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Simulation of a cold-stressed finger including the effects of wind, gloves, and cold-induced vasodilatation.

The thermal response of fingers exposed to cold weather conditions has been simulated. Energy balance equations were formulated, in a former study, for the tissue layers and the arterial, venous, and capillary blood vessels. The equations were solved by a finite difference scheme using the Thomas algorithm and the method of alternating directions. At this stage of development the model does not include any autonomic control functions. Model simulations assumed an electrical heating element to be embedded in the glove layers applied on the finger. A 1.3 W power input was calculated for maintaining finger temperatures at their pre-cold exposure level in a 0 degree C environment. Alternate assumptions of nutritional (low) and basal (high) blood flows in the finger demonstrated the dominance of this factor in maintaining finger temperatures at comfortable levels. Simulated exposures to still and windy air, at 4.17 m/s (15 km/h), indicated the profound chilling effects of wind on fingers in cold environments. Finally, the effects of variable blood flow in the finger, known as "cold-induced vasodilatation," were also investigated. Blood flow variations were assumed to be represented by periodic, symmetric triangular waves allowing for gradual opening-closing cycles of blood supply to the tip of the finger. Results of this part of the simulation were compared with measured records of bare finger temperatures. Good conformity was obtained for a plausible pattern of change in blood flow, which was assumed to be provided in its entirety to the tip of the finger alone.

Algorithms↗

Probability distributions for locations of calling animals, receivers, sound speeds, winds, and data from travel time differences.

A new nonlinear sequential Monte Carlo technique is used to estimate posterior probability distributions for the location of a calling animal, the locations of acoustic receivers, sound speeds, winds, and the differences in sonic travel time between pairs of receivers from measurements of those differences, while adopting realistic prior distributions of the variables. Other algorithms in the literature appear to be too inefficient to yield distributions for this large number of variables (up to 41) without recourse to a linear approximation. The new technique overcomes the computational inefficiency of other algorithms because it does not sequentially propagate the joint probability distribution of the variables between adjacent data. Instead, the lower and upper bounds of the distributions are propagated. The technique is applied to commonly encountered problems that were previously intractable such as estimating how accurately sound speed and poorly known initial locations of receivers can be estimated from the differences in sonic travel time from calling animals, while explicitly modeling distributions of all the variables in the problem. In both cases, the new technique yields one or two orders of magnitude improvements compared with initial uncertainties. The technique is suitable for accurately estimating receiver locations from animal calls.

Air↗

Virus transfer from surf to wind.

Bubbles in the sea surf adsorb and carry viruses to the surface where they are propelled into the air on tiny jets of seawater when the bubble bursts. The ejected jets become tiny drops of aerosol. The buble adsorption and virus concentration in the surf is analagous to industrial bubble levitation processes that concentrate metallic ores, enzymes, and finely divided organic crystals. Bubble levitation of viruses delibrately injected into the surf produced 200 times more virus per milliliter in the aerosol than were present in samples from the surf. Some aerosol drops created by the surf and carried by the wind fall out on the beach. The frequency of virus-bearing drops, that is, the number of plaques on seeded plates exposed on the beach, decreased exponentially with the distance downwind from the surf.

Aerosols↗

Wind speed limits to work under hot environments for clothed men.

Four heat-acclimated clothed young adult men exercised (treadmill) at metabolic rate of 191 W.m-2 (27% VO2 max), under five air temperatures (Ta) between 36 and 53 degrees C and three wind velocities (v), 1, 2, and 4 m.s-1, for 2 h. The 2nd h of each experiment involved progressive increases in the ambient vapor pressure (Pa) to force an upward inflection of the rectal temperature (Tre). The Tre point of inflection identified the critical Pa (Pcrit) for each Ta. The average mean skin temperature (Tsk = 36 degrees C for all Pcrit. Straight-line isotherms for Tsk = 36 degrees C, which agreed with the negative regressions of the Pcrit on Ta, represented the limits of exposure for Ta less than or equal to 44 degrees C. The slope characteristics of the isotherms corresponded with skin wettedness (w) of 0.94, 0.71, and 0.58, respectively, for v of 1, 2, and 4 m.s-1. For Ta greater than 44 degrees C the limit line corresponded with steeper negative regressions indicating a lower w than for Ta less than or equal to 44 degrees C. Despite the increase in the ambient evaporative capacity due to the higher v the limit lines describing exposure limits were not significantly different either at Ta less than or equal to 44 degrees C for v of 2 and 4 m.s-1 or at Ta greater than 44 degrees C for all three v.

