Biology subjects

Luro, A. B.

Publications and source records attributed to Luro, A. B..

3 recordsLinked to original sources

bioRxiv2021

Pressure for rapid and accurate mate recognition promotes avian-perceived plumage sexual dichromatism in true thrushes (genus: Turdus)

Ecological conditions limiting the time to find a compatible mate or increasing the difficulty in doing so likely promote the evolution of traits used for species and mate recognition. Conspicuous traits that signal an individuals species, sex, and breeding status reduce the challenge of identifying a compatible conspecific mate, and should be more common in migratory rather than sedentary species, species with shorter breeding seasons, and species breeding under high sympatry with many closely-related heterospecifics. Here, we tested this recognition hypothesis for promoting plumage sexual dichromatism in the true thrushes (Turdus spp.), a large and diverse genus of passerine birds. We used receptor-noise limited models of avian vision to quantify avian-perceived chromatic and achromatic visual contrasts between male and female plumage patches and tested the influence of breeding season length, spatial distribution, and sympatry with other Turdus species on plumage dichromatism. As predicted, we found that 1) true thrush species with migratory behaviour have greater plumage sexual dichromatism than non-migratory species, 2) species with longer breeding seasons have less plumage sexual dichromatism, and 3) greater numbers of Turdus thrush species breeding in sympatry is associated with more plumage sexual dichromatism. These results suggest that social recognition systems, including species and mate recognition, play a prominent role in the evolution of plumage sexual dichromatism in true thrushes.

evolutionary biology↗

bioRxiv2020

Visual acuity and egg spatial chromatic contrast predict egg rejection behavior of American robins

Color and spatial vision are critical for recognition and discrimination tasks affecting fitness, including finding food and mates and recognizing offspring. For example, as a counter defense to avoid the cost of raising the unrelated offspring of obligate interspecific avian brood parasites, many host species routinely view, recognize, and remove the foreign egg(s) from their nests. Recent research has shown that host species visually attend to both chromatic and spatial pattern features of eggs; yet how hosts simultaneously integrate these features together when recognizing eggs remains an open question. Here, we tested egg rejection responses of American robins (Turdus migratorius) using a range of 3D-printed model eggs covered with blue and yellow checkered patterns differing in relative square sizes. We predicted that robins would reject a model egg if they could visually resolve the blue and yellow squares as separate features or accept it if the squares blended together and appeared similar in color to the natural blue-green color of robin eggs as perceived by the avian visual system. As predicted, the probability of robins rejecting a model egg increased with greater sizes of its blue and yellow squares. Our results suggest that chromatic visual acuity and viewing distance have the potential to limit the ability of a bird to recognize a foreign egg in its nest, thus providing a limitation to host egg recognition that obligate interspecific avian brood parasites may exploit.

animal behavior and cognition↗

bioRxiv2018

Avian diet and foraging ecology constrain foreign egg recognition and rejection

Egg rejection is the most common defense against avian brood parasitism in which the host either removes the parasitic egg or deserts the parasitized clutch. The ability to recognize and reject a parasitic egg depends on bill morphology, sensory systems, and cognition, all of which are also shaped by other selective processes, such as foraging. This begs the question whether specific phenotypes associated with different foraging strategies and diets may constrain or facilitate egg recognition and rejection. Here, we propose a novel hypothesis that host species phenotypes related to foraging ecology and diet impose morphological and sensory constraints on the evolution of egg rejection. We conducted a comparative analysis of the adult diets and egg rejection rates of 165 current host and non-host species and found species that consume an animal and fruit dominated diet rather than seeds and grains, forage arboreally rather than aerially, and possess relatively larger body sizes have significantly higher egg rejection rates. As predicted, these results suggest that phenotypes related to specific diets and foraging strategies may differentially constrain or facilitate evolution of host egg rejection defenses against avian brood parasitism.

animal behavior and cognition↗