118 research outputs found

    Formation of Micropatches by Zooplankton-Driven Microturbulences

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    The distribution and behavior of tintinnids Stenosernella nucula have been measured in situ within a microlayer formed by 39 million individuals⋅liter–1 with an optical particle counting- and imaging-system. The parallel propulsions of the many animals add up and drive strong downwelling water currents. Preliminary results for swimming-speeds, -directions and organism-distributions are presented. Probably due to gyrotaxis (Kessler, 1985, 1986) or some unknown bio/physical processes the organisms are focused into their self-generated velocity profile. Similar phenomena have been described for very dense plankton cultures as “bioconvection” (Childress et al., 1975a, 1975b; Platt, 1961; Plesset and Winet, 1974; Plesset et al., 1975). The micropatches are 2–4 mm wide and 8–340 mm deep with organism concentrations up to 215 million tintinnids⋅liter–1. The flows form small convection cells similar to Langmuir- or Benard-cells with distances between the patches of 8–30 mm. At the edge of the downwelling areas water velocity increases from near zero to 2–3 mm per s over a vertical distance of less than 1 mm resulting in considerable shear. Some ecological consequences of these microturbulences and microdistributions for predator-prey relationships and particle transports in eutrophic estuaries are discussed

    In situ investigations on the respiration and behaviour of the eelpout Zoarces viviparus under short-term hypoxia

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    Respiration and activity of eelpouts Zoarces viviparus L. were measured in an underwater respiration chamber in Kiel Bay (Germany) under short-term hypoxia. Respiration and swimming activity both declined almost continuously with decreasing oxygen saturation..

    Size dissociation in krill swarms

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    Innermost stable circular orbits around magnetized rotating massive stars

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    In 1998, Shibata and Sasaki [Phys. Rev. D 58, 104011 (1998)] presented an approximate analytical formula for the radius of the innermost stable circular orbit (ISCO) of a neutral test particle around a massive, rotating and deformed source. In the present paper, we generalize their expression by including the magnetic dipole moment. We show that our approximate analytical formulas are accurate enough by comparing them with the six-parametric exact solution calculated by Pach\'on et. al. [Phys. Rev. D 73, 104038 (2006)] along with the numerical data presented by Berti and Stergioulas [MNRAS 350, 1416 (2004)] for realistic neutron stars. As a main result, we find that in general, the radius at ISCO exhibits a decreasing behavior with increasing magnetic field. However, for magnetic fields below 100GT the variation of the radius at ISCO is negligible and hence the non-magnetized approximate expression can be used. In addition, we derive approximate analytical formulas for angular velocity, energy and angular momentum of the test particle at ISCO.Comment: 8 pages, 3 figure

    Life in a warm deep sea: routine activity and burst swimming performance of the shrimp Acanthephyra eximia in the abyssal Mediterranean

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    Measurements of routine swimming speed, "tail-flip'' escape responses, and oxygen consumptions were made of the deep-sea shrimp Acanthephyra eximia using autonomous landers in the Rhodos Basin at depths of up to 4,400 m and temperatures of 13 - 14.5 degrees C. Routine swimming speeds at 4,200 m averaged 0.18 m s(-1) or 3.09 body lengths s(-1), approximately double those of functionally similar oceanic scavengers. During escape responses peak accelerations of 23 m s(-2) or 630.6 body lengths s(-2) were recorded, with animals reaching speeds of 1.61 m s(-1) or 34.8 body lengths s(-2). When compared to shallow-water decapods at similar temperatures these values are low for a lightly calcified shrimp such as A. eximia despite a maximum muscle mass specific power output of 90.0 W kg(-1). A preliminary oxygen consumption measurement indicated similar rates to those of oceanic crustacean scavengers and shallower-living Mediterranean crustaceans once size and temperature had been taken into account. These animals appear to have high routine swimming speeds but low burst muscle performances. This suite of traits can be accounted for by high competition for limited resources in the eastern Mediterranean, but low selective pressure for burst swimming due to reductions in predator pressure

    Early Measles Vaccination During an Outbreak in the Netherlands: Short-Term and Long-Term Decreases in Antibody Respo

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    Background. The majority of infants will not be protected by maternal antibodies until their first measles vaccination, between 12 and 15 months of age. This provides incentive to reduce the age at measles vaccination, but immunological consequences are insufficiently understood, and long-term effects are largely unknown. Methods. A total of 79 infants who received early measles vaccination between 6 and 12 months age and a second dose at 14 months of age were compared to 44 children in a control group who received 1 dose at 14 months of age. Measles virus–specific neutralizing antibody concentrations and avidity were determined up to 4 years of age. Results. Infants who first received measles vaccination before 12 months of age had a long-term decrease in the concentration and avidity of measles virus–specific neutralizing antibodies, compared with infants in the control group. For 11.1% of children with a first dose before 9 months of age, antibody levels at 4 years of age had dropped below the cutoff for clinical protection. Conclusions. Early measles vaccination provides immediate protection in the majority of infants but yields a long-term decrease in neutralizing antibody responses, compared to vaccination at a later age. Additional vaccination at 14 months of age does not improve this. Over the long term, this may result in an increasing number of children susceptible to measles

    Feeding behavior of the ctenophore Thalassocalyce inconstans : revision of anatomy of the order Thalassocalycida

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    © 2009 The Authors. This article is distributed under the terms of the Creative Commons Attribution Noncommercial License. The definitive version was published in Marine Biology 156 (2009): 1049-1056, doi:10.1007/s00227-009-1149-6.Behavioral observations using a remotely operated vehicle (ROV) in the Gulf of California in March, 2003, provided insights into the vertical distribution, feeding and anatomy of the rare and delicate ctenophore Thalassocalyce inconstans. Additional archived ROV video records from the Monterey Bay Aquarium Research Institute of 288 sightings of T. inconstans and 2,437 individual observations of euphausiids in the Gulf of California and Monterey Canyon between 1989 and 2005 were examined to determine ctenophore and euphausiid prey depth distributions with respect to temperature and dissolved oxygen concentration [dO]. In the Gulf of California most ctenophores (96.9%) were above 350 m, the top of the oxygen minimum layer. In Monterey Canyon the ctenophores were more widely distributed throughout the water column, including the hypoxic zone, to depths as great as 3,500 m. Computer-aided behavioral analysis of two video records of the capture of euphausiids by T. inconstans showed that the ctenophore contracted its bell almost instantly (0.5 s), transforming its flattened, hemispherical resting shape into a closed bi-lobed globe in which seawater and prey were engulfed. Euphausiids entrapped within the globe displayed a previously undescribed escape response for krill (‘probing behavior’), in which they hovered and gently probed the inner surfaces of the globe with antennae without stimulating further contraction by the ctenophore. Such rapid bell contraction could be effected only by a peripheral sphincter muscle even though the presence of circumferential ring musculature was unknown for the Phylum Ctenophora. Thereafter, several live T. inconstans were collected by hand off Barbados and microscopic observations confirmed that assumption.Supported by the David and Lucile Packard Foundation and NOAA Grant #NA06OAR4600091
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