The purpose of this blog is to organize and reorganize resources and my own work on the biology of Millepora spp. and their zooxanthellae.

Wednesday, August 27, 2025

Stepping back: What are Millepora spp.?

 

Fire corals Millepora spp. are cousins of the predominant reef corals, the Anthozoan Scleractinians.  Scleractinian reproductive biology has attracted attention partly because of mass spawning and multispecies mass spawning events.  Such spawning behavior---synchronized broadcast of eggs and sperm into the "water column" is common in marine species, particularly species that are attached to the sea bottom.  Among coral reef species, broadcast spawning is a prevalent reproductive strategy, partly because the reef is a bulwark of hungry animals, so it is believed that by broadcasting eggs and sperm can facilitate their escape until they are competent to make their way to a reef---the same or even another reef at great distance---and claim their own living spaces.  The literature of coral reef invertebrate and fish reproduction is vast, presenting a panoply of fascinating and diverse life patterns.  

 Millepora species hold a special interest in regard to their life histories.  They hold a large amount of space on coral reefs, wherever they occur.  They live a complex lifestyle, as both consumering---meeting some proportion of their nutritional needs by capturing plankton; and produccers---through their partnership with photosynthesizing zooxanthellae, which provide them with a preponderance of their needs.  They, like other reef-building corals---which likewise could not thrive and build massive reef frameworks without their zooxanthella partners---take on characteristics of both plants and animals.  Like plants, they obtain energy from the sun, and they are immobile, living in the shallow waters where sufficient sunlight exists to support photosynthesis; and at the same time, they possess all the characteristics of animals: their polyps can snag prey, their cells are of the animal type, without cell walls or photosynthesizing plastics.  Early naturalists noticed these peculiarities, and they were classified as Zoophytes---a living hybrid between animal and plant.   Their animal nature demanded them to be classified among the animal kingdom, however, and eventually, it was recognized that the comprised a unique kind of amalgam, as animals with single-celled dinoflagellates living within them. This relationship is more than a friendship---the coral cannot survive without it's partner, and the partner is specially adapted for life within animals and animal cells.  Such organisms are now identified as Holobionts, similar to Lichens, amalgams of fungus and alga partners.  

 Millepora holds a special interest among "corals."  Their general nature is so similar that one might be forgiven for classifying them together with Scleractinia, but a closer leads to a completely different conclusion: these are Hydrozoans, where Scleractinians are Anthozoans, both belonging to the Phylum Cnidaria---known for their stinging cells, their cnidae, or nematocysts.  Moreover, the life cycles of these Hydrozoans is very unlike that of  their cousins,  as Millepora species exhibits the same Alternation of Generations that is characteristic of many comon hydroids, between polyp and medusa.  Like butterflies and caterpillars, these alternate stages seem completely unlike each other.   The reproductive cycle of Millepora spp. invokes a medusoid to carry the gametes---egg and sperm---away from the colony, into the water column where they spawn within a matter of hours, and die (like ephemeral insects).  

 Millepora spp., like Scleractinians, create massive Calcium Carbonae skeletons, although the size of each polyp is less than 1mm across.  The name "Millepora" means, literally, thousand pores: the colony is peppered with numerous minute pores, ordinarily of two kinds: the gastropores---from which the larger of two types of polyps, the gastrozoids, the eating polyps, can access the exterior; and the dactylopores---home to the smaller dactylozoids, the stinging zooids.  These two types are arranged in cyclosystems,   a central gastropore encircled by  five or six dactylopores.  The colony, then, consists of one large organism comprised of a multitude of smaller specialized individuals, the zooids.  Like other hydrozoans, Millepora spp. also have a third kind of zooid: a medusoid.  This zooid develops only at certain times, and it does not have access to the exterior: this   zooid is the host to developing gametes; it has two tasks: to swim away from the colony at the appropriate moment, and to spawn.  Pretty obviously, this must be the adult, like the butterfly, where the colony serves as the relatively giant host of these minute adults.  

 The medusoid develops within a protective cocoon---the ampulla---a pit within the stony skeleton covered by a thin layer of calcium carbonate, isolated from the external world.  The medusoid  cannot access the outside environment; but at the time of its liberation, it is essential that it escape.  This is made possible because the cover of the ampulla dissolves in concert with the development of the gametes and the maturation of the  medusoid itself, as the moment   for the medusoid to carry the gametes away.  Remarkably, this concert is synchronized among other medusoids on this colony, as well as on other, nearby colonies, at the appropriate moment.  

