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	<title>marine sponges &#8211; Science</title>
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	<title>marine sponges &#8211; Science</title>
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		<title>Bright Orange Sponge Reveals Hidden Diversity in the Eastern Tropical Pacific</title>
		<link>https://scienmag.com/bright-orange-sponge-reveals-hidden-diversity-in-the-eastern-tropical-pacific/</link>
		
		<dc:creator><![CDATA[Gavin Prescott]]></dc:creator>
		<pubDate>Sun, 13 Sep 2026 02:24:31 +0000</pubDate>
				<category><![CDATA[Climate]]></category>
		<category><![CDATA[18S rRNA]]></category>
		<category><![CDATA[biodiversity]]></category>
		<category><![CDATA[Caribbean to Pacific sponge distribution]]></category>
		<category><![CDATA[COI]]></category>
		<category><![CDATA[coral reefs]]></category>
		<category><![CDATA[cryptic marine species identification]]></category>
		<category><![CDATA[Eastern Tropical Pacific]]></category>
		<category><![CDATA[Eastern Tropical Pacific marine biodiversity]]></category>
		<category><![CDATA[hidden marine species diversity]]></category>
		<category><![CDATA[integrative taxonomy]]></category>
		<category><![CDATA[integrative taxonomy in sponges]]></category>
		<category><![CDATA[Islas Marietas]]></category>
		<category><![CDATA[marine biodiversity in well-visited tropical coastlines]]></category>
		<category><![CDATA[marine sponge discovery]]></category>
		<category><![CDATA[marine sponges]]></category>
		<category><![CDATA[new species]]></category>
		<category><![CDATA[new sponge species Svenzea marialmae]]></category>
		<category><![CDATA[phylogenetics]]></category>
		<category><![CDATA[Scopalinidae]]></category>
		<category><![CDATA[sponge evolutionary relationships]]></category>
		<category><![CDATA[sponge morphological and genetic analysis]]></category>
		<category><![CDATA[sponge taxonomy and classification]]></category>
		<category><![CDATA[Svenzea marialmae]]></category>
		<category><![CDATA[tropical marine ecosystem exploration]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=200816</guid>

					<description><![CDATA[Scientists have described a new bright orange sponge species, Svenzea marialmae, marking the first record of the genus Svenzea in the Eastern Tropical Pacific.]]></description>
										<content:encoded><![CDATA[<p>Deep beneath the waves of Islas Marietas National Park, a vivid patch of orange clinging to a shaded cave wall has turned out to be far more than an attractive curiosity. Researchers working in the Central Mexican Pacific have described a brand-new species of marine sponge, Svenzea marialmae, and in doing so have recorded the genus Svenzea in the Eastern Tropical Pacific for the very first time. The discovery, published in the journal Discover Ecology, expands the known range of a sponge lineage previously confined to the Caribbean Sea, the South Atlantic and parts of the Indo-Pacific, and it underscores how much biodiversity still hides in plain sight along well-visited tropical coastlines.</p>
<p>Marine sponges are notoriously difficult to identify. Many species lack fixed, easily readable external characteristics, and their morphological traits can be ambiguous, variable with environment, or shared misleadingly among unrelated lineages. This has produced a long history of taxonomic confusion, misidentifications and inconsistent classification, particularly among so-called cryptic species that look nearly identical but differ genetically. In recent years, sponge systematics has been transformed by integrative approaches that pair careful morphological description with molecular tools, allowing researchers to delimit species and reconstruct evolutionary relationships with far greater confidence than morphology alone permits.</p>
<p>The new study focuses on the order Scopalinida, a group erected and redefined only in the last decade using both morphological and molecular evidence. Scopalinida contains a single family, Scopalinidae, which in turn holds just three genera: Scopalina, Stylissa and Svenzea. The genus Svenzea, named in honor of the Colombian spongiologist Sven Zea, was established in 2002 for reef-associated sponges whose classification had long bounced between the former order Halichondrida and the family Dictyonellidae. Its defining features include distinctive microanatomy, the arrangement of skeletal elements, the composition and shape of spicules, and the presence of granular cells observed in both adults and larvae, along with a larva of extraordinary size. The larvae of Svenzea zeai, at up to six millimeters long, are regarded as the largest documented for the entire phylum Porifera.</p>
