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Category: Marine biology

A tale of two algae, and a puzzle

Posted on 2015-06-182023-01-06 by Allison J. Gong

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:

Algae-covered rocks at Pistachio Beach, 18 June 2015. © Allison J Gong
Algae-covered rocks at Pistachio Beach
18 June 2015
© Allison J Gong

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:

Two unrelated but morphologically similar red algae, 18 June 2015. © Allison J. Gong
Two taxonomically unrelated but morphologically similar red algae
18 June 2015
© Allison J. Gong

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:

Plocamium pacificum at Davenport Landing, 17 June 2015. © Allison J. Gong
Plocamium pacificum at Davenport Landing
17 June 2015
© Allison J. Gong

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.

Plocamium pacificum (left) and a mystery look-alike (right), 18 June 2015. © Allison J. Gong
Plocamium pacificum (left) and a mystery look-alike (right)
18 June 2015
© Allison J. Gong

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!

Microcladia coulteri growing epiphytically on Mazzaella sp. 18 June 2015. © Allison J. Gong
Microcladia coulteri growing epiphytically on Mazzaella sp. at Pistachio Beach
18 June 2015
© Allison J. Gong

Finally, we have both specimens identified:

Plocamium pacificum (left) and Microcladia coulteri (right), 18 June 2015. © Allison J. Gong
Plocamium pacificum (left) and Microcladia coulteri (right)
18 June 2015
© Allison J. Gong

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?

Mystery red alga, 18 June 2015. © Allison J. Gong
Mystery red alga
18 June 2015
© Allison J. Gong

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.

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Branching out

Posted on 2015-06-162023-01-06 by Allison J. Gong

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.

Coralline rocks in seawater table at Long Marine Lab, 16 June 2015. © Allison J. Gong
Coralline rocks in seawater table at Long Marine Lab
16 June 2015
© Allison J. Gong

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:

Coralline rock bearing red and green filamentous algae, 16 June 2015. © Allison J. Gong
Coralline rock bearing red and green filamentous algae
16 June 2015
© Allison J. Gong

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:

Apical tip of Antithamnion defectum, 16 June 2015. © Allison J. Gong
Apical tip of Antithamnion defectum
16 June 2015
© Allison J. Gong

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.

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Growing fast

Posted on 2015-06-122023-01-06 by Allison J. Gong

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:

10-day-old bipinnaria larva of Pisaster ochraceus, 12 June 2015. © Allison J. Gong
Ventral view of 10-day-old bipinnaria larva of Pisaster ochraceus
12 June 2015
© Allison J. Gong

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!

10-day-old bipinnaria larva of Pisaster ochraceus, drawn from life. 12 June 2015. © Allison J. Gong
10-day-old bipinnaria larva of Pisaster ochraceus, drawn from life
12 June 2015
© Allison J. Gong

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!

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Green is the new sexy, Part II

Posted on 2015-06-112023-01-06 by Allison J. Gong

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.

Alternation_of_generations_simpler.svg

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!

Biflagellated gametes of Ulva sp., 11 June 2015. © Allison J. Gong
Biflagellated gametes of Ulva sp.
11 June 2015
© Allison J. Gong

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?

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Green is the new sexy, Part I

Posted on 2015-06-112023-01-06 by Allison J. Gong

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:

Specimen of Ulva sp. spawning, 11 June 2015. © Allison J. Gong
Specimen of Ulva sp. spawning
11 June 2015
© Allison J. Gong

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.

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Feeling blue?

Posted on 2015-06-102023-01-06 by Allison J. Gong

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.

Windrows of Velella velella (by-the-wind sailor) washed up on the beach at Point Piños, 9 May 2015. © Allison J. Gong
Windrows of fresh Velella velella (by-the-wind sailor) and algal detritus washed up on the beach at Point Piños
9 May 2015
© Allison J. Gong
Desiccated Velella velella on the beach at Franklin Point, 22 April 2015. © Allison J. Gong
Desiccated Velella velella on the beach at Franklin Point
22 April 2015
© Allison J. Gong

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:

Single Velella velella washed up on beach at Franklin Point, 22 April 2015. © Allison J. Gong
Single Velella velella washed up on beach at Franklin Point
22 April 2015
© Allison J. Gong

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.

Porpita porpita (left) and its predator, the nudibranch Glaucus atlanticus. Diameter of P. porpita approx. 2 cm.
Porpita porpita (left) and its predator, the nudibranch Glaucus atlanticus. Diameter of P. porpita approx. 2 cm.

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!

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Slow and steady (I think)

Posted on 2015-06-092023-01-06 by Allison J. Gong

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!

Front view of Pisaster ochraceus bipinnaria larva, age 7 days, 8 June 2015. © Allison J. Gong
Front (ventral) view of Pisaster ochraceus bipinnaria larva, age 7 days
8 June 2015
© Allison J. Gong

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:

Right side view of bipinnaria larva of Pisaster ochraceus, age 7 days. © Allison J. Gong
Right side view of Pisaster ochraceus bipinnaria larva, age 7 days.
© Allison J. Gong

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.

