Chemosynthetic primary production by microbes supports abundant faunal assemblages at deep-sea hydrothermal vents, with zonation of invertebrate species typically occurring along physico-chemical gradients. Recently discovered vent fields on the East Scotia Ridge (ESR) in the Southern Ocean represent a new province of vent biogeography, but the spatial dynamics of their distinct fauna have yet to be elucidated. This study determines patterns of faunal zonation, species associations, and relationships between faunal microdistribution and hydrothermal activity in a vent field at a depth of 2,400 m on the ESR. Remotely operated vehicle (ROV) dives obtained high-definition imagery of three chimney structures with varying levels of hydrothermal activity, and a mosaic image of >250 m2 of seafloor co-registered with temperature measurements. Analysis of faunal microdistribution within the mosaiced seafloor reveals a consistent pattern of faunal zonation with increasing distance from vent sources and peak temperatures. Assemblages closest to vent sources are visibly dominated by a new species of anomuran crab, Kiwa n. sp. (abundance >700 individuals m−2), followed by a peltospiroid gastropod (>1,500 individuals m−2), eolepadid barnacle (>1,500 individuals m−2), and carnivorous actinostolid anemone (>30 individuals m−2). Peripheral fauna are not dominated by a single taxon, but include predatory and scavenger taxa such as stichasterid seastars, pycnogonids and octopus. Variation in faunal microdistribution on chimneys with differing levels of activity suggests a possible successional sequence for vent fauna in this new biogeographic province. An increase in δ34S values of primary consumers with distance from vent sources, and variation in their δ13C values also indicate possible zonation of nutritional modes of the vent fauna. By using ROV videography to obtain a high-resolution representation of a vent environment over a greater extent than previous studies, these results provide a baseline for determining temporal change and investigations of processes structuring faunal assemblages at Southern Ocean vents.
Citation: Marsh L, Copley JT, Huvenne VAI, Linse K, Reid WDK, et al. (2012) Microdistribution of Faunal Assemblages at Deep-Sea Hydrothermal Vents in the Southern Ocean. PLoS ONE 7(10): e48348. doi:10.1371/journal.pone.0048348
Editor: Howard Browman, Institute of Marine Research, Norway
Received: July 6, 2012; Accepted: September 24, 2012; Published: October 29, 2012
Copyright: © 2012 Marsh et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The ChEsSo research programme was funded by a Natural Environment Research Council NERC Consortium Grant (NE/DO1249X/1) and supported by the Census of Marine Life and the Sloan Foundation, all of which are gratefully acknowledged. The authors also acknowledge NERC PhD studentships NE/D01429X/1(LM) and NE/F010664/1 (WDKR). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The abundant faunal assemblages colonising deep-sea hydrothermal vents are fuelled predominantly by chemosynthetic microbial primary production, typically using the oxidation of reduced inorganic compounds such as hydrogen sulfide at the mixing interface between hydrothermal vent fluids and seawater . Vent fauna utilise microbial primary production by direct consumption of free-living microorganisms (either filter feeding or grazing), through symbiotic relationships with microorganisms (either endosymbiotic or ectosymbiotic), or through a combination of both nutritional modes . Consequently, primary consumers often occur with extremely high population densities compared with non-chemosynthetic deep-sea environments, generally covering all available surfaces around vent fluid exits , . A main objective in ecological studies is to understand the factors determining the distribution and abundance of individual populations , and in dynamic environments such as hydrothermal vents, determining faunal distributions is a starting point for developing ecological understanding , , . Quantifying the composition and microdistribution of faunal assemblages at vents is also a prerequisite for understanding temporal patterns such as succession (e.g., , , , ), and the impact of anthropogenic activities such as the mining of seabed massive sulfide (SMS) deposits .
Within a single hydrothermal vent field, distribution patterns of species often match gradients in physicochemical conditions over spatial scales from a few centimetres to tens of metres or greater , . Zonation of faunal assemblages at deep-sea hydrothermal vents therefore occurs over similar spatial scales to those found on rocky intertidal shores . Proximity to and tolerance of vent effluent may be a primary factor in determining the extent to which species can exploit chemosynthetic primary production. Consequently, physicochemical factors appear to play important roles in determining the distribution patterns of species at vents , , , , , . The development of vent ecology has therefore mirrored that of rocky intertidal ecology , initially considering physical tolerance of conditions as a primary determinant of zonation patterns, and subsequently investigating the role of biological interactions (e.g., , , , ). Unlike the rocky intertidal environment, however, acquiring primary observational data at deep-sea vents is hampered by the relative inaccessibility of the environment, and refinements in the use of deep-submergence platforms are required to overcome this limitation , .
(Top-right) Ship acquired swath bathymetry of the ‘Devils Punchbowl’ collapsed caldera. Black outline denotes the E9 vent field and area of ROV-based swath. (Main bathymetric map) High-resolution ROV-acquired mulitbeam bathymetry of the E9 vent field. Waypoints denote areas of interest (A) Flat sheet lavas, typical background substrate of the E9 vent field (B) Most northern point of low-lying hydrothermal activity (C) “Twin Peaks” (D) “Black and White” (E) “Carwash” (F) “Temple” (G) “Marshland” (H) “Marsh Towers”; (I) “Ivory Towers” chimney complex (J) “Pagoda” chimney complex (K) “Launch Pad” chimney complex (L) “Needle” (M) “Windsor Castle”.
Since the first direct observations of deep-sea hydrothermal vent fields in the late 1970 s, several biogeographic provinces have been defined for vent fauna, which differ in the species composition of their assemblages , , , . The composition and microdistribution of assemblages have been studied at vent fields in these established provinces, but with differences in effort that reflect the history of vent exploration. In the eastern Pacific Ocean, there have been numerous studies of faunal microdistribution at vent fields on the East Pacific Rise and Juan de Fuca Ridge , , , , , , , , , , , , , , , , , , , , but fewer studies so far on the Mid-Atlantic Ridge , , , , , ,  and in Western Pacific back-arc basins , .
Dive 140, 2400 m depth, ROV heading 090° (B) “Carwash” 9.7 m edifice (−60°02.572, −29°58.904). Dive 140, 2401 m depth, ROV heading 128° (C) “Ivory Towers” 6.7 m edifice (−60°02.809, 29°58.708). Dive 142, 2395 m depth, ROV heading 090°.
Exploration of the East Scotia Ridge (ESR), an intermediate-rate back-arc spreading centre in the Southern Ocean  (Figure 1), has recently revealed vent fields inhabited by new, undescribed species of anomuran crab, eolepadid barnacle, lepetodrilid and peltospiroid gastropods, actinostolid anemones, and a stichasterid seastar, which represent a new province of vent biogeography . Here we: (i) describe the distribution of vent structures in the newly-discovered E9 vent field on the ESR; (ii) determine patterns of faunal zonation and species association in the E9 vent field, using refinements in videography from a deep-sea remotely operated vehicle (ROV); and (iii) examine relationships between faunal microdistribution, vent activity, and the trophic ecology of abundant primary consumers using carbon and sulphur stable isotope analyses. These studies therefore provide a first characterisation of faunal ecology in this new province of vent biogeography.
Dive 139, 2401 m depth. ROV heading 358°. Area mosaiced ~280 m2. Laser scale = 10 cm (A) unidentified Octopod (B) cluster of stichasterid seastars (C) pycnogonid genus Colessendeis sp. predating on actinostolid (D) small area of diffuse flow (E) barnacles on ‘y’ – shaped fracture (F) “Kiwa assemblage B” and “gastropod assemblage” (G) “Kiwa assemblage A” associated with peak ROV mounted CTD temperature measurement (6.03°C) (H) small area of diffuse flow in collapsed basalt.
Materials and Methods
Image Acquisition and Mosaicing
During research cruise 42 of the RRS James Cook (7th January –24th February 2010) the Isis ROV completed 9 dives with a total bottom time of 96 hours at the E9 vent field on the ESR (Figure 2). These dives included systematic videographic surveys of selected areas of the vent field. Surveys of horizontal substratum were undertaken using a downward-looking (seabed-perpendicular) 3-chip CCD (charge-coupled device) video camera (Insite Pacific Atlas). Two lasers, 0.1 m apart, were mounted parallel to the focal axis of the camera to provide scale in images. A CTD mounted to the starboard side of the ROV recorded water temperature at an altitude of 2 to 3 m above the seafloor during these horizontal mosaic surveys.
Unless stated otherwise, laser scale or scale bar = 10 cm (A) Anhydrite assemblage adjacent to Kiwa assemblage A (B) Kiwa assemblage B (C) gastropod assemblage (D) barnacle assemblage (E) anemone assemblage (F) Actinostolid observed egesting a Kiwa n. sp. carapace (indicated by white arrow) (G) Un-described seven-armed stichasterid seastar (H) Predatory seastar observed preying on a Kiwa n. sp. (I) On-board still image of Lepetodrilus n. sp. on carapace of large individual of Kiwa n. sp. 62 individuals counted, Scale = 5 cm (J) Lepetodrilus n. sp in association with the gastropod assemblage (5900–6200 individuals m−2).
