You know how the saying goes. I just wanted to share how beautiful this larva is.
I have nothing to add. More on Friday, probably.
Notes from a California naturalist
The nature of Nature
What a difference a week makes! The Pisaster larvae have grown and developed quite a bit since I looked at them a week ago. Here they are as little space ships again.
Since they are getting so big, Scott and I decided to redistribute the larvae from four jars into six. This will give them room to grow and ensure that they aren’t overcrowded. To do this we first concentrated them all into a single beaker, then divided the entire population into two jars, then subdivided each jar into three jars, for a total of six. See all the larvae in the beaker?
The largest larvae are ~1200 µm long, getting big enough to fill up the field of view under the lowest magnification of the compound microscope. The most noticeable difference from last time, aside from the overall increase in size, is that the ciliated band is becoming more lobed. These lobes will eventually be elaborated into the long arms of the mature brachiolaria larva (‘brach-‘ is Greek for ‘arm’). See below:
The other rather obvious development is that the left and right coeloms from the previous observation a week ago have fused together in the anterior (top of the picture) and posterior (bottom of the picture) region of the body.
From here on out the larvae won’t get too much bigger; if I remember correctly they’ll grow until they’re about 1500 µm long. Their brachiolar arms will get really long and pretty, though, greatly increasing the length of the ciliated band. Eventually their juvenile rudiments will form . . . but that’s a post for another day. More on that when it happens.
THE ANSWER TO YESTERDAY’S PUZZLE IS . . .
. . . drum roll, please . . .
Microcladia coulteri!
I showed you this:
but what you really needed to be certain of the ID was the rest of the photo:

Huzzah again for natural history! I love it when natural history provides the answer to a taxonomic or identification question. Sometimes you need to see the organism where it lives in order to understand what it’s all about. Quite a lot of modern biology has to do with grinding up organisms and examining their DNA; while I do appreciate the evolutionary and ecological insights these data provide, it’s really not my cup of tea. I’d rather spend my time looking at intact organisms than their molecules, and getting outdoors to see them in nature instead of running gels and staring at computer algorithms. As in most other walks of life, it takes many kinds of work to get at the whole picture in ecology, and I am grateful to be able to contribute a little piece to the puzzle.
If you visit the California rocky intertidal in the spring or summer, one of the first things you notice will be the macroalgae, or seaweeds. They are incredibly abundant and diverse this time of year, covering just about every bit of rock. In fact, in a landscape sense the only visible organisms are macroalgae and surfgrass:
Of the three major divisions of algae (the greens, browns, and reds), the red algae are the most diverse. We have several hundred species along the California coast, and while they don’t get as big as the kelps (which are brown algae) they display an astonishing assortment of morphologies, colors, and life history complexities. Almost all of the algae in the photo above are reds. The olive-greenish stuff? Yep, those are reds; multiple genera of reds, in fact. The dark brown things? Those are also reds, again representing more than one genus.
Within the incredible diversity of red algae, today I want to focus on two species: Microcladia coulteri and Plocamium pacificum. Both of these algae have delicate branching forms that make beautiful pressings. But despite their apparently similar morphologies, they represent different taxonomic orders and have completely different lifestyles. Let’s take a look at how similar they actually are:
Pretty tough to distinguish, aren’t they? The specimen on the left is a bit more robust in comparison, but if you had only one of these in front of you and nothing to compare it to you’d probably be hard-pressed to determine which species it is.
This is where an understanding of natural history becomes invaluable. Since these species are morphologically so similar to each other, an extremely helpful piece of information is where (and how) each one lives. In terms of habitat, these species can be found pretty much right next to each other, so that doesn’t help much. However, the surface on which each species grows tells you exactly what you need to know.
The specimen on the left in the photo above is Plocamium pacificum, a member of the taxonomic order Plocamiales. It lives from the mid-low intertidal to the shallow subtidal and is always attached to rocks, as you can see below:
The specimen on the left was taken from a thallus that was growing on a rock. This means that it is Plocamium pacificum. Now we can label our photograph with one name.
