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Publications (10 of 173) Show all publications
Biderre-Petit, C., Courtine, D., Hennequin, C., Galand, P. E., Bertilsson, S., Debroas, D., . . . Hochart, C. (2024). A pan-genomic approach reveals novel Sulfurimonas clade in the ferruginous meromictic Lake Pavin. Molecular Ecology Resources, 24(3), Article ID e13923.
Open this publication in new window or tab >>A pan-genomic approach reveals novel Sulfurimonas clade in the ferruginous meromictic Lake Pavin
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2024 (English)In: Molecular Ecology Resources, ISSN 1755-098X, E-ISSN 1755-0998, Vol. 24, no 3, article id e13923Article in journal (Refereed) Published
Abstract [en]

The permanently anoxic waters in meromictic lakes create suitable niches for the growth of bacteria using sulphur metabolisms like sulphur oxidation. In Lake Pavin, the anoxic water mass hosts an active cryptic sulphur cycle that interacts narrowly with iron cycling, however the metabolisms of the microorganisms involved are poorly known. Here we combined metagenomics, single-cell genomics, and pan-genomics to further expand our understanding of the bacteria and the corresponding metabolisms involved in sulphur oxidation in this ferruginous sulphide- and sulphate-poor meromictic lake. We highlighted two new species within the genus Sulfurimonas that belong to a novel clade of chemotrophic sulphur oxidisers exclusive to freshwaters. We moreover conclude that this genus holds a key-role not only in limiting sulphide accumulation in the upper part of the anoxic layer but also constraining carbon, phosphate and iron cycling.

Place, publisher, year, edition, pages
John Wiley & Sons, 2024
Keywords
freshwater, meromictic lake, pan-genome, sulphur oxidation, Sulfurimonas
National Category
Microbiology Environmental Sciences
Identifiers
urn:nbn:se:uu:diva-543223 (URN)10.1111/1755-0998.13923 (DOI)001137537300001 ()38189173 (PubMedID)
Available from: 2024-11-25 Created: 2024-11-25 Last updated: 2024-11-25Bibliographically approved
Nota, K., Orlando, L., Marchesini, A., Girardi, M., Bertilsson, S., Vernesi, C. & Parducci, L. (2024). Enriching barcoding markers in environmental samples utilizing a phylogenetic probe design: Insights from mock communities. ENVIRONMENTAL DNA, 6(4), Article ID e593.
Open this publication in new window or tab >>Enriching barcoding markers in environmental samples utilizing a phylogenetic probe design: Insights from mock communities
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2024 (English)In: ENVIRONMENTAL DNA, ISSN 2637-4943, Vol. 6, no 4, article id e593Article in journal (Refereed) Published
Abstract [en]

Hybridization capture is an emerging method making use of short oligonucleotide baits to enrich DNA libraries for genomic fragments of specific organisms thus enabling detection of their presence in environmental samples. Although it offers a primer-independent alternative to metabarcoding, little empirical work has been dedicated to characterizing the underlying biases and coupled implications for biological interpretation. Moreover, few published bioinformatic pipelines are available for designing polynucleotide capture baits from a reference sequence collection. We designed RNA-baits specifically targeting two chloroplast barcoding genes matK and rbcL to reveal the plant taxonomic diversity present in a given environmental sample. Our approach leverages the sensitivity of hybridization capture and the capacity of high-throughput DNA sequencing instruments. It builds on a new and universal method based on ancestral sequence reconstruction, ultimately limiting the number of bait-probes required and reducing experimental costs, while accessing high levels of taxonomic diversity. Our bait-set selectively targets four main plant orders (Fagales, Pinales, Asterales, and Poales), representing similar to 18% of all described vascular plants. This is achieved through the use of only 4084 baits, each 80 nucleotides in length (80-mer), capturing similar to 1.0-1.6 k nucleotide sequences from each taxon. Tests on mock communities revealed important factors influencing capture efficiency and relative abundance estimates, including GC-content, the overall target length per taxa, and the bait density and mean number of mismatches to the bait sequence. Our results show that hybridization capture, like metabarcoding, requires caution when interpreting results quantitatively within (paleo)-ecological studies. Biases detected in this work have the potential to be mitigated with bait designs that avoid extreme base compositional biases and balancing bait targets across taxa. However, we strongly recommend the use of mock communities and read simulations to quantify the accuracy of taxonomic representation when using new bait designs.

