Functional measurements of human ventral occipital cortex: retinotopy and colour

Human colour vision originates in the cone photoreceptors, whose spatial density peaks in the fovea and declines rapidly into the periphery. For this reason, one expects to find a large representation of the cone-rich fovea in those cortical locations that support colour perception. Human occipital cortex contains several distinct foveal representations including at least two that extend onto the ventral surface: a region thought to be critical for colour vision. To learn more about these ventral signals, we used functional magnetic resonance imaging to identify visual field maps and colour responsivity on the ventral surface. We found a visual map of the complete contralateral hemifield in a 4 cm(2) region adjacent to ventral V3; the foveal representation of this map is confluent with that of areas V1/2/3. Additionally, a distinct foveal representation is present on the ventral surface situated 3-5 cm anterior from the confluent V1/2/3 foveal representations. This organization is not consistent with the definition of area V8, which assumes the presence of a quarter field representation adjacent to V3v. Comparisons of responses to luminance-matched coloured and achromatic patterns show increased activity to the coloured stimuli beginning in area V1 and extending through the new hemifield representation and further anterior in the ventral occipital lobe.     

木聚糖酶活力测定条件研究

用DNS法测木聚糖酶活力,分析测定条件对测定结果的影响。结果表明,在不同的条件下测定酶活力会得到不同的木聚糖酶活力测定值。其中,酶液用量、酶解反应的时间对测定结果的影响较大,酶液稀释度、DNS显色时间、DNS的用量,对测定结果也有一定的髟响。测定木聚糖酶活力的适宜条件为：酶液量/1％木聚糖液量1/9(V／V);酶解反应时间：10min;DNS用量2—2．5ml;DNS显色时间2—5min。     

Colour vision: a clue to hue in v2

Where do our brains encode all the colours of the rainbow? We know the neural basis for colour opponency and colour contrast, and recent studies have now provided evidence for the representation of hue in cortical visual area V2.     

Mapping of contextual modulation in the population response of primary visual cortex

We review the evidence of long-range contextual modulation in V1. Populations of neurons in V1 are activated by a wide variety of stimuli outside of their classical receptive fields (RF), well beyond their surround region. These effects generally involve extra-RF features with an orientation component. The population mapping of orientation preferences to the upper layers of V1 is well understood, as far as the classical RF properties are concerned, and involves organization into pinwheel-like structures. We introduce a novel hypothesis regarding the organization of V1’s contextual response. We show that RF and extra-RF orientation preferences are mapped in related ways. Orientation pinwheels are the foci of both types of features. The mapping of contextual features onto the orientation pinwheel has a form that recapitulates the organization of the visual field: an iso-orientation patch within the pinwheel also responds to extra-RF stimuli of the same orientation. We hypothesize that the same form of mapping applies to other stimulus properties that are mapped out in V1, such as colour and contrast selectivity. A specific consequence is that fovea-like properties will be mapped in a systematic way to orientation pinwheels. We review the evidence that cytochrome oxidase blobs comprise the foci of this contextual remapping for colour and low contrasts. Neurodynamics and motion in the visual field are argued to play an important role in the shaping and maintenance of this type of mapping in V1.     

The clinical and functional measurement of cortical (in)activity in the visual brain, with special reference to the two subdivisions (V4 and V4 alpha) of the human colour centre.

We argue below that, at least in studying the visual brain, the old and simple methods of detailed clinical assessment and perimetric measurement still yield important insights into the organization of the visual brain as a whole, as well as the organization of the individual areas within it. To demonstrate our point, we rely especially on the motion and colour systems, emphasizing in particular how clinical observations predicted an important feature of the organization of the colour centre in the human brain. With the use of data from functional magnetic resonance imaging analysed by statistical parametric mapping and independent component analysis, we show that the colour centre is composed of two subdivisions, V4 and V4 alpha the two together constituting the V4 complex of the human brain. These two subdivisions are intimately linked anatomically and act cooperatively. The new evidence about the architecture of the colour centre might help to explain why the syndrome, cerebral achromatopsia, produced by lesions in it is so variable.     