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Early morning low tides are the best

Posted on 2015-06-052023-01-06 by Allison J. Gong

This morning I went on a solo trip to one of my favorite intertidal sites up the coast a bit. I’ve been busy with stuff at the marine lab and my house is a construction zone this summer so it was really nice being alone in nature for a couple of hours before most people had gotten out of bed.

I didn’t find what I was looking for but did see some great stuff that I wasn’t looking for, which is just as rewarding.

The approach to the beach over the dunes is always spectacular even on a gloomy morning. I find this color palette very soothing.

The hike over the dunes, 5 June 2015. © Allison J. Gong
The hike over the dunes
5 June 2015
© Allison J. Gong

The site itself is rocky with a sandy bottom. Depending on the severity of recent storm action there can be more or less sand. Winter storms wash sand away, while in the summer the sand tends to accumulate and can bury the rocks to surprising depths.

Surfgrass bed (Phyllospadix sp.) and rocks at Franklin Point, 5 June 2015. © Allison J. Gong
Surfgrass bed (Phyllospadix sp.) and rocks at Franklin Point
5 June 2015
© Allison J. Gong

It may be an optical illusion, but when I’m scrunched down in amongst the rocks it appears that the waves are breaking at heights quite a bit above my head. Most of the water’s force is dissipated as the waves wash over the rocks, and unless I’ve wandered out too far, by the time it gets to me all I need to worry about is whether the surge will overtop my boots. Which has indeed happened and makes for a cold squelchy morning.


And now for some happy snaps!

A small mid-intertidal pool at Franklin Point, 5 June 2015. © Allison J. Gong
An example of intertidal biodiversity at Franklin Point. The most conspicuous organisms are Ulva (sea lettuce), coralline algae (the pink stuff), small acorn barnacles, the tube-dwelling worm Phragmatopoma californica, and small anemones in the genus Anthopleura
5 June 2015
© Allison J. Gong
I love my hip boots!  © Allison J. Gong
I love my hip boots!
© Allison J. Gong
Pagurus hirsutiusculus hermit crab in shell of the snail Olivella biplicata, 5 June 2015. © Allison J. Gong
Pagurus hirsutiusculus hermit crab in shell of the snail Olivella biplicata
5 June 2015
© Allison J. Gong
A beautifully camouflaged kelp crab (Pugettia producta) hiding in plain sight, 5 June 2015. © Allison J. Gong
A beautifully camouflaged kelp crab (Pugettia producta) hiding in plain sight
5 June 2015
© Allison J. Gong

Because, really, doesn’t everybody have a favorite red alga? This is mine. It presses gorgeously and is so damn beautiful!

Erythrophyllum delesserioides, 5 June 2015. © Allison J. Gong
Erythrophyllum delesserioides
5 June 2015
© Allison J. Gong

At one point I saw a worm-like thing thrashing around in a shallow pool. Turns out it was a polychaete worm, probably in the genus Nereis, doing epic battle with a predatory nemertean worm (Paranemertes peregrina). By the time I figured out what was going on and stuck my camera in the water the interaction had more of less come to an end. The polychaete did get away without apparent damage, but it was moving pretty slowly afterward. In this video Nereis is the segmented worm that’s doing all the wiggling, and Paranemertes is the purple and beige unsegmented worm that you can sort of make out in the top of the frame. I wish I had been swifter on the uptake with the camera.


And the pièce de résistance for this trip:  A little sea hare! This guy was so small (about 2.5 cm long) that at first I thought it was a clump of red algae. Then I saw the little rhinophores (those ear-like projections that give them their common name) and recognized it as a sea hare. Amazingly cute!

A little sea hare (Aplysia sp.), 5 June 2015. © Allison J. Gong
A little sea hare (Aplysia sp.)
5 June 2015
© Allison J. Gong

I was lucky enough to capture some video of this critter crawling around.

Aside from the rhinophores it doesn’t look hare-like at all, does it? I wonder about common names sometimes.

All in all, it was a great morning. An early morning low tide is the best reason I can think of to crawl out of bed at 04:30!

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A glass half full

Posted on 2015-06-042023-01-06 by Allison J. Gong

It’s becoming quite clear that I don’t have to worry about having too many sea star larvae to deal with. While the embryos from my F1 x M1 (Purple x Purple) cross had hatched this morning, nothing from the F2 x M1 (Orange x Purple) cross looked promising. I’m about ready to write off these guys and dump them all down the drain, but will give them until tomorrow to pull themselves together and do something that doesn’t look all wonky.

In the meantime, it’s really fun looking at the good embryos from the F1 x M1 mating. They hatched out of their fertilization envelopes and have become elongated, sort of like stubby Tylenol caplets. This elongation defines a functional anterior-posterior axis, and the animal swims with its anterior end forward.

