Justin B. Ries

Last updated
Justin Baker Ries
English
Ries headshot zoom June2023.jpg
Born
NationalityAmerican
Alma mater Franklin and Marshall College Johns Hopkins University
Known forOcean acidification, biomineralization, and carbon sequestration research
Awards Phi Beta Kappa, Sigma Xi, Hanse-Wissenschaftskolleg Fellowship (Germany), Woods Hole Oceanographic Institution Ocean and Climate Change Postdoctoral Fellowship
Scientific career
FieldsOcean acidification, carbon sequestration, global warming, biomineralization, paleoceanography
Institutions Northeastern University, University of North Carolina at Chapel Hill, Woods Hole Oceanographic Institution, California Institute of Technology, Johns Hopkins University
Thesis Experiments on the effect of secular variation in seawater Mg/Ca (calcite and aragonite seas) on calcareous biomineralization  (2005)
Website rieslab.sites.northeastern.edu

Justin Baker Ries is an American marine scientist, best known for his contributions to ocean acidification, carbon sequestration, and biomineralization research.

Contents

Biography

Ries was born in Baltimore, Maryland, and attended the Friends School of Baltimore. He received a B.A. from Franklin and Marshall College and a Ph.D. from the Johns Hopkins University for a dissertation 'Experiments on the effect of secular variation in seawater Mg/Ca (calcite and aragonite seas) on calcareous biomineralization'. He received postdoctoral training at the Johns Hopkins University, the Woods Hole Oceanographic Institution, and the California Institute of Technology. Ries was a professor at the University of North Carolina at Chapel Hill for five years before becoming a professor at Northeastern University in 2013. At Northeastern, he is affiliated with the Department of Marine and Environmental Sciences, the Marine Science Center, and the Institute for Coastal Sustainability.

Major discoveries

Ries is best known for his contributions to ocean acidification and biomineralization research. He and his colleagues made the publicized and controversial discovery that anthropogenic CO2-induced ocean acidification does not negatively impact all species of marine calcifying organisms, but can also have neutral and even positive effects on some species. [1] [2] [3] [4] [5] [6] [7] [8] [9] Ries also discovered that ocean acidification can alter the shell mineralogy, [10] shell structure, [11] predator-prey dynamics, [12] [13] [9] [14] and calcifying fluid pH of marine organisms, and produced the first geochemical model of the calcifying fluid that could predict organisms' responses to future ocean acidification. [15] [16] Ries and colleagues are also credited with discovering that the current rate of CO2-induced ocean acidification is the fastest in Earth history [17] [18] [19] and that many species of marine calcifiers today inhabit seawater that is already undersaturated with respect to their shell mineral. [20] [21]

Inventions

Ries holds carbon sequestration patents describing biologically and geologically inspired methods for removing and mineralizing CO2 from the flue-streams of fossil-fuel-fired power plants and transoceanic vessels, production of carbon-negative cement, and alleviating bottlenecks in the global carbon cycle. [22] [23]

Honors

Honors include induction into the Phi Beta Kappa and Sigma Xi honor societies, receipt of the German Hanse-Wissenschaftskolleg  [ de ] Award [24] [25] and the Woods Hole Oceanographic Institution Ocean and Climate Change Postdoctoral Fellowship.

Related Research Articles

<span class="mw-page-title-main">Coccolithophore</span> Unicellular algae responsible for the formation of chalk

Coccolithophores, or coccolithophorids, are single-celled organisms which are part of the phytoplankton, the autotrophic (self-feeding) component of the plankton community. They form a group of about 200 species, and belong either to the kingdom Protista, according to Robert Whittaker's five-kingdom system, or clade Hacrobia, according to a newer biological classification system. Within the Hacrobia, the coccolithophores are in the phylum or division Haptophyta, class Prymnesiophyceae. Coccolithophores are almost exclusively marine, are photosynthetic, and exist in large numbers throughout the sunlight zone of the ocean.

<span class="mw-page-title-main">Lysocline</span> Depth in the ocean below which the rate of dissolution of calcite increases dramatically

The lysocline is the depth in the ocean dependent upon the carbonate compensation depth (CCD), usually around 5 km, below which the rate of dissolution of calcite increases dramatically because of a pressure effect. While the lysocline is the upper bound of this transition zone of calcite saturation, the CCD is the lower bound of this zone.