The specimen on the right was growing as an epiphyte (“on plant”) on a large blade of another red alga. This epiphytic lifestyle tells me that it is not Plocamium, but a species in the genus Microcladia in the taxonomic order Ceramiales. When I brought it into the lab to key it out I was able to identify it as Microcladia coulteri. Three cheers for natural history!
Here’s a picture of M. coulteri growing on blades of another red alga, Mazzaella sp. See how green the Mazzaella looks? Color isn’t the only factor that determines which major group an alga belongs to, and can in fact be quite deceiving!

Finally, we have both specimens identified:
Which is all well and good when you have two specimens in hand that you can compare directly to each other. But what if all you have is this little bit?
Would you say this is Plocamium, or Microcladia? What would you base your decision on? And how certain would you be?
Submit answers (with justifications!) in the Comments, and I’ll give you the answer tomorrow.
Today I decided to look at some scuzz growing in one of the seawater tables at the marine lab. This table is populated mostly by coralline rocks, although I have some pet chitons running around in it.
I picked out a promising rock and examined it under some decent light. Most of the rocks have at least some fuzzy red filamentous algae growing on them; this one also had a bit of a filamentous green, which made it a promising subject for photography. I already knew what the green was (Bryopsis corticulans) but didn’t recognize the filamentous red. The Bryopsis is in the lower right corner of the rock in the photo below:
What was noticeable about the Bryopsis and the mystery red is the difference in size. Bryopsis looks positively dainty until you compare it with the red. Wanting to take a closer look at the red, I plucked off a bit and mounted it on a microscope slide. This is really the only way to see what’s going on with these filamentous algae, and it works like a charm. You don’t have to make a cross-section or anything; you just put the piece in a drop of water, add a cover slip, and look at what you can get:
What first caught my eye was the rather simple branching pattern. The central axis is made up of roughly rectangular cells, each of which has two side branches that are opposite each other. Each of the side branches has branchlets on only the upper surface. Branching like this is relatively easy to draw (things spiralling around in three dimensions are really difficult for me), although my drawing isn’t nearly as pretty as the real thing.
This microscope view, along with my little sketches, provided me with enough information to key out this alga even though it didn’t have any reproductive structures. According to the dichotomous keys in Marine Algae of California* (the book that marine biologists refer to as the MAC, our Bible for identifying the algae) it is Antithamnion defectum. The MAC says that this species is common on other algae and can be found both intertidally and subtidally from southern British Columbia to Baja California. It could very well be that I see this species in the field, but these filamentous reds look pretty much the same, at least to my inexpert eye. It really does take a microscope to figure out what I’m looking at.
*Abbott, Isabella A. and George J. Hollenberg. Marine Algae of California. Stanford: Stanford University Press, 1976. Print.
Today my Pisaster ochraceus larvae are 10 days old. Although they seemed to be developing slowly, compared to the urchins that I’m more used to, in the past several days they have changed quite a bit. They’ve also been growing quickly, which makes me think that they’re off to a strong start. Of course, there’s still a lot of time for things to go wrong, as they have another couple of months in the plankton. However, at this point in time I feel optimistic about their chances.
In the dish under the dissecting scope they swim around like bizarre space ships. All the bits of detritus in the water add to the effect. The only thing missing is the sound effects.
The magnification of my dissecting scope goes up to 40X. To see any details of anatomy I have to use the compound microscope, through which I can see this, under 100X magnification:
Aside from the dramatic increase in overall size (almost 1 mm long now!), the larva’s body has gotten a lot more complicated. For one thing, the animal’s marginal ciliated band, which propels the larva through the water, has started becoming more elongate and elaborate. In this view the larva is lying on its back, and I have focused on the plane of its ventral surface. The left and right coeloms are in the plane of the dorsal surface, and thus are not really in focus. You should still be able to see how long they have gotten, though. Eventually they will fuse anteriorly to form a single cavity. The stomach of the larva has a nice green-golden color due to the food it has been eating. It makes perfect sense, as we are feeding them a cocktail of green algae and a diatom-like golden alga.
