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Creators/Authors contains: "Sipler, Rachel E"

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  1. null (Ed.)
    The Southern Ocean (SO) harbors some of the most intense phytoplankton blooms on Earth. Changes in temperature and iron availability are expected to alter the intensity of SO phytoplankton blooms, but little is known about how these changes will influence community composition and downstream biogeochemical processes. We performed light-saturated experimental manipulations on surface ocean microbial communities from McMurdo Sound in the Ross Sea to examine the effects of increased iron availability (+2 nM) and warming (+3 and +6 °C) on nutrient uptake, as well as the growth and transcriptional responses of two dominant diatoms, Fragilariopsis and Pseudo-nitzschia . We found that community nutrient uptake and primary productivity were elevated under both warming conditions without iron addition (relative to ambient −0.5 °C). This effect was greater than additive under concurrent iron addition and warming. Pseudo-nitzschia became more abundant under warming without added iron (especially at 6 °C), while Fragilariopsis only became more abundant under warming in the iron-added treatments. We attribute the apparent advantage Pseudo-nitzschia shows under warming to up-regulation of iron-conserving photosynthetic processes, utilization of iron-economic nitrogen assimilation mechanisms, and increased iron uptake and storage. These data identify important molecular and physiological differences between dominant diatom groups and add to the growing body of evidence for Pseudo-nitzschia ’s increasingly important role in warming SO ecosystems. This study also suggests that temperature-driven shifts in SO phytoplankton assemblages may increase utilization of the vast pool of excess nutrients in iron-limited SO surface waters and thereby influence global nutrient distribution and carbon cycling. 
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  2. Abstract Two oceanographic cruises were completed in September 2016 and August 2017 to investigate the distribution of particulate organic matter (POM) across the northeast Chukchi Shelf. Both periods were characterized by highly stratified conditions, with major contrasts in the distribution of regional water masses that impacted POM distributions. Overall, surface waters were characterized by low chlorophyll fluorescence (Chl Fl < 0.8 mg m−3) and particle beam attenuation (cp < 0.3 m−1) values, and low concentrations of particulate organic carbon (POC < 8 mmol m−3), chlorophyll and pheophytin (Chl + Pheo < 0.8 mg m−3), and suspended particulate matter (SPM ∼2 g m−3). Elevated Chl Fl and Chl + Pheo (∼2 mg m−3) values measured at mid‐depths below the pycnocline defined the subsurface chlorophyll maxima (SCM), which exhibited moderate POC (∼10 mmol m−3),cp(∼0.4 m−1) and SPM (∼3 g m−3). In contrast, deeper waters below the pycnocline were characterized by low Chl Fl and Chl + Pheo (∼0.7 mg m−3), highcp(>1.5 m−1) and SPM (>8 g m−3) and elevated POC (>10 mmol m−3). POM compositions from surface and SCM regions of the water column were consistent with contributions from active phytoplankton sources whereas samples from bottom waters were characterized by high Pheo/(Chl + Pheo) ratios (>0.4) indicative of altered phytoplankton detritus. Marked contrasts in POM were observed in both surface and middepth waters during both cruises. Increases in chlorophyll and POC consistent with enhanced productivity were measured in middepth waters during the September 2016 cruise following a period of downwelling‐favorable winds, and in surface waters during the August 2017 cruise following a period of upwelling‐favorable winds. 
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  3. Abstract. Marine diazotrophs convert dinitrogen (N2) gas intobioavailable nitrogen (N), supporting life in the global ocean. In 2012, thefirst version of the global oceanic diazotroph database (version 1) waspublished. Here, we present an updated version of the database (version 2),significantly increasing the number of in situ diazotrophic measurements from13 565 to 55 286. Data points for N2 fixation rates, diazotrophic cellabundance, and nifH gene copy abundance have increased by 184 %, 86 %, and809 %, respectively. Version 2 includes two new data sheets for the nifH genecopy abundance of non-cyanobacterial diazotrophs and cell-specific N2fixation rates. The measurements of N2 fixation rates approximatelyfollow a log-normal distribution in both version 1 and version 2. However,version 2 considerably extends both the left and right tails of thedistribution. Consequently, when estimating global oceanic N2 fixationrates using the geometric means of different ocean basins, version 1 andversion 2 yield similar rates (43–57 versus 45–63 Tg N yr−1; rangesbased on one geometric standard error). In contrast, when using arithmeticmeans, version 2 suggests a significantly higher rate of 223±30 Tg N yr−1 (mean ± standard error; same hereafter) compared to version 1(74±7 Tg N yr−1). Specifically, substantial rate increases areestimated for the South Pacific Ocean (88±23 versus 20±2 Tg N yr−1), primarily driven by measurements in the southwestern subtropics,and for the North Atlantic Ocean (40±9 versus 10±2 Tg N yr−1). Moreover, version 2 estimates the N2 fixation rate in theIndian Ocean to be 35±14 Tg N yr−1, which could not be estimatedusing version 1 due to limited data availability. Furthermore, a comparisonof N2 fixation rates obtained through different measurement methods atthe same months, locations, and depths reveals that the conventional15N2 bubble method yields lower rates in 69 % cases compared tothe new 15N2 dissolution method. This updated version of thedatabase can facilitate future studies in marine ecology andbiogeochemistry. The database is stored at the Figshare repository(https://doi.org/10.6084/m9.figshare.21677687; Shao etal., 2022). 
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