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Olá da Madeira! The island – a green paradise in the middle of the Atlantic Ocean – has been home to us for almost three months already. How the time flies!

We are Lara and Karo, one of 8 teams that currently conduct experiments all over the world as part of this year’s GAME project. Lara is a Marine Biology student currently enrolled at the University of Rostock and she is collecting data for her master thesis within the project. When she heard about GAME from her professor, she knew she had to be part of it! Karo is studying Biological Oceanography in Kiel. She found her passion for marine sciences quite recently and has never lived close to the ocean on beforehand. It was a dream of them both to join this project!

This year’s aim is – like in the previous years since 2021 – to investigate the effects of artificial light at night (or ALAN for short). We want to see how this phenomenon affects macroalgae in their ability to photosynthesize, grow and defend themselves against grazers. After an intense planning phase in March, during which we decided on the design of our experiments, we were more than glad to leave cold and grey northern Germany behind and escape into the sunny, subtropical climate of Madeira.

The city lights of Funchal are illuminating the coast at night. Photo: Team Madeira

Finding accommodation was not easy, but in the end, we found a nice flat in the capital city Funchal with (almost) an ocean view! More than this, we have a balcony where we’ve enjoyed many lengthy weekend breakfasts.

We had an enjoyable first week when we settled into our flat, scouted the city and tried to figure out the bus system, which proved to be kind of complicated, since there are so many different bus companies here. One thing we learned very quickly, though: walking on this island requires strong calves. Madeira is hills…hills…and more hills. This is why you hardly ever see local people walking here – sometimes you get funny looks when you are doing a typical German “Spaziergang” (which is more like a hike over here), and you really have to watch out not to get run over by a bus or a car.

Then, we finally met the team of the Marine and Environmental Science Centre “MARE”. In our first meeting, we sat together with our supervisors (who are all former GAME participants!) and discussed how we could make our experiments here successful. Everyone was excited and motivated to get our project started!

Not long after, we made our first trip to the laboratory where we are conducting our experiments together. It is located in Quinta do Lorde, a place on the easternmost part of the island. It is close to the peninsula “Ponta de São Lourenço” which offers stunning views over the rugged coastline of the volcanic island. This part of the island is very dry and it almost feels like you have stepped into a desert – quite the contrast to the rest of Madeira, which is a lush, green paradise. 

Could be on Mars…or Ponta de São Lourenço in the east of Madeira…, Photo: Team Madeira
… definitely feels very different from the lush, green forests of the rest of Madeira. Photo: Team Madeira
The marina in Quinta do Lorde, where the lab is located. Photo: Team Madeira

It is also the perfect spot for investigating ALAN, since it is very isolated and therefore mostly uninfluenced by nighttime illumination. Hence, the marine life here is not already adapted to light at night. The only downgrade is: the lab is located quite far away from Funchal, where we live. Most days, we have to take a bus that takes the scenic route and drives 1.5 hours along the coast, up and down the hills. At least we are rewarded with pretty ocean views during the drive – or we go for a little nap, especially after a long day in the lab. Thankfully, we can sometimes catch a ride in the car with our supervisors.

In the first weeks, we worked hard to build up our experimental set-up. Thanks to the great work of former GAME students, our lab is already equipped with most of the materials that we need, so we could quickly set up a flow-through system to supply running water to our algae. But we celebrated too soon: The complete water system of the lab had to be cleaned with bleach due to some pesky epiphytic growth and that meant that we had to re-do the flow through system again from scratch. We patiently cut tubes, and more tubes and connected them with little plastic suppliers, which let out filtered seawater to each of our 72 experimental tanks.

