Frontiers in Marine Science

Arctic ecosystems are critically endangered by rising temperatures and changing hydrography, especially the intrusion of increasingly warm water from the Atlantic Ocean known as Atlantification. In addition to housing fragile biodiversity, Arctic copepods and their lipids play a crucial role in cycling carbon by transporting carbon into the deep ocean through their diapausing behaviors. Here, we explored the lipidomes of the Arctic copepod Calanus glacialis, collected from three fjords around Svalbard during November 2022 when C. glacialis are known to be in diapause. These three field sites provide a natural laboratory experiment, as they are influenced by different water masses with varying degrees of Atlantic water, and experience vast differences in sea ice coverage over the year. These environmental differences were clearly reflected in the lipidomic analysis, with stations influenced most by Atlantic Warm Water having the lowest total lipid concentrations and the lowest accumulation of storage lipids necessary for entering diapause. Membrane lipids were a significant proportion of the Svalbard copepod lipidomes, with the highest ratios observed at the Atlantified site. The high membrane lipid and high triacylglycerol concentrations were interpreted as signs of active feeding. This was further corroborated by fatty acid composition analysis, which revealed dietary biomarkers of carnivory at Atlantified sites. The copepods from the site most insulated from Atlantic influence had more than double the amount of storage lipids per individual and fatty acids associated with diatom biomass, indicating assimilation in the spring. Ultimately, the decrease in lipid content observed in association with Atlantification around Svalbard will impact diapause patterns, as Calanus species need 20-30% more WE to successfully complete diapause. In turn, this will impact the magnitude of carbon sequestration through the seasonal lipid pump, not to mention having radiating effects through the Arctic food web where Calanus glacialis plays an important role. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=131 SRC="FIGDIR/small/738257v1_ufig1.gif" ALT="Figure 1"> View larger version (49K): org.highwire.dtl.DTLVardef@fc9321org.highwire.dtl.DTLVardef@1f6336org.highwire.dtl.DTLVardef@aaa3a1org.highwire.dtl.DTLVardef@dcd2a8_HPS_FORMAT_FIGEXP M_FIG C_FIG

Diatoms are major contributors to marine primary production, yet current approaches for monitoring their abundance and function rely on coarse satellite chlorophyll estimates or sparse cell count and carbon fixation measurements. Molecular markers are a promising approach for high-resolution measurement of both abundance and metabolic activity through analysis of environmental DNA (eDNA) and RNA (eRNA). We present an isothermal quantitative recombinase polymerase amplification (qRPA) assay targeting rbcL gene copies and transcripts of marine diatoms, operating at low temperature and producing results in less than 15 min. We demonstrate specificity and calibration across diverse diatom taxa, then apply the assay to eDNA and eRNA samples from the Mare Chiara Long-Term Ecological Research site in the Bay of Naples, Italy, alongside microscopy, chlorophyll, physicochemical, and carbon-fixation data. Diatom rbcL DNA tracked abundance across five orders of magnitude despite seasonal shifts in community composition. Combining molecular and optical data revealed increased cellular rbcL copies and chlorophyll in low-light winter populations, suggesting enhanced photosynthetic capacity despite lower abundance. Furthermore, rbcL RNA reflected total carbon fixation rates and identified populations with differing carbon fixation activity. These results support rapid, RPA-based rbcL quantification as a robust approach for biomolecular ocean observing.

The marine biodiversity inhabiting rocky shores in the Colombian Pacific remains largely undocumented, primarily due to geographic isolation, logistical challenges, and socio-political constraints. To address the existing knowledge gap, we conducted an expedition to enhance baseline biodiversity knowledge in rocky shores by integrating multiple complementary approaches, including visual censuses, specimen collection with morphological identification, environmental DNA (eDNA) metabarcoding and DNA barcodes. eDNA samples were collected at four coastal sites adjacent to rocky substrates, along with biological specimens obtained from fourteen locations through SCUBA diving at depths ranging from 1 to 25 meters. Tissue samples were subjected to genomic DNA isolation, followed by the generation and validation of cytochrome c oxidase subunit I (COI) barcode sequences, which were subsequently corroborated through taxonomic assessment to ensure accurate species identification. eDNA metabarcoding analyses yielded over 7 million high-quality sequence reads. Although taxonomic resolution at the species level was constrained by the limited completeness of reference sequence databases, a total of 106 species and 83 families were successfully identified, predominantly within the classes Actinopteri, Chondrichthyes, and marine mammals. From the 769 specimens obtained we generated 871 sequences, including 414 validated COI barcodes representing 76 species across 64 families. The integration of DNA barcoding and eDNA approaches resulted in over 1,400 taxonomic detections spanning five phyla, with only six species shared between methodologies. Richness and diversity varied among sites, and revealed significant differences along the coastline between Jurado and Cupica Gulf. All sequences were deposited in BOLDsystems database under the CCBIO project and were visualized through OBIS and GBIF databases. These findings provide the first molecular-based baseline for rocky shore biodiversity in the Colombian Pacific, highlighting the value of integrative approaches for monitoring and conservation.