Place, publisher, year, edition, pages
John Wiley & Sons, 2024
Keywords
capture bias, DNA barcoding, hybridization capture, shotgun metagenomics, target capture, target enrichment
National Category
Ecology
Identifiers
urn:nbn:se:uu:diva-538299 (URN)10.1002/edn3.593 (DOI)001300482200008 ()
Funder
EU, Horizon 2020, 101071707EU, Horizon 2020, 681605-PEGASUS
Available from: 2024-09-12 Created: 2024-09-12 Last updated: 2024-09-12Bibliographically approved
Florenza, J., Divne, A.-M. & Bertilsson, S. (2024). Fluorescently labeled prey surrogates in combination with fluorescence-activated cell sorting successfully discriminate actively feeding mixotrophs in a lake water sample. Limnology and Oceanography, 69(5), 1030-1044
Open this publication in new window or tab >>Fluorescently labeled prey surrogates in combination with fluorescence-activated cell sorting successfully discriminate actively feeding mixotrophs in a lake water sample
2024 (English)In: Limnology and Oceanography, ISSN 0024-3590, E-ISSN 1939-5590, Vol. 69, no 5, p. 1030-1044Article in journal (Refereed) Published
Abstract [en]

Mixotrophic protists are capable of acting both as primary producers and primary consumers at the base of the aquatic food web, thus constituting key organisms in ecosystems where they are abundant. However, their identity, abundance, ecological dynamics, and biogeochemical impact in aquatic ecosystems remain understudied in comparison to classically demarcated autotrophs or heterotrophs. In this study, we make use of fluorescently labeled prey and fluorescence-activated cell sorting to taxonomically identify actively-feeding individual mixotrophic flagellates from lake water. Replicated experiments were carried out to assess the performance of three different fluorescently labeled prey types and a fluorescent dye targeting food vacuoles. In the experiments, water from an oligotrophic lake was exposed independently to each type of reporter and cells were individually sorted based on fluorescent signals for predation and chlorophyll a. A total of 927 individual single cells were successfully recovered, with all fluorescent reporters exhibiting high sensitivity for putative mixotrophic taxa: overall, 87% of the occurrences could be assigned to dictyochophytes, 9% to chrysophytes, and 3% to dinoflagellates. As a result, we were able to detect cryptic diversity within pedinellid algae and report a Prorocentrum-like freshwater occurrence. We argue that this procedure can be a valuable tool to uncover relevant and unexpected active mixotrophic species in a wider range of aquatic environments, and could easily be coupled to other techniques to describe the finer details of the trophic status of aquatic microbial communities.

Place, publisher, year, edition, pages
John Wiley & Sons, 2024
National Category
Ecology
Identifiers
urn:nbn:se:uu:diva-542110 (URN)10.1002/lno.12545 (DOI)001184122500001 ()
Funder
EU, Horizon 2020, H2020-MSCA-ITN-2015-675752Swedish Research Council Formas, 2022-01211Swedish Research CouncilKnut and Alice Wallenberg FoundationSwedish Research Council, 2018-05973VinnovaSwedish Research Council Formas
Available from: 2024-11-13 Created: 2024-11-13 Last updated: 2024-11-13Bibliographically approved
Florenza, J. & Bertilsson, S. (2023). Choice of methodology and surrogate prey are decisive for the quality of protistan bacterivory rate estimates. Aquatic Microbial Ecology, 89, 43-53
Open this publication in new window or tab >>Choice of methodology and surrogate prey are decisive for the quality of protistan bacterivory rate estimates
2023 (English)In: Aquatic Microbial Ecology, ISSN 0948-3055, E-ISSN 1616-1564, Vol. 89, p. 43-53Article in journal (Refereed) Published
Abstract [en]

