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Selected AbstractsWhite background stimulates the food intake of a pleuronectiform fish the barfin flounder, Verasper moseri (Jordan and Gilbert)AQUACULTURE RESEARCH, Issue 6 2009Toshikazu Sunuma First page of article [source] Text binarization in color documentsINTERNATIONAL JOURNAL OF IMAGING SYSTEMS AND TECHNOLOGY, Issue 6 2006Efthimios Badekas Abstract This article presents a new method for the binarization of color document images. Initially, the colors of the document image are reduced to a small number using a new color reduction technique. Specifically, this technique estimates the dominant colors and then assigns the original image colors to them in order that the background and text components to become uniform. Each dominant color defines a color plane in which the connected components (CCs) are extracted. Next, in each color plane a CC filtering procedure is applied which is followed by a grouping procedure. At the end of this stage, blocks of CCs are constructed which are next redefined by obtaining the direction of connection (DOC) property for each CC. Using the DOC property, the blocks of CCs are classified as text or nontext. The identified text blocks are binarized properly using suitable binarization techniques, considering the rest of the pixels as background. The final result is a binary image which contains always black characters in white background independently of the original colors of each text block. The proposed document binarization approach can also be used for binarization of noisy color (or gray-scale) document images. Several experiments that confirm the effectiveness of the proposed technique are presented. © 2007 Wiley Periodicals, Inc. Int J Imaging Syst Technol, 16, 262,274, 2006 [source] Bone Loss, Weight Loss, and Weight Fluctuation Predict Mortality Risk in Elderly Men and WomenJOURNAL OF BONE AND MINERAL RESEARCH, Issue 8 2007Nguyen D Nguyen Abstract Low baseline BMD, rate of BMD loss, weight loss, and weight fluctuation are significant predictors of all-cause mortality in elderly men and women, independent of each other and of age, incident fracture, and concomitant diseases. Introduction: Although low BMD has been shown to be associated with mortality in women, the effect of BMD is affected by weight and weight change and the contribution of these factors to mortality risk, particularly in men, is not known. This study examined the association between baseline BMD, rate of bone loss, weight loss, and weight fluctuation and all-cause mortality risk in elderly men and women. Materials and Methods: Data from 1059 women and 644 men, ,60 years of age (as of 1989), of white background who participated in the Dubbo Osteoporosis Epidemiology Study were analyzed. All-cause mortality was recorded annually between 1989 and 2004. BMD at the femoral neck was measured by DXA (GE-LUNAR) at baseline and at approximately every 2 yr afterward. Data on incident osteoporotic fractures and concomitant diseases, including cardiovascular diseases, all types of cancer, and type I/II diabetes mellitus, was also recorded. Results: In the multivariable Cox's proportional hazards model with adjustment for age, incident fractures, and concomitant diseases, the following variables were independent risk factors of all-cause mortality in men: rate of BMD loss of at least 1%/yr, rate of weight loss of at least 1%/yr, and weight fluctuation (defined by the CV) of at least 3%. In women, in addition to the significant factors observed in men, lower baseline BMD was also an independent risk factor of mortality. In both sexes, baseline weight was not an independent and significant predictor of mortality risk. Approximately 36% and 22% of deaths in women and men, respectively, were attributable to the four risk factors. Conclusions: These data suggest that, although low BMD was a risk factor of mortality in women, it was not a risk factor of mortality in men. However, high rates of BMD loss, weight loss, and weight fluctuation were also independent predictors of all-cause mortality in elderly men and women, independent of age, incident fracture, and concomitant diseases. [source] Residual Lifetime Risk of Fractures in Women and Men,,JOURNAL OF BONE AND MINERAL RESEARCH, Issue 6 2007Nguyen D Nguyen Abstract In a sample of 1358 women and 858 men, ,60 yr of age who have been followed-up for up to 15 yr, it was estimated that the mortality-adjusted residual lifetime risk of fracture was 44% for women and 25% for men. Among those with BMD T-scores , ,2.5, the risks increased to 65% in women and 42% in men. Introduction: Risk assessment of osteoporotic fracture is shifting from relative risk to an absolute risk approach. Whereas BMD is a primary predictor of fracture risk, there has been no estimate of mortality-adjusted lifetime risk of fracture by BMD level. The aim of the study was to estimate the residual lifetime risk of fracture (RLRF) in elderly men and women. Materials and Methods: Data from 1358 women and 858 men ,60 yr of age as of 1989 of white background from the Dubbo Osteoporosis Epidemiology Study were analyzed. The participants have been followed for up to 15 yr. During the follow-up period, incidence of low-trauma, nonpathological fractures, confirmed by X-ray and personal interview, were recorded. Incidence of mortality was also recorded. BMD at the femoral neck was measured by DXA (GE-LUNAR) at baseline. Residual lifetime risk of fracture from the age of 60 was estimated by the survival