Ultrasonographic study of early embryonic loss induced by Actinomyces pyogenes in cattle.

Four cows were inoculated into the uterus with Actinomyces pyogenes between 30 and 41 days of gestation. Gross morphological changes were monitored by rectal palpation and with a realtime B-mode two-dimensional scanner with a 7.5 MHz transrectal linear transducer, shortly before infection and afterwards at three to 12 hours intervals. Two control groups of cows 27 to 50 days pregnant were used: two cows were inoculated with 6 ml of sterile saline into the uterine lumen and four cows were treated with cloprostenol (prostaglandin F2 alpha analogue). There was a change in the uterine fluid from a black, non-echogenic image before infection to a grey or cloudy echogenic image as early as 21 hours after infection. There was an increase in the thickness of the endometrium of the horns and body of the uterus. The embryonic membranes thickened and separated from the endometrium as early as four hours after infection, followed by cessation of the embryonic heart beat, opening of the cervix and abortion. Abortion was followed by an increase in the amount of echogenic intrauterine fluid leading to an increase in the size of the uterus, and the cervix remained open for at least eight days. The area of the corpus luteum remained greater than 2 cm2 throughout the whole period. Intrauterine inoculation with sterile saline had no effects, but the administration of cloprostenol was followed by the death of the embryo and abortion within 72 hours, and the regression of the corpus luteum from greater than 2 cm2 at treatment to 0.4 cm2, 24 hours after abortion.(ABSTRACT TRUNCATED AT 250 WORDS)     

Intramuscular anesthesia of bonito and Pacific mackerel with ketamine and medetomidine and reversal of anesthesia with atipamezole

OBJECTIVE: To determine anesthetic effects of ketamine and medetomidine in bonitos and mackerels and whether anesthesia could be reversed with atipamezole. DESIGN: Clinical trial. ANIMALS: 43 bonitos (Sarda chiliensis) and 47 Pacific mackerels (Scomber japonica). PROCEDURE: 28 bonitos were given doses of ketamine ranging from 1 to 8 mg/kg (0.5 to 3.6 mg/lb), i.m., and doses of medetomidine ranging from 0.2 to 1.6 mg/kg (0.1 to 0.7 mg/lb), i.m. (ratio of ketamine to medetomidine, 2.5:1 to 20:1). Doses of atipamezole equal to 1 or 5 times the dose of medetomidine were used. The remaining 15 bonitos were used to determine the anesthetic effects of ketamine at a dose of 4 mg/kg (1.8 mg/lb) and medetomidine at a dose of 0.4 mg/kg (0.2 mg/lb). The mackerels were given ketamine at doses ranging from 11 to 533 mg/kg (5 to 242 mg/lb) and medetomidine at doses ranging from 0.3 to 9.1 mg/kg (0.1 to 4.1 mg/lb; ratio of ketamine to medetomidine, 3:1 to 800:1). Doses of atipamezole equal to 5 times the dose of medetomidine were used. RESULTS: I.m. administration of ketamine at a dose of 4 mg/kg and medetomidine at a dose of 0.4 mg/kg in bonitos and ketamine at a dose of 53 to 228 mg/kg (24 to 104 mg/lb) and medetomidine at a dose of 0.6 to 4.2 mg/kg (0.3 to 1.9 mg/lb) in mackerels was safe and effective. For both species, administration of atipamezole at a dose 5 times the dose of medetomidine reversed the anesthetic effects. CONCLUSIONS AND CLINICAL RELEVANCE: Results suggest that a combination of ketamine and medetomidine can safely be used for anesthesia of bonitos and mackerels and that anesthetic effects can be reversed with atipamezole.     

Increased sacral screw purchase minimizes screw loosening in canine triple pelvic osteotomy

OBJECTIVE: To determine if screw loosening in triple pelvic osteotomies (TPO) is minimized when screws cranial to the ilial osteotomy had maximal sacral purchase. STUDY DESIGN: Prospective study. ANIMALS: Forty-six dogs with decreased acetabular coverage of the femoral head and minimal degenerative joint changes. METHODS: TPOs were performed where screws cranial to the ilial osteotomy were inserted to maximally engage sacral bone. Data collected were: use of ilial and ischial cerclage wire, screw length, ventrodorsal radiographic sacral width (most caudal aspect), pelvic canal diameter, and sacral penetration of the 3 cranial screws. On all subsequent radiographs, changes in screw position, pelvic canal diameter, and sacral purchase were noted. RESULTS: For 69 TPOs, 414 screws were used. Mean radiographic cranial screw length was 34.54 mm. Combined sacral depth of all 3 screws was 93.3% of sacral width. All osteotomies healed uneventfully. Twenty-four screws (6%) loosened with 12 being in the most cranial positions. Use of ischial or ilial cerclage wires did not statistically influence screw loosening. Pelvic diameter decreased by a mean of 7.79% from postoperative radiographs to the last radiographic recheck. CONCLUSIONS: By sufficiently engaging the sacrum with screws cranial to the ilial osteotomy, implant failures can be avoided and screw loosening minimized when a 6-hole TPO plate is used. CLINICAL RELEVANCE: To minimize screw-loosening in TPO, screws inserted cranial to the ilial osteotomy should be inserted to maximum sacral depth without penetrating the vertebral canal.     

