본 연구는 숲의 종류별로 숲의 이미지와 만족도 및 신체적․정서적 측면의 치유지각 효과를 분석하기 위하여 실시한 것이다. 숲의 종류는 편백나무숲, 졸참나무숲, 소나무숲으로 분류하였으며 단일 임상으로 이루어진 대상지를 선정하여 평가를 진행하였다. 평가는 각 숲별로 60명의 피험자에 의해 이루어졌으며 평균연령 68.6세이다. 편백나무숲은 쾌적하고 편안하며 친밀한 이미지, 졸참나무숲은 평범하면서도 안정된 개방적인 이미지, 소나무숲은 아 름답고 쾌적하며 자연스러운 이미지로 평가되었으며 숲의 이미지구조는 정연성, 어메니티, 공간특이성, 정감성 인자로 구분된다. 숲의 만족도는 졸참나무숲이 높게 평가되었다. 편백나무숲은 정연성 인자가, 졸참나무숲은 정연성 및 공간특 이성인자가, 소나무숲은 어메니티 인자가 만족도에 영향을 미친다. 모든 숲에서 피험자들은 신체적 ․정서적 측면에서 개선이 되었다는 치유효과를 지각하고 있으며 특히 정서적 측면에서 치유지각의 효과가 높다. 신체적 치유지각은 숲 종류별로 차이가 없었으나 정서적 측면에서는 소나무숲이 가장 높았으며 다음은 졸참나무숲, 편백나무숲 순으로 숲 종 류 상이에 유의적인 차이가 있었다. 숲 만족도와 정서적 측면의 치유효과 사이에는 정적인 상관 관계가 있었다.

We present a novel method to implement time-delayed propagation of radiation fields in cosmo- logical radiative transfer simulations. Time-delayed propagation of radiation fields requires construction of retarded-time fields by tracking the location and lifetime of radiation sources along the corresponding light-cones. Cosmological radiative transfer simulations have, until now, ignored this “light-cone effect” or implemented ray-tracing methods that are computationally demanding. We show that radiative trans- fer calculation of the time-delayed fields can be easily achieved in numerical simulations when periodic boundary conditions are used, by calculating the time-discretized retarded-time Green’s function using the Fast Fourier Transform (FFT) method and convolving it with the source distribution. We also present a direct application of this method to the long-range radiation field of Lyman-Werner band photons, which is important in the high-redshift astrophysics with first stars.

The brachiocephalic muscle in domestic mammals is formed as a homology of the sternocleidomastoid muscle and the clavicular part of the deltoid muscle since it results from reduction of the clavicle as a clavicular intersection. The cranial insertions of the brachiocephalic muscle vary among species in domestic mammals. In the dog, the brachiocephalic muscle comprises three parts, which arise from the clavicular intersection and insert at the humerus, the dorsal cervical raphe, and the mastoid process of the temporal bone. These three parts are named the cleidobrachial muscle, the cervical part of the cleidocephalic muscle, and the mastoid part of the cleidocephalic muscle, respectively. This complexity could confuse veterinarians and complicate surgical procedures in this area. Information about the normal structure of this muscle, and any variation therein, would help to avoid such situations. During dissections of a male cross-breed dog, we found that the brachiocephalic muscle had two bellies located on the mastoid part of the cleidocephalic muscle that extended from the clavicular intersection to the wing of the atlas and the mastoid process of the temporal bone. They were innervated by the accessory nerve and the ventral branches of the second, third, and fifth cervical nerves, and they were supplied by the ascending branch of the superficial cervical artery. These bellies were considered to be a rare variation of the muscle. This is the second report of a brachiocephalic muscle variation in a dog, in which the mastoid part of the cleidocephalic muscle was made of two bellies inserted independently. Such variations should be considered during anatomical dissections and surgical procedures.

