| Contributors | Affiliation | Role |
|---|---|---|
| Qin, Wei | University of Illinois Urbana-Champaign (UIUC) | Principal Investigator |
| Shen, Hui | University of Illinois Urbana-Champaign (UIUC) | Scientist, Contact |
| Soenen, Karen | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
At Stations 5, 8, and 13, one liter of seawater from each depth was collected by Niskin bottles attached at CTD, then filtered onto 0.22 μm Sterivex filters (GP-type, Millipore) and stored at −80 °C.
DNA was extracted using a modified manual extraction protocol as previously described (Urakawa et al. 2010). Archaeal and β-proteobacterial amoA genes were quantified by qPCR using primer sets CrenAmoAQ-F/CrenAmoAModR (Mincer et al. 2007) and AmoA1-F/AmoA2-R (Rotthauwe et al. 1997), respectively, on a LightCycler system (Roche), following previously described methods (Horak et al. 2013). Standard curve construction, amplification procedures, melting curves, and gel electrophoresis tests were carried out as previously described (Horak et al. 2013)
* Converted latitude and longitude values from degrees, minute, seconds to decimal degrees
* Rounded those fields to 7 decimals
* Renamed the column headers to comply with the database requirements (no spaces or special characters)
| Parameter | Description | Units |
| Datetime_of_sampling | Date and time of sampling in UTC time zone | unitless |
| Latitude | Latitude of sampling location | decimal degrees |
| Longitude | Longitude of sampling location | decimal degrees |
| Station_ID | Station identification | unitless |
| Depth_m | Depth of sampling | meters (m) |
| AOA_amoA_Calculated_Abundance | abundance of amoA genes of Ammonia Oxidizing Archaea (AOA) | copies per milliliter (copies/mL) |
| stdev_AOA | Standard deviation of abundance of amoA genes of AOA | copies per milliliter (copies/mL) |
| AOB_amoA_Calculated_Abundance | abundance of amoA genes of Ammonia Oxidizing Bacteria (AOB) | copies per milliliter (copies/mL) |
| stdev_AOB | Standard deviation of abundance of amoA genes of AOB | copies per milliliter (copies/mL) |
| Dataset-specific Instrument Name | |
| Generic Instrument Name | CTD - profiler |
| Generic Instrument Description | The Conductivity, Temperature, Depth (CTD) unit is an integrated instrument package designed to measure the conductivity, temperature, and pressure (depth) of the water column. The instrument is lowered via cable through the water column. It permits scientists to observe the physical properties in real-time via a conducting cable, which is typically connected to a CTD to a deck unit and computer on a ship. The CTD is often configured with additional optional sensors including fluorometers, transmissometers and/or radiometers. It is often combined with a Rosette of water sampling bottles (e.g. Niskin, GO-FLO) for collecting discrete water samples during the cast.
This term applies to profiling CTDs. For fixed CTDs, see https://www.bco-dmo.org/instrument/869934. |
| Dataset-specific Instrument Name | |
| Generic Instrument Name | Niskin bottle |
| Generic Instrument Description | A Niskin bottle (a next generation water sampler based on the Nansen bottle) is a cylindrical, non-metallic water collection device with stoppers at both ends. The bottles can be attached individually on a hydrowire or deployed in 12, 24, or 36 bottle Rosette systems mounted on a frame and combined with a CTD. Niskin bottles are used to collect discrete water samples for a range of measurements including pigments, nutrients, plankton, etc. |
| Dataset-specific Instrument Name | LightCycler system (Roche) |
| Generic Instrument Name | qPCR Thermal Cycler |
| Generic Instrument Description | An instrument for quantitative polymerase chain reaction (qPCR), also known as real-time polymerase chain reaction (Real-Time PCR). |
| Website | |
| Platform | R/V Kilo Moana |
| Start Date | 2013-08-07 |
| End Date | 2013-09-05 |
Microorganisms sustain the biogeochemical cycling of nitrogen, one of the most important nutrient cycles on earth. A key step in this cycle, the oxidation of ammonia to nitrite by autotrophic microorganisms, was for a century thought mediated by a few restricted bacterial genera. Significant ammonia oxidation, perhaps most, is now attributed to a previously enigmatic group of Archaea - the ammonia-oxidizing archaea (AOA) - of high abundance in both marine and terrestrial environments. The investigators prior physiological and environmental analyses, the foundation for this proposal, have shown that AOA are active within the marine photic zone and that their competitive fitness in the marine environment is at least in part attributable to an extremely high affinity for ammonia, growing at near maximum growth rates at concentrations of ammonia that would not sustain known bacterial ammonia oxidizers, and an unusual copper-based respiratory system that may render them more competitive in iron limited environments. The compelling inference from these prior analyses is that AOA alter and possibly control the forms of fixed nitrogen available to other microbial assemblages within the photic zone by converting ammonia, a nearly universally available form of nitrogen, into nitrite, a form only available to nitrite oxidizing bacteria and some phytoplankton. If correct, this has a significant impact on biodiversity.
