Wooster’s Fossil of the Week: A colonial scleractinian coral from the Pliocene of Cyprus

November 10th, 2013

Cladocora_585This week’s fossil is another from the collection made in 1996 on a Keck Geology Consortium expedition to Cyprus with Steve Dornbos as a Wooster student. Steve and I found a spectacular undescribed coral reef in the Nicosia Formation (Pliocene) near the village of Meniko (N 35° 5.767′, E 33° 8.925′). Finding a reef was a surprise because the unit is mostly quartz silt, which is not a sediment you usually associate with coral reefs. It was an advantage, though, because the silt was poorly lithified and could be easily removed from the fossils. The significance of this reef was that it represents the early recovery of marine faunas following the Messinian Salinity Crisis and the later refilling of the Mediterranean basin (the Zanclean Flood). Steve and I published our observations and analyses of this reef community in 1999.

The coral is a species of the genus Cladocora Ehrenberg, 1834. This genus, a member of the Family Caryophylliidae, ranges from the Late Cretaceous to today, so it is a hardy group. This may be because it is unusually diverse in its habits, ranging from the shallow subtidal down to at least 480 meters, and including both zooxanthellate (containing symbiotic photosynthesizing organisms called zooxanthellae) and azooxanthellate (with no such symbionts) species. Since our fossils lived in shallow water, they were almost certainly zooxanthellate.

(Courtesy of Wikimedia Commons user Esculapio)

(Courtesy of Wikimedia Commons user Esculapio)

Cladocora is still found today in the Mediterranean (see the above Cladocora caespitosa). Like all zooxanthellate scleractinian corals, these shallow species of Cladocora obtain their nutrition from the byproducts of their photosynthetic symbionts and a diet of small animals (mostly arthropods and larvae) they collect with their tentacles. These tentacles are lined with “stinging cells” called nematocysts.
CladocoraSpondylus_585Our Pliocene Cladocora formed the framework of a reef at least six meters high and 50 meters wide. It had many shelled organisms living entwined in the branches of the coral, like the bivalve Spondylus pictured above. You can see the corallites (individual tubes) embedded in the shell.
EhrenbergChristianGottfried_585Christian Gottfried Ehrenberg (1795-1876) named the genus Cladocora from specimens in the Red Sea. He was a German naturalist and explorer who is often credited with founding the field of micropaleontology (the study of microfossils such as foraminiferans, ostracodes and diatoms). He earned an M.D. at the University of Berlin and remained on the university staff for his entire career. He was no homebody, though, traveling as a scientist throughout the Mediterranean and Middle East, Central Asia and Siberia. (His first expedition to the Middle East was an adventure, as you can read at the link.) He was the first to prove that fungi reproduce via spores, to describe the anatomy of corals, and to identify plankton as the source for marine phosphorescence. Ehrenberg was also the first to discover microfossils in rocks, noting that some rocks (like chalk) are made almost entirely of them. His best known books include Reisen in Aegypten, Libyen, Nubien und Dongola (1828; “Travels in Egypt, Libya, Nubia and Dongola”) and Die Infusionsthierchen als volkommene Organismen (1838; “The Infusoria as Complete Organisms”). That last concept (“volkommene Organismen” or “complete organisms”) was his idea that even the smallest organisms had all the working organs of the largest. That one didn’t go so well!

References:

Cowper Reed, F.R. 1935. Notes on the Neogene faunas of Cyprus, III: the Pliocene faunas. Annual Magazine of Natural History 10 (95): 489-524.

Cowper Reed, F.R. 1940. Some additional Pliocene fossils from Cyprus. Annual Magazine of Natural History 11 (6): 293-297.

Dornbos, S.Q. and Wilson, M.A. 1999. Paleoecology of a Pliocene coral reef in Cyprus: Recovery of a marine community from the Messinian Salinity Crisis. Neues Jahrbuch für Geologie und Paläontologie, Abhandlungen 213: 103-118.

