<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>chlorophyll f &#8211; Science</title>
	<atom:link href="https://scienmag.com/tag/chlorophyll-f/feed/" rel="self" type="application/rss+xml" />
	<link>https://scienmag.com</link>
	<description></description>
	<lastBuildDate>Sat, 12 Sep 2026 23:46:32 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=7.1</generator>

<image>
	<url>https://scienmag.com/wp-content/uploads/2024/07/cropped-scienmag_ico-32x32.jpg</url>
	<title>chlorophyll f &#8211; Science</title>
	<link>https://scienmag.com</link>
	<width>32</width>
	<height>32</height>
</image> 
<site xmlns="com-wordpress:feed-additions:1">73899611</site>	<item>
		<title>Hidden Cyanobacteria That Harvest Far-Red Light Revealed in Taiwan&#8217;s Hot Springs</title>
		<link>https://scienmag.com/hidden-cyanobacteria-that-harvest-far-red-light-revealed-in-taiwans-hot-springs/</link>
		
		<dc:creator><![CDATA[Juliet Wilcox]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 23:46:32 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[16S rRNA gene]]></category>
		<category><![CDATA[16S rRNA gene classification]]></category>
		<category><![CDATA[apcE2]]></category>
		<category><![CDATA[biogeography]]></category>
		<category><![CDATA[chlorophyll f]]></category>
		<category><![CDATA[chlorophyll f and d]]></category>
		<category><![CDATA[Chroococcidiopsis]]></category>
		<category><![CDATA[Cyanobacteria]]></category>
		<category><![CDATA[extremophile microbes]]></category>
		<category><![CDATA[far-red light]]></category>
		<category><![CDATA[far-red light photosynthesis]]></category>
		<category><![CDATA[FaRLiP]]></category>
		<category><![CDATA[FaRLiP genetic program]]></category>
		<category><![CDATA[FRCI database]]></category>
		<category><![CDATA[geothermal ecosystems]]></category>
		<category><![CDATA[hot spring cyanobacteria]]></category>
		<category><![CDATA[hot springs]]></category>
		<category><![CDATA[microbial adaptation to extreme environments]]></category>
		<category><![CDATA[microbial distribution in hot springs]]></category>
		<category><![CDATA[microbial ecology]]></category>
		<category><![CDATA[microbial ecology Taiwan]]></category>
		<category><![CDATA[oxygenic phototrophs]]></category>
		<category><![CDATA[photosynthesis beyond visible spectrum]]></category>
		<category><![CDATA[Taiwan]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=199752</guid>

					<description><![CDATA[A validated 16S rRNA gene framework has revealed that far-red light-utilizing cyanobacteria in Taiwan's hot springs favor higher pH and lower temperatures, with distinct global biogeographic patterns.]]></description>
										<content:encoded><![CDATA[<p>Deep in the steaming runoff channels of Taiwan&#8217;s hot springs, a group of microbes has been quietly rewriting the rules of photosynthesis. These are the far-red light-utilizing cyanobacteria, or FRLCyano, organisms capable of extending oxygenic photosynthesis beyond the visible spectrum by deploying specialized chlorophylls and remodelled light-harvesting machinery. A new study led by Ying-Yang Li and Ming-Yang Ho of National Taiwan University, published in the journal Microbial Ecology, has mapped where these remarkable microbes live across Taiwanese geothermal ecosystems and identified the environmental conditions that govern their abundance. The work combines a customized 16S rRNA gene classification framework with independent functional validation, offering one of the most rigorous surveys to date of this enigmatic phototrophic lineage and revealing clear ecological rules that shape their distribution in some of the planet&#8217;s most extreme sunlit habitats.</p>
<p>Far-red light-utilizing cyanobacteria first came to prominence when researchers discovered that certain strains, when grown under light enriched in far-red wavelengths beyond roughly 700 nanometers, activate a coordinated genetic program known as FaRLiP, short for far-red light photoacclimation. This program replaces the standard photosynthetic apparatus with variants containing chlorophyll d and chlorophyll f, pigments that absorb light in the near-infrared range where conventional chlorophyll a is essentially blind. In nature, far-red light dominates in shaded environments such as under plant canopies, beneath microbial mat layers, and in the crevices of rocks where visible wavelengths are filtered out. For cyanobacteria living in dense hot spring mats, the ability to exploit these longer wavelengths can mean the difference between thriving and being starved of usable energy, making FRLCyano a potentially significant but historically underappreciated component of geothermal microbial communities.</p>