Surveys of upstanding structures such as vent chimneys were undertaken using a 1080i high-definition video camera (Insite Pacific Mini-Zeus) on a pan-and-tilt mount. For these surveys, this camera was configured to view horizontally forwards from the ROV, so that its focal axis was perpendicular to the vertical plane described by the movement of the vehicle during surveys. Once configured, the pan and tilt module was then fixed for the duration of the survey. Two lasers, 0.1 m apart, were mounted parallel to the focal axis of the camera to provide scale in images. Continuous CTD measurements of water temperature during imaging of vent chimneys cannot be related to the surfaces surveyed, because of the vertical advection of vent fluids.
(A) Barnacle assemblage with associated Lepetodrilus n. sp. 20,172–56,904 individuals m−2. (B) Line plot indicates the total number of limpets in each 5 cm increment towards an area of rising hydrothermal effluent. Bar plot indicates average number of limpets per capitula. Error bars are standard deviation.
Several criteria constrained the selection of edifices for vertical mosaicing surveys. As a result of ROV dive time limitations, only three upstanding structures could be surveyed. These three chimneys were selected to represent a range of levels of hydrothermal activity. For inter-chimney comparisons, the west face (approximate ROV heading 090°) was chosen, as this heading was most amenable to complete ROV transect lines in a vertical plane with no obstructions. Selecting the same cardinal face also minimises possible variations between faces that may result from the effects of background currents. These criteria resulted in the following three structures being surveyed: “Black & White”, “Carwash” and “Ivory Towers” (Figure 3).
(A) Assemblage distances from the vertical high-temperature black smoker exit on the “Black & White” edifice (B) Assemblage distances from the vertical diffuse flow exits on the “Carwash” edifice. (C) Assemblage distances from the horizontal diffuse flow exit indicated by ROV CTD peak temperature measurement on the “Twin Peaks” mosaic (see Figure 4 & Figure 8). (D) Image illustrating transition from assemblage to assemblage.
Temperature plot is an interpolation using data acquired from the ROV mounted CTD. (B) Digitised faunal assemblages of the “Twin Peaks” low-lying diffuse flow area. Assemblage types are colour coded and presented in the legend. Peripheral fauna are indicated using the following symbols (+) Kiwa n. sp. (○) unidentified Octopod (•) un-described Stichasterid seastar (x) Colessendeis sp. pycnogonid.
The Doppler velocity log (DVL) of the Isis ROV provided precise (<0.1 m in x, y, z directions) control of the position and movement of the vehicle during the acquisition of video imagery for both survey types. For surveys of horizontal surfaces, this precise control was used to maintain an altitude of 2 to 3 m above the seafloor. For surveys of vertical surfaces, the precision control of the ROV was used to maintain constant heading of camera view and maintain the position of the vehicle in a vertical plane parallel to the face of the chimney being surveyed. In both cases, DVL control was used to ensure survey lines with a minimum overlap of 50% in visible frames.
(A) “Ivory Towers” (B) “Black & White” (C) “Carwash” (D) Comparative bar chart of percentage surface coverage of defined faunal assemblages associated with each edifice.
Video media were then imported into a video editing software package (QuickTime Pro Version 7.6.6) and exported as a stills image sequence (full resolution 1080i HD images). These images were then used to construct mosaic images by manually aligning and superimposing frames in Adobe Photoshop CS5 extended (version 12.0×64). For mosaics of upstanding structures, where no relevant CTD data are available, video footage was reviewed simultaneously with the mosaicing process to identify and locate visible vent fluid sources including black smokers, active flanges, and areas of diffuse flow.
This spatial pattern of zonation radiates in both (A) horizontal and (B) vertical directions.
Definition and Quantification of Faunal Assemblages
Mosaic images constructed from ROV dive footage were used to define faunal assemblage types based on dominant visible species , . Voucher specimens of dominant species were collected during ROV dives and identified through morphological and molecular analyses . From these specimens, tissue samples were dissected for stable isotope analyses.
Areas occupied by different assemblage types were defined using Photoshop to delineate their extent in mosaic images. The area of each assemblage type was determined using the 0.1 m laser scale visible in images. Percentage cover of each assemblage type was then calculated for chimney surfaces as a 2D projection of the face of the vent structure , using the laser scale to correct for variation in the distance between the topography of the vent chimney and the vertical plane followed by the ROV.
On the surfaces of upstanding structures, the abundances of visually-identifiable species were estimated in each assemblage type by using the 0.1 m laser scale on areas chosen to be as perpendicular to the camera view as possible. Although the mosaics were used to define and digitise the faunal assemblages on each structure, all numerical data were collated from the original stills captures extracted from the raw high-definition video footage and reviewed on a high-resolution monitor. This removes any error of double counting of mobile megafauna, which could be an artefact from the mosaicing process. For some species where multi-layered aggregations may be present, the abundances reported are a “minimum abundance” based on the visible monolayer population. Distributions of assemblage types were compared with distances from identified visible sources of vent fluids on upstanding structures.
Faunal assemblages types were also identified in the mosaic images of horizontal surfaces based on dominant visible species . CTD data recorded during horizontal mosaic surveys were interpolated and contoured using Surfer 8.0 (Golden Software Inc). Interpolated data were co-registered with ROV position data in ArcMap 10 to enable comparison of distributions of assemblage types with variations in water temperature recorded by the CTD. The ROV position data were corrected to account for an offset between the locations of the CTD and camera on the vehicle.
Stable Isotope Analyses
Approximately 0.7 mg of powder was weighed into separate tin capsules for carbon stable isotope analysis (SIA). For sulphur SIA, 2 mg of sample and 4 mg of the catalyst vanadium pentoxide were weighed into each tin capsule. Stable carbon isotope ratios were measured by continuous-flow isotope ratio mass spectrometry using a Costech Elemental Analyser interfaced with Thermo Finnigan Delta Plus XP (Natural Environment Research Council, Life Sciences Mass Spectrometry Facility, SUERC, East Kilbride, United Kingdom). Two laboratory standards were analysed every ten samples in each analytical sequence. These alternated between paired alanine standards, of differing δ13C, and an internal laboratory gelatin standard. Sulphur SIA was conducted by Iso-Analytical (Crewe, United Kingdom) using a SERCON Elemental Analyser coupled to a Europa Scientific 20–20 Mass Spectrometer. Laboratory standards barium sulphate (two sets of differing δ34S) and silver sulfide were used for calibration and drift correction. An internal standard of whale baleen was used for quality control (n = 28, 16.34‰ ± s.d. 0.21). Stable isotope ratios were expressed in delta (δ) notation as parts per thousand/permil, (‰). All internal standards are traceable to the following international standards: v-PDB (Pee Dee Belemnite), NBS-127 (barium sulphate), IAEA-S-1 (silver sulfide) and IAEA-SO-5 (barium sulphate). An external standard of freeze dried and ground white fish muscle (Antimora rostrata) was also analysed (δ13C, n = 24, −18.94‰ ± s.d. 0.09; δ34S, n = 30, 18.20‰, ± s.d. 0.59).
Distribution and Setting of Vents in the E9 Vent Field
The E9 vent field (Figure 2; main) is located north of a collapse caldera (“Devil's Punchbowl”, Figure 2: top-right) on the axial high of the E9 ridge segment of the ESR, at depth ~2400 m. The distribution of active and inactive vent chimneys (Figure 2B–2M) within the field appears to be associated with fissures parallel to the ridge axis, running NNW from the edge of the caldera across a seafloor of predominantly flat sheet lavas (Figure 2, insert A; ). Background seawater temperature at the E9 vent field, in areas not influenced by hydrothermal activity, is typically −1.3°C and is influenced by lower Weddell Sea Deep Water .
Two active chimney structures occur in close proximity at the northern limit of the vent field. “Black & White” (Figure 2D) is a ~10 m high structure with multiple “black smoker” sources at its summit, emitting fluids with a maximum measured temperature of 380.2°C. Lower down the structure, flanges and beehives provide additional exits for hydrothermal fluids at lower temperatures. The “Black & White” structure also includes sulfide pinnacles that do not emit visible diffuse flow. A second vent chimney, “Carwash”, is located less than 5 m south of “Black & White”. “Carwash” (Figure 2E) is ~10 m high and surmounted by two chimneys that are no longer venting high-temperature fluids from their peaks. Cooler fluids (5–19°C) and visible “white smoke” emit from sources between the two chimney structures. Towards the lower part of the chimney, flanges provide further fluid exits.
In addition to chimney structures, the northern limit of the vent field includes three areas of abundant faunal populations associated with diffuse flow from fissures in sheet lavas. Two of these areas (including “Twin Peaks” Figure 2C) lie within 100 m north of “Black & White” and “Carwash”.
The southern area of the vent field is characterised by active and extinct chimneys and diffuse flow fields distributed parallel to the ridge axis. The “Marsh Towers” structure (Figure 2H) consists of two chimneys rising from a sulfide platform, which emit diffuse flow, but no visible black-smoker venting. “Marsh Land” (Figure 2G), an area of diffuse flow from fissures in basalts lies immediately to the west. “Ivory Towers” (Figure 2I) is located ~30 m south of “Marsh Towers” and is similarly formed of two chimney complexes on a sulfide platform. One chimney complex at “Ivory Towers” emits high temperature fluids (382.8°C) through a number of exits, including clusters of beehive diffusers. The other complex consists of five chimneys with bulbous tops that do not emit visible high-temperature fluids. Extensive venting does occur, however, from beehive diffusers and flanges at the sides of these chimneys. Several less active pinnacles also surround the main structures of “Ivory Towers”.
