Caribbean Sponge Research Articles

Fine‐grained sediment production by endolithic sponges on Caribbean coral reefs

AbstractEndolithic sponges are key players in carbonate cycling on coral reef systems. While their bioerosion of reef framework is relatively well studied, their role in biogenic sediment generation is poorly understood. In this study, the sedimentary attributes and production rates of eight Caribbean endolithic sponge species were characterized. The findings revealed notable species‐specific variations in sediment production rates (range: 1.0–6.3 kg CaCO3 m−2 yr−1), alongside consistency in sediment characteristics (modal sizes ranging from 39 to 48 μm). The species‐specific rates were used to explore reef‐scale variations in sponge‐derived sediment generation across 50 reef sites in the Mexican Caribbean. Significant between‐site variability was observed, with estimated annual sediment production ranging from < 0.01 to 0.84 kg m−2 of reef. Production was primarily driven by sponge abundance, with discernible spatial variations in the contributions of different species, which could be related to variability in local environmental conditions. The rapidity at which these sediment producers can utilize dead coral substrates, coupled with their positive response to the changing marine environment, highlights the growing importance of these sponges in modern degraded Caribbean reef systems.

Severe hurricanes increase recruitment and gene flow in the clonal sponge Aplysina cauliformis.

Upright branching sponges, such as Aplysina cauliformis, provide critical three-dimensional habitat for other organisms and assist in stabilizing coral reef substrata, but are highly susceptible to breakage during storms. Breakage can increase sponge fragmentation, contributing to population clonality and inbreeding. Conversely, storms could provide opportunities for new genotypes to enter populations via larval recruitment, resulting in greater genetic diversity in locations with frequent storms. The unprecedented occurrence of two Category 5 hurricanes in close succession during 2017 in the U.S. Virgin Islands (USVI) provided a unique opportunity to evaluate whether recolonization of newly available substrata on coral reefs was due to local (e.g. re-growth of remnants, fragmentation, larval recruitment) or remote (e.g. larval transport and immigration) sponge genotypes. We sampled A. cauliformis adults and juveniles from four reefs around St. Thomas and two in St. Croix (USVI). Using a 2bRAD protocol, all samples were genotyped for single-nucleotide polymorphisms (SNPs). Results showed that these major storm events favoured sponge larval recruitment but did not increase the genetic diversity of A. cauliformis populations. Recolonization of substratum post-storms via clonality was lower (15%) than expected and instead was mainly due to sexual reproduction (85%) via local larval recruitment. Storms did enhance gene flow among and within reef sites located south of St. Thomas and north of St. Croix. Therefore, populations of clonal marine species with low pelagic dispersion, such as A. cauliformis, may benefit from increased frequency and magnitude of hurricanes for the maintenance of genetic diversity and to combat inbreeding, enhancing the resilience of Caribbean sponge communities to extreme storm events.

Oceans May Have Already Seen 1.7�C of Warming

The global warming clock started ticking decades earlier than current estimates assume, according to Caribbean sponges.

Ocean acidification influences the gene expression and physiology of two Caribbean bioeroding sponges

IntroductionCoral reef ecosystems are experiencing increased rates of carbonate dissolution due to losses in live coral cover coupled with the impacts of ocean acidification (OA) on coral reef calcifiers and bioeroders. While the stimulating effect of OA on bioerosion has been demonstrated experimentally, predominantly in the Pacific, the underlying physiological and molecular mechanisms behind the response are still poorly understood.MethodsTo address this, we subjected common zooxanthellate (Cliona varians) and azooxanthellate (Pione lampa) Caribbean sponges to pre-industrial (8.15 pH), present-day (8.05 pH), and two future OA scenarios (moderate OA, 7.85 pH; extreme OA, 7.75 pH) and evaluated their physiological and transcriptomic responses.ResultsThe influence of OA on sponge bioerosion was nonlinear for both species, with the greatest total bioerosion and chemical dissolution rates found in the 7.85 pH treatment, then not increasing further under the more extreme 7.75 pH conditions. A trend towards reduced bioerosion rates in the 7.75 pH treatment occurred regardless of the presence of algal symbionts and suggests that the sponges may become physiologically impaired under prolonged OA exposure, resulting in diminished bioerosion potential. These findings were supported by the RNA-seq analysis, which revealed differentially expressed genes involved in a stress response to OA, in particular, suppressed metabolism.DiscussionThis may indicate that the sponges had reallocated energy resources towards more critical physiological needs in response to OA as a survival mechanism under stressful conditions. These data reveal that while the bioerosion rates of excavating sponges in Caribbean reef ecosystems may increase under moderate OA scenarios, this OA-stimulation may plateau or be lost at extreme end-of-century pH conditions, with implications for the dissolution and long-term persistence of reef habitat structures.

