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Tuesday, January 16, 2024

THE HAGFISH

Researchers sequence the first genome of myxini, the only vertebrate lineage that had no reference genome


Such finding, published in ‘Nature Ecology & Evolution’, is the work of an international consortium of more than 30 institutions from 7 countries around the world


Peer-Reviewed Publication

UNIVERSITY OF MALAGA

Researchers sequence the first genome of myxini, the only vertebrate lineage that had no reference genome 

VIDEO: 

AN INTERNATIONAL SCIENTIFIC TEAM MADE UP OF MORE THAN 40 AUTHORS FROM SEVEN DIFFERENT COUNTRIES, LED BY THE RESEARCHER AT THE UNIVERSITY OF MALAGA JUAN PASCUAL ANAYA, HAS MANAGED TO SEQUENCE THE FIRST GENOME OF THE MYXINI –ALSO KNOWN AS ‘HAGFISH’–, THE ONLY LARGE GROUP OF VERTEBRATES FOR WHICH THERE WAS NO REFERENCE GENOME OF ANY OF ITS SPECIES YET.

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CREDIT: UNIVERSITY OF MALAGA




An international scientific team made up of more than 40 authors from seven different countries, led by the researcher at the University of Malaga Juan Pascual Anaya, has managed to sequence the first genome of the myxini –also known as ‘hagfish’–, the only large group of vertebrates for which there was no reference genome of any of its species yet.

This finding, published in the scientific journal ‘Nature Ecology & Evolution’, has allowed deciphering the evolutionary history of genome duplications –number of times a genome is completely duplicated– that occurred in the ancestors of vertebrates, a group that comprises the human beings.

“This study has important implications in the evolutionary and molecular field, as it helps us understand the changes in the genome that accompanied the origin of vertebrates and their most unique structures, such as the complex brain, the jaw and the limbs”, explains the scientist of the Department of Animal Biology of the UMA Pascual Anaya, who has coordinated the research.

Thus, this study, which has taken almost a decade, has been carried out by an international consortium that includes more than 30 institutions from Spain, United Kingdom, Japan, China, Italy, Norway and the United States, including the University of Tokyo, the Japan research institute RIKEN, the Chinese Academy of Science and the Centre for Genomic Regulation in Barcelona, among others.

Ecological link

The myxini or ‘hagfish’ are a group of animals that inhabit deep ocean areas. Known for the amount of mucosa they release when they feel threatened –a focus of research of cosmetic companies– and, also, for their role as an ecological link in the seabed –since they are scavengers and are responsible for eliminating, among other things, the corpses of whales that end up at the bottom of the sea after dying–; hitherto their genome had not been sequenced due to its complexity, since they are composed of a large number of microchromosomes, which, in turn, are composed of repetitive sequences. This is in addition to the difficulty of accessing biological material.

“Besides, these microchromosomes are lost during the development of the animal, so that only the genital organs maintain a whole genome,” says Juan Pascual Anaya.

Genome duplications

To be more specific, for this study, in collaboration with the Chinese Academy of Science, the genome that has been sequenced is that of the Eptatretus burgeri, which lives in the Pacific, on the coasts of East Asia. To achieve this, the researchers generated data up to 400 times the size of its genome, using advanced techniques –Hi-C– of chromosomal proximity and managing to assemble it at chromosome level.

“This is important because it allowed us to compare, for example, the order of genes between this and the rest of vertebrates, including sharks and humans, and, thus, solve one of the most important open debates in genomic evolution: the number of genome duplications, and when these occurred during the origin of the different vertebrate lineages,” says the UMA scientist, who adds that thanks to this we now know that the common ancestor of all vertebrates derived from a species which genome was completely duplicated once.

Later, according to Pascual Anaya, the lineages that gave rise to modern mandibular and non-mandibular vertebrates separated, and each of these re-multiplied its genome independently: while the former, which include humans, duplicated it, the latter tripled it.