The larvae are very flexible and can be quite animated when they’re swimming around. They bend, scrunch up, and swallow food cells. They have already gotten so big that they take up much of the field of view under the microscope, even at the lowest magnification. Watch some larval gymnastics:
Part of the reason that I wanted to spawn Pisaster and raise the larvae this summer is that I want to put together a series of pen-and-ink drawings of the developmental stages. I did the same for the bat star Patiria miniata several years ago, but the Pisaster larvae will have longer and more elaborate arms when they mature; capturing these in drawings will be a challenge for me. I also hope to include the juveniles in this set of drawings. With that goal in mind, I’ve been sketching the larvae every few days, just to get some practice under my hand and remind myself what it feels like to draw. I’ve missed it!
For whatever reason, I really like how this sketch turned out. It’s not pretty, but it does truly represent what I saw under the microscope. I’m going to have to work on depicting three-dimensional structures on a two-dimensional page, which will take some practice. Fortunately I have several weeks to brush up on my skills!
Part of what makes the marine algae so fascinating to me is their life cycles. I’m intrigued by organisms that do things differently from us. And to be honest, from the perspective of someone who studies invertebrates and their life cycles, we humans are rather boring: we’re born into in one body, reproduce (maybe), and then die, all in the same body. Ulva, on the other hand, follows the typical plant example and has a life cycle that includes alternation of generations.
Without going into too much detail, let’s just say that Ulva has two generations within a single life cycle, one called a sporophyte and the other called a gametophyte. The difference between the sporophyte and gametophyte is the number of chromosome sets found in the cells of the respective generations: sporophytes have two sets of chromosomes per cell, a condition which we describe as being diploid (2n), while gametophytes are haploid (1n) and have only one set of chromosomes per cell. The diagram below lays it out nicely. Note that the gametophyte in the diagram is white, while the sporophyte is green.
The little white circles in the diagram above are the reproductive cells. These cells are produced by either the gametophyte (in the case of gametes) or the sporophyte (in the case of spores).
Now, determining if what you’re looking at is a sporophyte or gametophyte can be easy or difficult, depending on whether your species is isomorphic (‘same form’) or heteromorphic (‘other’ or ‘different form’). Unfortunately for us, Ulva happens to be isomorphic, which means that the sporophyte and gametophyte are for the most part morphologically indistinguishable. However, if you knew what kind of reproductive cells a particular generation produces, you could deduce whether that generation is a sporophyte or a gametophyte, right? So, is there any way to determine whether a 2.5 µm cell is a spore or a gamete?
Yes, there is! In the group of algae that includes Ulva the spores are quadriflagellate, which is just a fancy way of saying that each one bears four flagella. The gametes are biflagellate, having (you guessed it) two flagella. Now it’s just a matter of counting flagella on these tiny reproductive cells released by the specimen of Ulva in my bowl.
And voilà!
It’s clear that these cells have only two flagella, right? This means that they are gametes, not spores, and the thallus that produced them was the gametophyte!
Pretty dang nifty, isn’t it?
I was making my last run through the wet lab today, about to head off to forage for lunch before a meeting elsewhere, when I saw this in one of my bowls:
This is one of my feeding treatments for the juvenile urchins. The sheet of green stuff is Ulva sp., a green alga several species of which grow locally in the intertidal. You also see it in harbors and estuaries. This particular bit was growing ferally in one of the large outdoor tanks in an area of the marine lab called the tank farm.
You can see that the algal body (called a thallus) has a fairly distinct edge, except for the parts that the urchins have munched through. Can you also see the cloudy pale green water that runs sort of horizontally across the middle third of the bowl? That’s the stuff that caught my eye. After glancing at the clock I figured I had just enough time to take a quick peek under the scope, and if I really didn’t care about eating lunch I could even snap a few pictures and still make it to my meeting on time. Anyone who knows me personally understands that I organize my life around food and the next time I get to eat. The fact that I was willing to forego lunch to look at this green spooge should tell you how exciting this was.