Effects of sponge-to-sponge contact on the microbiomes of three spatially competing Caribbean coral reef species.

Sponges perform important ecosystem functions, host diverse microbial symbiont communities (microbiomes), and have been increasing in density on Caribbean coral reefs over the last decade. Sponges compete for space in coral reef communities through both morphological and allelopathic strategies, but no studies of microbiome impacts during these interactions have been conducted. Microbiome alterations mediate spatial competition in other coral reef invertebrates and may similarly impact competitive outcomes for sponges. In this study, we characterized the microbiomes of three common Caribbean sponges (Agelas tubulata, Iotrochota birotulata, and Xestospongia muta) observed to naturally interact spatially in Key Largo, Florida (USA). For each species, replicate samples were collected from sponges in contact with neighbors at the site of contact (contact) and distant from the site of contact (no contact), and from sponges spatially isolated from neighbors (control). Next-generation amplicon sequencing (V4 region of 16S rRNA) revealed significant differences in microbial community structure and diversity among sponge species, but no significant effects were observed within sponge species across all contact states and competitor pairings, indicating no large community shifts in response to direct contact. At a finer scale, particular symbiont taxa (operational taxonomic units at 97% sequence identity, OTUs) were shown to decrease significantly in some interaction pairings, suggesting localized effects for specific sponge competitors. Overall, these results revealed that direct contact during spatial competition does not significantly alter microbial community composition or structure of interacting sponges, suggesting that allelopathic interactions and competitive outcomes are not mediated by microbiome damage or destabilization.

The influence of sponge-dwelling gobies (Elacatinus horsti) on pumping rates of Caribbean sponge hosts, Aplysina lacunosa and Aplysina archeri

The influence of sponge-dwelling gobies (Elacatinus horsti) on pumping rates of Caribbean sponge hosts, Aplysina lacunosa and Aplysina archeri

Microbiome diversity and metabolic capacity determines the trophic ecology of the holobiont in Caribbean sponges

Sponges are increasingly recognized as an ecologically important taxon on coral reefs, representing significant biomass and biodiversity where sponges have replaced scleractinian corals. Most sponge species can be divided into two symbiotic states based on symbiont community structure and abundance (i.e., the microbiome), and are characterized as high microbial abundance (HMA) or low microbial abundance (LMA) sponges. Across the Caribbean, sponge species of the HMA or LMA symbiotic states differ in metabolic capacity, as well as their trophic ecology. A metagenetic analysis of symbiont 16 S rRNA and metagenomes showed that HMA sponge microbiomes are more functionally diverse than LMA microbiomes, offer greater metabolic functional capacity and redundancy, and encode for the biosynthesis of secondary metabolites. Stable isotope analyses showed that HMA and LMA sponges primarily consume dissolved organic matter (DOM) derived from external autotrophic sources, or live particulate organic matter (POM) in the form of bacterioplankton, respectively, resulting in a low degree of resource competition between these symbiont states. As many coral reefs have undergone phase shifts from coral- to macroalgal-dominated reefs, the role of DOM, and the potential for future declines in POM due to decreased picoplankton productivity, may result in an increased abundance of chemically defended HMA sponges on tropical coral reefs.

