Effects of Susceptibility of Test Plants on Modes of Cucumovirus Transmission by Myzus persicae

In sequential transmission tests of Peanut stunt virus S (PSV-S) and Cucumber mosaic virus V (CMV-V) using Myzus persicae, these viruses behave as a semipersistent virus in Phaseolus vulgaris, but as a nonpersistent virus in Nicotiana tabacum, regardless of the species of plant used as the virus source. In addition, viruliferous aphids retained virus infectivity and transmitted it to P. vulgaris, even after they lost infectivity to N. tabacum. Apparently, the mode of transmission by the aphids differs depending on the plant species used for the assay. After mechanical inoculation with purified PSV-S or CMV-V, P. vulgaris appeared more susceptible to PSV-S than N. tabacum. However, the susceptibility to CMV-V appeared similar in both assay plants. Received 22 May 2000/ Accepted in revised form 14 September 2000     

Comparison of time budget of behaviors between penned and ranged young cattle focused on general and oral behaviors

To consider cattle welfare, time budget of behaviors of young cattle in pen and pasture conditions were compared. Behavioral observations of 103 steers in seven pens and 1136 steers in six ranges were performed during daylight over 3 days in each rearing condition. The pen condition had Japanese Black × Holstein cross, and the pasture conditions had assorted breeds of Angus, Murray Grey, Shorthorn, Hereford, Santa Gertrudis and their crosses aged 5–15 months. The ranges varied in vegetation from extensive native pasture to intensive improved pasture. The daytime proportion of behaviors and activity patterns were compared between rearing conditions. The proportion of walking was much lower in the pen condition (1.0 ± 0.2%) compared to all pasture conditions (at least 9.4 ± 4.0%; all P < 0.05), but grooming (5.9 ± 1.2%), investigating (2.5 ± 0.2%) and tongue playing (1.1 ± 0.2%) covered the loss. Fluctuation patterns of the proportions of eating (P < 0.001) and resting (P < 0.001) were different between pen and pasture conditions, whereas the pattern of the proportion of walking was not different. The proportion of eating in the pen condition (32.4 ± 0.3%) was not different to that in one on the farm (42.2 ± 12.6%), which had a thick improved pasture. However, the proportion of eating in the pen condition (32.4 ± 0.3%) was lower than that in two farms (58.8 ± 5.0% and 61.6 ± 16.5%) with low pasture availability (both P < 0.05). The proportions of oral behaviors such as self‐grooming (3.9 ± 1.0%), allogrooming (2.0 ± 0.2%), licking objects (1.3 ± 0.4%) and tongue‐playing (1.1 ± 0.2%) compensated for the lack of eating. These results indicate that we can learn a well‐balanced proportion of behaviors for cattle by making comparisons of time budget of behaviors and activity pattern between various rearing conditions. In addition, it is indicated that cattle under pen conditions under a restricted feeding period might compensate for a lower time spent feeding by performing other oral behaviors.     

Use of a box to prevent agonistic behavior after regrouping in isolated and non-isolated pigs

The effects of a box in the pen on the agonistic behavior of pigs after regrouping was determined in 24 pigs from five litters that were kept in three pens after weaning. For the experiment, the pigs were allocated to six pens with four animals each and kept with their peers for 2 weeks. The lightest pig from each pen was removed and isolated for 2 weeks, and then regrouped with its original peers. At the time of regrouping, half of the pens were equipped with the box. The number and duration of agonistic behavior events were particularly large and long in the pen without a box on the first day after regrouping, and for the isolated pig on the first day (all P  < 0.05). The number of times the box was accessed was large for the isolated pig on the first day after regrouping ( P  < 0.01). The number of agonistic behavior events and the times the box was accessed was correlated on the first day after regrouping ( r _s = 0.79, P  < 0.01). The number of agonistic behavior events on the first day after regrouping was greater in the pens without a box than in the pens with a box ( P  < 0.01). It was suggested that the box had the effect of reducing agonistic behavior after regrouping.     

Assessing the end-point temperature of heated fish and shellfish meats

ABSTRACT: Attempts have been made to assess the end-point temperature (EPT) of heated fish and shellfish meats by using the coagulation method together with sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE) analysis and enzyme activity determination. Unfrozen and frozen fish and shellfish meats were heat-treated at different selected temperatures with 0, 15 or 30 min holding times. Proteins were extracted with NaCl solution. The coagulation method was able to determine EPT of heated fish and shellfish meats between 60 and 67°C. SDS-PAGE patterns of the filtrates from heated meats were closely related to the results of the coagulation method and enzyme activity determination. Two proteins responsible for producing coagulum of fish meat extracts seem to be lactate dehydrogenase (LDH) and glyceraldehyde phosphate dehydrogenase (GAPDH). End-point temperatures determined by these methods were not significantly different between unfrozen and frozen samples. On the contrary, a highly thermostable protein with a molecular mass of 35 kDa was detected in heated shellfish meats up to 108°C. In scallop adductor muscle, this highly thermostable protein was found to be the tropomyosin subunit from its amino acid composition and their partial sequences. Tropomyosin could be used as an EPT indicator up to 108°C for heated shellfish meats.     

