3,939 research outputs found

    Scale-eating cichlids: from hand(ed) to mouth

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    Two recent studies in BMC Biology and Evolution raise important questions about a textbook case of frequency-dependent selection in scale-eating cichlid fishes. They also suggest a fascinating new line of research testing the effects of handed behavior on morphological asymmetry

    Dissociation Quotients of Malonic Acid in Aqueous Sodium Chloride Media to 100°C1

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    The first and second molal dissociation quotients of malonic acid were measured potentiometrically in a concentration cell fitted with hydrogen electrodes. The hydrogen ion molality of malonic acidJbimalonate solutions was measured relative to a standard aqueous HCI solution from 0 to 100°C over 25° intervals at five ionic strengths ranging from 0.1 to 5.0 molal (NaCl). The molal dissociation quotients and available literature data were treated in the all anionic form by a seven-term equation. This treatment yielded the following thermodynamic quantities for the first acid dissociation equilibrium at 25°C: log K1a = -2.852 ± 0.003. ΔH1̊a = 0.1 ±0.3 kJ-mol-1. ΔS1̊a = -54.4±1.0 J-mol-1-K-1 and ΔCp̊,1a = -185±20 J-mol-1-K-1. Measurements of the bimalonatelmalonate system were made over the same intervals of temperature and ionic strength. A similar regression of the present and previously published equilibrium quotients using a seven- term equation yielded the following values for the second acid dissociation equilibrium at 25°C: log K2a = -5.697 ± 0.001. ΔH2̊a = -5.13±0.11 kJ-mol-1, ΔS2̊a = -126.3±0.4 J-mol-1-K-1. and ΔCp̊,2a = -250+10 J-mol-1-K-1

    Dissociation Quotients of Malonic Acid in Aqueous Sodium Chloride Media to 100°C1

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    The first and second molal dissociation quotients of malonic acid were measured potentiometrically in a concentration cell fitted with hydrogen electrodes. The hydrogen ion molality of malonic acidJbimalonate solutions was measured relative to a standard aqueous HCI solution from 0 to 100°C over 25° intervals at five ionic strengths ranging from 0.1 to 5.0 molal (NaCl). The molal dissociation quotients and available literature data were treated in the all anionic form by a seven-term equation. This treatment yielded the following thermodynamic quantities for the first acid dissociation equilibrium at 25°C: log K1a = -2.852 ± 0.003. ΔH1̊a = 0.1 ±0.3 kJ-mol-1. ΔS1̊a = -54.4±1.0 J-mol-1-K-1 and ΔCp̊,1a = -185±20 J-mol-1-K-1. Measurements of the bimalonatelmalonate system were made over the same intervals of temperature and ionic strength. A similar regression of the present and previously published equilibrium quotients using a seven- term equation yielded the following values for the second acid dissociation equilibrium at 25°C: log K2a = -5.697 ± 0.001. ΔH2̊a = -5.13±0.11 kJ-mol-1, ΔS2̊a = -126.3±0.4 J-mol-1-K-1. and ΔCp̊,2a = -250+10 J-mol-1-K-1

    Precision metering of microliter volumes of biological fluids in micro-gravity

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    Concepts were demonstrated and investigated for transferring accurately known and reproducible microliter volumes of biological fluids from sample container onto dry chemistry slides in microgravity environment. Specific liquid transfer tip designs were compared. Information was obtained for design of a liquid sample handling system to enable clinical chemical analysis in microgravity. Disposable pipet tips and pipet devices that were designed to transfer microliter volumes of biological fluid from a (test tube) sample container in 1-G environment were used during microgravity periods of parabolic trajectories of the KC-135 aircraft. The transfer process was recorded using charge coupled device camera and video cassette equipment. Metering behavior of water, a synthetic aqueous protein solution, and anticoagulated human blood was compared. Transfer of these liquids to 2 substrate materials representative of rapidly wettable and slowly wettable dry chemistry slide surface was compared

    Cadmium Malonate Complexation in Aqueous Sodium Trifluoromethanesulfonate Media to 75°C; Including Dissociation Quotients of Malonic Acid

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    The molal formation quotients for cadmium-malonate complexes were measured potentiometrically from 5 to 75°C, at ionic strengths of 0.1, 0.3, 0.6 and 1.0 molal in aqueous sodium trifluoromethanesulfonate (NaTf) media. In addition, the stepwise dissociation quotients for malomc acid were measured in the same medium from 5 to 100°C, at ionic strengths of 0.1, 0.3, 0.6, and 1.0 molal by the same method. The dissociation quotients for malonic acid were modeled as a function of temperature and ionic strength with empirical equations formulated such that the equilibrium constants at infinite dilution were consistent, within the error estimates, with the malonic acid dissociation constants obtained in NaCl media. The equilibrium constants calculated for the dissociation of malonic acid at 25°C and infinite dilution are log K1a = -2.86 ± 0.01 and log K2a = -5.71 ± 0.01. A single Cd-malonate species, CdCH2C2O4, was identified from the complexation study and the formation quotients for this species were also modeled as a function of temperature and ionic strength. Thermodynamic parameters obtained by differentiating the equation with respect to temperature for the formation of CdCH2C2O4 at 25°C and infinite dilution are: log K = 3.45 ± 0.09, ΔH° = 7 ± 6 kJ-mol-1, ΔS° = 91 ± 22 J-K-1-mol-1, and ΔC°p = 400 ± 300J-K-1-mol-1

    Handling Trajectory Uncertainties for Airborne Conflict Management

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    Airborne conflict management is an enabling capability for NASA's Distributed Air-Ground Traffic Management (DAG-TM) concept. DAGTM has the goal of significantly increasing capacity within the National Airspace System, while maintaining or improving safety. Under DAG-TM, autonomous aircraft maintain separation from each other and from managed aircraft unequipped for autonomous flight. NASA Langley Research Center has developed the Autonomous Operations Planner (AOP), an onboard decision support system that provides airborne conflict management (ACM) and strategic flight planning support for autonomous aircraft pilots. The AOP performs conflict detection, prevention, and resolution from nearby traffic aircraft and area hazards. Traffic trajectory information is assumed to be provided by Automatic Dependent Surveillance Broadcast (ADS-B). Reliable trajectory prediction is a key capability for providing effective ACM functions. Trajectory uncertainties due to environmental effects, differences in aircraft systems and performance, and unknown intent information lead to prediction errors that can adversely affect AOP performance. To accommodate these uncertainties, the AOP has been enhanced to create cross-track, vertical, and along-track buffers along the predicted trajectories of both ownship and traffic aircraft. These buffers will be structured based on prediction errors noted from previous simulations such as a recent Joint Experiment between NASA Ames and Langley Research Centers and from other outside studies. Currently defined ADS-B parameters related to navigation capability, trajectory type, and path conformance will be used to support the algorithms that generate the buffers

    Morphology of the ferritin iron core by aberration corrected scanning transmission electron microscopy

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    As the major iron storage protein, ferritin stores and releases iron for maintaining the balance of iron in fauna, flora, and bacteria. We present an investigation of the morphology and iron loading of ferritin (from equine spleen) using aberration-corrected high angle annular dark field scanning transmission electron microscopy. Atom counting method, with size selected Au clusters as mass standards, was employed to determine the number of iron atoms in the nanoparticle core of each ferritin protein. Quantitative analysis shows that the nuclearity of iron atoms in the mineral core varies from a few hundred iron atoms to around 5000 atoms. Moreover, a relationship between the iron loading and iron core morphology is established, in which mineral core nucleates from a single nanoparticle, then grows along the protein shell before finally forming either a solid or hollow core structure
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