ABSTRACT: Microeukaryote predation on bacteria is a fundamental phenomenon to understand energy and nutrient dynamics at the base of the aquatic food web. To date, the most prevalent way to estimate grazing rates is by using epifluorescence microscopy to enumerate ingestion events of fluorescently labelled tracers (FLTs) after short-term incubation experiments. However, this approach can be sensitive to the type of FLT, requires skillful preparation of the samples and is limited to small sample sizes. We tested the susceptibility of rate estimates to the choice of prey and made a side-by-side comparison between microscopy and flow cytometry when recording ingestion by a bacterivorous flagellate. Short-term uptake experiments were established using 5 types of FLTs differing in quality (living, dead or inert) and size (large or small), with <i>Ochromonas triangulata</i> as a model flagellate. The experiments showed that (1) each of the different prey types yielded different clearing rates, ranging from 0.5 to 3.6 nl cell<sup>-1</sup> h<sup>-1</sup>, with the largest differences (3-fold or higher) between small prey (lower rates) and large prey (higher rates); (2) the cytometry estimate differed significantly from the microscopy estimate in 3 out of 4 experimental configurations; and (3) the precision of the cytometric analysis was greater, with >3-fold higher uncertainty associated with microscopy counting. Our results validate that flow cytometry provides a more precise bacterivory estimate, and that the choice of FLT influences the grazing rate estimate to a high extent regardless of the analytical method used.

Place, publisher, year, edition, pages
Inter-Research Science Publisher, 2023
Keywords
Bacterivory rates, Fluorescently labelled tracers, FLB, Flow cytometry, Ochromonas triangulata
National Category
Ecology Microbiology
Identifiers
urn:nbn:se:uu:diva-500711 (URN)10.3354/ame01996 (DOI)000989677200001 ()
Available from: 2023-04-21 Created: 2023-04-21 Last updated: 2023-06-28Bibliographically approved
Wernroth, L., Peura, S., Hedman, A. M., Hetty, S., Vicenzi, S., Kennedy, B., . . . Fall, T. (2022). Development of gut microbiota during the first 2 years of life. Scientific Reports, 12(1), Article ID 9080.
Open this publication in new window or tab >>Development of gut microbiota during the first 2 years of life
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2022 (English)In: Scientific Reports, E-ISSN 2045-2322, Vol. 12, no 1, article id 9080Article in journal (Refereed) Published
Abstract [en]

8Although development of microbiota in childhood has been linked to chronic immune-related conditions, early childhood determinants of microbiota development have not been fully elucidated. We used 16S rRNA sequencing to analyse faecal and saliva samples from 83 children at four time-points during their first 2 years of life and from their mothers. Our findings confirm that gut microbiota in infants have low diversity and highlight that some properties are shared with the oral microbiota, although inter-individual differences are present. A considerable convergence in gut microbiota composition was noted across the first 2 years of life, towards a more diverse adult-like microbiota. Mode of delivery accounted for some of the inter-individual variation in early childhood, but with a pronounced attenuation over time. Our study extends previous research with further characterization of the major shift in gut microbiota composition during the first 2 years of life.

Place, publisher, year, edition, pages
Springer Nature, 2022
National Category
Microbiology in the medical area
Identifiers
urn:nbn:se:uu:diva-470208 (URN)10.1038/s41598-022-13009-3 (DOI)000803920600048 ()35641542 (PubMedID)
Funder
Swedish National Infrastructure for Computing (SNIC), sens2018616Swedish Research Council, 2018-05973
Available from: 2022-03-21 Created: 2022-03-21 Last updated: 2022-10-20Bibliographically approved
Nota, K., Klaminder, J., Milesi, P., Bindler, R., Nobile, A., van Steijn, T., . . . Parducci, L. (2022). Norway spruce postglacial recolonization of Fennoscandia. Nature Communications, 13, Article ID 1333.
Open this publication in new window or tab >>Norway spruce postglacial recolonization of Fennoscandia
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2022 (English)In: Nature Communications, E-ISSN 2041-1723, Vol. 13, article id 1333Article in journal (Refereed) Published
Abstract [en]

Contrasting theories exist regarding how Norway spruce (Picea abies) recolonized Fennoscandia after the last glaciation and both early Holocene establishments from western microrefugia and late Holocene colonization from the east have been postulated. Here, we show that Norway spruce was present in southern Fennoscandia as early as 14.7 ± 0.1 cal. kyr BP and that the millennia-old clonal spruce trees present today in central Sweden likely arrived with an early Holocene migration from the east. Our findings are based on ancient sedimentary DNA from multiple European sites (N = 15) combined with nuclear and mitochondrial DNA analysis of ancient clonal (N = 135) and contemporary spruce forest trees (N = 129) from central Sweden. Our other findings imply that Norway spruce was present shortly after deglaciation at the margins of the Scandinavian Ice Sheet, and support previously disputed finds of pollen in southern Sweden claiming spruce establishment during the Lateglacial.