Acclimatization↗

Metabolic power of European starlings Sturnus vulgaris during flight in a wind tunnel, estimated from heat transfer modelling, doubly labelled water and mask respirometry.

It is technically demanding to measure the energetic cost of animal flight. Each of the previously available techniques has some disadvantage as well advantages. We compared measurements of the energetic cost of flight in a wind tunnel by four European starlings Sturnus vulgaris made using three independent techniques: heat transfer modelling, doubly labelled water (DLW) and mask respirometry. We based our heat transfer model on thermal images of the surface temperature of the birds and air flow past the body and wings calculated from wing beat kinematics. Metabolic power was not sensitive to uncertainty in the value of efficiency when estimated from heat transfer modelling. A change in the assumed value of whole animal efficiency from 0.19 to 0.07 (the range of estimates in previous studies) only altered metabolic power predicted from heat transfer modelling by 13%. The same change in the assumed value of efficiency would cause a 2.7-fold change in metabolic power if it were predicted from mechanical power. Metabolic power did not differ significantly between measurements made using the three techniques when we assumed an efficiency in the range 0.11-0.19, although the DLW results appeared to form a U-shaped power-speed curve while the heat transfer model and respirometry results increased linearly with speed. This is the first time that techniques for determining metabolic power have been compared using data from the same birds flying under the same conditions. Our data provide reassurance that all the techniques produce similar results and suggest that heat transfer modelling may be a useful method for estimating metabolic rate.

Analysis of Variance↗

Horizontal flight of a swallow (Hirundo rustica) observed in a wind tunnel, with a new method for directly measuring mechanical power.

A swallow flying in the Lund wind tunnel was observed from the side and from behind, by two synchronised high-speed video cameras. The side-view camera provided a record of the vertical position of a white mark, applied to the feathers behind and below the eye, from which the vertical acceleration was obtained. The rear-view camera provided measurements of the mean angle of the left and right humeri above horizontal. From these data, the force acting on the body, the moment applied by each pectoralis muscle to the humerus and the rotation of the humerus were estimated and used to analyse the time course of a number of variables, including the work done by the muscles in each wing beat. The average mechanical power turned out to be more than that predicted on the basis of current estimates of body drag coefficient and profile power ratio, possibly because the bird was not flying steadily in a minimum-drag configuration. We hope to develop the method further by correlating the mechanical measurements with observations of the vortex wake and to apply it to birds that have been conditioned to hold a constant position in the test section.

Animals↗

Flexibility in flight behaviour of barn swallows (Hirundo rustica) and house martins (Delichon urbica) tested in a wind tunnel.

The flight behaviour of barn swallows (Hirundo rustica) and house martins (Delichon urbica) was tested in a wind tunnel at 15 combinations of flight angles and speeds. In contrast to that of most other small passerines, the intermittent flight of hirundines rarely consists of regular patterns of flapping and rest phases. To vary mechanical power output, both species used intermittent flight, controlling the number of single, pulse-like wingbeats per unit time. House martins in descent tended to concentrate their wingbeats into bursts and performed true gliding flight during rest phases. Barn swallows mainly performed partial bounds during brief interruptions of upstrokes, which they progressively prolonged with decreasing flight angle. Thus, identification of distinct flapping phases to calculate wingbeat frequencies was not feasible. Instead, an effective wingbeat frequency for flight intervals of 20 s, including partial bounds, was introduced. The effective wingbeat frequencies of house martins (N=3) ranged from 2 to 10.5 s(-1), those of barn swallows (N=4) from 2.5 to 8.5 s(-1). In both hirundine species, effective wingbeat frequency was found to decrease almost linearly with decreasing flight angle. With changes in air speed, wingbeat frequency varied according to a U-shaped curve, suggesting a minimum power speed of roughly 9 m s(-1). The duration of the down- and upstrokes varied systematically depending on flight angle and air speed.