Evolutionary impact

An analysis of the functionality of genomes, based on extremely rare samples of myxini embryos, carried out in the prestigious laboratory of Professor Shigeru Kuratani of RIKEN; and a study on the possible impact of genome duplications on each vertebrate, developed together with the Professor at the University of Bristol and member of the Royal Society Phil Donoghue, complete this multidisciplinary research that is key to understanding the evolutionary history of vertebrates, since it provides perspectives on the genomic events that, probably, drove the appearance of important characteristics of vertebrates, such as brain structure, sensory organs or neural crest cells, among them, an increase in regulatory complexity, that is, a greater number of switches that turn genes on/off.

Juan Pascual Anaya is a scientist of the Department of Animal Biology of the University of Malaga. He studies the evolution of innovative structures that appear in different animal lineages, mainly vertebrates, for example, blood cells and the process by which they are produced, as well as other structures such as the origin of legs, hands or jaws.

He holds a degree in Biology from the University of Malaga and a PhD in Genetics from the University of Barcelona (2010). He held a postdoctoral position for 5 years, until 2015, at the RIKEN center in Japan, in the laboratory of Professor Shigeru Kuratani, where he became independent as a Permanent Scientific Researcher until 2021, year in which he returned to the UMA as a senior researcher of the ‘Beatriz Galindo’ grant program.

To be more specific, for this study, in collaboration with the Chinese Academy of Science, the genome that has been sequenced is that of the Eptatretus burgeri, which lives in the Pacific, on the coasts of East Asia. To achieve this, the researchers generated data up to 400 times the size of its genome, using advanced techniques –Hi-C– of chromosomal proximity and managing to assemble it at chromosome level.


An international scientific team made up of more than 40 authors from seven different countries, led by the researcher at the University of Malaga Juan Pascual Anaya, has managed to sequence the first genome of the myxini –also known as ‘hagfish’–, the only large group of vertebrates for which there was no reference genome of any of its species yet.

An international scientific team made up of more than 40 authors from seven different countries, led by the researcher at the University of Malaga Juan Pascual Anaya, has managed to sequence the first genome of the myxini –also known as ‘hagfish’–, the only large group of vertebrates for which there was no reference genome of any of its species yet.

CREDIT

University of Malaga








No One Is Prepared for Hagfish Slime

It expands by 10,000 times in a fraction of a second, it’s 100,000 times softer than Jell-O, and it fends off sharks and Priuses alike.
A car is covered in hagfish, and slime, after an accident on Highway 101. (Reuters)

ATLANTIC
JANUARY 23, 2019

At first glance, the hagfish—a sinuous, tubular animal with pink-grey skin and a paddle-shaped tail—looks very much like an eel. Naturalists can tell the two apart because hagfish, unlike other fish, lack backbones (and, also, jaws). For everyone else, there’s an even easier method. “Look at the hand holding the fish,” the marine biologist Andrew Thaler once noted. “Is it completely covered in slime? Then, it’s a hagfish.”

Hagfish produce slime the way humans produce opinions—readily, swiftly, defensively, and prodigiously. They slime when attacked or simply when stressed. On July 14, 2017, a truck full of hagfish overturned on an Oregon highway. The animals were destined for South Korea, where they are eaten as a delicacy, but instead, they were strewn across a stretch of Highway 101, covering the road (and at least one unfortunate car) in slime.

Typically, a hagfish will release less than a teaspoon of gunk from the 100 or so slime glands that line its flanks. And in less than half a second, that little amount will expand by 10,000 times—enough to fill a sizable bucket. Reach in, and every move of your hand will drag the water with it. “It doesn’t feel like much at first, as if a spider has built a web underwater,” says Douglas Fudge of Chapman University. But try to lift your hand out, and it’s as if the bucket’s contents are now attached to you.