Place, publisher, year, edition, pages
Springer NatureSpringer Nature, 2022
National Category
Ecology
Identifiers
urn:nbn:se:uu:diva-467857 (URN)10.1038/s41467-022-28976-4 (DOI)000769063600023 ()35288569 (PubMedID)
Funder
Swedish Research Council, 2017-04548Swedish Research Council, 2018-05973Knut and Alice Wallenberg Foundation
Available from: 2022-02-17 Created: 2022-02-17 Last updated: 2024-01-15Bibliographically approved
Patriarca, C., Sedano Núñez, V. T., Garcia, S. L., Bergquist, J., Bertilsson, S., Sjöberg, P. J. R., . . . Hawkes, J. A. (2021). Character and environmental lability of cyanobacteria-derived dissolved organic matter. Limnology and Oceanography, 66(2), 496-509
Open this publication in new window or tab >>Character and environmental lability of cyanobacteria-derived dissolved organic matter
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2021 (English)In: Limnology and Oceanography, ISSN 0024-3590, E-ISSN 1939-5590, Vol. 66, no 2, p. 496-509Article in journal (Refereed) Published
Abstract [en]

Autotrophic dissolved organic matter (DOM) is central to the carbon biogeochemistry of aquatic systems, and the full complexity of autotrophic DOM has not been extensively studied, particularly by high‐resolution mass spectrometry (HRMS). Terrestrial DOM tends to dominate HRMS studies in freshwaters due to the propensity of such compounds to ionize by negative mode electrospray, and possibly also because ionizable DOM produced by autotrophy is decreased to low steady‐state concentrations by heterotrophic bacteria. In this study, we investigated the character of DOM produced by the widespread cyanobacteria Microcystis aeruginosa using high‐pressure liquid chromatography—electrospray ionization—high‐resolution mass spectrometry. M. aeruginosa produced thousands of detectable compounds in axenic culture. These compounds were chromatographically resolved and the majority were assigned to aliphatic formulas with a broad polarity range. We found that the DOM produced by M. aeruginosa was highly susceptible to removal by heterotrophic freshwater bacteria, supporting the hypothesis that this autotroph‐derived organic material is highly labile and accordingly only seen at low concentrations in natural settings.

Place, publisher, year, edition, pages
John Wiley & SonsWiley, 2021
National Category
Analytical Chemistry
Identifiers
urn:nbn:se:uu:diva-410263 (URN)10.1002/lno.11619 (DOI)000577965400001 ()
Funder
Knut and Alice Wallenberg Foundation, 2013.0091The Royal Swedish Academy of Sciences, CR2019‐0060Swedish Research Council, 2015‐4870Swedish Research Council, 2017‐04422Swedish Research Council, 2018‐04618
Available from: 2020-05-14 Created: 2020-05-14 Last updated: 2024-01-15Bibliographically approved
Scharnweber, K., Peura, S., Attermeyer, K., Bertilsson, S., Bolender, L., Buck, M., . . . Székely, A. J. (2021). Comprehensive analysis of chemical and biological problems associated with browning agents used in aquatic studies. Limnology and Oceanography: Methods, 19(12), 818-835
Open this publication in new window or tab >>Comprehensive analysis of chemical and biological problems associated with browning agents used in aquatic studies
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2021 (English)In: Limnology and Oceanography: Methods, E-ISSN 1541-5856, Vol. 19, no 12, p. 818-835Article in journal (Refereed) Published
Abstract [en]

Inland waters receive and process large amounts of colored organic matter from the terrestrial surroundings. These inputs dramatically affect the chemical, physical, and biological properties of water bodies, as well as their roles as global carbon sinks and sources. However, manipulative studies, especially at ecosystem scale, require large amounts of dissolved organic matter with optical and chemical properties resembling indigenous organic matter. Here, we compared the impacts of two leonardite products (HuminFeed and SuperHume) and a freshly derived reverse osmosis concentrate of organic matter in a set of comprehensive mesocosm- and laboratory-scale experiments and analyses. The chemical properties of the reverse osmosis concentrate and the leonardite products were very different, with leonardite products being low and the reverse osmosis concentrate being high in carboxylic functional groups. Light had a strong impact on the properties of leonardite products, including loss of color and increased particle formation. HuminFeed presented a substantial impact on microbial communities under light conditions, where bacterial production was stimulated and community composition modified, while in dark potential inhibition of bacterial processes was detected. While none of the browning agents inhibited the growth of the tested phytoplankton Gonyostomum semen, HuminFeed had detrimental effects on zooplankton abundance and Daphnia reproduction. We conclude that the effects of browning agents extracted from leonardite, particularly HuminFeed, are in sharp contrast to those originating from terrestrially derived dissolved organic matter. Hence, they should be used with great caution in experimental studies on the consequences of terrestrial carbon for aquatic systems.