The influences of diurnal variability and ocean acidification on the bioerosion rates of two reef-dwelling Caribbean sponges.

Ocean acidification (OA) is expected to modify the structure and function of coral reef ecosystems by reducing calcification, increasing bioerosion, and altering the physiology of many marine organisms. Much of our understanding of these relationships is based on experiments with static OA treatments, although evidence suggests that the magnitude of diurnal fluctuations in carbonate chemistry may modulate the calcification response to OA. These light-mediated swings in seawater pH are projected to become more extreme with OA, yet their impact on bioerosion remains unknown. We evaluated the influence of diurnal carbonate chemistry variability on the bioerosion rates of two Caribbean sponges: the zooxanthellate Cliona varians and azooxanthellate Cliothosa delitrix. Replicate fragments from multiple colonies of each species were exposed to four precisely controlled pH treatments: contemporary static (8.05 ± 0.00; mean pH ± diurnal pH oscillation), contemporary variable (8.05 ± 0.10), future OA static (7.80 ± 0.00), and future OA variable (7.80 ± 0.10). Significantly enhanced bioerosion rates, determined using buoyant weight measurements, were observed under more variable conditions in both the contemporary and future OA scenarios for C. varians, whereas the same effect was only apparent under contemporary pH conditions for C. delitrix. These results indicate that variable carbonate chemistry has a stimulating influence on sponge bioerosion, and we hypothesize that bioerosion rates evolve non-linearly as a function of pCO2 resulting in different magnitudes and directions of rate enhancement/reduction between day and night, even with an equal fluctuation around the mean. This response appeared to be intensified by photosymbionts, evident by the consistently higher percent increase in bioerosion rates for photosynthetic C. varians across all treatments. These findings further suggest that more variable natural ecosystems may presently experience elevated sponge bioerosion rates and that the heightened impact of OA enhanced bioerosion on reef habitat could occur sooner than prior predictions.

Sponge holobionts shift their prokaryotic communities and antimicrobial activity from shallow to lower mesophotic depths

In this study, we used 16S rRNA gene amplicon sequencing to investigate prokaryotic community composition of the Caribbean sponges Xestospongia muta and Agelas sventres from three depth ranges: < 30 m (shallow), 30–60 m (upper mesophotic), and 60–90 m (lower mesophotic). The prokaryotic community in shallow samples of X. muta was enriched in Cyanobacteria, Chloroflexota, and Crenarchaeota compared to samples from mesophotic depths, while mesophotic samples of X. muta were enriched in Acidobacteriota. For A. sventres, relative abundance of Acidobacteriota, Chloroflexota, and Gammaproteobacteria was higher in shallow samples, while Proteobacteria and Crenarchaeota were enriched in mesophotic A. sventres samples. Antimicrobial activity was evaluated by screening crude extracts of sponges against a set of Gram-positive and Gram-negative bacteria, a yeast, and an oomycete. Antibacterial activities from crude extracts of shallow sponge individuals were generally higher than observed from mesophotic individuals, that showed limited or no antibacterial activities. Conversely, the highest anti-oomycete activity was found from crude extracts of X. muta individuals from lower mesophotic depth, but without a clear pattern across the depth gradient. These results indicate that sponge-associated prokaryotic communities and the antimicrobial activity of sponges change within species across a depth gradient from shallow to mesophotic depth.