Populations are exposed to multiple anthropogenic stressors simultaneously; however, the combined effects are poorly understood. Climate change is starkly impacting marine ecosystems and consequently fishes, with warming temperatures and increases in frequencies and durations of extreme climate events. Concurrently, plastics, such as nylon used in fishing industries, are contaminating marine waters at unprecedented levels, with detrimental effects on fishes. Here we studied the cumulative effects of warming and nylon microplastic fibres on the behavior and physiology of threespine stickleback (Gasterosteus aculeatus) by exposing fish to conditions of 15{degrees}C and 20{degrees}C and nylon concentrations of 0, 1, 10, and 100 mg/g (mg nylon/g food) for 4 weeks. Feeding rates responded complexly to multiple stressors, as increasing concentrations of plastic reduced feeding rates, with warming having an antagonistic effect. Furthermore, we observed "coughing" behaviors in response to ingestion of microfibres and a unique reselection tendency of food items previously selected by conspecifics. Under warming conditions, critical thermal maximum (CTmax) increased; however, exposure to plastics led to reductions in CTmax and thermal safety margins. Given these results, we anticipate reduced acclimation capacities, greater anxiety, and reductions in foraging efficiencies with increasing concentrations of plastic. Cumulatively, these stressors will yield greater energetic trade-offs and decreased accuracy in food selection with stark implications for marine ecosystem dynamics.

Experimentally evolved, heat-tolerant algal symbionts (heat-evolved; HE) offer a promising means of enhancing coral holobiont thermotolerance under rapidly warming oceans. However, translating their benefits into restoration practices requires scalable delivery methods. Coral tissue fusion may provide one such pathway by facilitating HE symbiont transfer to wild corals; however, its feasibility remains largely untested. As an initial test, we paired adult isografts of Galaxea fascicularis and Psammocora columna hosting HE Cladocopium proliferum (SS8) with chemically bleached, SS8-naive recipients. Fusion was first observed after three days in G. fascicularis and nine days in P. columna. In both species, fusion was followed by increased pigmentation and photochemical efficiency at the recipients fusion interface relative to distal tissue and unfused controls. After [~]50 days, SS8 was detected at low levels (<3.5%) in 15/19 fused G. fascicularis recipients, although detection was also common among unfused horizontal-transmission controls maintained in the same water column (13/18). These findings provide the first empirical evidence that conspecific coral tissue fusion is associated with localised physiological recovery and can coincide with HE symbiont acquisition, while highlighting the need to distinguish tissue-mediated transfer from background horizontal transmission. Fusion may therefore represent a complementary pathway for beneficial symbiont delivery in assisted-evolution frameworks.

Coral reef monitoring needs scalable, non-invasive tools to complement resource-intensive traditional survey methods. Passive Acoustic Monitoring (PAM) offers a promising supplement, but its effectiveness is limited by the difficulty of attributing recorded sounds to species outside of previously well-characterized taxa. Using Omnidirectional Underwater Passive Acoustic Cameras (UPAC-360), we identified sounds from 31 reef fish species across 14 families on the Kona coast of Hawaii Island, including 13 not previously documented as soniferous. By releasing video and audio specimens, we have created the largest open-access collection of in-situ reef fish sounds to date for the Pacific. A subset of acoustically distinctive taxa--such as Hawaiian Dascyllus (Dascyllus albisella), Lei Triggerfish (Sufflamen bursa), soldierfishes (Myripristis spp.), wrasses, and herbivorous grazers--were identifiable in PAM recordings through manual acoustic and spectrogram review. Through identifying particular sounds linked to species with different ecological roles, these sounds have the potential to serve as indicators of reef function to increase the information and value coming from PAM surveys of Hawaiian and Pacific coral reefs.

