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Herrera, S.

Publications and source records attributed to Herrera, S..

At least 19 recordsLinked to original sources

Stepping-stone population structure and sidespread clonality of the mesophotic octocoral Swiftia exserta in the warm temperate northwest Atlantic

Isolated mesophotic banks form spatially discrete networks of patchy ecosystems along continental shelves. Their long-term persistence depends on connectivity among populations of the dominant coral species that structure these communities. Yet the scale of larval-mediated gene flow across these networks remains poorly characterized. Similarly, the extent to which clonal propagation shapes local population dynamics is unresolved, leaving the relative contributions of sexual and asexual reproduction to population maintenance an open question. Here, population genomics and high-resolution (1km) biophysical larval dispersal modeling are integrated to resolve the genetic connectivity and clonal dynamics of Swiftia exserta, a key habitat-forming octocoral, across 13 mesophotic banks spanning the U.S. Gulf and eastern coast within the Warm Temperate Northwest Atlantic (WTNWA) coastal and shelf biogeographic province. Genome-wide SNP markers derived from Restriction-site Associated Sequencing (RADseq) were genotyped across 288 individuals. About 40% of individuals belonged to clonal genets confined to single banks within meters of one another, indicating that asexual propagation sustains local density but plays no detectable role in inter-bank connectivity. Population genetic analyses pointed to isolation by distance as the primary structuring force, with the majority of molecular variance residing within rather than among populations. The west-most population, East Flower Garden Banks, was the most differentiated population in the WTNWA Northern Gulf ecoregion, reflecting its peripheral position within the bank network. The Edisto population from the WTNWA Carolinian ecoregion, was distinct from all others, implicating the Florida Peninsula as a phylogeographic barrier. Biophysical particle-tracking simulations independently recovered the same spatial structure, with modeled larval exchange consistent with the genomic signal across the bank network. These findings reveal that S. exserta persists across the northern WTNWA province through a dual reproductive strategy of clonality at the bank scale and episodic larval exchange at the network scale, with implications for the conservation and management of mesophotic octocoral metacommunities.

ecology↗

Ca. Steroidedax gorgoniicola, a heterotrophic coral associate with horizontally acquired genes from Endozoicomonadaceae

Corals associate with many bacteria whose evolutionary histories and holobiont roles are unknown due to a lack of genomic resources. An example is the BD1-7 clade, which is found in some microbial metabarcoding libraries of corals and has been speculated to be phototrophic. To evaluate its phylogenetic position and assess its metabolic capabilities, we assembled and annotated the genome of an octocoral associate classified as BD1-7. Its full genome revealed that it instead represents a distinct and divergent clade of widespread coral associates. We propose the name Ca. Steroidedax gorgoniicola for this associate of Swiftia exserta. Unlike the true BD1-7 clade, its genome encoded no pathways to generate ATP from light and instead reveals that it is likely a heterotroph that can degrade steroids, chitin, and collagen as well as produce toxins or antimicrobial compounds and detoxify several reactive oxygen and nitrogen species. In addition, we identified several genes that were likely horizontally transmitted from Endozoicomonadaceae, including transposases and genes involved in virulence and cell adhesion. This work sheds light on the potential role of horizontal genetransfer in the evolution of symbiosis and highlights the importance of obtaining genomes to resolve coral-associated lineages and their metabolic capabilities.

microbiology↗

High Connectivity, Local Signatures: Genomic and Otolith Evidence from Reef-Associated Snappers.

Connectivity in reef-associated fishes emerges from processes operating across multiple spatial and temporal scales, yet these processes are rarely evaluated jointly. Here, we integrated genome-wide single-nucleotide polymorphisms (SNPs) data and otolith elemental signatures to examine connectivity in Red Snapper (Lutjanus campechanus) and Vermilion Snapper (Rhomboplites aurorubens) across 14 reefs and banks from the Flower Garden Banks National Marine Sanctuary and neighboring banks to the east. We tested whether genomic variation revealed population structure across geographic and depth gradients (shallow, upper mesophotic, and lower mesophotic), whether otolith chemistry captured fine-scale site-specific patterns of environmental exposure and habitat use not resolved by genetic markers alone, and how these complementary signals related to spatial variation in age structure and growth dynamics. Genome-wide SNP data revealed little detectable spatial genetic structure across the sampled banks in either species. In contrast, otolith microchemistry revealed pronounced site-associated environmental structuring, indicating that individuals experience localized habitat conditions within a regionally connected system. Red Snapper exhibited otolith signatures consistent with reef-associated environments, whereas Vermilion Snapper showed more variable elemental signatures, indicating exposure to a broader or more heterogeneous range of habitats. Spatial variation in age structure and growth provided additional demographic context, indicating that local differences among banks can emerge despite weak genomic differentiation. Together, these results show that fine-scale ecological and demographic differentiation can exist within a genetically connected system and that otolith chemistry provides critical information on post-settlement processes at scales not captured by genetic markers alone. By linking regional genomic connectivity with otolith-derived habitat signatures and demographic variation, this integrative framework provides a more comprehensive basis for understanding resilience and informing fisheries management in shelf-edge reef systems.

