Evidence map›Paper›PMID 39676451›Full record

ArticleSmall methods2025

A High-Resolution Microscopy System for Biological Studies of Cold-Adapted Species Under Physiological Conditions.

Anne-Pia M Marty, Edward N Ward, Jacob R Lamb, Francesca W van Tartwijk, Lloyd S Peck, Melody S Clark, Clemens F Kaminski

Abstract read
In one paragraph

Article in Small methods, 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
  2. Challenges and limitations for live cell imaging in extreme cold.Methods and applications in fluorescence · 2026
    Article
  3. Article
  4. Article
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

7 authors.

Anne-Pia M MartyDepartment of Chemical Engineering and Biotechnology, University of Cambridge, Phillipa Fawcett Drive, Cambridge, CB3 0AS, UK.ORCID 0009-0008-8018-8600
Edward N WardDepartment of Chemical Engineering and Biotechnology, University of Cambridge, Phillipa Fawcett Drive, Cambridge, CB3 0AS, UK.ORCID 0000-0002-9078-9716
Jacob R LambDepartment of Chemical Engineering and Biotechnology, University of Cambridge, Phillipa Fawcett Drive, Cambridge, CB3 0AS, UK.ORCID 0009-0003-5804-679X
Francesca W van TartwijkDepartment of Chemical Engineering and Biotechnology, University of Cambridge, Phillipa Fawcett Drive, Cambridge, CB3 0AS, UK.ORCID 0000-0002-9795-2571
Lloyd S PeckBritish Antarctic Survey, High Cross, Madingley Road, Cambridge, CB3 0ET, UK.ORCID 0000-0003-3479-6791
Melody S ClarkBritish Antarctic Survey, High Cross, Madingley Road, Cambridge, CB3 0ET, UK.
Clemens F KaminskiDepartment of Chemical Engineering and Biotechnology, University of Cambridge, Phillipa Fawcett Drive, Cambridge, CB3 0AS, UK.ORCID 0000-0002-5194-0962

Funding

British Antarctic SurveyEngineering and Physical Sciences Research Council EP/H018301/1Engineering and Physical Sciences Research Council EP/L015889/1Medical Research Council MR/K015850/1Medical Research Council MR/K02292X/1Vice Chancellors Award and School of Technology, University of Cambridge, and the Engineering and Physical Sciences Research Council Centre for Doctoral Training in Sensor Technologies for a Healthy and Sustainable Future EP/S023046/1Wellcome TrustWellcome Trust 3-3249/Z/16/Z
6 · The paper itself

Abstract

The Antarctic seabed harbors significant biodiversity, and almost 90% of oceanic environments are permanently below 5 °C (i.e., deep sea and polar regions). However, organisms whose entire lifecycle occurs around 0 °C are understudied, leaving this large and diverse proportion of the global biome poorly understood. To address this question at the cellular level, tools are required for high-resolution imaging of biological systems under physiological conditions. This poses severe technical challenges. High-resolution imaging objectives require short working distances and immersion media, causing rapid heat transfer from the microscope to the sample. This affects the viability of live specimens and the interpretability of results. Here, we present a method for high-fidelity imaging of live biological samples at temperatures of around, or below, 0 °C. It relies on hardware additions to traditional microscopy, namely as a cooling collar, 10% ethanol as an immersion medium, and nitrogen flow to reduce condensation It can be straightforwardly implemented on different microscopy modalities, including super-resolution imaging. The method is demonstrated in live cell cultures derived from Antarctic fish and highlights the need to maintain physiological conditions for these fragile samples. Future applications include evolutionary biology, biophysics and biotechnology.

Indexed as

Adaptation, PhysiologicalCold TemperatureMicroscopyAnimalsAntarctic RegionsFishescold‐adaptationextremophilesoptical microscopysuper‐resolutiontemperature

Identifiers

PMID39676451
PMCPMC12103227

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Registered trials

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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.