Relationship between the flavonoid composition and flower colour variation in Victoria

• Victoria (Nymphaeaceae), an annual or perennial aquatic plant genus, contains only two species: V. amazonica (Poepp.) J. C. Sowerby and V. cruziana A. D. Orb. Both species have large floating leaves and variable flower colour. Both Victoria species are night bloomers, which have white petals on the first blooming night that then turn pink or ruby red on the second blooming day. The mechanism of the colour change of Victoria petals during anthesis is still unclear.
• In this study, flavonoids in Victoria petals of both species were evaluated and quantified by high‐performance liquid chromatography with photodiode array detection (HPLC‐DAD) and by ultra‐performance liquid chromatography coupled with tandem mass spectrometry (UPLC‐MS/MS) for the first time.
• In total, 14 flavonoids were detected in Victoria petals, including 4 anthocyanins and 10 flavonols. The flavonoid compositions differed across the two species, resulting in different colours between the inner and outer petals. With increased anthocyanin content across blooming days, the colour of Victoria flowers changed over time.
• The results of this study will improve understanding of the chemical mechanism of colour formation and lay the foundation for selective colour breeding in Victoria.

     

The anatomical basis of sexual dichromatism in non-iridescent ultraviolet-blue structural coloration of feathers

Despite extensive research on the evolution of avian dichromatism, the anatomical bases for differences between the sexes in species with structurally coloured plumage remain largely unknown. Using full‐spectrum spectrometry and transmission electron microscopy, we compared the colour and morphology of rump feathers of male and female eastern bluebirds (Sialia sialis). The ultraviolet (UV)‐blue feather colour in this species is caused by coherent scattering of light within the medullary ‘spongy layer’ of feather barbs. This spongy layer lies beneath a keratin cortex and on top of a layer of melanin granules that surround a hollow central vacuole. Irregularly shaped electron‐dense regions are present within the cortex. Male and female S. sialis differed substantially in their plumage colour and feather structure. A backwards logistic regression predicted sex with 100% accuracy using the colour variables brightness, UV‐violet (UV‐V) chroma and spectral saturation. A second backwards logistical regression predicted sex with 100% accuracy using relative cortex area and size of air spaces. Thus, S. sialis are dimorphic both in colour and in the structures causing this colour. Multiple regression analyses using data pooled from both sexes indicated that multiple features of feather barb structure contributed to colour variation in complex ways. Brightness was negatively related to the relative surface area of cortex in barb cross‐sections. Hue was positively related and UV‐V chroma was negatively related to the distance between scattering elements (i.e. keratin rods and air spaces) in the spongy layer. In contrast, hue was negatively related and UV‐V chroma was positively related to the thickness of the spongy layer. UV‐V chroma was also negatively related to the relative area of electron‐dense regions in the cortex. Spectral saturation was negatively related to the distance between scatterers and the standard error of the size of air spaces. These results suggest that the dimensions of spongy‐layer elements are critical to colour production, but that UV‐blue coloration can also be modified by the cortex and the thickness of the spongy layer. © 2005 The Linnean Society of London, Biological Journal of the Linnean Society, 2005, 84 , 259–271.     

Film Reviews

The Chemistry of the Cell. Produced by Technical and Scientific Films Ltd., for E.F.V.A. and Educational Films of Scotland. Part 1 : The Structure of Protein and Nucleic Acids Sound, colour, 22 min

The Birth of the Red Kangaroo. 16 mm, sound, colour, 21 min. Produced by Commonwealth Scientific & Industrial Research Organisation Film Unit, Australia

Embryonic Development of the Light Brown Apple Moth. 16 mm, sound, black and white, 18 min. Produced by Commonwealth Scientific & Industrial Research Organisation Film Unit, Australia

Biology by Enquiry. 16 mm, sound, black and white, 17 min. Produced by the Nuffield Foundation

Animals Breathe in Many Ways. 16 mm, sound, colour, 10 min. Produced by Film Associates of California, U.S.A.

Life Story of a Moth. 16 mm, sound, colour, 11 min. Produced by Encyclopaedia Britannica     

Visual processing levels revealed by response latencies to changes in different visual attributes.