Two further active structures occur in close proximity ~50 m south of “Ivory Towers”. At “Pagoda” (Figure 2J), buoyant high-temperature vent fluid pools beneath a series of flanges. Similar flange-trapped pools occur at “Launch Pad” ~10 m to the west (Figure 2K), where there is also a single black-smoker chimney. The southernmost limit of the vent field is marked by several inactive structures, ~100 m south of “Pagoda”: “Needle” (Figure 2L) and “Windsor Castle” (Figure 2M).
Definition of Faunal Assemblages at E9 Vent Field
Vertical mosaic images were obtained at three vent edifices: the “Black & White” vent chimney (east and west faces; Mosaic Figure 3A), the “Carwash” vent chimney (west face; Mosaic Figure 3B), and “Ivory Towers” (north, south, east and west face; Mosaic Figure 3C). Three horizontal mosaic surveys were also completed: one at the NW corner of the “Black & White” vent chimney (resulting in a high-definition mosaic image of 17 m x 13 m of seafloor), and two in the Twin Peaks area (26 m x 7 m and 13 m x 29 m; Figure 4).
The fauna of the E9 vent field are visually dominated by four taxa: an undescribed species of anomuran crab of the genus Kiwa; an undescribed species of peltospiroid gastropod; an undescribed species of eolepadid barnacle of the genus Vulcanolepas; and undescribed species of actinostolid anemones. Initial morphological and molecular phylogenetic analyses are consistent with these taxa representing new species , and they are therefore referred to here as putative new species (e.g. “Kiwa n. sp.”). Although formal descriptions are required to confirm actual species identities, these dominant taxa can clearly be distinguished from each other in video imagery. Other fauna present among aggregations of the dominant taxa include an undescribed species of limpet of the genus Lepetodrilus, and at least three species of the pycnogonid genus Sericosura. An undescribed seven-armed sea star from the family Stichasteridae is also present towards the base of chimneys and peripheral to areas of low-temperature diffuse venting. Other common peripheral fauna include two species of the pycnogonid genus Colessendeis, the brisingid seastar Freyella sp., an unidentified species of octopus, and zoarcid fish.
Video analyses define seven assemblage types at the E9 vent field, based either on the fauna visibly dominating their biomass or the substratum type where no fauna were present (Table 1 and Figure 5; names of each faunal assemblage type are derived from their dominant taxon). In areas immediately surrounding high-temperature fluid exit, heating of seawater results in the precipitation of an anhydrite layer around the vent opening . The “anhydrite assemblage” is typically devoid of organisms with the exception of occasional mats of white filamentous bacteria and occasional large individuals of Kiwa n. sp. with white filamentous bacteria growing on the carapace (Figure 5A).
Surfaces adjacent to areas of exposed anhydrite are dominated by Kiwa n. sp. The “Kiwa assemblage” can be divided into three subtypes based on average size of individuals and proximity to vent fluid exits. “Kiwa assemblage A” contains the largest individuals (47±0.8 mm mean carapace length.; Figure 5A), often with filamentous bacteria on their carapace when in close proximity to vent fluid sources, but individuals occur in low population densities (minimum reported 65 individuals m−2 for “Black & White”). At greater distance from fluid exits, but still within areas of visible diffuse flow, “Kiwa assemblage B” is dominated by smaller individuals (30±0.8 mm mean carapace length; Figure 5B) occurring at higher population densities (minimum 533 individuals m−2 for “Black & White”). Here Kiwa n. sp. occur in multilayer aggregations and have carapaces devoid of visible filamentous bacteria. Adjacent to “Kiwa assemblage B” but at greater distance from visible vent fluid sources, “Kiwa assemblage C” consists of juvenile specimens (12±0.4 mm mean carapace length) in abundant aggregations (minimum 4017 individuals m−2 for “Black & White”). In each of these assemblages, the only other visible faunal species is the limpet Lepetodrilus n. sp., on the carapaces of Kiwa n. sp. (Figure 5I). The maximum number of Lepetodrilus n. sp. recorded on the carapace of a collected specimen was 62 individuals and was similar to the 69 individuals counted from video imagery.
Surrounding the “Kiwa assemblage”, though still within areas of visible diffuse flow, the undescribed peltospiroid genus dominates the “gastropod assemblage” (Figure 5C), as multilayer aggregations (minimum reported abundance 1062 individuals m−2 for “Carwash”) and occasional chains of individuals hanging from the edges of hydrothermal structures. Other conspicuous fauna within the “gastropod assemblage” include Lepetodrilus n. sp. on the shells of the gastropods (minimum estimated abundance from video analysis was 5900–6200 individuals m−2; Figure 5J). Occasional individuals of Sericosura spp. pycnogonids and Kiwa n. sp. were also observed moving over the surfaces of the gastropod aggregations.
Beyond the gastropod assemblage, the fauna are visually dominated by the eolepadid cirripede Vulcanolepas n. sp., forming the “barnacle assemblage” (Figure 5D; minimum reported abundance 893 individuals m−2 for “Carwash”). Although the barnacles are not basally attached in areas of diffuse flow, their capitula typically occur above areas of diffuse venting. Lepetodrilus n. sp. occur at high abundance on the barnacles (estimates of abundances from video observations: 20 172 to 56 904 individuals m−2; Figure 6A), with the greatest numbers on the capitula of barnacles that are exposed to diffuse flow (Figure 6B). Actinostolid anemones and Kiwa n. sp. are also occasionally present among the barnacles.
Actinostolid anemones subsequently dominate the fauna at greater distance from fluid sources, defining an “anemone assemblage” (Figure 5E). Pacmanactis n. spp. are the most abundant anemones in this assemblage (minimum reported abundance 34 individuals m−2 for “Carwash”), but Marianactis n. sp. may also be present. A specimen of Pacmanactis n. sp. was observed egesting a carapace of Kiwa n. sp. (Figure 5F).
Vent structures also include some areas of visible exposed substratum but no obviously dominant or abundant faunal taxon, for example occupied by patches of visible microbial mats and sparse juvenile Vulcanolepas n. sp. These areas are defined as “substratum assemblage”. Finally, a “peripheral assemblage” occurs in areas where there is no visible influence of hydrothermal activity in substratum type (i.e. absence of anhydrite) or fluid sources. This assemblage includes individuals of seven-armed stichasterid seastars (Figures 5G and 5H) and fauna not present in other assemblages such as Colossendeis spp. pycnogonids, which were observed feeding on peripheral actinostolids (Figure 4C). Occasional small Kiwa n. sp. (carapace length <50 mm) were also observed in the “peripheral assemblage”.
Zonation of Faunal Assemblages at E9 Vent Field
The faunal assemblages at the E9 vent field show a repeatable pattern of zonation around vent fluid sources in vertical and horizontal directions (Figure 7). The horizontal mosaic survey at “Twin Peaks” (Figures 4 and 8) show the “Kiwa assemblage” and “gastropod assemblage” associated with areas of highest temperature recorded by ROV-mounted CTD (“Kiwa assemblage”: up to 3.6 m maximum distance from peak temperature record; “gastropod assemblage”: up to 4.3 m maximum distance from peak temperature record). With increasing distance from these areas, faunal composition changes into “barnacle assemblage” (between 0.9 m minimum to 9.9 m maximum distance from peak temperature record) followed by “anemone assemblage” (between 1.1 m minimum to 13.2 m maximum distance from peak temperature record), with eventual gradation into “peripheral assemblage” where stichasterid seastars are prevalent (beyond 2.7 m minimum distance from peak temperature record). Stichasterids occur as solitary individuals, but also in small aggregations (closest proximity 0.11 m between centres of individual disks).
On upstanding structures where mosaic images were obtained, the same zonation is apparent with distance above, below and lateral to vent sources where substratum is available for fauna to occupy (Figure 7). In addition, the western faces of the three surveyed vent structures, (“Ivory Towers”, “Black & White” and “Carwash”) show differences in the number and type of visible vent sources (Figure 9). These structures also exhibit differences in percentage cover of assemblage types in the 2D projections of their mosaiced faces (Figure 9; Table 2).
The western face of “Ivory Towers” exhibits fifteen visible fluid flow exits across its projected mosaic area, and the highest proportion of “anhydrite assemblage” (Figure 9A). The “anhydrite assemblage” bordering high-temperature fluid sources covers 19% of the projected mosaic area. Adjacent to these patches, “Kiwa assemblages” account for 21% coverage (“Kiwa assemblage A”: 12%; “Kiwa assemblage B”: 9%; “Kiwa assemblage C”: absent; Figure 9A). The “gastropod assemblage” covers 24% of the total projected mosaic area, occurring towards the base of the mosaiced structure at greater distance from visible fluid flow exits. The remainder of the projected mosaic area is classified as “substratum assemblage” (36%). The “barnacle assemblage” and “anemone assemblage” are absent from the mosaiced area of the “Ivory Towers” structure.
