There is so much going on in the world of solar slugs! I came across a couple of nice videos, and thought I’d share.
A broad collection of European slug scientists has launched a project to sequence the genome of Elysia timida. That will be a wonderful resource for all of us who are interested in slug science. The video below provides an explanation of the motivation, along with excellent general information.
The video below does a great job of describing the biology of E. viridis, with some beautiful footage. Can you see the minor error? (Hint: what is it eating?)
Elysia and related sacoglossans are beautiful and interesting, but their use of stolen chloroplasts puts them in a class above your average green sea slug. How the slugs accomplish this, and what function it serves, are coming into focus very slowly.
It has been known for a long time that kleptoplasts remain alive and functional in many Elysia species, but the idea that they can rely on the chloroplasts for all of their energy needs (the “crawling leaves” hypothesis) appears to be wrong, or at least overly simple. The inadequacy of the crawling leaf theory got me thinking about a possible role for kleptoplasts as factories for making defensive chemicals. There was support in the literature (e.g., Trench et al., 1972; Ireland and Scheuer, 1975), and I was interested enough to organize a student journal club on chemical ecology, and prepare experiments to test the connection between kleptoplasty and predation in Bahia de los Angeles in summer 2018.
To introduce the students to the journal club format, and to some important Elysia concepts, I presented the following paper by Baumgartner, Pavia and Toth from PLoS One, published in 2015. The paper has restored some of my faith that kleptoplasty provides a substantial metabolic benefit to the host slug.
They performed a series of experiments to ask a straightforward question: Do kleptoplasts provide usable energy to E. viridis?
The main characters in Baumgartner et al., 2015. Codium (upper left), Cladophora (lower left), and Elysia viridis (right). Images of algae are from AglaeBase, and E. viridis is from Scottish Nudibranchs.
E. viridis‘ gets kleptoplasts from at least two of its natural food plants, Codium and Cladophora, and they differ in their viability in the slug. Chloroplasts from Codium are highly functional, whereas those from Cladophora do not function well after being eaten. This provides a natural experiment, in which one can compare the effects of light on the growth of slugs fed Codium (highly productive kleptoplasts) versus those fed Cladophora (little contribution from photosynthesis). Importantly, the slugs in these experiments are not starved, so the authors are looking at the effects of photosynthesis over and above the energy and nutrients gained from feeding.
They tested the following hypotheses:
E. viridis were divided into four groups: Those eating Codium,under high light (~100 μmol quanta m-2 s-1) or low light (~6 μmol quanta m-2 s-1); and those eating Cladophora in high or low light
In the first experiment, they examined the effect of illumination on growth of the slugs. Rather than simply looking at growth rate, they used a measure called Growth Efficiency (GE), which calculated the amount of growth of the slugs as a function of how much the slugs ate.
Step 1: calculate slug Growth Rate (GR) = (Mend-Mbefore)/t, where M = mass and t = time
Step 2: calculate Consumption Rate (CR). For this they needed to either measure the change in mass over time (Codium), or the number of damaged cells (Cladophora). They had to use two different measures because the structures of the two species of algae posed different challenges. They used algae kept without slugs as a control for the effect of time.
Step 3: Calculate GE = GR/CR, yielding the number of milligrams (mg) of slug growth per gram of algae consumed (Codium) or per 1000 cells consumed (Cladophora). Because they were comparing the effect of light intensity on slugs fed the two algae, the different units used for consumption did not cause problems.
Figure 1A shows that slugs fed Codium show significantly better growth efficiency in high light than in low light. Those feeding on Cladophora show no difference in two conditions. The kleptoplasts from Codium contributed more to the growth of the slugs in bright light, which suggests that photosynthesis is producing energy that the slugs could use for growth.
However, they needed to be sure that the kelptoplasts from Codium were truly more functional than those from Cladophora, so they measured photosynthetic ability of chloroplasts and kleptoplasts using PAM fluorometry. The absorbance and fluorescence of chlorophyll can be used to measure the health of chloroplasts, and to calculate the relative electron transport rate (rETR), a measure of carbon fixation and therefore energy production.
