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Heat flow in the Western Arctic Ocean (Amerasian Basin)

From 1963 to 1973 the U.S. Geological Survey (USGS) measured heat flow at 356 sites in the Amerasian Basin (Western Arctic Ocean) from a drifting ice island (T-3). The resulting measurements, which are unevenly distributed on Alpha-Mendeleev Ridge (AMR) and in Canada and Nautilus basins, greatly expand available heat flow data for the Arctic Ocean. Average T-3 heat flow is ~54.7 ± 11.3 mW m-2, and Nautilus Basin, including Mendeleev Plain, is the only well-surveyed area (~13% of data) with significantly higher average heat flow (63.8 mW m-2). Heat flow and bathymetry are not correlated at a large scale, and turbiditic surficial sediments (Canada and Nautilus basins) have higher heat flow than the sediments that blanket the AMR. Thermal gradients are mostly near-linear, implying that conductive heat transport dominates and that near-seafloor sediments are in thermal equilibrium with overlying bottom waters. Combining the heat flow data with modern seismic imagery suggests that some of the observed heat flow variability may be explained by local changes in sediment thickness or lithology or the presence of basement faults that channel circulating seawater. A thermal model that incorporates thermal conductivity variations along a profile from Canada Basin (thick sediment on mostly oceanic crust) to Alpha Ridge (thin sediment over thick magmatic units associated with the High Arctic Large Igneous Province) predicts heat flow lower than that observed on Alpha Ridge. This, along with other observations, implies that circulating fluids modulate conductive heat flow and contribute to high variability in the T-3 dataset. .

Journal of Geophysical Research B: Solid Earth

Seafloor fluid seeps on Kimki Ridge, offshore southern California: Links to active strike-slip faulting

The Kimki Ridge fluid seeps are located in western Catalina Basin about 60 km southwest of the southern California mainland and at a water depth of approximately 1100 m. Multichannel seismic reflection profiles collected by the U.S. Geological Survey (USGS) in 2014 show acoustic transparency within the Kimki Ridge, suggesting the possibility of fluid seeps and possible sub-seafloor fluid pathways. Subsequent multibeam bathymetric and backscatter intensity data collected during a cooperative University of Washington/USGS cruise in early 2016 show subtle seafloor buildups with high acoustic backscatter (reflectivity) in three places along Kimki Ridge, supporting the existence of fluid seepage. A Remotely Operated Vehicle (ROV) dive, conducted as part of the Nautilus Exploration Program, took place in August 2016 to confirm the presence of these previously unknown seeps and document their characteristics as well as those of any associated biological communities. Two of the three seeps were explored by ROV, and showed abundant evidence of fluid seepage, including characteristic algal mats, chemosynthetic clams, and authigenic carbonate formation. The seeps are comprised of carbonate buildups 1–3 m thick and 300–500 m across. Within these areas, we interpret broad crater-like depressions 30–50 m across and 1–2 m deep to be individual seep vents. The seep areas appear to be broad zones of diffuse seepage that support chemosynthetic biologic communities; however, active venting was not observed. Geochemical analyses of rock samples collected from the seeps indicate microbially driven anaerobic oxidation of methane at or near the sediment water interface. Seismic-reflection profiles show chimney-like fluid pathways along the limbs and in the axis of the fold forming Kimki Ridge, and evidence of methane in shallow sediments can be traced into the adjacent Catalina Basin. A system of closely spaced faults located at the axis of the Kimki Ridge anticline may serve as pathways to allow fluid flow to the seafloor. Our data are consistent with other studies that suggest that transpression is an important component in the formation and localization of fluid seeps in a strike-slip setting, implying that seep formation may be a common occurrence at fault stepovers or transpressional bends in strike-slip systems.

California

Colored shaded-relief bathymetry, acoustic backscatter, and selected perspective views of the northern part of the California Continental Borderland, southern California

The California Continental Borderland is the complex continental margin in southern California that extends from Point Conception southward into northern Baja California (Fisher and others, 2009). This colored shaded-relief bathymetry map of the northern continental borderland in southern California was generated primarily from multibeam-echosounder data collected by the University of Washington in 2016, the Ocean Exploration Trust-Nautilus Exploration Program in 2015–17, and the National Oceanic and Atmospheric Administration in 2017. These datasets were processed in part by the U.S. Geological Survey. Additional smaller amounts of publicly available multibeam-bathymetry data collected by other federal and local agencies, academic institutions, and private firms were also incorporated into this map. Since the production of this map, other multibeam-bathymetry data have been collected in this region.