 My study focused on this unique character of Millepora spp., that as the egg and sperm have matured toward the point of readiness, the ampulla dissolves, making possible the escape of the medusoid.  By examining skeletal fragments, collected over a period of months, it should be possible to determine the time of reproductive activity.  

 

A very important question arises: how are these developments all synchronized on the reef?  Because Millepora spp. are gonochoristic---each colony bearing either male or female gametes---unless this process is tightly orchestrated, fertilization will fail.  Not only that, but synchronized timing is necessary to ensure maximal efficiency in success of spawning. 


Saturday, March 22, 2025

It's that time of year. A perplexing question: when will be Millepora platyphylla first go off, on Guam, in Spring 2025?

 [This blog is intended to store keepers, both my own work, and found material.  ]

 [Update, 6 April 2025: My gut feeling trends toward the next mass release of medusoids on Guam about three to five days after the next Full Moon--between April 18 and 18, 2025.]  

 

It is the second day of spring, 2025.  I am in California.  In 2023 and 2024, I wrote lengthy pieces around my predictions for potential dates for Millepora platyphylla's reproductive output.  I still have received no affirmation or confutation of my predictions.  

2025 presents a baffling puzzle.  Let me explain briefly.

 In 1984, soon after my arrival at the University of Guam Marine Laboratory, to commence graduate study.  Professor Richard Randall took me aside and suggested that corals would make a good thesis study.   I told him I was interested in reproductive timing, and I probably told him that I was interested in Tridacnid clams.  He called attention to an important detail of the life history, the fact that the hard parts (the skeleton) of these species bear markers of reproductive status: ampullae, small pits in which develop the medusoids---the reproducing adult stage.  I could easily, so I reasoned, collect a few small fragments of these corals every time I snorkeled.  This would make an interesting side project, requiring little effort.  After a year or two, I would have sufficient fragments to study them and perform a statistical analysis of the times of reproductive effort.  

Indeed, I began collecting fragments, cleaning them in Professor Randall's blue tank of Calcium Hypochlorite (swimming pool bleach) on the lanai, behind his lab.  I enjoyed snorkeling, and did so frequently during the coming months.  Over time;  I visited a number of reefs.  Over time a number of fragments (each between a couple of inches and perhaps 8 inches across) accumulated over the months in a large drawer in my desk.  Each of them bore pencil markings recording the place and date of collection. 

In April of 1985, about 3 or 4 days after Full Moon, a fellow student invited me to join his party on a night fishing foray in Southern Guam, and I tagged along.  By this time I had developed an efficient technique for collecting my fragments.  A fellow student, Doug Markell, introduced me to the use of a child's swim ring as a flotation collar for the five gallon white buckets that were ubiquitous and  cheap at local hardware stores.   Spare flashlights and large Ziploc bags, a geologist's hammer, a  masonry chisel, and a handmade acrylic slate made up my kit.  I probably was a hindrance to my friend and his cousins, but by the time I left the water I brought a few bags of seawater and fragments to my car.  

I was amazed: as I prepared to treat the specimens, in the beam of the flashlight could be seen swarms of medusoids in some of the bags!  Statistics would not be necessary to determine at least one date of reproductive effort!  

This was the first event I was to observe.  The next morning, I visited several of my snorkeling spots along the West (leeward) coast of Guam, and at each site, evidence presented itself that indicated recent spawning.  It seemed to me that such an event would be tightly syncronized, to ensure successful fertilization.  (You see, each medusoid is either male or female, and I had read reports that these ephemeral adults did not more than a few hours.)  

I kept on it, collecting fragments into the summer and fall.   I observed the sibling species M. dichotoma, with medusoids popping out of their ampullaee, swarmed by young Oxymonacanthus sp. filefish.  Could it be that these fish timed their production of young to coincide with the availability of such a food source?  The mouths, after all, of these young fishes were undoubtedly the ideal size to suck the medusoids out of their holes. 

As it happened, my study of Millepora spp. intensified, and I began to learn to prepare the tissues for microscopic study.  I had spent time at UCSB, during my last year prior to graduation, learning about microscopic methods that, I reasoned, would be possible even on a remote island.  My interest in reproductive timing led me to research methods for study of neurosecretion, which involved release of hormones that stimulated the development of gametes, a process called gametogenesis.  The next year found me in the microscope laboratory, processing specimens of Millepora spp.  

