'''Short description:''' You can find here the biogeochemistry non assimilative hindcast simulation GLOBAL_REANALYSIS_BIO_001_018 at 1/4° over period 1998 - 2016. Outputs are delivered as monthly mean files with Netcdf format (CF/COARDS 1.5 convention) on the native tripolar grid (ORCA025) at ¼° resolution with 75 vertical levels. This simulation is based on the PISCES biogeochemical model. It is forced offline at a daily frequency by the equivalent of the GLOBAL-REANALYSIS-PHYS-001-009 physics product but without data assimilation. '''Detailed description: ''' There are 8 different datasets: * dataset-global-nahindcast-bio-001-018-no3 containing : nitrate concentration * dataset-global-nahindcast-bio-001-018-po4 containing : phosphate concentration * dataset-global-nahindcast-bio-001-018-si containing : silicate concentration * dataset-global-nahindcast-bio-001-018-o2 containing : dissolved oxygen concentration * dataset-global-nahindcast-bio-001-018-fe containing : iron concentration * dataset-global-nahindcast-bio-001-018-chl containing : chlorophyll concentration * dataset-global-nahindcast-bio-001-018-phyc containing : carbon phytoplankton biomass * dataset-global-nahindcast-bio-001-018-pp containing : primary production The horizontal grid is the standard ORCA025 tri-polar grid (1440 x 1021 grid points). The three poles are located over Antarctic, Central Asia and North Canada. The ¼ degree resolution corresponds to the equator. The vertical grid has 75 levels, with a resolution of 1 meter near the surface and 200 meters in the deep ocean.Biogeochemical and physical simulations start at rest (cold start) in December 1991. The spin-up period consists of 5 years of interannual simulation between 1992 and 1997. The simulation period covers the ocean color era (1998 – 2016).The biogeochemical model used is PISCES (Aumont, in prep). It is a model of intermediate complexity designed for global ocean applications (Aumont and Bopp, 2006) and is part of NEMO modeling platform. It has 24 prognostic variables and simulates biogeochemical cycles of oxygen, carbon and the main nutrients controlling phytoplankton growth (nitrate, ammonium, phosphate, silicic acid and iron). The model distinguishes four plankton functional types based on size: two phytoplankton groups <nowiki>(small = nanophytoplankton and large = diatoms)</nowiki> and two zooplankton groups <nowiki>(small = microzooplankton and large = mesozooplankton).</nowiki>Prognostic variables of phytoplankton are total biomass in C, Fe, Si (for diatoms) and chlorophyll and hence the Fe/C, Si/C, Chl/C ratios are variable. For zooplankton, all these ratios are constant and total biomass in C is the only prognostic variable. The bacterial pool is not modeled explicitly. PISCES distinguishes three non-living pools for organic carbon: small particulate organic carbon, big particulate organic carbon and semi-labile dissolved organic carbon. While the C/N/P composition of dissolved and particulate matter is tied to Redfield stoichiometry, the iron, silicon and carbonate contents of the particles are computed prognostically. Next to the three organic detrital pools, carbonate and biogenic siliceous particles are modeled. Besides, the model simulates dissolved inorganic carbon and total alkalinity. In PISCES, phosphate and nitrate + ammonium are linked by constant Redfield ratio <nowiki>(C/N/P = 122/16/1)</nowiki>, but cycles of phosphorus and nitrogen are decoupled by nitrogen fixation and denitrification. Biogeochemical model PISCES (NEMO3.5) is forced offline by daily fields of the physical model NEMO (OPA module in the NEMO platform) without any assimilation of physical data. The main features of this dynamical ocean are: * NEMO 3.1 * Atmospheric forcings from 3-hourly ERA-Interim reanalysis products, CORE bulk formulation * Vertical diffusivity coefficient is computed by solving the TKE equation * Tidal mixing is parameterized according to the works of Bessières et al. (2008) and Koch-Larrouy et al, (2006). * Sea-Ice model: LIM2 with the Elastic-Viscous-Plastic rheology * Initial conditions: Levitus 98 climatology for temperature and salinity, patched with PHC2.1 for the Arctic regions, and Medatlas for the Mediterranean Sea. A special treatment is done on vertical diffusivity coefficient (Kz): the daily mean is done on Log10(Kz) after a filtering of enhanced convection (Kz increased artificially to 10 m2.s-1 when the water column is unstable). The purpose of this Log10 is to average the orders of magnitudes and to give more weight to small values of vertical diffusivity. The atmospheric forcing fields are daily averages from ERA-Interim reanalysis product (CORE bulk formulation). Boundary fluxes account for nutrient supply from three different sources: Atmospheric deposition (Aumont et al., 2008), rivers for nutrients, dissolved inorganic carbon and alkalinity (Ludwig et al., 1996; Mayorga et al., 2010) and inputs of Fe from marine sediments. Nutrient and freshwater inflows by rivers are colocalized. River and dust inputs are balanced with sediment trapping of NO3, Si and Carbon. An annual and global value of atmospheric carbon dioxide is imposed at sea surface.