Place, publisher, year, edition, pages
John Wiley & Sons, 2021
National Category
Ecology
Identifiers
urn:nbn:se:uu:diva-461034 (URN)10.1002/lom3.10463 (DOI)000711887000001 ()
Funder
Knut and Alice Wallenberg Foundation, KAW 2013.0091Swedish Research Council FormasEU, FP7, Seventh Framework Programme
Available from: 2021-12-10 Created: 2021-12-10 Last updated: 2024-01-15Bibliographically approved
Mehrshad, M., Lopez-Fernandez, M., Sundh, J., Bell, E., Simone, D., Buck, M., . . . Dopson, M. (2021). Energy efficiency and biological interactions define the core microbiome of deep oligotrophic groundwater. Nature Communications, 12(1), Article ID 4253.
Open this publication in new window or tab >>Energy efficiency and biological interactions define the core microbiome of deep oligotrophic groundwater
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2021 (English)In: Nature Communications, E-ISSN 2041-1723, Vol. 12, no 1, article id 4253Article in journal (Refereed) Published
Abstract [en]

While oligotrophic deep groundwaters host active microbes attuned to the low-end of the bioenergetics spectrum, the ecological constraints on microbial niches in these ecosystems and their consequences for microbiome convergence are unknown. Here, we provide a genome-resolved, integrated omics analysis comparing archaeal and bacterial communities in disconnected fracture fluids of the Fennoscandian Shield in Europe. Leveraging a dataset that combines metagenomes, single cell genomes, and metatranscriptomes, we show that groundwaters flowing in similar lithologies offer fixed niches that are occupied by a common core microbiome. Functional expression analysis highlights that these deep groundwater ecosystems foster diverse, yet cooperative communities adapted to this setting. We suggest that these communities stimulate cooperation by expression of functions related to ecological traits, such as aggregate or biofilm formation, while alleviating the burden on microorganisms producing compounds or functions that provide a collective benefit by facilitating reciprocal promiscuous metabolic partnerships with other members of the community. We hypothesize that an episodic lifestyle enabled by reversible bacteriostatic functions ensures the subsistence of the oligotrophic deep groundwater microbiome. Ecological constraints on microbial niches in oligotrophic deep groundwaters remain elusive. This study provides support for the existence of a common core microbiome in two deep groundwater biomes of the Fennoscandian Shield using a genome-resolved, integrated omics analysis.

Place, publisher, year, edition, pages
Springer Nature, 2021
National Category
Microbiology
Identifiers
urn:nbn:se:uu:diva-453773 (URN)10.1038/s41467-021-24549-z (DOI)000675329200009 ()34253732 (PubMedID)
Funder
Swedish Research Council, 2018-04311Swedish Research Council, 2017-04422Swedish Research Council, 2014-4398Swedish Research CouncilSwedish National Infrastructure for Computing (SNIC), b2013127Swedish National Infrastructure for Computing (SNIC), SNIC 2019/3-22Swedish National Infrastructure for Computing (SNIC), SNIC 2020/5-19Knut and Alice Wallenberg FoundationSwedish Nuclear Fuel and Waste Management Company, SKBThe Crafoord Foundation, 20180599The Crafoord Foundation, 20130557Carl Tryggers foundation , KF16: 18Science for Life Laboratory - a national resource center for high-throughput molecular bioscience
Note

These authors contributed equally: Maliheh Mehrshad, Margarita Lopez-Fernandez

Available from: 2021-10-12 Created: 2021-10-12 Last updated: 2024-01-15Bibliographically approved
Garcia, S. L., Mehrshad, M., Buck, M., Tsuji, J. M., Neufeld, J. D., McMahon, K. D., . . . Peura, S. (2021). Freshwater Chlorobia Exhibit Metabolic Specialization among Cosmopolitan and Endemic Populations. mSystems, 6(3), Article ID e01196-20.
Open this publication in new window or tab >>Freshwater Chlorobia Exhibit Metabolic Specialization among Cosmopolitan and Endemic Populations
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2021 (English)In: mSystems, E-ISSN 2379-5077, Vol. 6, no 3, article id e01196-20Article in journal (Refereed) Published
Abstract [en]

