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Methane seeps harbor uncharacterized animal–microbe symbioses with unique nutritional strategies. Three undescribed sea spider species (family Ammotheidae; genusSericosura) endemic to methane seeps were found along the eastern Pacific margin, from California to Alaska, hosting diverse methane- and methanol-oxidizing bacteria on their exoskeleton. δ¹³C tissue isotope values of in situ specimens corroborated methane assimilation (−45‰, on average). Live animal incubations with¹³C-labeled methane and methanol, followed by nanoscale secondary ion mass spectrometry, confirmed that carbon derived from both compounds was actively incorporated into the tissues within five days. Methano- and methylotrophs of the bacterial families Methylomonadaceae, Methylophagaceae and Methylophilaceae were abundant, based on environmental metagenomics and 16S rRNA sequencing, and fluorescence and electron microscopy confirmed dense epibiont aggregations on the sea spider exoskeleton. Egg sacs carried by the males hosted identical microbes suggesting vertical transmission. We propose that these sea spiders farm and feed on methanotrophic and methylotrophic bacteria, expanding the realm of animals known to harness C1 compounds as a carbon source. These findings advance our understanding of the biology of an understudied animal lineage, unlocking some of the unique nutritional links between the microbial and faunal food webs in the oceans. 

Methane seeps harbor uncharacterized animal–microbe symbioses with unique nutritional strategies. Three undescribed sea spider species (family Ammotheidae; genus Sericosura) endemic to methane seeps were found along the eastern Pacific margin, from California to Alaska, hosting diverse methane-and methanol-oxidizing bacteria on their exoskeleton. δ13C tissue isotope values of in situ specimens corroborated methane assimilation (−45‰, on average). Live animal incubations with 13C-labeled methane and methanol, followed by nanoscale secondary ion mass spectrometry, confirmed that carbon derived from both compounds was actively incorporated into the tissues within five days. Methano-and methylotrophs of the bacterial families Methylomonadaceae, Methylophagaceae and Methylophilaceae were abundant, based on environmental metagenomics and 16S rRNA sequencing, and fluorescence and electron microscopy confirmed dense epibiont aggregations on the sea spider exoskeleton. Egg sacs carried by the males hosted identical microbes suggesting vertical transmission. We propose that these sea spiders farm and feed on methanotrophic and methylotrophic bacteria, expanding the realm of animals known to harness C1 compounds as a carbon source. These findings advance our understanding of the biology of an understudied animal lineage, unlocking some of the unique nutritional links between the microbial and faunal food webs in the oceans. 

Methane seeps are highly productive ecosystems that provide carbon sequestration services, host diverse communities including endemic species, and serve as habitats for commercial fisheries. Little is known about the economic value the public places on them. Discrete Choice Experiments (DCEs) are administered to a sample of Costa Rican taxpayers to evaluate their willingness to pay (WTP) in monetary terms using tradeoffs made in a survey context involving three of the main attributes of methane seep ecosystems to provide insights for future conservation and management efforts. Extensive effort is devoted to understanding how Costa Ricans view different aspects of the deep sea. We find that they associate it with strange animals, natural resources, the unknown, and being far from reach. Perhaps surprisingly, they underestimate how much they know about the deep sea. We find that WTP for methane seep protection is the highest for programs that protect seeps with endemic species, followed by seeps with high climate change mitigation potential and commercial fishing habitat. Higher-income groups and women are more likely to prefer options that increase the current level of protection. We discuss how science communication and community engagement contribute to care expressed toward the deep sea. 

Chemosynthetic ecosystems host unique geological, biogeochemical, microbial and faunistic settings, which provide key ecosystem services for human wellbeing. In the Argentine continental margin, the existence of chemosynthetic ecosystems is still unknown. We present the first finding of chemosynthetic ecosystems in the Argentine deep sea. We assessed and compared biological and geological settings for cold seeps at Malvinas Basin and Colorado Basin and a control site (no gas) at Colorado Basin. We found two cold seeps with crater-like geomorphic features (pockmarks) of 500-m and 1000-m diameter at depths of ⁓500 m. Both cold seeps exhibited methane gas bubbles trapped at the surface of the seafloor, one exhibited seepage into the water column. Cold seeps hosted dense benthic macroinvertebrates (≥300 μm) assemblages consisting mainly of polychaetes, peracarid crustaceans and mollusks. The fauna from Argentinean seeps exhibited δ13C and δ15N stable isotope signatures indicative of multiple trophic levels, supported by both chemosynthetic and photosynthetic sources of energy. The difference in bubbling to the water column was not associated with different trophic input of chemosynthetically-derived sources of energy, suggesting that gas input is mediated by the bubbles trapped in the seafloor sediments. The presence of gas bubbles trapped in the surface sediments of the ocean floor allowed the detection of ecological and trophic characteristics of active chemosynthetic ecosystems. Integration of the sub-bottom dimension can help improve our understanding of the interactions of chemosynthetic ecosystems with seafloor fluid flow in a more reliable manner than the gas plumes. These cold seeps host significant biodiversity and ecosystem functions of the deep ocean. They fall within areas tendered for oil and gas industry development, but have not been a focus of conservation efforts to date. Information provided here can inform effective conservation actions and improve our understanding of the distribution of chemosynthetic ecosystems worldwide. 

Despite their small individual size, marine prokaryotic and eukaryotic microbes can form large 3D structures and complex habitats. These habitats contribute to seafloor heterogeneity, facilitating colonization by animals and protists. They also provide food and refuge for a variety of species and promote novel ecological interactions. Here we illustrate the role of microbes as ecosystem engineers and propose a classification based on five mtypes of habitat: microbial mats, microbial forests, microbial-mineralized habitats, microbial outcrops and microbial nodules. We also describe the metabolic processes of microbial habitat formers and their ecological roles, highlighting current gaps in knowledge. Their biogeography indicates that these habitats are widespread in all oceans and are continuously being discovered across latitudes and depths. These habitats are also expected to expand under future global change owing to their ability to exploit extreme environmental conditions. Given their high ecological relevance and their role in supporting endemic species and high biodiversity levels, microbial habitats should be included in future spatial planning, conservation and management measures. 

Deep-sea chemosynthesis-based ecosystems support unique biological communities, but human impacts are an increasing threat. Understanding the life-history traits of species from deep-sea chemosynthesis-based ecosystems can help to develop adequate management strategies, as these can have impacts on ecological responses to changes in the environment. Here we examined the occurrence of sexual dimorphism in the yeti crab Kiwa puravida , an endemic species from the Costa Rican Pacific margin that aggregates at active methane seeps and depends on chemosynthetic bacteria for nutrition. The two morphological features examined included the claws, suspected to be under sexual selection and used for defense, and the carpus of the second pereopod not suspected to be under sexual selection. A total of 258 specimens, 161 males, 81 females, 16 juveniles, were collected from Mound 12 at 1,000-1,040 m depth in 2017 and 2018 and analyzed. We found that males have larger and wider claws than females, while there were no differences in carpus length. These results suggest that claw weaponry is under sexual selection in K . puravida , which is probably related to the mating system of this deep-sea species. This is the first attempt to study the reproductive biology of K . puravida , and additional observations will be necessary to shed more light on this matter.