The slime looks revolting, but it’s also one of nature’s more wondrous substances, unlike anything else that’s been concocted by either evolution or engineers. Fudge, who has been studying its properties for two decades, says that when people first touch it, they are invariably surprised. “It looks like a bunch of mucus that someone just sneezed out of their nose,” he says. “That’s not at all what it’s like.”

For a start, it’s not sticky. If there wasn’t so damn much of it, you’d be able to wipe it off your skin with ease. The hagfish themselves scrape the slime off their skin by tying a knot in their bodies and sliding it from head to tail.

The slime also “has a very strange sensation of not quite being there,” says Fudge. It consists of two main components—mucus and protein threads. The threads spread out and entangle one another, creating a fast-expanding net that traps both mucus and water. Astonishingly, to create a liter of slime, a hagfish has to release only 40 milligrams of mucus and protein—1,000 times less dry material than human saliva contains. That’s why the slime, though strong and elastic enough to coat a hand, feels so incorporeal.

Indeed, it’s one of the softest materials ever measured. “Jell-O is between 10,000 and 100,000 times stiffer than hagfish slime,” says Randy Ewoldt from the University of Illinois at Urbana-Champaign, who had to invent new methods for assessing the substance’s properties after conventional instruments failed to cope with its nature. “When you see it in a bucket, it almost still looks like water. Only when you stick your hand in and pick it up do you find that it’s a coherent thing.”

The proteins threads that give the slime cohesion are incredible in their own right. Each is one-100th the width of a human hair, but can stretch for four to six inches. And within the slime glands, each thread is coiled like a ball of yarn within its own tiny cell—a feat akin to stuffing a kilometer of Christmas lights into a shoebox without a single knot or tangle. No one knows how the hagfish achieves this miracle of packaging, but Fudge just got a grant to test one idea. He thinks that the thread cells use their nuclei—the DNA-containing structures at their core—like a spindle, turning them to wind the growing protein threads into a single continuous loop.
A microscope image of a hagfish’s coiled slime thread (Courtesy of Douglas Fudge)

Once these cells are expelled from the slime glands, they rupture, releasing the threads within them. Ewoldt’s colleague Gaurav Chaudhury found that despite their length, the threads can fully unspool in a fraction of a second. The pull of flowing water is enough to unwind them. But the process is even quicker if the loose end snags on a surface, like another thread, or a predator’s mouth.

Being extremely soft, the slime is very good at filling crevices, and scientists had long assumed that hagfish use it to clog the gills of would-be predators. That hypothesis was only confirmed in 2011, when Vincent Zintzen from the Museum of New Zealand Te Papa Tongarewa finally captured footage of hagfish sliming conger eels, wreckfish, and more. Even a shark was forced to retreat, visibly gagging on the cloud of slime in its jaws.

“We were blown away by those videos,” Fudge says, “but when we really looked carefully, we noticed that the slime is released after the hagfish is bitten.” So how does the animal survive that initial attack? His colleague Sarah Boggett showed that the answer lies in their skin. It’s exceptionally loose, and attaches to the rest of the body at only a few places. It’s also very flaccid: You could inject a hagfish with an extra 40 percent of its body volume without stretching the skin. The animal is effectively wearing a set of extremely loose pajamas, Fudge says. If a shark bites down, “the body sort of squishes out of the way.”

That ability makes hagfish not only hard to bite, but also hard to defend against. Calli Freedman, another member of Fudge’s team, showed that these animals can wriggle through slits less than half the width of their bodies. In the wild, they use that ability to great effect. They can hunt live fish by pulling them out of sandy burrows. And if disturbed by predators, they can dive into the nearest nook they find. Perhaps that’s why, in 2013, the Italian researcher Daniela Silvia Pace spotted a bottlenose dolphin with a hagfish stuck in its blowhole.