A rod-shaped, Gram-negative chlorpyrifos-methyl (CM) degrading bacterium (designated strain KR200) was isolated from a Korean rice paddy soil and was further tested for its substrate specificity against 11 insecticides and its sensitivity against eight commercial antibiotics. Based on morphological, biochemical, and molecular characteristics, this bacterium showed greatest similarity to members of the order Flavobacteriales and was shown to be most closely related to members of the Chryseobacterium proteolyticum group. Strain KR200 hydrolyzed CM to 3,5,6-trichloro-2-pyridinol (TCP) but could not degrade TCP further. The isolate was also able to degrade chlorpyrifos, dicrotophpos, monocrotophos, and carbaryl at 300 μg mL–1 but diazinon, dimethoate, and furathiocarb at 100μg mL–1. The ability to degrade CM was found to be encoded on the chromosome. Genes encoding resistance to amphotericin B, polymixin B sulfate, and tetracycline were also located on the chromosome. This bacterium merits further study as a potential biological agent for the remediation of soil, water, or crop contaminated with organophosphorus (OP) compounds because of its greater biodegradation activity and its broad specificity against a range of OP insecticides.

The toxicity of cade oil (Juniperus oxycedrus), its constituents and structurally related compounds toward adult house dust mite Dermatophagoides farina was examined. Results were compared with two commercially available acaricides, benzyl benzoate and deet. The cade oil constituents were identified by GC-MS analysis. Citral (LC50, 1.13 μg cm–2) and methyleugenol (LC50, 5.78 μg cm–2) were the most toxic compounds, followed by eugenol (LC50,12.52 μg cm–2), nerol (LC50, 21.4 μg cm–2) and terpinen-4-ol (LC50, 29.55 μg cm–2) were shown significant mortality against adult of D. farina. Toxicity of citral, methyleugenol were higher than that of benzyl benzoate, and above listed compounds was all more toxic than deet. Given the result of vapour-phase mortality tests that these compounds were more toxic in closed containers than in open ones, we concluded that vapour action plays a great role in their mode of delivery. Cade applied as 3 and 4% experimental sprays provided 96 and 100% mortality against the mites respectively, whereas permethrin (cis:trans, 25:75) 2.5 g/l spray treatment resulted in 17% mortality. Cade oil, and its constituents shown their potentials as effective alternatives for harmful synthetic acaricides for the control of Dermatophagoides populations as fumigants in contact and therefore illustrated the need for further study of this essential oil.

Alzheimer’s disease (AD) is the most common type of presenile and senile dementia. Human β-amyloid precursor cleavage enzyme (BACE-1) is a key enzyme responsible for amyloid plaque production. We assessed anti-BACE-1 and behavioral activities of curcuminoids from Curcuma longa, curcumin (CCN), demethoxycurcumin (DMCCN), and bisdemethoxycurcumin (BDMCCN) against AD fly models. Neuro-protective ability of curcuminoids was assessed using fly model system overexpressing BACE-1 and its substrate APP in compound eyes and entire neurons. BDMCCN has the strongest inhibitory activity toward BACE-1 with 17 μM IC50, which was 20 and 13 times lower than those of CCN and DMCCN respectively. Expression of APP/BACE-1 resulted in the progressive and measurable defects in morphology of eyes and locomotion. Supplementing diet with either 1 mM BDMCCN or CCN rescued APP/BACE1 expressing flies and kept them from developing both morphological and behavioral defects. Structural characteristics and hydrophobicity appear to play a role in determining inhibitory potency of curcuminoids on BACE-1.

An assessment is made of the anti-proliferative activity of cicada slough-derived materials against 10 human cancer cell lines, including PC-3 and DU145 prostate cancer cell lines, using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay. Results were compared with those of the commercially available anticancer agent with broad spectrum cisplatin. The ethanol extract of Cryptotympana spp. slough was proved to have anti-proliferative activity against A549 lung, AGS stomach, PC-3 and DU145 prostate, Hela cervix, HT-29 colon, MCF-7 breast, and SK-Hep-1 liver cancer cell lines except for Hep-2 larynx and SK-OV-3 ovary cancer cell lines. The biologically active constituent was characterized as the nonprotein α-amino acid theanine [2-amino-4-(ethylcarbamoyl)butyric acid] by spectroscopic analysis, including EI-MS and NMR. Theanine was isolated from the cicada slough as a new cytotoxic principle. Fifty percent inhibition concentration (IC50) values of the constituent against PC-3 was 6.52 μg/mL, respectively. The activity of theanine (IC50,6.52μg/mL) did not differ significantly from that of the anticancer agent cisplatin (IC50,7.39μg/mL) toward PC-3. In conclusion, further studies on the cicada slough-derived materials containing theanine as potential anticancer products or a lead molecule for the prevention or eradication from human prostate cancer.