Reliability of stock size estimates from adaptive framework virtual population analysis

ABSTRACT:   The stock size estimates from adaptive framework virtual population analysis are sometimes very sensitive to the model's assumptions. The uniqueness and precision of stock size estimates from adaptive framework virtual population analysis are examined analytically and numerically. The results indicate that (i) when the fishing mortalities remain constant for all years, the stock size estimates are not determined uniquely without additional assumptions, and (ii) when the cumulative fishing mortalities are similar among cohorts, the precision of stock size estimates will be poor, even if the abundance indices are precise and informative. For the precise estimation of stock size, it is necessary that fishing mortalities vary among years, that cumulative fishing mortalities vary among cohorts and that auxiliary information such as selectivity is available in addition to precise abundance indices.     

Cloning of estrogen receptor-β cDNA of common Japanese conger Conger myriaster and expression of the gene during oocyte development

ABSTRACT:   Estrogen receptor (ER) cDNA was cloned from the liver of common Japanese conger Conger myriaster . Common Japanese conger ER cDNA contains 2543 nucleotides including an open reading frame that encodes 596 amino acids, with a molecular weight of 66.1 kDa. The deduced amino-acid sequence of the common Japanese conger ER shares 85% identity with that of eel Anguilla japonica ER-β, and 39–46% and 53–59% identity with the deduced sequences of ER-α and ER-β of other species, respectively. In a phylogenetic analysis, the common Japanese conger ER was found to cluster with the ER-β of other species. The common Japanese conger ER-β also has six domains (A–F), which are conserved in the nuclear receptor superfamily. The amino-acid sequences in the C and E domains were highly conserved between common Japanese conger ER-β and other ER. However, the other domains showed low homology. In the female common Japanese conger, ER-β mRNA was highly expressed in the liver and pituitary gland. The expression levels of the ER-β gene increased from the oil droplet stage to the primary yolk globule stage and were maintained until the migratory nucleus stage.     

Immunohistochemical detection of cellular prion protein (PrPc) in the rat central nervous system

A simple conventional method of immunohistochemistry (i.e. fixing the frozen sections in cold methanol) was used to determine the immunolocalization of cellular prion protein (PrPc), with good results. In the rat cerebrum, the cytoplasm of neural cells in the cortex and corpus stratum, pia mater, membrane limitans gliae superficialis, choroid plexus and blood vessel wall were immunostained. The formation of network structures of immunostained neural and/or glial fibers in the cerebral cortex was also observed. These immunostained network structures of neural and/or glial fibers were also observed in cultured neural cells. The results suggest that fixation of frozen sections and cultured cells with cold methanol is a useful method for detecting the immunolocalization of PrPc and that PrPc exists in the various components of the central nervous system of the rat.     

Central estrogen action sites involved in prepubertal restraint of pulsatile luteinizing hormone release in female rats

The present study aimed to determine estrogen feedback action sites to mediate prepubertal restraint of gonadotropin-releasing hormone (GnRH)/luteinizing hormone (LH) release in female rats. Wistar-Imamichi strain rats were ovariectomized (OVX) and received a local estradiol-17β (estradiol) or cholesterol microimplant in several brain areas, such as the medial preoptic area (mPOA), paraventricular nucleus, ventromedial nucleus and arcuate nucleus (ARC), at 20 or 35 days of age. Six days after receiving the estradiol microimplant, animals were bled to detect LH pulses at 26 or 41 days of age, representing the pre- or postpubertal period, respectively. Estradiol microimplants in the mPOA or ARC, but not in other brain regions, suppressed LH pulses in prepubertal OVX rats. Apparent LH pulses were found in the postpubertal period in all animals bearing estradiol or cholesterol implants. It is unlikely that pubertal changes in responsiveness to estrogen are due to a change in estrogen receptor (ER) expression, because the number of ERα-immunoreactive cells and mRNA levels of Esr1, Esr2 and Gpr30 in the mPOA and ARC were comparable between the pre- and postpubertal periods. In addition, kisspeptin or GnRH injection overrode estradiol-dependent prepubertal LH suppression, suggesting that estrogen inhibits the kisspeptin-GnRH cascade during the prepubertal period. Thus, estrogen-responsive neurons located in the mPOA and ARC may play key roles in estrogen-dependent prepubertal restraint of GnRH/LH secretion in female rats.     

Long-term stock assessment and growth changes of the Japanese sardine (Sardinops melanostictus) in the Sea of Japan and East China Sea from 1953 to 2006

We estimated the stock size of Japanese sardine ( Sardinops melanostictus ) in the Sea of Japan and East China Sea since 1953 using cohort analysis based on the changes of growth patterns. Growth of Japanese sardine, estimated by using annual rings on archived scales since 1961, showed that body lengths were extremely stunted in the 1980–1987 year-classes. The body length at age 3 from February to April in the 1980–1987 year-classes, a period when the stock size exceeded 4 million tons, was 180.0 ± 2.6 mm (mean ± SD), and in the other year-classes was 195.1 ± 7.6 mm. The body length at age 3 and wet weight of zooplankton in August in the offshore area of the Sea of Japan had a significantly positive correlation. We assumed three scenarios for maturation ratios, and estimated Ricker's spawner–recruitment relationships. We analyzed the correlations between logarithmic recruitment residuals (LNRR) and environmental factors in winter, represented by the North Pacific index (NPI), Aleutian low pressure index (ALPI), Pacific decadal oscillation (PDO), monsoon index (MOI), Arctic oscillation (AO) and Southern oscillation index (SOI). Significant correlations were observed between MOI and LNRR and between AO and LNRR. A combination of strong MOI and weak AO would increase the biomass of phytoplankton and zooplankton and subsequently increase the recruitment of Japanese sardine.