RESUMO
From well-controlled long creep tests, we show that the residual apparent yield stress observed with soft-jammed systems along smooth surfaces is an artifact due to edge effects. By removing these effects, we can determine the stress solely associated with steady-state wall slip below the material yield stress. This stress is found to vary linearly with the slip velocity for a wide range of materials whatever the structure, the interaction types between the elements and with the wall, and the concentration. Thus, wall slip results from the laminar flow of some given free liquid volume remaining between the (rough) jammed structure formed by the elements and the smooth wall. This phenomenon may be described by the simple shear flow in a Newtonian liquid layer of uniform thickness. For various systems, this equivalent thickness varies in a narrow range (35±15 nm).
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To what extent are aqueous foams prone to clogging? Foam permeability is measured as a function of particulate loading (trapped hydrophilic particles) under conditions where the particle to bubble size ratio is allowed to increase when the number of particles per bubble is fixed. In addition to experiments performed on the foam scale, we investigated experimentally and numerically the hydrodynamic resistance of a single foam node loaded with one particle. It is shown that, with respect to solid porous media, aqueous foams clog more efficiently due to two reasons: (i) the deformation of interfaces allows for larger particles to be incorporated within the interstitial network and (ii) the interfacial mobility contributes to lowering of the reduced permeability.
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Although extensively studied in the past, drainage of aqueous foams still offers major unaddressed issues. Among them, the behaviour of foam films during drainage has great significance as the thickness of the films is known to control the Ostwald ripening in foams, which in turn impacts liquid drainage. We propose a model relating the films' behavior to the liquid flow in foam channels. It is assumed that Marangoni-driven recirculation counterflows take place in the transitional region between the foam channel and the adjoining films, and the Gibbs elasticity is therefore introduced as a relevant parameter. The velocity of these counterflows is found to be proportional to the liquid velocity in the channel. The resulting channel permeability is determined and it is shown that Marangoni stresses do not contribute to rigidify the channel's surfaces, in strong contrast with the drainage of horizontal thin liquid films. New experimental data are provided and support the proposed model.
Assuntos
Modelos Químicos , Soluções/química , Tensoativos/química , Substâncias Viscoelásticas/química , Elasticidade , Reologia , Propriedades de SuperfícieRESUMO
We perform forced-drainage experiments in aqueous foams and compare the results with data available in the literature. We show that all the data can be accurately compared together if the dimensionless permeability of the foam is plotted as a function of liquid fraction. Using this set of coordinates highlights the fact that a large part of the published experimental results corresponds to relatively wet foams (epsilon approximately 0.1). Yet, most of the foam drainage models are based on geometrical considerations only valid for dry foams. We therefore discuss the range of validity of the different models in the literature and their comparison to experimental data. We propose extensions of these models considering the geometry of foam in the relatively wet-foam limit. We eventually show that if the foam geometry is correctly described, forced drainage experiments can be understood using a unique parameter --the Boussinesq number.
Assuntos
Teste de Materiais , Permeabilidade , Biofísica/métodos , Ecologia , Modelos Estatísticos , Reologia , Propriedades de Superfície , Tensão SuperficialRESUMO
A polymerase chain reaction-based method was used to generate a Drosophila melanogaster antennal cDNA library from which head cDNAs were subtracted. We identified five cDNAs that code for antennal proteins containing six cysteines in a conserved pattern shared with known moth antennal proteins, including pheromone-binding proteins. Another cDNA codes for a protein related to vertebrate brain proteins that bind hydrophobic ligands. In all, we describe seven antennal proteins which contain potential signal peptides, suggesting that, like pheromone-binding proteins, they may be secreted in the lumen of olfactory hairs. The expression patterns of these putative odorant-binding proteins define at least four different subsets of olfactory hairs and suggest that the Drosophila olfactory apparatus is functionally segregated.
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Drosophila melanogaster/metabolismo , Receptores Odorantes/biossíntese , Sequência de Aminoácidos , Animais , Sequência de Bases , Clonagem Molecular , Primers do DNA , DNA Complementar/biossíntese , DNA Complementar/metabolismo , Drosophila melanogaster/genética , Expressão Gênica , Biblioteca Gênica , Dados de Sequência Molecular , Família Multigênica , Odorantes , Mucosa Olfatória/metabolismo , Especificidade de Órgãos , Reação em Cadeia da Polimerase , Sinais Direcionadores de Proteínas/biossíntese , Homologia de Sequência de AminoácidosRESUMO
This paper deals with the drainage of liquid foams. The liquid velocity is known to be related to viscous dissipation occurring within the elements of the liquid network, i.e. the channels and the nodes. When compared together, available values for the hydrodynamic resistance of a foam node appear to span over more than one order of magnitude. To clarify this point, we propose an alternative experimental method to estimate the value of this parameter. In contrast to previous experimental work performed on the foam scale, the node resistance is not treated as a fitting parameter, but instead it is measured directly on the microscopic scale. The results allow a consistent range of values to emerge for this parameter.
