Abstract. We present a summary of biomass data for 11 plankton functional types (PFTs) plus phytoplankton pigment data, compiled as part of the MARine Ecosystem biomass DATa (MAREDAT) initiative. The goal of the MAREDAT initiative is to provide, in due course, global gridded data products with coverage of all planktic components of the global ocean ecosystem. This special issue is the first step towards achieving this. The PFTs presented here include picophytoplankton, diazotrophs, coccolithophores, Phaeocystis, diatoms, picoheterotrophs, microzooplankton, foraminifers, mesozooplankton, pteropods and macrozooplankton. All variables have been gridded onto a World Ocean Atlas (WOA) grid (1 • × 1 • × 33 vertical levels × monthly climatologies). The results show that abundance is much better constrained than their carbon content/elemental composition, and coastal seas and other high productivity regions have much better coverage than the much larger volumes where biomass is relatively low. The data show that (1) the global total heterotrophic biomass (2.0-4.6 Pg C) is at least as high as the total autotrophic biomass (0.5-2.4 Pg C excluding nanophytoplankton and autotrophic dinoflagellates); (2) the biomass of zooplankton calcifiers (0.03-0.67 Pg C) is substantially higher than that of coccolithophores (0.001-0.03 Pg C); (3) patchiness of biomass distribution increases with organism size; and (4) although zooplankton biomass measurements below 200 m are rare, the limited measurements available suggest that Bacteria and Archaea are not the only important heterotrophs in the deep sea. More data will be needed to characterise ocean ecosystem functioning and associated biogeochemistry in the Southern Hemisphere and below 200 m. Future efforts to understand marine ecosystem composition and functioning will be helped both by further archiving of historical data and future sampling at new locations.Microzooplankton database:

Abstract. Pteropods are a group of holoplanktonic gastropods for which global biomass distribution patterns remain poorly described. The aim of this study was to collect and synthesise existing pteropod (Gymnosomata, Thecosomata and Pseudothecosomata) abundance and biomass data, in order to evaluate the global distribution of pteropod carbon biomass, with a particular emphasis on temporal and spatial patterns. We collected 25 939 data points from several online databases and 41 scientific articles. These data points corresponded to observations from 15 134 stations, where 93 % of observations were of shelled pteropods (Thecosomata) and 7 % of non-shelled pteropods (Gymnosomata). The biomass data has been gridded onto a 360 × 180• grid, with a vertical resolution of 33 depth levels. Both the raw data file and the gridded data in NetCDF format can be downloaded from PANGAEA, doi:10.1594/PANGAEA.777387. Data were collected between 1950-2010, with sampling depths ranging from 0-2000 m. Pteropod biomass data was either extracted directly or derived through converting abundance to biomass with pteropod-specific length to carbon biomass conversion algorithms. In the Northern Hemisphere (NH), the data were distributed quite evenly throughout the year, whereas sampling in the Southern Hemisphere (SH) was biased towards winter and summer values. 86 % of all biomass values were located in the NH, most (37 %) within the latitudinal band of 30-60• N. The range of global biomass values spanned over four orders of magnitude, with mean and median (non-zero) biomass values of 4.6 mg C m −3 (SD = 62.5) and 0.015 mg C m −3 , respectively. The highest mean biomass was located in the SH within the 70-80• S latitudinal band (39.71 mg C m −3 , SD = 93.00), while the highest median biomass was in the NH, between 40-50• S (0.06 mg C m −3 , SD = 79.94). Shelled pteropods constituted a mean global carbonate biomass of 23.17 mg CaCO 3 m −3 (based on non-zero records). Total biomass values were lowest in the equatorial regions and equally high at both poles. Pteropods were found at least to depths of 1000 m, with the highest biomass values located in the surface layer (0-10 m) and gradually decreasing with depth, with values in excess of 100 mg C m −3 only found above 200 m depth.Tropical species tended to concentrate at greater depths than temperate or high-latitude species. Global biomass levels in the NH were relatively invariant over the seasonal cycle, but more seasonally variable in the SH.The collected database provides a valuable tool for modellers for the study of marine ecosystem processes and global biogeochemical cycles. By extrapolating regional biomass to a global scale, we established global pteropod biomass to add up to 500 Tg C.

We characterize the realized ecological niches of 133 phytoplankton taxa in the open ocean based on observations from the MAREDAT initiative and a statistical species distribution model (MaxEnt). The models find that the physical conditions (mixed layer depth, temperature, light) govern large-scale patterns in phytoplankton biogeography over nutrient availability. Strongest differences in the realized niche centers were found between diatoms and coccolithophores. Diatoms (87 species) occur in habitats with significantly lower temperatures, light intensity and salinity, with deeper mixed layers, and with higher nitrate and silicate concentrations than coccolithophores (40 species). However, we could not statistically separate the realized niches of coccolithophores from those of diazotrophs (two genera) and picophytoplankton (two genera). Phaeocystis (two species) niches only clearly differed from diatom niches for temperature. While the realized niches of diatoms cover the majority of niche space, the niches of picophytoplankton and coccolithophores spread across an intermediate fraction and diazotroph and colonial Phaeocystis niches only occur within a relatively confined range of environmental conditions in the open ocean. Our estimates of the realized niches roughly match the predictions of Reynolds' C-S-R model for the global ocean, namely that taxa classified as nutrient stress tolerant have niches at lower nutrient and higher irradiance conditions than light stress tolerant taxa. Yet, there is considerable within-class variability in niche centers, and many taxa occupy broad niches, suggesting that more complex approaches may be necessary to capture all aspects of phytoplankton ecology.

Abstract. Coccolithophores are calcifying marine phytoplankton of the class Prymnesiophyceae. They are considered to play an import role in the global carbon cycle through the production and export of organic carbon and calcite. We have compiled observations of global coccolithophore abundance from several existing databases as well as individual contributions of published and unpublished datasets. We make conservative estimates of carbon biomass using standardised conversion methods and provide estimates of uncertainty associated with these values. The quality-controlled database contains 57 321 individual observations at various taxonomic levels. This corresponds to 11 503 observations of total coccolithophore abundance and biomass. • S, with declines towards both the equator and the poles. Biomass estimates between the equator and 40•

Living shorelines are a type of estuarine shoreline erosion control that incorporates native vegetation and preserves native habitats. Because they provide the ecosystem services associated with natural coastal wetlands while also increasing shoreline resilience, living shorelines are part of the natural and hybrid infrastructure approach to coastal resiliency. Marshes created as living shorelines are typically narrow (< 30 m) fringing marshes with sandy substrates that are well flushed by tides. These characteristics distinguish living shorelines from the larger meadow marshes in which most of the current knowledge about created marshes was developed. The value of living shorelines for providing both erosion control and habitat for estuarine organisms has been documented but their capacity for carbon sequestration has not. We measured carbon sequestration rates in living shorelines and sandy transplanted Spartina alterniflora marshes in the Newport River Estuary, North Carolina. The marshes sampled here range in age from 12 to 38 years and represent a continuum of soil development. Carbon sequestration rates ranged from 58 to 283 g C m-2 yr-1 and decreased with marsh age. The pattern of lower sequestration rates in older marshes is hypothesized to be the result of a relative enrichment of labile organic matter in younger sites and illustrates the importance of choosing mature marshes for determination of long-term carbon sequestration potential. The data presented here are within the range of published carbon sequestration rates for S. alterniflora marshes and suggest that wide-scale use of the living shoreline approach to shoreline management may come with a substantial carbon benefit.