Lara adjusting the flow-through system and Karo and Patrício connecting the lights. Photo: Team Madeira

To give our algae as much light as possible, so that they are able to happily photosynthesize, we decided to order more LED lamps. One thing we did not anticipate: Madeira is located in the middle of the Atlantic Ocean, around 1000 km from the European coastline (the African coast is actually closer!), so equipment can take a loooong time to arrive. We were lucky that our lamps arrived “only” 3 weeks later, but already we faced the next challenge: connecting our lights to the control unit, with which we want to regulate the light intensity that our algae will be exposed to, proved to be more difficult than we had previously thought. However, with the help of the lab technician Patrício we quickly found a solution!

Finally, our finished setup! Photo: Team Madeira

When we weren’t diligently building our set-up, we spent our days snorkelling in different places on the south coast of the island, looking for algae “candidates” that we could use in our experiments. Easier said than done, because the waters around Madeira are depleted in nutrients and large macroalgae are rare to find. We quickly decided on using Halopteris scoparia, a brown macroalgae that is quite abundant in the upper subtidal and therefore possible for us to collect while snorkelling. Another (particularly interesting) candidate is Rugulopteryx okamurae, an invasive brown alga, that has first been introduced on the north coast of Madeira in 2021 and since then spread rapidly – it is even growing on the pontoons in the marina outside our lab. It could be especially interesting to investigate how this species reacts to ALAN in comparison to native algae.

A photo from snorkelling – the green-looking algae are Rugulopteryx individuals, the reddish alga is Asparagopsis (which was sadly not a fit for our experiment, because they are not seasonal anymore and bleached quickly after we arrived on the island). Photo: Team Madeira

Since we want to investigate how ALAN affects the defence capacity of our algae, we also had to find suitable grazers (=algae eaters). Our options were less than ideal: Should we use sea urchins (even though they are very hungry and consume our algae in too large amounts) or intertidal snails (even though this makes less sense ecologically, because our algae come from the subtidal). In the end, we decided on the sea urchin Paracentrotus lividus, which we can easily collect in the tide pools next to our lab. Did we say easy? – To get the hang of how to sample these little algae eaters took some blood, sweat and tears. Equipped with forks and buckets; after waiting for low tide to arrive, we wade into the tide pools and try to gently (or not so gently) persuade our sea urchins to come out of the holes in the rock that they like to sit in. We always take good care not to injure or stress them too much, but some unfortunately have already met their fate.

Our grazer Paracentrotus lividus: Sea urchins like to put on little hats to protect themselves. Photo: Team Madeira
The tide pools near our lab. Photo: Team Madeira

Before we could start with the main experiments, we had to test a few things. For instance, how much and when the sea urchins eat and how much the algae photosynthesize. To find this out, we carried out some pilot studies – more or less successfully. During one of our pilot studies all our sea urchins mysteriously died, probably after some contamination[LM1] [LH2]  of the water. In addition to this, our method for measuring the oxygen production initially did not work, because the oxygen values we measured did not stabilize and photosynthesized waaaay too slowly despite looking perfectly healthy. After many hours of trial and error, we fortunately found a way that should allow us to accurately assess the oxygen evolution. For this[LM3] , we increased the light intensity to help the algae photosynthesize more quickly and also got a multi-position magnetic stirrer where we can put multiple of our containers with algae on simultaneously. A little magnetic bar keeps the water in the containers in constant motion, resulting in more stable oxygen measurements.

The magnetic stirrer with our containers on it – under the green mesh a magnetic bar is constantly stirring the water. Photo: Team Madeira

Furthermore, we have another nice tool available here. It is a PAM, which is short for Pulse Amplitude Modulation. Behind this rather complicated name lies a technology with which we can assess how well our algae are absorbing sunlight for photosynthesis and ultimately determine their health status. Because no one in the institute had used the device before, we had to do a lot of headache-inducing reading (the 200-page manual is not easy to understand) and carry out some test runs to get prepared for the measurements. Our weekly meetings with the other GAME participants became crucial for discussing challenges and brainstorming solutions together – so far this project has been a huge learning curve for the both of us.

