<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Federico Baltar | Amano Lab | Hokkaido University</title><link>https://amanoresearch.com/authors/federico-baltar/</link><atom:link href="https://amanoresearch.com/authors/federico-baltar/index.xml" rel="self" type="application/rss+xml"/><description>Federico Baltar</description><generator>HugoBlox Kit (https://hugoblox.com)</generator><language>en-us</language><lastBuildDate>Tue, 01 Jul 2025 00:00:00 +0000</lastBuildDate><item><title>The contribution of pelagic fungi to ocean biomass</title><link>https://amanoresearch.com/publication/stix-202507-fungi/</link><pubDate>Tue, 01 Jul 2025 00:00:00 +0000</pubDate><guid>https://amanoresearch.com/publication/stix-202507-fungi/</guid><description/></item><item><title>Anaplerotic processes are key contributors to dark carbon fixation in the ocean</title><link>https://amanoresearch.com/publication/amano-202409-dark-carbon/</link><pubDate>Wed, 25 Sep 2024 00:00:00 +0000</pubDate><guid>https://amanoresearch.com/publication/amano-202409-dark-carbon/</guid><description>&lt;p&gt;Abstract Anaplerotic carbon fixation is ubiquitous in heterotrophic organisms including those
inhabiting the ocean1. Despite its prevalence, the drivers of this process and its significance in
ocean carbon cycling remain poorly understood2,3. Here we combined global ocean metatranscriptomic
analysis, laboratory experiments on a bacterial model strain, and microautoradiography combined with
catalyzed reporter deposition fluorescence in situ hybridization (MICRO-CARD-FISH) on marine
microbial communities, to uncover the global prevalence of anaplerotic processes in oceanic dark
dissolved inorganic carbon (DIC) fixation. Metatranscriptomic analysis revealed high expression
levels of key anaplerotic genes, especially in mesopelagic waters, comparable to those of photo- and
chemolithoautotrophic DIC fixation genes. Alteromonas emerged as the main contributor to anaplerotic
DIC fixation gene expression, highlighting its role in DIC assimilation in the global ocean.
Laboratory incubations with a marine Alteromonas representative confirmed their capability to fix
DIC, which varied with organic matter availability and temperature. MICRO-CARD-FISH on oceanic
samples revealed that Alteromonas contributed 0–40% (14 ± 16%, mean ± s.d.) to the dark DIC fixation
in the pelagic ocean. Considering that Alteromonas is an obligate heterotroph lacking
chemoautotrophic DIC fixation genes, its contribution to DIC fixation should be attributed to
anaplerotic processes. Based on these results, we estimated a contribution of anaplerotic processes
to dark DIC fixation of 0–0.5 C Pg y-1 in the global dark ocean. Yet, since Alteromonas is not the
only taxon performing anaplerotic DIC fixation, our results represent a baseline conservative
estimate. Collectively, our findings place anaplerotic DIC fixation as a relevant processes in the
oceanic carbon cycling.&lt;/p&gt;</description></item><item><title>Metaproteomic analysis decodes trophic interactions of microorganisms in the dark ocean</title><link>https://amanoresearch.com/publication/zhao-202407-metaproteomic/</link><pubDate>Tue, 30 Jul 2024 00:00:00 +0000</pubDate><guid>https://amanoresearch.com/publication/zhao-202407-metaproteomic/</guid><description>&lt;p&gt;Proteins in the open ocean represent a significant source of organic matter, and their profiles
reflect the metabolic activities of marine microorganisms. Here, by analyzing metaproteomic samples
collected from the Pacific, Atlantic and Southern Ocean, we reveal size-fractionated patterns of the
structure and function of the marine microbiota protein pool in the water column, particularly in
the dark ocean (&amp;gt;200 m). Zooplankton proteins contributed three times more than algal proteins to
the deep-sea community metaproteome. Gammaproteobacteria exhibited high metabolic activity in the
deep-sea, contributing up to 30% of bacterial proteins. Close virus-host interactions of this taxon
might explain the dominance of gammaproteobacterial proteins in the dissolved fraction. A high
urease expression in nitrifiers suggested links between their dark carbon fixation and zooplankton
urea production. In summary, our results uncover the taxonomic contribution of the microbiota to the
oceanic protein pool, revealing protein fluxes from particles to the dissolved organic matter pool.&lt;/p&gt;</description></item><item><title>A ubiquitous gammaproteobacterial clade dominates expression of sulfur oxidation genes across the mesopelagic ocean</title><link>https://amanoresearch.com/publication/baltar-202304-sulfur/</link><pubDate>Mon, 24 Apr 2023 00:00:00 +0000</pubDate><guid>https://amanoresearch.com/publication/baltar-202304-sulfur/</guid><description/></item><item><title>Autofluorescence Is a Common Trait in Different Oceanic Fungi</title><link>https://amanoresearch.com/publication/breyer-202108-fungi/</link><pubDate>Sun, 29 Aug 2021 00:00:00 +0000</pubDate><guid>https://amanoresearch.com/publication/breyer-202108-fungi/</guid><description>&lt;p&gt;Natural autofluorescence is a widespread phenomenon observed in different types of tissues and
organisms. Depending on the origin of the autofluorescence, its intensity can provide insights on
the physiological state of an organism. Fungal autofluorescence has been reported in terrestrial and
human-derived fungal samples. Yet, despite the recently reported ubiquitous presence and importance
of marine fungi in the ocean, the autofluorescence of pelagic fungi has never been examined. Here,
we investigated the existence and intensity of autofluorescence in five different pelagic fungal
isolates. Preliminary experiments of fungal autofluorescence at different growth stages and nutrient
conditions were conducted, reflecting contrasting physiological states of the fungi. In addition, we
analysed the effect of natural autofluorescence on co-staining with DAPI. We found that all the
marine pelagic fungi that were studied exhibited autofluorescence. The intensity of fungal
autofluorescence changed depending on the species and the excitation wavelength used. Furthermore,
fungal autofluorescence varied depending on the growth stage and on the concentration of available
nutrients. Collectively, our results indicate that marine fungi can be auto-fluorescent, although
its intensity depends on the species and growth condition. Hence, oceanic fungal autofluorescence
should be considered in future studies when fungal samples are stained with fluorescent probes
(i.e., fluorescence in situ hybridization) since this could lead to misinterpretation of results.&lt;/p&gt;</description></item></channel></rss>