California

Distribution of deep-water scleractinian and stylasterid corals across abiotic environmental gradients on three seamounts in the Anegada Passage

In the Caribbean Basin the distribution and diversity patterns of deep-sea scleractinian corals and stylasterid hydrocorals are poorly known compared to their shallow-water relatives. In this study, we examined species distribution and community assembly patterns of scleractinian and stylasterid corals on three high-profile seamounts within the Anegada Passage, a deep-water throughway linking the Caribbean Sea and western North Atlantic. Using remotely operated vehicle surveys conducted on the E/V Nautilus by the ROV Hercules in 2014, we characterized coral assemblages and seawater environmental variables between 162 and 2,157 m on Dog Seamount, Conrad Seamount, and Noroît Seamount. In all, 13 morphospecies of scleractinian and stylasterid corals were identified from video with stylasterids being numerically more abundant than both colonial and solitary scleractinians. Cosmopolitan framework-forming species including Madrepora oculata and Solenosmilia variabilis were present but occurred in patchy distributions among the three seamounts. Framework-forming species occurred at or above the depth of the aragonite saturation horizon with stylasterid hydrocorals being the only coral taxon observed below Ωarag values of 1. Coral assemblage variation was found to be strongly associated with depth and aragonite saturation state, while other environmental variables exerted less influence. This study enhances our understanding of the factors that regulate scleractinian and stylasterid coral distribution in an underreported marginal sea and establishes a baseline for monitoring future environmental changes due to ocean acidification and deoxygenation in the tropical western Atlantic.

Puerto Rico

Characterization of deep-sea coral and sponge communities in Greater Farallones National Marine Sanctuary: Point Arena South Essential Fish Habitat Conservation Area and New Amendment 28 Areas

This report summarizes samples collected during a remotely operated vehicle (ROV) cruise conducted in October 2019 on board E/V Nautilus. Areas sampled in Greater Farallones National Marine Sanctuary included areas proposed for fisheries management zoning in the Point Arena South (PAS) Essential Fish Habitat Conservation Area (EFH). Dive planning targeted habitats and biological communities of corals, sponges, and fishes in relation to the new, 2020 configuration of PAS EFH (hereafter referred to as PAS), which includes areas once closed to commercial bottom trawling and now opened to bottom trawling, once opened to bottom trawling and now closed, or that remain closed to commercial bottom trawling. Particular interest was given to enumerating deep-sea corals and sponges (DSCS) in these areas as they are long-lived, slow-growing species that are vulnerable to impacts from bottom trawling. Fish species were also enumerated. These data provide the most recent assessment and characterization for a portion of these areas before the final ruling on Amendment 28 went into effect on January 1, 2020 (50 C.F.R. part 660). A total of seven sponge specimens were collected on this mission, some of which could potentially be new species, such as the large yellow ‘plate’-shaped sponge and the ‘palm frond’ morphology of the predatory sponge Asbestopluma , documented on both dives. Six coral collections were made, including three types of red Swiftia sp. gorgonians (two had fan-shaped morphology and one had branched morphology) with different polyp colors. A high diversity of fishes, particularly groundfish, were documented across the entire PAS area. The findings from this cruise will be provided to NOAA’s National Marine Fisheries Service to help them identify biologically complex areas of the seafloor that are most sensitive to bottom trawling and aid in the ongoing management of this designated essential fish habitat conservation zone. Habitat data from these surveys will be used to confirm substrate prediction models that can be used to predict DSCS habitats where there is a dearth of visual observations.