And the next year, 1986, I was not disappointed.  Millepora platyphylla went off about 4 or 5 nights after Full Moon, but in March.  My collecting and study now became the entire focus of my time, even until I left Guam in November 1986.  

A hypothesis about timing.

These observations  led me to hypothesize that Millepora platyphylla released the medusoids in either late March or early April, three to five nights after Full Moon, just after dusk.  The date of this event would be some time during a window in the calendar, depending on when Full Moon fell.  I did not realize at the time that this mode of timing conincides in at least some details to the timing of many marine invertebrates, including Scleractinian corals, the kind that gets most of the attention, due to mass spawnings at various places around the world.  Easter, in fact, is reckoned by a similar algorithm, sometimes in March  and sometimes in April.

 Perplexing Question

 
This year Full Moon falls near the middle of March and again in April.  One is baffled.  
 
???

 

 

Monday, June 24, 2024

Structure of the ampullae of Millepora spp. is defined by the structure of the tissues.

An earlier post presented an image of the degradation of the tissue overlying the ampulla---and hence medusoid---of Millepora sp. cf. platyphylla.  An image of lower magnification of the identical slide shows the structure that has been compromised, toward the periphery of the hollow that is the ampulla.  Pylons remain beyond the central part of the disk.



Below, another image, this time of a male medusoid gives a better idea of the structure of tissues of an intact covering of an ampulla.  The pylon-like structure is clearly identifiable.  Individual spermatozoa are also clearly visible.





Friday, June 21, 2024

Ampullae of Millepora spp: Decalcification Prior to Liberation/Escape of Medusoids


This image signals a hallmark event in the life history of Millepora spp., as one of several propitious sections with views of a Millepora sp. (probably M. platyphylla) collected in 1986, likely at Toguan Bay, Guam.  This study derived from the plan to use the condition of hard-part specimens---presence of open ampullae---as an indicator of reproductive activity, as an approach to determining the timing of reproductive activity.  Once open ampullae had been observed, and certain signs in  colonies, in situ,  interest was aroused in histological study of the structural changes.  This slide represents a proof of concept of this approach.  e of  image is the beginning of a story, involving timing of reproductive activity of these spp.; development of medusoids---inside protective cavities, the ampullae; and the dissolution of the coverings of ampullae to allow the medusoids to escape.  

Millepora spp. are colonial calcifying hydroids, exhibiting alternation of generations; each colony bears either male or female medusoids. the "adult" form that spawns within a few hours of liberation into the water column, each of them less than 1mm in diameter.  In order to facilitate successful spawning between ephemeral medusoids, which live a number of hours, they must swarm in the water column en masse. This requires a tight synchrony in time of release.    

 



Distal part of medusoid, degrading covering, concomitant with decalicification of ampulla cover.  Two tentacles shown with developing nematocysts.





Wednesday, February 28, 2024

Briefly: A note from the Coral List about Millepora spp. decline in the Red Sea

On a mailing list a recent post to a discussion thread about effects of warming on coral reefs included this remark:

 

... There was a massive coral bleaching south of latitude 20 degrees (Al Lith) during the 2023 summer, correlating with water temperatures of 33-34 degrees. Many of the bleached corals have subsequently died and there has also been a near-complete loss of Millepora hydrozoans.

 

I had lunch next to Zvi Dubinsky, at the International Coral Reef Symposium on Guam, in 1992.  I discussed my interest in Millepora spp.  He said: "Millepora is always the first to go."

 

 


 




Note about Millepora taxonomy

 History of the taxonomy of Genus Millepora is tortured.   In the mid-20th Century, work by Hulbrandt Boschma resulted in the separation of the Genus into a number of species that are, substantially, still recognized today.  Hickson had synonymized all species of Millepora as ecomorphs of M. alcicornis. 

 In 1898, Hickson decided that the variations in morphology were due to environmental factors and that Millepora alcicornis was the valid name for all these species. This conclusion has since been questioned.

                                          ---Wikipedia

A number of workers have recently applied molecular methods to the classification of Millepora spp., and to be sure some question has been cast on the global homogeneity of, for example, Millepora platyphylla and especially M. dichotoma.  

Sidney Hickson was a  widely recognized zoological authority.  A lesson can be drawn by looking at the number of workers---themselves also authorities---who accepted the word of Hickson without, it seems, questioning the validity of a remarkable act of mass synonymization of a suite of species as ecomorphs of a single species.    Hickson could do no wrong.  