The picocyanobacterium Prochlorococcus is a fundamental contributor to ocean primary productivity. While its free-living population has been extensively studied, primarily using flow cytometric analyses, the size and distribution of its particle-associated population is not well understood. Using filter fractionated samples from cruises in the Pacific Ocean, Atlantic Ocean, and Mediterranean Sea, we generated metagenomic data using internal standards, yielding absolute genome equivalent counts of Prochlorococcus cells in different size fractions. We used these data to model a relationship between relative and absolute genome equivalent counts, yielding a correction factor that we validated using published datasets. We then applied the correction factor to size-fractionated global metagenomic data from the TARA Oceans Project, which has widespread Prochlorococcus cells in size fractions >1.6 m throughout the transects, to calculate the fraction of the total Prochlorococcus population in large size fractions. The ''particle-associated'' population fraction increased with net primary productivity. Dissolved inorganic carbon was also directly correlated with increased particle association, which, combined with other evidence, could indicate an association with upwelling. We also examined the relationship between particle-associated population and carbon export at 150 m by incorporating published estimates of carbon flux based on TARA optical scattering data. This study highlights the potential importance of particle-associated Prochlorococcus to carbon flux in marine ecosystems and offers a way to convert relative to absolute genome equivalents of microorganisms in archival metagenomic datasets.

Thermal history provenancing can guide the choice of parental broodstock for selective breeding of corals from distinct reefs and has been proposed as an intervention for enhancing climate resilience. However, the genetic and molecular mechanisms underlying resultant offspring responses to heat stress, particularly during early life stages, remain poorly understood. Here, we generated Acropora tersa larvae and recruits by crossing parental colonies from the historically warmer Martin Reef and cooler Davies Reef and assessed the effects of within- and between-reef crosses on genetic diversity and transcriptional responses to heat stress. Genome-wide single nucleotide polymorphism analyses showed that broodstock from Martin and Davies Reefs were weakly differentiated (FST = 0.008) and exhibited comparable heterozygosity, as did all larval offspring groups. Transcriptomic analyses of recruits exposed to heat stress (32 {degrees}C for 36 days) revealed that both within- and between-reef offspring groups activated conserved stress-response pathways, with seven genotype-independent heat-responsive genes detected across all offspring groups. Differential expression and enrichment analyses showed induction of defence, protein homeostasis, intracellular transport, and metabolic processes alongside repression of growth- and signalling-related functions, consistent with the Type A General Coral Stress Response. Taken together, these findings suggest that the benefits of thermal history provenancing-informed selective breeding may be limited in low-differentiation systems and that targeted pre-screening of broodstock may help capture functional genetic variation relevant to restoration applications.

The global coral reef crisis has prompted restoration initiatives worldwide. Targeting the coral larval stage is among the most scalable approaches as recruitment operates over large spatial scales. It thus represents one of the best levers for coral population recovery. Active coral larval seeding has shown considerable success, and passive substrate engineering has emerged as a promising complementary strategy. Coral settlement modules featuring helix recesses have increased settlement and survival by up to 80-fold on small experimental units, but whether these results translate to tools deployable at the scale of thousands of units, remains yet an open question. Here, we transferred structural features from successful experimental coral settlement designs into production-ready concrete modules to (i) evaluate coral recruitment on five designs at four reef sites differing in flow regime and coral cover over one year; (ii) compare production-scale performance against experimental clay modules and natural reef substrate; and (iii) identify key parameters for large-scale production. The helix recess geometry of coral settlement modules outperformed the featureless control design approximately 20-fold and exceeded natural reef recruitment at least 3- to 32-fold. The helix features were successfully transferred from experimental clay to production-scale concrete modules, yielding comparable settlement densities when standardized to crevice length, which proved to be the biologically relevant unit of available habitat. Production feasibility was demonstrated by producing 690 modules for deployment on a hybrid reef on the west side of Oahu, Hawaii. The passive coral larval recruitment approach presented here could substantially improve the logistical and economic feasibility of large-scale coral reef restoration. This approach requires neither coral larval rearing, handling, nor coral fragmenting, and is compatible with active larval seeding where genetic diversity or larvae supply are limiting factors. The coral settlement modules can be cast in standardized concrete molds at precast facilities. Modules have demonstrated consistent coral recruitment enhancement across reef environments with contrasting flow and coral cover. Deploying mixed arrays of helix-recess structures with designs offering multi-level complexity and three-dimensional rugosity maximizes outcomes for coral, fish, and invertebrate communities simultaneously. Site selection is the most critical deployment decision and should consider larval supply, hydrodynamics, and substrate stability which drive recruitment outcomes more than design choice alone. The modules offer a range of application potential, ranging from integration into existing coastal infrastructure over stand-alone reef restoration approaches, to substrate-consolidating interconnected arrangements.