ecology↗

Argentina Explores Its Bathyal and Abyssal Zone for the First Time Using an ROV: New Biodiversity Discoveries and Unprecedented Public Engagement

Between July 23 and August 12, 2025, members of the scientific group Grupo de Estudios del Mar Profundo de Argentina (GEMPA) and collaborators conducted the Talud Continental IV expedition in the Mar del Plata Canyon. The expedition was conducted aboard the R/V Falkor (too) in partnership with Schmidt Ocean Institute (SOI), marking the first deployment of a Remotely Operated Vehicle (ROV) in Argentinean bathyal and abyssal waters. The Mar del Plata Canyon was explored in 2012 and 2013 by CONICET researchers using bottom trawls aboard the R/V Puerto Deseado (CONICET, Argentina). This new expedition combined high-definition video surveys, acoustic seafloor mapping, and physicochemical water-column characterization, with in situ sensing and sampling of fauna (animal specimens, zooplankton, and environmental DNA), water, sediments, and rock to characterize biodiversity and habitats between 880 and 3900 m. The expedition revealed extensive Bathelia cold-water coral reefs, soft-coral gardens, and more than 40 species suspected to be new to science, six of which have already been formally described. Anthropogenic debris, including plastics and fishing gear, was recorded at multiple stations, reaching even the deepest sites, underscoring the extent of human influence on these environments. The Talud Continental IV expedition was successful both scientifically and in promoting deep-ocean literacy and engagement, with broad outreach conducted through SOIs outreach and community engagement programs. The Ship-to-Shore program connected scientists on board with students and educators through live interactive sessions, engaging over 900 students from 19 institutions across Argentina and the United States. The live ROV divestreams, broadcast through SOIs YouTube and Twitch platforms, reached record levels of public engagement, with [~]19 million total views by July 23rd. The national and international press responded with extensive coverage and interview requests, resulting in over 3,900 international stories. Scientists continued to engage with the public after the expedition through talks at schools and public institutions. The expeditions achievements promise to usher in a new era of scientific discovery in the Southwestern Atlantic and underscore the value of integrating exploration, conservation, and outreach to inspire wonder and curiosity about the deep-sea in society. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=179 SRC="FIGDIR/small/726651v3_ufig1.gif" ALT="Figure 1"> View larger version (138K): org.highwire.dtl.DTLVardef@1457548org.highwire.dtl.DTLVardef@116f19aorg.highwire.dtl.DTLVardef@14fbb26org.highwire.dtl.DTLVardef@187c3a4_HPS_FORMAT_FIGEXP M_FIG C_FIG

ecology↗

Depth-dependent eDNA abundances across ecosystems inform deep-sea sampling strategies

Environmental DNA (eDNA) surveys are increasingly used to assess marine biodiversity and inform deep-sea environmental decision-making, including mineral resource management and fisheries oversight. Yet standard low-volume protocols inherited from coastal work may be inadequate at depth, and recent findings indicate that depth- and productivity-aware sampling, often requiring high-volume in situ filtration, is needed, but no quantitative framework links depth and ecosystem context to defensible filtration volume targets. We compiled 841 eDNA samples from eight expeditions across the North Atlantic, Wider Caribbean, and Pacific (surface to 4000 m) to quantify how recoverable eDNA scales with depth and surface productivity, and to derive depth- and productivity-aware sampling targets. Total eDNA concentration declined with depth as a power law, with attenuation exponents (b) modulated by surface productivity: most gradual in eutrophic waters (b = 0.67), intermediate in mesotrophic (b = 0.90), and steepest in oligotrophic systems (b = 1.25); volume-weighted models explained 66 to 88% of the variance. At a fixed extract-concentration target, required filtration volumes diverged ~7-fold between oligotrophic and eutrophic systems at 200 m and ~38-fold at 4000 m. Conventional Niskin sampling therefore undersamples deep-sea biodiversity, particularly in mid- to low-productivity systems. Among laboratory parameters, the assay-specific extract-concentration target exerted greater leverage on required volume than extraction efficiency or elution volume. Volume-aware sampling paired with optimized recovery should be routine in deep-sea eDNA surveys.