Plume Layer Influences the Amazon Reef Sponge Microbiome Primary Producers

Symbiont relationships between corals and photosynthetic microorganisms sustain coral reef existence. However, the Great Amazon Reef System (GARS) stays under a plume layer that attenuates the entry of light, and instead of corals, sponges are the major reef epifauna, for which little is known about the function of the associated microbiome. Here, we used genome-resolved metagenomics to investigate how the sponge microbiome supports its host and overcomes the reduced light availability, recovering 205 MAGs from Agelas and Geodia sponges with completeness &amp;gt;70% and contamination &amp;lt;10%. Beta diversity estimates based on the 16S rRNA genes indicated the microbiomes of Amazon and Caribbean sponges to be distinct (P&amp;lt;0.01), with heterotrophic lifestyles being prevalent in Amazon sponge microbiomes (P&amp;lt;0.05). Nevertheless, genes indicating the carbon fixation pathways 3-Hydroxypropionate/4-Hydroxybutyrate cycle, 3-Hydroxypropionate bicycle, Reductive Tricarboxylic Acid Cycle, and Calvin-Benson-Bassham cycle could be recovered in low abundance. The presence of Cyanobacteria, represented by both 16S rRNA analyses and low-quality MAGs indicated light incidence on the reef. The metabolic profile shows that the GARS sponge microbiome had genes for sulfate reduction, sulfur oxidation, nitric oxide reduction, ammonia oxidation, nitrate reduction, nitrite ammonification, nitrite oxidation, and nitrite reduction, indicating that the microbiome might play a role in detoxification of the holobiont. We conclude, that neither the plume-limited photosynthesis of the sponge microbiome nor the primary producers sustain the organic carbon input for the sponges, which likely live off plume-associated organic carbon and their heterotrophic microbiota.

Cophylogeny and convergence shape holobiont evolution in sponge-microbe symbioses.

Symbiotic microbial communities of sponges serve critical functions that have shaped the evolution of reef ecosystems since their origins. Symbiont abundance varies tremendously among sponges, with many species classified as either low microbial abundance (LMA) or high microbial abundance (HMA), but the evolutionary dynamics of these symbiotic states remain unknown. This study examines the LMA/HMA dichotomy across an exhaustive sampling of Caribbean sponge biodiversity and predicts that the LMA symbiotic state is the ancestral state among sponges. Conversely, HMA symbioses, consisting of more specialized microorganisms, have evolved multiple times by recruiting similar assemblages, mostly since the rise of scleractinian-dominated reefs. Additionally, HMA symbioses show stronger signals of phylosymbiosis and cophylogeny, consistent with stronger co-evolutionary interaction in these complex holobionts. These results indicate that HMA holobionts are characterized by increased endemism, metabolic dependence and chemical defences. The selective forces driving these patterns may include the concurrent increase in dissolved organic matter in reef ecosystems or the diversification of spongivorous fishes.

Diversity and time-series analyses of Caribbean deep-sea coral and sponge assemblages on the tropical island slope of Isla de Roat\xe1n, Honduras

Shore-based submersible operations, from 2006 to 2020, have allowed us to examine megabenthic assemblages along the island margin of Isla de Roatán from depths of about 150 to 750 m, including repeated observations of the same organisms. These dives were used to photo-document a diverse benthic assemblage and observe the health and condition of the sessile fauna in a well-explored but relatively undocumented area of the Mesoamerican Reef. Samples were collected by dip net, and some dives profiled the water column chemistry in the year 2011. The deep-sea coral assemblage observed off Roatan exhibits high abundance and diversity. The sessile habitat-forming taxa consist primarily of at least 20 different octocorals (e.g., Plexauridae, Primnoidae, Coralliidae, Isididae, and Ellisellidae) and 20 different sponges each (Demospongiae and Hexactinellida), with several known and unknown taxa of Zoantharia, Antipatharia (Bathypathes spp), and Scleractinia (e.g., Desmophyllum pertusum, Dendrophyllia alternata, Madracis myriaster, and solitary taxa). Crinoidea were also abundant and diverse, represented by at least nine species. Epifaunal assemblages associated with corals include at least 24 macroinvertebrate species dominated by Asteroschema laeve (Ophiuroidea) and Chirostylus spp. (Decapoda: Anomura). Repeated observations of a few large octocoral colonies over many years illustrate patterns of predation, recolonization, and epibiont host fidelity, including a 14-year record of decline in a plexaurid octocoral (putatively Paramuricea sp.) and loss of its resident ophiuroids. The shore-based submersible provides a practical and relatively inexpensive platform from which to study coral and sponge assemblages on a deep tropical island slope. The deep-sea coral gardens are likely to harbor new species and new discoveries if more samples can be acquired and made available for taxonomic research.