<p>Despite decades of study, only seven species of Svenzea had ever been described, and none had been recorded anywhere along the Eastern Tropical Pacific. That gap made the Mexican Pacific an intriguing frontier. Between July and November 2024, a team led by Eric Bautista-Guerrero of the Universidad de Guadalajara collected samples by SCUBA diving at depths of three to eight meters in the coral community known as Plataforma Pavonas, within Islas Marietas National Park in Bahía de Banderas. The site, where live pocilloporid coral cover is roughly eleven percent and sponges account for only about one percent, proved to host an abundant, widely distributed sponge growing over semi-shaded substrates, cave walls and vertical rock formations.</p>
<p>Underwater, the sponge is unmistakable: a thickly encrusting, irregularly massive animal ten to twenty-five centimeters across and two to three centimeters high, glowing bright orange in life and fading to beige in alcohol preservation. Its surface is smooth but microscopically hispid, densely pierced with incurrent pores and marked by bifurcated exhalant channels that lead to elevated, translucent chimney-like oscula. Under the microscope, the internal architecture revealed a cavernous choanosomal skeleton of disorganized, multispicular tracts, bundles of three to six needle-like spicules cemented by spongin fibers, ascending toward the surface. The spicules themselves, slender styles in two size categories measuring roughly 413 to 551 micrometers long, proved to be significantly larger than those of any previously known Svenzea species, and the complete absence of oxea, a second spicule type common in relatives, provided another decisive clue.</p>
<p>The team did not stop at adults. Using plankton nets towed by a diver around the coral community, they captured free-swimming larvae in full planktonic condition and raised them for observation. The larvae are bright orange, elongated to ovoid, and slightly flattened at the posterior pole, giving them a pyriform, or pear-shaped, appearance. Measuring 710 to 766 micrometers in length, they are uniformly covered in fine cilia about 24 micrometers long and swim in counterclockwise spirals, sometimes pausing or sinking before resuming their corkscrew journey. Their clear anterior-posterior polarity and cylindro-conical body plan echo the unusual parenchymella larvae documented in other scopalinid sponges, although the new species&#8217; larvae are far smaller than the giant larvae of the Caribbean Svenzea zeai, which reach over six millimeters in length.</p>
<p>To place the new species on the sponge tree of life, the researchers extracted DNA from three adults and two larvae and amplified two independent genetic markers: the mitochondrial cytochrome c oxidase subunit I gene, COI, and the nuclear small-subunit ribosomal RNA gene, 18S. Sequences were aligned against a comprehensive set of Scopalinidae sequences from public databases, and phylogenetic trees were reconstructed using both maximum likelihood and Bayesian inference methods. The two approaches produced congruent topologies, and both markers placed Svenzea marialmae firmly within a well-supported clade containing Svenzea, Scopalina and Stylissa, confirming its membership in the family Scopalinidae and its distinction from the family Dictyonellidae, to which some of its relatives were once assigned.</p>
<p>The genetic evidence was strikingly specific. Based on COI sequences, the new species is closest to the Caribbean sponge Svenzea cristinae, with a genetic distance of just 0.052, followed by an undescribed Svenzea and Svenzea zeai, while showing much larger distances from all species of Scopalina and Stylissa. The 18S data told the same story, yielding the lowest interspecies distance, a mere 0.005, between Svenzea marialmae and Svenzea cristinae. Intriguingly, the two markers disagreed on one point: COI recovered Svenzea as monophyletic while 18S suggested it is paraphyletic, a discrepancy the authors attribute to the scarcity of Scopalinida sequences in public databases and to the possibility that some Scopalina species, such as S. goletensis and S. kuyamu, may have been misidentified. Resolving this will require additional genetic markers, but the congruence of the adult and larval sequences within a single clade provides strong evidence that both life stages belong to the same new species.</p>