Animals↗

Wind direction coding in the cockroach escape response: winner does not take all.

Cockroaches respond to the approach of a predator by turning away and then running. Three bilateral pairs of giant interneurons are involved in determining the direction of the sensory stimulus and setting the turn direction. Each of these six interneurons has a different directional response to wind stimuli. We have tested whether these six cells use a winner-take-all mechanism to perform this directional determination: that is, each of these cells suppressing the motor response that each of the other cells promotes. Such a mechanism is found in similar behaviors of some other animals. By adding spikes to identified giant interneurons through intracellular stimulation during the sensory-induced behavior and analyzing the resulting directional leg movements, we find that a winner-take-all is not used in this system. Rather, directional determination appears to be based on collaborative calculation of direction by the giant interneurons as a group.

Action Potentials↗

Reducing hydraulic short-circuiting in maturation ponds to maximize pathogen removal using channels and wind breaks.

This paper reports the impact of four sequential maturation pond interventions on the removal of thermotolerant "faecal" coliform bacteria at a full scale WSP system in tropical Colombia. Each intervention was designed to increase hydraulic retention time and was followed by continuous physico-chemical logging and meteorological monitoring, and simultaneous tracer studies to define hydraulic retention time, flow paths and dispersion. Inlet and outlet monitoring showed that, primarily due to hydraulic short-circuiting, the open maturation pond only achieved a 90% reduction in thermotolerant "faecal" coliforms. By contrast, an in-pond batch decay rate study for thermotolerant faecal coliforms showed that a 1 log (90%) reduction was achieved every 24 hours for 4 days at 26 degrees C, so that the maximum theoretical efficiency would be a 2.6 log reduction (99.7%) if hydraulic efficiency was perfect for plug flow. The second intervention was the conversion of the maturation pond to a parallel series of three open channels to attempt to control short-circuiting and convert to plug flow. The channels raised performance to 96%. The introduction of top baffles, at the end of the first and second channels, to attempt to further reduce the effect of surface and sub-surface flow on short-circuiting, actually reduced performance to 92.64%, and were removed. The final intervention, a 2.1 m high wind break around the maturation channels raised efficiency to 98.13%; this performance is almost a half log (0.47) greater than the efficiency (95.1%) predicted from Marais' equation for a completely mixed reactor, and 0.77 log greater than recorded in the open pond. The results have fundamental implications for improving WSP efficiency, for meeting re-use guidelines, for savings in land area and improvement of design of WSPs; they also highlight short-comings in the indiscriminate use of the Marais design equation for faecal coliform removal.

Colombia↗

[Release of radioactive aerosols from the object "shelter" during strong winds].

Results of measurements of radionuclide and disperse compositions of aerosols in ventilation system "Bypass" of the object "Shelter" of the Chernobyl NPP are presented. The Bypass is used for releasing contaminated air from the destroyed reactor of Block-IV to the atmosphere. In aerosols, the experimentally found ratio of 137Cs concentration to the sum of beta-emitting radionuclides more than 1.5 times exceeds the calculated ratio for nuclear fuel (in December, 2003). Using the data of meteorological station "Chornobyl", which situated 15 km SE from the Chernobyl NPP, we found that the wind with mean velocity of 4-5 m/sec or more and gusts of 10-11 m/sec led to increasing the aerosol concentration in the Bypass by more than power of magnitude. With the help of filter pack technique sizes of aerosol particles--the carriers of Chernobyl's radioactivity--were measured. It was found that the range of activity median aerodynamical diameter (AMAD) is 2-5 microns.

Aerosols↗

Dust pollution: effect of grain size in the transportation and deposition by wind.