Lung cancer caused by diverse changes in cells resulted by exposure to carcinogens found in tobacco smoke, the environment, or sequential accumulation of genetic changes to the normal epithelial cells of the lung. An assessment was made of the anti-proliferative activity of constituents from silkworm feces against 11 human cancer cell lines, including A549 and H727 lung cancer cell lines, using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay. The ethanol extract of silkworm feces was proved to have anti-proliferative activity against all 11 species of human cancer cell lines. The biologically active constituent was characterized as vomifoliol (blumenol A) (1) and stigmasterol (2) by spectroscopic analysis ,including MS and NMR. In conclusion, global efforts to reduce the level of antitcancer agents justify further studies on the silkworm feces-derived materials containing vomifoliol and stigmasterol as potential anticancer products or lead compounds for the prevention or eradication from human lung cancer.

The toxicity of bay leaf (Pimenta racemosa) and palmorasa (Cymbopogon martini) essential oils, and its constituents, and structurally related compounds to adult American house dust mites, Dermatophagoides farinae was examined. Both bay leaf (24 h LC50, 131.95 μg/cm2) and palmorosa (24 h LC50, 116.10 μg/cm2) essential oils were toxic to mites. The most active principles were determined to be citral, methyleugenol, eugenol, and geranyl acetate from both bay leaf and palmorosa oils. Citral (24 h LC50, 1.13 μg/cm2), methyl eugenol (5.78 μg/cm2), eugenol (24 h LC50, 12.52 μg/cm2) and geranyl acetate (24 h LC50, 18.79 μg/cm2) were the most toxic. The toxicity of these compounds was more toxic than that of commercially available acaricides such as, benzylbenzoate (LC50,8.41μg/cm2) and deet (37.67 μg/cm2). Potent toxicity was also observed with nerol, linalool and geraniol (LC50, 21.44–54.61 μg/cm2). These compounds were consistently more toxic in closed versus open containers, indicating that their mode of delivery was largely a result of vapour action. Both bay leaf and palmorosa oil, and their constituents shown their potentials as effective alternatives for harmful synthetic acaricides for the control of Dermatophagoides populations as fumigants in contact and therefore illustrated the need for further study of these essential oils.

An assessment was made of beta-site amyloid precursor protein (APP) cleaving enzyme (BACE1) inhibitory, feeding, climbing activities and lifespan of the diarylalkyls curcumin (CCN), demethoxycurcumin (DCCN) and bisdemethoxycurcumin (BDCCN) identified in the rhizomes of Curcuma longa. Based on IC50 values, BDCCN (0.024 mM) was the most inhibitory constituent, followed by DCCN (0.31 mM) and CCN (0.59 mM). Overall the three curcuminoids were significantly less inhibitory than BACE1 inhibitor IV isophthalamide (8.5 × 10-5 mM). The expression of human APP and BACE1 in compound eye of Drosophila melangaster presented rough abnormal ommatidial lattice. Co-expression of APP and BACE1 within the developing nervous system of drosophila showed climbing defects. These transgenic flies kept on media containing 1 mM of CCN and BDCCN were observed to ameliorate eye degeneration, significantly suppress locomotive dysfunctions, and increase media life time, as well as isophthalamide. CCN and BDCCN as human BACE1 inhibitory constituents may be used as potential therapeutics or lead molecules to develop Alzheimer's disease treatment drugs.

Inhibition of acetylcholinesterase (AChE) is one of the important modes of action available for the control of insects. An assessment was made of the electric eel AChE inhibitory activity of 55 endophytic fungi isolated from the leaves of Huperzia serrata collected in Eunshi, Hubei Province, China. Of 55 mycelial extracts and 55 ethyl acetate-soluble fractions from liquid culture of the fungi, the ethyl acetate-soluble fraction of strain ES056 exhibited strong AChE inhibitory activity (88%) at a concentration of 100 μg/mL. Based on morphological characteristics and nuclear ribosomal DNA ITS sequence analysis, this fungus showed greatest similarity to members of the order Eurotiales and was shown to be most closely related to members of the Aspergillus aculeatus group. It was designated Aspergillus sp. MY056. This strain merits further study as a potential anti-AChE product.