Bottom trawls have been used for centuries, yet studies of their impact on marine ecosystems have largely been restricted to recent decades. Here, we reconstruct fishing effort for the international trawler fleets in the North Sea from the age of sail to early steam trawling, by synthesising historical data describing vessel numbers and specifications, gear dimensions, fishing grounds, and operational characteristics. The trawler fleet increased from ca 800 sailing vessels in the 1820s to ca 3500 at the peak in sail trawling in the 1880s. Subsequently, steam trawling fleets emerged, increasing to almost 2000 vessels in the 1910s, while sailing fleets declined. Trawling grounds, covering ca 7% of the North Sea in 1820s, expanded from coastal to offshore grounds, reaching ca 25% in the 1880s, and 46% in the 1910s after the transition to steam trawling. Using a hydro- and aerodynamic approach to model the wind conditions required for sail trawling, we show that about 55% to 80% of the time at sea was suitable for trawling, providing a new quantitative basis for estimating historical fishing effort. The surface area swept by the trawl per year increased from 35,000 km2 in 1820s to 225,000 km2 in 1880s and 500,000 km2 in 1910s, corresponding to ca 60% of present levels. The trawling intensity (swept area ratio) varied between 0.9-1.7 year-1 in the era of sail, increasing to ca 2.0 in the 1910s. The trawling footprint (unique area trawled) increased to 160,000 km2, about half the present level.

Crown-of-thorns sea star (CoTS), Acanthaster cf. solaris, outbreaks are a major cause of hard coral cover decline across the west Pacific, threatening coral reefs. Coral taxa vary in susceptibility to CoTS predation from preferred (Acropora spp.) to non-preferred (Porites spp.), yet the mechanisms underlying these differences are poorly understood. We investigated coral defenses during an ongoing CoTS outbreak in Mo'orea, French Polynesia by examining gene expression (including putative toxin genes) in healthy and actively predated colonies of a preferred (Acropora hyacinthus) and a non-preferred (Porites sp.) coral prey species. During predation, A. hyacinthus exhibited molecular signatures of cellular stress responses involving oxidative stress signalling, inflammation, and tissue proteolysis. In contrast, Porites sp. showed enrichment of genes involved in mitochondrial metabolic adjustment and aerobic metabolism, suggesting metabolic compensation to maintain cellular function. Furthermore, A. hyacinthus demonstrated a reactive defense behaviour by differentially expressing toxins (e.g., kunitz-type neurotoxins) while Porites sp. employed constitutive expression of all putative toxins regardless of active predation, suggesting a proactive defense strategy. Together, these findings suggest that preferred and non-preferred coral prey exhibit fundamentally different molecular and defensive strategies during CoTS predation, shedding light on the evolutionary arms race between corals and their predators.

Lipid peroxidation (LPO) is widely used as a biomarker of oxidative stress in coral bleaching research, yet its measurement remains poorly standardized across the field. A systematic review of the coral LPO literature reveals substantial variation in methodological approaches, including tissue fraction analysis, lysis protocols, assay choice, and normalization metrics, confounding cross-study comparison and obscuring the biological interpretation of results. We experimentally investigate two key sources of variation: the use of bulk holobiont vs separated host and algal symbiont fractions, and the choice of normalization metric. To do so, we used Montastraea cavernosa (n = 6 colonies) exposed to ambient (28C), heat stress (30.5C), and heat stress + artificial upwelling (AU; heat stress intermitted by daily pulses of cooler water, 30.5/27.5C) conditions in a controlled mesocosm experiment. Using a TBARS-based MDA assay with a lysis buffer optimized for coral tissue, we measured LPO separately in coral host and algal symbiont fractions across four time points throughout the day. Host MDA remained stable across all treatments and time points, consistent with either sufficient antioxidant buffering capacity or thermal acclimation over the experimental period. Algal symbiont MDA, in contrast, exhibited pronounced diel and treatment-specific dynamics, and the two fractions responses were decoupled from one another. Normalizing MDA to coral surface area instead of total protein content produced largely consistent diel and treatment patterns, but the two metrics diverged at specific time points, indicating that normalization choice is not interchangeable and can itself affect interpretation. Together, our literature review and empirical results demonstrate that host and algal symbiont LPO dynamics are not comparable when aggregated and argue for host-symbiont fraction separation and consistent, explicitly reported normalization as minimum standards for interpretable and cross-comparable coral LPO measurement.