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The pervasive occurrence of circadian clocks throughout the living world underlines their adaptive value. Nonetheless, there is surprisingly little evidence for a negative impact, on any animal species, of a constant discrepancy between the environmental and endogenous periods. Male Drosophila melanogaster per mutants with altered circadian periods were compared to the wild type in two different LD schedules. Life span was used as a global index of physiological adaptation. The life span of the mutants was significantly reduced by up to 15% for the flies whose period differs most from that of the wild type. A reduction was observed even when flies were kept in an LD schedule fitting a mutant period. The LD schedule made no significant difference on its own, but the authors found evidence for an interaction between genotype and LD schedule in determining life span. These results are consistent with the importance of the circadian clock in maintaining internal temporal order independent of environmental cycles. Nonetheless, a large difference between the environmental and endogenous periods has a measurable impact.
Assuntos
Ritmo Circadiano/genética , Ritmo Circadiano/fisiologia , Mutação/fisiologia , Alelos , Animais , Drosophila melanogaster , Feminino , Genótipo , Longevidade/fisiologia , Masculino , SobrevidaRESUMO
We have measured the spectrum of velocity fluctuations in a granular system confined to a vertical plane and driven into a homogeneous, steady state by strong vertical vibration. The distribution of horizontal velocities is not Maxwell-Boltzmann and is given by P(v) = Cexp[-beta(|v|/sigma)(alpha)] where alpha = 1.55+/-0.1 at all frequencies and amplitudes investigated, and also for varying boundary conditions. The deviation from Maxwell-Boltzmann statistics occurs in the absence of spatial clustering and does not result from an inhomogeneous average over regions of varying local density. Surprisingly, P(v) has the same shape over a wide range of densities.
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The final stages of a coin spinning on a flat surface have recently been proposed [H.K. Moffatt, Nature (London) 404, 833 (2000)] as an example of a finite-time singularity, wherein the precession rate of the symmetry axis of the coin diverges as it comes to a stop. We report measurements by high-speed video imaging of the rolling motion of disks and rings on a variety of surfaces. We find that the precession rate, Omega, diverges as a power law in time: Omega(t) proportional, variant (t-t(o))(-1/n), where t(o) is the instant the motion ceases. The exponent n varies between 2.7 and 3.2 under different experimental conditions. The value of n, as well as the systematic dependence of precession rate on coefficients of friction, establishes that the primary mechanism of energy dissipation is rolling friction rather than air drag, as previously suggested.
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A forced Ostwald ripening experiment is performed on a single foam bubble. The bubble size is followed as the system is wetted with a constant liquid flow rate delivered from one of the bubble Plateau borders. Obtained ripening velocities cannot be described with a model based on a constant film thickness assumption. Within these well-controlled experimental conditions, the film thickness is measured and found to depend on the imposed liquid flow rate. It is shown that the bubble growth rate is well predicted as the films thickness evolution is explicitly introduced in the ripening model. Finally, it is suggested that existing results for the coarsening of draining foams could be understood following the approach validated on the bubble scale.
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Liquid foams were recognized early to be porous materials, as liquid flowed between the gas bubbles. Drainage theories have been established, and foam permeability has been modeled from the microscopic description of the equivalent pores geometry, emphasizing similarities with their solid counterparts. But to what extent can the theoretical work devoted to the permeability of solid porous materials be useful to liquid foams? In this article, the applicability of the Carman-Kozeny model on foam is investigated. We performed measurements of the permeability of foams with nonmobile surfactants, and we show that, in introducing an equivalent specific surface area for the foam, the model accurately describes the experimental data over two orders of magnitude for the foam liquid fraction, without any additional parameters. Finally, it is shown that this model includes the previous permeability models derived for foams in the dry foams limit.
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This chapter summarizes our present knowledge about the master clock of the fruit fly at the neuronal level. The clock is organized in distinct groups of interconnected pacemaker neurons with different functions. All of these neurons appear to communicate with one another in order to produce the species-specific activity rhythm, which is organized in morning (M) and evening (E) activity bouts. These two activity components are differentially influenced by distinct groups of pacemaker neurons reminiscent of the Pittendrigh-Daan dual oscillator model. In the original work (Grima et al. 2004; Stoleru et al. 2004), the ventrolateral (LN(v)) and dorsolateral (LN(d)) plus some dorsal groups (DN) of clock neurons have been defined as M and E cells, respectively. We further specify that the clock neurons belong to the M and E oscillators and define a more complex picture of the Drosophila brain clock.
