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Loning, H.

Publications and source records attributed to Loning, H..

3 recordsLinked to original sources

Communication networks of wild zebra finches (Taeniopygia castanotis)

Communication networks are widespread across species, permitting information flow and facilitating social connections across space and time. In birds, communication networks are well studied in territorial species with long-range songs connecting individuals across space, where unintended listeners extract information from others signalling interactions. Yet, acoustic signals also play important social roles at short range, forming communication networks that connect individuals within larger social units. Wild zebra finches (Taeniopygia castanotis) provide a unique model system to examine such communication networks in a non-territorial species. Zebra finches breed in loose colonies in the Australian arid zone, move around in pairs or small groups, and gather at social hotspots, thus forming dynamic, potentially multi-level, societies. Here, we quantified singing activity and connectivity using the individually distinctive male song recorded at two breeding sub-colonies and three social hotspots over one to three days. We identified 1,835 song bouts from 163 males based on spectrographic similarities and we assessed within and between individual song assignments with a deep learning model (BirdNET). We constructed communication networks based on temporal singing proximity at shared locations: social hotspots and breeding colonies. We reveal higher singing activity at social hotspots than at breeding sites, with almost no dawn song at either site. Singing peaked later, yet at different times of day between breeding sites and social hotspots. Communication networks, with distinct males singing in close temporal proximity, were apparent in both contexts, with larger networks at hotspots. These networks included some individuals that sang together repeatedly at either site, but overall networks were not strongly nested, with only very few males maintaining associations across breeding colonies and hotspots. These networks may facilitate synchronised foraging and breeding as adaptations to a harsh and unpredictable environment. Additionally, our approach offers a novel road map for widening the understanding of communication networks.

animal behavior and cognition↗

Zebra finches produce intralaryngeal laminar flow whistles during panting

Birds and mammals converged upon the same physical mechanism of vocal fold vibration to produce their broad range of voiced sounds critical to communication1. The frequency range of vocal fold vibration is limited per species by biophysical constraints to 3-4 octaves2. However, recent work reported vocalizations in zebra finches with apparent fundamental frequencies of 7-11 kHz3 that far exceed the range of regular calls and song (0.5-1.5 kHz)4,5. These "heat" or "incubation" calls are suggested to have close-range communicative relevance in the global temperature rise context3,6, but their acoustics are poorly described and by what biophysical mechanism they are produced remains unknown. We recorded heat calls in adult zebra finches in vivo and show they are extremely soft, frequency-modulated calls with source levels of 13.9 {+/-} 3.3 dB SPL at one meter with dominant frequencies of 6.8 {+/-} 0.6 kHz. Through a series of in vitro experiments, we establish that these calls are aerodynamic whistles produced inside the avian larynx, not syrinx, during inspiration. Respiratory air flow during whistle production is an order of magnitude higher than song and consistent with thermal panting for evaporative cooling6,7. Laryngeal geometry and dimensional flow analysis suggest that these whistles are laminar flow whistles that occur when a flow boundary layer is in a transition phase from laminar to turbulent flows8,9. Birds, like some rodents10-12, are thus able to produce both voiced sounds and aerodynamical whistles in their vocal tract.

physiology↗

Constant companions: Wild zebra finch pairs display extreme spatial cohesion

Many animals maintain long-term monogamous partnerships, but the extent to which partners associate varies substantially and has implications for the scope of cooperation between pair members. Zebra finches (Taeniopygia castanosis) are monogamously paired for life and maintain continuous partnerships, raising questions as to if and how they maintain pair cohesion despite being nonterritorial and having only short-range acoustic signals. While zebra finches are the best studied songbird in captivity, their social and spatial behaviour in the wild is poorly understood. Determining pair cohesion in songbirds to date has almost exclusively been studied at specific locations where pairs would be expected to meet, such as nesting or feeding sites, without quantifying broader movements. Here, we used solar-powered automated tracking to simultaneously monitor the movements of radio-tagged zebra finch pairs during periods with breeding activity. We reveal extremely high spatial cohesion with pairs using nearly identical home ranges and maintaining close spatial proximity across large areas. This characterisation of extremely high spatio-temporal coordination of zebra finch pairs provides important insights into the operation and benefits of monogamous relationships in highly mobile taxa, such as birds.

animal behavior and cognition↗