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  1. Abstract

    Students lose interest in science as they progress from elementary to high school. There is a need for authentic, place‐based science learning experiences that can increase students' interest in science. Scientists have unique skillsets that can complement the work of educators to create exciting experiences that are grounded in pedagogy and science practices. As scientists and educators, we co‐developed a lesson plan for high school students on the Eastern Shore of Virginia, a historically underserved coastal area, that demonstrated realistic scientific practices in students' local estuaries. After implementation of the lesson plan, we observed that students had a deeper understanding of ecosystem processes compared to their peers who had not been involved, were enthusiastic about sharing their experiences, and had a more well‐rounded ability to think like a scientist than before the lesson plan. We share our experiences and five best practices that can serve as a framework for scientists and educators who are motivated to do similar work. Through collaboration, scientists and educators have the potential to bolster student science identities and increase student participation in future scientific endeavors.

     
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    Free, publicly-accessible full text available February 2, 2025
  2. Free, publicly-accessible full text available March 1, 2025
  3. Phytoplankton and sea ice algae are traditionally considered to be the main primary producers in the Arctic Ocean. In this Perspective, we explore the importance of benthic primary producers (BPPs) encompassing microalgae, macroalgae, and seagrasses, which represent a poorly quantified source of Arctic marine primary production. Despite scarce observations, models predict that BPPs are widespread, colonizing ~3 million km2of the extensive Arctic coastal and shelf seas. Using a synthesis of published data and a novel model, we estimate that BPPs currently contribute ~77 Tg C y−1of primary production to the Arctic, equivalent to ~20 to 35% of annual phytoplankton production. Macroalgae contribute ~43 Tg C y−1, seagrasses contribute ~23 Tg C y−1, and microalgae-dominated shelf habitats contribute ~11 to 16 Tg C y−1. Since 2003, the Arctic seafloor area exposed to sunlight has increased by ~47,000 km2y−1, expanding the realm of BPPs in a warming Arctic. Increased macrophyte abundance and productivity is expected along Arctic coastlines with continued ocean warming and sea ice loss. However, microalgal benthic primary production has increased in only a few shelf regions despite substantial sea ice loss over the past 20 y, as higher solar irradiance in the ice-free ocean is counterbalanced by reduced water transparency. This suggests complex impacts of climate change on Arctic light availability and marine primary production. Despite significant knowledge gaps on Arctic BPPs, their widespread presence and obvious contribution to coastal and shelf ecosystem production call for further investigation and for their inclusion in Arctic ecosystem models and carbon budgets.

     
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    Free, publicly-accessible full text available March 12, 2025
  4. Abstract

    As part of a long-term study on the effects of nitrogen (N) loading in a shallow temperate lagoon, we measured rates of N2fixation associated with seagrass (Zostera marina) epiphytes during the summer from 2005 to 2019, at two sites along a gradient from where high N groundwater enters the system (denoted SH) to a more well-flushed outer harbor (OH). The data presented here are the first such long-term N2fixation estimates for any seagrass system and one of the very few reported for the phyllosphere in a temperate system. Mean daily N2fixation was estimated from light and dark measurements using the acetylene reduction assay intercalibrated using both incorporation of15N2into biomass and a novel application of the N2:Ar method. Surprisingly, despite a large inorganic N input from a N-contaminated groundwater plume, epiphytic N2fixation rates were moderately to very high for a seagrass system (OH site 14-year mean of 0.94 mmol N m−2 d−1), with the highest rates (2.6 mmol N m−2 d−1) measured at the more N-loaded eutrophic site (SH) where dissolved inorganic N was higher and soluble reactive phosphorus was lower than in the better-flushed OH. Over 95% of the total N2fixation measured was in the light, suggesting the importance of cyanobacteria in the epiphyte assemblages. We observed large inter-annual variation both within and across the two study sites (range from 0.1 to 2.6 mmol N fixed m−2d−1), which we suggest is in part related to climatic variation. We estimate that input from phyllosphere N2fixation over the study period contributes on average an additional 20% to the total daily N load per area within the seagrass meadow.