“Black & White” exhibits an archetypal chimney structure, with venting occurring from eleven visible fluid flow sources at its peak and from flanges below (Figure 9B). All assemblage types from “Kiwa assemblage A” to “anemone assemblage” are present in the mosaiced area of the western face of this structure. “Kiwa assemblage” types account for a total of 21% of the projected mosaic area (“Kiwa assemblage A”: 11%; “Kiwa assemblage B”: 8%; “Kiwa assemblage C”: 2%; Figure 9B), while the “gastropod assemblage” and “barnacle assemblage” cover 2% and 6% respectively. The “anemone assemblage” occupies 9%, occurring towards the base of the chimney. The remainder (62%) of the projected mosaic area at “Black & White” is represented by “substratum assemblage”, for example below the main active chimney where surfaces are occupied by occasional bacterial mats and sparse small barnacles.
Eight point sources of vent fluids were visible on the western side of “Carwash”, and there is no visible high-temperature venting (Figure 9C). “Kiwa assemblage B” covers 14% of the projected mosaic area, and occurs largely between the two relict pinnacles of the structure. Here fluid exits may be obscured from visual recognition, by dispersal of diffuse flow through dense aggregations of Kiwa n. sp. and neighbouring peltospiroid gastropods. The “gastropod assemblage” accounts for 23% of the projected mosaic area at “Carwash”. In contrast with “Ivory Towers” and “Black & White”, the “barnacle assemblage” accounts for 47% of the projected mosaic area at “Carwash”. Towards the base of the structure, the “anemone assemblage” occupies 8% of the projected mosaic area, and the “substratum assemblage” only represents 7%, in contrast with the other mosaiced structures. The remaining 1% of surveyed surface on this structure was represented by the “anhydrite assemblage”.
Carbon and sulphur isotope composition of dominant primary consumers.
Across the faunal assemblages identified at the E9 vent field, the visually dominant taxa show an increase in δ34S values with distance from visible vent fluid source. Kiwa n. sp. sampled from the “Kiwa assemblage” exhibited a mean δ34S (s.d.) of 3.06±1.12 (n = 52), while peltospiroid gastropods from the “gastropod assemblage” showed a mean δ34S of 4.12±0.93 (n = 37), and the mean δ34S of Vulcanolepas n. sp. from the “barnacle assemblage” was 8.13±2.95 (n = 46).
The dominant primary consumers among assemblage types also varied in mean δ13C values. The mean δ13C (s.d.) value of Kiwa n. sp. from the “Kiwa assemblage” was −10.64±0.74, while the value for peltospiroid gastropods from the “gastropod assemblage” was −30.71±0.70. The mean δ13C of Vulcanolepas n. sp. from the “barnacle assemblage” was −24.46±2.52, intermediate to the values shown by the Kiwa n. sp. and peltospiroids.
Faunal Assemblages at a Vent Field in the Southern Ocean
The fauna occupying the E9 hydrothermal vent field on the East Scotia Ridge belong to a proposed new Southern Ocean province of vent biogeography . The assemblages at the E9 vent field include aggregations of a new species of anomuran crab, Kiwa n. sp., and video mosaicing of vent structures shows that this species occurs at abundances of >700 individuals m−2 in close proximity to vent fluid sources. Two other species of Kiwa are known to occur in chemosynthetic environments. Kiwa hirsuta occurs at hydrothermal vents on the Pacific-Antarctic Ridge, but at lower population densities (0.1 to 0.2 individuals m−2) towards the periphery of vent fields . Kiwa puravida occurs at cold seeps on the Costa Rica margin, but has not been observed in extensive aggregations similar to those of the Kiwa species at the E9 vent field . Recently, specimens superficially resembling Kiwa n. sp. have also been found in close proximity to active vent sources at a vent field on the SW Indian Ridge, though at population densities at least an order of magnitude lower than those observed at the E9 vent field in the Southern Ocean (Copley & Marsh, pers. obs.). The galatheid Shinkaia crosnieri found in the Okinawa Trough back-arc basin of the western Pacific  is the only other anomuran known to occur in dense aggregations (exceeding 560 individuals m−2) in close proximity to vent fluid sources .
The ventral surface of Shinkaia crosnieri is covered in plumose setae, similar to Kiwa n. sp., and S. crosnieri has been observed “combing out” these setae using its third maxilliped to transfer epibiotic bacteria to its mouth . Carbon radioisotope uptake and stable isotope studies confirm that S. crosneiri obtains nutrition from harvesting epibiotic bacteria in this fashion , . Kiwa hirsuta and K. puravida are thought to harvest epibiotic bacteria similarly from the setae on their chelipeds, although this has only been demonstrated for K. puravida . The chelipeds of Kiwa n. sp. are not conspicuously setose and much shorter in proportional length than those of K. hirsuta and K. puravida, but its ventral surface is densely covered in setae unlike other Kiwa species. Filamentous bacteria associated with these ventral setae suggest that Kiwa n. sp. may also feed on epibiotic bacteria .
Assemblages dominated by other decapod crustaceans occur in close proximity to vent fluid sources at some Atlantic and Indian Ocean vents. Alvinocarid shrimp of the genus Rimicaris occur at high densities close to vent sources at depths greater than 3000 m on the Mid-Atlantic Ridge (R. exoculata, 1500–2500 individuals m−2; , , ), on the Central Indian Ridge (R. kairei; , , , ), and on the Mid-Cayman Spreading Centre (R. hybisae, 2000 individuals m−2; , ). In contrast, the substratum adjacent to high-temperature fluid exits on vent chimneys at east and northeast Pacific ridge vent fields is typically occupied by alvinellid polychaetes (~2000 individuals m−2; ).
Among taxa occupying a similar position in faunal zonation at vents in other biogeographic provinces, Rimicaris exoculata are also thought to derive nutrition from epibiotic bacteria , , , which may include methanotrophs at vent fields in ultramafic settings , and a nutritional role of epibiotic bacteria is also indicated for the polychaete Alvinella pompejana . The δ13C values of Kiwa n. sp. sampled from the “Kiwa assemblage” at the E9 vent field are similar to values found in other vent species thought to feed on an epibiont flora dominated by epsilon-Proteobacteria , , , , although the epibiont flora associated with the ventral setae of Kiwa n. sp. have not yet been characterised.
The occurrence of Kiwa n. sp. at the E9 vent field extends from aggregrations around vent fluid sources to individuals in peripheral areas. Direct temperature probe measurements of the “Kiwa assemblages” defined by video mosaicing of vent structures ranged from 10.1 to 12.6°C. Lower temperatures of −0.11 to 1.02°C were recorded by the ROV-mounted CTD where individual Kiwa n. sp. occur in the periphery of the vent field (Figure 8), but these temperature data are not directly representative of conditions inhabited by the animals because of the elevated position of the CTD sensor on the ROV. Lithodid crabs are the other anomuran taxon known to maintain adult populations in deep Antarctic waters south of the Polar Front , although a squat lobster, Munidopsis albatrossae, has also been recorded from the Bellingshausen Sea . However, lithodid crabs appear to be excluded at temperatures lower than 0.5°C . Explanations for a general absence of reptant decapods from deep Antarctic waters include their inability to regulate haemolymph magnesium concentrations, resulting in loss of activity and death at cold temperatures , . The elevated temperatures recorded directly by temperature probe in areas occupied by “Kiwa assemblages” may exclude these aggregations from this limitation.
The “gastropod assemblage” at the E9 vent field is visually dominated by an undescribed species of peltospiroid and occurs adjacent to “Kiwa assemblages” but, at greater distance from visible vent fluid sources. Peltospiroid gastropods are a geographically widespread taxon at hydrothermal vents, and occur in a similar position in vent faunal zonation at several vent fields on the Central Indian Ridge (undescribed “scaly foot” gastropod; , ) and on the Juan de Fuca Ridge in the northeast Pacific (Depressigyra globulus; , ). At the 9°N vent field on the East Pacific Rise, three species of peltospiroid are associated with the “alvinellid zone” but do not dominate its assemblages . Two morphospecies of peltospiroid are also abundant at newly-explored vents on the SW Indian Ridge (Copley & Marsh, pers. obs.), and another peltospiroid occurs in high abundance at a vent field north of the Azores on the Mid-Atlantic Ridge . Physico-chemical tolerances are thought to be important in defining gastropod microdistributions within hydrothermal vent fields, although other factors such as biological interactions and microbial flora may also be important , , . The δ13C values of peltospiroid gastropods from the “gastropod assemblage” are similar to those of other taxa with endosymbionts dominated by gamma-Proteobacteria, such as the gastropod Ifremeria nautilei  and some Bathymodiolus spp mussels , , .
The sessile filter-feeding stalked barnacle Vulcanolepas n. sp. dominates the third assemblage away from visible vent fluid sources in video mosaics at the E9 vent field. Eolepadid barnacles occupy a similar position in faunal zonation at vent fields on the Central Indian Ridge , , , SW Indian Ridge (Copley & Marsh, pers. obs), and several back-arc basins of the western Pacific ,  where similar abundances have been recorded to those reported at the ESR .
