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UrduA new paper that examines two foram species found that they demonstrated great metabolic versatility to flourish in hypoxic and anoxic sediments where there is little or no dissolved oxygen, inferring that the forams’ contribution to the marine ecosystem will increase with the expansion of oxygen-depleted habitats.
In addition, the paper found that the multiple metabolic strategies that these forams exhibit to adapt to low and no oxygen conditions are changing the classical view about the evolution and diversity of eukaryotes. That classical view hypothesizes that the rise of oxygen in Earth’s system led to the acquisition of oxygen-respiring mitochondria, the part of a cell that generates most of the chemical energy that powers a cell’s biochemical reactions. The forams in the study represent “typical” mitochondrial-bearing eukaryotes. However, these two forams respire nitrate and produce energy in the absence of oxygen, with one colonizing an anoxic environment, often with high levels of hydrogen sulfide, a chemical compound typically toxic to eukaryotes.
“Benthic foraminifera represent truly successful microbial eukaryotes with diverse and sophisticated metabolic adaptive strategies” that scientists are just beginning to discover, the authors noted in the paper, Multiple integrated metabolic strategies allow foraminiferal protists to thrive in anoxic marine sediments appearing in Science Advances.
This is important because scientists have studied forams extensively for interpreting past oceanographic and climate conditions. Scientists largely have assumed that forams evolved after oxygen was on the planet and likely require oxygen to survive. However, finding that forams can perform the processes described “throws a whole new wrench in interpretations of past environmental conditions on Earth, driven by the foram fossil record,” said co-author and project leader Joan Bernhard, senior scientist in the Geology and Geophysics Department at the Woods Hole Oceanographic Institution (WHOI).
Bernhard said that over the past several decades she has worked to establish that forams can live where there is little or no oxygen. “We never knew exactly why forams can live where there isn’t any oxygen until molecular methods got good enough that we could really start to ask some of these questions. This is our first paper that’s coming out with some of these insights,” she said. Bernhard added that with thousands of foram species living today, and with hundreds of thousands extinct, it is likely that this is “the tip of the iceberg” in terms of possibly discovering other metabolic strategies invoked by these forams.
Specific insights from the paper pertain to two highly successful benthic foraminiferal species that inhabit hypoxic or anoxic sediments in the Santa Barbara Basin, a sort of natural laboratory off the coast of California for studying the impact of oxygen depletion in the ocean.
Through gene expression analysis of the two species—Nonionella stella and Bolivina argentea—scientists found different successful metabolic adaptations that allowed the forams to succeed in oxygen-depleted marine sediments and identified candidate genes involved in anaerobic respiration and energy metabolism.
The N. stella is a sort of kleptomaniac, utilizing a technique to steal chloroplasts—the structure in a cell where photosynthesis occurs—from a particular diatom genus. What makes this particularly interesting is that N. stella lives well below what is considered to be the zone where photosynthesis can happen. The authors noted that there has been discussion in the literature questioning the functionality of these kleptoplasts in the Santa Barbara Basin N. stella but the new results show that these kleptoplasts are firmly functional, although exact metabolic details remain elusive.
In addition, the scientists found that the two foram species in the study use different metabolic pathways to incorporate ammonium into organic nitrogen in the form of glutamate, a metabolic strategy that was not previously known to be performed by these organisms.
“The metabolic variety suggests that at least some species of this diverse protistan group will withstand severe deoxygenation and likely play major roles in oceans affected by climate change,” the authors wrote.
The study “gives the scientific community a new direction for research,” said lead author Fatma Gomaa, who, at the time of the study, was a postdoctoral investigator at the Geology and Geophysics Department at WHOI. “We are now starting to learn that there are microeukaryotes living in habitats similar to those in Earth’s early history that are performing very interesting biological functions. Learning about these forams is very intriguing and will shed light on how early eukaryotes evolved.”
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About Woods Hole Oceanographic Institution
The Woods Hole Oceanographic Institution (WHOI) is a private, non-profit organization on Cape Cod, Massachusetts, dedicated to marine research, engineering, and higher education. Established in 1930, its primary mission is to understand the ocean and its interaction with the Earth as a whole, and to communicate an understanding of the ocean’s role in the changing global environment. WHOI’s pioneering discoveries stem from an ideal combination of science and engineering—one that has made it one of the most trusted and technically advanced leaders in basic and applied ocean research and exploration anywhere. WHOI is known for its multidisciplinary approach, superior ship operations, and unparalleled deep-sea robotics capabilities. We play a leading role in ocean observation and operate the most extensive suite of data-gathering platforms in the world. Top scientists, engineers, and students collaborate on more than 800 concurrent projects worldwide—both above and below the waves—pushing the boundaries of knowledge and possibility. For more information, please visit www.whoi.edu