<p>Morphologically, the new sponge walks a fascinating line between its named relatives. Its skeletal architecture, prominent dendritic spongin fibers cored by long styles over a basal spongin plate, resembles that of Scopalina species, and its thin cushions, conulose surface and bright orange color closely recall the Caribbean Scopalina ruetzleri. Yet it lacks the oxeas and other spicule modifications seen in that species, and it differs sharply from the erect, flabellate Stylissa, whose choanosome is supported by confusedly plumoreticulate spicule tracts. Against its congeners, the comparisons are equally decisive: Svenzea tubulosa is tubular with smaller styles, Svenzea flava bears blunt-ended styloids, Svenzea germanyanezi is a tiny cave-dweller with two categories of oxea, and Svenzea zeai carries short styles and a purple-brown, volcano-like form. Only the combination found in the Mexican specimens, giant styles, no oxeas and vivid orange pigmentation, defines the new species.</p>
<p>Beyond its taxonomic significance, the discovery carries a dedication with deep personal meaning. The species epithet marialmae honors María del Rocío Troncoso González, mother of co-author Dr. Alma Paola Rodríguez-Troncoso, a marine biologist who has spent two decades conserving and restoring the coral communities of Islas Marietas National Park and strengthening biodiversity management in this Marine Protected Area. The type specimens are deposited in the Colección de Esponjas del Pacífico Mexicano at the Institute of Marine Sciences of the National Autonomous University of Mexico, and all genetic sequences have been archived in GenBank, making the data freely available for future studies.</p>
<p>The broader implications reach well beyond one sponge. By raising the global count of Svenzea species to eight and establishing the first documented record of the genus in the Eastern Tropical Pacific, the study fills a conspicuous biogeographic gap and hints at unrecognized evolutionary connections across ocean basins, the new species&#8217; closest relative after all lives on the far side of the American continent in the Caribbean. It also validates the combined use of mitochondrial and ribosomal markers alongside morphological and reproductive characters as a robust framework for testing phylogenetic hypotheses in Demospongiae, reducing the uncertainty of misidentifications that has long plagued sponge taxonomy. For the coral reefs of the Mexican Pacific, the message is clear: even in a marine protected area studied for decades, an abundant, brightly colored animal can remain formally unknown to science. As integrative taxonomy spreads to underexplored regions, researchers expect many more such surprises, each one refining our understanding of how sponge diversity evolved and how these ecologically important filter feeders are distributed across the world&#8217;s tropical seas.</p>
<p><strong>Subject of Research:</strong> Taxonomic and molecular description of a new marine sponge species of the genus Svenzea from coral communities in the Eastern Tropical Pacific</p>
<p><strong>Article Title:</strong> New insights into the diversity of Scopalinida (Porifera: Demospongiae) in the Eastern Tropical Pacific</p>
<p><strong>Article References:</strong> Bautista-Guerrero, E., Marin-Ramirez, M. F., Carballo, J. L., Rodríguez-Troncoso, A. P., &amp; Santiago-Valentín, J. D. (2026). New insights into the diversity of Scopalinida (Porifera: Demospongiae) in the Eastern Tropical Pacific. <em>Discover Ecology, 2</em>(1), Article 13. <a href="https://doi.org/10.1007/s44396-026-00031-2" rel="noopener noreferrer">https://doi.org/10.1007/s44396-026-00031-2</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44396-026-00031-2" rel="noopener noreferrer">10.1007/s44396-026-00031-2</a></p>
<p><strong>Keywords:</strong> marine sponges, Svenzea marialmae, Scopalinidae, Eastern Tropical Pacific, new species, integrative taxonomy, phylogenetics, COI, 18S rRNA, coral reefs, Islas Marietas, biodiversity</p>