More commonly, these creatures burrow into dead or dying animals, in search of flesh to scavenge. They can’t bite; instead, they rasp away at carcasses with a plate of toothy cartilage in their mouths. The same traveling knots they use to de-slime themselves also help them eat. They grab into a cadaver, then move a knot from tail to head, using the leverage to yank out mouthfuls of meat. They can also eat by simply sitting inside a corpse, and absorbing nutrients directly through their skin and gills. The entire hagfish is effectively a large gut, and even that is understating matters: Their skin is actually more efficient at absorbing nutrients than their own intestines.

Hagfish on display at a seafood market (Elizabeth Beard / Getty)

Hagfish are so thoroughly odd that biologists have struggled to clearly work out how they’re related to other fish, and to the other backboned vertebrates. Based on their simple anatomy, many researchers billed the creatures as primitive precursors to vertebrates—an intermediate form that existed before the evolution of jaws and spinal columns.

But a new fossil called Tethymyxine complicates that story. Hailing from a Lebanese quarry, and purchased by researchers at a fossil show in Tucson, Arizona, the Cretaceous-age creature is clearly a hagfish. It has a raspy cartilage plate in its mouth, slime glands dotting its flanks, and even chemicals within those glands that match the composition of modern slime. By comparing Tethymyxine to other hagfish, Tetsuto Miyashita from the University of Chicago concluded that these creatures (along with another group of jawless fish, the lampreys) are not precursors to vertebrates, but actual vertebrates themselves.

Such work is always contentious, but it fits with the results of genetic studies. If it’s right, then hagfish aren’t primitive evolutionary throwbacks at all. Instead, they represent a lineage of vertebrates that diverged from all the others about 550 million years ago, and lost several traits such as complex eyes, taste buds, scales, and perhaps even bones. Maybe those losses were adaptations to a life spent infiltrating carcasses in the dark, deep ocean, much like their flaccid, nutrient-absorbing skins are. “Hagfishes might look primitive; they’re actually very specialized,” Miyashita adds.

Their signature slime might have also evolved as a result of that lifestyle, as a way of fending off predators that were competing for cadavers. “Everything about hagfish is weird,” says Fudge, “but it all kind of fits.”


Ed Yong is a former staff writer at The Atlantic. He won the Pulitzer Prize for Explanatory Reporting for his coverage of the COVID-19 pandemic.

Friday, February 26, 2021

New research on hagfish provides insight into evolutionary origin of the eye

U of A biologists studying hagfish eyes uncover unexpected similarities to those of other vertebrates, including humans.

UNIVERSITY OF ALBERTA

Research News

IMAGE

IMAGE: AN ADULT HAGFISH IN A CONTAINER FILLED WITH SEA WATER. NEW U OF A RESEARCH REVEALS UNEXPECTED SIMILARITIES BETWEEN THE EYES OF HAGFISH AND THOSE OF OTHER VERTEBRATES INCLUDING HUMANS,... view more 

CREDIT: RYAN WAYNE

The answer to the age-old mystery of the evolutionary origins of vertebrate eyes may lie in hagfish, according to a new study by biologists at the University of Alberta.

"Hagfish eyes can help us understand the origins of human vision by expanding our understanding of the early steps in vertebrate eye evolution," explained lead author Emily Dong, who conducted the research during her graduate studies with Ted Allison, a professor in the Faculty of Science and member of the U of A's Neuroscience and Mental Health Institute. "Our findings solidify the hagfish's place among vertebrates and open the door to further research to uncover the finer details of their visual system."

For years, hagfish eyes were thought to be different from those of vertebrates--so the researchers were surprised to discover hagfish eyes contain many of the same features. These include neurons that connect light-sensitive photoreceptors to ganglion cells, continued growth of the eye late into adulthood, and a hidden layer of support cells that are prominent in other vertebrates and are key to photoreceptor function.

"This is important because it broadens the picture of early vertebrate eye evolution," explained Dong. "The fossil record can only provide us limited information, because soft tissues like eyes do not preserve well. And so we look to living members of these early lineages, such as the hagfish."

