Connect with us

Biology

“Symbiotic Swirls: How Physical Forces Encouraged Evolution of Multicellular Life”

A study presents a striking example of cooperative organization among cells as a potential force in the evolution of multicellular life. The study is based on the fluid dynamics of cooperative feeding by Stentor, a relatively giant unicellular organism.

Avatar photo

Published

on

The evolution of multicellularity has long been a puzzle for biologists. While we often associate being bigger and multicellular with advantages, 80 percent of life on Earth consists of single-celled organisms that thrive in conditions lethal to any beast. A new study from the Marine Biological Laboratory (MBL) sheds light on how physical forces may have contributed to the emergence of multicellular life.

Researchers led by Shashank Shekhar, Assistant Professor of Physics at Emory University, studied the fluid dynamics of cooperative feeding by Stentor, a relatively giant unicellular organism. Their findings, published in Nature Physics, provide striking evidence for the role of physical forces in the evolution of multicellular life.

Stentors are trumpet-shaped, single-celled organisms that can grow up to 2 mm long. In their native habitat of ponds or lakes, they attach one end (the holdfast) to leaves or twigs while the other end sways freely, creating a vortex of water to suck in food with their cilia-lined mouth.

When Stentors are dropped into a dish of pond water, they quickly form dynamic colonies where cells don’t actually attach to each other but touch together on the glass. By quantifying fluid flows, the team showed that two neighboring Stentors can double the flow rate of water into their mouths, allowing them to suck in more prey and faster-swimming prey by creating stronger vortexes.

However, the feeding benefits accrued by two neighboring Stentor aren’t equal; the weaker Stentor gains more from teaming up than the stronger one does. They display what Shekhar calls “she loves me, she loves me not” behavior: when paired Stentors sway their trumpet ends together, their fluid flows increase but then oscillate, pulling their mouths apart again.

To answer this, the researchers turned to mathematical modeling of fluid dynamics across the colony led by co-authors Hanliang Guo and Eva Kanso. They confirmed a “promiscuity” in the colony where individuals keep switching between neighboring partners, resulting in all cells gaining stronger feeding flows on average.

In an evolutionary context, this makes sense as individuals are expected to seek the most favorable energetic payoff by associating with a neighboring individual that benefits them most. You might look at them as always attempting to optimize their income,” said John Costello of Providence College.

The researchers noted that when they give Stentors plenty of food, they remain attached and feed in colonies. But when food becomes scarce, the Stentors detach and go into individual foraging mode. This behavior is reminiscent of humans who collaborate and cooperate when resources are plentiful but turn to individualism when resources reduce.

In other models of early multicellular life, such as green algae Volvox cateri, cells that failed to divide properly eventually evolved a matrix between them, forming a colony of genetically identical cells which later differentiated. However, the ephemeral Stentor colonies are formed not of clones but of genetically distinct individuals.

Shekhar thinks their Stentor model precedes other models of early multicellularity (which is believed to have evolved at least 25 times in different lineages). This study suggests that multicellularity wasn’t done permanently yet” and that the evolution of complex life forms may be a more gradual process than previously thought.

Animals

A “Roadmap” to Understanding the Fruit Fly Brain: Breakthrough Study Reveals Comprehensive Insights into Entire Nervous System

Researchers have gained comprehensive insights into the entire nervous system of the fruit fly (Drosophila melanogaster). The study describes in detail the neurons that span the entire nervous system of the adult fruit fly. The researchers also compared the complete set of neural connections (the connectome) in a female and a male specimen — and identified differences.

Avatar photo

Published

on

The fruit fly (Drosophila melanogaster) has long been a model organism for scientists studying genetics, development, and behavior. However, despite its importance, the intricacies of the fruit fly’s nervous system have remained somewhat of a mystery – until now. Researchers at Leipzig University and other institutions have made a groundbreaking discovery, publishing a study in Nature that provides comprehensive insights into the entire nervous system of the adult fruit fly.

For the first time, scientists have mapped out the neural connections (the connectome) in a female and a male specimen, revealing differences between the two sexes. This breakthrough is a significant step forward in understanding the complex interactions within the fruit fly’s brain and nervous system.

The study, led by Dr. Katharina Eichler from Leipzig University, involved analyzing three connectomes: one female brain data set and two nerve cord data sets (one male, one female). The researchers used light microscopy to identify all neurons in the neck of the fruit fly that could be visualized using this technique.

This allowed them to analyze the circuits formed by these cells in their entirety. When comparing male and female neurons, the scientists identified sex-specific differences for the first time. They found previously unknown cells that exist only in one sex and are absent in the other.

One notable example is a descending neuron known as aSP22, which communicates with neurons present only in females. This finding provides an explanation for the behavioral differences observed when this neuron is active: female flies extend their abdomen to lay eggs, while males curl theirs forward to mate.

The study’s findings are significant not only because they provide a comprehensive overview of the fruit fly connectome but also because they offer a “roadmap” for future research. By understanding the intricate connections within the nervous system, scientists can design more intelligent experiments to investigate the function of individual neurons or entire circuits – saving time and resources.

As Eichler notes, now that the technical challenges in analyzing the fruit fly’s nervous system have been overcome, her research group is working on two new data sets covering the entire central nervous system of both a female and a male specimen. This continued research will undoubtedly shed more light on the complexities of the fruit fly brain and its implications for our understanding of nervous systems in general.