Figure 2 shows that kleptoplasts from Codium responded to intense illumination with a strong increase in rETR, consistent with increased growth efficiency being caused by increased photosynthesis of healthy kleptoplasts. Kleptoplasts from Cladophora had low rETR regardless of lighting, correlating well with the lack of effect of intense light on growth efficiency of E. viridis. These observations support the idea that photosynthesis by kleptoplasts contributes to slug growth.
Just in case the increased growth rate of E. viridis was due to some other benefit provided by Codium, they measured nutritional quality of the two algal species.
In all cases, the nutritional value of Cladophora was as high or higher than that of Codium (Figure 3), so there was no evidence that Codium was intrinsically more nutritious. Importantly, Panel 3N shows chloroplasts in Cladophora increased rETR in response to more intense light. Therefore, the poor performance of Cladophora-derived kleptoplasts (Figure 2B) is likely to result from degradation inside the slug.
The evidence therefore supports the authors’ hypotheses, and they conclude that E. viridis derive measurable metabolic benefits from photosynthesizing kleptoplasts. Whereas Slugs feeding on Cladophora receive nutrients by digesting the cellular contents (including the chloroplasts), those feeding on Codium get an extra boost from products produced by active, healthy kleptoplasts.
Overall, the experiments seemed well-executed and convincing, with the only caveat being that the slugs fed Codium and Cladophora were collected on those species and not randomly assigned to the groups. There remains at least a formal possibility that the groups represent two populations of slugs that metabolize chloroplasts differently.
This brings us back to the the role of kleptoplasty in the biology of Elysia. It could be:
We should bear in mind that parsimony may not equal truth, and there is no reason to believe that only one of these answers is correct for all species and life stages.
I recently had an epiphany about how to grow Bryopsis more efficiently. In retrospect, it was pretty obvious, and I wonder why it took 2 years to get to this point.
It seemed as though culturing adequate Bryopsis was under control. However, there’s nothing like 6+ weeks of travel to turn things upside-down. I had hired a service to come in and keep things going while I was away, but their primary task was to prevent biological meltdown, or worse, a big salty disaster that would have me forever on the naughty list of the facilities people. I am happy to say, there were no smelly or wet disasters.
Unfortunately, I was not there to give the algae cultures the kind of attention they need, and by the time I was back in the office, the system was overrun with Derbesia, and the slugs had devoured the Bryopsis that I had left for them. The 20-gallon slug tank and both algae culture tanks were full of felty, green hair algae. In retrospect, I should have taken photos, but I was more focused on cleaning up the mess and getting ready to teach a summer class.
Over a week or so, I pulled out the algae tanks off the system, cleaned out at least two pounds of green glop, salvaged the remaining Bryopsis, and set the tanks back up. Somewhere along the line, I came across a few posts about “algae reactors,” cylindrical chambers with water flowing through and some sort of light source. My first thought was “maybe I should buy one of those things.” Then I remembered that I had two media reactors sitting idly in the basement. They are clear cylinders, designed to have water flow through them, which is exactly what I wanted.
The amount of Bryopsis remaining was so small that it didn’t seem worthwhile to have two algae tanks. Instead, I shut down the 10-gallon tank and stuck some of the remaining algae into a reactor. The reactor was hooked up to one of the valves, and connected to the drain, and sat under the grow light where the 10-gallon tank had been.
Within a week or so, it became clear that the experiment was working, so I added the second reactor. I had enough Bryopsis to harvest some for the slugs, and the culture in the first reactor had seeded a sponge that I could use to start the second reactor.
It was working. Time to make things a little less clumsy. I built a rack from 3/4″ PVC, setting the reactors at an angle to optimize the connections to the input valves and drains.
Things went so well, I begged a few unused reactors from local aquarists. This one is from Alan (of unidentified algae fame), and I have one more waiting in the wings.
