Diurnal variation of the melanin-concentrating hormone level in the hypothalamus.

Melanin-concentrating hormone (MCH), the neuropeptide produced mainly in the hypothalamus, plays an operative role in regulating food intake and the sleep/wake cycle. Considering that these physiological functions pursue diurnal variations, we checked whether the total hypothalamic MCH level depends on the time of the day. The aggregated MCH peptide content of the whole MCH neuron population was significantly higher at the end of the sleeping period (lights on), than at the end of the active period (lights off). This result, together with earlier observations, indicates that in contrast to the MCH gene expression, the level of MCH peptide is object of circadian variation in the hypothalamus.

An unexpected advantage of whiteness in horses: the most horsefly-proof horse has a depolarizing white coat.

White horses frequently suffer from malign skin cancer and visual deficiencies owing to their high sensitivity to the ultraviolet solar radiation. Furthermore, in the wild, white horses suffer a larger predation risk than dark individuals because they can more easily be detected. In spite of their greater vulnerability, white horses have been highly appreciated for centuries owing to their natural rarity. Here, we show that blood-sucking tabanid flies, known to transmit disease agents to mammals, are less attracted to white than dark horses. We also demonstrate that tabanids use reflected polarized light from the coat as a signal to find a host. The attraction of tabanids to mainly black and brown fur coats is explained by positive polarotaxis. As the host's colour determines its attractiveness to tabanids, this parameter has a strong influence on the parasite load of the host. Although we have studied only the tabanid-horse interaction, our results can probably be extrapolated to other host animals of polarotactic tabanids, as the reflection-polarization characteristics of the host's body surface are physically the same, and thus not species-dependent.

Experimental evidence that stripes do not cool zebras.

There are as many as 18 theories for the possible functions of the stripes of zebras, one of which is to cool the animal. We performed field experiments and thermographic measurements to investigate whether thermoregulation might work for zebra-striped bodies. A zebra body was modelled by water-filled metal barrels covered with horse, cattle and zebra hides and with various black, white, grey and striped patterns. The barrels were installed in the open air for four months while their core temperature was measured continuously. Using thermography, the temperature distributions of the barrel surfaces were compared to those of living zebras. The sunlit zebra-striped barrels reproduced well the surface temperature characteristics of sunlit zebras. We found that there were no significant core temperature differences between the striped and grey barrels, even on many hot days, independent of the air temperature and wind speed. The average core temperature of the barrels increased as follows: white cattle, grey cattle, real zebra, artificial zebra, grey horse, black cattle. Consequently, we demonstrate that zebra-striped coats do not keep the body cooler than grey coats challenging the hypothesis of a thermoregulatory role of zebra stripes.

Why do horseflies need polarization vision for host detection? Polarization helps tabanid flies to select sunlit dark host animals from the dark patches of the visual environment.

Horseflies (Tabanidae) are polarotactic, being attracted to linearly polarized light when searching for water or host animals. Although it is well known that horseflies prefer sunlit dark and strongly polarizing hosts, the reason for this preference is unknown. According to our hypothesis, horseflies use their polarization sensitivity to look for targets with higher degrees of polarization in their optical environment, which as a result facilitates detection of sunlit dark host animals. In this work, we tested this hypothesis. Using imaging polarimetry, we measured the reflection-polarization patterns of a dark host model and a living black cow under various illumination conditions and with different vegetation backgrounds. We focused on the intensity and degree of polarization of light originating from dark patches of vegetation and the dark model/cow. We compared the chances of successful host selection based on either intensity or degree of polarization of the target and the combination of these two parameters. We show that the use of polarization information considerably increases the effectiveness of visual detection of dark host animals even in front of sunny-shady-patchy vegetation. Differentiation between a weakly polarizing, shady (dark) vegetation region and a sunlit, highly polarizing dark host animal increases the efficiency of host search by horseflies.

Wall thickness of gas- and marrow-filled avian long bones: measurements on humeri, femora and tibiotarsi in crows (Corvus corone cornix) and magpies (Pica pica).