Study of movement of dust and sand by wind to far off places is seldomly reported in literature. To overcome this problem, modelling was done and investigations were carried out under reasonable physical constraints. After conducting a theoretical analysis, an outcome is reported in this paper which cues for a need of further study.

Air Pollutants↗

Airborne pollen sampling in Manoa Valley, Hawaii: effect of rain, humidity and wind.

Kramer-Collins pollen sampling was conducted over 24 hours for 25 consecutive months at two valley sites in Honolulu. Of 1,059 expected samples, 699 (66.0%) were collected. Only 25 were considered excellent, i.e., eight three-hour collection bands. Twenty eight were considered good, ie., two to six bands. The difficulties in the study were associated with the weather directly (17.5%), the power source (3.9%), inadequancy of the samplers (63.1%) and the inexperience of technicians (15.3%). Sampler problems were also indirectly attributable to the high humidity, rain and wind, which differed at the two sites.

Air Movements↗

A two-dimensional water-quality model for a winding and topographically complicated river.

In this paper, a two-dimensional numerical calculation algorithm for water-quality modeling is presented. The algorithm is designed specifically for river systems with complicated geometric conditions. When velocity field data of the river are not available, the numerical calculation algorithm for the water-quality modeling can be used to project river-water quality by using a topographic map of the river course and a finite element method. The calculation results of the water-quality model can show the concentration fields of various pollutants. The water-quality model was applied to a case-study in the Hengyang City section of Xiangjiang River in Hunan Province, China. The river under consideration is winding and has an isle between two branches. In 1995, Chinese government secured a World Bank loan to conduct a Waterways Project in the study region. It was expected that construction works in the river section might affect water quality. Given that the project would change the hydrological regime of the river system and discharges, and so would affect water quality, there would be a need for model results that would predict the water-quality impacts of the Waterways Project. In particular, the study intended to apply the model to identify changes in river-water quality associated with the construction of Dayuandu navigation key project. It is hoped that the numerical calculation algorithm for the water-quality modeling presented in this paper can also be applied to other shallow rivers with similar topographical conditions.

Algorithms↗

Output connections of a wind sensitive interneurone with motor neurones innervating flight steering muscles in the locust.

The output connections of a bilaterally symmetrical pair of wind-sensitive interneurones (called A4I1) were determined in a non-flying locust (Schistocerca gregaria). Direct inputs from sensory neurones of specific prosternal and head hairs initiate spikes in these interneurones in the prothoracic ganglion. The interneurone with its axon in the right connective makes direct, excitatory connections with the two mesothoracic motor neurones innervating the pleuroaxillary (pleuroalar, M85) muscle of the right forewing, but not with the comparable motor neurones of the left forewing. The connections can evoke motor spikes. The interneurones also exert a powerful, but indirect effect on the homologous metathoracic pleuroaxillary motor neurones (muscle 114), and a weaker, indirect effect on subalar motor neurones of the hindwings. No connections or effects were found with other flight motor neurones, or motor neurones innervating hindleg muscles, including common inhibitor 1 which also innervates the pleuroaxillary muscle. One thoracic interneurone with its cell body in the right half of the mesothoracic ganglion and with its axon projecting ipsilaterally to the metathoracic ganglion receives a direct input from the right A4I1 interneurone. These restricted output connections suggest a role for the A4I1 interneurones in flight steering.

Animals↗

Sensory projections from the wind-sensitive head hairs of the locust Schistocerca gregaria. Distribution in the central nervous system.

The neurones from the wind-sensitive hairs on the locust head have been filled with cobalt chloride and intensified with silver. All the neurones project through the brain to the suboesophageal ganglion, some continue to the prothoracic ganglion and a few as far as the mesothoracic ganglion. Three different types of projection are described and a regrouping is proposed of Weis-Fogh's five hair fields into three areas. The distribution of the neurones from these areas is described in relation to other structures in the ganglion and is discussed in relation to the function of the hair fields in stability control and grooming.

Animals↗