Hagfish are the most ancient line of vertebrates still living today, representing vertebrates before the evolutionary appearance of the jaw or paired fins, such as limbs. As a result, studying hagfish provides important information about early evolution in vertebrates, setting the foundation for what scientists can learn by studying other animal models such as zebrafish and mice.

"The data shed light on the confusing and dimly lit evolutionary origins of the vertebrate eye," added Allison, professor in the Department of Biological Sciences and Dong's master's supervisor.

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Dong is now a PhD student at the University of Toronto. The research was funded by the Natural Sciences and Engineering Research Council of Canada and the Bamfield Marine Sciences Centre.

The study, "Vertebrate features revealed in the rudimentary eye of the Pacific hagfish (Eptatretus stoutii)," was published in Proceedings of the Royal Society B.

Sunday, January 11, 2026

 

Revealing the diversity of olfactory receptors in hagfish and its implications for early vertebrate evolution




University of Tsukuba
Inshore hagfish (Eptatretus burgeri) 

image: 

Inshore hagfish (Eptatretus burgeri)

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Credit: Tsukuru Maeda





Tsukuba, Japan—Animals, including humans, rely on their sense of smell to locate food, avoid predators, and communicate. This sensory ability depends on specialized receptor proteins. In vertebrates, four major receptor families mediate olfaction; these include olfactory receptors (ORs), vomeronasal type 1 receptors (V1Rs), vomeronasal type 2 receptors (V2Rs), and trace amine-associated receptors (TAARs). However, the evolutionary origin and early diversification patterns of these receptor classes remain poorly understood.

In this study, University of Tsukuba researchers examined the hagfish genome for genes linked to ORs. In total, they identified 48 OR genes, 2 V1R genes, a surprisingly large set of 135 V2R genes, and no TAAR gene. Subsequent expression analyses confirmed that most of these genes were actively expressed in the olfactory organ, indicating that they may play functional roles in smell perception. Notably, the presence of true V2Rs in hagfish overturns the long-standing assumption that these receptors evolved only in jawed vertebrates. Conversely, the results of this study suggest that functional V2Rs were already present in the common ancestor of all vertebrates and that they subsequently diversified in a lineage-specific manner. Overall, this discovery provides critical insight into the evolution of vertebrate olfaction and underscores the importance of hagfish as a model for reconstructing the sensory biology of early vertebrates.

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This work was supported by the Grant-in-Aid for the Japan Society for the Promotion of Science (JSPS; Grant Numbers JP20K15855, JP22K15164, JP24K09556, and JP24H01538 to D.G.S, and JP19K16178 to Y.Y.) and by the Sasakawa Scientific Research Grant from The Japan Science Society (Grant Number 2023-4098 to H.K.).

 

Original Paper

Title of original paper:
Hagfish olfactory repertoire illuminates lineage-specific diversification of olfaction in basal vertebrates

Journal:
iScience

DOI:
10.1016/j.isci.2025.114118

Correspondence

Assistant Professor SUZUKI, Daichi G.
Institute of Life and Environmental Sciences, University of Tsukuba

KARIYAYAMA, Hirofumi
(Current position: Visiting Researcher of the RIKEN Center for Biosystems Dynamics Research (BDR))
Graduate School of Comprehensive Human Sciences, University of Tsukuba

Assistant Professor YAMAGUCHI, Yoko
Institute of Agricultural and Life Sciences, Academic Assembly, Shimane University

Related Link

Institute of Life and Environmental Sciences

Monday, October 16, 2023

 

Marine "Biomimetics" Could Be the Blue Economy's Next Big Hit

Humpback whale calf, Tonga, 2015 (GRID-Arendal / Glenn Edney / CC BY NC SA 2.0) 
Humpback whale calf, Tonga, 2015. The bumps on the whale's head reduce drag and have inspired many engineered applications (GRID-Arendal / Glenn Edney / CC BY NC SA 2.0) 

PUBLISHED OCT 9, 2023 2:32 PM BY CHINA DIALOGUE OCEAN

 

[By Emma Bryce]

Deep in the Pacific Ocean, a strange, diaphanous balloon drifts by. Inside, tunnels and chambers coil like a miniature floating Guggenheim around the talented architect within: a tadpole-like creature called a larvacean. Incredibly, the organism has crafted this entire structure out of mucus.