Wooster’s Fossil of the Week: A carnivorous snail from the Pliocene of Cyprus

October 20th, 2013

Euthria Gray 1850 Pliocene Cyprus_585These drab and worn shells from the Pliocene of Cyprus are the remains of deadly little snails still around today. They are from an unknown species of the genus Euthria Gray, 1850. (Sometimes Euthria is considered a subgenus of Buccinulum.) They are fossil whelks (Family Buccinidae) from the Nicosia Formation coral reef community described in earlier posts and in a paper by Dornbos and Wilson (1999).

Whelks are carnivorous snails of a group formerly known as the neogastropods. They have an incredible underwater sense of smell through an organ known as the osphradium, enabling them to track down prey items such as clams, other snails, and carrion. (Yes, “tracking down” mostly sessile critters does seem to lack a bit in drama.) With their radulae (essentially tooth-bearing ribbons) they can drill through thick shells. Some are known to cause extensive damage in oyster farms. Their characteristic boreholes have been found in shells since the Cretaceous.

Euthria is very widespread today, and contains innumerable species poorly separated from each other by shell morphology. No doubt some later genetic study will show that the genus consists of relatively few species with considerable ecophenotypic variability.
John Edward Gray 1851Euthria was described by the English naturalist John Edward Gray (1800-1875) in 1850. Gray, who eventually became a fellow of the Royal Society, started his zoological career in a classic way: he volunteered to collect insects for the British Museum in London when he was just 15 years old. He joined the Museum officially in 1824 and stayed there for 50 years, publishing hundreds of papers on zoological topics, from reptiles and birds to snails and clams. Oddly enough, for all his scientific fame, he is also recognized as the first postage stamp collector. In 1840 he purchased a group of Penny Black stamps in order to save them as curiosities rather than use them for mailing.

References:

Beets, C. 1987. Notes on Buccinulum (Gastropoda, Buccinidae), a reappraisal. Scripta Geologica 82: 83-100.

Cowper Reed, F.R. 1935. Notes on the Neogene faunas of Cyprus, III: the Pliocene faunas. Annual Magazine of Natural History 10 (95): 489-524.

Cowper Reed, F.R. 1940. Some additional Pliocene fossils from Cyprus. Annual Magazine of Natural History 11 (6): 293-297.

Dornbos, S.Q. and Wilson, M.A. 1999. Paleoecology of a Pliocene coral reef in Cyprus: Recovery of a marine community from the Messinian Salinity Crisis. Neues Jahrbuch für Geologie und Paläontologie, Abhandlungen 213: 103-118.

Fraussen, K. 2002. A new Euthria (Gastropoda: Buccinidae) from New Caledonia. Gloria Maris. Tijdschrift uitgegeven door de Belgische Vereniging voor Conchyliologie 41: 70-74.

Petit, R.E. 2012. John Edward Gray (1800–1875): his malacological publications and molluscan taxa. Zootaxa 3214: 1-125.

Zunino, M. and Pavia, G. 2009. Lower to Middle Miocene Mollusc assemblages from the Torino Hills (NW Italy): Synthesis of new data and chronostratigraphical arrangement. Rivista Italiana di Paleontologia e Stratigrafia 115: 349-370.

Wooster’s Fossil of the Week: A gastropod/coral/hermit crab combination from the Pliocene of Florida

October 6th, 2013

Septastrea marylandica_585These two shells show a lovely symbiosis between shallow marine hermit crabs and encrusting scleractinian corals. I was first introduced to the concept of “pagurized” shells by my friends Paul Taylor and Sally Walker. They showed me the many ways by which shells that were carried around by hermit crabs display particular evidence of this specific use, from characteristic wear patterns to patterns of encrustation and boring. Further, there are some situations, such as that shown above, where encrusters and hermit crabs have developed a mutually beneficial relationship that may have even been depended upon by the crabs.

What we have here are gastropod (snail) shells that have been completely encrusted by the scleractinian coral Septastrea marylandica (Conrad, 1841). These are found in great abundance in the Pliocene Pinecrest Sand (foraminiferal zone N20) near Fruitville, Sarasota County, Florida. What is most cool is that the corals have completely encrusted these spiraling snail shells and more. If you look carefully at the aperture of the specimen on the left you see the lower surface of the coral with no snail shell. The coral had encrusted the whole shell and continued to grow from the original aperture outward, elongating the twisting tube farther than the snail ever grew. Why (and how) did it do this?