ecology↗

Novel insights into conserved biomineralization mechanisms revealed from a cold-water scleractinian coral skeletal proteome

Stony corals exhibit striking morphological plasticity across diverse environments and trophic strategies, raising fundamental questions about the conservation of their biomineralization machinery. Here, we characterize the skeletal organic matrix proteome of the cold-water, asymbiotic coral Desmophyllum pertusum and compare it with skeletal proteomes from a facultatively photosymbiotic temperate coral and an obligately photosymbiotic subtropical coral. Despite pronounced differences in habitat, symbiotic status, and skeletal micro-density, we observe convergence on a conserved "biomineralization toolkit". Comparative proteomics, genomics, and structural predictions reveal that this toolkit integrates diverse acidic matrix proteins, carbonic anhydrases, adhesion and structural proteins, and signaling components with multiple cellular export pathways. Together, these findings redefine coral biomineralization as a dynamic, coordinated network of cellular pathways rather than a static assemblage of matrix components. The symbiont-free model D. pertusum provides a mechanistic framework for dissecting coral calcification across environments and for assessing the resilience of this conserved machinery.

biochemistry↗

Lysosomal Expansion Compartments Mediate Zinc and Copper Homeostasis in Caenorhabditis elegans

Zinc is an essential transition metal that participates in many biological processes. In C. elegans, excess zinc is stored in lysosomes in intestinal cells; this process involves increasing the expression of the zinc transporter CDF-2 and remodeling of lysosomes characterized by an increase in the volume of the expansion compartment. To determine if this is a more general property, we investigated other metals. Here we report that lysosomes are remodeled in response to excess copper, manganese, and cadmium, with each metal causing an increase in the volume of the expansion compartment. Mutants with a reduced number of lysosomes were hypersensitive to growth retardation caused by excess copper and manganese, suggesting metal toxicity is prevented by metal sequestration in lysosomes. Using a novel method to analyze isolated lysosomes by X-ray Fluorescence Microscopy we demonstrated that zinc, copper and manganese are detectable in the lumen of lysosomes. To further analyze copper, we examined localization of CUA-1.1, a copper transporter that moves copper into the lumen of lysosomes. Like the zinc transporter CDF-2, CUA-1.1 localizes to both the acidified and expansion compartments in excess copper. These results indicate that the same intestinal lysosomes store zinc, copper and manganese. Lysosome remodeling characterized by an increase in volume of the expansion compartment is not specific to zinc but is a more general phenomenon during metal storage in lysosomes.

