Soil compactness predicts above-below ground community structure, but
not nematode microbiome patterns in desert habitats
Abstract
Soil microorganisms, including prokaryotes and eukaryotes, represent a
large fraction of global terrestrial biodiversity. These organisms and
their microbiomes play critical roles in ecosystem functioning and
services and are essential to soil health. Soil biodiversity is governed
by above-ground and below-ground factors, which create specific habitat
conditions that structure soil communities. However, the compounded
effects of such environmental drivers are often understudied, thus
limiting our understanding of processes governing soil biodiversity,
especially in desert habitats. Here we show that above- and below-ground
factors shape prokaryotic and microeukaryotic communities, but these
environmental factors do not appear to structure invertebrate-associated
microbiomes. By integrating metabarcoding and morphological datasets, we
found that soil compactness is a major factor structuring prokaryote and
microeukaryote assemblages and influences the abundance of genes
involved in nutrient cycling and organic matter decomposition. Despite
having lower nitrogen levels, compacted soils displayed significantly
higher alpha-diversity than uncompacted habitats across datasets.
Different bacterial clades were enriched within specific nematode
lineages (Plectids and Tylenchids) highlighting potentially new
species-specific nematode-associated taxa. The data suggests that
nematode microbiomes are less impacted by the same environmental drivers
of the soil bacterial community and respond to microscale variations
among sampling sites. The prevalence of functionally diverse
invertebrate-associated bacteria (Mycobacterium) in the nematode
microbiome suggests that these microbial communities benefit the host.
Our findings highlight the importance of assessing above- and
below-ground effects to elucidate patterns of microbial community
assembly in terrestrial habitats, and how fine-scale analyses are
critical for understanding patterns of host-associated microbiomes.