<span class="mw-page-title-main">Alkalinity</span> Capacity of water to resist changes in pH that would make the water more acidic

Alkalinity (from Arabic: القلوية, romanized: al-qaly, lit. 'ashes of the saltwort') is the capacity of water to resist acidification. It should not be confused with basicity, which is an absolute measurement on the pH scale. Alkalinity is the strength of a buffer solution composed of weak acids and their conjugate bases. It is measured by titrating the solution with an acid such as HCl until its pH changes abruptly, or it reaches a known endpoint where that happens. Alkalinity is expressed in units of concentration, such as meq/L (milliequivalents per liter), μeq/kg (microequivalents per kilogram), or mg/L CaCO3 (milligrams per liter of calcium carbonate). Each of these measurements corresponds to an amount of acid added as a titrant.

<span class="mw-page-title-main">Ocean acidification</span> Decrease of pH levels in the ocean

Ocean acidification is the ongoing decrease in the pH of the Earth's ocean. Between 1950 and 2020, the average pH of the ocean surface fell from approximately 8.15 to 8.05. Carbon dioxide emissions from human activities are the primary cause of ocean acidification, with atmospheric carbon dioxide levels exceeding 410 ppm. CO2 from the atmosphere is absorbed by the oceans. This produces carbonic acid which dissociates into a bicarbonate ion and a hydrogen ion. The presence of free hydrogen ions lowers the pH of the ocean, increasing acidity. Marine calcifying organisms, such as mollusks and corals, are especially vulnerable because they rely on calcium carbonate to build shells and skeletons.

The carbonate compensation depth (CCD) is the depth, in the oceans, at which the rate of supply of calcium carbonates matches the rate of solvation. That is, solvation 'compensates' supply. Below the CCD solvation is faster, so that carbonate particles dissolve and the carbonate shells (tests) of animals are not preserved. Carbonate particles cannot accumulate in the sediments where the sea floor is below this depth.

<span class="mw-page-title-main">Rhodolith</span> Calcareous marine nodules composed of crustose red algae

Rhodoliths are colorful, unattached calcareous nodules, composed of crustose, benthic marine red algae that resemble coral. Rhodolith beds create biogenic habitat for diverse benthic communities. The rhodolithic growth habit has been attained by a number of unrelated coralline red algae, organisms that deposit calcium carbonate within their cell walls to form hard structures or nodules that resemble beds of coral.

<span class="mw-page-title-main">Carbonate–silicate cycle</span> Geochemical transformation of silicate rocks

The carbonate–silicate geochemical cycle, also known as the inorganic carbon cycle, describes the long-term transformation of silicate rocks to carbonate rocks by weathering and sedimentation, and the transformation of carbonate rocks back into silicate rocks by metamorphism and volcanism. Carbon dioxide is removed from the atmosphere during burial of weathered minerals and returned to the atmosphere through volcanism. On million-year time scales, the carbonate-silicate cycle is a key factor in controlling Earth's climate because it regulates carbon dioxide levels and therefore global temperature.

Marine chemistry, also known as ocean chemistry or chemical oceanography, is influenced by plate tectonics and seafloor spreading, turbidity currents, sediments, pH levels, atmospheric constituents, metamorphic activity, and ecology. The field of chemical oceanography studies the chemistry of marine environments including the influences of different variables. Marine life has adapted to the chemistries unique to Earth's oceans, and marine ecosystems are sensitive to changes in ocean chemistry.

<span class="mw-page-title-main">Effects of climate change on oceans</span> Overview of all the effects of climate change on oceans

There are many effects of climate change on oceans. One of the main ones is an increase in ocean temperatures. More frequent marine heatwaves are linked to this. The rising temperature contributes to a rise in sea levels. Other effects include ocean acidification, sea ice decline, increased ocean stratification and reductions in oxygen levels. Changes to ocean currents including a weakening of the Atlantic meridional overturning circulation are another important effect. All these changes have knock-on effects which disturb marine ecosystems. The main cause of these changes is climate change due to human emissions of greenhouse gases. Carbon dioxide and methane are examples of greenhouse gases. This leads to ocean warming, because the ocean takes up most of the additional heat in the climate system. The ocean absorbs some of the extra carbon dioxide in the atmosphere. This causes the pH value of the ocean to drop. Scientists estimate that the ocean absorbs about 25% of all human-caused CO2 emissions.