molecular biology↗

Deep-sea siliceous sponges harbor distinct and functionally diverse microbiomes

Sponges, phylum Porifera, are long-lived and basal-branching metazoans that play important roles in ocean biogeochemistry and host diverse microbial communities. Siliceous sponges form a major clade of the Porifera, yet their microbiome is not well-characterized, particularly in the deep ocean. Here, we used shotgun metagenomics to investigate the composition of the microbial communities of 13 siliceous sponges collected from four sites near Puerto Rico from depths ranging from 400-1900 meters. Nine of the sponges in this study are from five sponge family taxa that have not previously been sequenced using shotgun metagenomics. We assembled a total of 176 metagenome-assembled-genomes from 20 bacterial and 1 archaeal phyla. Ammonia-oxidizing archaea (AOA) Nitrosopumilaceae dominated most siliceous sponge microbial communities and was strikingly the sole symbiont associated with one sponge (Farrea). Overall, microbiome diversity was relatively low across siliceous sponges, except for a Phloeodictyidae, which was likely a high microbial abundance (HMA) sponge. Our results suggest that host sponge phylogeny may shape microbial community structure, with limited evidence for environmental influence. The sponge-associated microbial communities contained genetic capabilities for diverse metabolic functions, particularly contributing to the carbon, nitrogen, and sulfur cycles. In addition to the AOA, evidence of potential for microbial autotrophy was found through the presence of genes for RuBisCO, methanotrophy, and ATP citrate lyase. These results reveal both conserved relationships and metabolic flexibility across siliceous sponge lineages, suggesting unique evolutionary dynamics and demonstrating the importance of microbial metabolism to sponge host health and nutrient cycling in the oligotrophic deep ocean. ImportanceMarine sponges, emerging [~]600 million years ago, have close relationships with microorganisms, but the microbiome of deep-sea siliceous sponges is not well understood. Siliceous sponges play essential roles in deep-sea ecosystems by providing habitats for other metazoans and mediating carbon, nitrogen, and sulfur cycling, yet they remain some of the least studied sponges. By shotgun sequencing DNA from 13 siliceous sponges collected near Puerto Rico, this study found that host sponge phylogeny influences microbial community composition and structure. Ammonia-oxidizing archaea dominated the microbial communities associated with marine sponges, likely playing key roles in utilizing metabolic byproducts and supporting host health. Other microbes also contributed to nutrient cycling and contained the potential to fix carbon, suggesting metabolic flexibility which may benefit sponge hosts in low-resource environments. These findings emphasize the ecological importance of siliceous sponge-microbe symbioses and contribute to our understanding of the drivers shaping their structure and function.

microbiology↗

Environmental filtering shapes patch dynamics across isolated mesophotic reefs

Mesophotic coral ecosystems (MCEs; [~]30-150 m) are major but poorly understood benthic habitats. We used Autonomous Reef Monitoring Structures (ARMS) and integrated metabarcoding (mtCOI, 18S), image analysis, and hydrodynamic modeling across six mesophotic banks in the Gulf of Mexico to test whether community assembly is governed by environmental filtering or dispersal limitation. Local environmental conditions explained nearly twice as much compositional variance as geographic effects. Differences in depth and turbidity predicted community dissimilarity up to tenfold better than geographic distance. Turbidity, driven by the benthic nepheloid layer (BNL), was the dominant filter, while depth effects were weaker and taxon-specific. Hydrodynamic simulations revealed dispersal is variable but not limiting. These findings identify the BNL as a key physical driver linking shelf oceanography, biodiversity, and ecosystem function. Suspended particle dynamics associated with BNLs merit integration into conservation planning as critical mediators of ecological connectivity in mesophotic and other patchy reef systems globally. TeaserSuspended particle layers, not dispersal barriers, determines which species colonize mesophotic coral reefs on the TX-LA continental shelf.

ecology↗

Coordination of Anle138b to Silver Results in Selective Reduction of a C-terminal truncated Alpha-synuclein Protein and Increased Aggregate Size

Parkinsons disease (PD) is a prevalent age-related neurodegenerative syndrome, partially thought to be caused by a decrease in alpha-synuclein proteostasis. Anle138b = 5-(1,3-benzodioxol-5-yl)-3-(3-bromophenyl)-1H-pyrazole (HL), is undergoing clinical trials as a promising mitigator of alpha-synuclein aggregation. Because complexation to metals is known to modulate the activity of several drugs, we have prepared and characterized: H2L(ClO4), [CuI({micro}-L)]3, and [AgI({micro}-L)]3. To better understand the bioviability of these compounds, we monitored their effects in a cell culture model of alpha-synuclein protein aggregation using human alpha-synuclein pre-formed fibrils (PFFs). Using two different anti-alpha-synuclein antibodies, our data suggests that [AgI({micro}-L)]3 decreases a C-terminal truncated protein that is approximately 12.4 kDa, as well as increases the size and alters the shape of PFF-induced aggregates. This indicates that [AgI({micro}-L)]3 impacts aggregation in a manner different from HL and may serve as a novel tool for studying C-terminal truncation related aggregation chemistry. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=101 SRC="FIGDIR/small/679869v1_ufig1.gif" ALT="Figure 1"> View larger version (18K): org.highwire.dtl.DTLVardef@4bbda5org.highwire.dtl.DTLVardef@8fc0b7org.highwire.dtl.DTLVardef@1b561f5org.highwire.dtl.DTLVardef@1322902_HPS_FORMAT_FIGEXP M_FIG C_FIG

biochemistry↗

A 3-genes interferon signature predicts sustained complete remission in pediatric AML patients