     
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  5. Coastal landscapes are naturally shifting mosaics of distinct ecosystems that are rapidly migratingwith sealevel rise. Previous work illustrates that transitions among individual ecosystems have disproportionate impacts on the global carbon cycle, but this cannot address nonlinear interactions between multiple ecosystems that potentially cascade across the coastal landscape. Here, we synthesize carbon stocks, accumulation rates, and regional land cover data over 36 years (1984 and 2020) for a variety of ecosystems across a large portion of the rapidly transgressing mid-Atlantic coast. The coastal landscape of the Virginia Eastern Shore consists of temperate forest, salt marsh, seagrass beds, barrier islands, and coastal lagoons. We found that rapid losses and gains within individual ecosystems largely offset each other, which resulted in relatively stable areas for the different ecosystems, and a 4% (196.9 Gg C) reduction in regional carbon storage. However, new metrics of carbon replacement times indicated that it would take only 7 years of carbon accumulation in surviving ecosystems to compensate this loss. Our findings reveal unique compensatory mechanisms at the scale of entire landscapes that quickly absorb losses and facilitate increased regional carbon storage in the face of historical and contemporary sea-level rise. However, the strength of these compensatory mechanisms may diminish as climate change exacerbates the magnitude of carbon losses. 
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    Free, publicly-accessible full text available September 15, 2024
  6. Abstract

    Megaripples are current‐generated seafloor bedforms of well‐sorted sand or gravel and wavelengths over 1 m. In this aquatic eddy covariance study, we measured large rates of benthic primary production and respiration for a shallow‐water sandy megaripple field exposed to strong tidally driven currents and intense sunlight. Current and light were the main short‐term drivers of a highly dynamic oxygen exchange. Daytime oxygen release as high as 300 mmol m−2 d−1and nighttime oxygen uptake up to −100 mmol m−2 d−1were likely sustained by current‐driven transport of oxygen, nutrients, and organic matter (fuel) into and out of the sand and superimposed by rapid internal cycling. Seasonal differences in temperature (45%) and light (69%) between April and September were the main long‐term drivers of substantially greater rates of gross primary production and respiration in September. The megaripples functioned as an intense metabolic hotspot with carbon cycling rates larger than those of most near‐shore sediments.

     
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  7. Abstract

    The aquatic eddy covariance technique is increasingly used to determine oxygen (O2) fluxes over benthic ecosystems. The technique uses O2measuring systems that have a high temporal and numerical resolution. In this study, we performed a series of lab and field tests to assess a new optical submersible O2meter designed for aquatic eddy covariance measurements and equipped with an existing ultra‐high speed optical fiber sensor. The meter has a 16‐bit digital‐to‐analog‐signal conversion that produces a 0–5 V output at a rate up to 40 Hz. The device was paired with an acoustic Doppler velocimeter. The combined meter and fiber‐optic O2sensor's response time was significantly faster in O2‐undersaturated water compared to in O2‐supersaturated water (0.087 vs. 0.12 s), but still sufficiently fast for aquatic eddy covariance measurements. The O2optode signal was not sensitive to variations in water flow or light exposure. However, the response time was affected by the direction of the flow. When the sensor tip was exposed to a flow from the back rather than the front, the response time increased by 37%. The meter's internal signal processing time was determined to be ~ 0.05 s, a delay that can be corrected for during postprocessing. In order for the built‐in temperature correction to be accurate, the meter should always be submerged with the fiber‐optic sensor. In multiple 21–47 h field tests, the system recorded consistently high‐quality, low‐noise O2flux data. Overall, the new meter is a powerful option for collecting robust aquatic eddy covariance data.

     
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  8. Aquatic eddy covariance (AEC) is increasingly being used to study benthic oxygen (O 2 ) flux dynamics, organic carbon cycling, and ecosystem health in marine and freshwater environments. Because it is a noninvasive technique, has a high temporal resolution (∼15 min), and integrates over a large area of the seafloor (typically 10–100 m 2 ), it has provided new insights on the functioning of aquatic ecosystems under naturally varying in situ conditions and has given us more accurate assessments of their metabolism. In this review, we summarize biogeochemical, ecological, and biological insightsgained from AEC studies of marine ecosystems. A general finding for all substrates is that benthic O 2 exchange is far more dynamic than earlier recognized, and thus accurate mean values can only be obtained from measurements that integrate over all timescales that affect the local O 2 exchange. Finally, we highlight new developments of the technique, including measurements of air–water gas exchange and long-term deployments. 
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