The PIs will use the most recent technological advances in protein and high throughput sequencing to evaluate the significance of nitrification in shaping biodiversity (genomic and metagenomics), activity (transcriptome, proteome and stable isotope probing), and in controlling availability of an important trace element (copper). In turn, by resolving the environmental and biotic variables that influence the diversity, distribution and activity of AOA, they will advance general understanding of their taxonomy. More directly, functional knowledge of the contribution of AOA to regenerated nitrate will improve estimates of new ocean production ("biological pump") based on nitrate assimilation, which in the past has mostly neglected the importance of nitrification as a major source of nitrate. Together these studies will transform understanding of the marine nitrogen cycle, estimates of new production, and will ultimately provide a better understanding of the impact of human activity on this critical nutrient cycle.
The nitrogen cycle has been profoundly affected by anthropogenic inputs of reactive nitrogen into terrestrial, marine, and atmospheric systems having, or predicted to have, major impacts on marine biological production, increased N20 emissions, nitrogen pollution, and eutrophication. Likewise, there is a poor understanding of the relationship between nitrogen cycling and productivity in marine ecosystems. Marine systems are increasingly affected by ocean acidification and by atmospheric inputs of reactive nitrogen. Since both changes greatly alter nitrogen available to microorganisms, the characterization of the response of these environmentally relevant AOA is of tremendous relevance to understanding the affect of acidification and anthropogenic nitrogen inputs on major ocean processes.
The proposed project encompasses and integrates the three dimensions (functional genetic, and taxonomic) of biodiversity. First, the project is framed by function: microbial control of one of the most important nutrient cycles on earth, the nitrogen-cycle. Second, it is motivated by recent genetic analyses that associate activities of a novel clade of Archaea (provisionally assigned to a new kingdom within the Archaea, the Thaumarchaeota) with control of ammonia oxidation in the ocean. Third, it is built upon a compelling synthesis of physiological and environmental data that lead to its central hypothesis that by altering and possibly controlling the form of nitrogen, the AOA also alter biodiversity and ecological function in one of the most productive environments on earth. It identifies a specific taxonomic imperative. The tremendous genetic diversity among the globally abundant AOA catalogued almost exclusively by gene sequencing surveys and therefore lacking formal description makes it essential to resolve membership into ecologically relevant groups or clades as a prelude to developing a formal taxonomy. The investigators have assembled a group of researchers with specific expertise in each of dimension and uniquely qualified to address the research objectives outlined in an integrative way.
(adapted from the NSF Synopsis of Program)
Dimensions of Biodiversity is a program solicitation from the NSF Directorate for Biological Sciences. FY 2010 was year one of the program. [MORE from NSF]
The NSF Dimensions of Biodiversity program seeks to characterize biodiversity on Earth by using integrative, innovative approaches to fill rapidly the most substantial gaps in our understanding. The program will take a broad view of biodiversity, and in its initial phase will focus on the integration of genetic, taxonomic, and functional dimensions of biodiversity. Project investigators are encouraged to integrate these three dimensions to understand the interactions and feedbacks among them. While this focus complements several core NSF programs, it differs by requiring that multiple dimensions of biodiversity be addressed simultaneously, to understand the roles of biodiversity in critical ecological and evolutionary processes.
| Funding Source | Award |
|---|---|
| NSF Division of Ocean Sciences (NSF OCE) |