The immunological composition of the microenvironment has shown relevance for diagnosis, prognosis, and therapy in solid tumors but remains underexplored in acute leukemias. We investigated the significance of acute myeloid leukemia (AML) bone marrow microenvironment in predicting chemosensitivity and long-term remission in pediatric patients. We analyzed 32 non-promyelocytic pediatric AML patients at diagnosis using NanoString PanCancer IO 360 assay, RNA sequencing, and deep-phenotype flow cytometry analyses. The findings were validated using the pediatric TARGET AML dataset. A short signature of three interferon (IFN)-related genes (GBP1, PARP12, TRAT1) distinguished patients with chemosensitive disease and reduced minimal residual disease after induction chemotherapy. The signature stratified patients overall, and within the clinically defined "standard-risk" group, patients with high gene expression at diagnosis had significantly longer overall survival. The leukemia microenvironment associated with this signature showed enrichment of non-exhausted CD4+ and CD8+ T cytotoxic lymphocytes and expansion of CD8+ T effector memory cells re-expressing CD45RA (TEMRA) in patients with a favorable prognosis. Our results show the importance of the bone marrow microenvironment in pediatric AML and provide tools for a refined stratification of "standard-risk" patients, lacking adequate risk-oriented therapies. They also offer a promising guide for tackling immune pathways and exploiting immune-targeted therapies. Statement of significanceWe identified a novel three-gene IFN-related signature that distinguished pediatric AML patients by chemosensitivity and remission outcomes. It stratified patients across all risk groups, including the "standard-risk" group, with high expression linked to a T-cell-enriched microenvironment and longer survival. This signature may enhance risk stratification and guide targeted immunotherapy.

cancer biology↗

Environmental DNA Transport at an Offshore Mesophotic Bank in the Northwestern Gulf of Mexico

Environmental DNA (eDNA) offers a powerful, non-invasive means of assessing biodiversity in marine ecosystems, yet the spatial resolution of eDNA remains poorly understood. We investigated the vertical and horizontal dispersion of eDNA from an isolated mesophotic coral reef (Bright Bank) in the stratified offshore waters of the northern Gulf of Mexicos shelf edge. We conducted comprehensive vertical and horizontal water column eDNA sampling across multiple radial directions and depths. We characterized invertebrate communities using a paired metabarcoding approach targeting broad (18S) and taxon-specific (28S) markers. We found that vertical transport of benthic eDNA was limited by water column stratification, with distinct benthic community signals confined to the near-bottom layers. In contrast, horizontal dispersal of eDNA extended beyond at least 1.5 km, though the prevalence of eDNA from benthic invertebrates declined with increasing distance from the bank. Taxon-specific primers showed greater detection sensitivity and dispersal range, particularly for benthic corals, than primers that are used to broadly assess eukaryotic biodiversity. These findings demonstrate that water column structure and marker selection critically influence the spatial interpretation of marine eDNA data. The study represents a snapshot of late-summer conditions. Seasonal variability should be considered in future studies. Our results provide a realistic framework for integrating eDNA into offshore environmental surveillance, biodiversity monitoring, and spatial management.

ecology↗

Cross-reactivity of rPvs48/45, a recombinant Plasmodium vivax protein, with sera from Plasmodium falciparum endemic areas of Africa

BackgroundPs48/45, a Plasmodium gametocyte surface protein, is a promising candidate for malaria transmission-blocking (TB) vaccine. Due to its relevance for a multispecies vaccine, we explored the cross-reactivity and TB activity of a recombinant P. vivax Ps48/45 protein (rPvs48/45) with sera from P. falciparum-exposed African donors. MethodsrPvs48/45 was produced in Chinese hamster ovary cell lines and tested by ELISA for its cross-reactivity with sera from Burkina Faso, Tanzania, Mali, and Nigeria - In addition, BALB/c mice were immunized with the rPvs48/45 protein formulated in Montanide ISA-51 and inoculated with a crude extract of P. falciparum NF-54 gametocytes to evaluate the parasite-boosting effect on rPvs48/45 antibody titers. Specific anti-rPvs48/45 IgG purified from African sera was used to evaluate the ex vivo TB activity on P. falciparum, using standard mosquito membrane feeding assays (SMFA). ResultsrPvs48/45 protein showed cross-reactivity with sera of individuals from all four African countries, in proportions ranging from 94% (Tanzania) to 40% (Nigeria). Also, the level of cross-reactive antibodies varied significantly between countries (p<0.0001), with a higher antibody level in Mali and the lowest in Nigeria. In addition, antibody levels were higher in adults ([&ge;] 17 years) than young children ([&le;] 5 years) in both Mali and Tanzania, with a higher proportion of responders in adults (90%) than in children (61%) (p<0.0001) in Mali, where male (75%) and female (80%) displayed similar antibody responses. Furthermore, immunization of mice with P. falciparum gametocytes boosted anti-Pvs48/45 antibody responses, recognizing P. falciparum gametocytes in indirect immunofluorescence antibody test. Notably, rPvs48/45 affinity-purified African IgG exhibited a TB activity of 61% against P. falciparum in SMFA. ConclusionAfrican sera (exposed only to P. falciparum) cross-recognized the rPvs48/45 protein. This, together with the functional activity of IgG, warrants further studies for the potential development of a P. vivax and P. falciparum cross-protective TB vaccine.