The oriental tobacco budworm, Helicoverpa assulta, is an oligophagous insect feeding on a few species of Solanaceae plants, including Nicotina tabacum. This study investigated the relationship between H. assulta and plants, focusing on oviposition preference and larval performance of the specialist in host and non-host plants. (1) In choice experiments, N. tabacum and Phaseolus vulgaris were put in a cage with 5 females and 10 males. Most of eggs (ca. 98%) were layed in N. tabacum, whereas few eggs in P. vulgaris. (2) In non-choice experiments, N. tabacum, Datura stramonium, or P. vulgaris was individually put in a cage with 3 females and 6 males, resulting that N. tabacum was the most preferred host, followed by D. stramonium and P. vulgaris. Oviposition was delayed about 2 days in P. vulgaris (a non-host plant) compared to the two host plants. (3) Larval performances were also compared with the three plants. Larval growth was better in N. tabacum followed by D. stramonium and P. vulgaris, High mortality (ca. 100%) of larvae was observed in P. vulgaris, suggesting toxic component(s) derived from the non-host plant might cause the death. The ovipositional avoidance in P. vulgaris is current being investigated to search for the oviposition deterrent, which could be useful for the environment-friendly pest management of H. assulta.

An assessment was made of the toxicity of hiba, Thujopsis dolabrata var. hondai, oil and 24 oil constituents and control efficacy of four experimental spray formulations containing the oil (0.5. 1, 2, and 3% sprays) to adult American house dust mite (AHDM), Dermatophagoides farinae, and copra mite (CM), Tyrophagus putrescentiae. Results were compared with those of three conventional acaricides benzyl benzoate, N,N-diethyl-3-methylbenzamide (deet), and permethrin. Based on 24 h LC50 values, (–)-thujopsene was the most toxic constituent against AHDM (9.82 μg/cm2) and CM (10.92 μg/cm2) and the toxicity of the compound was nearly identical to that of benzyl benzoate (9.33 and 10.14 μg/cm2). High toxicity was also observed with (–)-(E)-pinocarveol, carvacrol, (+)-terpinen-4-ol, β-thujaplicin, cedrol, α-terpineol, (+)-ledene, thymol, and 2,4-di-tert-butylphenol against both mite species (LC50, 11.92–19.19 and 12.49–22.97 μg/cm2). These constituents were more toxic than deet (LC50, 35.53 and 38.42 μg/cm2). Hiba applied as 2 and 3% sprays provided >95% mortality against both mite species, whereas permethrin (cis:trans, 25:75) 2.5 g/L spray treatment resulted in ca 11% mortality. Global efforts to reduce the level of highly toxic synthetic acaricides in indoor environments justify further studies on hiba oil preparations containing the constituents described as potential contact-action fumigants or lead molecules for the control of mite populations.

The yellow fever mosquito, Aedes aegypti, is a vector for transmitting dengue fever and yellow fever. An assessment was made of the histopathological and molecular effects of pellitorine, an isobutylamide alkaloid, on third instar Ae. aegypti larvae. At 5 mg/L concentration of pellitorine, whole body of the treated larvae became dark in color, particularly damaged thorax and abdominal regions. Pellitorine targeted mainly on midgut epithelium and anal gills, indicating variably dramatic degenerative responses of the midgut through a sequential epithelial disorganization. The anterior and posterior midgut was entirely necrosed, bearing only gut lumen residues inside the peritrophic membranes. Pellitorine caused comprehensive damage of anal gill cells and branches of tracheole and the debris was found in hemolymph of anal gills. RT-PCR analysis indicates that the compound inhibited gene expression encoding V-type H+-ATPase and aquaporine 4 after treatment with 2.21 mg/L pellitorine. The results provide a fact that pellitorine merits further study as a potential larvicide with a specific target site or a lead molecule for the control of mosquito populations.

Coevolution is a large part of evolution and the patterns of adaptation and speciation may be modified by coevolution processes. The arms races between insects and plants in natural system are one of coevolutionary processes and the mechanistic and predictive processes of the system may be helpful to understand the interaction between host plants and herbivores in agricultural systems. Furthermore, human activities may give direct and/or indirect effects on ecological and evolutionary processes in natural and agricultural ecosystems and have selection power as well as natural selection. Recent studies showed that the fundamental principles of evolution – variation (genetic difference, phenotypic plasticity, epigenetic change, and nongenetic inheritance), selection (directional or fluctuating), connectivity and eco-evolutionary dynamics – are important to understand the interplay between insects and plants. The coevolutionary processes between plants and herbivores were also interpreted by the geographic mosaic theory. The evolutionary effects on ecological dynamics in natural ecosystems were classified four categories: trophic specialization, evolution of defense, interaction outcome and loss of traits in absent of interaction. It was reviewed that it is necessary to consider the ecological response in evolutionary studies as well as evolutionary variation in ecological researches.