The answer is that the shells were occupied by hermit crabs. The corals extended the aperture of the shell with the crab shuffling about in the opening. The crabs gained the advantage of a shell that essentially grew along with them, meaning they did not have to make the dangerous switch to a larger shell as often. The corals gained by being carried about into diverse microenvironments, extending their feeding possibilities. Nice arrangement, and elegant fossils to show it.
Septastrea closeSeptastrea marylandica (Conrad, 1841) is a scleractinian coral. We’ve seen this order before on this blog, but usually as a recrystallized version of the original aragonitic shell. In these specimens the aragonite is still preserved in excellent detail. Each of the individual “cups” (corallites) above contained a single coral polyp in life. The radiating vertical walls are called septa and are related to the original soft parts of the polyps. The polyps extended tentacles from these corallites into the surrounding seawater. The tentacles were lined (as they are today) with stinging cells called nematocysts for subduing very small items of prey, such as larvae or tiny arthropods. Corals thus represent an ecological group of sessile benthic epifaunal predators. Sessile means stationary, benthic means on the seafloor, and epifaunal means on the surface of the seafloor (that is, not in the substrate itself). Curiously, then, these corals that encrusted shells with hermit crabs in them became in a sense vagrant rather than benthic because they were moved about on the seafloor. You don’t hear about vagrant benthic corals very often!

References:

Allmon, W.D. 1993. Age, environment and mode of deposition of the densely fossiliferous Pinecrest Sand (Pliocene of Florida): Implications for the role of biological productivity in shell bed formation. Palaios 8: 183-201.

Darrell, J.G. and Taylor, P.D. 1989. Scleractinian symbionts of hermit crabs in the Pliocene of Florida. Memoir of the Association of Australasian Palaeontologists 8:115–123.

Laidre, M.E. 2012. Niche construction drives social dependence in hermit crabs. Current Biology 22: R861–R862.

Petuch, E J. 1986. The Pliocene reefs of Miami: Their geomorphological significance in the evolution of the Atlantic coastal ridge, southeastern Florida, USA. Journal of Coastal Research 2: 391-408.

Taylor, P.D. and Schindler, K.S. 2004. A new Eocene species of the hermit-crab symbiont Hippoporidra (Bryozoa) from the Ocala Limestone of Florida. Journal of Paleontology 78: 790-794.

Vermeij , G.J. 2012. Evolution: Remodelling hermit shellters. Current Biology 22: R882-R884. [Really. The title is spelled exactly this way.]

Walker, S.E. 1992. Criteria for recognizing marine hermit crabs in the fossil record using gastropod shells. Journal of Paleontology 66: 535-558.

Wooster’s Fossil of the Week: A delicate brachiopod from the Pliocene of Cyprus

September 22nd, 2013

Terebratulid Pliocene CyprusThese thin-shelled brachiopods were collected in the summer of 1996 on a Keck Geology Consortium project in Cyprus. Strangely enough, they were the first brachiopods I had ever seen in the Cenozoic. These are ventral valves of the terebratulid Maltaia pajaudi García–Ramos, 2006. On the left is the external view, and on the right is the internal. In the internal view at the top (posterior) portion of the shell you can see the rounded pedicle opening and two teeth of the hinge mechanism that articulated the valves.

The fieldwork that summer was with three students: Steve Dornbos (’97) of Wooster, Ellen Avery of Bryn Mawr, and Lorraine Givens of SUNY-Buffalo State. We found hundreds of gorgeous fossils, many of which have been described in these webpages. All are from the Nicosia Formation (Pliocene) exposed on the Mesaoria Plain in the center of Cyprus near the village of Meniko. The brachiopods above were found at a site we termed “Pelican-Brachiopod” that had 37 different fossil species. It was an unusual paleocommunity with large numbers of predatory gastropods, many of which left their marks as boreholes in shells. We figured from the microfossils present, as well as the fine silty sediment, that this fauna lived in relatively deep waters, probably several hundred meters. We had other Nicosia Formation sites in very shallow waters (including a coral reef), so we were able to show considerable paleoenvironmental diversity in this thick unit.
G. Arthur Cooper and the "Emerald Queen"The Mediterranean brachiopod genus Maltaia was named in 1983 by the famous American paleontologist G. Arthur Cooper (1902-2000). I actually met the man in 1977 when I was an undergraduate attending the North American Paleontological Convention in Lawrence, Kansas. I was awestruck because he was legendary for his prodigious systematic work with brachiopods, especially those of the Permian in western Texas. The classic photo above shows him in the field with his Smithsonian Institution vehicle he named the “Emerald Queen”.