The species question of corals in general is a thorny one.  Even the definition of species needs to be examined, when discussing corals.  The fact of mass spawning of numerous species of corals at various places, including the Great Barrier Reef, and Guam, for example, would seem to leave open the possibility, in my mind, of hybridization. 

In his treatment of _The Species Problem in Millepora,  Boschma he discussed  characters that could distinguish various Millepora species, citing Hickson's earlier list:


  • The form of the corallum
  • The texture of the corallum and its surface
  • The size of the pores
  • The shape of the pores
  • The degree of isolation of the cycles
  • The relative number of Dactylopores and Gastropores
  • The distribution of the pores in various parts of the corallum
  • The Presence or absence of ampullae
  • The anatomy of the soft parts
  • The stinging properties
  • The distribution of the various forms in different parts of the reefs
 

 In one paper, Duchassiang and Michelotti (in 1864) named "not less than 22 (or 24) West Indian species."  (Boschma,  Very few have not tripped over the thorny problem of the species of Millepora.  

 

To be extended.  Boschma's paper is noteworthy.  

 Boschma, Hilbrand. "The species problem in Millepora." Zoologische Verhandelingen 1, no. 1 (1948): 1-116.

Randomly, here is a reference to Arigoni et al, a recent approach to systematics of Millepora spp.

 Arrigoni, Roberto ; Maggioni, Davide ; Montano, Simone et al. / An integrated morpho-molecular approach to delineate species boundaries of Millepora from the Red Sea. In: Coral Reefs. 2018 ; Vol. 37, No. 4. pp. 967-984.

 Boisson et al. approached the species of Millepora at Reunion in a similar manner:

Boissin, E., J. K. L. Leung, V. Denis, Chloé A-F. Bourmaud, and Nicole Gravier-Bonnet. "Morpho-molecular delineation of structurally important reef species, the fire corals, Millepora spp., at Réunion Island, Southwestern Indian Ocean." Hydrobiologia 847, no. 5 (2020): 1237-1255.
 

 Another parallel:

Manchenko, Gennady P., Alexander V. Moschenko, and Vyatcheslav S. Odintsov. "Biochemical genetics and systematics of Millepora (Coelenterata: Hydrozoa) from the shore of south Vietnam." Biochemical systematics and ecology 21, no. 6-7 (1993): 729-735.

 

 

 

 



 



Friday, February 2, 2024

A lost slide found: Some thoughts: Putative Dying Dinoflagellaes; and Overview Images of Zooid Distribution

 As I was cleaning out my drawers, a slide appeared, caked in grime, that I had carefully labelled at some point using a crow quill pen wit, waterproof drawing ink, coated with clear nail polish.  The label provides the following information:  

Slide    : 530 ["A"]

Colony: Tog BE

Date.    : 15 April 1986

                    Fixative:  Bouin's 

                    Stain.    : #2 = Hematoxylin and Eosin

  

Green Cells: Putative dying Dinoflagellates, and date Medusae were Liberated

This slide is particularly interesting because of the date, and the presence of clusters of green entities that are probably deteriorating dinoflagellate symbionts.  Full Moon that month was on March 26 (need to double check this).   Medusae would have been liberated between 2 and 5 days after Full Moon.  This specimen may have been taken 20 days after Full Moon.  





Why are these clusters interesting?  Seeing the date, I have at least one new hypothesis to test:

 Since this date is 20 after full moon and the liberation of medusa was two to five days after Full Moon, does this suggest that after liberation, the entire colony reorganizes itself, the symbionts in certain regions being killed off?

I will revisit this idea at another time.

 Overviews of zooid distribution: a cyclosystem and random dactylozoids.


Two images are presented here of the same area of the slide mentioned above.  Actually, the date is inconsequential, as I was merely aiming for an, if one will, aerial overview of a small region, including a single Gastrozoid and its associates, the Dactylozoids, arranges in a Cyclosystem, .  The first is a single  brightfield image taken through a 4X AmScope objective; the second image is a 4x4 panorama assembled through Helicon Focus, software I have also used to take focus stacks of especially Millepora spp. skeletal material.  

Image I: A single brightfield image, 4X.  

I have not yet inserted a scale bar.





Image II: Darkfield panorama of 16 images taken at a higher magnification.

Panorama built up from 16 (4x4) images.  16X Objective.