Light has a significant impact on many aspects of avian biology, physiology and behaviour. An increasing number of studies show that illumination may positively influences birds’ offspring fitness by e.g. acceleration of embryo development, stimulation of skeleton growth or regulation of circadian rhythm. Because nest cavities have especially low illumination, suitable light levels may be especially important for species which nest there. We may therefore expect that birds breeding in relatively dim conditions should prefer brighter nest sites and/or evolve behavioral mechanisms to secure sufficient light levels in the nest. Using nest boxes with modified internal illumination, we experimentally tested whether light regime is a cue for nest site selection of secondary cavity-nesting species. Additionally, we investigated whether nest building strategies are tuned to internal illumination. Our results demonstrate that, nest boxes with elevated illumination were chosen twice as often as dark nest boxes. Moreover, birds built higher nests in dark nest boxes than birds in boxes with elevated illumination, which suggests a mechanism of compensating for low light conditions. Our results provide the first experimental support for the idea that nest site choice and nest building behaviour in cavity-nesting birds are influenced by ambient illumination.

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Nocturnal bird species possess special adaptations to maximise visual efficiency under low light levels. However, some typically diurnal species also experience low‐light environments. For example, cavity‐nesting Passerines raise broods in dark cavities and search for food in light‐abundant surroundings. It is not clear whether they possess special adaptations for low light vision or breed in cavities at the expense of impaired parental care. In this study, we tested whether light conditions affect the provisioning efficiency of great tits. We experimentally tested how the level of natural and artificially increased illumination inside nest boxes affects parental feeding duration, frequency and timing. We monitored 15‐h of provisioning activity of great tit parents when nestlings were day seven post hatch. We used traditional ‘dark’ nest boxes and ‘bright’ nest boxes with increased illumination obtained by using semi‐transparent plastic windows. The duration of single feedings were, on average, shorter in brightened nest boxes compared to dark ones. This difference tended to be higher early in the morning and in the evening, when the illumination in dark nest boxes was the lowest. Nest box type, however, did not influence feeding frequency or times of the onset and the end of feeding. Our findings provide new evidence for impaired efficiency of parental care due to lowered light conditions. Further research is needed to test whether prolonged feeding duration has negative effects on adult time budgets and nestling energy expenditures.

Surveys of terrestrial microinvertebrate morphometry, especially spatial patterns of body size at wider geographical scales, including the polar regions, are very scarce. In this study, we focused on Tardigrada, common limno-terrestrial microinvertebrates. Considering Bergmann's rule, originally formulated for endothermic animals, we tested the hypothesis that body length of limno-terrestrial tardigrades augments with increasing latitude and decreasing temperature. Since some of our sampling areas adjoined seabird colonies, we also explored the effects of nutrients from seabird guano deposits. Individual body length of Testechiniscus spitsbergensis was measured in populations obtained from seven localities distributed along a latitudinal gradient extending from 45°N (northern Italy) to 79°N (northern Svalbard), and for Pilatobius recamieri from three localities in Svalbard (77°N-80°N). Considering both latitude and proximity to a seabird colony there were significant effects of locality on the body length of T. spitsbergensis; however, no clear pattern of increasing individual body size with increasing latitude could be detected. Immense differences in body size may be a signal for cryptic species diversity within this genus. No effect of latitude, or proximity to a seabird colony, on the body length of Arctic populations of P. recamieri was documented. Evidently, there is no tendency towards body size increase along the latitudinal gradient in either T. spitsbergensis or P. recamieri. Our study, and recent literature, indicates that larger body size in polar regions reported for several groups of micro-fauna may be a taxon-dependent response, and cannot be taken as a universally applicable rule for limnoterrestrial animals.

Our current understanding of the function of coordinated acoustic displays usually comes from studies conducted over a short period of the breeding season. However, the function of particular types of vocalizations may vary according to sex and context, and such displays can extend beyond the time of reproduction. To fully understand this phenomenon, analyses of year-round singing behavior are required. In the current study, we focused on a small, year-round territorial Afrotropical songbird, Chubb’s Cisticola (Cisticola chubbi). We analyzed the structure of songs during the breeding season as well as year-round changes in the proportion of solos, duets, and choruses to investigate the potential function(s) of each type of vocalization. We found that: (1) females produced whistling notes, while males generated trilling ones; (2) up to five individuals formed coordinated choruses, and (3) individuals were always near to each other during cooperative singing. Over the course of a year, the majority of syllables recorded were duets (82%), with rarer choruses (16%) and extremely rare solos (2%). Outside of the breeding season, males produced the most solos, while females produced more at the beginning of the breeding season. The proportion of choruses was highest at the end of breeding season. Frequent year-round production of duets and choruses strongly supports territory defense as the main function of joint singing, while the highest proportion of choruses at the end of the breeding season suggests that offspring take part in the chorus. To better understand cooperative singing, it is essential to extend our looking beyond the breeding season.