analysis taking into account the competing risk of death. Results: After adjusting for competing risk of death, the RLRF for women and men from age 60 was 44% (95% CI, 40,48) and 25% (95% CI, 19,31), respectively. For individuals with osteoporosis (BMD T-scores , ,2.5), the mortality-adjusted lifetime risk of any fracture was 65% (95% CI, 58,73) for women and 42% (95% CI, 24,71) for men. For the entire cohort, the lifetime risk of hip fracture was 8.5% (95% CI, 6,11%) for women and 4% (95% CI, 1.3,5.4%) for men; risk of symptomatic vertebral fracture was 18% (95% CI, 15,21%) for women and 11% (95% CI, 7,14%) for men. Conclusions: These estimates provide a means to communicate the absolute risk of fracture to an individual patient and can help promote the identification and targeting of high-risk individuals for intervention. [source] Demonstration of Postsynaptic Receptor Plasticity in an Amphibian Neuroendocrine InterfaceJOURNAL OF NEUROENDOCRINOLOGY, Issue 11 2002B. G. Jenks Abstract Pituitary pars intermedia melanotrope cells are often used as a model to study mechanisms of neuroendocrine integration. In the amphibian Xenopus laevis, the synthesis and release of ,-melanophore-stimulating hormone (,-MSH) from these cells is a dynamic process dependent upon the colour of background. In animals on a black background, there is a higher level of synthesis and secretion of ,-MSH than in animals on a white background, and, consequently, there is skin darkening in animals on a black background. The melanotropes are innervated by hypothalamic neurones that produce neuropeptide Y (NPY), a peptide that inhibits ,-MSH secretion via the NPY Y1 receptor. The inhibitory neurones have a higher expression of NPY in animals adapted to a white background and both the size and the number of inhibitory synapses on the melanotrope cells are enhanced. The purpose of the present study was to determine if this presynaptic plasticity displayed by the inhibitory neurones is reciprocated by postsynaptic plasticity (i.e. if there is an enhanced expression of the Y1 receptor in melanotropes of animals adapted to a white background). For this purpose quantitative real-time reverse transcriptase-polymerase chain reaction was used to determine the level of Y1 receptor mRNA in melanotropes of animals undergoing the process of background adaptation. The results showed that there is a higher Y1 receptor mRNA expression in melanotropes of white-adapted animals. We conclude that the inhibitory neuroendocrine interface in the Xenopus pars intermedia displays postsynaptic plasticity in response to changes of background colour. To our knowledge, this is the first demonstration of a physiological environmental change leading to changes in postsynaptic receptor expression in a fully identified vertebrate neuroendocrine reflex. [source] Impact of Background on Color Performance of False Clownfish, Amphiprion ocellaris, CuvierJOURNAL OF THE WORLD AQUACULTURE SOCIETY, Issue 6 2009Inayah Yasir Color performance of false clownfish, Amphiprion ocellaris, Cuvier was first examined at four color backgrounds (blue, green red, and white) for 4 wk, then all fish were transferred to a white background for another 4 wk to test whether the impact of background colors on fish skin could have a lasting effect when the environment colors are changed. The experiment was conducted in 10-L rectangular plastic buckets with three replicates. Thirty fish were stocked in each bucket and three fish were randomly sampled from each tank in Weeks 1, 4, and 8. The color hue, saturation, and brightness were quantified using image analysis. In addition to the whole body analysis, each fish image was divided into ventral and dorsal parts to examine the body position-dependent response. Furthermore, color differences among the dorsal fin, anal fin, ventral fin, and caudal fin were also quantified. Blue or green background enhanced red orange color on fish skin, whereas white background made fish color brighter. Irrespective of background color, the dorsal side of fish exhibited more red orange, but the color was less bright and less saturated than that of ventral side. Upper fins (dorsal and caudal fins) were more red orange in a blue background than in a white background. Transferring fish from colored backgrounds to a white background made the fish skin and fins brighter, the color of ventral body and ventral fins less saturated, and the bottom fins more yellow orange. The results indicate that blue or green background could strengthen the orange color, whereas white background made fish color less saturated but brighter. The impact of background on the performance of fish color is temporary and likely to disappear when environmental color changes. [source] Limits of spherical blur determined with an adaptive optics mirrorOPHTHALMIC AND PHYSIOLOGICAL OPTICS, Issue 3 2009David A. Atchison Abstract We extended an earlier study (Vision Research, 45, 1967,1974, 2005) in which we investigated limits at which induced blur of letter targets becomes noticeable, troublesome and objectionable. Here we used a deformable adaptive optics mirror to vary spherical defocus for conditions of a white background with correction of astigmatism; a white background with reduction of all aberrations other than defocus; and a monochromatic background with reduction of all aberrations other than defocus. We used seven cyclopleged subjects, lines of three high-contrast letters as targets, 3,6 mm artificial pupils, and 0.1,0.6 logMAR letter