (1.66 +/- 0.08 mg/kg i.m.) was sufficient for reversal. The eland were intermittently restrained in a hydraulic squeeze chute for serial blood sample collection via jugular venipuncture during immobilization and up to 48 hr post-immobilization. The quantification of carfentanil and naltrexone in the plasma was performed by liquid chromatography and mass spectroscopy methods. Carfentanil was rapidly absorbed following administration, with the peak plasma concentration (C(max)) at 13.8 min. Naltrexone was readily absorbed and reached C(max) at 23.4 +/- 16.8 min after administration. All animals stood 2.7 +/- 2.2 min after naltrexone administration. Carfentanil has a half-life of 7.7 hr, whereas naltrexone has a much shorter half-life of 3.7 hr. Although respiratory rates appeared to fluctuate widely among animals, heart rates and body temperature remained stable throughout the immobilization. Renarcotization was not noted as a major complication.

OBJECTIVE:To determine the pharmacokinetics of marbofloxacin after single IV and orally administered doses in blue and gold macaws.ANIMALS:10 healthy blue and gold macaws.PROCEDURES:In a crossover study, marbofloxacin (2.5 mg/kg) was administered orally (via crop gavage) to 5 birds and IV to 5 birds. Blood samples were obtained at 0, 0.5, 1, 3, 6, 12, 24, 48, 72, and 96 hours after marbofloxacin administration. After a 4-week washout period, the study was repeated, with the first 5 birds receiving the dose IV and the second 5 birds receiving the dose orally. Serum marbofloxacin concentrations were quantitated by use of a validated liquid chromatography-mass spectrometry assay.RESULTS:After oral administration, mean +/- SD area under the curve was 7.94 +/- 2.08 microg.h/mL, maximum plasma concentration was 1.08 +/- 0.316 microg/mL, and bioavailability was 90.0 +/- 31%. After IV administration of marbofloxacin, the apparent volume of distribution was 1.3 +/- 0.32 L/kg, plasma clearance was 0.29 +/- 0.078 L/h/kg, area under the curve was 9.41 +/- 2.84 microg.h/mL, and the harmonic mean terminal half-life was 4.3 hours.CONCLUSIONS AND CLINICAL RELEVANCE:Single IV and orally administered doses of marbofloxacin were well tolerated by blue and gold macaws. The orally administered dose was well absorbed. Administration of marbofloxacin at a dosage of 2.5 mg/kg, PO, every 24 hours may be appropriate to control bacterial infections susceptible to marbofloxacin in this species.

ABSTRACTAims Hantaviruses are zoonotic, aetiological agents maintained by rodents of the family Muridae. The occurrence of hantavirus in rodent hosts has been correlated to a number of climatic and environmental factors, including landscape structure. To date, most of these correlative studies have been conducted at moderate to fine spatial resolution. Our aim is to determine whether land cover classes defined at a mapping resolution of 1 km2are associated with rodents with antibodies to hantavirus in Paraguay.Location The Republic of Paraguay.Methods A total of 362 rodents from 10 species known to host hantaviruses were tested for the presence of hantavirus antibodies, resulting in 27 seropositive individuals. This data base was then combined with a map of six land cover types derived from coarse resolution remote sensing data to create a series of contingency tables, which were used to relate serostatus to land cover type using nonparametric tests of proportions and qualitative comparison of observed and expected values.Results There was a significant difference in habitat association between seropositive and seronegative rodents when species were pooled. Seropositive rodents were found with disproportionately high frequency in areas where human disturbance in the form of intensive and mosaic agricultural landscapes was present.Main conclusions Human‐disturbed land cover classes have a detectable relationship to the hantavirus serostatus of host population rodents when observed at coarse spatial resolutions. Although coarse‐grained analysis does not lead to any conclusions as to why agricultural land cover is more likely to harbour seropositive rodents, the relationship between them could form the basis for a monitoring system designed to relate land cover change to potential viral outbreaks in rodents and humans.

Objective-To determine the plasma pharmacokinetics and synovial fluid concentrations after oral administration of single and multiple doses of celecoxib in Greyhounds. Animals-7 adult Greyhounds. Procedures-Dogs received celecoxib (median dose, 11.8 mg/kg [range, 11.5 to 13.6 mg/kg], PO, q 24 h) for 10 days. Blood samples were collected prior to administration of celecoxib and serially for 24 hours after the 1st and 10th doses were administered. A synovial joint catheter was placed into a stifle joint in each dog for collection of synovial fluid samples. Concentrations of celecoxib in plasma and synovial fluid were quantified by use of a validated liquid chromatography/mass spectrometry method. Identification of hydroxy- and carboxyl-celecoxib in plasma and synovial fluid was also performed, Pharmacokinetic parameters were determined by use of noncompartmental analysis. Results-Administration of multiple doses of celecoxib resulted in a significant decrease (40%) in median area under the curve (AUC) values and a corresponding decrease in median maximum concentrations (C-max; 2,620 to 2,032 ng/mL) between the 1st and 10th doses. Synovial fluid concentrations were less than the corresponding plasma concentrations at all times except 24 hours after administration of the 10th dose of celecoxib. Conclusions and Clinical Relevance-Celecoxib distributes into the synovial fluid of Greyhounds. Although the exact mechanism for the decreases in AUC and C-max is not known, results suggested that the plasma pharmacokinetics of celecoxib are different after administration of multiple doses in Greyhounds. These findings warrant further investigation on the absorption, distribution, metabolism, and elimination of celecoxib in Greyhounds and other breeds of dogs.

OBJECTIVE:To determine pharmacokinetics and tissue concentrations of azithromycin in ball pythons (Python regius) after IV or oral administration of a single dose.ANIMALS:2 male and 5 female ball pythons.PROCEDURES:Using a crossover design, each snake was given a single dose of azithromycin (10 mg/kg) IV. After a 4-week washout period, each snake was given a single dose of azithromycin (10 mg/kg) orally. Blood samples were collected prior to dose administration and 1, 3, 6, 12, 24, 48, 72, and 96 hours after azithromycin administration. Azithromycin was quantitated by use of liquid chromatography-mass spectrometry.RESULTS:After IV administration, azithromycin had an apparent volume of distribution of 5.69 L/kg and a plasma clearance of 0.19 L/h/kg. Harmonic means for the terminal half-life were 17 hours following IV administration and 51 hours following oral administration. Mean residence times were 37 and 94 hours following IV and oral administration, respectively. Following oral administration, azithromycin had a peak plasma concentration (Cmax) of 1.04 microg/mL, a time to Cmax of 8.4 hours, and a prolonged mean absorption time of 57 hours. Mean oral bioavailability was 77%. Tissue concentrations ranged from 4 to 140 times the corresponding plasma concentration at 24 and 72 hours after azithromycin administration.CONCLUSIONS AND CLINICAL RELEVANCE:Azithromycin is well absorbed and tolerated by ball pythons. On the basis of plasma pharmacokinetics and tissue concentration data, we suggest an azithromycin dosage in ball pythons of 10 mg/kg, orally, every 2 to 7 days, depending upon the site of infection and susceptibil ity of the infective organism.