Posts Tagged ‘marine biology’

Coral Problems

Friday, December 17th, 2010

Hi Folks,

A most interesting and interesting article discussing the problems with identifying stony corals, in particular, some species of Hawai’ian Montipora has recent been published.

The background for the article is that last year several parties petitioned to have 83 stony corals to be listed under the United States Endangered Species Act. The National Marine Fisheries Service (NMFS), a branch of the National Oceanic and Atmospheric Administration (NOAA) is charged with assessing the coral species in question to determine, among other things, if they actually are endangered.  If the corals are listed, the act is supposed to provide some more protection for the species, and probably most importantly, designate critical habitat for these corals.

Of course, the whole “assessment” process ultimately depends upon somebody’s ability to identify individual colonies of coral species in question and that, in turn, depends upon the validity scientific description of those species.  The basic fundamental issues are:

1) Is the given species well-enough described to be reliably identified?  Keep in mind, that by being listed on the petition, at least somebody thinks the indivual colonies in that species can be identified.

2) If the species is identifable, can it be assessed to determine if it is endangered?

The article discussed in the Coral feature was officially published on 2 December, 2010, in the electronic (online and free access) peer-reviewed journal, PLoS One:

 

Forsman ZH, Concepcion GT, Haverkort RD, Shaw RW, Maragos JE, et al. (2010) Ecomorph or Endangered Coral? DNA and Microstructure Reveal Hawaiian Species Complexes: Montipora dilatata/flabellata/turgescens & M. patula/verrilli PLoS ONE 5(12): e15021. doi:10.1371/journal.pone.

I urge you all to read, at least, the Abstract (= the authors’ short summery) of the article, but I am also a realist and realize that while a few of you will look at the Abstract, and some of you may actually read or download and save the article, most people who scan this blog probably won’t.

So…

Here is a brief summary of the summary – if you will, an abstracted abstract.  And if this is creative document would it then be “abstract art?”    Yeah, I know, “Boo!… hiss!”

The researchers examined the genetic codes for a relatively large number of well-known and well-characterised proteins found in the corals’ cells, as well, they also looked at how the subcellular structures called mitochondria vary genetically between the samples.  They also microscopically compared, in fine detail, some of the visible physical structures of each specimen.  

When added together, these different examinations revealed four distinct groupings of specimens (called “clades”), and when each specimen was identified with traditional taxonomic methods, the four clades contained these species: I) M. patula/M. verrilli, II) M. cf. incrassata, III) M. capitata, IV) M. dilatata/M. flabellata/M. cf. turgescens.  So, sophisticated statistical analyses of skeletal microstructure and genetics separated specimens of 7 “species,” based on traditional taxonomy, into 4 groups that represent -probably- actual groups.  I think whether or not one wants to consider that each of these groups represents a species is probably dependent on how one feels about this type of analysis.  To me, yup, I’ll buy in to consideration of each group as representation of a species.  The microcharacters of the size and shape of verrucae or papillae were the only reliable physical characters that could be used in identifying the groups, while gross features such as any aspect of colony-level morphology was so highly variable as to be useless.

The authors noted that previous studies on how observable structures in corals vary from specimen to specimen have revealed that fragments taken from the same colony can exhibit strikingly different growth forms if grown in different environments.   Additionally, the extent of both genetic and morphological intraspecific variation in corals is poorly understood. This is clearly creates problems for assessment of species in the context of the Endangered Species Act as  structurally-based taxonomy – not molecular or genetic information – is the current basis for estimating species distributions, abundance, and extinction risk.

This study identified no fixed genetic or fine-scale morphological differences between M. flabellata, M. cf. turgescens, and M. dilatata, or between M. patula and M. verilli; in other words, these 5 named species appear to be only 2 natural species.  The authors noted that the geographic ranges of these groups are likely to extend beyond Hawai’i into the central Pacific and that individuals within “species” of these complexes are either actively interbreeding (which means they are not separate species), or they are from separate species that are very closely related (e.g., evolutionarily separated within the last one million years) and cannot be distinguished from one another.  Now that these complexes have been identified, work is needed to determine if the nominal species within each complex freely interbreed.