Photosynthetic bacteria from the class Chlorobia (formerly phylum Chlorobi) sustain carbon fixation in anoxic water columns. They harvest light at extremely low intensities and use various inorganic electron donors to fix carbon dioxide into biomass. Until now, most information on the functional ecology and local adaptations of Chlorobia members came from isolates and merely 26 sequenced genomes that may not adequately represent natural populations. To address these limitations, we analyzed global metagenomes to profile planktonic Chlorobia cells from the oxyclines of 42 freshwater bodies, spanning subarctic to tropical regions and encompassing all four seasons. We assembled and compiled over 500 genomes, including metagenome-assembled genomes (MAGs), single-amplified genomes (SAGs), and reference genomes from cultures, clustering them into 71 metagenomic operational taxonomic units (mOTUs or “species”). Of the 71 mOTUs, 57 were classified within the genus Chlorobium, and these mOTUs represented up to ∼60% of the microbial communities in the sampled anoxic waters. Several Chlorobium-associated mOTUs were globally distributed, whereas others were endemic to individual lakes. Although most clades encoded the ability to oxidize hydrogen, many lacked genes for the oxidation of specific sulfur and iron substrates. Surprisingly, one globally distributed Scandinavian clade encoded the ability to oxidize hydrogen, sulfur, and iron, suggesting that metabolic versatility facilitated such widespread colonization. Overall, these findings provide new insight into the biogeography of the Chlorobia and the metabolic traits that facilitate niche specialization within lake ecosystems.

IMPORTANCE The reconstruction of genomes from metagenomes has helped explore the ecology and evolution of environmental microbiota. We applied this approach to 274 metagenomes collected from diverse freshwater habitats that spanned oxic and anoxic zones, sampling seasons, and latitudes. We demonstrate widespread and abundant distributions of planktonic Chlorobia-associated bacteria in hypolimnetic waters of stratified freshwater ecosystems and show they vary in their capacities to use different electron donors. Having photoautotrophic potential, these Chlorobia members could serve as carbon sources that support metalimnetic and hypolimnetic food webs.

Place, publisher, year, edition, pages
American Society for MicrobiologyAmerican Society for Microbiology, 2021
Keywords
Chlorobia, freshwater, photosynthetic bacteria, planktonic
National Category
Microbiology
Identifiers
urn:nbn:se:uu:diva-458706 (URN)10.1128/mSystems.01196-20 (DOI)000709811800011 ()33975970 (PubMedID)
Funder
Knut and Alice Wallenberg Foundation, KAW 2013.0091Swedish Research CouncilSwedish Research Council FormasSwedish National Infrastructure for Computing (SNIC), SNIC2020/5-19Science for Life Laboratory, SciLifeLabThe Royal Swedish Academy of Sciences
Available from: 2021-11-25 Created: 2021-11-25 Last updated: 2024-01-15Bibliographically approved
Projects
Biogeokemiska processer - småskaliga mekanismer med effekt på storskaliga system för perioden 2008-07-01--2011-06-30. [2008-01293_VR]; Uppsala UniversityProbing seasonal and diurnal dynamics in bacterial and archaeal freshwater communities: building a lake microbial observatory [2008-04359_VR]; Uppsala UniversityAmundsen Sea Polynya International Research Expedition (ASPIRE): Patchiness and significance of microbial communities controlling the Southern Ocean carbon cycle [2008-06430_VR]; Uppsala UniversityNiche separation and substrate specialization in heterotrophic freshwater bacterioplankton [2009-03784_VR]; Uppsala UniversityHow is organic matter degradation sustained across redox gradients: community shifts or adaptation? [2012-03892_VR]; Uppsala UniversityFlow sorter for single cell genomics of microorganisms from the environment [2012-05095_VR]; Uppsala UniversityPHYTOREV: A coordinated effort to understand genomic changes in revived diatom and phytoplankton populations from Baltic Sea sediments in light of environmental change [21-RN-0003_OSS]; Södertörn UniversityWoodenLeg: Reducing Legionella in pulp- and paper-mill wastewater treatment [2023-01638_Formas]; Uppsala University
Organisations
Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0002-4265-1835

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