Visual latencies, and their variation with stimulus attributes, can provide information about the level in the visual system at which different attributes of the image are analysed, and decisions about them made. A change in the colour, structure or movement of a visual stimulus brings about a highly reproducible transient constriction of the pupil that probably depends on visual cortical mechanisms. We measured this transient response to changes in several attributes of visual stimuli, and also measured manual reaction times to the same stimulus changes. Through analysis of latencies, we hoped to establish whether changes in different stimulus attributes were processed by mechanisms at the same or different levels in the visual pathway. Pupil responses to a change in spatial structure or colour are almost identical, but both are ca. 40 ms slower than those to a change in light flux, which are thought to depend largely on subcortical pathways. Manual reaction times to a change in spatial structure or colour, or to the onset of coherent movement, differ reliably, and all are longer than the reaction time to a change in light flux. On average, observers take 184 ms to detect a change in light flux, 6 ms more to detect the onset of a grating, 30 ms more to detect a change in colour, and 37 ms more to detect the onset of coherent motion. The pattern of latency variation for pupil responses and reaction times suggests that the mechanisms that trigger the responses lie at different levels in cortex. Given our present knowledge of visual cortical organization, the long reaction time to the change in motion is surprising. The range of reaction times across different stimuli is consistent with decisions about the onset of a grating being made in V1 and decisions about the change in colour or change in motion being made in V4.     

Vipera pontica sp.n., a new viper species in the kaznakovi group (Reptilia, Viperidae) from northeastern Turkey and adjacent Transcaucasia

Vipera pontica sp.n. from northeastern Turkey and Transcaucasia is a member of the Vipera kaznakovi group characterized by partial fragmentation of frontal and parietals, sharp canthus rostralis, and a colour pattern on the head of the Vipera dinnicki type. It differs from all vipers in the Near and Middle East in having an upturned but hornless snout, and in a number of scalation and colour pattern characters. It is most similar to the west European V. aspis, but differs in having a yellow green tail tip, more loreals and fewer subcaudals. The affinities to the latter species as well as to V. barani are discussed.     

Hoverflies are imperfect mimics of wasp colouration

Many Batesian mimics are considered to be inaccurate copies of their models, including a number of hoverfly species which appear to be poor mimics of bees and wasps. This inaccuracy is surprising since more similar mimics are expected to deceive predators more frequently and therefore have greater survival. One suggested explanation is that mimics which appear inaccurate to human eyes may be perceived differently by birds, the probable agents of selection. For example, if patterns contain an ultra-violet (UV) component, this would be visible to birds but overlooked by humans. So far, indirect comparisons have been made using human and bird responses to mimetic stimuli, but direct colour measurements of mimetic hoverflies are lacking. We took spectral readings from a wide range of hoverfly and wasp patterns. They show very low reflectance in the UV range, and do not display any human-invisible colour boundaries. We modelled how the recorded spectra would be perceived by both birds and humans. While colour differences between wasps and hoverflies are slightly more distinct according to human visual abilities, bird vision is capable of discriminating the two taxa in almost all cases. We discuss a number of factors that might make the discrimination task more challenging for a predator in the field, which could explain the apparent lack of selection for accurate colour mimicry.     

Mapping the variation in spider body colouration from an insect perspective

Colour variation is frequently observed in spiders. Such variation can impact fitness by affecting the way spiders are perceived by relevant observers such as prey (i.e. by resembling flower signals as visual lures) and predators (i.e. by disrupting search image formation). Verrucosa arenata is an orb-weaving spider that presents colour variation in a conspicuous triangular pattern on the dorsal part of the abdomen. This pattern has predominantly white or yellow colouration, but also reflects light in the UV part of the spectrum. We quantified colour variation in V. arenata from images obtained using a full spectrum digital camera. We obtained cone catch quanta and calculated chromatic and achromatic contrasts for the visual systems of Drosophila melanogaster and Apis mellifera. Cluster analyses of the colours of the triangular patch resulted in the formation of six clusters and three clusters in the colour space of D. melanogaster and A. mellifera, respectively. Significant differences were found between morphs for both visual systems in contrasts between the colour pattern and two backgrounds against which it would be viewed. Yellow spiders showed higher chromatic contrast than white spiders, while white spiders showed higher achromatic contrast. Therefore, there are perceptual differences between V. arenata colour morphs in the visual systems of potential relevant observers which could pose an important selective pressure on this trait. A variation in the contribution of colour channels to the colour pattern observed in colour maps constructed from reflectance values of individual pixels could influence the way the pattern is perceived, and its resemblance to attractive flower signals.     