<span class="mw-page-title-main">Oceanic carbon cycle</span> Ocean/atmosphere carbon exchange process

The oceanic carbon cycle is composed of processes that exchange carbon between various pools within the ocean as well as between the atmosphere, Earth interior, and the seafloor. The carbon cycle is a result of many interacting forces across multiple time and space scales that circulates carbon around the planet, ensuring that carbon is available globally. The Oceanic carbon cycle is a central process to the global carbon cycle and contains both inorganic carbon and organic carbon. Part of the marine carbon cycle transforms carbon between non-living and living matter.

<span class="mw-page-title-main">Shell growth in estuaries</span>

Shell growth in estuaries is an aspect of marine biology that has attracted a number of scientific research studies. Many groups of marine organisms produce calcified exoskeletons, commonly known as shells, hard calcium carbonate structures which the organisms rely on for various specialized structural and defensive purposes. The rate at which these shells form is greatly influenced by physical and chemical characteristics of the water in which these organisms live. Estuaries are dynamic habitats which expose their inhabitants to a wide array of rapidly changing physical conditions, exaggerating the differences in physical and chemical properties of the water.

Estuarine acidification happens when the pH balance of water in coastal marine ecosystems, specifically those of estuaries, decreases. Water, generally considered neutral on the pH scale, normally perfectly balanced between alkalinity and acidity. While ocean acidification occurs due to the ongoing decrease in the pH of the Earth's oceans, caused by the absorption of carbon dioxide (CO2) from the atmosphere, pH change in estuaries is more complicated than in the open ocean due to direct impacts from land run-off, human impact, and coastal current dynamics. In the ocean, wave and wind movement allows carbon dioxide (CO2) to mixes with water (H2O) forming carbonic acid (H2CO3). Through wave motion this chemical bond is mixed up, allowing for the further break of the bond, eventually becoming carbonate (CO3) which is basic and helps form shells for ocean creatures, and two hydron molecules. This creates the potential for acidic threat since hydron ions readily bond with any Lewis Structure to form an acidic bond. This is referred to as an oxidation-reduction reaction.

<span class="mw-page-title-main">Freshwater acidification</span>

Freshwater acidification occurs when acidic inputs enter a body of fresh water through the weathering of rocks, invasion of acidifying gas, or by the reduction of acid anions, like sulfate and nitrate within a lake. Freshwater acidification is primarily caused by sulfur oxides (SOx) and nitrogen oxides (NOx) entering the water from atmospheric depositions and soil leaching. Carbonic acid and dissolved carbon dioxide can also enter freshwaters, in a similar manner associated with runoff, through carbon dioxide-rich soils. Runoff that contains these compounds may incorporate acidifying hydrogen ions and inorganic aluminum, which can be toxic to marine organisms. Acid rain is also a contributor to freshwater acidification. It is created when SOx and NOx react with water, oxygen, and other oxidants within the clouds.

<span class="mw-page-title-main">Ocean acidification in the Great Barrier Reef</span> Threat to the reef which reduces the viability and strength of reef-building corals

Ocean acidification threatens the Great Barrier Reef by reducing the viability and strength of coral reefs. The Great Barrier Reef, considered one of the seven natural wonders of the world and a biodiversity hotspot, is located in Australia. Similar to other coral reefs, it is experiencing degradation due to ocean acidification. Ocean acidification results from a rise in atmospheric carbon dioxide, which is taken up by the ocean. This process can increase sea surface temperature, decrease aragonite, and lower the pH of the ocean. The more humanity consumes fossil fuels, the more the ocean absorbs released CO₂, furthering ocean acidification.

<span class="mw-page-title-main">Marine biogenic calcification</span> Shell formation mechanism

Marine biogenic calcification refers to the production of calcium carbonate by organisms in the global ocean.

