Published February 12, 2024 | Version v1
Dataset Open

Energy input, habitat heterogeneity, and host specificity on avian haemosporidian diversity at continental scales

  • 1. Instituto de Ecología
  • 2. National Autonomous University of Mexico
  • 3. Institute for Scientific and Technological Research
  • 4. University of South Florida

Description

The correct identification of biotic and abiotic drivers affecting parasite diversity and assemblage composition at different spatial scales is crucial for understanding how pathogen distribution responds to anthropogenic disturbance and climate change. Here, we used a database of avian haemosporidian parasites to identify such drivers and their effect on the taxonomic and phylogenetic diversity of genera Plasmodium, Haemoproteus, and Leucocytozoon from three zoogeographic regions. We explored how parasite diversity is related to energy input (i.e., temperature, precipitation, and potential evapotranspiration [PET]), to habitat heterogeneity (i.e., climatic seasonality, vegetation density, ecosystem heterogeneity, human disturbance, and host richness), and to a novel assemblage-level metric related to parasite niche overlap (degree of generalism). We found that the relative importance of the predictors differed between the three studied parasite genera and across diversity metrics. Among the most consistent predictors, host richness was positively related to the taxonomic diversity of the three genera. Energy input and human footprint explained the phylogenetic diversity of Haemoproteus. Finally, the degree of generalism explained the diversity of Plasmodium and Leucocytozoon. Our results suggest that different dimensions of haemosporidian diversity are shaped by energy input, host heterogeneity, and assembly processes related to parasite resource use within local parasite assemblages.

Notes

Funding provided by: CONACYT
Crossref Funder Registry ID: http://dx.doi.org/10.13039/501100003141
Award Number:

Methods

We acquired records from MalAvi, a global database with at least 2400 haemosporidian lineages of mtDNA sequences of a cytochrome b (cyt-b) gene fragment (479 bp) that has been used as a barcode. We considered each haplotype as a unique parasite lineage and in the case of duplicated sequences with different names, we randomly assigned duplicated sequences to the same lineage name. We then downloaded the Host and Sites Table (accessed on March 2023), we validated geographic coordinates at country level, final table had 10302 records based on 286 references published between 2006 and 2023.     

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Additional details

Related works

Is derived from
10.5281/zenodo.10642584 (DOI)