Here, oyster larval developmental abnormalities within a New England hatchery were linked to a common UV sterilization technique that has been used for over 20 years. Because of the known link between phytoplankton oxylipins and egg mortality in copepods, we hypothesized that UV pretreatment of seawater results in the production of oxylipins that inhibit larval digestion of microalgae. We used lipidomics to observe changes in the organic compounds dissolved in estuarine seawater when filtered and when filtered and pretreated with UV. UV treatment resulted in an increase in the relative abundance of oxylipins associated with cyanobacteria, fungi, and macroalgae in 2020, whereas oxylipins typically produced by diatoms were more abundant in the UV treatments from 2021. Oxylipin concentrations were higher in 2020, when the hatchery reported the most severe problems with larval development. Removing the UV step allowed continued larval production in both years. However, the lack of UV sterilization led to an unidentified bacterial pathogen in 2021, which nearly decimated the overall seasonal production of oyster seed. To follow up in a more controlled environment, the larvae were exposed to exogenous oxidized lipids, which resulted in the same digestive syndrome and histological symptoms as the endogenous suite of compounds produced by UV. Further investigation of the lipidomes revealed that oxylipins were only one class of potentially harmful compounds linked to UV sterilization, and the dissolved concentrations of secondary metabolites associated with higher plants, a wide range of pharmaceuticals, and anthropogenic organic pollutants also increased under UV light. Future efforts will explore the sources of these compounds, the mechanisms by which they inhibit oysters, and whether this is an emerging environmental problem for other ecosystems and shellfish hatcheries. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=137 SRC="FIGDIR/small/738347v1_ufig1.gif" ALT="Figure 1"> View larger version (37K): org.highwire.dtl.DTLVardef@43d06corg.highwire.dtl.DTLVardef@2894daorg.highwire.dtl.DTLVardef@449e59org.highwire.dtl.DTLVardef@f81983_HPS_FORMAT_FIGEXP M_FIG C_FIG

Shifts from coral-dominated to macroalgal-dominated reef systems have become increasingly common in many coastal regions worldwide. Coral-macroalgal interactions have been shown to be generally detrimental to coral health, with macroalgal allelopathic compounds able to exert serious and even lethal effects on coral at various stages of growth and development. Previous studies have shown that the coral-associated microbial communities play important roles in coral health and mitigating external environmental stress, including macroalgal contact stress. However, it remains unclear whether changes in the coral microbiome have an influence on the Symbiodiniaceae community composition, and if such changes subsequently affect coral health. In this study, we examined changes in both the coral microbiome and the Symbiodiniaceae communities of two Singaporean coral species (Pocillopora acuta and Merulina ampliata) when exposed to both direct and water-mediated macroalgal contact with Lobophora sp. This was investigated using 16S rRNA gene amplicon sequencing to characterize the coral microbiome, and ITS2 variable region sequencing to profile the Symbiodiniaceae communities. Although no significant differences were observed for the coral microbiomes and Symbiodiniaceae communities at both alpha-and beta- diversity levels between control and macroalgal contact treated fragments within each coral species, inter-colony variations in responses to macroalgal contact were observed for both the coral microbiome and Symbiodiniaceae communities of M. ampliata. These results suggest that coral colonies vary in the mechanisms that allow mitigation of the effects of macroalgal contact, and in their resilience to macroalgal-induced stress.

