Virtual forest: design and evaluation of a walk-through system for forest education

Forest education is generally conducted in a real forest to provide learners a direct experience with reality. However, often it is not easy to participate in forest education programs carried out in remote places due to distance, limited time, or economic or physical restrictions. Therefore, we developed a walk-through system for forest education in a virtual forest and evaluated its educational efficacy as well as usability through indoor experiments. The virtual forest was constructed with omnidirectional images taken in a forest using a digital camera with an omnidirectional vision sensor. The results of the postquestionnaire showed that the developed system was highly evaluated by the participants in the experiments in terms of educational efficacy and enjoyment. Also, comparison of results of prequestionnaire and postquestionnaire showed that it had educational value. On the other hand, some technical problems in the developed system were revealed. For example, 45.0% of the participants answered that the walk-through in the virtual forest did not proceed with sufficient smoothness, and encountered unexpected slowdowns and stops. In addition, image quality was not high enough to identify small objects in the virtual forest. Regardless of these problems, we believe that the computer-based forest education was successful because 88.3% of the participants answered that they would like to join a similar program again and 90.0% answered that they would like to visit the real forest that the virtual forest imitated.     

Diagnostic imaging of intra-abdominal cyst in heifer using the computed tomography

A 10-month-old Japanese black heifer was diagnosed as having an intra-abdominal cyst using computed tomography (CT). Through a posterior ventral midline incision, the cyst was removed, and the heifer completely recovered after the surgery. CT scans enabled detection of the intra-abdominal cyst and measurements of the diameter of the cyst before the surgery.     

Deficient proliferation and apoptosis in the granulosa and theca interna cells of the bovine cystic follicle

The aim of the present study was to examine the frequencies of cell proliferation and death of granulosa and theca interna layers during development of cystic follicles in order to understand the mechanisms of cystic follicle formation. Paraffin sections of cystic follicles were immunostained with antibodies against proliferating cell nuclear antigen (PCNA) and cleaved caspase-3 in order to observe proliferating and apoptotic cells, respectively. The concentrations of estradiol-17beta and progesterone in the follicular fluid of these follicles were measured by ELISA. The granulosa and theca interna layers contained both PCNA- and caspase-3-positive cells, although their numbers were limited. There was significant negative correlation between the estradiol-17beta and progesterone concentrations in the follicular fluid. Regression analysis revealed no significant correlation, except for that between the PCNA-positive cells in the theca interna and the caspase-3-positive cells in the granulosa layer. These results indicate that the granulosa and theca interna cells of the cystic follicle show weak proliferative activity and low apoptotic frequency; this implies that the cystic follicle grows slowly and then maintains a static condition without degeneration, which leads to long-term persistence of the follicle.     

UV-B irradiation retards chlorophyll degradation in lime (Citrus latifolia Tan.) fruit

Peel yellowing is a major postharvest problem of lime fruit. Research was conducted to control peel yellowing by UV-B irradiation. Mature green lime fruit were irradiated with UV-B doses at 0 (control), 8.8, and 13.2 kJ m^?2 and then stored at 25 °C in darkness. UV-B treatment at 8.8 kJ m^?2 efficiently delayed the decrease of chlorophyll content. A high level of chlorophyllide a accumulated in mature green fruit and then gradually decreased with the progress of peel yellowing. The chlorophyllide a level was higher in 8.8 kJ m^?2 UV-B-treated fruit than it was in the controls. The pheophorbide a level declined in lime fruit treated with 8.8 kJ m^?2 UV-B, especially during the development of yellowing. In addition, the pheophytin a level increased by 8.8 kJ m^?2 UV-B treatment at the late period of storage. We concluded that UV-B treatment effectively suppressed chlorophyll degradation in mature green lime during storage, which suggests that UV-B irradiation is a usable method for prolonging the postharvest life of lime fruit.     

Cultivation of corneal epithelial cell sheets on canine amniotic membrane

Objective To develop and assess canine corneal epithelial cell sheets cultivated from limbal stem cells on amniotic membrane. Procedures Canine corneal limbal segments were obtained from six beagle dogs. Cryopreserved denuded amniotic membranes (obtained from Miniature Dachshund and Cavalier King Charles Spaniel breeds) from which the epithelial cells were removed were used as scaffolds. The limbal segments were cultured on these amniotic membranes with 3T3 feeder cells for 2 weeks. The harvested corneal epithelial cell sheets were stained with H&E for histologic analysis. The harvested sheets were analyzed immunohistochemically using a corneal epithelium‐specific marker keratin 3(K3) and putative stem cell markers ABCG2, p63, and vimentin. Results Cultivated cells from the corneal limbal tissues reached confluency in 7–8 days. The cultivated cells adhered to the denuded amniotic membrane and formed a sheet. The cultivated cell sheet was transparent and consisted of five to eight layers. K3 was observed in all layers and ABCG2, p63, and vimentin were notably present in the basal layer of the cultivated canine epithelium by immunofluorescence. Conclusions Canine corneal epithelial cells were successfully cultivated on the canine amniotic membrane. The cultivated epithelial sheets contained putative stem cells in the basal layer and had a stratified epithelium.     

Lodging resistance locus prl5 improves physical strength of the lower plant part under different conditions of fertilization in rice (Oryza sativa L.)

High fertilizer application rates increase grain yield and biomass in rice, but reduces lodging resistance. Lodging resistance locus prl5 enhances pushing resistance through delaying leaf senescence and increasing carbohydrate reaccumulation in stems. This study demonstrates the effects of prl5 under different levels of Nitrogen·Phosphorus·Potassium basal fertilizer application using a chromosome segment substitution line based on the genetic background of Koshihikari, which contains prl5. High fertilizer application rates enhanced pushing resistance of the lower part, but did not consistently affect the pushing resistance of the whole plant. Independent of fertilizer application rates, prl5 enhanced pushing resistances of both the lower part and the whole plants. Plant height, biomass and grain yield were increased by high fertilizer application rates, but stem diameter and the dry weight of basal culms did not show consistent increases as determined over a period of 2 years. In leaves just after heading, chlorophyll (Chl) contents, rather than Rubisco contents, were correlated with fertilizer application rates. At the fully ripe stage, fertilizer application did not affect Chl and Rubisco contents in leaves, while prl5 increased the contents in the second leaf. High fertilizer application rates did not affect the concentration of non-structural carbohydrates (NSCs) in basal culms, but prl5 increased them at the fully ripe stage. These results suggest that fertilizer application reduces lodging resistance by highly elevating the center of gravity, but that prl5 can counteract this effect by enhancing the physical strength of the lower part through delaying leaf senescence and increasing NSC reaccumulation in culms without any effects of different fertilizer application rates.     

红星苹果花柱S-核酸酶的分离与纯化

采用多种蛋白分离纯化技术，结合生物鉴定方法，成功地从红星苹果（Malus domestica Borkh．）花柱中纯化出了一类与自交不亲和性识别反应相关的花柱蛋白。通过聚丙烯酰胺凝胶和等电聚焦电泳分析，确定该蛋白分子量为26和28kD，等电点为10．2和10．4，为碱性蛋白；核糖核酸酶活性染色和N-末端序列分析结果显示具有核酸酶活性，且与其它蔷薇科植物花柱S-核酸酶N-末端氨基酸序列同源性较高。