'''DEFINITION''' The temporal evolution of thermosteric sea level in an ocean layer is obtained from an integration of temperature driven ocean density variations, which are subtracted from a reference climatology to obtain the fluctuations from an average field. The products used include three global reanalyses: GLORYS, C-GLORS, ORAS5 (GLOBAL_MULTIYEAR_PHY_ENS_001_031) and two in situ based reprocessed products: CORA5.2 (INSITU_GLO_PHY_TS_OA_MY_013_052) , ARMOR-3D (MULTIOBS_GLO_PHY_TSUV_3D_MYNRT_015_012). Additionally, the time series based on the method of von Schuckmann and Le Traon (2011) has been added. The regional thermosteric sea level values are then averaged from 60°S-60°N aiming to monitor interannual to long term global sea level variations caused by temperature driven ocean volume changes through thermal expansion as expressed in meters (m). '''CONTEXT''' The global mean sea level is reflecting changes in the Earth’s climate system in response to natural and anthropogenic forcing factors such as ocean warming, land ice mass loss and changes in water storage in continental river basins. Thermosteric sea-level variations result from temperature related density changes in sea water associated with volume expansion and contraction (Storto et al., 2018). Global thermosteric sea level rise caused by ocean warming is known as one of the major drivers of contemporary global mean sea level rise (Cazenave et al., 2018; Oppenheimer et al., 2019). '''CMEMS KEY FINDINGS''' Since the year 2005 the upper (0-700m) near-global (60°S-60°N) thermosteric sea level rises at a rate of 1.0 ± 0.2 mm/year. Note: The key findings will be updated annually in November, in line with OMI evolutions. '''DOI (product):''' https://doi.org/10.48670/moi-00239

'''DEFINITION''' The global annual chlorophyll anomaly is computed by subtracting a reference climatology (1997-2014) from the annual chlorophyll mean, on a pixel-by-pixel basis and in log10 space. Both the annual mean and the climatology are computed employing ESA Ocean Colour Climate Change Initiative (ESA OC-CCI, Sathyendranath et al., 2018a) global products (i.e. using the standard OC-CCI chlorophyll algorithms, OCI) as distributed by CMEMS. '''CONTEXT''' Phytoplankton – and chlorophyll concentration as a proxy for phytoplankton – respond rapidly to changes in their physical environment. Some of those changes are seasonal and are determined by light and nutrient availability (Racault et al., 2012). By comparing annual mean values to a climatology, we effectively remove the seasonal signal, while retaining information on potential events during the year. Chlorophyll anomalies can be correlated to climate indexes in particular regions, such as the ENSO index in the equatorial Pacific (Behrenfeld et al. 2006; Racault et al., 2012) and the IOD index in the Indian Ocean (Brewin et al., 2012). It is important to study chlorophyll anomalies in consonance with sea surface temperature and sea level anomalies, as increases in chlorophyll are generally consistent with decreases in SST and sea level anomalies, suggesting an increase in mixing and vertical nutrient transport (von Schuckmann et al., 2016). '''CMEMS KEY FINDINGS''' The average global chlorophyll anomaly 2019 is -0.02 log10(mg m-3), with a maximum value of 1.7 log10(mg m-3) and a minimum value of -3.2 log10(mg m-3). That is to say that, in average, the annual 2019 mean value is slightly lower (96%) than the 1997-2014 climatological value. The positive signals reported in 2016 and 2017 (Sathyendranath et al., 2018b) in the southern Pacific Ocean could still be observed in the 2019 map, while the significant negative anomalies in the tropical waters of the northern Pacific Ocean were also detected to a lesser extent. Areas showing a change of anomaly sign from 2019 include the southern coast of Japan (no anomaly to positive) and the tropical Atlantic (anomalies close to zero for 2019). A marked increase in chlorophyll concentration was observed during 2019 in the Great Australian Bight, while negative anomalies became stronger in the Guatemala Basin and the region south of the Gulf of Guinea and, with values of chlorophyll reaching as low as 30% of the climatological value (anomaly < -0.5 log10(mg m-3)). The persistent positive anomalies in the higher latitudes of the North Atlantic (> 40°) match the cooling observed in the 2018 and previous years SST anomaly maps.