Assuntos
Ritmo Circadiano/fisiologia , Drosophila melanogaster/anatomia & histologia , Drosophila melanogaster/fisiologia , Neurônios/fisiologia , Animais , Relógios Biológicos/genética , Relógios Biológicos/fisiologia , Encéfalo/anatomia & histologia , Encéfalo/citologia , Encéfalo/fisiologia , Ritmo Circadiano/genética , Proteínas de Drosophila/genética , Proteínas de Drosophila/fisiologia , Drosophila melanogaster/genética , Genes de Insetos , Modelos Neurológicos , Mutação , Neuropeptídeos/genética , Neuropeptídeos/fisiologia , FotoperíodoRESUMO
The structure and function of the human Y chromosome have been approached by molecular genetics. The use of Y-derived DNA probes to analyze the Y chromosome of patients with sexual differentiation abnormalities allowed the construction of a deletion map localizing TDF (testis determining factor) in the terminal part of the short arm. These studies culminated recently in the isolation of a candidate gene for the TDF locus. Nevertheless, the existence of a related locus on the X chromosome does not fit with the simple hypothesis of a single Y-located gene for testis differentiation. The finding of a strictly homologous region at the tip of the short arms of X and Y chromosomes allowed the characterization of another major property of the sex chromosomes. These so called pseudoautosomal DNA sequences show only a partial sex linkage and can be exchanged between X and Y chromosomes during male meiosis. Genetic analysis and determination of the physical length of the pseudoautosomal region show that it is subjected in male meiosis, to a recombination rate about 20 times higher than the mean value of the human genome. In 1966, Ferguson-Smith proposed that an abnormal cross-over was responsible for both types of sex inversions in humans: XX males and XY females. Segregation analysis of the pseudoautosomal loci in these patients has demonstrated the validity of this hypothesis and shown the existence of sex inversions unrelated to the TDF locus. The construction of a detailed map of the human Y chromosome enables the search for new genes (H-Y antigen, fertility gene(s]. The finding of several homologous regions on the sex chromosomes confirms the hypothesis of a common origin and should help to understand the establishment of sex determination and X inactivation mechanisms during mammalian evolution.
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Análise para Determinação do Sexo , Cromossomo Y/fisiologia , Deleção Cromossômica , Mapeamento Cromossômico , Troca Genética , DNA/genética , Proteínas de Ligação a DNA/genética , Transtornos do Desenvolvimento Sexual/genética , Feminino , Antígeno H-Y/genética , Humanos , Fatores de Transcrição Kruppel-Like , Masculino , Meiose , Homologia de Sequência do Ácido Nucleico , Aberrações dos Cromossomos Sexuais/genética , Fatores de Transcrição , Cromossomo X/ultraestrutura , Cromossomo Y/ultraestruturaRESUMO
Circadian rhythms of locomotor activity and eclosion in Drosophila depend upon the reciprocal autoregulation of the period (per) and timeless (tim) genes. As part of this regulatory loop, per and tim mRNA levels oscillate in a circadian fashion. Other cycling transcripts may participate in this central pacemaker mechanism or represent outputs of the clock. In this paper, we report the isolation of Crg-1, a new circadianly regulated gene. Like per and tim transcript levels, Crg-1 transcript levels oscillate with a 24 h period in light:dark (LD) conditions, with a maximal abundance at the beginning of the night. These oscillations persist in complete darkness and depend upon per and tim proteins. The putative CRG-1 proteins show some sequence similarity with the DNA-binding domain of the HNF3/fork head family of transcription factors. In the adult head, in situ hybridization analysis reveals that per and Crg-1 have similar expression patterns in the eyes and optic lobes.
Assuntos
Relógios Biológicos , Ritmo Circadiano , Proteínas de Drosophila , Drosophila/genética , Genes de Insetos , Fatores de Transcrição/genética , Processamento Alternativo , Sequência de Aminoácidos , Animais , Sequência de Bases , Sítios de Ligação , Clonagem Molecular , DNA Complementar , Proteínas de Ligação a DNA/genética , Drosophila melanogaster/genética , Fatores de Transcrição Forkhead , Expressão Gênica , Sequências Hélice-Volta-Hélice , Fator 3-gama Nuclear de Hepatócito , Dados de Sequência Molecular , Proteínas Nucleares/genética , Fases de Leitura Aberta , Proteínas Circadianas Period , RNA , Homologia de Sequência de AminoácidosRESUMO
The expression of the period (per) gene of Drosophila melanogaster has been studied by in situ hybridization in the adult's head, where it is required for the fly to exhibit behavioral circadian rhythms. We have used non-radioactive in situ hybridization to obtain a high sensitivity and specificity on head sections, with single cell resolution. Consistent with previous per protein- or per reporter gene-expression, per-expressing cells were detected in the optic lobes and the central brain, as well as in the head sensory organs: eyes, ocelli, maxillary palps and proboscis. In the brain and the eyes, circadian fluctuations of the per mRNA abundance were observed in different per expressing cells.