<span class="mw-page-title-main">Silica cycle</span> Biogeochemical cycle

The silica cycle is the biogeochemical cycle in which biogenic silica is transported between the Earth's systems. Silicon is considered a bioessential element and is one of the most abundant elements on Earth. The silica cycle has significant overlap with the carbon cycle and plays an important role in the sequestration of carbon through continental weathering, biogenic export and burial as oozes on geologic timescales.

<span class="mw-page-title-main">Ocean acidification in the Arctic Ocean</span>

The Arctic ocean covers an area of 14,056,000 square kilometers, and supports a diverse and important socioeconomic food web of organisms, despite its average water temperature being 32 degrees Fahrenheit. Over the last three decades, the Arctic Ocean has experienced drastic changes due to climate change. One of the changes is in the acidity levels of the ocean, which have been consistently increasing at twice the rate of the Pacific and Atlantic oceans. Arctic Ocean acidification is a result of feedback from climate system mechanisms, and is having negative impacts on Arctic Ocean ecosystems and the organisms that live within them.

<span class="mw-page-title-main">Human impact on marine life</span>

Human activities affect marine life and marine habitats through overfishing, habitat loss, the introduction of invasive species, ocean pollution, ocean acidification and ocean warming. These impact marine ecosystems and food webs and may result in consequences as yet unrecognised for the biodiversity and continuation of marine life forms.

<span class="mw-page-title-main">Particulate inorganic carbon</span>

Particulate inorganic carbon (PIC) can be contrasted with dissolved inorganic carbon (DIC), the other form of inorganic carbon found in the ocean. These distinctions are important in chemical oceanography. Particulate inorganic carbon is sometimes called suspended inorganic carbon. In operational terms, it is defined as the inorganic carbon in particulate form that is too large to pass through the filter used to separate dissolved inorganic carbon.

<span class="mw-page-title-main">Great Calcite Belt</span> High-calcite region of the Southern Ocean

The Great Calcite Belt (GCB) refers to a region of the ocean where there are high concentrations of calcite, a mineral form of calcium carbonate. The belt extends over a large area of the Southern Ocean surrounding Antarctica. The calcite in the Great Calcite Belt is formed by tiny marine organisms called coccolithophores, which build their shells out of calcium carbonate. When these organisms die, their shells sink to the bottom of the ocean, and over time, they accumulate to form a thick layer of calcite sediment.

References

  1. Ries, Justin B.; Cohen, Anne L.; McCorkle, Daniel C. (2009-12-01). "Marine calcifiers exhibit mixed responses to CO2-induced ocean acidification". Geology. 37 (12): 1131–1134. Bibcode:2009Geo....37.1131R. doi:10.1130/G30210A.1. ISSN   0091-7613.
  2. "Giant Lobsters From Rising Greenhouse Gases?". NPR.org. Retrieved 2017-12-15.
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  5. Heffernan, Olive (2009-12-10). "Consider the lobster". Nature Reports Climate Change. 1 (1001): 2. doi: 10.1038/climate.2010.130 .
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  11. Horvath, Kimmaree M.; Castillo, Karl D.; Armstrong, Pualani; Westfield, Isaac T.; Courtney, Travis; Ries, Justin B. (2016). "Next-century ocean acidification and warming both reduce calcification rate, but only acidification alters skeletal morphology of reef-building coral Siderastrea siderea". Scientific Reports. 6 (1): 29613. Bibcode:2016NatSR...629613H. doi:10.1038/srep29613. ISSN   2045-2322. PMC   4965865 . PMID   27470426.
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  17. Hönisch, Bärbel; Ridgwell, Andy; Schmidt, Daniela N.; Thomas, Ellen; Gibbs, Samantha J.; Sluijs, Appy; Zeebe, Richard; Kump, Lee; Ries, Justin B. (2012-03-02). "The Geological Record of Ocean Acidification" (PDF). Science. 335 (6072): 1058–1063. Bibcode:2012Sci...335.1058H. doi:10.1126/science.1208277. hdl:1983/24fe327a-c509-4b6a-aa9a-a22616c42d49. ISSN   0036-8075. PMID   22383840. S2CID   6361097.
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