At this point, it was clear that my former method of rearing Bryopsis in aquaria was not very efficient. Raising Bryopsis in reactors allows me to play with growth parameters, like flow and nutrients, much more easily. Further, keeping multiple separate cultures will make it much easier to eradicate unwanted algae. At some point, it should be straightforward to maintain cultures free of unwanted algae and invertebrate pests (I am all for biodiversity, except when it eats slug larvae) by UV sterilizing the water going into the chambers.
As far as I can tell, this was a successful experiment, so I converted the 15 gallon algae tank into the second slug tank, shutting down the 10-gallon slug tank.
When I walked in today, the system had two slug tanks (top and middle left), and one remaining algae tank (top right)
Five hours of cleaning and rearranging later, there were two slug tanks and three algae reactors. In the process, the system now has two fewer circulation pumps and one fewer light fixture.
Current slug system arrangement. Two tanks for slugs and and their food on top, three reactors in the middle, and room to expand. 8/5/17.
In the future, you can expect a few more reactors. Now it’s time to play with parameters to maximize algae growth. Maybe we’ll finally see some consistent egg production from the slugs.
Every 5 or 6 years, we end up exploring someplace a little more exotic. This year, we decided to go to Madagascar, and we arranged for a driver and accommodations for about 10 days of overland travel and saw some incredible people, landscapes, and wildlife. We’re still sorting through the photos of lemurs, chameleons, villages, and vistas, and it is likely to take some time.
Of course, you don’t come to this web site for the lemurs.
Because we were traveling all the way to an island in the tropical Indian Ocean, I pushed for a stretch of diving at the end. When we were planning the trip, I asked our tour operator, Cactus Tours (an excellent Madagascar-based company) to arrange for some diving at the island of Nosy Be, at the north end of Madagascar. We ended up spending a few days in Nosy Be, and had three days and two night of diving on a sailing catamaran.
After bouncing around in a four-wheel drive for over a week, it was pure luxury to be on the boat. For just the two of us, there was a driver, cook, and a very experienced and knowledgeable dive master, all arranged through Madavoile Cruises. We had six excellent dives, and were completely blown away by the diversity of corals, fish and invertebrates.
Our dive guide, Nicolas, figured out pretty quickly that I wanted to see nudibranchs and sea slugs, and he did not disappoint. The photos below were taken with an Olympus Tough TG-4 camera, which is rated to 50 feet without a housing. Because the housing was clumsy, we took the unhoused camera as deep as 65 feet, which worked just fine despite its increasingly strident warnings. Identifications are based largely on a digital version of Gosliner et al’s “Nudibranch and Sea Slug Identification” and the Sea Slugs from Reunion Island Web site, which is an excellent reference for the southwest Indian Ocean. Please let me know if you believe a species to be misidentified.
Although we saw plenty of Caulerpa, Halimeda and other macroalgae, and looked very hard for Elysia, we came up empty. At Nosy Sakatia, we spent our last morning snorkeling with the turtles before we dove, and I was pleased to see a wide expanse of turtle grass (Thalassia) and manatee grass (Syringodium), which had some excellent growths of Halimeda incrassata.
Unfortunately, I did not get to spend hours searching the seagrass beds. Watching the biggest green turtles I had ever seen graze right in front of me was a nice consolation. It is hard to get a sense of just how big these monsters are from a photograph.
I did find one sacoglossan, Plakobranchus ocellatus, on the reef at Sakatia Arch. Unfortunately, the camera housing I was using for the dive had fogged, so it is a lousy photo. Just not the trip for sap-sucking slugs, I guess.
In addition to the plentiful slugs, there were quite a few flatworms pretending to be nudibranchs. All were in the genus Pseudoceros, and all were found in Humann and Deloach’s Reef Creature Identification book, which has an impressive section on flatworms.
As described in the previous post, I had very modest goals for this summer in Bahia. Because I am getting more interested in the role of kleptoplasty in chemical defense, I thought it would be worth assessing the palatability of Elysia diomedea. Some Elysia species are known to taste bad because of chemicals assimilated from their food plants (see, e.g., Rasher et al., described in this post). E. diomedea is known to produce interesting derivatives of plant compounds (e.g., Ireland et al., 1978, J. Am. Chem. Soc. 100:1002), but, as far as I can tell, there is no evidence regarding the slugs’ palatability.