“This is an animal without legs, arms, or eyes, and it secretes this complex house of mucus around itself,” explains Joost Daniels, a research engineer. Daniels is part of a team at the Monterey Bay Aquarium Research Institute that has 3D modelled these structures, which they’ve christened ‘snot palaces’. Their modelling work, carried out at the institute’s Bioinspiration Lab, revealed how the larvacean uses its tail to pump detritus-filled water through the passageways of the snot palace, using it like a filter to snag food.

The magnificent structure could inspire inventions on land. “This could be very interesting for very efficient vehicle propulsion or other pumping systems. There are lots of medical applications as well,” says Daniels.

Such innovations belong to the growing collection of ‘biomimetic’ products – which mimic the form, structure, or function of organisms. Taking inspiration from nature isn’t new, but marine biomimetics is relatively nascent partly because just 5% of the ocean has been explored. And yet, “the ocean is where all life started, and where a lot of things have evolved from,” says Daniels, which creates huge potential for discovery in its vast depths.

Researchers think that, as discoveries related to marine biomimetics grow, they could contribute billions to the economy annually, with applications across diverse industries including energy, transport, pharmaceuticals, and deep-sea exploration. This could also serve as a more sustainable source of marine revenue than industries like deep-sea mining, believes Robert Blasiak, a researcher in the sustainable management of ocean resources at the Stockholm Resilience Centre. “I think it gives a bit of a different flavour to how we can explore this ‘final frontier’,” he says.

Wild inventions

It was Blasiak’s personal enthusiasm for the subject that drove him to start cataloguing marine biomimetic inventions, which together with his colleagues he described in a 2022 research article. The paper explored a glittering array of innovations – some under development, and several already on the market.

One of them takes inspiration from the tapering fins of the humpback whale. These leviathans glide effortlessly through the water, despite having knobbly fins that look like they would slow them down. In the early 2000s, engineers discovered that those bumps, called tubercles, actually generate lift, reducing drag in the water. This has since inspired the design of bumpy fan blades and surfboard fins, as well as patents to apply tubercles to wind farms.

Another source of inspiration is shark skin, which bristles with billions of microscopic scales called denticles. Arranged in a diamond pattern and imprinted with peaks and troughs, these channel water and allow the animals to glide seamlessly through it. This structure has inspired new car tyres that aim to reduce the risk of aquaplaning, and materials for aircraft that streamline airflow and cut carbon emissions by 1.1%. Sharks aren’t coated in algae and barnacles, Blasiak explains, because their “skin is very hard for stuff to settle on, to actually stick to.” Materials scientists have replicated this microscopic architecture in antibacterial surfaces for hospitals, and antifouling materials to protect ships from organisms that may latch on to their hulls, affecting their speed and seaworthiness.

Meanwhile, animals such as the ram’s horn squid have inspired better ways to explore the ocean itself. The creature controls its buoyancy with the help of an internal coil-shaped shell containing gas-filled compartments. As the squid grows, explains Blasiak, more of these compartments appear. Most famously, these inspired the submersible used by filmmaker James Cameron to travel to the bottom of the Mariana Trench.

In 2021, scientists successfully mimicked the jelly-like structure of the deep sea snailfish to create a remotely operated soft robot, made of flexible materials, capable of withstanding the crushing ocean pressure at depths of 11,000 metres.

