How do parents recognize their offspring when the cost of making a recognition error is high? Avian brood parasite-host systems have been used to address this question because of the high cost of parasitism to host fitness. We discovered that superb fairy-wren (Malurus cyaneus) females call to their eggs, and upon hatching, nestlings produce begging calls with key elements from their mother's "incubation call." Cross-fostering experiments showed highest similarity between foster mother and nestling calls, intermediate similarity with genetic mothers, and least similarity with parasitic Horsfield's bronze-cuckoo (Chalcites basalis) nestlings. Playback experiments showed that adults respond to the begging calls of offspring hatched in their own nest and respond less to calls of other wren or cuckoo nestlings. We conclude that wrens use a parent-specific password learned embryonically to shape call similarity with their own young and thereby detect foreign cuckoo nestlings.
Species hybridization can lead to fitness costs, species collapse, and novel evolutionary trajectories in changing environments. Hybridization is predicted to be more common when environmental conditions change rapidly. Here, we test patterns of hybridization in three sympatric tree finch species (small tree finch Camarhynchus parvulus, medium tree finch Camarhynchus pauper, and large tree finch: Camarhynchus psittacula) that are currently recognized on Floreana Island, Galápagos Archipelago. Genetic analysis of microsatellite data from contemporary samples showed two genetic populations and one hybrid cluster in both 2005 and 2010; hybrid individuals were derived from genetic population 1 (small morph) and genetic population 2 (large morph). Females of the large and rare species were more likely to pair with males of the small common species. Finch populations differed in morphology in 1852-1906 compared with 2005/2010. An unsupervised clustering method showed (a) support for three morphological clusters in the historical tree finch sample (1852-1906), which is consistent with current species recognition; (b) support for two or three morphological clusters in 2005 with some (19%) hybridization; and (c) support for just two morphological clusters in 2010 with frequent (41%) hybridization. We discuss these findings in relation to species demarcations of Camarhynchus tree finches on Floreana Island.
The fly, Philornis downsi Dodge & Aitken, was first collected in 1964 on the Galápagos Islands and is now widespread across the archipelago. Virtually nothing is known about the behaviour and ecology of the fly as well as for the genus in general. Here, we describe all larval instars for the first time, and discuss infection intensity and impacts of parasitism on nestling survival of Darwin's finches. Adult P. downsi are non-parasitic free-living flies, whereas the larvae are obligate blood-feeding parasites on nestling birds. The larvae show a marked shift in their host site specificity--a novel finding for the genus Philornis: the first and early second larval instars live as agents of myiasis in finch nostrils and other tissues, while the older second and third instar larvae reside in the nest material and feed externally on the blood of nestlings, leading to blood losses in nestlings of 18-55%. Pupation occurs in the bottom layer of the nest. The combined effects of tissue damage by the endoparasitic instar larvae and anaemia by nest-dwelling haematophagous instar larvae account for the high nestling mortality (76%) due to Philornis parasitism. This represents the highest mortality by Philornis reported in the literature and emphasizes the extremely serious threat this parasite poses for the endemic passerine fauna of the Galápagos Islands.
Parasites place their hosts under strong selection for adaptive traits that increase parasite resistance. The initial impact of invasive parasites has rarely been observed and can be particularly strong on naïve hosts with limited prior exposure to parasites.Philornis downsiis an introduced fly to the Galapagos Islands whose parasitic larvae cause high mortality in nestlings of Darwin's finches. We used a within-nest camera system and nest monitoring data to examine this new host–parasite interaction in the wild. ManyP. downsiflies entered finch nests with incubated eggs or nestlings but only when parent finches were not present. ParasiticP. downsilarvae were observed to emerge from the nest base at night to feed both internally and externally on nestlings. Adult and nestling Darwin’s finches exhibit grooming and avoidance behaviours in the presence ofP. downsiparasites. Specifically, in nests with high parasite intensity, nestlings increased self-preening behaviour, ate larvae and stood on top of one another. Female finches probed into their nestling’s nares (first instar larvae reside in the nares) and probed into the nest base (second and third larvae reside in the nest base during the day). These findings shed light on the emergence of anti-parasite behaviour as well as host–parasite relationships after recent parasitism in a naïve host.
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