(It turns out that a few minutes later the person I was supposed to meet with e-mailed me and asked to postpone our meeting until next week. Yes! This means actual quality time with the microscope and the spooge.)
Here’s what a spawning green alga looks like:
That undulating column on the left side is a stream of reproductive cells being released by the thallus. And yes, those are my little urchins chowing down. They like eating Ulva much better than the coralline rocks they’d been subsisting on until recently.
Under the compound scope at 400X magnification, the reproductive cells look like this:
The tiny little cells zooming around are about 2.5 µm long. The way they swim suggests that they have flagella. Do they look familiar?
They should. They look a lot your typical flagellated animal sperms! I don’t think it’s a coincidence that my first thought upon seeing the green stuff in the bowl was “Spooge!”
But here’s where it gets tricky. For algae, looking and acting like sperm doesn’t mean that something is sperm. More on that in the next post.
This spring and summer the local beaches have at times been covered by what appear to be small, desiccated, blue or white potato chips. They would typically be seen in windrows at and just below the high-tide line, or blown into piles. The most recently washed up ones are a dark blue-violet color, while the ones that have been on the beach for more than a day or two are faded to white.

These animals are Velella velella, commonly called by-the-wind sailors. Taxonomically they are in the Class Hydrozoa of the Phylum Cnidaria. Other members of this class are the colonial hydroids and siphonophores (such as the Portuguese man-o’-war, Physalia) as well as the freshwater hydras that you may have played around with in high school. Technically speaking, Velella isn’t a jellyfish. Actually, if we want to get uber-technical about it, there’s no such thing as a jellyfish at all; or if there is, it’s a vertebrate (i.e., some kind of actual fish) rather than a cnidarian. Most of the gelatinous creatures that people generally refer to as “jellyfish” are in fact the medusae of cnidarians.
That said, Velella is a special kind of hydrozoan. Its body consists of an oblong disc, 3-10 cm long, with tentacles and such hanging down and a sail sticking up. The little sail catches the wind that propels the animal:
How do so many of these animals end up on the beach? The answer is that they float on the surface of the ocean and are at the mercy of the winds, hence their common name. This is an extremely specialized habitat called the neuston. Organisms living here have to be adapted to both aerial and marine factors. In fact, the blue pigment in these animals is thought to act as a sunscreen, reflecting the blue (and probably UV) wavelengths and protecting the underlying cells. We all know that UV radiation damages DNA, right? That’s why we wear sun protection. Other cnidarian inhabitants of the neuston are things like Physalia and Porpita porpita (blue buttons), which are also blue in color. A former boss of mine used to say that for every hydroid there’s a nudibranch that lives on it, eats it, and looks just like it. Porpita isn’t exactly a hydroid, but it does have a predatory nudibranch, Glaucus atlanticus, which is (of course) blue-purple! Glaucus eats Velella, too.

The Monterey Bay Aquarium Research Institute (MBARI) has, of course, one of the best video explanations of what Velella is all about. I certainly can’t do any better, so you should watch this:
By the way, MBARI’s YouTube channel is like marine biology and oceanography porn. Just sayin’. If you have some time to kill on the Internet, you could certainly do worse than to spend it there!
Today the Pisaster larvae that Scott and I are following are a week old. Happy birthday, little dudes! Yesterday we did the twice-weekly water change and looked at them. They’re getting big fast since we started feeding them on Saturday when their mouths finally broke through. At this stage they are sort of jellybean-shaped and extremely flexible–they don’t have the calcified skeletal rods that sea urchin larvae have so they bend and flex quite a lot. They are also beautifully transparent, which allows us to see their guts in fine detail. We can even watch them swallow food cells!
In profile view you can see that the larvae are shaped sort of like fat C’s. Here’s a side view of a different individual:
In the short term (over the next couple of weeks or so) the larvae will continue to get longer. Their guts won’t change much, but their coelomic systems will develop and become more complex. I’ll try to capture that in photos and drawings to share with you.