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A standard-free method for hoof samples taken from cattle such as cow, calf, pony and sheep has been developed in order to estimate the state of health of these animals. The standard-free method developed for human nails was confirmed to be applicable to quantitative analysis of hoof samples since the shape of continuous X-rays is almost the same for nail and hoof taken from these ungulate animals. Accuracy and sensitivity of the present standard method were examined by comparing the results with those obtained by an internal-standard method combined with a chemical-ashing method, and it is confirmed that the method is applicable to hoof samples taken from domestic animals of many species. The method allows us to quantitatively analyze untreated hoof samples and to prepare the targets without complicated preparation technique which often brings ambiguous factors such as elemental loss from the sample and contamination of the sample during preparation procedure. It is also confirmed that halogens, which are important elements for estimating the state of health and are mostly lost during chemical-ashing, can be analyzed without problem by the present method. It is found that elemental concentration of more than twenty elements can be constantly analyzed and it is expected to be quite useful in order to estimate the state of health and to make diagnosis of domestic animals. It is also confirmed that elemental concentration of essential elements in hoof is not so changed depending on the positions in the sliced sample along both horizontal and vertical axis.

To establish the proper analgesic method by electroacupuncture (EA) for bovine surgery, the analgesic effect of dorsal and lumbar acupoints, in addition to the combination with dorsal and lumbar acupoints, were investigated in the present study. Four Korean native cattle (two males and two females) and 24 Holstein-Friesian cattle (all females) were used. The experimental animals were divided into four groups according to used acupoints: dorsal acupoint group (Tian Ping [GV-20] and Bai Hui [GV-5]: 7 heads), lumbar acupoint group (Yap Pang 1 [BL-21], Yao Pang 2 [BL-23], Yao Pang 3 [BL-24] and Yao Pang 4 [BL-25]; 5 heads), dorsal-lumbar acupoint group (Yao Pang 1 [BL-21], Yao Pang 2 [BL-23], Yao Pang 3 [BL-24] and Bai Hui [GV-5]; 8 heads) and control group (non-acupoints, the last intercostals space and the femoral area; 3 heads). The acupoints were stimulated with currents of 2–6 V (30 Hz) in dorsal acupoint group, 0.5–2.0 V (30 Hz) in lumbar acupoint group and 0.3–2.5 V (30 Hz) in dorsal-lumbar acupoint group. Recumbency time was 10 seconds to 1 minute (except one case) and induction time of analgesia was approximately 1 to 6 minutes in dorsal acupoint group. Analgesic effect was systemic, including the extremities in dorsal acupoint group. During the EA, the consciousness was evident and blepharo-reaction was still present under EA in dorsal acupoint group. During the surgery, grades of analgesic effect were 6 excellent (6/7, 87.5%) and 1 good (1/7, 14.3%). In addition, induction time for analgesia was about 10 minutes in both lumbar and dorsal-lumbar acupoint groups. Analgesic areas were found in abdominal areas from the last intercostal spaces to the femoral areas, except lower abdomen in lumbar and lumbar-dorsal acupoint groups. The consciousness was evident and standing position was maintained during EA stimulation in contrast to that of dorsal excellent (1/5, 20.0%), 3 good (3/5, 60.0%) and 1 poor (1/5, 20.0%) in the lumbar acupoint group. Additionally, grades of analgesic effect were 4 excellent (4/8, 50.0%), 3 good (3/8, 37.5%) and 1 poor (1/8, 12.5%). On the other hand, pain was present and analgesia was not accomplished under EA stimulation in control group. In conclusion, analgesia by EA was effective with decreasing order of dorsal acupoint > dorsal-lumbar acupoint > lumbar acupoint among groups. It was considered that dorsal acupoint group might be useful for operation with recumbent position, and lumbar and dorsal-lumbar acupoint groups might be proper for operation with standing position.

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Bluetongue is an arthropod-borne disease in domestic and wild ruminants caused by bluetongue virus (BTV), and it leads to great economic loss worldwide. Previous studies showed that BTV in ruminants in Taiwan was often subclinical infection. The aim of this study was to determine the current status (years 2016–2017) of BTV infection in ruminants in Taiwan, to compare it to the results of a large-scale study conducted in the year 2003, and to investigate whether new viral strains exist. Competitive ELISA tests of serum samples for anti-BTV-VP7 group-specific antibody revealed seropositive rates of 26.7% in cattle by head, similar to 32.7% in the year 2003, suggestive of a BTV-vector-host (cattle) dynamic balance. In goats, the seropositive rate was 18.6%, slightly increased from 8.2% in the year 2003, suggestive of a slow but active infection taking place. This notion was supported by the detection of VP1 gene nucleic acid from whole blood in six out of 29 seropositive goats by reverse transcription–polymerase chain reaction. However, no new virus strain was isolated from embryonating chicken embryos (ECEs) inoculation. Alignment of VP7 amino acid sequences revealed that Taiwan and Japan isolates possessed three specific amino acids on sites No. 82 (arginine), No. 328 (aspartate), and No. 336 (glutamine), which are different from many countries. In a three-dimensional model, these amino acids were located closely on the middle lateral surface of VP7 trimers. Since VP7 is a major outer protein engaged in entry into insect cells and a strong T cell response inducer, these differences likely indicate the result of positive selection of local vectors and hosts in Taiwan.

Rates of selected soil nitrogen transforming processes as well as kinetic parameters of denitrification enzymes were determined in a cattle overwintering area. Soils from three localities differently impacted by the cattle (severe, moderate, control with no impact) were examined. In cattle-influenced soils, total N, organic C and pH were significantly increased. Consequently rates of potential mineralization, nitrifying enzyme activity and denitrifying enzyme activity (DEA) were enhanced compared to control, while potential nitrogenase activity was lowered in both soils influenced by cattle. The soils differed substantially in DEA, which was about 60 ng N₂O-Ng dw^-1h^-1 in control soil but 3 times and 34 times higher in moderately and severely impacted soils, respectively. The soils also exhibited significantly different maximum reaction velocity (V) and Michaelis-Menten constant (K_m) of enzymes responsible for reduction either of nitrate to nitrous oxide or of nitrous oxide to di-nitrogen. Results suggest that the cattle-induced stress alters the functioning of soil microbial community.