An assessment was made of the biological control potential of mud loaches, Misgurnus mizolepis, toward Culex pipiens molestus, in laboratory condition and septic tank and rainwater storage tank (RST) systems. Results were compared with those of temephos 20% emulsifiable concentrate (EC) and Bacillus thuringiensis israelensis (BTI). In the laboratory tests, all M. mizolepis survived on waters from the settling tank of aerobic septic tank (AST), sump tank of AST, and RST. However, all M. mizolepis died within 3 h after introduction in the settling tank and sump tank waters of anaerobic septic tank (AnAST). Gill or dorsal fin inflammation was detected in the dead mud loaches. M. mizolepis consumed an average of 968–1087, 901–986, and 993–1087 of 1500 third instars of Cx. p. molestus in AST settling tank, AST sump tank, and RST waters, respectively. In the AST and RST systems, predation of Cx. p. molestus by mud loaches at a release rate of 900 larvae/fish resulted in complete mosquito control from the first wk after treatment through the end of the survey period for 16 wk. The average mosquito reduction rates by temephos 20% EC and BTI treatments were 28.6 and 2.1% 2 wk post-treatment, respectively. Mud loaches merit further study as a potential biological control agent for the control of mosquito populations in light of global efforts to reduce the level of highly toxic synthetic insecticides in the aquatic environment.

The toxicity of materials derived from the seed of Pongamia pinnata to third instars of insecticide-susceptible Culex pipiens pallens and Aedes aegypti and wild Aedes albopictus was examined using a direct contact bioassay. Results were compared with those of the currently used insecticides fenthion and temephos. The active principles of Pongamia pinnata were identified as the karanjin (1), karanjachromene (2), pongamol (3), pongarotene (4), oleic acid (5), and palmitic acid (6) by spectroscopic analysis. Based on 24 h LC50 values, karanjin (14.61 and 16.13 mg/L) was the most toxic compound, followed by oleic acid (18.07 and 18.45 mg/L) and karanjachromene (18.74 and 20.57 mg/L). These constituents were less toxic than either fenthion (LC50, 0.0031 and 0.0048 mg/L) or temephos (0.021 and 0.050 mg/L) against Ae. aegypti and Cx. p. pallens. Low toxicity was produced by pongamol (LC50, 23.95 and 25.76 mg/L), pongarotene (25.52 and 37.61 mg/L), and palmitic acid (34.50 and 42.96 mg/L). Against A. alpopictus instars, oleic acid (LC50, 18.79 mg/L) was most toxic. Low toxicity was observed with the other five constituents (LC50, 35.26- 85.61 mg/L). P. pinnata seed-derived active principles, particularly karanjin, karanjachromene, and oleic acid, merits further study as potential mosquito larvicides for the control of mosquito populations in light of global efforts to reduce the level of highly toxic synthetic larvicides in the aquatic environment.

The toxicity of red pine needle hydrodistillate (RPN-HD), 19 RPN-HD constituents and 12 structurally related compounds and control efficacy of four experimental spray formulations containing RPN-HD (0.5. 1, 2 and 3% sprays) to adult Dermatophagoides farinae was evaluated. RPN-HD (24 h LC50,68.33 μg cm–2) was toxic. Menthol was the most toxic compound (12.69 μg cm–2) and the toxicity of this compound and benzyl benzoate did not differ significantly from each other. High toxicity was also produced by α-terpineol, bornyl acetate, geranyl acetate, thymol, linalyl acetate, terpinyl acetate, citral, linalool and camphor (18.79–36.51 μg cm–2). These compounds were more toxic than either deet or dibutyl phthalate. In vapour-phase mortality tests, these compounds were consistently more toxic in closed versus open containers, indicating that their mode of delivery was largely a result of vapour action. RPN-HD 3% experimental spray provided 95% mortality against adult D. farinae, whereas permethrin (cis:trans,25:75)2.5gL–1 spray treatment resulted in 0% mortality. In the light of global efforts to reduce the level of highly toxic synthetic acaricides in indoor environments, RPN-HD and the compounds described merit further study as potential biocides for the control of Dermatophagoides populations as fumigants with contact action.