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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.

Many bird species have experienced short- or long-term population declines. However, the mechanisms and reasons underlying such negative changes are often not fully understood, making it difficult to identify effective conservation measures to recover populations. In this study, we focused on local changes in the abundance and distribution of calling male Corncrakes Crex crex in relation to: (1) within- and between-season site fidelity of adult males, (2) spatial distribution of territories in consecutive years and (3) the effect of habitat conditions on population size. We counted the number of calling males at ten randomly selected study plots (1 km2) in 2014–2018. Additionally, males were caught and individually marked in years 2015–2017. We found significant between-year changes in Corncrake abundance, from a 34% decrease to a 21% increase. On average, 32% of males established territories in the same locations as males recorded in the previous year. Breeding site fidelity was very low, with only 2–5% of males recaptured in the following year. Males selected areas characterized by higher values of NDVI (Normalized Difference Vegetation Index–higher values indicate more biomass) than on average within the study area. Population size in a particular year was significantly affected by the NDVI of the previous year but not by the NDVI in the current breeding season. We suppose that Corncrakes may exhibit a nomadic breeding behavior, and settle at territories when they encounter optimal habitat conditions. Moreover, as population size was negatively correlated with habitat conditions at the beginning of the previous breeding season, we suppose that local population changes may reflect more general trends in a whole population rather than local breeding success. Therefore, we highlight the need for better knowledge of Corncrake dispersal within the main European population and for the coordination of monitoring and conservation efforts, especially in those regions where most Corncrakes breed.

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