<p>The central obstacle to studying these organisms has always been detection. Traditional approaches rely on pigment analysis or on culturing strains under far-red light in the laboratory, both of which are time-consuming and prone to systematic bias. Many cyanobacteria express the FaRLiP program only inducibly, meaning the characteristic chlorophyll f signature appears only when cells are actually exposed to far-red light, so culture-dependent surveys can easily miss species whose induction conditions were not replicated. As a result, the true abundance and diversity of FRLCyano in the environment has likely been underestimated. The Taiwanese team addressed this gap by applying the Far-Red Cyanobacteria Identification framework, or FRCI, a customized 16S rRNA gene database and classification pipeline designed to flag cyanobacterial lineages with known far-red light capabilities directly from environmental sequence data, bypassing the need for cultivation or pigment measurements altogether.</p>
<p>Applying FRCI to a comprehensive dataset of 16S rRNA gene amplicons from Taiwanese hot springs, the researchers identified 11 distinct FRLCyano amplicon sequence variants across the sampled geothermal sites. Taxonomically, these variants were primarily affiliated with two cyanobacterial genera: Leptolyngbya, a group of thin filamentous forms common in microbial mats, and Calothrix, a genus of heterocyst-forming filamentous cyanobacteria. The detection of these lineages across multiple springs suggests that far-red-capable phototrophs are a recurring feature of Taiwan&#8217;s geothermal landscapes rather than isolated curiosities. Because the identification rests on phylogenetic placement within a curated database rather than on visible pigment expression, the approach can detect organisms even when their far-red machinery is dormant at the time of sampling, providing a more complete census than pigment-based methods alone.</p>
<p>A crucial strength of the study lies in its validation strategy. Because any classification scheme built on 16S rRNA gene data carries the risk of false positives, the team cross-checked their FRCI results against two independent lines of functional evidence. First, they tested for consistency with apcE2, a gene that encodes the far-red-specific form of a phycobilisome linker protein and serves as a reliable molecular marker of the FaRLiP program. This marker had not been incorporated into the initial FRCI framework, so agreement between the two methods represents a genuine independent confirmation. Second, the researchers examined the relationship between FRLCyano abundance and chlorophyll f concentrations measured in the samples, finding a significant positive correlation. Together, these validations demonstrate that the 16S-based classification is not merely a statistical artifact but genuinely tracks organisms equipped for far-red photosynthesis in the wild.</p>
<p>With a validated detection method in hand, the team turned to the ecological question of what controls FRLCyano distribution. The analysis revealed that relative abundance of these organisms is driven by two environmental variables acting in opposite directions: higher pH and lower temperature. In practical terms, far-red light-utilizing cyanobacteria in Taiwanese hot springs favor the cooler, more alkaline end of the geothermal gradient. This pattern makes physiological sense. Photosynthetic machinery, particularly the protein-pigment complexes of the FaRLiP program, is vulnerable to thermal denaturation, and extremely hot spring waters exclude most oxygenic phototrophs entirely. Alkaline conditions, meanwhile, may favor cyanobacterial growth more broadly, consistent with the well-known prevalence of cyanobacterial mats in alkaline geothermal systems worldwide. The finding provides a predictive framework: researchers hunting for FRLCyano should prioritize moderate-temperature, alkaline springs rather than the hottest vents.</p>