Molecular phylogenetics of Vulcanolepas n. sp. from the E9 vent field indicates that it is most closely related to V. osheai from the Brothers Caldera on Kermadec Ridge in the SW Pacific . The cirral setae of V. osheai harbour filamentous bacteria, and stable isotope and fatty acid analyses indicate that V. osheai derives nutrition from these epibionts . Eolepadid barnacles at other vents also harbour filamentous bacteria on elongated cirral setae and may be capable of feeding on finer particles than other deep-sea barnacles . The stable isotope composition of eolepadid barnacles from vents on the Central Indian Ridge is consistent with nutrition from epibiotic bacteria in addition to filter feeding . The δ13C values of Vulcanolepas n. sp. from the “barnacle assemblage” suggests a similar mixed nutritional mode for eolepadid barnacles at the E9 vent field.
In the “barnacle assemblage” and “gastropod assemblage” defined by video mosaicing, lepetodrilid limpets are the numerically dominant species, occurring at high abundances on the peduncles and capitula of the eolepadids, the shells of the peltospiroids, and also occasionally on the carapaces of individual Kiwa n. sp., both in the “Kiwa assemblages” and in the periphery of the E9 vent field. Lepetodrilids are a numerically dominant component of the fauna in zones comparable to the “barnacle assemblage” at some vent fields in other regions, for example on the northern East Pacific Rise  and Juan de Fuca Ridge . Although the proximity of lepetodrilid species closest to vent sources may be determined by tolerance of hydrothermal conditions , their distribution is often widespread across other faunal assemblages at vent fields elsewhere .
The “anemone assemblage” defined by video mosaicing occurs beyond the “barnacle assemblage” at greater distance from visible vent fluid sources in the E9 vent field, and is the most peripheral assemblage type dominated by a single taxon. Actinostolids occupy a similar position in faunal zonation at several vent fields in other biogeographic provinces, either dominating peripheral zones (e.g. TAG hydrothermal mound, Mid-Atlantic Ridge ; Rose Garden, Galapagos Rift ; Kairei and Edmond fields, Central Indian Ridge , ) or surfaces at low temperatures (Ashadze-1, Mid-Atlantic Ridge ). The abundances of actinostolids in the “anemone assemblage” at the E9 vent field (33–44 individuals m−2) are comparable with anemone abundances reported on the Mid-Atlantic Ridge at the TAG hydrothermal mound (~20 individuals m−2; ) and Ashadze-1 (32 individuals m−2; ), and at the Beebe Vent Field on the Mid-Cayman Spreading Centre (>20 individuals m−2; ). The observation of an anemone egesting a carapace of Kiwa n. sp. at the E9 vent field is consistent with a general recognition of actinostolids as secondary consumers at vents .
The “peripheral assemblage” defined by horizontal video mosaicing at the E9 vent field is characterised by the occurrence of secondary consumers such as octopus, seven-armed stichasterid asteroids and Colessendeis spp. pycnogonids (Figure 4A, 4B and 4C). Specimens of the suspension-feeding brisingid genus Freyella were also present on inactive structures in the southern sector of the E9 vent field (“Needle” and “Windsor Castle”, Figures 2L and 2M). Predators, scavengers and suspension-feeders known from non-vent environments are known to occur opportunistically in the periphery of vent fields . Whether taxa only observed in the “peripheral assemblage” at the E9 vent field can be considered “vent endemic” is therefore not clear, even where stable isotope values indicate nutrition ultimately derived from chemosynthetic sources of carbon fixation .
Overall, although the fauna present at the E9 vent field are distinct from those of other biogeographic provinces at species level, it is clear that they exhibit similarities in zonation patterns at higher taxonomic levels. Similarities in zonation at disparate locations may result from family-level constraints of physical tolerances to physico-chemical gradients at vents, and/or family-level similarities in trophic ecology. However, the families that dominate the assemblages at the E9 vent field do not always co-occur at vents in other biogeographic provinces. Currently, a zonation dominated by peltospiroids, eolepadids, and actinostolids with increasing distance from vent sources is only known at vent fields on the Central Indian Ridge , . At family level, the E9 vent field is distinct in the high abundance of kiwaid crabs in close proximity to high-temperature vent sources, not previously observed for other kiwaid species, and only known for one other anomuran species at vent examined so far .
Microdistribution Patterns Revealed by Large-scale Video Mosaicing at a Vent Field
There is a consistent pattern of faunal zonation at the E9 vent field, transitioning between assemblage types with increasing distance from vent fluid sources (Figure 10). Faunal zonation occurs in both vertical and horizontal directions around “black smoker” sources and areas of visible diffuse flow (Figure 7). The importance of thiothrophic nutrition for primary consumers may decline with distance from vent fluid sources, as indicated by the increase in δ34S values across the zonation of their assemblages . There are variations, however, in the coverage of surfaces by different assemblage types on individual chimneys surveyed at the E9 vent field (Figure 9). These chimneys vary in the occurrence of visible fluid sources and predominance of focused high-temperature venting or lower-temperature diffuse flow.
The western face of “Ivory Towers” exhibits the highest concentration of high-temperature fluid flow exits and the highest proportion of “anhydrite assemblage” among the structures surveyed, and the faunal zonation only extends to the “gastropod assemblage” in the mosaiced area. At “Black and White”, most venting occurs as “black smoker” activity at the peak of the structure, immediately surrounded by “Kiwa assemblages”. With most sources of buoyant vent fluid concentrated at the top of this structure, much of the lower chimney is uncolonised by faunal assemblages, with small patches of “barnacle assemblage” on relict pinnacles above other vent fluid sources.
At “Carwash”, there are no visible sources of high-temperature vent fluids, and no visible venting at the peaks of its two sulfide pinnacles. Instead, venting occurs as diffuse flow from the central and lower portions of the structure. More than 90% of its surveyed area is covered by faunal assemblages, dominated by the “barnacle assemblage” (Figure 9D). Zonation from “Kiwa assemblage” to “barnacle assemblage” occurs repeatedly across the lower structure around individual sources of visible vent fluids. Dense faunal aggregations also disperse vent fluids laterally from their sources in this area, and there may be additional fluid flow exits in this area that are obscured by faunal aggregations. A similar dispersion of vent fluids by mussel beds at Rose Garden on the Galapagos Rift has been proposed to extend the seawater-effluent interface and thereby increase habitat for vent fauna .
Surveying several structures with different level and types of activity in the E9 vent field reveals a possible successional pattern in faunal colonisation as activity at a particular structure declines. Nascent vent structures with high levels of “black smoker” venting may resemble “Ivory Towers” in assemblage types and coverage, while structures where high-temperature activity is waning may resemble “Carwash”. “Black & White” may represent a transition between these two extremes. This successional pattern can be tested on future visits to the E9 vent field, using the large-scale high-definition video mosaics compiled here as a baseline to assess faunal change.
Variations in faunal microdistribution patterns at the E9 vent field appear to be aligned with temperature gradients, where CTD temperature data are available for large-scale mosaic surveys of horizontal surfaces (Figure 8). Temperature is often used as a proxy for physico-chemical conditions at vents, and considered to represent the primary abiotic drivers in the spatial structuring of vent assemblages (e.g., , , , , , ). However, biological processes may also be important in structuring faunal assemblages in vent environments (e.g., , , , , , , , ), but subsequent investigation of these processes usually requires ecological experimentation at the seafloor .
Here, large-scale, high-definition video mosaicing at the E9 vent field has enabled detailed determination and quantification of faunal zonation and microdistribution patterns over a similar spatial scale to studies in accessible intertidal environments. Determining patterns of spatial variation is a prerequisite for elucidating processes  and a necessary first step in understanding the ecology of a new province of vent biogeography. Although the presence/absence of species is used to distinguish biogeographic provinces, such information does not represent all aspects of ecological similarity or difference. There are some similarities at family level in the zonation of assemblages at the E9 vent field and those of other provinces, but also some differences. Determining such patterns at a global scale, and understanding their genesis, represents a goal for vent ecology beyond the mapping of biogeographic distributions.
The authors would like to thank the Master and crew of the RRS James Cook for their outstanding support and efforts during expedition JC042 in the Southern Ocean. We also thank the staff of National Marine Facilities at the National Oceanography Centre for logistic and shipboard support. Special thanks also to the pilots and technical teams of ROV Isis, who undertook the deep-sea sampling and adapted the vehicle for detailed videography surveys. This is ChEsSO publication #2.
Conceived and designed the experiments: LM JTC WDKR CJS. Performed the experiments: LM JTC WDKR CJS. Analyzed the data: LM JTC VAIH WDKR CJS. Contributed reagents/materials/analysis tools: LM JTC VAIH KL WDKR ADR CJS PAT. Wrote the paper: LM JTC. Participants on JC042: LM JTC VAIH KL WDKR ADR CJS PAT.
- 1. Jannasch HW, Wirsen CO (1979) Chemosynthetic primary production at East Pacific seafloor spreading centres. Bioscience 29: 592–598. doi: 10.2307/1307765
- 2. De Busserolles F, Sarrazin J, Gauthier O, Gelinas Y, Fabri MC, et al. (2009) Are spatial variations in the diets of hydrothermal fauna linked to local environmental conditions? Deep Sea Res Part 2 Top Stud Oceanogr 56: 1649–1664. doi: 10.1016/j.dsr2.2009.05.011
- 3. Hessler RR, Smithey WM (1983) The distribution and community structure of megafauna at the Galapagos Rift hydrothermal vents. In: Rona PA, Bostrom K, Laubier L, Smith KL, editors. Hydrothermal processes at seafloor spreading centers. New York: Plenum Press. 735–770.