The best part of a day in the lab is cuddling Quintinha, the lab cat. Photo: Team Madeira

Our lunch breaks we share with the lizards. Fun fact: there are more lizards than mice on Madeira! They are called Madeira lizards (Teira dugesii) and they are endemic to some of the Macaronesian islands. They are very curious creatures – especially when we unpack our food. They sometimes even like to jump on our feet, but you have to watch out that they don’t crawl inside your backpack, and you accidentally take home a new pet.

A lizard sharing our lunch with us. Photo: Team Madeira

When we are not in the lab, we also know how to have fun (not that being in the lab is not fun). Madeira is an island full of amazing places and activities, and it’s a hiker’s paradise! There are a lot of different routes to explore, very famous are “levada” walks here. Levadas are old, narrow water channels that wind through the mountains. They were constructed to carry water from the misty mountains down to the drier parts of the island to water the crops of the farmers. You can walk along these levadas and enjoy the views over the island!

The path along the levada das 25 fontes. Photo: Team Madeira

Besides doing a lot of hiking and training our calves, we have spotted some dolphins, explored different beaches, and even got swept up in the European Championships fever. Since Madeira is Cristiano Ronaldo’s birthplace, people here (young and old) are fans, and we joined the locals cheering for the Portuguese soccer team. Of course, we also had to try Madeira’s famous “poncha”, a traditional drink with rum and fresh fruit juice – typically lemon, orange, or – our favourite – maracuja. Another drink is Nikita, which is a mixture of pineapple juice, ice cream and beer. It tastes… well… interesting, as Karo’s face in the picture shows.

Karo trying Nikita. Photo: Team Madeira
During whale watching we saw spotted dolphins (Stenella frontalis)! Photo: Team Madeira

Madeira’s climate is perfect for growing all kinds of tropical fruits and other plants. What people keep as house plants in Germany, grows here in ditches next to the road, or in the size of trees – Monstera leaves get almost bigger than oneself! We also tried some fruits here that we have never seen before in our life. Our flatmate’s supervisor even has avocado trees in his backyard, which we sometimes get a share of – a luxury we will sorely miss back in Germany.

The local farmers market where both tourists and locals love to buy all kinds of fruits and vegetables. Photo: Team Madeira
Almost every garden has their own little banana plantation. Photo: Team Madeira
House plants like this Monstera can grow huuuge here. Photo: Team Madeira

Another thing we learned here: you can never trust the weather forecast. In Funchal, situated on the south coast, the weather is usually pretty dry and sunny. However, it’s a different story for the North coast, where it rains more frequently, and temperatures are cooler. But even here on the sunny south coast, you never know what to wear. You could burn under the African sun or in the next second freeze from the wind, especially in the evenings, when the sun is already down. The onion-principle (a German favourite) really proves best.

We have been really enjoying our time here so far and we are sure by the end of September we will not want to go back to Germany. We have finished the first experiment and are soon starting the second one, we are excited to see what happens!

Lights, Algae, Action! Researching light pollution in the middle of the Atlantic

Ocean Acidification

New Friends, New Addresses

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The JOIDES Resolution (JR) was a renowned, international, scientific research ship. It was home to over 190 expeditions, each sailing for 60 days at a time without docking. Scientists and crew members from all over the world met to discover Earth’s secrets through studying ocean cores. Every two months the JR would get a new crew, sailing to an entirely new place. This once in a lifetime experience forms special and unforgettable social connections.

Since working on the JR I’ve kept those connections strong with snail mail. I have always been an avid penpal, so meeting new friends means new addresses to send my letters and postcards to. Experiences like sailing on the JOIDES Resolution or participating in programs like OCEAN CORE Academy is one of the ways I’ve met people from all over the world.

