Evidence map›Paper›PMID 40808488›Full record

ArticleEnvironmental science & technology2025

Investigating the Stability of Individual Carboxylate-Rich Alicyclic Molecules Under Simulated Environmental Irradiation and Microbial Incubation Conditions.

Alexander J Craig, Mahsa Norouzi, Paul Löffler, Foon Yin Lai, Rim Mtibaà, Eva Breyer, Federico Baltar, Lindon W K Moodie, Jeffrey A Hawkes

Abstract read
In one paragraph

Article in Environmental science & technology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Alexander J CraigAnalytical Chemistry, Department of Chemistry BMC, Uppsala University, Uppsala 752 37, Sweden.ORCID 0000-0002-8107-6378
Mahsa NorouziAnalytical Chemistry, Department of Chemistry BMC, Uppsala University, Uppsala 752 37, Sweden.
Paul LöfflerDepartment of Aquatic Sciences and Assessment, Swedish University of Agricultural Sciences, Box 7050, Uppsala 750 07, Sweden.ORCID 0000-0003-1959-0752
Foon Yin LaiDepartment of Aquatic Sciences and Assessment, Swedish University of Agricultural Sciences, Box 7050, Uppsala 750 07, Sweden.
Rim MtibaàFungal & Biogeochemical Oceanography Group, Department of Functional and Evolutionary Ecology, University of Vienna, Vienna 1030, Austria.
Eva BreyerFungal & Biogeochemical Oceanography Group, Department of Functional and Evolutionary Ecology, University of Vienna, Vienna 1030, Austria.
Federico BaltarFungal & Biogeochemical Oceanography Group, Department of Functional and Evolutionary Ecology, University of Vienna, Vienna 1030, Austria.
Lindon W K MoodieDrug Design and Discovery, Department of Medicinal Chemistry, Uppsala University, Uppsala 752 37, Sweden.ORCID 0000-0002-9500-4535
Jeffrey A HawkesAnalytical Chemistry, Department of Chemistry BMC, Uppsala University, Uppsala 752 37, Sweden.ORCID 0000-0003-0664-2242

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding dissolved organic matter (DOM) relies on the development of methods capable of navigating its complexity. Although analytical techniques have continually advanced, the fate of individual compound classes remains nearly impossible to track with the current technology. Previously, we reported the synthesis of carboxylate-rich alicyclic molecule (CRAM) compounds that shared more similar analytical features with DOM than previously available standards. Here, we adopt an alternative approach to the conventional use of DOM as a bulk material by subjecting our synthesized CRAM compounds to simulated solar irradiation and microbial incubation experiments alongside molecules with chosen biological or chemical relevance. Irradiation experiments typically showed that compounds bearing only carboxylic acids and/or alcohols on a saturated carbon backbone were the most resistant to photochemical degradation but also that some of the investigated CRAM analogues were notably more stable in the presence of DOM. Within microbial incubations, all of our synthesized CRAMs were entirely stable after 8 months in various aquatic settings. These sets of experiments provide support for the proposed stability of CRAM within the environment as well as providing a platform from which a more diverse set of molecules can be used to assist in probing the stability of DOM.

Indexed as

Carboxylic AcidsDissolved Organic MatterCarboxylic AcidsDissolved Organic Mattercarboxylate-rich alicyclic moleculesdissolved organic mattermass spectrometrymicrobial incubationssimulated irradiationstability

Identifiers

PMID40808488
PMCPMC12392460

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.