immunology↗

Nuclear eDNA Metabarcoding Primers for Anthozoan Coral Biodiversity Assessment

The distributions of anthozoan corals are under-characterized due to their wide bathymetric range, occurrences in remote locales, and difficulties of identification from morphology alone. Environmental DNA (eDNA) sequencing promises to be a non-invasive strategy to complement conventional approaches for mapping and monitoring coral communities. Primers for eDNA meta-barcoding have been designed to amplify nuclear and mitochondrial DNA barcodes in shallow scleractinians and mitochondrial MutS in deep-sea octocorals. However, a comprehensive method for eDNA meta-barcoding from all anthozoan corals, including black corals, has not been developed. We leveraged a sequence database of global coral collections, from shallow water to the deep sea, to design new PCR primers for coral eDNA sequencing that target the 28S rRNA gene. We tested the performance of these primers by amplifying and sequencing eDNA from water samples collected in the Gulf of Mexico near mesophotic and deep-sea corals that were also imaged, sampled, and sequenced. Sequencing libraries produced using the primers were highly enriched in coral eDNA, with up to 99.8% of the reads originating from corals. Further, the 28S barcode amplified using the primers distinguished coral genera. We recovered amplicon sequencing variants (ASVs) identical to DNA barcodes derived from Sanger sequencing and genome skimming of corals sampled at the same field sites. This new eDNA meta-barcoding strategy permits targeted eDNA sequencing of black corals, octocorals, and scleractinians at sites where they co-occur and expands our current toolkit for mapping and monitoring coral communities in shallow coral reefs and the deep sea.

ecology↗

Skimming genomes for systematics and DNA barcodes of corals

1: Numerous genomic methods developed over the past two decades have enabled the discovery and extraction of orthologous loci to help resolve phylogenetic relationships across various taxa and scales. Genome skimming (or low-coverage whole genome sequencing) remains a low-cost, promising method to not only extract high-copy loci, but also 100s to 1000s of phylogenetically informative single-copy nuclear loci (e.g., ultraconserved elements [UCEs] and exons) from contemporary and historical museum samples. The subphylum Anthozoa, which includes important ecosystem engineers (e.g., stony corals, black corals, anemones and octocorals) in the marine environment, is in critical need of phylogenetic resolution and thus might benefit from a genome-skimming approach. 2: Genome skimming was conducted on 242 hexacorals and octocorals collected from 1890 to 2022. Using previously developed target-capture baitsets, we bioinformatically obtained UCEs and exons from the genome-skimming data and incorporated them with data from previously published target-capture studies. We also extracted partial to whole mitogenomes and nuclear rRNA genes from the skim data. 3: The mean number of UCE and exon loci extracted from the genome skimming data was 1,837 {+/-} 662 SD for octocorals and 1,422 {+/-} 720 loci for hexacorals; phylogenetic relationships were well resolved within each class. A mean of 1,422 {+/-} 720 loci were obtained from the historical museum specimens, with 1,253 loci recovered from the oldest specimen collected in 1886 and 1,336 loci recovered from a holotype. The nuclear rRNA genes and the majority of mitochondrial genes were successfully obtained from >95% of samples. Out of 99 circularized mitogenomes, 88% were recovered in samples from which we obtained >15M paired-end (PE) reads (>30M total reads); there was more variability in whether mitogenomes were circularized or not in samples with <15M PE reads. 4: Bioinformatically pulling UCEs, exons, mitochondrial genomes, and nuclear rRNA genes from genome skimming is a viable and low-cost option for phylogenetic studies. This approach can be used to review and support taxonomic revisions and reconstruct evolutionary histories, including historical museum and type specimens.

