A total of 550 fertile chicken eggs (White Leghorn) were exposed to a radiofrequency (RF) electromagnetic field of 1.25 GHz (continuous wave) at six different power flux densities in the range of 9.0-0.75 mW/cm(2). The eggs were exposed either continuously throughout the whole 21 days of incubation (long-term exposure) or in a short-term exposure (1-2 h/day). The temperatures of the embryonic tissue and the amniotic fluid, respectively, were measured with inserted temperature probes. This study was designed to investigate the relationship between exposure and temperature changes in exposed tissues, without considering biological and medical effects. This knowledge is of general interest for studies of nonthermic teratological or embryo-lethal effects of exposure to electromagnetic fields (EMFs). Throughout the entire 21 days of embryonic development, the mean temperature increases in the eggs during the exposure were found to be up to 0.25 degrees C for a power flux density of 1.25 mW/cm(2) and increased to 2.3 degrees C for 9.0 mW/cm(2). The corresponding maximum whole-body SARs for the embryos over the 21 days of embryonic development were 1.45 and 10.44 W/kg, respectively. At 0.75 mW/cm(2) (0.87 W/kg) the extent of the RF-field induced hyperthermia was within the measurement accuracy (+/-0.1 degrees C) of the temperature probes used in the tests. The field-induced temperature increase was greatest in the first week of incubation and was less pronounced in the last (third) week before hatching. In both the short- and the long-term exposures, the temperature of the exposed tissue and the amniotic fluid, respectively, reached its maximum (asymptotic) approximately 40-50 min after the RF field was switched on. After the field was switched off, the temperature inside the exposed eggs returned to its initial value within 40-50 min.
After pinealectomy, young pied flycatchers tested in the geomagnetic field have been found to be disoriented. In order to examine the possible role of the pineal hormone melatonin, handraised flycatchers were pinealectomized (PX) at the age of 8 weeks. From the day of operation onward, the PXMEL group received 100 µg of melatonin every evening 1 h before darkness, the PXSOL group was injected with the solvent only, and the PX group was untreated. Unoperated birds served as controls. During the following autumn migration, the birds were tested for directional preference in the local geomagnetic field, in the absence of visual cues. The controls were oriented in the species-specific southwesterly direction; pinealectomized birds without additional melatonin (PXSOL, PX) did not show directional preferences. The PXMEL birds that had received daily injections of melatonin also showed significant southwesterly tendencies; their orientation did not differ from that of the controls. This indicates that melatonin is involved in migratory orientation, either in the processes of expressing the genetically encoded information on the migratory course as a direction with respect to the geomagnetic field or in the time programme controlling the specific migratory direction at a given time.
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