Absorption of CO2 by global oceans is decreasing pH resulting in ocean acidification (OA). Impacts on shellfish have been documented in ecologically and commercially important species. We examined the influence of diet and OA between two populations of red abalone (Haliotis rufescens) a species of aquaculture importance and declining wild populations. Populations experience different exposure histories: strong upwelling (Van Damme, California [VD]) historically exposed to low-pH conditions and weak-intermittent upwelling (Santa Barbara, California [SB]). Abalone were cultured under control-pH or OA-conditions and fed crustose coralline algae (CCA) or diatoms used in aquaculture. We tested treatment effects of population, settlement diet, and OA-exposure on survival as influenced by larval-energy stores. Survival in both populations was enhanced by CCA when cultured under both treatment conditions; however, by later stages, this effect remained only for SB. SB had reduced post-settlement survival when cultured under OA-conditions, whereas post-settlement survival of VD was not. Diet affected the relationship between larval-energy and post-settlement survival; a positive relationship when fed diatoms and a negative relationship with CCA. The relationship between larval energy and post-settlement survival was stronger in VD. CCA enhanced juvenile growth in SB cultured abalone at both three-months and one-year post-settlement. Settlement diets can reduce the impacts of OA on early-life stages of abalone, but population differences driven by underlying energetics affect the consistency of this outcome. These findings illuminate the impacts from OA, suggesting populations may be at risk, and inform strategies for developing and sustaining shellfish aquaculture in the face of changing ocean conditions.

Sexual coral propagation is an emerging technique capable of producing large numbers of corals for coral transplantation and reef rehabilitation. In contrast to asexual coral propagation, sexual propagation increases genotypic diversity and can be used for selective breeding to enhance coral heat tolerance or other desirable traits. However, implementation at meaningful ecological scales is hindered by high mortality during early life stages, high costs associated with nursery rearing facilities, and labour-intensive outplanting methods. To overcome these issues, we developed the CoralAssist Plug (CAP), a ceramic device designed for the rapid and cost-effective outplanting of sexually propagated corals in large numbers that maximises post-outplant survivorship. CAPs combine three important functional features: 1) built-in microrefugia to protect juvenile corals from grazing, 2) a relatively small size, 3 by 1 cm, that is easy to handle and stack efficiently without compromising the survivorship of corals, and 3) a hole in the middle that facilitates handling and attachment. CAPs were settled with Acropora aff. digitifera and outplanted to a reef crest after 1 to 6 months of ex situ nursery rearing. A 3-person dive team was able to outplant ~120 CAPs in one 90-minute shallow dive (just over 2 minutes per CAP per person). With longer nursery durations of 6 months, it was possible to achieve 36 % yield (i.e., the proportion of devices with a surviving coral) 4-years post-outplant. With nursery durations shortened to 1 month, we were able to attain 24 % yield 3-years post-outplant. Microrefugia significantly enhanced post-outplant survivorship leading to an 11 % increase in yield 4 years post outplant compared to devices without microrefugia. Outplanted corals that had reached adult size, were self-attached and were reproductively mature after 4 years. Our results suggest that CAPs can play a meaningful role in reef rehabilitation by efficiently introducing sexually propagated corals into natural populations with clear applications to assisted evolution techniques, such as selective breeding.

Phenotypic plasticity is a critical strategy for sessile marine invertebrates that cannot escape changing environmental conditions. For corals facing intensifying climate change, the molecular mechanisms that generate and regulate acclimatory responses are central to understanding performance and persistence. MicroRNAs (miRNAs), small non-coding RNAs that regulate gene expression via translational repression and transcript degradation, are compelling candidates for mediating such plasticity, but their role in coral biology remains poorly characterized. Here, we use Astrangia poculata, a temperate coral that endures annual temperature ranges exceeding 25{degrees}C, to investigate the potential for miRNA-mediated plasticity across seasonal and thermal contexts. We exposed adult aposymbiotic colonies to ambient seasonal temperatures ([~]5-22{degrees}C) and a chronic +3{degrees}C warming treatment from February to August 2021, sampling monthly for physiological analyses and at three time points (February, June, August) for molecular analyses. Seasonal change drove significant shifts in photosynthesis, respiration, and soluble protein, whereas the +3{degrees}C treatment had minimal physiological effect. RNA-seq analysis identified the strongest response across seasons, with transcriptional functional enrichment shifting from protein homeostasis, and cellular integrity in the winter, to immunity, metabolism, and reproduction in the summer. We identified 51 miRNAs in A. poculata, 46 of which are novel to this species, providing the first characterization of the miRNA repertoire in this species. Target prediction and co-expression analyses revealed that while mRNA-miRNA networks maintain a stable infrastructure across seasons and treatments, specific interactions are rewired to drive seasonal biology. This dynamic regulation suppresses energy-intensive cell division and morphogenesis during winter quiescence, while shifting to regulate tissue remodeling and reproduction genes during the summer. These results establish miRNAs as seasonal gene regulators in a temperate coral and suggest that the molecular infrastructure underlying its plasticity may also confer resilience to moderate thermal stress.