Variability in antimicrobial chemical defenses in the Caribbean sponge Agelas tubulata: implications for disease resistance and resilience

Sponges in the genus Agelas produce a diversity of bromopyrrole alkaloid secondary metabolites, some of which are known to inhibit predators and pathogens. Selective pressures on sponges to produce chemical defenses vary in time and space, often resulting in differences in the production of secondary metabolites. To characterize intraspecific variation in these compounds, we generated metabolomic profiles of the Caribbean sponge A. tubulata across spatial gradients, including multiple sites in Belize and Grand Cayman, and depths ranging from 15 to 61 m in Grand Cayman. Samples were also analyzed from a reciprocal transplant experiment across shallow (22 m) to mesophotic (61 m) reefs. We found quantitative, but not qualitative, differences in metabolite profiles across sites and depths, with 9 metabolites contributing to that variation. In addition, transplanting sponges across depths resulted in significant changes in concentrations of the metabolite sceptrin. Sponge extracts exhibited antibacterial activity against a panel of marine and human pathogens. Multiple regression analyses showed that different metabolites were associated with antibacterial activity against different pathogens. The strongest compound-specific relationship was a negative effect of oroidin on the growth of Serratia marcescens, and purified oroidin was found to inhibit S. marcescens growth in a dose-dependent manner. Overall, A. tubulata exhibits intraspecific variability in the production of antibacterial secondary metabolites across sites and depths that signals selective responses to its environment. Given the current increase in sponge densities, and incidence of disease on coral reefs, these data have implications for disease resistance and resilience of sponges in the Anthropocene.

Depth-dependent trophic strategies of Caribbean sponges on mesophotic coral reefs

Mesophotic coral reef ecosystems (MCEs) are characterized by gradients in irradiance, temperature and trophic resources. As depth increases on Caribbean mesophotic reefs, particulate organic matter increases while dissolved organic matter decreases, and the increase in particulate organic matter is directly related to the increase in sponge abundances and growth rates on MCEs. To further understand the trophic ecology of sponges, changes in microbiome composition and function, stable isotopic composition and proximate biochemical composition of 4 Caribbean reef sponges (Amphimedon compressa, Agelas tubulata, Plakortis angulospiculatus and Xestospongia muta) were quantified along a shallow to mesophotic depth gradient on Grand Cayman Island. Increases in δ15N for all sponges were observed as depth increased, indicating an increasing reliance on heterotrophic food resources. Species-specific changes in symbiotic microbial community composition were also observed as depth increased, and the predicted functional genes associated with nitrogen and carbon cycling showed species-specific changes between depths. Regardless of species-specific changes in microbiome community structure or function, or whether sponges were classified as high microbial or low microbial abundance, sponges increased their consumption of particulate organic matter with increasing depth into the lower mesophotic zone.

Plastics in Porifera: The occurrence of potential microplastics in marine sponges and seawater from Bocas del Toro, Panamá.

Microplastics (MP) are now considered ubiquitous across global aquatic environments. The ingestion of MP by fish and other marine vertebrates is well studied, but the ingestion of MP by marine invertebrates is not. Sponges (Phylum Porifera) are particularly understudied when it comes to MP ingestion, even though they are widely distributed across benthic habitats, can process large volumes of seawater, and can retain small particles within their water filtration systems. This study examines the presence of potential MP (PMP) in wild marine sponges and seawater collected in Bocas del Toro, Panamá. Subsurface seawater and tissue from six common Caribbean sponge species was collected in Saigon Bay, a heavily impacted, shallow-water coral reef. Seawater samples were filtered onto glass fiber filters to retain any PMP present and sponge tissue was digested with bleach, heated and filtered. Filters were examined using fluorescence microscopy to quantify PMP. An average of 107 ± 25 PMP L–1 was detected in seawater from Saigon Bay with particles ranging in size between 10 μm and ~3,000 μm. The number of PMP found in sponge tissue ranged between 6 ± 4 and 169 ± 71 PMP g–1 of dry tissue. Most particles found in sponge samples were very small (10–20 μm), but fibers greater than 5,000 μm were detected. Our results indicate that PMP exists within the tissues of the sponges we studied, but future studies should confirm the presence of MP in sponges using chemical analysis. Most importantly, the discrepancy between low levels of PMP in our sponge samples and high levels in the surrounding seawater highlights the potential for sponges to resist and/or egest MP. Finally, we provide a critical evaluation of our methods to improve their use in future MP work with benthic marine organisms.