California

Cascadia Margin cold seeps: Subduction zone fluids, gas hydrates, and chemosynthetic habitats

Priority Geographic Area: The outer continental shelf and upper continental slope from Canada/U.S. border offshore Washington State to the Mendocino Fracture Zone (Northern California), entirely within the U.S. Exclusive Economic Zone (EEZ), from the outermost shelf to at least 2000 m water depth (Figure 1). Description of Priority Area: Since 2015, over a thousand water column gas plumes originating at seafloor gas seeps have been discovered landward of the Cascadia deformation front (e.g., Embley et al., 2016; Johnson et al., 2015, 2019; Merle and Embley, 2016; NA-95 Cruise Report, 2018; Riedel et al., 2018), adding to those that had long been known on Hydrate Ridge (e.g., Heeschen et al., 2003; Tréhu et al., 2004). The recently-discovered seeps stretch from offshore Vancouver Island to the Mendocino Fracture Zone and from the outer shelf to ~2000 m water depth, occurring both landward and seaward of the nominal limit for gas hydrate stability zone on the upper continental slope (Figure 1). Hundreds of seeps likely remain undiscovered. Water column imaging is incomplete both within the target geographic area and farther seaward, between the 2000 m isobath and the deformation front, which is the subject of an imaging study described in a white paper by Watt et al. The recently-discovered Cascadia Margin cold seeps partially overlap an important active margin gas hydrate province (Spence et al., 2001; Tréhu et al., 2003, 2004), as well as an area where sediments on the North American plate are folded and faulted and affected by fluids generated in the subduction complex beneath the Cascadia forearc (e.g., Saffer and Tobin, 2011). Several Ocean Drilling Program expeditions have focused on hydrate systems offshore Vancouver and Oregon (e.g., Riedel et al., 2009; Tréhu et al., 2004) and on the connection between the shallow and deep hydrogeologic systems. Cabled observatories now continuously monitor physical, chemical, and venting processes on south Hydrate Ridge (OOI; e.g., Philip et al., 2016a) and offshore Vancouver Island (NEPTUNE; e.g. Römer et al., 2016). Outside of these well-studied gas hydrate areas, a subset of the recently-discovered Cascadia seeps, including some that we visited with R/V Falkor in 2019 (e.g., https://schmidtocean.org/cruise/methane-seeps-at-edge-of-hydrate-stability/), also likely emit methane associated with shallow subseafloor gas hydrate systems. Other seeps are delivering not only methane, but also deep-derived gases (Baumberger et al., 2018, 2020) to the seafloor. Many Cascadia Margin seeps have also been recognized at water depths too shallow (e.g., 175 m) to be connected to gas hydrate dynamics. These seeps are postulated to be emitting gas and fluids that originated deep in accretionary wedge before migrating up normal faults generated during forearc extension associated with large earthquakes (Johnson et al., 2019). Only a small fraction of the recently discovered U.S. Cascadia Margin water column gas plumes has so far been verified by ROVs (Hercules from E/V Nautilus in 2016 and 2018; SuBastian from R/V Falkor in 2018 and 2019) to correspond to seafloor seeps. Careful scientific mapping, investigation, and sampling at the seeps have also been limited (e.g., Baumberger et al., 2018, 2020; Merle and Embley, 2016; Seabrook et al., 2018; Greinert et al. 2019). This white paper focuses on expanding exploration of already-identified U.S. Cascadia Margin cold seeps through a multipronged and multidisciplinary discovery program that could be accomplished with a variety of NOAA assets. The goals of the proposed exploration activities are to develop high-resolution maps of seep fields from deep ocean vehicles; to verify (and sample) seafloor gas emissions at the locations of water column plumes for compositional and isotopic studies; to map, sample, and conduct analyses on chemosynthetic communities and deep-sea coral habitats near seep sites to document species distributions and habitats as a function of depth and latitude along the margin; to collect seep geologic samples that can constrain the timing of methane emissions through geochronology; and to record environmental data (e.g., CTD) near the seafloor and in the water column above the seeps. Seafloor mapping using shipboard systems (multibeam/backscatter) would be needed to characterize seafloor features near seep sites. Water column imaging (EK60/80 and/or multibeam WCD data) conducted before and after seafloor explorations would capture active methane plumes and constrain temporal variations in seep emissions (e.g., Kannberg et al., 2013; Philip et al., 2016a, 2016b), which are known to vary on time scales as rapid as tidal cycles on this margin (e.g., Römer et al., 2016). What are the characterization and data needs in this area? Check all that apply: __x_ Biology, Geology, Physical Oceanography, Chemistry ___ Marine Archaeology ___ Other Provide a list or brief description of the data needed within this area, from your perspective: 1. Water column backscatter to image active gas plumes 2. High-resolution multibeam bathymetry, seafloor backscatter, and shallow sub-bottom imaging 3. Visual characterization and ground truthing of potential seeps, including high-resolution mapping and photography from near-seafloor vehicles; collection of seep-associated species, corals, sediments, authigenic carbonates, gases, and seawater Describe relevance to national security, conservation, and/or the economy: The Cascadia margin seeps provide significant ecosystem services, including habitat for commercially important fishes and support for diversity along the continental margin. Methane seeps are also biological hotspots for krill, plankton, and crustaceans, which in turn sustain higher trophic levels (e.g., whales). Methane-derived authigenic carbonates serve as a hard substrate for deep-sea corals and sponges on millennial time scales. The studies proposed here will elucidate the relationship among seep environments, deep-sea corals, sponges, fisheries, and other organisms and provide new insight into subduction zone and hydrate-associated fluids in this important seismogenic zone. The studies address fishery management concerns and inform future conservation of sensitive species (e.g., deep-sea corals) and benthic habitats. From your perspective, what makes this area unique? The Cascadia Margin seeps are a critical component of the leaky margin that stretches from Baja California to the Aleutian Arc along the Pacific coastline of North America. Cold seeps have been intensely studied on the Gulf of Mexico and U.S. Atlantic passive margins with a focus on chemosynthetic communities, deep-sea corals, and leakage of microbially-generated and/or thermogenic hydrocarbons; however, the recently-discovered Cascadia Margin seeps, as well as active margin seep systems in general, remain more poorly characterized. Such seeps not only contribute to the ocean carbon cycle (e.g., Pohlman et al., 2011), thereby fueling the base of the food chain in these settings, but also emit subduction zone fluids that provide clues about processes within the seismogenic zone and the accretionary complex. The Cascadia seeps area allows both biological (e.g., benthic habitats, coral distributions) and physical processes (e.g., generation of subduction zone fluids) to be studied along both depth (perpendicular to the deformation front) and latitudinal gradients.