Now that the JR is retired, there is no more scientific research drilling being done through the International Ocean Discovery Program (IODP). But, there is still plenty to learn from ocean cores, and plenty of people to meet through programs like OCEAN CORE Academy (OCA). OCA is an annual summer opportunity from the U.S. Scientific Support Program (USSSP) that hosts undergraduates interested in geoscience related careers. Students can apply to this program for a chance to research and study data recovered from cores originally brought up by the JR, now located at the Gulf Coast Repository (GCR) in College Station, Texas. Students also practice forms of science communication with the guide of mentors. As a science communicator and fan of snail mail, I ran a craft night teaching students how to make and send science-themed postcards.

Fig. 1) students using watercolor to paint onto 4 by 6 inch board paper, a photo of a thin section slide is in the background. Photo by Dr. Leah Joseph.

For this project, we based the cover image of the postcards off of rock thin section slides. These slides are a slice of a hard rock or mineral that’s been glued to a microscope slide, sanded to 0.03 millimeter thickness, and polished. Thin section slides are used to identify grain size, shape, color, and other physical properties. This helps scientists understand the textural relationships between the rocks and determine the origin or evolution of the parent rock. Thin sections can also be helpful for identifying minerals using cross polarized light (XPL). XPL reduces light reflection and glare, commonly used for sunglasses and professional photography, but in a polarizing microscope, XPL is used to create a dark field causing certain minerals to appear brighter and more visible. Different colors are associated with different minerals, and as the stage of the microscope rotates, light passes through the slide in unique ways aiding scientists with identification. Identifying minerals can help scientists in understanding more about where the rocks came from and how old they are. These thin sections are not only informative, but are incredibly beautiful, making unique and stunning postcard covers.

     

Fig. 2) Examples of thin section slides under a XPL microscope, bronzitite (left) and gabbro (right). Sourced from here.

After the OCA students finished their paintings, my home-made “post card” stamps go on the back, a stamp gets added, and they’re ready to be mailed out. Although most OCA participants this year were U.S. based, they came from all over, ranging from Staten Island to San Francisco to Arizona to Connecticut. In addition to one mentor from New Zealand!  For many of these students this was their first time traveling on their own, and their first time forming long-distance connections. With these scientific postcards, OCA students can stay connected by reminding each other of the science they learned together. My experience on the JR taught me great things about geological research, but it also gave me life long connections that I cherish. Although the JR is gone, its legacy lives on in our memories and the ways we stay connected with friends. I’m grateful to know that even without an international ship, I’m still able to add friends to my address book.

     

Fig. 3) Examples of participant made postcards

Written by Kellan Moss

New Friends, New Addresses

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Ocean Acidification

Color Traditions with Munsell Soil-Color Charts

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Fig. 1) an open page of the Munsell Soil-Color Chart book

The Munsell Color Chart has been the national standard and official color system for soil research in the U.S. since the 1930s. For nearly 100 years, geologists and soil scientists have taken these color chip pages into the field to better understand the Earth they are studying, so it comes as no surprise that it is the standard for recording ocean cores brought up by the JOIDES Resolution.

Upon first glance, these charts may look like a page of free paint sample strips you can find at your local hardware store, but they are critical to classifying sediment and understanding the environments they came from and can cost several hundred dollars. The Munsell Color System is a method of numerically describing colors. It specifies colors based on hue, value, and chroma and measures them in a three dimensional space. Hue refers to the dominant color of the soil, value is the lightness of the color (scaled 0-10; 0 being black and 10 being white), and chroma is the intensity or saturation of the color.

Fig. 2) A 3D model representation of the Munsell Color System

There are five primary hues, red, yellow, green, blue, and purple, and five intermediate hues, which are a combination of primary hues such as yellow-red (YR) or green-yellow (GY). The hue of a color is represented as a ring and as the rings go up and down a vertical axis, the value of the color changes. As the color moves horizontally from the vertical axis, chroma or saturation becomes stronger or weaker. A color is specified by listing the three numbers or letters for hue, value, and chroma in that order. In the soil color chart, these number letter combinations correspond with a color. For instance, in figure 1, a 7.5YR 5/6 is also called “strong brown” (seen on the left page, bottom right). The names of colors used in weekly expedition reports are not arbitrary or subjective, they are specific and can be easily and accurately charted by anyone with a Munsell Chart reading the report.