]]></content:encoded>
					
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">200816</post-id>	</item>
		<item>
		<title>Last-Resort Antibiotic Resistance Genes Are Spreading Through Brazil&#8217;s Coastal Waters</title>
		<link>https://scienmag.com/last-resort-antibiotic-resistance-genes-are-spreading-through-brazils-coastal-waters/</link>
		
		<dc:creator><![CDATA[Juliet Wilcox]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 14:20:44 +0000</pubDate>
				<category><![CDATA[Earth Science]]></category>
		<category><![CDATA[antibiotic resistance in marine environments]]></category>
		<category><![CDATA[Antimicrobial Resistance]]></category>
		<category><![CDATA[antimicrobial resistance in seawater]]></category>
		<category><![CDATA[Brazil coastal water pollution]]></category>
		<category><![CDATA[challenges in combating multidrug-resistant bacteria]]></category>
		<category><![CDATA[colistin]]></category>
		<category><![CDATA[detection of resistance genes in pristine ecosystems]]></category>
		<category><![CDATA[Enterobacter]]></category>
		<category><![CDATA[environmental spread of colistin resistance]]></category>
		<category><![CDATA[Fernando de Noronha]]></category>
		<category><![CDATA[global dissemination of antibiotic resistance]]></category>
		<category><![CDATA[Guanabara Bay]]></category>
		<category><![CDATA[impact of antimicrobial resistance on public health]]></category>
		<category><![CDATA[integrons]]></category>
		<category><![CDATA[Klebsiella pneumoniae]]></category>
		<category><![CDATA[marine microbiology]]></category>
		<category><![CDATA[marine sponge microbiome resistance]]></category>
		<category><![CDATA[marine sponges]]></category>
		<category><![CDATA[mcr genes]]></category>
		<category><![CDATA[mcr genes in coastal bacteria]]></category>
		<category><![CDATA[One Health]]></category>
		<category><![CDATA[plastic pollution]]></category>
		<category><![CDATA[resistance genes on marine plastic litter]]></category>
		<category><![CDATA[spread of last-resort antibiotics]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=195351</guid>

					<description><![CDATA[Researchers found mobile colistin resistance genes in bacteria from water, plastic litter, and marine sponges across Brazilian coastal sites, including pristine areas, revealing ocean environments as widespread reservoirs of last-resort antibiotic resistance.]]></description>
										<content:encoded><![CDATA[<p>Scientists surveying Brazil&#8217;s coastline have uncovered an unsettling truth about the ocean: bacteria carrying genes that confer resistance to colistin, one of the world&#8217;s last-line antibiotics, are far more widespread in marine environments than previously believed. A research team led by investigators from the Universidade Federal do Rio de Janeiro screened more than 1,500 bacterial strains isolated from seawater, floating plastic litter, and marine sponges across five sampling regions, and found that mobile colistin resistance genes, known as mcr genes, were present at every single site examined. The findings, published in the journal Ocean Microbiology, reveal that even ecosystems considered pristine and far from urban pollution harbor these resistance determinants, underscoring how deeply antimicrobial resistance has penetrated the natural world.</p>
<p>Colistin, also called polymyxin E, occupies a special and precarious position in modern medicine. It is a cationic polypeptide that attacks the outer membrane of Gram-negative bacteria, and after decades of limited use because of kidney toxicity, it was reintroduced in recent years as a final defense against multidrug-resistant infections. With few new antibiotics in the development pipeline, clinicians increasingly depend on colistin when carbapenem-resistant pathogens strike hospital patients. The emergence of bacteria that resist this drug is therefore not a routine scientific concern but a genuine emergency in global public health, and the new study demonstrates that the ocean may be serving as an unexpected reservoir and highway for the genes responsible.</p>