Fortunately for me, there is a relatively easy way to get a quick sense of their palatability. When snorkeling at the field station, one is generally followed by a small parade of large bullseye puffers (Sphoeroides annulatus) waiting for tasty morsels to be stirred up. What would happen if I dropped a slug in the water column and allowed the fish to eat it? One might expect a puffer to eat anything.
After a day in the field, I had time for a snorkel, so it was a perfect opportunity. After a short survey along the subtidal, I found a few Elysia in a small bunch of Codium (surprise!). I pulled out this little beauty, apologized to her and carried her to the surface.
If you click the link below for the short video (note: large-ish file), it is pretty clear that the puffer does not find the little Elysia to its liking.
Not only one, but three puffers rejected the Elysia. After the first spat out the slug, a second tried it, then a third. In no case did one of the puffers as much as chew, they rejected it as soon as it was in their mouths. Very good for the slug, and suggests that it may be something secreted in the mucus that repels the fish. One might also conclude that puffers don’t learn from their friends, since each had to try it.
Based on one slug (but three puffers), we can tentatively conclude that E. diomedea tastes bad. Are the bad tasting compounds derived from products made by the kleptoplasts?
Nature is perverse.
We’re back in Bahia de los Angeles, on the east coast of Baja California, Mexico. For the two previous years, I have had to suffer for a while before finding any Elysia diomedea. It was rather nerve wracking, because I needed them for research projects each of those years.
Because of time constraints, my goals this year are to help my friend, Dr. Drew Talley, with his long term research, and to discuss plans for student Elysia projects in summer 2018 with Ocean Discovery Institute.
We had some complications at the border, because the Mexican authorities had some reservations about some equipment that was being used by one of the other research groups. We were allowed to proceed after a few hours dealing with paperwork, but were delayed to the point that we had to stop along the way for the night.
We arrived without further incident, unloaded equipment and belongings, started setting up the station, had a great meal in town, we went to bed for the night. It was amazing to be back under all the stars, listening to the ocean and the occasional breathing of a marine mammal.
We woke up to a classic sunrise, and soon we were on the islands, setting traps for insect surveys and savoring the bay and the scenery.
After returning to the station, we ran some errands, followed by a little open time to get in the water. Although I may try a few extremely simple preliminary experiments, my work here does not depend on finding them. Naturally, that means they were abundant in the shallows in front of the station. I found the first within five minutes, and saw at least six within the half hour allotted for the survey.
They looked darker than the slugs we found last summer, but, as was true last summer, all were on or near Codium.
Keeping fingers crossed for a chance to test some ideas about chemical camouflage.
Just when I thought I had it all figured out.
After struggling for way too long, I finally got reliable growth of Bryopsis in the algae culture tanks by providing strong lighting, balanced nutrients, along with very intense water movement. Bryopsis grew well, although Derbesia also started to thrive and needed periodic removal, so I figured I was close to the magic formula.
10 gallon slug tank a few weeks after system revamp. Sponge-covered circulation pump visible at right, and a small clump of Bryopsis in rear center. 3/8/17.
Imagine my surprise when Bryopsis started to thrive, largely without contamination by dinoflagellates or Derbesia, in the slug culture tanks. In the 20 gallon long, the algae that was transferred on the plastic racks started to grow and spread, despite constant grazing from the resident E. clarki. In the 10 gallon, a few scraps growing on some of the macroalgae grew to fill almost half the tank.
10 gallon slug tank, showing heavy growth of Bryopsis after a few months. Other algae are doing fine, but the Bryopsis is taking over. 5/9/17
This has made the single E. crispata very happy. She has grown considerably, and her color is amazing. Will post a photo when she comes out of the algae far enough to be photographed.