<p>The study did not stop at Taiwan&#8217;s borders. By extending the FRCI framework to publicly available hot spring datasets from around the world, the researchers uncovered distinct biogeographical signatures in the global distribution of far-red light-utilizing cyanobacteria. The most striking of these was the rarity of Fischerella, a genus of morphologically complex, multiseriate filamentous cyanobacteria known to include far-red-capable members, in Taiwanese springs compared with hot spring communities in other regions. Such geographic patterning suggests that dispersal limitation, historical contingency, or regionally distinct environmental filters shape which FRLCyano lineages colonize a given geothermal field. Biogeography, often assumed to matter little for microorganisms given their enormous populations and ready dispersal, appears to leave a measurable imprint on this functional group, echoing a broader theme in microbial ecology that microbial distributions are not always cosmopolitan.</p>
<p>Cultivation also earned its place in the study. Alongside the sequence-based survey, the team isolated a novel far-red light-utilizing strain, Chroococcidiopsis sp. GD1, from the Taiwanese samples. Chroococcidiopsis is a genus of desiccation- and radiation-tolerant unicellular cyanobacteria famous for surviving in some of Earth&#8217;s most inhospitable niches, from hot deserts to the deep subsurface, and its appearance in a hot spring adds another extreme environment to the genus&#8217;s portfolio. The successful isolation of GD1 underscores a point the authors emphasize throughout: sequence-based detection and culture-based characterization are complementary, not interchangeable. Sequencing can reveal who is present, but only cultivation allows researchers to test physiology directly, confirm far-red photoacclimation experimentally, and preserve a living reference strain for future work on the biochemistry of chlorophyll f-containing photosystems.</p>
<p>The broader significance of this research extends beyond Taiwan&#8217;s geothermal fields. Far-red photosynthesis has attracted intense interest for applications in agricultural engineering, where introducing chlorophyll f-based machinery into crop plants has been proposed as a way to deepen light penetration through dense canopies and boost photosynthetic efficiency. It also bears on astrobiology, since organisms that can photosynthesize under the redder light of M-dwarf stars or beneath layers of attenuating material are prime models for photosynthesis on other worlds. A robust, multi-method validated framework for detecting FRLCyano in the environment, as this study delivers, is a prerequisite for understanding how widely this expanded form of photosynthesis is deployed across Earth&#8217;s biosphere. By showing that a curated 16S rRNA gene database, validated against apcE2 and chlorophyll f, can reliably census these organisms, the Taiwanese team has given the field a scalable tool, and by pinning down pH and temperature as key correlates, they have told future explorers exactly where to look next.</p>
<p><strong>Subject of Research:</strong> Ecological distribution and environmental drivers of far-red light-utilizing cyanobacteria in hot spring ecosystems</p>
<p><strong>Article Title:</strong> Ecological Distribution and Environmental Correlates of Far-red Light-utilizing Cyanobacteria in Taiwan’s Hot Springs</p>
<p><strong>Article References:</strong> Li, Y.-Y., Ko, J.-T., Chen, P.-Y., Chen, T.-L., Liu, P.-Y., &amp; Ho, M.-Y. (2026). Ecological Distribution and Environmental Correlates of Far-red Light-utilizing Cyanobacteria in Taiwan’s Hot Springs. <em>Microbial Ecology</em>. <a href="https://doi.org/10.1007/s00248-026-02873-5" rel="noopener noreferrer">https://doi.org/10.1007/s00248-026-02873-5</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s00248-026-02873-5" rel="noopener noreferrer">10.1007/s00248-026-02873-5</a></p>
<p><strong>Keywords:</strong> cyanobacteria, far-red light, chlorophyll f, FaRLiP, hot springs, 16S rRNA gene, FRCI database, apcE2, biogeography, Taiwan, Chroococcidiopsis, microbial ecology</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">199752</post-id>	</item>
	</channel>
</rss>