Cooper earned his B.S. degree at Colgate University with a chemistry major in 1924. He did his PhD work at Yale University with the epic paleontologists Carl O. Dunbar and Charles Schuchert, earning his degree in 1929. He loved brachiopods and was encouraged to pursue them by Schuchert. Cooper joined the paleontological staff at the United States National Museum in 1930, flourishing there through his retirement in 1974 into active emeritus status. He named hundreds of new fossil brachiopods during his career. I would not be surprised to hear he has the record of new fossil taxonomic descriptions. He was much honored in his time, including receipt of the second Paleontological Society medal in 1964.

References:

Bitner, M.A. and Martinell, J. 2001. Pliocene brachiopods from the Estepona Area (Málaga, South Spain). Revista Española de Paleontología 16: 177-185.

Bitner, M.A. and Moissette, P. 2003. Pliocene brachiopods from north-western Africa. Geodiversitas 25: 463-479.

Cooper, G.A. 1983. The Terebratulacea (Brachiopoda), Triassic to Recent: A study of the brachidia (loops). Smithsonian Contributions to Paleobiology 50: 1–445.

Dornbos, S.Q. and Wilson, M.A. 1999. Paleoecology of a Pliocene coral reef in Cyprus: Recovery of a marine community from the Messinian Salinity Crisis. Neues Jahrbuch für Geologie und Paläontologie, Abhandlungen 213: 103-118.

Toscano-Grande, A., et al. 2010. Neogene brachiopods from the southwestern Guadalquivir basin (south Spain). Revista Mexicana de Ciencias Geologicas 27: 254-263.

Wooster’s Fossil of the Week: A crab’s meal from the Pliocene of Cyprus

August 25th, 2013

Astraea rugosa side view_585This week’s fossil was collected on a Keck Geology Consortium expedition to Cyprus in the summer of 1996. My Independent Study student on that adventure was Steve Dornbos (’97), now a professor at the University of Wisconsin, Milwaukee (and a new father!). The other students on our paleontological project were Ellen Avery and Lorraine Givens. One day Steve and I stumbled across a beautifully-exposed coral reef weathering out of the silty Nicosia Formation (Pliocene) on the hot and dry Mesaoria Plain in the center of the island near the village of Meniko (N 35° 5.767′, E 33° 8.925′). The significance of this reef was that it represents the early recovery of marine faunas following the Messinian Salinity Crisis and the subsequent refilling of the basin (the dramatic Zanclean Flood). Steve and I published our observations and analyses of this reef community in 1999.

Our featured fossil is the herbivorous turbinid gastropod Astraea rugosa (Linnaeus, 1767). That beautiful generic name means “star-maiden” in Greek and was originally used by Linnaeus in homage to the mythological Astraea, daughter of Zeus (maybe) and a “celestial virgin”. The species name rugosa means “rough” or “wrinkled”, in reference to the many ridges on the shell. The common name for this species, which is still alive today (as you can see in this video) is “rough star”.

What was most interesting to Steve and me was how this shell is broken. Most of the shell appears to have been peeled away, leaving the central axis and top in excellent shape. This is characteristic of crab predation. The crab, usually using one enlarged claw, peels the shell open by breaking it at the aperture and moving up the spiral. Eventually it hits the terrified snail pulled up as far as it could go in its twisty spiral of doom.
Astraea_Screen Shot 2013-08-22 at 8.37.54 PM copyThe image above, from this Spanish webpage, shows one of the further defenses Astraea rugosa had against crab predation: a thick calcareous operculum blocking the aperture like a heavy door. In some places these opercula are commonly preserved, but we found only a few and could not associate them with any particular species.
Astraea rugosa apical_585Finally, here is the top view of Astraea rugosa from the Pliocene of Cyprus. There is wonderful detail still preserved in the apical region of the shell, including characteristic star-like projecting spines.

