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Es beginnt der zweite Teil unserer Forschungsreise. Wir fahren im Moment Richtung Norden in die Labradorsee. Inzwischen ist es mit einer Lufttemperatur um 4°C richtig kalt geworden. Wir sind auf dem Weg zum 53. Breitengrad. Dort liegen fest verankerte Geräte, die zum Beispiel Temperatur, Salzgehalt, Sauerstoff und Strömungsgeschwindigkeiten messen können. Man kann sich das so vorstellen, dass die Messgeräte aufgereiht sind, wie an einer langen Perlenkette. An einem Ende der „Perlenkette“ befindet sich ein Anker, der alles an einer spezifischen Position festhält. Durch Schwimmkörper, die zwischen den Messgeräten positioniert sind, bekommt die ganze Kette Auftrieb und schwebt dadurch senkrecht in der Wassersäule. Diese sogenannten Verankerungen können 2-3 km lang sein und sind das erste Ziel unserer Reise.

Seit 1997 befinden sich Teile der Verankerungen schon an dieser Stelle in der Labradorsee und werden im Abstand von 2 Jahren kontrolliert. Die Position wurde aus gutem Grund gewählt. Die Labradorsee ist ein bedeutender Ort für die Zirkulation des gesamten Ozeans, denn hier befindet sich ein Ort an dem neues Tiefenwasser gebildet wird. Aufgrund von Dichteänderungen sinkt dabei sauerstoffreiches, kaltes und salzreiches Wasser ab. Die Stelle, an der sich die Verankerungen befinden ist besonders, da sich dort ein Knotenpunkt verschiedener Strömungen befindet. Alle dichten Wassermassen des Nordatlantiks kommen hier zusammen und bilden den westlichen Randstrom, der in der Tiefe Richtung Süden fließt. Durch die lange Messreihe ist es möglich Schwankungen in dieser Bildung der Wassermassen zu dokumentieren, was zum Beispiel Schlussfolgerungen über die Stärke des Golfstroms ermöglichen kann. So können auf lange Sicht potenzielle Auswirkungen des Klimawandels auf die Ozeanzirkulation abgeleitet werden.

Schwimmkörper treiben nach dem Auftauchen auf dem Wasser (Foto: Abed Hassoun)
Schwimmkörper aufgereiht an Deck (Foto: Abed Hassoun)
Das oberste Element wird seitlich am Schiff angenommen und zum Heck geführt, wo anschließend die ganze Kette in Empfang genommen wird. (Foto: Grete Boskamp)
Mit Hilfe von Winde und Kran werden die Schwimmkörper an Bord gebracht. (Foto: Grete Boskamp)

In den nächsten Tagen werden wir die Verankerungen aus dem Wasser holen, gegebenenfalls reparieren, die Daten aus den Messgeräten auslesen und alles am Ende wieder ins Wasser werfen. Dieser Prozess läuft eigentlich immer gleich ab. Zuerst wird vom Schiff aus ein akustisches Signal ins Wasser gesendet. Dieses Signal löst die Verbindung zwischen Anker und dem Kabel mit den Messgeräten. Die Verankerung fängt dann an, zur Wasseroberfläche aufzusteigen – das liegt an den zu Anfang bereits erwähnten Schwimmkörpern. Anschließend wird von der Brücke Ausschau gehalten, wo die Verankerung genau an die Oberfläche treibt. Dann wird alles Stück für Stück an Bord geholt, gesäubert und demontiert. Erst, wenn die Messgeräte wieder mit neuen Batterien bestückt und die Daten ausgelesen sind, wird alles wieder zusammengebaut und Stück für Stück wieder ins Wasser gelassen. Als allerletztes wird der Anker ins Wasser gesetzt. Er fällt zum Meeresboden und zieht die Verankerung unaufhaltsam mit nach unten.

Abhängig von der Länge, braucht man einige Stunden für diesen Prozess. Pro Tag werden im Idealfall 1-3 Verankerungen abgefertigt. Eine wichtige Rolle spielt bei dieser Arbeit das Wetter. Drei Dinge sind hierbei wichtig: gute Sichtbedingungen, möglichst wenig Welle und Tageslicht. Im Moment ist der Nebel unser größter Gegenspieler, doch meistens verzieht er sich den Tag über und stört uns nur noch, beim Sterne oder Sonnenuntergang beobachten.

Mooring works

The second part of our research journey begins. We are currently heading north to the Labrador Sea. In the meantime, it has become really cold with an air temperature around 4°C. We are on our way to the 53rd latitude. This is the location of permanently anchored measurement devices that can measure, for example, temperature, salinity, oxygen and flow velocities. One can imagine that the measuring instruments are lined up, as if on a long chain of beads. At one end of the “pearl chain” there is an anchor that holds everything in a specific position. With the help of floating devices positioned between the measuring instruments, the entire chain receives buoyancy and thus floats vertically in the water column. These so-called moorings can be 2-3 km long and are the first destination of our trip.

Since 1997, parts of the moorings have been located at this point in the Labrador Sea and are checked at intervals of 2 years. The position was chosen for good reason. The Labrador Sea is an important place for the circulation of the entire ocean, because here is a place where new deep water is formed. Due to changes in density, oxygen-rich, cold and salt-rich water sinks. The location where the moorings are located is special, since there is a junction of different currents. All the dense water masses of the North Atlantic come together here and form the deep western boundary current, which flows in depth southward. Due to the long series of measurements, it is possible to document fluctuations in this formation of the water masses, which can, for example, allow conclusions about the strength of the Gulf Stream. In this way, in the long term, potential effects of climate change on ocean circulation can be deduced.

Floating devices passing by on the surface (Foto: Abed Hassoun)
Floating devices on deck after recovery of the mooring. (Foto: Abed Hassoun)
The uppermost element is caught at the side of the ship and brought to the rear of the ship. (Foto: Grete Boskamp)
Floating devices are retrieved with a winch. (Foto: Grete Boskamp)

Over the next few days we will take the moorings out of the water, repair them if necessary, read the data from the measuring devices and finally throw everything back into the water. This process is usually always the same. First, an acoustic signal is sent into the water from the ship. This signal breaks the connection between the anchor and the cable with the measuring devices. The mooring then begins to rise to the water surface – this is due to the floats mentioned at the beginning. Then we look out from the bridge to see exactly where the mooring is floating to the surface. Then everything is brought on board piece by piece, cleaned and dismantled. Only when the measuring devices have been fitted with new batteries and the data has been read out will everything be reassembled and put back into the water piece by piece. The very last thing to do is to put the anchor in the water. It falls to the seabed and inexorably pulls the mooring down with it.

Depending on the length of the mooring, this process takes several hours. Ideally, 1-3 anchorings are completed per day. The weather plays an important role in this work. Three things are important here: good visibility, as little waves as possible and daylight. At the moment the fog is our biggest opponent, but it usually disappears during the day and only disturbs us when we are watching the stars or the sunset.

Verankerungsarbeit

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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