Finally, the authors note:

Unfortunately, this study provides little guidance for determining if these specific species are valid and should be listed under the ESA, but perhaps more importantly; it highlights major gaps in the present understanding of species as opposed to population-level variation in corals. This study is an example of how knowledge of species boundaries in corals is not only necessary for understanding patterns and processes of biodiversity and evolution, but is essential for conservation.

In short, the article is a “fun read.” 

One of the many take home messages is obviously that corals are exceptionally difficult critters to identify.  Generally, if we choose the proper characters, we can identify them to genus.  Beyond that… don’t even try.  As it stands now, we have so few data across the range of most tropical stony reef-forming (and presumably, non-reef forming as well) corals, that distinguishing any specific species is an impossible task. 

Enjoy the article!!

Cheers,

Angels of Death

Wednesday, December 15th, 2010

Hi Folks,

Here are a couple of great links pirated from the Deep Sea News blog.

The subject of that blog’s discussion is what the author calls “sea angels,” rather beautiful predatory swimming snails in the genus Clione.   Embedded below is a movie of one swimming lifted from YouTube.   These pretty liddle snails were called “sea butterflies” in the Pacific NW – off the British Columbia and Washington coasts, where I had many chances to observe them, both during and after my graduate studies.

In that area, the common species reaches lengths of about 2 cm – 3cm, roughly an inch or so, but most of the individuals I have seen have been smaller.   These are shell-less snails, found in the water of the colder oceans through out the world.  They swim all their lives.

“Sea angels” and “sea butterflies” ….. ah…. such cute names…

Sorta like calling a hunting tiger, “Fluffy,” or a semi-starved, very hungry, fresh-from-hibernation-and-in-a-(REALLY)-bad-mood Grizzly bear, “Snuggles.”  

Individuals in Clione species snails are specialized predators that appear obligately bound to eat only another pelagic swimming snail.  At least that is the reading from the snail biology gospel; in reality I don’t think they have been studied well enough to know if they have any alternative prey.   While Clione individuals lack shells, their prey do have shells and look rather like a regular snail; both species have large extensions of their foot which they flap like wings.  This gives all of these snails the group name of Pteropods, or “wing-foot,” snails. 

I have embeded another movie, this one showing Clione individuals attacking and eating their prey, Limacina.  And as you watch the movie, I think you will see why I consider the name of Sea Angel to be a bit…. inappropriate.  Unless, that is, it is modified to be the “Sea Angel of Death.”

Swimmers near bathing beaches should be thankful that Clione individuals don’t reach about 2 m long (6.6 ft) and have a taste for humans.

A few times when I was teaching a course about Marine Invertebrates at a university field station/marine laboratory on Vancouver Island, I was lucky enough to be able to have had my theaching assistants collect some individuals both Clione and Limacina within a day or two of one another.   For the class, I would take a large graduated cylinder – these are about 3 feet long and several inches in diameter.  And then I would put in one or two Clione individuals and let them become acclimated, typically that only took a minute or two.  Then I would have the students gather around, and would introduce two or three Limacina.   The rapidity and apparent “ferociousness” (this is a anthropomorphic adjective, but after watching the Clione at work, it seemed to fit, but probably a better adjective is “efficiency”) of the attack would typically leave the students, quite literally, speechless.

Most of the time marine biologists (and I suppose other folks who see such things) typically regard snail predation as a slow and rather leisurely process (albeit animals like Cone snails will also demonstrate the other extreme).  After all, an oyster drill (a muricid whelk) drilling a hole through a bivalve shell is hardly action that is exciting, except, perhaps, to the participants.  