Major effect of retinal short-chain dehydrogenase reductase (RDHE2) on bovine fat colour

Beef with yellow fat is considered undesirable by consumers in most European and Asian markets. β-Carotene is the major carotenoid deposited in the adipose tissue and milk fat of cattle (Bos taurus), which can result in the yellowness. The effects of retinal short-chain dehydrogenase reductase (RDHE2) and β, β-carotene 9',10-dioxygenase (BCO2) were considered jointly as major candidate genes for causing the yellow fat colour, based on their genomic locations in the fat colour quantitative trait loci (QTL) and their roles in the metabolism of β-carotene. In a secondary pathway, BCO2 cleaves β-carotene into retinoic acid, the most potent form of vitamin A. RDHE2 converts trans-retinol to trans-retinal, a less active form of vitamin A. We evaluated the effects of two amino acid variants of the RDHE2 gene (V6A and V33A) along with a mutation in the BCO2 gene that results in a stop codon (W80X) in seven cattle populations. The RDHE2 V6A genotype affected several fat colour traits but the size of the effect varied in the populations studied. The genotype effect of the RDHE2 V33A variant was observed only in New Zealand samples of unknown breed. In general, the individual effects of RDHE2 V6A and V33A SNPs genotypes were greater in the random New Zealand samples than in samples from pedigreed Jersey-Limousin backcross progeny, accounting for 8-17 % of the variance in one population. Epistasis between the BCO2 W80X and RDHE2 variants was observed, and in some populations this explained more of the variation than the effects of the individual RDHE2 variants.     

Synaesthetic Colour in the Brain: Beyond Colour Areas. A Functional Magnetic Resonance Imaging Study of Synaesthetes and Matched Controls

Background

In synaesthesia, sensations in a particular modality cause additional experiences in a second, unstimulated modality (e.g., letters elicit colour). Understanding how synaesthesia is mediated in the brain can help to understand normal processes of perceptual awareness and multisensory integration. In several neuroimaging studies, enhanced brain activity for grapheme-colour synaesthesia has been found in ventral-occipital areas that are also involved in real colour processing. Our question was whether the neural correlates of synaesthetically induced colour and real colour experience are truly shared.

Methodology/Principal Findings

First, in a free viewing functional magnetic resonance imaging (fMRI) experiment, we located main effects of synaesthesia in left superior parietal lobule and in colour related areas. In the left superior parietal lobe, individual differences between synaesthetes (projector-associator distinction) also influenced brain activity, confirming the importance of the left superior parietal lobe for synaesthesia. Next, we applied a repetition suppression paradigm in fMRI, in which a decrease in the BOLD (blood-oxygenated-level-dependent) response is generally observed for repeated stimuli. We hypothesized that synaesthetically induced colours would lead to a reduction in BOLD response for subsequently presented real colours, if the neural correlates were overlapping. We did find BOLD suppression effects induced by synaesthesia, but not within the colour areas.

Conclusions/Significance

Because synaesthetically induced colours were not able to suppress BOLD effects for real colour, we conclude that the neural correlates of synaesthetic colour experience and real colour experience are not fully shared. We propose that synaesthetic colour experiences are mediated by higher-order visual pathways that lie beyond the scope of classical, ventral-occipital visual areas. Feedback from these areas, in which the left parietal cortex is likely to play an important role, may induce V4 activation and the percept of synaesthetic colour.     

Melanocortin 1 receptor (MC1R), pigmentary characteristics and sun exposure: Findings from a case–control study of diffuse large B-cell and follicular lymphoma

The relationship between skin cancer and non-Hodgkin lymphoma (NHL) suggests common genetic, host or environmental causes. Ultraviolet radiation (UVR), pigmentary characteristics have been linked with both malignancies, and for skin cancer, the melanocortin 1 receptor (MC1R) which influences pigmentation has also been implicated. This paper reports on the relationship between MC1R, skin, hair and eye colour, time spent outdoors, and diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL). Persons carrying MC1R homozygote variant alleles at R151C, R160W, D294H and D84E were more likely to have fair skin, red hair and to spend less time outdoors than those who did not. The variant allele at V92M was associated with FL (odds ratio (OR) = 1.61, 95% confidence interval (CI) 1.08–2.39) and the r:wild type genotype with DLBCL (OR = 0.58, 95% CI 0.38–0.89). Interactions between MC1R genotypes and skin colour influenced DLBCL risk; the RR genotype increased risk in individuals with medium or dark skin, based on 5 cases and no controls, but decreased risk among those of fair skin. On the whole, DLBCL and FL risk were not related to genetic variation in MC1R, pigmentation or time spent outdoors.     

