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Abstract Human activity changes multiple factors in the environment, which can have positive or negative synergistic effects on organisms. However, few studies have explored the causal effects of multiple anthropogenic factors, such as urbanization and invasive species, on animals and the mechanisms that mediate these interactions. This study examines the influence of urbanization on the detrimental effect of invasive avian vampire flies (Philornis downsi) on endemic Darwin's finches in the Galápagos Islands. We experimentally manipulated nest fly abundance in urban and non‐urban locations and then characterized nestling health, fledging success, diet, and gene expression patterns related to host defense. Fledging success of non‐parasitized nestlings from urban (79%) and non‐urban (75%) nests did not differ significantly. However, parasitized, non‐urban nestlings lost more blood, and fewer nestlings survived (8%) compared to urban nestlings (50%). Stable isotopic values (δ15N) from urban nestling feces were higher than those from non‐urban nestlings, suggesting that urban nestlings are consuming more protein. δ15N values correlated negatively with parasite abundance, which suggests that diet might influence host defenses (e.g., tolerance and resistance). Parasitized, urban nestlings differentially expressed genes within pathways associated with red blood cell production (tolerance) and pro‐inflammatory response (innate immunological resistance), compared to parasitized, non‐urban nestlings. In contrast, parasitized non‐urban nestlings differentially expressed genes within pathways associated with immunoglobulin production (adaptive immunological resistance). Our results suggest that urban nestlings are investing more in pro‐inflammatory responses to resist parasites but also recovering more blood cells to tolerate blood loss. Although non‐urban nestlings are mounting an adaptive immune response, it is likely a last effort by the immune system rather than an effective defense against avian vampire flies since few nestlings survived.
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Cigarette tobacco reduces the survival of an invasive parasite that affects Darwin’s finches
Invasive parasites are a major threat to biodiversity worldwide, so understanding the factors that control them is necessary to improve the health of affected host species. In the Galápagos Islands, the invasive nest ectoparasite, the avian vampire fly (Philornis downsi), is causing up to 100% mortality in nestling Darwin’s finches. However, urban finch nests have fewer flies than non-urban finch nests. One explanation is that finches incorporate cigarette butts into their nests, which can decrease nest parasite abundance for other bird species. For our study, we exposed larval flies to cigarette tobacco-treated (concentrated or diluted) or untreated cotton, then characterized pupation success, pupal deformities and success, and adult fly eclosure success and size. The influence of moisture on the effect of tobacco treatment on fly health was also determined. Flies reared in the tobacco treatments as larvae had lower pupation success, larger pupal volume, and a higher prevalence of pupal deformities compared to control flies, regardless of moisture treatment. Furthermore, we found that tobacco-treated flies had lower eclosure success. In fact, very few tobacco-treated flies survived to adulthood. We also collected finch nests and quantified the prevalence and mass of cigarette butts and abundance of flies in the nests. Although most urban finch nests contain cigarette butts (73%), the mass of cigarette butts was very low and did not correlate with fly abundance. Compared to past studies, finch nests require ten times as many cigarette butts to affect fly survival. Although tobacco can negatively affect vampire flies, finches likely do not incorporate enough cigarette butts to affect fly fitness.
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- Award ID(s):
- 1949858
- PAR ID:
- 10496501
- Publisher / Repository:
- Springer Link
- Date Published:
- Journal Name:
- Biological Invasions
- ISSN:
- 1387-3547
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1007/s10530-024-03278-6