Then, if you are very lucky, you get to see something like Clione attacking a Limacina.  Wow!!!  It kinda blows away the stereotypes and misconceptions…

If you think about this system, wherein one pelagic snail lives by preying only on another pelagic snail, a bit further, I think it is really cause for wonder.  At best, Clione – the predators – are found in aggregations (I really don’t think one could call them “schools,” or “herds” or “flocks”) or patches maybe several meters in volume, and with a few snails per cubic meter.  More often the patches arel larger a few hundred meters on a side, and the density is one or two snails per 5 or 10 cubic meters.

So… lots of water… not many predators….just swimmin’ along being their little sea angelic selves, and with a LOT of water between them.  

Now… the prey – and the same sort of situation.  Lots of water, not many prey.

Two diffuse patches of animals in a very large body of water, what are the odds that any one snail of either species will encounter an individual of the other species?

Well, the odds have to be pretty good or the animals wouldn’t be here!  But still, it is not like these are pedestrians on the sidewalk along a busy street bumping into one another. 

I don’t know of any research that has been done investigating these interactions ecologically in nature.  I suspect the logistics of such research would make it prohibitively expensive (lots of ship time, for example), but the questions raised by the necessity of such interactions are really pretty interesting, I think you will agree.

Perhaps they are being studied at the present.  The author of Deep Sea News blog mentions a student/researcher/photographer, Natalia Chervyakova of Moscow University, who has taken some images of Clione feeding in nature – an amazingly difficult proposition.  Here are some of her images from the White Sea.  These are some of the most spectacular underwater macro photographic images I have ever seen.   And having taken thousands of underwater shots, including a number of planktonic macro shots, I can attest to the skill and effort involved and demonstrated by these images.  I would have killed to have been able to get one – 1 – image like these.  I would have killed a lot more, to have had the skill to be able to do it repeatedly.

Finally, shelled pteropods, similar to Limacina in some regards, are at the base of the zooplankton food chain throughout much of the world’s ocean.  They are especially abundant in the very rich fishery regions of the cold temperate and boreal seas, where they eat phytoplankton and convert it into their tissue. In turn they are eaten by many other organisms.  Two or three times removed, they are the fish flesh or krill that is harvested for human consumption or use, to say nothing of the top predators in those ecosystems, whose trophic position has been usurped by humans.   These pteropods have aragonitic shells, and as the oceans acidify they will be amongst the first to be affected by this interesting tiny experiment in the alteration of the ocean’s physical parameters.  “Affected” … A nice polite word for “Exterminated” by both human action (the addition of massive amounts of excessive carbon dioxide to the atmosphere) and inaction (no attempt to slow down those additions).

The sheer and utter stupidity of the human species, both individually and collectively is truly mind-boggling.  Here we are, well on our way into the sixth major mass extinction event in the Earth’s existence, and politicians play games of posturing over public images and the majority of the public wastes its time paying attention to the foibles of ephemeral pseudo-entertainer or some ridiculous sporting event.  I guess over the symbolic grave of humanity, our epitaph should be, “Considering their potential and abilities, they had their priorities straight.”

Until later,

Cheers,

It Happened One Night

Saturday, April 3rd, 2010
    
It Happened One Night…2nd Edition.

This is the second version of this essay, the first one was destroyed when my blog had to be wiped as a result of being hacked, see the previous post for details.  I did not keep a record of the images that I had placed in the previous version, so if you read the previous version and had a favorite image, and it is not here, please contact me and I will see what I can do about inserting it. 

A couple of squid near the breeding assemblage

About 25 years ago I was teaching Marine Invertebrate Zoology at the Bamfield Marine Station (the name has been since changed to the Bamfield Marine Science Centre), a university-run marine teaching and research laboratory facility.  This facility is located on the shores of Bamfield Inlet, a small embayment on the south side of Barkley Sound near the southwest corner of Vancouver Island.  That particular year the course ran from late April until early June and was supposed to be a total immersion course – the students lived, breathed, ate, slept, and dreamed about invertebrates.  In this year, by late May, I was casting around for something of special interest for the students to work on, something above and beyond the “standard” course offerings.   