We studied how the ratio K of the internal to external diameter of gas- and marrow-filled avian long bones follows the biomechanical optima derived for tubular bones with minimum mass designed to fulfil various mechanical requirements. We evaluated radiographs of numerous humeri, femora and tibiotarsi in Corvus corone cornix and Pica pica. The K-values of the gas-filled humerus (K=0.78+/-0.03) and the marrow-filled femur (K=0.79+/-0.02) in Corvus are practically the same, while K of the marrow-filled tibiotarsus (K=0.71+/-0.04) is significantly smaller. The same is true for the gas-filled humerus (K=0.78+/-0.02) and the marrow-filled femur (K=0.77+/-0.02) and tibiotarsus (K=0.67+/-0.05) in Pica. K in Corvus is slightly larger than K in Pica, but the differences are statistically not significant. The standard deviation DeltaK of the tibiotarsi (DeltaK=0.04-0.05) is approximately two times as large as that of the humeri (DeltaK=0.02-0.03) and femora (DeltaK=0.02) in both species. Accepting the assumption of earlier authors that the ratio Q of the marrow to bone density is 0.5, our data show that the marrow-filled tibiotarsi of Corvus and Pica are optimized for stiffness, while the marrow-filled femora are far from any optimum. The relative wall thickness W=1-K of the gas-filled avian humeri studied is much larger than the theoretical optimum W*=1-K*=0.07, and thus these bones are thicker-walled than the optimal gas-filled tubular bone with minimum mass.

Testing the biomechanical optimality of the wall thickness of limb bones in the red fox (Vulpes vulpes).

The optimum for the ratio K of the internal to external diameter of a marrow-filled tubular bone with minimum mass designed to withstand a given type of strength (yield/fatigue, stiffness, fracture or impact) depends on Q = rhom/rhob only, where rhom and rhob are the densities of marrow and bone. With computer-assisted evaluation of radiographs of 62 femurs in the red fox (Vulpes vulpes) we measured the values of K. The mean and standard deviation of K are 0.68 and 0.036, and K changes in the rather wide range from 0.59 to 0.74. Accepting the assumption of earlier authors that Q = 0.50 or 0.44, our data would support the hypothesis that the fox femurs are optimized to withstand yield, fatigue or stiffness strengths. However, since the Q-values are unknown, the possibility cannot be excluded that any studied fox bone with an appropriately selected Q-value is optimized for any strength type. Assuming Q = 0.50 or 0.44, the relative mass increments mu of the investigated fox bones are smaller than 5% under all four mechanical conditions. The evolutionary relevance of such tiny mu-values is questionable.

Glial fibrillary acidic protein immunoreactivity in the rat suprachiasmatic nucleus: circadian changes and their seasonal dependence.

The pacemaker of the biological clock, the suprachiasmatic nucleus (SCN) of the hypothalamus, was studied in intact male rats to determine its immunoreactivity to glial fibrillary acidic protein (GFAP), a specific marker of astrocytes. Animals were kept under 12-h light-dark cycles in synchrony with day-night periods. Immunohistochemical reactions were carried out at midday and late at night in both winter (January) and summer (July). In winter, GFAP immunoreactivity was found to be low during the day and high at night. The findings were reversed in summer, when GFAP immunoreactivity was high during the day and low at night. Increased GFAP immunoreactivity appeared in the form of an abundance of thick immunopositive fibres rather than of cell bodies. This was interpreted as a hypertrophy of pre-existing astrocytes due to alternating photic stimulation conveyed by retinofugal fibres to the SCN. The observed seasonal reversal in the direction of GFAP oscillations raises the possibility that a circannual timer exists outside the SCN.

How does the relative wall thickness of human femora follow the biomechanical optima? An experimental study on mummies.

We studied how the ratio (K) of the internal:external diameter of human femora follows the biomechanical optima derived earlier by other researchers for marrow-filled tubular bones with circular cross section and minimum mass designed to withstand yield and fatigue, or stiffness, or bending fracture, or impact strengths. With evaluation of radiographs of 107 femora from 57 human mummies the values of K were measured. We found that K(posterior)=0.498+/-0.085 for the posterior radiographic view, and K(medial)=0.589+/-0.070 for the medial view with K(min)=0.345 and K(max)=0.783. The theoretical optima for K depend on the ratio (Q) of the marrow:bone density. Accepting the assumption of earlier authors that Q=0.50, our data show that human femora are optimised to withstand bending fracture, or yield and fatigue strengths. There were no sex-, age- and length-specific differences in K, and the means of K of the right and left femora of individuals were statistically not significantly different. The biomechanical optimization for K of human femora is not finely tuned. Compared with fox femora, K of human femora follows the biomechanical optimum to a much lesser extent. Although the relative wall thickness W=1-K of human femora are optimised, the very low relative mass increment due to deviation of K from the optimum and the considerable intraspecific variance of K make it probable that an accurate optimization of the relative wall thickness is irrelevant in humans.