The role of disturbance severity and canopy closure on standing crop of understory plant species in ponderosa pine stands in northern Arizona,USA

Concerns about the long-term sustainability of overstocked dry conifer forests in western North America have provided impetus for treatments designed to enhance their productivity and native biodiversity. Dense forests are increasingly prone to large stand-replacing fires; yet, thinning and burning treatments, especially combined with other disturbances such as drought and grazing, may enhance populations of colonizing species, including a number of non-native species. Our study quantifies plant standing crop of major herbaceous species across contrasting stand structural types representing a range in disturbance severity in northern Arizona. The least disturbed unmanaged ponderosa pine stands had no non-native species, while non-native grasses constituted 7–11% of the understory plant standing crop in thinned and burned stands. Severely disturbed wildfire stands had a higher proportion of colonizing native species as well as non-native species than other structural types, and areas protected from grazing produced greater standing crop of native forbs compared to grazed unmanaged stands. Standing crop of understory plants in low basal area thinned and burned plots was similar to levels on wildfire plots, but was comprised of fewer non-native graminoids and native colonizing plants. Our results also indicate that size of canopy openings had a stronger influence on standing crop in low basal area plots, whereas tree density more strongly constrained understory plant standing crop in dense stands. These results imply that treatments resulting in clumped tree distribution and basal areas <10 m² ha⁻¹ will be more successful in restoring native understory plant biomass in dense stands. Multiple types and severity of disturbances, such as thinning, burning, grazing, and drought over short periods of time can create greater abundance of colonizing species. Spreading thinning and burning treatments over time may reduce the potential for non-native species colonization compared to immediately burning thinned stands.     

Rainforest litter quality and chemical controls on leaf decomposition with near‐infrared spectrometry

Plant‐litter chemical quality is an important driver of many ecosystem processes, however, what actually constitutes high‐ or low‐quality litter (chemical potential for fast and slow decomposition, respectively) is often interpreted by the indices available. Here, near‐infrared spectroscopy (NIRS) was used to explore leaf‐litter chemical quality and the controls on decomposition in the tropical rainforest region of north Queensland Australia. Leaf‐litter samples from litterfall collections and litterbag studies were used. NIRS was used to calibrate the chemical compositions of the material (N, P, C, Mg, Ca, acid detergent fiber, acid detergent lignin, α‐cellulose, and total phenolics) from a smaller sample set covering the spectral range in the full set of samples. Calibrations were compared for both separate (local) and combined models, for litterbags, and litterfall. Coefficients of determination (r²) in the local models ranged from 0.88 (litterbag Mg) to 0.99 (litterfall N), with residual prediction deviation ratios > 3 for all constituents except Mg (≈ 2.5). Mass loss in the litterbags was strongly related to the NIR spectra, with model r²'s of 0.75 (in situ leaves) and 0.76 (common control leaf). In situ decomposability was determined from modeling the initial NIR spectra prior to decomposition with litterbag exponential‐decay rates (model r² of 0.81, n = 85 initial samples). A best subset model including litter‐quality, climate, and soil variables predicted decay better than the NIR decomposability model (r² = 0.87). For litter quality alone the NIR model predicted decay rate better than all of the best predictive litter–chemical quality indices. The decomposability model was used to predict in situ decomposability in the litterfall samples. The chemical variables explaining NIR decomposability for litterfall were initial P, C, and phenolics (linear model r² = 0.80, n = 2471). NIRS is a holistic technique that is just as, if not more accurate, than litter–chemical quality indices, when predicting decomposition and decomposability, shown here in a regional field study.     

Detection and quantification of equine herpesvirus-1 viremia and nasal shedding by real-time polymerase chain reaction.