Art in Endoscopy: Natural analogies.

This papilla with an impacted stone was observed during ERCP. The image was so extraordinary that we wondered whether any similar image might exist in nature. We therefore contacted an expert in the biological field, Dr. Conxita Avila from the Department of Evolutionary Biology, Ecology and Environmental Sciences, and Biodiversity Research Institute (IrBIO), University of Barcelona. She replied that our image was certainly reminiscent of a marine animal, for example a sponge. There are curious analogies amongst biological forms, as Ernst Haeckel said in his book Kunstformen der Natur [Art Forms in Nature]. Our image of the papilla resembles this one of the Caribbean sponge, Mycale laxissima, https://spongeguide.uncw.edu/imageinfo.php?img=319 (photographer Sven Zea; The Sponge Guide, Universidad Nacional de Colombia).

Targeted predator defenses of sponges shape community organization and tropical marine ecosystem function

AbstractDefenses that target particular consumers often influence community organization, ecosystem function, and diversity maintenance. In coral reef, mangrove, and seagrass ecosystems, sponges affect substratum stability, water clarity, diversity of associated species, and survival of habitat‐providing organisms, key roles not duplicated by other organisms. Whether and how predators control sponges are much disputed. Substantial ecosystem consequences of losing or gaining sponges motivated definitive experiments on how predators control sponge distribution and abundance. Caribbean sponges of 94 species representing 13 taxonomic orders and three linked habitats (coral reefs, mangroves, and seagrass meadows) were exposed to seven predator species representing different habitats and degrees of spongivory in 4,493 in situ trials. The resulting data force reassessment of popular interpretations of several patterns and processes. Contrary to extract pellet assays that declare most sponges deterrent, 78% of these 94 species were eaten by at least one predator. But “palatability” is consumer dependent: a sponge species eaten by one predator can be rejected by other predators, and predator species differed in what sponges they ate in 55.4% (214/392) of pairwise comparisons between predators. Because spongivore species are usually restricted to particular habitats, they impose abrupt boundaries on sponges’ habitat distributions, reflecting inverse relationships between accessibility and palatability to each predator. Thus a seagrass‐dwelling starfish eats only 9% of seagrass sponge species, but 70% of coral reef species, and 78% of mangrove species. Reef‐dwelling angelfishes completely consume only 13% of reef species, but 29% of seagrass species, and 63% of mangrove species. Defenses that target specific predators reveal that spongivore influence on community organization cannot be inferred from extract pellet/omnivore assays that assume defenses target all predators equally. In fact, pellet data wrongly predicted actual consumption of living sponges of that pellet's species in 43% of field experiments with spongivores. In contrast with herbivore–plant interactions, opportunistic spongivory is at least as important as routine spongivory for community organization and ecosystem function. Potential for loss of key functional roles of sponges, if opportunistic predators gain access to sponge species that lack defenses against them, must inform conservation plans for coral reef, mangrove, and seagrass ecosystems.