<p>The mechanics of colistin resistance matter for understanding why the new results are so significant. Resistance can arise in two ways. Intrinsic resistance develops through chromosomal mutations that alter lipid A, the lipopolysaccharide component of the bacterial outer membrane that colistin targets, reducing the drug&#8217;s ability to bind. Acquired resistance, by contrast, depends on the horizontal transfer of mcr genes, usually carried on plasmids, which are mobile DNA elements that can shuttle between bacterial cells. Since the discovery of the mcr-1 gene in Escherichia coli plasmids a decade ago, researchers have identified ten mcr variants, from mcr-1 through mcr-10, and watched them disperse across continents, animal populations, and clinical settings. What remained poorly understood was how extensively these genes had colonized marine ecosystems.</p>
<p>To answer that question, the Brazilian team designed a natural experiment spanning roughly 330 kilometers of the Rio de Janeiro coastline plus the Fernando de Noronha Archipelago, a volcanic island group about 360 kilometers offshore in the Western Atlantic. Their sampling sites deliberately covered a gradient of human influence. At one extreme sat Bom Jesus Cove in Guanabara Bay, a tropical urban estuary receiving raw sewage, oils, and industrial contaminants from Rio de Janeiro city. At the other extreme lay the submarine caves of Fernando de Noronha, protected within a national marine park and accessible only by SCUBA diving. Between those poles, the researchers sampled the Cagarras Archipelago, a no-take marine protected area unfortunately positioned near the Ipanema submarine sewage outfall; the biodiverse waters of Arraial do Cabo, including the Gruta Azul submarine cave; and Ilha Grande Bay, one of the world&#8217;s largest tropical bays, which faces growing pressure from coastal settlements and maritime traffic.</p>
<p>The laboratory work was methodical and technically demanding. From 1,550 total bacterial isolates, the team focused on 308 Gram-negative bacilli identified as potential hosts of acquired colistin resistance determinants. Bacteria were cultured on Luria Bertani and MacConkey agar from water samples, washed and swabbed from pieces of floating plastic, and extracted from sponge tissue through serial dilution across four growth media. Identification proceeded by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry on a Bruker Microflex LT platform, and DNA was extracted using a thermal lysis protocol with Chelex 100 resin. Polymerase chain reaction screening then probed each strain for eight mcr variants, and any positive strains were tested further for beta-lactamase genes, quinolone resistance genes, aminoglycoside resistance genes, sulfonamide resistance genes, and class 1, 2, and 3 integron-integrase genes.</p>
<p>The results were striking in both breadth and detail. Of the 308 potential host strains, 101 carried at least one mcr variant, generating 128 total gene occurrences. Water samples contributed 59.4 percent of the positive strains, plastic litter 35.6 percent, and marine sponges 5.0 percent. The mcr-9 variant dominated with 33 occurrences, followed by mcr-3 with 23, mcr-2 with 18, and mcr-1 with 17. That mcr-9 topped the list is noteworthy because global metagenomic surveys have often ranked mcr-1 as the most dispersed variant. The mcr-9 gene is known to circulate on IncHI2 plasmids that interconnect human, animal, and environmental isolates, suggesting an efficient dissemination network that the ocean may now be extending.</p>
<p>The bacterial hosts carrying these genes were equally concerning. Among ten identified genera, Enterobacter, Acinetobacter, Vibrio, and Klebsiella predominated. Enterobacter species alone accounted for 31 strains and harbored the greatest mcr diversity, with every variant except mcr-5 and mcr-7 detected in the genus. More alarming still, mcr-positive Enterobacter was not confined to polluted Bom Jesus Cove but turned up in marine sponges and cave waters in Fernando de Noronha, an area with restricted human access. One Enterobacter hormaechei strain, isolated from a sponge in Sapata Cave, simultaneously carried mcr-2, mcr-9, and the sulfonamide resistance gene sul1. Four strains carried three mcr variants at once, including Klebsiella pneumoniae isolates from pristine sponges and from floating plastic, and an Enterobacter cloacae from Noronha water. Both K. pneumoniae and E. cloacae belong to the notorious ESKAPE group of pathogens, and their carriage of multiple resistance genes in aquatic matrices highlights the risk of waterborne transmission to humans.</p>