For about a week, we had been seeing a few squids swimming near the water’s surface next to the dock.  This was unusual, so I decided to go diving and see if I could see what they were up to.  These animals were Loligo opalescens, the “Pacific Market Squid” harvested in huge numbers near Monterey, California for calamari.  At the time, the southern populations were pretty well known, but not much was known about the northern populations. The local lore was that the squids, occasionally, would spawn in the inlet.  If spawning was to occur, I thought it would be nice to document this for a couple of reasons.  First – it would be ultimately cool to be in a squid spawning aggregation.  Second – I thought I might get some nice images that I could use in lectures.  Third – I thought I might be able to interest a few of the students in doing some actual research on some small aspect of the spawning.  All-in-all, if I could carry it off, it would be a win-win-win situation.  The only problem was trying to predict when the  animals would spawn, and then coming up with a scientifically valid short research project.   

Prior to this one particular morning, we had been seeing a few scattered squids near the surface in the inlet.  These surface-swimming animals were fully-grown, about 30 cm (1 foot) long, and bright white, so they were quite evident in the dark water of the inlet.  About 10 o’clock, after my lecture for the day was over, I wandered down to the dock, and noticed that the squids were present in larger than “normal” shoals, maybe up to 30 to 50 animals in each fast moving school, so I thought this would be worth a look.  I asked around and found a dive partner and dock tender, and we plopped ourselves in the water about 30 minutes after 10 AM.  To document our dive, I took along my underwater camera system, which consisted of an Olympus OM-2 in an Ikelite housing, with two strobes attached; one triggered by the camera and the other slaved to the first one.  The film was Kodachrome-64, my film of choice for underwater photography.  

Solitary Loligo opalescens

Dropping down to the bottom, at a depth of about 17m to 18 m (55-60 ft), we found a small mass of squids in a frenzy of activity.  As a result, I started my personal frenzy of activity taking some images.  It soon became evident that a couple of individuals were spawning, but that most of the animals were just “interested” observers, squid voyeurs, I guess.  I documented a solitary female spawning and depositing her egg capsules.  I presumed copulation had already taken place, as I saw no obvious mating activity.  I had seen movies of some squid spawning aggregations, and it was obvious that what we were watching was not a normal spawning event.  However, I thought it might be a precursor to the “real” action.       

Solitary Female Loligo opalescens Spawning. Note The Extruded Egg Capsule Between Her Arms.

Solitary Female Ovipositing. Note Egg Capsule Between Her Arms.

Same Individual As In The Previous Figure. Note The Egg Capsule.

Egg Capsules Deposited By The Single Female Over The Course Of Her Spawning

Egg Capsules Produced By The Single Female Over The Course Of Her Spawning.,

For about a week the people of the village of Bamfield had been catching squid by jigging for them near the government-owned docks in town.  So, after seeing the events off of the laboratory dock, I thought that there might be a small mass spawning event occurring near the dock in the upcoming evening.  It would be a “small” event simply because the area was constrained.  The inlet was not wide and was relatively shallow, about 18 m (60 ft) deep at its maximum in that area.  I arranged for another dive buddy and boat tender and we went down to the town docks about 10:30 pm to do our dive.  As usual, I took my camera system along to document interesting “happenings.”   

When we arrived at the scene, the fishermen already there said that jigging was “slow.”  Squids were visible, but sparse, and not many had come into the area where the fishermen were.  To avoid upsetting the fishermen, we dove well away from them.  This also prevented us from being “jigged.”  Having a sharp squid jig tear open and flood one’s (very) expensive dry suit can really ruin the experience of the moment!   

When we first got into the water, few Loligo were around, but within a couple of minutes they started to aggregate around us, probably attracted by our diving lights, and the large pile of rocks on the bottom nearby.  At first there were just a few solitary individuals, then a few doublets, and then quartets, and then … large groups; Too large and too fast to count.  All of a sudden the action began.   