BOOK REVIEWS

Book reviewed in this article:
THE BULBOUS PLANTS OF TURKEY. Brian Mathew and Turhan Baytop. 132 pp. 120 colour and 18 black and white photographs
FLOWERING PLANTS OF THE WORLD. Consultant Editor, V.H. Heywood. 335 pp. Number of colour and half-tone illustrations; numerous maps
SOUTH AFRICA'S PROTEACEAE: KNOW THEM AND GROW THEM. Marie Vogts, with photography by C. Paterson-Jones
Trees and shrubs cultivated in Ireland. Compiled by Mary Forrest, edited by E.C. Nelson     

中国新纪录属犁沟蚁属(膜翅目,蚁科)及一新种记述

记述中国新纪录属犁沟蚁属Vombisidris Bolton及1新种暗腹犁沟蚁V.umbrabdomina sp.nov..新种与V.nahet Bolton相似,但中胸背板背面观两侧轻度隆起,不呈钝角状,触角柄节较长,体黄褐色,后腹部深褐色,深于头和并腹胸.模式标本保存于广西师范大学昆虫标本室.     

孟德尔豌豆基因克隆的研究进展及其在遗传学教学中的应用

150多年前, 孟德尔进行了豌豆7对相对性状的杂交试验, 发现了遗传学的两个基本规律。1900年, 孟德尔定律被重新发现以后, 人们从生理生化、细胞和分子水平等不同层次上对豌豆的这7个性状进行了深入研究。近年, 随着分子生物学技术的发展, 已有种子形状(R)、茎的长度(Le)、子叶颜色(I)和花的颜色(A)等4个性状的基因被克隆; 未成熟豆荚的颜色(Gp)、花的着生位置(Fa)和豆荚形状(V)的基因已被定位在各自的连锁群上。4个孟德尔基因的鉴定和克隆加深了人们对基因概念的理解：如基因功能的多样性、在分子水平上基因变异原因的多样性、显性和隐性的分子实质等。在遗传学教学中, 把孟德尔基因克隆和研究的最新进展介绍给学生, 在分子水平上诠释经典遗传规律, 有助于提高学生的学习兴趣, 帮助学生全面把握从形式遗传学到分子遗传学的内容和遗传学的发展方向。     

Ultraviolet mutagenesis of the cellulase producer Aspergillus niger using protoplasts

Abstract Ultraviolet mutagenesis of Aspergillus niger strain O97 was achieved using protoplasts. Protoplasts of A. niger O97 showed the same ultraviolet killing kinetics as intact cells. After mutagenesis, several mutants were found in regenerated collonies. These mutants differ from the original strain in spore colour and cellulase-producing ability. The most active strain, designated 97V3-3 has an altered spore colour, and its carboxymethylcellose-hydrolysing, filter-paper-degradation, cotton-de-gradation and β-glucosidase activities were increased by 45.4%, 19.1%, 28.2% and 18.2%, respectively.     

Editor's Note

A new species of Apobaetis is described based on nymphs and male imago, and the male imago of A. fiuzai. Specimens were collected in the state of Amazonas, northern region of Brazil. Apobaetis hamadae sp. n. can be easily distinguished from the other congeners by the following combination of characteristics: male imago: (1) abdominal colour pattern; (2) area between forceps not excavated medially. Nymphs: (1) distal margin of labrum with shallow medial emargination and with four to five spatulated setae near midline; (2) maxillary palp 1.4× longer than galea-lacinia; (3) tarsal claws 1.2× times longer than tarsus. The male imago of A. fiuzai can be easily distinguished by the following characteristics: (1) abdominal colour pattern; (2) area between segments I of forceps with a deep V emargination.