Quantifying sponge host and microbial symbiont contribution to dissolved organic matter uptake through cell separation

Sponge-microbe symbioses underpin the ecological success of sponges in many aquatic benthic ecosystems worldwide. These symbioses are often described as mutually beneficial, but identifying positive symbiotic interactions and quantifying the contribution of partners to physiological processes is challenging. For example, our understanding of the relative contribution of sponge cells and their microbial symbionts to the uptake and exchange of dissolved organic matter (DOM)—a major component of sponge diet—is limited. Here, we combined host-symbiont cell separation with pulse-chase isotopic labelling in order to trace the uptake of13C- and15Nenriched DOM into sponge cells and microbial symbionts of the encrusting Caribbean spongesHaliclona vansoestiandScopalina ruetzleri, which are low microbial abundance (LMA) species. Sponge cells were responsible for &gt;99% of DOM assimilation during the pulse-chase experiment for both sponge species, while the contribution of symbiotic microbes to total DOM uptake was negligible (&lt;1%). Nitrogen derived from DOM was translocated from sponge cells to microbial cells over time, indicating processing of host nitrogenous wastes by microbial endosymbionts. Thus, host cells drive DOM uptake in these species, while microbial symbionts may aid in the recycling of host-waste products. Our findings highlight the ability of sponges to derive nutrition by internalizing dissolved compounds from their environment and retaining nutrients via host-microbe interactions.

Trophic ecology of Caribbean sponges in the mesophotic zone

AbstractSponges are a crucial component of Caribbean coral reef ecosystem structure and function. In the Caribbean, many sponges show a predictable increase in percent cover or abundance as depth increases from shallow (&lt; 30 m) to mesophotic (30–150 m) depths. Given that sponge abundances are predicted to increase in the Caribbean as coral cover declines, understanding ecological factors that control their distribution is critical. Here we assess if sponge cover increases as depth increases into the mesophotic zone for three common Caribbean reef sponges, Xestospongia muta, Agelas tubulata, and Plakortis angulospiculatus, and use stable isotope analyses to determine whether shifts in trophic resource utilization along a shallow to mesophotic gradient occurred. Ecological surveys show that all target sponges significantly increase in percent cover as depth increases. Using bulk stable isotope analysis, we show that as depth increases there are increases in the δ13C and δ15N values, reflecting that all sponges consumed more heterotrophic picoplankton, with low C:N ratios in the mesophotic zone. However, compound‐specific isotope analysis of amino acids (CSIA‐AA) shows that there are species‐specific increases in δ13CAA and δ15NAA values. Xestospongia muta and P. angulospiculatus showed a reduced reliance on photoautotrophic resources as depth increased, while A. tubulata appears to rely on heterotrophy at all depths. The δ13CAA and δ15NAA values of these sponges also reflect species‐specific patterns of host utilization of both POM and dissolved organic matter (DOM), its subsequent re‐synthesis, and translocation, by their microbiomes.

Oceanographic features and limited dispersal shape the population genetic structure of the vase sponge Ircinia campana in the Greater Caribbean

Understanding population genetic structure can help us to infer dispersal patterns, predict population resilience and design effective management strategies. For sessile species with limited dispersal, this is especially pertinent because genetic diversity and connectivity are key aspects of their resilience to environmental stressors. Here, we describe the population structure of Ircinia campana, a common Caribbean sponge subject to mass mortalities and disease. Microsatellites were used to genotype 440 individuals from 19 sites throughout the Greater Caribbean. We found strong genetic structure across the region, and significant isolation by distance across the Lesser Antilles, highlighting the influence of limited larval dispersal. We also observed spatial genetic structure patterns congruent with oceanography. This includes evidence of connectivity between sponges in the Florida Keys and the southeast coast of the United States (>700 km away) where the oceanographic environment is dominated by the strong Florida Current. Conversely, the population in southern Belize was strongly differentiated from all other sites, consistent with the presence of dispersal-limiting oceanographic features, including the Gulf of Honduras gyre. At smaller spatial scales (<100 km), sites showed heterogeneous patterns of low-level but significant genetic differentiation (chaotic genetic patchiness), indicative of temporal variability in recruitment or local selective pressures. Genetic diversity was similar across sites, but there was evidence of a genetic bottleneck at one site in Florida where past mass mortalities have occurred. These findings underscore the relationship between regional oceanography and weak larval dispersal in explaining population genetic patterns, and could inform conservation management of the species.