Rising ocean temperatures disrupt previously stable coral-microbe interactions, leading to widespread coral mortality and threatening reef ecosystems worldwide. Growing evidence demonstrates the coral microbiome, including protists, plays a critical role in the host response to thermal stress. Specifically, corallicolids (Phylum: Apicomplexa) are positively correlated with thermal stress mortality in soft corals. This study investigates changes in the eukaryotic microbiome of the stony coral, Pocillopora damicornis, across an experimental thermal stress event. Using anti-metazoan 18S rRNA gene metabarcoding, protist communities were assessed at four time-points during experimental thermal stress. Outside of the Symbiodiniaceae, a prominent shift in microbiome composition during thermal stress was observed, most notably a significant increase and dominance in Corallicolida abundance in heat-stressed corals, while other protists declined substantially. Increased corallicolid abundance concurrent with bleaching suggests an overlooked compounding stressor beyond the loss of algal symbionts during heat stress. These results contrast with previous research on Pocillopora microbiomes showing prokaryotic community stability throughout stress, and support the hypothesis that thermal stress may alter the coral-corallicolid relationship, potentially shifting corallicolids from a commensal to a parasitic role, and synergistically contributing to coral mortality during and after heat stress. This work provides critical insight into the role of protists in marine holobionts, supports their inclusion in future microbiome studies, and informs strategies to improve coral resilience under climate change.

The growing demand for sustainable aquafeeds has intensified interest in alternative protein ingredients capable of reducing reliance on fishmeal without compromising fish performance. Here, we evaluated microbial community-based single-cell protein (SCP) as a fishmeal substitute in juvenile Asian seabass (Lates calcarifer) diets in two independent feeding trials of juvenile fish conducted over 49 and 56 days, respectively and compared them to a previous study that lasted 24 days. SCP was produced from nutrient-rich soybean-processing side streams by microbial communities in fermenters and incorporated into experimental diets at inclusion levels ranging from 10% to 100% fishmeal replacement. In the 24-day trial, a diet containing 50% fishmeal replacement with lab-scale produced SCP achieved 100% survival and a feed conversion ratio (FCR), specific growth rate (SGR), and weight gain comparable to the fishmeal control diet. In the 49-day trial using pilot-scale produced SCP, a 50% fishmeal replacement also maintained an FCR and feed intake comparable to the control, whereas complete replacement reduced feed intake and growth performance. In a 56-day pilot-scale trial that used 500-L fish tanks, diets containing up to 50% fishmeal replacement maintained comparable survival, weight gain, and SGR, although moderately higher FCR values were observed at higher SCP inclusion levels. Proximate composition and essential amino acid profiles of fish fed control or SCP-containing diets were comparable. Genome-resolved metagenomic analyses revealed diverse microbial taxa associated with the SCP. Collectively, these findings support microbial community-based SCP as a scalable and reproducible alternative protein platform for aquaculture feeds across independent trials and production scales.

New maritime regulations restricting high-sulfur fuels have led to the transition to new low sulfur fuel oils (LFSOs). We do not know how LSFOs will behave in marine environments and how they will respond to available remediation strategies, presenting an environmental risk. The risk will be even higher in the remote high Arctic, especially along the Northwest Passage (NWP), for which an increase in shipping traffic is expected by the end of the century. In this study, we evaluated the long-term (one year) biodegradation potential of the native microbial community of NWP beach sediment using in situ mesocosm experiments with two different types of LSFOs: a marine gas oil (Marine diesel) and an ultra-low sulfur fuel oil (ULSFO). We observed that the lighter Marine diesel was biodegraded better (72.0%) than the heavier ULSFO (32.5%). We described composition of the microbial community of the mesocosms using 16S rRNA gene amplicon sequencing and observed a decrease in microbial diversity for the fuel-treated samples compared to the untreated controls. Despite the decrease in overall diversity, we observed significantly higher abundances of known hydrocarbon degrading microbes (e.g., Oleispira, Altererythrobacter, Gilvibacter, Pseudohongiella) in the fuel mesocosms. Our study showed the potential to implement biodegradation as a remediation strategy under the cold and oligotrophic environmental conditions present throughout the NWP. However, we also observed that microbes on their own cannot degrade the entirety of the removed fuel and other types of remediation will need to be considered to complement the natural biodegradation observed here.