Gastrulating embryo of Pisaster ochraceus, 4 June 2015. © Allison J. Gong
Gastrulating embryo of Pisaster ochraceus
4 June 2015
© Allison J. Gong

Gastrulation is the process of forming the first larval gut, or archenteron. Remember how yesterday the embryo was a hollow ball of cells called a blastula? In these echinoderms gastrulation is simply an invagination into the blastula. Imagine poking your finger into an inflated balloon:  The balloon is the blastula and your finger forms an invagination, or channel, through it. In embryos, gastrulation begins at a site on the blastula called the blastopore; this is where you’d stick your finger into the balloon in our analogy.

Most animal guts have two openings, a mouth and an anus. You understand what happens at each of those openings. The archenteron is a gut, one of whose openings is the blastopore. The fate of said blastopore is to be either the mouth end or the anus end of the archenteron. In echinoderms, the major invertebrate phylum that makes up a larger grouping of animals called the deuterostomes, the blastopore becomes the anus, with the mouth breaking through as the process of gastrulation finishes. And lest you think that possessing an anus before a mouth is somehow less evolved than the reverse would be, you might be interested in knowing that we humans are also deuterostomes. That’s right, each of you reading this blog, as well as the one who writes it, built an anus first and a mouth second.

These sea star embryos swim really fast! I had to squash them under a cover slip to snap some halfway decent pictures, and even then it wasn’t easy to slow them down or chase them around on the slide. You can get a feel for how fast they can move in this short video clip:

The archenteron appears to wobble because it doesn’t go straight through from the blastopore to the apex of the embryo. The mouth will break through along one of the sides, resulting in a curved gut. I suspect that when I look at the embryos tomorrow they will have graduated to the status of larvae, with complete guts. Then I get to start feeding them and watching them grow.

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Questions and answers

Posted on 2015-06-04 by Allison J. Gong

I’ve been fielding questions about my recent sea star spawning work from people I’ve shared this blog with, which is a lot of fun! To streamline things and make the info available to anybody who might be following, I decided to put together a very brief FAQ-like post to address the most recent questions.

Question:  Can you watch the eggs divide in real time?

In a time-lapse sense you can watch cleavage divisions occur, but not in real time. What I can do is set up a slide on the microscope and leave it there for a while. The gradually warming temperature speeds up development to the point that I can sort of see the division in real time. Of course, the danger is that the embryo will cook on the slide. I generally figure that once I’ve pipetted some embryos onto a slide and dropped a cover slip on top of them, they’re goners (it’s not really possible to remove the cover slip without damaging the cells underneath it) so I feel marginally less bad about sacrificing a few to the gods of observation.

Questions:  I’m fairly certain that the stars can go back to the sea, but are you able to keep their eggs with them, too? How difficult is that transport?

Actually, my scientific collecting permit specifically states that I’m not allowed to return animals to the wild. If I needed to, I could apply for additional permits but it has never been necessary for the work I do. Surplus eggs and larvae, therefore, are discharged into the seawater outflow at the lab and do return to the ocean but the parents remain in my care.

Question:  Are orange and purple stars usually able to cross with each other?

As far as anyone has been able to determine, the color of stars has zero effect on whether two individuals’ gametes are able to do the nasty together. The sea stars that I’m working with–Pisaster ochraceus, the ochre star–are broadcast spawners, meaning that each individual spews his/her gametes into the water, where fertilization and development occur. The stars are also synchronous spawners, meaning that if one individual in an area begins spawning other stars in the immediate vicinity will also spawn. After all, it does take two to tango, and to spawn while nobody else does is a tremendous waste of energy.

So yes, a purple star and an orange star should be able to mate without any problems… at least not any problems due to the parents’ colors.

Question:  If so, what color do they end up being, statstically?

This is a very interesting question. Two of my colleagues are going to spawn Patiria miniata (bat stars) next week to address this. Their plans are to cross a Blue female with an Orange male, an Orange female with a Blue male, and both pure-color matings. They did a preliminary version of this experiment a couple of years ago but didn’t end up with enough juveniles at a size that color could be ascertained; thus they couldn’t calculate any statistically meaningful color ratios.

Questions:  Do you suppose that the wasting disease could be now in the genetic makeup? Any thoughts (unofficial of course) about this?

My thought is sort of the opposite, actually. The animals that we brought in from the field are all survivors of SSWS; if anything, I’d expect them to be resistant to whatever causes the plague, and to (hopefully) pass on this resistance to their offspring. Of course, there’s no way of knowing if and how exposure to SSWS affects the quality of the gametes. It’s quite possible that these survivors are less fit after the SSWS outbreak than they were before.

Question:  Purple Male with Purple Female developed well and purple Male with Orange female didn’t…some sort of incompatibility?

Well, given what I saw today the Orange (female) x Purple (male) cross almost certainly did not work. Fertilization occurred, but almost none of the embryos had any indication of normal development. Since we know the Purple male was able to mate successfully with the Purple female, we can infer that his sperm were fine. It could be that there was something going on with the Orange female’s eggs; there were a lot of them, but maybe their quality just wasn’t very good. Or perhaps we somehow mistreated and wrecked them the other day.

Any other questions? Use the Comments section to ask them, and I’ll address them in a future post.

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