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Ritmo Circadiano/fisiologia , Drosophila melanogaster/genética , Proteínas Nucleares/genética , Animais , Proteínas de Drosophila , Drosophila melanogaster/fisiologia , Cabeça , Hibridização In Situ , Proteínas Circadianas PeriodRESUMO
Two pseudoautosomal loci DXYS15 and DXYS17 from the pairing region of the human sex chromosomes display a high variability with at least eight alleles each. The structural elements responsible for the polymorphisms have been isolated and sequenced. In both cases the variations result from DNA rearrangements occurring in tandemly repeated sequences (minisatellites) of 21-29 nucleotides for DXYS15 and 28-33 nucleotides for DXYS17. At reduced stringency, the DXYS15 minisatellite detects other hypervariable sequences located in other parts of the genome and hence represents a new family of minisatellites. In contrast to most other known hypervariable families, the DXYS15 hypervariable sequence displays a very high AT content.
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DNA Satélite/genética , Polimorfismo Genético , Cromossomos Sexuais , Alelos , Sequência de Bases , Feminino , Variação Genética , Humanos , Masculino , Hibridização de Ácido NucleicoRESUMO
A repeated DNA element (STIR) interspersed in Xp22.3 and on the Y chromosome has been used as a tag to isolate seven single-copy probes from the human sex chromosomes. The seven probes detect X-specific loci located in Xp22.3. Using a panel of X-chromosomal deletions from X-Y interchange sex reversals (XX males and XY females), these X-specific loci and some additional ones were mapped to four contiguous intervals of Xp22.3, proximal to the pseudoautosomal region and distal to STS. The construction of this deletion map of the terminal part of the human X chromosome can serve as a starting point for a long-range physical map of Xp22.3 and for a more accurate mapping of genetic diseases located in Xp22.3.
Assuntos
Sondas de DNA , Proteínas de Ligação a DNA/genética , Aberrações dos Cromossomos Sexuais/genética , Translocação Genética , Cromossomo X/ultraestrutura , Cromossomo Y/ultraestrutura , Animais , Deleção Cromossômica , Mapeamento Cromossômico , Cricetinae , Cricetulus , Sondas de DNA/genética , Feminino , Marcadores Genéticos , Humanos , Células Híbridas , Fatores de Transcrição Kruppel-Like , Masculino , Sequências Repetitivas de Ácido Nucleico , Fatores de TranscriçãoRESUMO
A family of DNA loci (DNF28) from the pseudoautosomal region of the human sex chromosomes is characterized by a repeated element (STIR: subtelomeric interspersed repeat) which detects homologous sequences in the telomeric regions of human autosomes by in situ hybridization. Several STIR elements from both the pseudoautosomal region and terminal parts of autosomes were cloned and sequenced. A conserved 350 bp sequence and some characteristic structural differences between the autosomal and pseudoautosomal STIRs were observed. Screening of the DNA sequence databases with a consensus sequence revealed the presence of STIRs in several human loci localized in the terminal parts of different chromosomes. We mapped single copy probes flanking the cloned autosomal STIRs to the subtelomeric parts of six different chromosomes by in situ hybridization and genetic linkage analysis. The linkage data show a greatly increased recombination frequency in the subtelomeric regions of the chromosomes, especially in male meiosis. The STIR elements, specifically located in subtelomeric regions, could play a role in the peculiar recombination properties of these chromosomal regions, e.g. by promoting initiation of pairing at meiosis.
Assuntos
Sequências Repetitivas de Ácido Nucleico , Cromossomo X , Sequência de Aminoácidos , Animais , Sequência de Bases , Southern Blotting , Mapeamento Cromossômico , Clonagem Molecular , Cricetinae , DNA/genética , DNA/isolamento & purificação , Sondas de DNA , Feminino , Biblioteca Gênica , Humanos , Células Híbridas/citologia , Sistemas de Informação , Masculino , Meiose , Metáfase , Dados de Sequência Molecular , Hibridização de Ácido Nucleico , Valores de Referência , Homologia de Sequência do Ácido NucleicoRESUMO
A single obligatory recombination event takes place at male meiosis in the tips of the X- and Y-chromosome short arms (i.e. the pseudoautosomal region). The crossover point is at variable locations and thus allows recombination mapping of the pseudoautosomal loci along a gradient of sex linkage. Recombination at male meiosis in the terminal regions of the short arms of the X and Y chromosomes is 10- to 20-fold higher than between the same regions of the X chromosomes during female meiosis. The human pseudoautosomal region is rich in highly polymorphic loci associated with minisatellites. However, these minisatellites are unrelated to those resembling the bacterial Chi sequence and which possibly represent recombination hotspots. The high recombination activity of the pseudoautosomal region at male meiosis sometimes results in unequal crossover which can generate various sex-reversal syndromes.