California, Oregon, Washington

New distribution record for the rare limpet Acroloxus coloradensis (Henderson, 1930) (Gastropoda: Acroloxidae) from Montana

The Rocky Mountain Capshell, Acroloxus coloradensis (Henderson, 1930), the only North American member of the basommatophoran family Acroloxidae, is broadly distributed across southern Canada and south into the Rocky Mountains in the USA (Turgeon et al., 1998; Lee and Ackerman, 2000). Despite its wide geographic range, A. coloradensis has been documented from < 30 locations, mostly in British Columbia, Alberta, Ontario, and Quebec (Lee and Ackerman, 2000; Anderson, 2005). Relict populations of A. coloradensis in the USA have been documented from only 6 sites in Colorado and 2 sites in Glacier National Park (Glacier NP), Montana (Anderson, 2005; Ellis et al., 2004). In Glacier NP, A. coloradensis was first reported from Lost Lake (Figure 1; Russell and Brunson, 1967). A second population in the park was discovered in Trout Lake in 2001 (Ellis et al., 2004). In both lakes, A. coloradensis was found primarily under rocks and other cover objects.

Montana

Demographic responses to density-dependence by two populations of the Florida Tree Snail, Liguus fasciatus (Gastropoda: Orthalicidae), in Everglades National Park

D uring May-October 1996, we captured and individually marked and released Florida Tree Snails, Liguus fasciatus, from two sites, a subclimax hammock and a large isolated wild tamarind tree, in the Long Pine Key region of Everglades National Park. Populations shared the same two dominant morphs, castaneozonatus and. cingulatus, both of which are strong colonizers. Monthly survivorship between the two sites were comparable, although annual survivorship was lower on the isolated tree. Intersite differences in growth rates were equivocal. The populations differed with respect to number of morphs, population size, and population structure. The hammock site was a subclimax hammock with a large and stable bell-shaped population structure comprising nine morphs. In contrast, the population structure of the single tree was highly skewed, with many young individuals produced, intermediate ages absent, and few large adults of larger asymptotic size present. Number of snails/m was higher on the isolated tree. Demographic studies of the Florida Tree Snail are uncommon. Our findings corroborate certain aspects of the ecology of this species and clarify two different demographic responses, one of stability, and one of apparent resource limitation whose demography represents opportunities for colonization.

Florida