<p>The co-occurrence of resistance genes painted an even darker picture. Nearly half of the mcr-positive strains, 46.5 percent, also carried other antimicrobial resistance genes or integron-integrases, with sulfonamide resistance genes, particularly sul1, the most frequent companions, followed by the beta-lactamase genes blaTEM and blaSHV. In Bom Jesus Cove, the team detected the carbapenemase gene blaKPC alongside mcr-3 in Enterobacter bugandensis and Raoultella ornithinolytica strains, a combination that effectively eliminates two of the last therapeutic options for infections caused by these organisms. Integron-integrases, genetic platforms that capture and shuffle gene cassettes, co-occurred with mcr exclusively in the polluted cove, suggesting bacterial adaptation to intense anthropogenic selective pressure. Because changes in membrane permeability in mcr-positive bacteria can reduce sensitivity to multiple drugs, these combinations can compound into true multidrug resistance, complicating treatment of hospital-associated infections.</p>
<p>The gradient of pollution left a measurable fingerprint on the data. In Bom Jesus Cove, 27 of 104 water-isolated strains tested positive for mcr, and 36 of 82 strains from floating plastic litter carried the genes, a prevalence of roughly 44 percent that represents the highest in the study. The finding positions plastic debris as both a reservoir and a vector for antimicrobial resistance, offering microbes a stable, drifting substrate on which biofilms can form, exchange genes, and travel with currents. At the Cagarras Archipelago, 40 percent of water-isolated strains were positive despite formal protection, a legacy of the nearby sewage outfall. Arraial do Cabo showed 36.5 percent prevalence among water isolates and Ilha Grande Bay 36.3 percent. In Fernando de Noronha, prevalence dropped to about 5 percent of candidate host strains, with two of 17 water isolates and five of 15 sponge isolates positive, proving that resistance persists even where human pressure is minimal.</p>
<p>What emerges from the study is a warning that antimicrobial surveillance cannot remain confined to clinics and farms. Marine sponges, submarine caves, and drifting plastic are now documented hotspots of colistin resistance, and the genes involved sit on mobile elements capable of jumping into human pathogens. The Brazilian coastline, with its juxtaposition of dense urban pollution and remote protected archipelagos, offered an ideal natural laboratory, but the pattern it revealed is almost certainly global. The researchers argue for integrated monitoring programs that treat the ocean as a critical node in the antimicrobial resistance network, alongside conservation strategies that reduce sewage discharge and plastic pollution. As colistin remains a last resort for patients out of options, every mcr gene circulating in seawater, attached to plastic, or sheltering inside a sponge represents a card stacked against future medicine, and the ocean, it turns out, is dealing them freely.</p>
<p><strong>Subject of Research:</strong> Distribution of mobile colistin resistance (mcr) genes in bacteria from Brazilian marine environments</p>
<p><strong>Article Title:</strong> Widespread occurrence of mobile colistin resistance genes in Brazilian marine environments</p>
<p><strong>Article References:</strong> Brunelli, R. C., de Jesus Carvalho Baptista, T. V., de Oliveira Nithack Marques, M., da Silva Oliveira Alves, G., Abdon, B. B., Mello, M. P., Paranhos, R., Gallo, M. N., Vinzon, S. B., Lage, A., Sandes, J., Muricy, G., Klautau, M., Lopes, M. V., Dias, G. R., Canellas, A. L. B., &amp; Laport, M. S. (2025). Widespread occurrence of mobile colistin resistance genes in Brazilian marine environments. <em>Ocean Microbiology, 1</em>(1), Article 3. <a href="https://doi.org/10.1186/s44375-025-00003-z" rel="noopener noreferrer">https://doi.org/10.1186/s44375-025-00003-z</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1186/s44375-025-00003-z" rel="noopener noreferrer">10.1186/s44375-025-00003-z</a></p>
<p><strong>Keywords:</strong> antimicrobial resistance, colistin, mcr genes, marine microbiology, plastic pollution, Guanabara Bay, Fernando de Noronha, Enterobacter, Klebsiella pneumoniae, integrons, marine sponges, One Health</p>
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