Continue Reading

Biodiversity

Unveiling Hidden Gems: Two New Crocodile Species Discovered in Mexico

Biologists have discovered two previously unknown species of crocodiles, one living on the island of Cozumel and the other on the atoll of Banco Chinchorro, both off the Yucat n Peninsula. The findings challenge long-held assumptions about the American crocodile (Crocodylus acutus) and highlight the urgent need for conservation efforts, the researchers say.

Avatar photo

Published

on

The American crocodile, a species once thought to be widespread across the Caribbean, Central America, and Mexico’s Pacific coast, has been hiding secrets. Researchers from McGill University, in collaboration with Mexican scientists, have made a groundbreaking discovery that challenges long-held assumptions about this iconic creature. Two previously unknown species of crocodiles have been found on the island of Cozumel and the atoll of Banco Chinchorro, both located off the Yucatán Peninsula.

“Biodiversity is disappearing faster than we can discover what we’re losing,” said Biology Professor Hans Larsson, the principal investigator. “Most species of crocodiles are already endangered, and rapid shoreline development threatens nearly every population. Our research aimed to uncover the true diversity of crocodiles on these isolated islands.”

Larsson and his team analyzed the genetic sequences of crocodile populations from Cozumel and Banco Chinchorro. By comparing these sequences to those of crocodiles across the Caribbean, Central America, and Mexico’s Pacific coast, they found striking levels of genetic differentiation, leading them to conclude that these populations were not simply variants of Crocodylus acutus.

“These results were totally unexpected,” former Larsson graduate student and lead author José Avila-Cervantes said. “We assumed Crocodylus acutus was a single species ranging from Baja California to Venezuela and across the Caribbean. Our study is the first to extensively explore genomic and anatomical variation in these animals.”

This discovery has significant conservation implications, as the newly identified species live in small, isolated populations, each numbering fewer than 1,000 breeding individuals. While both populations appear stable, their limited numbers and habitat restrictions make them vulnerable.

“The rapid loss of biodiversity can only be slowed if we know what species are most at risk,” said Larsson. “Now that we recognize these crocodiles as distinct species, it’s crucial to protect their habitats. Limiting land development and implementing careful conservation strategies on Cozumel and Banco Chinchorro will be key to ensuring their survival.”

The research was conducted with the help of local colleagues, including Pierre Charruau at El Colegio de la Frontera Sur in Mexico. The team captured and released crocodiles, collecting blood and scale samples for analysis. Genetic sequencing was carried out at McGill by José Avila-Cervantes during his graduate studies, with additional research on skull morphology by fellow McGill graduate student Hoai-Nam Bui.

This research was funded by the Canadian Foundation for Innovation, the Digital Research Alliance of Canada), the Comisión Nacional para el Conocimiento y Uso de la Biodiversidad, and the Natural Sciences and Engineering Research Council of Canada.

Continue Reading

Biochemistry

Unraveling Nature’s Secret: How Velvet Worm Slime Could Revolutionize Sustainable Materials Design

A new discovery about the slime ejected by velvet worms could revolutionize sustainable material design. The findings outline how a naturally occurring protein structure, conserved across species from Australia, Singapore and Barbados over nearly 400 million years of evolution, enables the slime’s transformation from liquid to fiber and back again. It’s a discovery that could inspire next-generation recyclable bioplastics.

Avatar photo

Published

on

The discovery of the remarkable properties of velvet worm slime has sent shockwaves through the scientific community, offering new hope for sustainable material design. Researchers from McGill University have made a groundbreaking find that could lead to the development of next-generation recyclable bioplastics.

Velvet worms, small caterpillar-like creatures found in humid forests of the southern hemisphere, possess an extraordinary ability – their slime can transform from liquid to fibre and back again. This remarkable property has puzzled scientists for centuries, but a team led by Matthew Harrington, a chemistry professor and Canada Research Chair in green chemistry, has finally decoded the molecular structure behind this phenomenon.

Using protein sequencing and AI-driven structure prediction (AlphaFold), the researchers identified previously unknown proteins in the slime that function similarly to cell receptors in the immune system. These receptor proteins appear to link large structural proteins during fibre formation, enabling the slime’s remarkable reversibility.

The implications of this discovery are profound. Traditional plastics and synthetic fibres require energy-intensive processes to manufacture and recycle, often involving heat or chemical treatments. In contrast, the velvet worm uses simple mechanical forces – pulling and stretching – to generate strong, durable fibres from biorenewable precursors, which can later be dissolved and reused without harmful byproducts.

While a plastic bottle that dissolves in water may seem like an impractical solution, Harrington believes that adjusting the chemistry of this binding mechanism could overcome this limitation. The team’s next challenge will be to experimentally verify the binding interactions and explore whether the principle can be adapted for engineered materials.

The study was co-authored by researchers from McGill University and Nanyang Technological University (NTU) in Singapore, highlighting the importance of international collaboration in addressing pressing global challenges.

As Harrington aptly puts it, “Nature has already figured out a way to make materials that are both strong and recyclable. By decoding the molecular structure of velvet worm slime, we’re now one step closer to replicating that efficiency for the materials we use every day.”

Continue Reading

Trending