This photograph shows two big and two
little Pyrocystis noctiluca. Credit: Prakash lab / Stanford University
Many
plankton journey from the cold, dark depths of our oceans to the surface, only
to eventually drift down again into the darkness in a perpetual rhythm. Yet,
how single-celled phytoplankton, most of which have no appendages to help them
swim, make this pilgrimage has remained a mystery.
In a paper published October
17 in Current Biology, researchers
describe a species of bioluminescent phytoplankton, called Pyrocystis
noctiluca, that balloons to six times their original size of a few hundred
microns.
This massive inflation allows the
plankton to journey up to 200 meters toward the ocean's surface to capture
sunlight, then sink back, showcasing a unique strategy for long-distance ocean
travel.
Phytoplankton are, on average, 5–10%
heavier than seawater, meaning that if they want to remain at the surface to
photosynthesize, they have to find a way to best gravity.
"We decided to work on things that
seemingly have no appendages to swim," says senior author Manu Prakash, a
marine biologist and bioengineer at Stanford University.
"What we have discovered in this
paper is that these P. noctiluca cells are like little submarines that can
control their density so precisely that they can choose where they want to be
in the water column."
On a research vessel off the coast of Hawaii, Prakash and a
postdoctoral fellow at Stanford University, Adam Larson , one of the first
authors on the study, stumbled upon a bloom of P. noctiluca and surprisingly
found two very different sizes in their nets.
"It took a while to piece together why until we recorded the videos where we saw the cells doing this massive inflation," says Larson. "It can happen quite suddenly, so if you sleep by the microscope for 10 minutes, you might miss it."
This video shows dividing Pyrocystis noctiluca.
Credit: Larson et al./Current Biology
To test what effects this rapid
growth might have on the plankton, the research team utilized their novel
"gravity machine."
"The gravity machine allows us
to see a single cell at subcellular resolution in an infinite water
column," says Prakash.
"It's a little bit like a
Ferris wheel for gerbils or mice but for a single cell. It's the size of a
dinner plate and rotates, so the cell doesn't know that it's not climbing or
sinking in its own frame of reference."
By altering water pressure and density within the gravity machine, the team
can create a virtual reality environment mimicking the ocean's depths. With the
machine, the team discovered that inflated cells were less dense than the
surrounding seawater, letting them escape the downward pull of gravity and
float toward the virtual surface.
Further investigation showed this
expansion happens as a natural part of the plankton's cell cycle. Once a single-celled plankton divides into two, an
internal structure called a vacuole, a kind of flexible water tank, filters in
fresh water, causing the two new cells to massively grow in size.
These two daughter cells, now swelled with the lighter freshwater, sail
upward. "What we realized is that this is a very clever way to essentially
slingshot in the ocean during cell division," Prakash says.
"So, what happens during
normal time? You're making a lot of proteins, you have tons of sunlight, and
you make a lot of biomass until you get heavier and you sink. Then, you do cell
division in the deeper waters and use inflation to get back to the size of the
mother."
The entire cell cycle takes roughly
seven days, coinciding with the plankton's vertical pursuit of light and
nutrients. "You can then see how this cell cycle could have evolved,"
says Prakash.
"I think this is the first time we have clear evidence that the cell cycle, which is such a fundamental mechanism of controlling a cell and cell division, is possibly controlled by an ecological parameter."
This video shows the Pyrocystis cell cycle.
Credit: Larson et al./Current Biology
With these insights in mind, using
a theoretical framework, the team discovered the ecological parameter acting
as a fundamental limit driving this evolution.
"All cells experience a gravitational pull downward, and unless they or subsequent progeny
fight back, they will sink forever to the bottom of the ocean in a
gravitational trap," says postdoctoral fellow Rahul Chajwa, the other
first author of the study, also at Stanford University.
Now, using the results from the
gravity machine, as well as their ecological and physiological observations,
the research team has developed a mathematical framework that could be
generalized and applied to all plankton in the ocean.
For future projects, Prakash's lab
is looking to uncover hidden mysteries of a vast number of plankton that may
use the new biochemistry to regulate density and move up and down the water
column.
"We have roughly around 600
species in our Behavioral Atlas right now, and we are systematically measuring
all kinds of mechanisms. It's turning out that there are four or five different
tricks all co-evolving for this function. I think one of the threads that's
really fun is that we have a long list of organisms to study; because there are
millions of species that live in the ocean, this is the tip of the
iceberg."
Hongquan Li, a graduate student in
the Prakash lab, is also an author on the study.
by Cell Press
Source: Plankton balloon to six times their size in newly discovered mode of oceanic travel (phys.org)
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