- 4. Tunnicliffe V (1991) The biology of hydrothermal vents - ecology and evolution. Oceanography and Marine Biology 29: 319–407.
- 5. Paine RT (1974) Intertidal community structure - experimental studies on relationship between a dominant competitor and its principal predator. Oecologia 15: 93–120. doi: 10.1007/bf00345739
- 6. Underwood AJ, Chapman MG, Connell SD (2000) Observations in ecology: you can't make progress on processes without understanding the patterns. J Exp Mar Bio Ecol 250: 97–115. doi: 10.1016/s0022-0981(00)00181-7
- 7. Van Dover CL, Lutz RA (2004) Experimental ecology at deep-sea hydrothermal vents: a perspective. J Exp Mar Bio Ecol 300: 273–307. doi: 10.1016/j.jembe.2003.12.024
- 8. Govenar B (2010) Shaping vent and seep communities: habitat provision and modification by foundation species. In: Vent and Seep Biota: Aspects from Microbes to Ecosystems. 403–432.
- 9. Hessler RR, Smithey WM, Boudrias MA, Keller CH, Lutz RA, et al. (1988) Temporal change in megafauna at the Rose Garden hydrothermal vent (Galapagos Rift - Eastern Tropical Pacific). Deep Sea Res Part 1 Oceanogr Res Pap 35: 1681–1709. doi: 10.1016/0198-0149(88)90044-1
- 10. Sarrazin J, Robigou V, Juniper SK, Delaney JR (1997) Biological and geological dynamics over four years on a high-temperature sulfide structure at the Juan de Fuca Ridge hydrothermal observatory. Mar Ecol Prog Ser 153: 5–24. doi: 10.3354/meps153005
- 11. Shank TM, Fornari DJ, Von Damm KL, Lilley MD, Haymon RM, et al. (1998) Temporal and spatial patterns of biological community development at nascent deep-sea hydrothermal vents (9°50'N, East Pacific Rise). Deep Sea Res Part 2 Top Stud Oceanogr 45: 465–515. doi: 10.1016/s0967-0645(97)00089-1
- 12. Cuvelier D, Sarrazin J, Colaco A, Copley JT, Glover AG, et al. (2011) Community dynamics over 14 years at the Eiffel Tower hydrothermal edifice on the Mid-Atlantic Ridge. Limnol Oceanogr 56: 1624–1640. doi: 10.4319/lo.2011.56.5.1624
- 13. Van Dover CL (2011) Mining seafloor massive sulphides and biodiversity: what is at risk? ICES J Mar Sci 68: 341–348. doi: 10.1093/icesjms/fsq086
- 14. Johnson KS, Childress JJ, Beehler CL (1988) Short-term temperature variability in the Rose Garden hydrothermal vent field - an unstable deep-sea environment. Deep Sea Res Part 1 Oceanogr Res Pap 35: 1711–1721. doi: 10.1016/0198-0149(88)90045-3
- 15. Johnson KS, Childress JJ, Beehler CL, Sakamoto CM (1994) Biogeochemistry of hydrothermal vent mussel communities: The deep-sea analogue to the intertidal zone. Deep Sea Res Part 1 Oceanogr Res Pap 41: 993–1011. doi: 10.1016/0967-0637(94)90015-9
- 16. Johnson KS, Childress JJ, Hessler RR, Sakamotoarnold CM, Beehler CL (1988) Chemical and biological interactions in the Rose Garden hydrothermal vent field, Galapagos spreading centre. Deep Sea Res Part 1 Oceanogr Res Pap 35: 1723–1744. doi: 10.1016/0198-0149(88)90046-5
- 17. Fisher CR, Childress JJ, Arp AJ, Brooks JM, Distel D, et al. (1988) Microhabitat variation in the hydrothermal vent Mussel, Bathymodiolus thermophilus, at the Rose Garden vent on the Galapagos Rift. Deep Sea Res Part 1 Oceanogr Res Pap 35: 1769–1791. doi: 10.1016/0198-0149(88)90049-0
- 18. Sarrazin J, Juniper SK, Massoth G, Legendre P (1999) Physical and chemical factors influencing species distributions on hydrothermal sulfide edifices of the Juan de Fuca Ridge, Northeast Pacific. Mar Ecol Prog Ser 190: 89–112. doi: 10.3354/meps190089
- 19. Desbruyeres D, Biscoito M, Caprais JC, Colaco A, Comtet T, et al. (2001) Variations in deep-sea hydrothermal vent communities on the Mid-Atlantic Ridge near the Azores plateau. Deep Sea Res Part 1 Oceanogr Res Pap 48: 1325–1346. doi: 10.1016/s0967-0637(00)00083-2
- 20. Luther GW, Rozan TF, Taillefert M, Nuzzio DB, Di Meo C, et al. (2001) Chemical speciation drives hydrothermal vent ecology. Nature 410: 813–816. doi: 10.1038/35071069
- 21. Van Dover CL, Trask JL (2000) Diversity at deep-sea hydrothermal vent and intertidal mussel beds. Mar Ecol Prog Ser 195: 169–178. doi: 10.3354/meps195169
- 22. Mullineaux LS, Fisher CR, Peterson CH, Schaeffer SW (2000) Tubeworm succession at hydrothermal vents: use of biogenic cues to reduce habitat selection error? Oecologia 123: 275–284. doi: 10.1007/s004420051014
- 23. Micheli F, Peterson CH, Mullineaux LS, Fisher CR, Mills SW, et al. (2002) Predation structures communities at deep-sea hydrothermal vents. Ecol Monogr 72: 365–382. doi: 10.2307/3100095
- 24. Mullineaux LS, Peterson CH, Micheli F, Mills SW (2003) Successional mechanism varies along a gradient in hydrothermal fluid flux at deep-sea vents. Ecol Monogr 73: 523–542. doi: 10.1890/02-0674
- 25. Yoerger DR, Kelley DS, Delaney JR (2000) Fine-scale three-dimensional mapping of a deep-sea hydrothermal vent site using the Jason ROV system. Int J Rob Res 19: 1000–1014. doi: 10.1177/02783640022067931
- 26. Tyler PA, German CR, Ramirez-Llodra E, Van Dover CL (2003) Understanding the biogeography of chemosynthetic ecosystems. Oceanologica Acta 25: 227–241. doi: 10.1016/s0399-1784(02)01202-1
- 27. Tunnicliffe V, McArthur AG, McHugh D (1998) A biogeographical perspective of the deep-sea hydrothermal vent fauna. Adv Mar Biol 34: 353–442. doi: 10.1016/s0065-2881(08)60213-8
- 28. Van Dover CL, German CR, Speer KG, Parson LM, Vrijenhoek RC (2002) Evolution and biogeography of deep-sea vent and seep invertebrates. Science 295: 1253–1257. doi: 10.1126/science.1067361
- 29. Bachraty C, Legendre P, Desbruyeres D (2009) Biogeographic relationships among deep-sea hydrothermal vent faunas at global scale. Deep Sea Res Part 1 Oceanogr Res Pap 56: 1371–1378. doi: 10.1016/j.dsr.2009.01.009
- 30. Vrijenhoek RC (2010) Genetic diversity and connectivity of deep-sea hydrothermal vent metapopulations. Mol Ecol 19: 4391–4411. doi: 10.1111/j.1365-294x.2010.04789.x
- 31. Hessler RR, Smithey WMJ, Keller CH (1985) Spatial and temporal variation of giant clams tube worms and mussels at deep-sea hydrothermal vents. In: ) Bulletin of the Biological Society of Washington Hydrothermal vents of the Eastern Pacific: an overview (Jones ML, ed. 6: 411–428.
- 32. Van Dover CL (2003) Variation in community structure within hydrothermal vent mussel beds of the East Pacific Rise. Mar Ecol Prog Ser 253: 55–66. doi: 10.3354/meps253055
- 33. Dreyer JC, Knick KE, Flickinger WB, Van Dover CL (2005) Development of macrofaunal community structure in mussel beds on the northern East Pacific Rise. Mar Ecol Prog Ser 302: 121–134. doi: 10.3354/meps302121
- 34. Govenar B, Le Bris N, Gollner S, Glanville J, Aperghis AB, et al. (2005) Epifaunal community structure associated with Riftia pachyptila aggregations in chemically different hydrothermal vent habitats. Mar Ecol Prog Ser 305: 67–77. doi: 10.3354/meps305067
- 35. Sarrazin J, Walter C, Sarradin P-M, Brind'Amour A, Desbruyeres D, et al. (2006) Community structure and temperature dynamics within a mussel assemblage on the Southern East Pacific Rise. Cah Biol Mar 47: 483–490.