evolutionary biology↗

A seascape approach to the microbial biogeography of mesophotic and deep-sea octocorals

Coral-associated microbiomes vary greatly between colonies and localities with functional consequences on the host. However, the full extent of variability across the ranges of most coral species remains unknown, especially in corals living in deep waters. Here we characterized the microbiomes of four octocoral species from mesophotic and deep-sea habitats in the northern Gulf of Mexico, Muricea pendula, Swiftia exserta, Callogorgia delta, and Paramuricea biscaya using 16S metabarcoding. We tested for microbiome differentiation between and within species, examining the influence of the corals genotype and environmental factors that vary with depth (53-2224 m) and geographic location (over 680 m). Coral microbiomes were often dominated by amplicon sequence variants whose abundances varied across hosts ranges including corallicolids, Endozoicomonas, members of the Mollicutes, and the BD1-7 clade. Coral species, depth, and geographic location significantly affected diversity, microbial community composition, and the abundance of individual microbes. Differences in host genotype, bottom temperature, and surface primary productivity could explain part of the variation associated with depth and geographic location. Altogether, this work demonstrates that the microbiomes of corals vary substantially across their ranges with potential functional consequences, identifies important ecological drivers in mesophotic and deep-sea corals, and can inform restoration efforts.

microbiology↗

Genome assembly of the deep-sea coral Lophelia pertusa

Like their shallow-water counterparts, cold-water corals create reefs that support highly diverse communities, and these structures are subject to numerous anthropogenic threats. Here, we present the genome assembly of Lophelia pertusa from the southeastern coast of the USA, the first one for a deep-sea scleractinian coral species. We generated PacBio CLR data for an initial assembly and proximity ligation data for scaffolding. The assembly was annotated using evidence from transcripts, proteins, and ab initio gene model predictions. This assembly is comparable to high-quality reference genomes from shallow-water scleractinian corals. The assembly comprises 2,858 scaffolds (N50 1.6 Mbp) and has a size of 556.9 Mbp. Approximately 57% of the genome comprises repetitive elements and 34% of coding DNA. We predicted 41,089 genes, including 91.1% of complete metazoan orthologs. This assembly will facilitate investigations into the ecology of this species and the evolution of deep-sea corals.

genomics↗

Improved biodiversity detection using a large-volume environmental DNA sampler with in situ filtration and implications for marine eDNA sampling strategies

Metabarcoding analysis of environmental DNA samples is a promising new tool for marine biodiversity and conservation. Typically, seawater samples are obtained using Niskin bottles and filtered to collect eDNA. However, standard sample volumes are small relative to the scale of the environment, conventional collection strategies are limited, and the filtration process is time consuming. To overcome these limitations, we developed a new large - volume eDNA sampler with in situ filtration, capable of taking up to 12 samples per deployment. We conducted three deployments of our sampler on the robotic vehicle Mesobot in the Flower Garden Banks National Marine Sanctuary in the northwestern Gulf of Mexico and collected samples from 20 to 400 m depth. We compared the large volume ([~]40 - 60 liters) samples collected by Mesobot with small volume ([~]2 liters) samples collected using the conventional CTD - mounted Niskin bottle approach. We sequenced the V9 region of 18S rRNA, which detects a broad range of invertebrate taxa, and found that while both methods detected biodiversity changes associated with depth, our large volume samples detected approximately 66% more taxa than the CTD small volume samples. We found that the fraction of the eDNA signal originating from metazoans relative to the total eDNA signal decreased with sampling depth, indicating that larger volume samples may be especially important for detecting metazoans in mesopelagic and deep ocean environments. We also noted substantial variability in biological replicates from both the large volume Mesobot and small volume CTD sample sets. Both of the sample sets also identified taxa that the other did not - although the number of unique taxa associated with the Mesobot samples was almost four times larger than those from the CTD samples. Large volume eDNA sampling with in situ filtration, particularly when coupled with robotic platforms, has great potential for marine biodiversity surveys, and we discuss practical methodological and sampling considerations for future applications.

ecology↗