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Volcanic eruptions directly triggered ocean acidification during Early Cretaceous

First study to use stable calcium and strontium isotopes to examine oceanic anoxic event

Around 120 million years ago, the earth experienced an extreme environmental disruption that choked oxygen from its oceans.

Known as oceanic anoxic event (OAE) 1a, the oxygen-deprived water led to a minor — but significant — mass extinction that affected the entire globe. During this age in the Early Cretaceous Period, an entire family of sea-dwelling nannoplankton virtually disappeared.

By measuring calcium and strontium isotope abundances in nannoplankton fossils, Northwestern earth scientists have concluded the eruption of the Ontong Java Plateau large igneous province (LIP) directly triggered OAE1a. Roughly the size of Alaska, the Ontong Java LIP erupted for seven million years, making it one of the largest known LIP events ever. During this time, it spewed tons of carbon dioxide (CO2) into the atmosphere, pushing Earth into a greenhouse period that acidified seawater and suffocated the oceans.

“We go back in time to study greenhouse periods because Earth is headed toward another greenhouse period now,” said Jiuyuan Wang, a Northwestern Ph.D. student and first author of the study. “The only way to look into the future is to understand the past.”

Volcanic eruptions directly triggered ocean acidification during Early Cretaceous
Calcium carbonate samples from a sediment core drilled from the mid-Pacific Mountains.
Credit: Northwestern University

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The study was published online last week (Dec. 16) in the journal Geology. It is the first study to apply stable strontium isotope measurements to the study of ancient ocean anoxic events.

Andrew Jacobson, Bradley Sageman and Matthew Hurtgen — all professors of earth and planetary sciences at Northwestern’s Weinberg College of Arts and Sciences — coauthored the paper. Wang is co-advised by all three professors.

Clues inside cores

Nannoplankton shells and many other marine organisms build their shells out of calcium carbonate, which is the same mineral found in chalk, limestone and some antacid tablets. When atmospheric CO2 dissolves in seawater, it forms a weak acid that can inhibit calcium carbonate formation and may even dissolve preexisting carbonate.

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To study the earth’s climate during the Early Cretaceous, the Northwestern researchers examined a 1,600-meter-long sediment core taken from the mid-Pacific Mountains. The carbonates in the core formed in a shallow-water, tropical environment approximately 127 to 100 million years ago and are presently found in the deep ocean.


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“When you consider the Earth’s carbon cycle, carbonate is one of the biggest reservoirs for carbon,” Sageman said. “When the ocean acidifies, it basically melts the carbonate. We can see this process impacting the biomineralization process of organisms that use carbonate to build their shells and skeletons right now, and it is a consequence of the observed increase in atmospheric CO2 due to human activities.”

Strontium as corroborating evidence

Several previous studies have analyzed the calcium isotope composition of marine carbonate from the geologic past. The data can be interpreted in a variety of ways, however, and calcium carbonate can change throughout time, obscuring signals acquired during its formation. In this study, the Northwestern researchers also analyzed stable isotopes of strontium — a trace element found in carbonate fossils — to gain a fuller picture.

“Calcium isotope data can be interpreted in a variety of ways,” Jacobson said. “Our study exploits observations that calcium and strontium isotopes behave similarly during calcium carbonate formation, but not during alteration that occurs upon burial. In this study, the calcium-strontium isotope ‘multi-proxy’ provides strong evidence that the signals are ‘primary’ and relate to the chemistry of seawater during OAE1a.”

“Stable strontium isotopes are less likely to undergo physical or chemical alteration over time,” Wang added. “Calcium isotopes, on the other hand, can be easily altered under certain conditions.”


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The team analyzed calcium and strontium isotopes using high-precision techniques in Jacobson’s clean laboratory at Northwestern. The methods involve dissolving carbonate samples and separating the elements, followed by analysis with a thermal ionization mass spectrometer.

Researchers have long suspected that LIP eruptions cause ocean acidification. “There is a direct link between ocean acidification and atmospheric CO2 levels,” Jacobson said. “Our study provides key evidence linking eruption of the Ontong Java Plateau LIP to ocean acidification. This is something people expected should be the case based on clues from the fossil record, but geochemical data were lacking.”

Modeling future warming

By understanding how oceans responded to extreme warming and increased atmospheric CO2, researchers can better understand how earth is responding to current, human-caused climate change. Humans are currently pushing the earth into a new climate, which is acidifying the oceans and likely causing another mass extinction.

“The difference between past greenhouse periods and current human-caused warming is in the timescale,” Sageman said. “Past events have unfolded over tens of thousands to millions of years. We’re making the same level of warming (or more) happen in less than 200 years.”


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“The best way we can understand the future is through computer modeling,” Jacobson added. “We need climate data from the past to help shape more accurate models of the future.”

Source

Northwestern University

Journal Reference

Stable Ca and Sr isotopes support volcanically triggered biocalcification crisis during Oceanic Anoxic Event 1a

Abstract

Large igneous province (LIP) eruptions are hypothesized to trigger biocalcification crises. The Aptian nannoconid crisis, which correlates with emplacement of the Ontong Java Plateau and Oceanic Anoxic Event 1a (OAE 1a, ca. 120 Ma), represents one such example.

The Ca isotope (δ44/40Ca) system offers potential to detect biocalcification fluctuations in the rock record because Ca isotope fractionation is sensitive to precipitation rate. However, other primary and secondary processes, such as input-output flux perturbations and early diagenesis, can produce similar signals.

Here, we exploit emergent properties of the stable Sr isotope (δ88/86Sr) system to resolve the origin of δ44/40Ca variability during OAE 1a. This study reports high-precision thermal ionization mass spectrometry (TIMS) δ44/40Ca, δ88/86Sr, and 87Sr/86Sr records for Hole 866A of Ocean Drilling Program Leg 143 drilled in Resolution Guyot, mid-Pacific Ocean.


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The samples span ~27 m.y. from the Barremian (ca. 127 Ma) to the Albian (ca. 100 Ma). The δ44/40Ca and δ88/86Sr secular trends differ from the 87Sr/86Sr record but mimic each other. δ44/40Ca and [Sr], as well as δ44/40Ca and δ88/86Sr, strongly correlate and yield slopes predicted for kinetic control, which demonstrates that variable mass-dependent fractionation rather than end-member mixing dominated the isotopic relationship between carbonates and seawater.

Positive δ44/40Ca and δ88/86Sr shifts that begin before OAE 1a and peak within the interval are consistent with reduced precipitation rates. All results combined point to a cascade of effects on rate-dependent Ca and Sr isotope fractionation, which derive from the dynamic interplay between LIP eruptions and biocalcification feedbacks.

Ibezim chukwuemerie

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