- 36. Mills SW, Mullineaux LS, Tyler PA (2007) Habitat associations in gastropod species at east Pacific rise hydrothermal vents (9°50 ' N). Biological Bulletin 212: 185–194. doi: 10.2307/25066601
- 37. Lutz R, Shank T, Luther GW, Vetriani C, Tolstoy M, et al. (2008) Interrelationships between vent fluid chemistry, temperature, seismicactivity and biological community structure at a mussel-dominated, deep-sea hydrothermal vent along the East Pacific Rise. J Shellfish Res 27: 177–190. doi: 10.2983/0730-8000(2008)27[177:ibvfct]2.0.co;2
- 38. Matabos M, Le Bris N, Pendlebury S, Thiebaut E (2008) Role of physico-chemical environment on gastropod assemblages at hydrothermal vents on the East Pacific Rise (13°N/EPR). J Mar Biol Assoc U.K. 88: 995–1008. doi: 10.1017/s002531540800163x
- 39. Sarrazin J, Juniper K (1999) Biological characteristics of a hydrothermal edifice mosaic community. Mar Ecol Prog Ser 185: 1–19. doi: 10.3354/meps185001
- 40. Govenar BW, Bergquist DC, Urcuyo IA, Eckner JT, Fisher CR (2002) Three Ridgeia piscesae assemblages from a single Juan de Fuca Ridge sulphide edifice: structurally different and functionally similar. Cah Biol Mar 43: 247–252.
- 41. Tsurumi M, Tunnicliffe V (2001) Characteristics of a hydrothermal vent assemblage on a volcanically active segment of Juan de Fuca Ridge, northeast Pacific. Canadian J Fish Aquac 58: 530–542. doi: 10.1139/f01-005
- 42. Tsurumi M, Tunnicliffe V (2003) Tubeworm-associated communities at hydrothermal vents on the Juan de Fuca Ridge, northeast Pacific. Deep Sea Res Part 1 Oceanogr Res Pap 50: 611–629. doi: 10.1016/s0967-0637(03)00039-6
- 43. Urcuyo IA, Massoth GJ, Julian D, Fisher CR (2003) Habitat, growth and physiological ecology of a basaltic community of Ridgeia piscesae from the Juan de Fuca Ridge. Deep Sea Res Part 1 Oceanogr Res Pap 50: 763–780. doi: 10.1016/s0967-0637(03)00061-x
- 44. Bergquist DC, Eckner JT, Urcuyo IA, Cordes EE, Hourdez S, et al. (2007) Using stable isotopes and quantitative community characteristics to determine a local hydrothermal vent food web. Mar Ecol Prog Ser 330: 49–65. doi: 10.3354/meps330049
- 45. Copley JT, Tyler PA, Murton BJ, VanDover CL (1997) Spatial and interannual variation in the faunal distribution at Broken Spur vent field (29°N, Mid-Atlantic Ridge). Mar Biol 129: 723–733. doi: 10.1007/s002270050215
- 46. Desbruyeres D, Almeida A, Biscoito M, Comtet T, Khripounoff A, et al. (2000) A review of the distribution of hydrothermal vent communities along the northern Mid-Atlantic Ridge: dispersal vs. environmental controls. Hydrobiologia 440: 201–216. doi: 10.1007/978-94-017-1982-7_19
- 47. Cuvelier D, Sarrazin J, Colaco A, Copley J, Desbruyeres D, et al. (2009) Distribution and spatial variation of hydrothermal faunal assemblages at Lucky Strike (Mid-Atlantic Ridge) revealed by high-resolution video image analysis. Deep Sea Res Part 1 Oceanogr Res Pap 56: 2026–2040. doi: 10.1016/j.dsr.2009.06.006
- 48. Gebruk A, Fabri MC, Briand P, Desbruyeres D (2010) Community dynamics over a decadal scale at Logatchev, 14°45 ' N, Mid-Atlantic Ridge. Cah Biol Mar 51(4), 383–388.
- 49. Fabri MC, Bargain A, Briand P, Gebruk A, Fouquet Y, et al. (2011) The hydrothermal vent community of a new deep-sea field, Ashadze-1, 12°58 ' N on the Mid-Atlantic Ridge. J Mar Biol Assoc U.K 91: 1–13. doi: 10.1017/s0025315410000731
- 50. Podowski EL, Moore TS, Zelnio KA, Luther GW, Fisher CR (2009) Distribution of diffuse flow megafauna in two sites on the Eastern Lau Spreading Center, Tonga. Deep Sea Res Part 1 Oceanogr Res Pap 56: 2041–2056. doi: 10.1016/j.dsr.2009.07.002
- 51. Tokeshi M (2011) Spatial structures of hydrothermal vents and vent-associated megafauna in the back-arc basin system of the Okinawa Trough, western Pacific. J Oceanogr 67: 651–665. doi: 10.1007/s10872-011-0065-9
- 52. Livermore RA, Cunningham AP, Vanneste L, Larter R (1997) Subduction influence on magma supply at the East Scotia Ridge Earth Planet Sci Lett. 150: 261–275. doi: 10.1016/s0012-821x(97)00074-5
- 53. Rogers AD, Tyler PA, Connelly DP, Copley JT, James R, et al. (2012) The discovery of new deep-sea hydrothermal vent communities in the southern ocean and implications for biogeography. PLoS Biology 10: e1001234. doi: 10.1371/journal.pbio.1001234
- 54. Naveira Garabato AC, McDonagh EL, Stevens DP, Heywood KJ, Sanders RJ (2002) On the export of Antarctic Bottom Water from the Weddell Sea. Deep Sea Res Part 2 Top Stud Oceanogr 49 (21), 4715–4742.
- 55. Tivey MK, Olson LO, Miller VW, Light RD (1990) Temperature measurements during initiation and growth of a black smoker chimney. Nature 346, 51–54.
- 56. MacPherson E, Jones W, Segonzac M (2005) A new squat lobster family of Galatheoidea (Crustacea, Decapoda, Anomura) from the hydrothermal vents of the Pacific-Antarctic Ridge. Zoosystema 27: 709–723.
- 57. Thurber AR, Jones WJ, Schnabel K (2011) Dancing for food in the deep sea: bacterial farming by a new species of yeti crab. PLoS ONE 6(11): e26243 doi:10.1371/journal.pone.0026243. doi: 10.1371/journal.pone.0026243
- 58. Baba K, Williams AB (1998) New galatheoidea (Crustacea, Decapoda, Anomura) from hydrothermal systems in the West Pacific Ocean: Bismarck Archipelago and Okinawa trough. Zoosystema 20: 143–156.
- 59. Van Dover CL, Fry B, Grassle JM, Haumphris S, Rona PA (1988) Feeding biology of the shrimp Rimicaris exoculata at hydrothermal vents on the mid-Atlantic ridge. Marine Biology 98: 209–216. doi: 10.1007/bf00391196
- 60. Gebruk AV, Chevaldonne P, Shank T, Lutz RA, Vrijenhoek RC (2000) Deep- sea hydrothermal vent communities of the Logatchev area (14°45'N, Mid-Atlantic Ridge): diverse biotopes and high biomass. J Mar Biol Assoc U.K 80: 383–393. doi: 10.1017/s0025315499002088
- 61. Hashimoto J, Ohta S, Gamo T, Chiba H, Yamaguchi T, et al. (2001) First hydrothermal vent communities from the Indian Ocean discovered. Zoolog Sci 18: 717–721. doi: 10.2108/zsj.18.717
- 62. Van Dover CL, Humphris SE, Fornari D, Cavanaugh CM, Collier R, et al. (2001) Biogeography and ecological setting of Indian Ocean hydrothermal vents. Science 294: 818–823. doi: 10.1126/science.1064574
- 63. Watabe H, Hashimoto J (2002) A new species of the genus Rimicaris (Alvinocarididae : Caridea : Decapoda) from the active hydrothermal vent field, “Kairei field,” on the Central Indian Ridge, the Indian Ocean. Zoolog Sci 19: 1167–1174. doi: 10.2108/zsj.19.1167
- 64. Nakamura K, Watanabe H, Miyazaki J, Takai K, Kawagucci S, et al. (2012) Discovery of new hydrothermal activity and chemosynthetic fauna on the Central Indian Ridge at 18° - 20°S. PLoS one 7: e32965. doi: 10.1371/journal.pone.0032965
- 65. Nye V, Copley J, Plouviez S (2011) Verity Nye, Jon Copley and Sophie Plouviez A new species of Rimicaris (Crustacea: Decapoda: Caridea: Alvinocarididae) from hydrothermal vent fields on the Mid-Cayman Spreading Centre, Caribbean. J Mar Biol Assoc U.K Available on CJO 2011.