sizes. Subjects used a method of adjustment to control the defocus component of the mirror to set the ,just noticeable', ,just troublesome' and ,just objectionable' defocus levels. For the white-no adaptive optics condition combined with 0.1 logMAR letter size, mean ,noticeable' blur limits were ±0.30, ±0.24 and ±0.23 D at 3, 4 and 6 mm pupils, respectively. White-adaptive optics and monochromatic-adaptive optics conditions reduced blur limits by 8% and 20%, respectively. Increasing pupil size from 3,6 mm decreased blur limits by 29%, and increasing letter size increased blur limits by 79%. Ratios of troublesome to noticeable, and of objectionable to noticeable, blur limits were 1.9 and 2.7 times, respectively. The study shows that the deformable mirror can be used to vary defocus in vision experiments. Overall, the results of noticeable, troublesome and objectionable blur agreed well with those of the previous study. Attempting to reduce higher-order aberrations or chromatic aberrations, reduced blur limits to only a small extent. [source] Endothelin receptor B2 (EDNRB2) is associated with the panda plumage colour mutation in Japanese quailANIMAL GENETICS, Issue 2 2007M. Miwa Summary The panda mutant in Japanese quail (Coturnix japonica) displays spots of wild-type plumage on a white background and is controlled by an autosomal recessive allele (s). The dotted white is controlled by a third allele (sdw) of the s locus with sdw/sdw quail having less pigmentation than s/s quail. We mapped the s locus to the Japanese quail chromosome 4 (CJA04) in a previous study. The orthologous region of the chicken (Gallus gallus) genome includes endothelin receptor B2 (EDNRB2), an avian-specific paralog of endothelin receptor B (EDNRB). EDNRB mutations in mammals retard the migration of neural crest cells (NCCs), which results in a spotted coat colour and an enteric nervous defect. In the present study, we investigated the association between the s locus and EDNRB2 in Japanese quail. Sequence comparison among transcripts from livers of wild-type, panda and dotted white quail revealed a nucleotide substitution (c.995G>A) leading to a p.R332H amino acid change that was specific to panda, whereas no amino acid substitution was found in dotted white birds. The amino acid position 332 is located in the sixth transmembrane domain and is highly conserved in both avian and mammalian endothelin receptors. The A allele at nucleotide position 995 was specific to panda (s/s) birds among 10 strains, and was mapped to the same chromosomal region as the s locus. Quantitative RT-PCR revealed that EDNRB2 transcripts were reduced in both panda and dotted white mutants compared with wild-type. However, there was no difference between the early embryos of wild-type and panda with respect to the migration of NCCs. The genetic association of EDNRB2 with plumage colour in birds was found for the first time in this study. [source] Effects of cage netting colour and density on the skin pigmentation and stress response of Australian snapper Pagrus auratus (Bloch & Schneider, 1801)AQUACULTURE RESEARCH, Issue 13 2008Ben J Doolan Abstract The unnaturally dark pigmentation of cultured Australian snapper Pagrus auratus can be improved through dietary astaxanthin supplementation and by holding fish in tanks with a white background. The practical application of these laboratory-based findings was examined with two experiments to establish if the advantages of transferring fish to light coloured tanks before harvest could be achieved on-farm using white cages and to determine the effects of fish density on skin colour. For the first experiment, snapper (mean TL=29.7 cm) were transferred from a commercial snapper sea cage to black or white netted cages and fed diets supplemented with unesterified astaxanthin (supplied as Lucantin® Pink, BASF) at 0 or 39 mg kg,1 for 42 days. Skin colour was measured using the CIE (black,white), (green,red), (blue,yellow) colour scale. Snapper held in white netting cages became significantly lighter (higher ) than snapper held in black cages; however, values were not as high as previous laboratory-based studies in which snapper were held in white plastic-lined cages. Snapper fed astaxanthin displayed significantly greater and values, and total carotenoid concentrations after 42 days. In addition, total carotenoids were higher in fish from black than white cages. The second experiment was designed to investigate whether density reduced the improvements in skin colour achieved by holding fish in white coloured cages and whether cage colour affected stress. Snapper (mean weight=435 g) were acclimated to black cages and fed 39 mg kg,1 astaxanthin for 44 days before transferring to black or white plastic-lined cages at 14 (low), 29 (mid) or 45 (high) kg m,3 for 7 days after which time skin colour, plasma cortisol and plasma glucose concentrations were measured. Skin lightness () was greater in snapper transferred to white plastic-lined cages with the lightest coloured fish obtained from the lowest density after 7 days. Density had no effect on plasma cortisol or glucose levels after 7 days, although plasma cortisol was elevated in snapper from black cages. For improved skin colouration we recommend feeding unesterified astaxanthin at 39 mg kg,1 for approximately 6 weeks and transferring snapper to white plastic-lined cages or similar at low densities for short periods before harvest rather than producing fish in white netting sea cages subject to biofouling. [source] | |||||||||||||