Useful or Just Tradition?

The Munsell Color System has limitations. There are a distinct number of samples and the spacing between colors are large, making it difficult to measure thresholds. This inspired new color measuring methods to develop like CIELAB. Read more about CIELAB and what it means here (blog post “Color Science and Ocean Cores”). Changes to the Munsell system were made, doubling the number of hues in Munsell’s original book from 20 to 40, but CIELAB was already on its way to mainstream.

However, it’s still true that Munsell has been the soil color standard for nearly 100 years. That’s 100 years of geological and earth science research using this method of recording color. If scientists were to change to a system like CIELAB, it would mean having to constantly convert units when comparing previous research. Scientists compare and reference previous work all the time. Comparing sediment core colors from different sites can help support their own scientific findings. So switching to a different color recording method would mean converting all previous research. But is that a good enough reason to stick to tradition?

CIELAB creates a standard observer, which is an averaging of color matching that helps set a base value for recordings. This helps create the most accurate color reading on something such as an ocean core. Using color charts opens up the possibility for disagreements as no two human eyes see colors the same. And this really happens! In 2024 while aboard the JOIDES Resolution, EXP401 sedimentologists held long discussions about shades of grey they were recording differently.

Fig. 3) Photos of “The Great Grey Debate” on EXP401 by Dr. Patty Standring

Machines can record accurately and consistently, so why not switch to CIELAB? Well, expensive machines that use CIELAB, like the Section Half Multi-Sensor Logger (SHMSL) take anywhere from seven minutes to hours, recording only one core at a time. When on a two month cruise, pulling up hundreds of meters of core, time is crucial. Cores dry out and potentially change color as they dry, so it’s important to record fresh colors.

The color of a core can tell scientists so much information so quickly.

“Gradual color changes helped us to identify where we saw facies changes on a larger scale. There were very obvious cyclical color changes at Site U1385 that helped establish that the cores preserved a really good orbitally-driven sediment record. Color differences are also really useful when looking at different grain sizes that help identify turbidites and other sedimentary structures, and burrows from bioturbating organisms,” (Standring)

It’s important that scientists record these fresh colors as quickly and efficiently as possible. Although debates about the color grey can happen, these color discussions and international collaborations are what scientific research is all about. After 100 years, Munsell will stay the golden standard, not because it’s what we’ve always done, but because it’s still the best.

Written by Kellan Moss

Thank you to Dr. Patty Standring and Natacha Fabregas for help with this research

Sources:

Berns, R. S. (2016). Color science and the visual arts a guide for conservators, curators, and the curious. Los Angeles Getty Conservation Institute.

EXP 401 Sedimentologists: Dr. Patty Standring ad Natacha Fabregas

Featured Image: MerlinOne Archive

Fig. 1 Image: Here

Fig. 2 Image: Here

Fig. 3 Images: Dr. Patty Standring from EXP401

Color Traditions with Munsell Soil-Color Charts

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Ribbegople, Rippenqualle or Comb Jelly: Whatever You Call Mnemiopsis leidyi, You Should Be Concerned

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In early July at Kerteminde, most of the individuals I observed were longer than 10 cm, including one close to 15 cm. Their size, and their timing, deserve immediate attention.

⚠ One out of many large speciments I got from Kerteminde (Javidpour, July 2026)

It does not matter whether you call it ribbegople in Danish, Rippenqualle in German or comb jelly in English. The species is the same: Mnemiopsis leidyi. And what I have observed in Kerteminde this summer should concern us. During our current summer field course at the Marine Research Centre, I have repeatedly seen unusually large individuals of M. leidyi around the pier. Most of the animals I observed were longer than 10 cm, even bigger than the one I photographed.