Although the spawning aggregation appeared terribly chaotic, with thousands – yes, thousands – of Loligo jetting around from all directions and bumping into each other and us, after a bit of observation, it became clear that what appeared to be an unruly affair was really quite well “choreographed.” 

From the outside in…   

The animals approached the spawning site alone or in small groups of up to about ten individuals.  As they approached they had normal coloration; brown to reddish brown tones predominated on the bodies and the arms’ outer surfaces.    

A Squid Pair Above The Main Spawning Site

A Quartet Of Squid Approaching The Spawning Site.

At the outermost region of the spawning site, about 5 to 6 m (15 to 20 feet) above it, the individuals were actively fighting with one another to find a mate.  Females were “attacked” by males that wished to mate with them, and often two or more males fought each other for each female.  This was a brutal, winner-take-all, competition!  Skin was ripped off and the combatants used their beaks to rip pieces of flesh from their opponents.  The females were NOT passive participants in this rough foreplay; they were actively fighting as well.  Presumably, the strongest, most fit male prevailed.  During this activity, both males and females were white.  They did not flash or change colors.   

Mating/Foreplay Damage Making the mate choice - maybe... Lots of action here.

Foreplay - but getting near the final choice of mates. Note the bite damage on the male (lower animal).

Precopulation - "Foreplay" - Two Males and One Female

Loligo opalescens foreplay or copulation well above the egg deposition site

 As the combat continued, the participants got closer and closer to the bottom, and eventually one male prevailed.  He got into the oviposition position; holding the female from behind and below, with his eight arms wrapped around her.  Copulation, the transfer of a spermatophore (sperm packet) from the male to the female, occurred once this posture was stabilized.  The animals were now about 3 m (10 feet) above the bottom.  Once he was securely holding his mate, the male’s color pattern changed from pure white all over, to having a white body and reddish-brown tentacles.  The female remained totally white.  Once this color pattern was established all other males avoided the pair, and ceased jostling the resident male for possession of his female.  I suspect the color pattern change was THE signal that mating had occurred and that this particular female was no longer available.   

Mated Pairs Depositing Egg Capsules.

After the male’s color changed, he did all of the subsequent swimming for the pair.  He moved the female to the oviposition site and began to push her into the mass of egg capsules that were already at the site.  As they approached the site, the female extruded and formed an egg capsule which was held in her arms.  Once the male pushed her into the egg capsule mass, or onto any other acceptable area, the female wrapped the distal, adhesive and ropelike, end of the egg capsule around anything, such as other egg capsules, a sunken twig, a rock, a diver’s mask strap, which would hold it in place.   

The egg deposition frenzy, overall there were hundreds of pairs of squid at this one small site.

Egg Capsule Deposition

Frenzied action a couple of meters above the main egg capsule mass

Spawning pairs and the main egg capsule mass.

  When first formed, these egg capsules were about the size of one’s little finger, but they became larger as they absorb water.  From subsequent studies, part of the project we later did, I found that each egg capsule in this region contained about 150 eggs, sequestered within a series of protective – and toxic – membranous coverings.  I was unable to count the number of egg capsules produced by any specific single female, the situation was just too chaotic for that.  In the California areas other studies found that each female produced about 20 capsules.  If the same number was produced by these northern Loligo, each female would deposit about 3000 eggs in her one night stand.  

Newly deposited egg capsules

Egg Masses The Day After Spawning. The Masses Are About A Meter Thick.

After the final capsule was deposited, the male released the female and they both slowly departed the area.  The males seemed to be a bit more active and I surmised that at least some of them might try to mate again, as each one produces numerous spermatophores, and they only use one per female.  However, the action was so frenzied that I was unable to follow any given squid more than a few seconds, so it is possible that one shot was all the males had.  The females appeared to be totally spent; they swam erratically and weakly.  They often travelled only a short distance prior to settling to the bottom and dying.  The males probably swam a few more hours, at best, but they, too, don’t survive long.  Individuals of both genders are badly injured by the experience.   