Equine herpesvirus-1 (EHV-1) infection is common in young horses throughout the world, resulting in respiratory disease, epidemic abortion, sporadic myelitis, or latent infections. To improve on conventional diagnostic tests for EHV-1, a real-time polymerase chain reaction (PCR) technique was developed, using primers and probes specific for the EHV-1 gB gene. Amplification efficiencies of 100% +/- 5% were obtained for DNA isolated from a plasmid, infected peripheral blood mononuclear cells (PBMCs), and nasal secretions from infected ponies. The dynamic range of the assay was 8 log10 dilutions, and the lower limit of detection was 6 DNA copies. Fifteen ponies, seronegative for EHV-1, were experimentally infected with EHV-1, and nasal samples were used to quantify shedding of virus by both virus isolation and real-time PCR analysis. Virus isolation identified nasal shedding of EHV-1 in 12/15 ponies on a total of 25 days; real-time PCR detected viral shedding in 15/15 ponies on 75 days. Viremia was quantified using PBMC DNA, subsequent to challenge infection in 3 additional ponies. Viremia was identified in 1/3 ponies on a single day by virus isolation; real-time PCR detected viremia in 3/3 ponies on 17 days. When real-time PCR was used to analyze PBMC DNA from 11 latently infected ponies (documented by nested PCR), EHV-1 was not detected. We conclude that real-time PCR is a sensitive and quantitative test for EHV-1 nasal shedding and viremia and provides a valuable tool for EHV-1 surveillance, diagnosis of clinical disease, and investigation of vaccine efficacy.     

Using 3D animations to teach intracellular signal transduction mechanisms: taking the arrows out of cells

Traditional methods of teaching intracellular biological processes and pathways use figures or flowcharts with the names of molecules linked with arrows. Many veterinary students, presented with such material, simply memorize the names or chemical structures of the molecules and are then likely to forget the material once the examination is completed. To address this problem, the authors designed, created, and field-tested new teaching media that incorporate realistic three-dimensional (3D) animations depicting the dynamic changes that occur in intracellular molecules during cellular activation. Testing found that veterinary students taught using traditional teaching media (e.g., lectures, handouts, textbooks) are proficient in memorizing the names and order of intracellular molecules but unable to appreciate the interactions between these elements or their spatial relationships within cells. In contrast, more than 90% of veterinary students taught using 3D animations not only recall the facts about the intracellular elements but also develop accurate mental images of the interactions among these molecules and their spatial relationships. These findings strongly suggest that the comprehension of complex biological processes by veterinary students can be enhanced by the use of dynamic 3D depictions of these processes in the classroom.     

Effects of perioperative saphenous and sciatic nerve blocks,lumbosacral epidural or morphine–lidocaine–ketamine infusion on postoperative pain and sedation in dogs undergoing tibial plateau leveling osteotomy

ObjectiveTo compare the quality of postoperative analgesia and sedation after preoperative saphenous and sciatic nerve blockade, preoperative lumbosacral epidural injection and perioperative intravenous (IV) morphine, lidocaine and ketamine infusions in dogs undergoing stifle arthroscopy and tibial plateau leveling osteotomy (TPLO) under general anesthesia.Study designProspective, blinded, randomized, clinical comparison study.AnimalsA total of 45 dogs weighing 33.9 (15.9–56.7) kg and aged 5.2 (1.0–12.0) years, mean (range), undergoing elective unilateral TPLO for spontaneous cranial cruciate ligament rupture.MethodsClient-owned dogs were enrolled. Dogs were randomly assigned to one of three groups: group MLK, perioperative IV morphine, lidocaine and ketamine infusion; group EPID, lumbosacral epidural with ropivacaine and morphine; or group SSNB, saphenous and sciatic nerve blockade with ropivacaine. Routine stifle arthroscopy followed by TPLO surgery was performed. Sedation and pain scores were assessed at 0, 2, 4, 8 and 24 hours following extubation. Rescue analgesia was administered as prescribed by Glasgow composite pain score–short form score >5.ResultsSedation scores for MLK were higher than EPID and SSNB. Pain scores for SSNB were lower than those for EPID and MLK. No significant differences were found in anesthesia duration or surgery duration among groups. No dogs required rescue analgesia.Conclusions and clinical relevanceAlthough analgesia was adequate in all groups, the best combination of analgesia without increased sedation was recorded for SSNB.