Many more biomimetic inventions are in the works. Materials scientists are developing hyper-strong materials for buildings based on the chitin structure of the mantis shrimp’s crack-resistant club. Others have found unlikely fashion inspiration in the slime-producing hagfish, whose goo contains thousands of silken but powerful strands that could inspire next-generation textiles. Elsewhere, researchers have patented the unique water-repelling proteins in byssus threads – the strong filaments that tether mussels to rocks – which could lead to corrosion-resistant steel for ships.

Big money in the blue economy

Marine biomimetics could generate significant revenue through novel products, designs, patents, and by reducing maintenance and materials costs in several industries, Blasiak believes. One significant area is shipping, which spends US$30 billion a year dealing with the added fuel and cleaning costs of biofouling by barnacles and other creatures. Biomimetic antifoulants, such as sharkskin-inspired coatings, could offset this expense, while also supplying the marine coatings industry that is worth nearly $15 billion.

According to Blasiak’s research, biomimetics could add billions to the tissue-engineering industry, which generated sales of $9 billion in 2017, with corals and sponges becoming increasingly important ingredients. Underwater robotics, meanwhile, is projected to reach almost $7 billion by 2025. And, in 2010, researchers estimate that cancer drugs derived from yet-to-be-discovered compounds in marine organisms could be worth between $0.5 trillion and $5.7 trillion.

Yet this huge potential is being overlooked, Blasiak believes. “All these conceptualisations of the ocean economy, they’re all looking at fisheries, cruise tourism, containerships, mining of aggregates – but they’re never looking at biomimetics,” he says. In his view, not only can marine biomimetics contribute significantly to economic growth, it also aligns with the emerging ‘blue economy’ – growth that’s derived from the sustainable use of the ocean’s resources.

Sharing the ocean’s treasures

But there are growing concerns about how to share these benefits fairly. Blasiak has found that 98% of the several thousand patent applications related to marine genetic resources belong to institutions in just 10 countries. Typically, ocean discoveries are made by a small number of wealthy nations, often off the shores of less wealthy nations.

The highly productive seas surrounding the Caribbean are one example, says Judith Gobin, a professor of marine biology at the University of the West Indies in Trinidad and Tobago. “If you look [at] the literature, you will see [that] quite a few commercial drugs, already on the market, have been found from Caribbean sponges [and] organisms,” she says. “And a lot of it, we in the Caribbean weren’t even aware of.” She describes some of these scientific expeditions as “ships passing in the night,” explaining that even though they were legal, they have failed to share their benefits.

The inequality has only grown as wealthier nations have been able to advance into the little-explored deep sea that often falls beyond the jurisdiction of any one nation. But Gobin is hopeful that the recently agreed High Seas Treaty will start to even out this playing field. She explains that the historic treaty, formally adopted in June this year, includes requirements to share the scientific and financial benefits of any marine genetic resources discovered in the high seas. Gobin participated in the treaty negotiations as an adviser with CARICOM, an intergovernmental organisation that represents the interests of Caribbean countries.

More important than financial benefits is the treaty’s hard-won obligation for countries to share resources, she says. Ideally, this means that future marine expeditions led by wealthy nations will be treated as an opportunity to bring scientists from developing nations on board, to share training, technologies, and expertise. “Let’s get the local scientists involved, and then let’s build the capacity,” Gobin says.

According to Blasiak, it’s this spirit of shared curiosity and discovery that drives marine biomimetics in the first place, and which he believes could turn it into a force for the good of the ocean. “I think that one of the most attractive things about biomimetics is that it first requires you to look at the natural world, to interact with it, be curious about it, and try to understand it better,” he says. “That’s the starting point for caring about the ocean, and then for thinking we should be stewards of it.”

Emma Bryce is a freelance journalist who covers stories focused on the environment, conservation and climate change. 

This article appears courtesy of China Dialogue Ocean and may be found in its original form here

Top image: Humpback whale calf, Tonga, 2015 (GRID-Arendal / Glenn Edney / CC BY NC SA 2.0ww.grida.no/resources/3544