Yes, yes, a pier observation is not a formal population survey….I know. We still need systematic sampling to determine the abundance, distribution and size structure of the population. Nevertheless, the observation is striking because both the size of the animals and the timing of their appearance are unusual, said by someone who is studying this species for the last 20 years.

This is happening earlier than expected

In previous years, the maximum population size of M. leidyi generally occurred several weeks later, mainly during August and early September. Our previous research, including work based on daily sampling, showed a clear seasonal development of the population. The timing varies among years and is influenced by environmental conditions, including winter temperature. Temperature is particularly important because it strongly affects the metabolism of M. leidyi. At warmer temperatures, individuals use their carbon reserves much faster and therefore require more food to maintain themselves and grow. This year, however, the pattern appears to be different. We are seeing very large individuals already in early July. We do not yet know whether this is a local aggregation, an unusually early bloom, transport from another area, particularly favourable feeding conditions or a combination of these factors. But it is a signal that deserves attention.

What does it take to grow by one centimetre?

It is tempting to ask how much energy an individual needs to add one centimetre to its body. The answer is not straightforward because one centimetre of length is not a fixed amount of biomass. Growing from 5 to 6 cm is not the same as growing from 14 to 15 cm…OK? However, we can make a rough carbon-budget calculation using a published relationship between the length and body-carbon content of M. leidyi:

Body carbon in milligrams = 0.0017 × body length in millimetres²·⁰¹³⁸

According to this relationship, an individual measuring 10 cm contains approximately 18.1 mg of carbon. At 11 cm, it contains about 21.9 mg. Adding this single centimetre therefore represents an increase of approximately 3.8 mg of body carbon. If we assume that the animal assimilates approximately 40% of the carbon it consumes, it would need to ingest at least ~10 mg of prey carbon to produce this additional tissue. Using an approximate value of 1 micrograms of carbon for a small copepod, this would correspond to more than 10,000 copepods.

For an already large individual growing from 14 to 15 cm, the estimated increase is approximately 5.3 mg of body carbon. At the same assimilation efficiency, that would require at least 13.3 mg of prey carbon: the equivalent of roughly 15,000 small copepods.

These calculations are only rough, conservative estimates. They are not complete energy budgets. They do not include the food needed for respiration, movement, reproduction, mucus production, excretion or unsuccessful feeding. The real prey requirement would therefore be considerably higher. The important point is that an individual measuring 15 cm represents a substantial transfer of material from the surrounding planktonic food web into gelatinous biomass. One additional centimetre is not “just” one centimetre.

Our students are tracing the food web

The timing of these observations coincides with our summer field course. The students are now collecting M. leidyi, fish, other gelatinous organisms and potential prey for stable-isotope analysis. By comparing carbon and nitrogen isotope values, we hope to obtain a rough picture of the relationships within the local food web. Carbon isotopes can help us trace the original sources of the material entering the food web, while nitrogen isotopes can provide information about relative trophic position.

This will not give us a direct photograph of one organism eating another. Stable-isotope values represent assimilated food over time, and their interpretation depends on appropriate baselines and turnover rates. Nevertheless, combined with information about size, abundance, prey availability and experimental feeding, they can help us understand where M. leidyi is obtaining its biomass and which organisms may be affected. …In simple terms, we are trying to determine who might be eating whom, and where this unusually large population fits into the food web.

Competition with fish is only part of the problem

The concern is not limited to competition for zooplankton. Mnemiopsis leidyi consumes copepods and other small planktonic animals that are also important food for pelagic fish. When the ctenophores are abundant, they can therefore compete directly with fish for prey. Our experiments have also demonstrated that M. leidyi can potentially feed directly on the early life stages of fish. In the study by my previous PhD student, the ctenophores captured and digested Baltic herring yolk-sac larvae. Predation was related to ctenophore size and was not simply eliminated when alternative copepod prey were available. This means that M. leidyi may/can affect fish populations in two ways: by consuming the food needed by fish and by consuming fish eggs or larvae directly.