The tanks are all plumbed together, so they all receive the same nutrient input. The slug tanks receive somewhat less light than the algae culture tanks. The spectrum of the lights in the slug tanks is broader, with more green, yellow and UV, mostly because that is nicer for my eyes when I look at the tanks. Finally, the circulation is considerably less intense. The algae tanks are blasted with propeller pumps and wavemakers, while circulation to each of the slug tanks is only provided by a single Maxi-Jet 600 (600 liters per hour output), with the intake slug-proofed by a strainer and sponge, and the output directed through a Hydor Flo to provide swirling motion.
Parts of a slug-proof circulation system. The intake of the Maxi-Jet powerhead is covered by a strainer and a sponge, because a strainer alone will not prevent injury to slow, squishy, dumb slugs. The output goes through a Hydor Flo rotating deflector to provide surgy motion.
Assembled Elysia circulator. In the slug system, each one is anchored to the glass with a magnetic holder.
Because even these relatively small pumps give the slugs a bit of a wild ride, they are only turned on for 15 minutes of every hour. Quick summary: despite my beliefs to the contrary, it is possible for Bryopsis to grow strongly with modest water movement.
Although I am pleased that there is now abundant food for the slugs, it does bother me that I still do not understand all of the factors affecting growth of Bryopsis. Previously, Bryopsis struggled in conditions that were largely similar. If I get a chance before leaving for Baja this week, I’ll make yet another deep dive into the system logs to determine which parameters may have changed. The luxuriant growth has emboldened me to order a few more E. clarki, so that the colony can be going full steam by the end of the summer.
To many, this post is akin to “how to give fleas to your dog,” or “how to grow ragweed.” Bryopsis is a benthic (substrate-associated) genus of algae that most aquarists dread seeing in their tanks. Bryopsis can thrive in reef aquaria, to the point that it can smother and kill corals. Many methods of eradication have been explored, including near-toxic levels of magnesium, and the anti-fungal medication fluconazole.
On the other hand, I really want the stuff. As far as I can tell, it is the favorite food of Elysia clarki. E. clarki will eat other macroalgae, such as Penicillus, Avrainvillea or Halimeda, but, given the choice, they will go straight for Bryopsis and stay there. Further, they have consistently produced eggs only at times when they have had unlimited availability of Bryopsis. One of my primary goals is to maintain a self-sustaining colony of slugs, so I very much want a constant, adequate supply of algae.
I’d be perfectly happy if I could count on the outbreaks of local aquarists to supply my needs. Unfortunately, sources have been spotty. My primary source, Justin, who had a beautiful outbreak in a 500-gallon tank, unfortunately managed to get his infestation under control. He swears the controlling factor for him is the level of phosphate; if PO4 levels creep up, he gets an outbreak. Others have provided quality material as well, but not as consistently. Yet others have offered species that turn out not to be Bryopsis. The take home lesson is that people who are trying to eradicate something are not the most dependable source.
How hard can the stuff be to grow? It is a pest, after all. Like any aquatic plant, it needs light, nutrients, and circulation. It gets a little more difficult when you try to provide for the plants’ requirements on a consistent basis. As far as I can tell (and PLEASE email or comment if I am wrong), nobody has published specific requirements of Bryopsis for PAR (photosynthetically-available radiation), macronutrients (e.g., carbon, nitrogen, phosphorous), or micronutrients (like iron, copper and cobalt). When marine aquarists have outbreaks, much of the nutrient load is derived from fish food (well, really fish poop), which is not measured. In fact, most reef aquaria don’t have Bryopsis outbreaks, which suggests that the unlucky few have managed to combine all the right ingredients. For a constant supply of Bryopsis, I need to provide for all of its needs.
If I wanted to grow phytoplankton, the single-cell, free-floating relatives of Bryopsis, I would be in luck. Because of the important role of phytoplankton in our oceans, and because there is a growing industry using them to generate hydrocarbons from sunlight, growing conditions have been explored and published at length. The most popular formula is Guillard’s F/2, so named because it consists of his formula F diluted to 50% (Guillard & Ryther, 1962, Can. J. Microbiol. 8:229), is readily available through suppliers such as Florida Aqua Farms, or even Ebay. The formula provides a balanced blend of nitrogen and phosphorous (with an option to add silicon if you want to grow diatoms), along with a mix of trace elements and vitamins. Mix it up, add a starter of the phytoplankton of your choice, bubble in some CO2 as a carbon source, and you’ll soon have a thriving culture of green water.