- 66. Connelly DP, Copley JT, Murton BJ, Stansfield K, Tyler PA, et al. (2012) Hydrothermal vent fields and chemosynthetic biota on the world's deepest seafloor spreading centre. Nat Commun 3 620 doi: 10.1038/ncomms1636. doi: 10.1038/ncomms1636
- 67. Chevaldonne P, Jollivet D (1993) Videoscopic study of deep-sea hydrothermal vent alvinellid polychaete populations: Biomass estimation and behaviour. Mar Ecol Prog Ser 95: 251–262. doi: 10.3354/meps095251
- 68. Miyake H, Kitada M, Tsuchida S, Okuyama Y, Nakamura K-I (2007) Ecological aspects of hydrothermal vent animals in captivity at atmospheric pressure. Mar Ecol 28: 86–92. doi: 10.1111/j.1439-0485.2006.00115.x
- 69. Watsuji TO, Nakagawa S, Tsuchida S, Toki T, Hirota A, et al. (2010) Diversity and function of epibiotic microbial communities on the galatheid crab. Microbes Environ 25(4): 288–294. doi: 10.1264/jsme2.me10135
- 70. Tsuchida S, Suzuki Y, Fujiwara Y, Kawato M, Uematsu K, et al. (2011) Epibiotic association between filamentous bacteria and the vent-associated galatheid crab, Shinkaia crosnieri (Decapoda: Anomura). J Mar Biol Assoc U.K 91: 23–32. doi: 10.1017/s0025315410001827
- 71. Polz MF, Robinson JJ, Cavanaugh CM, Van Dover CL (1998) Trophic ecology of massive shrimp aggregations at a Mid-Atlantic Ridge hydrothermal vent site. Limnol Oceanogr 43: 1631–1638. doi: 10.4319/lo.1922.214.171.1241
- 72. Petersen JM, Dubilier N (2009) Methanotrophic symbioses in marine invertebrates. Environ Microbiol Rep 1: 319–335. doi: 10.1111/j.1758-2229.2009.00081.x
- 73. Guri M, Durand L, Cueff-Gauchard V, Zbinden M, Crassous P, et al. (2012) Acquisition of epibiotic bacteria along the life cycle of the hydrothermal shrimp Rimicaris exoculata. ISME J 6: 597–609. doi: 10.1038/ismej.2011.133
- 74. Gaudron SM, Lefebvre S, Jorge AN, Gaill F, Pradillon F (2012) Spatial and temporal variations in food web structure from newly-opened habitat at hydrothermal vents. Mar Environ Res 77: 129–140. doi: 10.1016/j.marenvres.2012.03.005
- 75. Van Dover CL (2002) Trophic relationships among invertebrates at the Kairei hydrothermal vent field (Central Indian Ridge). Marine Biology 141: 761–772. doi: 10.1007/s00227-002-0865-y
- 76. Thatje S, Arntz WE (2004) Antarctic reptant decapods: more than a myth? Polar Biol 27: 195–201. doi: 10.1007/s00300-003-0583-z
- 77. García Raso JE, García Muñoz JE, Manjón Cabeza ME (2008) First record of Munidopsis albatrossae (Crustacea: Decapoda: Galatheidae) from Antarctic waters. Polar Biol 31: 1281–1285. doi: 10.1007/s00300-008-0476-2
- 78. Hall S, Thatje S (2011) Temperature-driven biogeography of the deep-sea family Lithodidae (Crustacea: Decapoda: Anomura) in the Southern Ocean. Polar Biol 34: 363–370. doi: 10.1007/s00300-010-0890-0
- 79. Portner HO (2001) Climate change and temperature-dependent biogeography: oxygen limitation of thermal tolerance in animals. Naturwissenschaften 88: 137–146. doi: 10.1007/s001140100216
- 80. Wittmann AC, Hel C, Poertner HA, Sartorius FJ (2010) Ion regulatory capacity and the biogeography of Crustacea at high southern latitudes. Polar Biol 33: 919–928. doi: 10.1007/s00300-010-0768-1
- 81. Bates AE, Tunnicliffe V, Lee RW (2005) Role of thermal conditions in habitat selection by hydrothermal vent gastropods. Mar Ecol Prog Ser 305: 1–15. doi: 10.3354/meps305001
- 82. Wheeler AJ, Benzie JAH, Carlsson J, Collins P, Copley J, et al. (2011) Moytirra: a newly discovered hydrothermal vent field on the mid-Atlantic Ridge between the Azores and Iceland. InterRidge Newsletter 20: 37–39. doi: 10.1002/ggge.20243
- 83. Suzuki Y, Kojima S, Watanabe H, Suzuki M, Tsuchida S, et al. (2006) Single host and symbiont lineages of hydrothermal vent gastropods Ifremeria nautilei (Provannidae): biogeography and evolution. Mar Ecol Prog Ser 315: 167–175. doi: 10.3354/meps315167
- 84. Colaco A, Dehairs F, Desbruyeres D (2002) Nutritional relations of deep-sea hydrothermal fields at the Mid-Atlantic Ridge: a stable isotope approach. Deep Sea Res Part 1 Oceanogr Res Pap 49: 395–412. doi: 10.1016/s0967-0637(01)00060-7
- 85. Duperron S (2010) The Diversity of Deep-Sea Mussels and Their Bacterial Symbioses. In: Vent and Seep Biota: Aspects from Microbes to Ecosystems. 137–167.
- 86. Southward AJ, Newman WA (1998) Ectosymbiosis between filamentous sulphur bacteria and a stalked barnacle (Scalpellomorpha, Neolepadinae) from the Lau Back Arc Basin, Tonga. Cah Biol Mar 39: 259–262.
- 87. Suzuki Y, Suzuki M, Tsuchida S, Takai K, Horikoshi K, et al. (2009) Molecular investigations of the stalked barnacle Vulcanolepas osheai and the epibiotic bacteria from the Brothers Caldera, Kermadec Arc, New Zealand. J Mar Biol Assoc U.K 89: 727–733. doi: 10.1017/s0025315409000459
- 88. Tunnicliffe V, Southward AJ (2004) Growth and breeding of a primitive stalked barnacle Leucolepas longa (Cirripedia: Scalpellomorpha: Eolepadidae: Neolepadinae) inhabiting a volcanic seamount off Papua New Guinea. J Mar Biol Assoc U.K 84: 121–132. doi: 10.1017/s0025315404008987h
- 89. Lee RW (2003) Thermal tolerances of deep-sea hydrothermal vent animals from the Northeast Pacific. Biological Bulletin 205: 98–101. doi: 10.2307/1543230
- 90. Rona PA, Klinkhammer G, Nelsen TA, Trefry JH, Elderfield H (1986) Black smokers, massive sulphides and vent biota at the Mid-Atlantic Ridge. Nature 321: 33–37. doi: 10.1038/321033a0
- 91. Copley JTP, Jorgensen PBK, Sohn RA (2007) Assessment of decadal-scale ecological change at a deep mid-Atlantic hydrothermal vent and reproductive time-series in the shrimp Rimicaris exoculata. J Mar Biol Assoc U.K 87: 859–867. doi: 10.1017/s0025315407056512
- 92. López-González P, Segonzac M, (2006) Cnidaria, Anthozoa, Actinaria. In: Desbruyères D, Segonzac M, Bright M, editors. Handbook of Deep-Sea Hydrothermal Vent Fauna. Densia 18 65–71.
- 93. Gebruk AV, Galkin SV, Vereshchaka AL, Moskalev LI, Southward AJ (1997) Ecology and biogeography of the hydrothermal vent fauna of the Mid-Atlantic Ridge. Adv Mar Biol 32: 93–144. doi: 10.1016/s0065-2881(08)60016-4
- 94. Erickson KL, Macko SA, Van Dover CL (2009) Evidence for a chemoautotrophically based food web at inactive hydrothermal vents (Manus Basin). Deep Sea Res Part 2 Top Stud Oceanogr 56: 1577–1585. doi: 10.1016/j.dsr2.2009.05.002
- 95. Fry B, Gest H, Hayes JM (1983) Sulfur isotopic compositions of deep-sea hydrothermal vent animals. Nature 306: 51–52. doi: 10.1038/306051a0
- 96. Sarradin PM, Caprais JC, Briand P, Gaill F, Shillito B, et al. (1998) Chemical and thermal description of the environment of the Genesis hydrothermal vent community (13°N, EPR). Cah Biol Mar 39: 159–167.
- 97. Sarradin PM, Caprais JC, Riso R, Kerouel R, Aminot A (1999) Chemical environment of the hydrothermal mussel communities in the Lucky Strike and Menez Gwen vent fields, Mid Atlantic ridge. Cah Biol Mar 40: 93–104.
- 98. Henry MS, Childress JJ, Figueroa D (2008) Metabolic rates and thermal tolerances of chemoautotrophic symbioses from Lau Basin hydrothermal vents and their implications for species distributions. Deep Sea Res Part 1 Oceanogr Res Pap 55: 679–695. doi: 10.1016/j.dsr.2008.02.001
- 99. Gebruk AV, Southward EC, Kennedy H, Southward AJ (2000) Food sources, behaviour, and distribution of hydrothermal vent shrimps at the Mid-Atlantic Ridge. J Mar Biol Assoc U.K 80: 485–499. doi: 10.1017/s0025315400002186
- 100. Levesque C, Juniper SK, Marcus J (2003) Food resource partitioning and competition among alvinellid polychaetes of Juan de Fuca Ridge hydrothermal vents. Mar Ecol Prog Ser 246: 173–182. doi: 10.3354/meps246173
- 101. Lenihan HS, Mills SW, Mullineaux LS, Peterson CH, Fisher CR, et al. (2008) Biotic interactions at hydrothermal vents: Recruitment inhibition by the mussel Bathymodiolus thermophilus. Deep Sea Res Part 1 Oceanogr Res Pap 55: 1707–1717. doi: 10.1016/j.dsr.2008.07.007
- 102. Podowski EL, Ma S, Luther GW III, Wardrop D, Fisher CR (2010) Biotic and abiotic factors affecting distributions of megafauna in diffuse flow on andesite and basalt along the Eastern Lau Spreading Center, Tonga. Mar Ecol Prog Ser 418: 25–U445. doi: 10.3354/meps08797