New Egg Capsules, The Day After Deposition, My Dive Partner For Scale.

During the flurry of spawning activity predators made their appearance.  In the area where I was diving these predators were seals and California sea lions which would come blasting through the spawning masses biting up squid as they went.  Fortunately, they decided big ugly divers in rubber suits didn’t match their search image of calamari.  In other areas, larger sharks, such as blue sharks, will also come into the spawning squid schools, but, blissfully, I didn’t see any of those in the aggregations I dove in. 

After the spawning was over, the bottom was littered with egg capsule masses and dead or dying squid.  Over the week following the spawning, some of my associates and students and I did some diving to make measurements of the squid egg masses.  Scattered all over the bottom, from just below lowest low water to beyond diver depth, were small individual egg capsule aggregations.  Each of these covered about 0.3 square meters, (about 3 square feet) and there were about 1.3 of them per square meter (10 square feet).  I collected some of these aggregations, and found that each contained, on the average, about 1,940 capsules.  Each capsule contained about 150 eggs, meaning each capsule mass was the result of 194 squid pairs, and contained 291,000 eggs.   

Dead squid the morning after the spawning event.

Mass of dead squid, the morning after.

 We did diving surveys to determine the extent of the night’s spawning activity.  This particular night’s spawning aggregation extended along about 11 km (7 miles) of the southern edge of Barkley sound.  The largest egg mass we found in a quantitative survey area was 69 square meters or 742 square feet, however, we saw some much larger egg masses.  Unfortunately, these were seen during the spot surveys for determining the whole area covered by the spawning aggregation, and we could not return to them.  We estimated the largest measured spawning aggregation was result of 24,000 spawning pairs of Loligo, and based our quantitative measurements of small egg mass abundance we estimated that during that one night of spawning, in the Bamfield area, over 64,000,000 squids spawned!   

Urticina corieaca, a sand dwelling anemone, and squid corpses. It normally would eat squid, but was sated the next morning.

 Loligo opalescens eggs take about six weeks to hatch in that region, and some of the egg masses were followed for that length of time.  After hatching, the remnants of the membranous egg coverings were still noticeable on the bottom for another several weeks in places.  As long as the egg capsule membranes were intact, nothing was seen eating the eggs.  Stupidly, I did not wear gloves during my initial examination of the egg capsules and the eggs when I was tearing and cutting open the egg capsule membranes.  After a few minutes of handling the membranes my fingers lost feeling, and a few minutes after that my hands became numb and immobile.  The area of numbness continued to expand until finally my arms became numb up to the elbows.  It took about 2 to 3 hours before the feeling slowly returned to my arms and hands.  Obviously, whatever is in the membranes would be effective at deterring predation.  In over 100 diver hours of examining the capsule masses, no animals were seen eating the eggs, although we saw many animals positioned on or in the masses.  If egg capsules were torn or cut open underwater, red rock crab individuals, Cancer productus, rapidly approached and started eating the eggs or developing embryos, further illustrating the protective function of the capsular membranes.  The long decay period for the membranes after the squids had hatched also indicated that the membranes contained either or both antifungal and antibacterial agents.   

A sunflower star, Pycnopodia helianthoides, on an egg capsule mass. The star was not eating them.

Old egg capsules, near hatching. They absorb water and are about three times the size they were when deposited.

During the several weeks it takes them to hatch, other animals in the area seem to consider the toxic egg capsules as "just part of the habitat."

 Reference:   

Shimek, R. L., D. Fyfe, L. Ramsey, A. Bergey, J. Elliott, and S. Guy.  1984.  A note on the spawning of the north Pacific market squid Loligo opalescens(Berry, 1911) in Barkley Sound, Vancouver Island, Canada.  Fishery Bulletin.  82:445-446.