I started dosing the Florida Aqua Farms version (“Plant Fuel Too”) almost a year and a half ago, using the complete dry mix (minus silicates). The Bryopsis started to look darker and happier pretty quickly. Perhaps unsurprisingly, there was also a phyoplankton bloom that turned the water green and generated a layer of green scum on the surface of the water. Also, the added nutrients seemed to increase levels of nuisances like cyanobacteria (a.k.a., red slime algae). That would have all been tolerable, but the biggest sticking point was that Bryopsis would go through cycles of boom and bust, which is not conducive to long-term management of a slug colony. I needed to get the right balance of nutrients that would get the Bryopsis to grow maximally and out-compete the species I don’t want.
With all of the possible factors (e.g., light, circulation, temperature, nutrients) to be within the right ranges, there were a lot of variables to play with:
In order to separate the variables a bit better, I started using Florida Aqua Farms original “Plant Fuel,” which contains all of the trace elements and vitamins, but no nitrogen or phosphate. That would allow me to play with levels of trace elements, N, and P separately. I also added a source of carbon. Because white vinegar is cheap, always available, and is readily broken down into CO2 by bacteria, it seemed like a good choice.
By adjusting the relative input of all four ingredients (C, N, P and trace elements), combined with very high flow in the algae culture tank, I was able to get significantly better growth. The final improvement was something that I had not expected to have such an impact: rebuilding the system. Within about a week of the big move, the algae was thriving on the racks of plastic eggcrate I was using as a substrate. I suspect that the 50% water change and improvements to circulation in the new system played a large part in the improved growth.
By growing on plastic racks, Bryopsis cultures can be moved to slug tanks to be consumed, and then removed for regrowth.
So we’re making forward progress. We are controlling the growth of food algae to the point where it seems to be sustainable. As a side benefit, the other macroalgae are also thriving. For example, the three deep green Penicillus in the photo below are new sprouts from the ratty old plant in the center.
At the moment (and likely to change) the system receives major elements at the (molar) ratio of 150:30:1 C:N:P. This is roughly in the range reported for other macroalgae, and does not support much growth of cyanobacteria or phytoplankton. In other words, it looks like I am providing nutrients at about the rate at which the are being consumed by the desired algae.
There is still plenty of room for improvement. The priority for the moment is eliminating or reducing dinoflagellates in the algae culture tanks. They do not seem to cause too much trouble in the slug tanks, but they form a slimy film on the Bryopsis in the culture tanks, presumably reducing growth, competing for nutrients, and producing toxins.
Dinoflagellates at low magnification. They can be seen as strings of brown dots surrounding the green algae branches. 4/11/17
At higher magnification they are kind of pretty. Based on the shape, size and general appearance, it looks a lot like Ostreopsis ovata (Faust and Gulledge, 2002, Contr. U.S. Natl. Herb. 42: 1-144). Like many dinoflagellates, O. ovata produces toxins, some of which are toxic to mice (Nakajima et al., 1981, Okinawa Bull. Jpn. Soc, Sci. Fish. 47: 1029). The effects on slugs or other invertebrates is not known.
DInoflagellate from Bryopsis tank, 400X magnification. Gold color is from densely packed chloroplasts. 4/6/17.
At the moment, I have reduced the photoperiod (the time the lights are on), and am rinsing the Bryopsis racks in clean artificial seawater periodically to reduce the population. At some point, it might be necessary to use harsher methods, such as antibiotics (metronidazole seems to affect dinoflagellates somewhat specifically) or starting a clean culture of Bryopsis and preventing entry of other species using UV sterilization.
For now, there is plentiful food for the slugs, which is a step forward.
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