February 6, 2023

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Researchers reveal a bottleneck for the self-purification capacity of deep lakes

Evolutionary history of planktonic Nitrososphaerota in lacustrine systems. (A) Metagenome sampling locations of freshwater lakes (n = 14) and brackish lakes/inland seas (n = 6) lakes, from which MAGs were reconstructed or publicly available. (B) Phylogenomic maximum-likelihood (ML) tree of Nitrososphaerota based on 122 conserved archaeal single-copy genes. The ML tree was rooted using 38 euryarchaeotal genomes following Ren et al. Branches are collapsed to genus level for brevity. Values in parentheses indicate the number of genomes in lineages containing lacustrine Nitrososphaerota, with corresponding genus-level taxa highlighted in blue. The closed black circles indicate nodes with bootstrap support of ≥80% [Shimodaira-Hasegawa-like approximate likelihood ratio (SH)] and ≥95% (UFBoot). For a full-size tree, see fig. S2. The scale bar [in (B)] shows the number of amino acid sequence substitutions per variable site. Credit: Science Advances (2023). DOI: 10.1126/sciadv.adc9392
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Evolutionary history of planktonic Nitrososphaerota in lacustrine systems. (A) Metagenome sampling locations of freshwater lakes (n = 14) and brackish lakes/inland seas (n = 6) lakes, from which MAGs were reconstructed or publicly available. (B) Phylogenomic maximum-likelihood (ML) tree of Nitrososphaerota based on 122 conserved archaeal single-copy genes. The ML tree was rooted using 38 euryarchaeotal genomes following Ren et al. Branches are collapsed to genus level for brevity. Values in parentheses indicate the number of genomes in lineages containing lacustrine Nitrososphaerota, with corresponding genus-level taxa highlighted in blue. The closed black circles indicate nodes with bootstrap support of ≥80% [Shimodaira-Hasegawa-like approximate likelihood ratio (SH)] and ≥95% (UFBoot). For a full-size tree, see fig. S2. The scale bar [in (B)] shows the number of amino acid sequence substitutions per variable site. Credit: Science Advances (2023). DOI: 10.1126/sciadv.adc9392

Microorganisms help to keep the water of lakes clean. In the process, they also detoxify the nitrogen compound ammonium, which is introduced into water bodies by fertilizers, for example, and is also produced naturally by metabolic processes.

An international team led by the German Collection of Microorganisms and Cell Cultures (DSMZ) with IGB researchers Hans-Peter Grossart and Danny Ionescu has now shown that this detoxification of ammonium in the depths of European lakes is only sustained by an extremely small number of specific archaebacteria species.

Ammonium is a nitrogen compound that is toxic to aquatic life in high concentrations and contaminates drinking . It is formed during decomposition of organic matter in the water column and also enters lakes and rivers as agricultural fertilizer from terrestrial areas in the catchment. Fortunately, the self-purifying power of exists in the form of countless microorganisms that break down ammonium.

In the deep layers of nutrient-poor lakes with large bodies of water (such as Lake Constance and many other pre-Alpine lakes), archaebacteria perform this function. They convert ammonium to nitrate, which is then used to produce N2 nitrogen—a major component of air.

Only about one to 15 different species of ammonium-degrading archaebacteria in deep lakes worldwide

The researchers studied the biodiversity and evolutionary history of ammonium-oxidizing archaebacteria in deep lakes on five continents. They were able to show that the species diversity of these archaea in lakes worldwide averages only about one to 15 species. In European lakes, the is even highly clonal and has little genomic microdiversity.

"This species poverty makes the self-purifying power of deep lakes potentially vulnerable to and contrasts with where a much higher species diversity of this group of microorganisms prevails," explains Hans-Peter Grossart, co-author of the study published in the journal Science Advances.

Selection pressure from habitat change from sea to freshwater

The team also found an explanation for this species paucity: colonization of freshwaters always originated from . However, due to the much lower salt concentrations in freshwaters, the archaea had to undergo major changes to their cell structure, which they only managed to do a few times during evolution. "This selection pressure probably prevented a broader diversity of ammonium-oxidizing archaea from colonizing freshwaters," says Danny Ionescu, another co-author of the study.

The researchers were surprised by the finding that the predominant freshwater species in Europe has hardly changed in the 13 million years since its occurrence and has spread quasi-clonally from Europe to Asia. The authors assume that low nutrients combined with low temperature of 4 degrees Celsius below the thermocline and some more limiting factors of the studied lakes prevents high growth rates and associated evolutionary changes.

These archaebacteria are thus trapped in a state of low genetic diversity. Because the effects of climate change are more pronounced in freshwater than in marine habitats, which is associated with a loss of biodiversity, it remains unclear how the extremely species-poor and evolutionarily static freshwater archaea will respond to changes caused by global warming and overfertilization of agricultural land.

More information: David Kamanda Ngugi et al, Postglacial adaptations enabled colonization and quasi-clonal dispersal of ammonia-oxidizing archaea in modern European large lakes, Science Advances (2023). DOI: 10.1126/sciadv.adc9392

Journal information: Science Advances

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