Neurobiological substrates of dread

Given the choice of waiting for an adverse outcome or getting it over with quickly, many people choose the latter. Theoretical models of decision-making have assumed that this occurs because there is a cost to waiting-i.e., dread. Using functional magnetic resonance imaging, we measured the neural responses to waiting for a cutaneous electric shock. Some individuals dreaded the outcome so much that, when given a choice, they preferred to receive more voltage rather than wait. Even when no decision was required, these extreme dreaders were distinguishable from those who dreaded mildly by the rate of increase of neural activity in the posterior elements of the cortical pain matrix. This suggests that dread derives, in part, from the attention devoted to the expected physical response and not simply from fear or anxiety. Although these differences were observed during a passive waiting procedure, they correlated with individual behavior in a subsequent choice paradigm, providing evidence for a neurobiological link between the experienced disutility of dread and subsequent decisions about unpleasant outcomes.     

Biomass Production and Net Ecosystem Exchange Following Defoliation in a Wet Sedge Community

Riparian ecosystems provide many ecosystem services, including serving as an important forage resource for livestock grazing operations. We evaluated defoliation impacts on above- and belowground production, and net ecosystem exchange of CO₂ (NEE), in a wet sedge (Carex nebrascensis Dewey)-dominated plant community. In June or July of 2004–2005, experimental plots were clipped to 10 cm stubble height and paired control plots left unclipped. All plots were clipped to 2.5 cm in mid-September, and end-of-season and season-long aboveground production calculated. Root ingrowth cores were used to estimate annual root production and root length density (RLD). A portable gas exchange system and plexiglass chamber were used to measure NEE in 2005. An elevated water table in 2005 vs. 2004 was associated with higher (P &spilt; 0.001) season-long aboveground production (about double), but lower (P ≤ 0.05) belowground production (about half). Total productivity did not differ between years, but below-:aboveground ratios were 3× higher in 2004 vs. 2005. RLD was not different between years (P &spigt; 0.05). Clipping reduced (P ≤ 0.05) end-of-season aboveground standing crop by 33% to 73% depending on clipping month and year. Effects of clipping month on season-long aboveground production were inconsistent between years; June clipping decreased (P ≤ 0.05) production (-10%) in 2005 and July clipping decreased (P ≤ 0.05) production (-25%) in 2004. NEE for June-clipped plots recovered within 1 mo of clipping, whereas NEE for plots clipped in July remained below unclipped levels at the end of the growing season. Water table levels strongly influenced below-:aboveground ratios, although total production was relatively stable between years. Year effects overwhelmed clipping effects on season-long aboveground production. Defoliation after mid-summer did not allow recovery of photosynthetic capacity by the end of the growing season, suggesting the potential for long-term impact with regular late-season defoliation.     

Restoring the Sagebrush Component in Crested Wheatgrass–Dominated Communities

Monotypic stands of crested wheatgrass (Agropyron cristatum [L] Gaertm. and Agropyron desertorum [Fisch.] Schult.), an introduced grass, occupy vast expanses of the sagebrush steppe. Efforts to improve habitat for sagebrush-associated wildlife by establishing a diverse community of native vegetation in crested wheatgrass stands have largely failed. Instead of concentrating on a diversity of species, we evaluated the potential to restore the foundation species, Wyoming big sagebrush (Artemisia tridentata spp. wyomingensis [Beetle & A. Young] S. L. Welsh), to these communities. We investigated the establishment of Wyoming big sagebrush into six crested wheatgrass stands (sites) by broadcast seeding and planting seedling sagebrush across varying levels of crested wheatgrass control with glyphosate. Planted sagebrush seedlings survived at high rates (～ 70% planted sagebrush survival 3 yr postplanting), even without crested wheatgrass control. However, most attempts to establish sagebrush by broadcast seeding failed. Only at high levels of crested wheatgrass control did a few sagebrush plants establish from broadcasted seed. Sagebrush density and cover were greater with planting seedlings than broadcast seeding. Sagebrush cover, height, and canopy area were greater at higher levels of crested wheatgrass control. High levels of crested wheatgrass control also created an opportunity for exotic annuals to increase. Crested wheatgrass rapidly recovered after glyphosate control treatments, which suggests multiple treatments may be needed to effectively control crested wheatgrass. Our results suggest that planting sagebrush seedlings can structurally diversify monotypic crested wheatgrass stands to provide habitat for sagebrush-associated wildlife. Though this is not the full diversity of native functional groups representative of the sagebrush steppe, it is a substantial improvement over other efforts that have largely failed to alter these plant communities. We also hypothesize that planting sagebrush seedlings in patches or strips may provide a relatively inexpensive method to facilitate sagebrush recovery across vast landscapes where sagebrush has been lost.