A recent study by Lucila Sobrero and colleagues in Argentina, within the native range of M. leidyi, found a similar pattern. Their experiments showed size-dependent predation on fish eggs and larvae. Larger ctenophores consumed more eggs. Some eggs were later regurgitated, but many were no longer viable, while fish larvae were retained and digested. These findings are particularly relevant to what we are observing in Kerteminde. The size of an individual is not merely an interesting measurement. It can influence what that individual is capable of capturing and how strongly it affects the surrounding ecosystem. A population consisting of fewer but much larger individuals may still exert substantial pressure on zooplankton, fish eggs and fish larvae.

We need to investigate use, not only control

For several years, I have tried to obtain funding to investigate innovative approaches to this invasive species.

Once M. leidyi is well established, we may not be able to control its regional spread or completely prevent its blooms. But that does not mean that we have no options. We should investigate whether at least part of this recurring biomass can be collected and converted into something useful.

This is not a proposal for a miracle solution. Any utilisation strategy would have to be tested carefully. It must not encourage the further spread of the species, create damaging bycatch or provide an economic incentive to maintain an invasive population. We also need to understand the environmental costs of collection, transport and processing.

But these are exactly the questions that research funding should allow us to answer.

So far, my attempts to secure support for this work have been unsuccessful. Funding agencies do not seem to sense the urgency of studying approaches whose benefits may not be immediate or easily visible. and EPAs do not have any resource to invest in this part. The contrast with events on land is striking. This week, the oak processionary moth, the so-called “larva from hell”, has attracted considerable attention in Odense. Its microscopic hairs can cause rashes and allergic reactions, residents have reported serious discomfort, and a kindergarten has reportedly had to close temporarily. Those concerns are real and deserve a response.

But the case also illustrates how differently we react to environmental threats.

When the impact appears visibly on human skin, the urgency is immediately understood. When ecological damage develops below the surface of the sea, in the form of disappearing zooplankton, altered food webs, consumed fish eggs or reduced larval survival, it is much easier to overlook.

Marine ecosystem changes are often gradual, underwater and largely invisible to the public. By the time their consequences become obvious, the opportunity for early and relatively inexpensive action may already have passed.

Concern does not mean panic

One photograph and a series of observations from one pier do not prove that an ecological crisis is underway. I am not suggesting that they do. But science should not have to wait for undeniable damage before investigation becomes urgent.

The unusually large M. leidyi appearing in Kerteminde this July give us an opportunity to act early. We need systematic monitoring of their abundance and size distribution. We need to measure the available prey field. We need to determine their trophic position and investigate possible consequences for fish recruitment. And we need to explore whether biomass that we may be unable to prevent could be collected and used responsibly.

Whatever language we use and whatever name we give it, the message is the same:

We should measure early, investigate early and support innovative solutions while the warning is still only a warning, not after it has become a crisis.

Relevant publications

Javidpour, J. et al. (2009). “Seasonal changes and population dynamics of the ctenophore Mnemiopsis leidyi after its first year of invasion in the Kiel Fjord, Western Baltic Sea.” Biological Invasions.

Javidpour, J. et al. (2020). “Cannibalism makes invasive comb jelly, Mnemiopsis leidyi, resilient to unfavourable conditions.” Communications Biology.

Stoltenberg, I. et al. (2024). “Predation on Baltic Sea yolk-sac herring larvae (Clupea harengus) by the invasive ctenophore Mnemiopsis leidyi.” Fisheries Research.

Sobrero, L. et al. (2025). “Predatory impact on ichthyoplankton by Mnemiopsis leidyi is size-dependent: an experimental approach.” Marine Ecology Progress Series.

Ribbegople, Rippenqualle or Comb Jelly: Whatever You Call Mnemiopsis leidyi, You Should Be Concerned

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