We’ll see more fossils from the Pliocene of Cyprus in this space!

References:

Cowper Reed, F.R. 1935. Notes on the Neogene faunas of Cyprus, III: the Pliocene faunas. Annual Magazine of Natural History 10 (95): 489-524.

Cowper Reed, F.R. 1940. Some additional Pliocene fossils from Cyprus. Annual Magazine of Natural History 11 (6): 293-297.

Dornbos, S.Q. and Wilson, M.A. 1999. Paleoecology of a Pliocene coral reef in Cyprus: Recovery of a marine community from the Messinian Salinity Crisis. Neues Jahrbuch für Geologie und Paläontologie, Abhandlungen 213: 103-118.

Sediments, fossils and vistas at the Capo Milazzo Peninsula, Sicily

June 9th, 2013

1. Capo Milazzo 060913CATANIA, SICILY, ITALY–This was the last day of our International Bryozoology Association pre-conference field trip through Sicily. We had an excellent time and covered an extraordinary amount of territory on this large Mediterranean island. We started our final day on the Capo Milazzo Peninsula in the northeastern portion of Sicily. The view above is looking north from the base of the with the main lighthouse on the right and bay on the left. Just peeking around the headland in the distance is one of the Aeolian Islands. We climbed down to study the rocks in the middle distance.
2. Eckart Conglomerate 060913One of the most striking units we saw was this Pliocene conglomerate at the base of a small paleobasin cut into a Paleozoic metamorphic complex. The clasts are a variety of metamorphic rocks, from high-grade schists and gneisses to low-grade greenstones. Eckart Hakansson for scale.
3. Closer conglomerate 060913This is a closer view of the conglomerates. The matrix is a foraminiferan-rich marl almost identical to the marl which lies above it (see the next image).
4. Foram Marl 060913This Pleistocene (Gelasian) marl above the conglomerates is almost 95% planktonic foraminiferans, or at least it looks that way with a handlens. There are some other fossils (see below) and a few sand-sized lithic fragments, but otherwise this is a foraminiferan ooze deposit.
5. Pliocene marl octocorals 060913Besides the foraminiferans, the most common fossils in the Pliocene marls on the Capo Milazzo Peninsula are these stick-like objects. They are gorgonian octocoral internodes, probably from the species Keratoisis melitensis. I grabbed a handful and thereby tripled Wooster’s collection of fossil octocorals.
6. Pleistocene bored Miocene 060913Included in the marls are these cobbles and boulders of Miocene limestones slumped in from the slopes above. They often have large borings from lithophagid bivalves (producing Gastrochaenolites) and a smaller background boring by clionaid sponges (making Entobia).
7. Stromboli 060913There are spectacular views from Capo Milazzo. This is looking north at the volcanic island of Stromboli. We spent a long time staring at it because every half-hour or so it spouts steam and smoke for a few seconds. I didn’t get to see an event, but there was a continual very light plume blowing from the right to the left.
8. Mark Stromboli 060913This is the only time I handed my camera to a colleague and asked for my picture taken. I couldn’t resist a view with Stromboli in the background. I also wanted to show off my new Italian hat. (I lost my regular and well-worn field hat somewhere along the way.)
9. Etna Smoking 060913As we were leaving the peninsula, Mount Etna to the south let out a large puff of steam and gases into the murky air.
10. Hotel in Milazzo 060913Finally, a few shots from today to show a bit how our field trip worked. Above is our hotel in Milazzo, typical of the places we stayed around Sicily. Note all the little Fiat cars. In every city and town these cars were constantly buzzing by.
11. Bus interior 060913This is a view from my seat in our bus. Our intrepid leader Antonietta Rosso from the University of Catania is speaking in the microphone. We are very grateful to her for her planning, energy and good humor. My legs here, by the way, are extending well into the aisle because they just did not fit in these tiny Italian seats.
12. Field trip lecture 060913Antonietta Rosso is here giving us a field lecture before we descend down to the Capo Milazzo outcrops. The man taking photographs in the background is a keen Italian amateur who was very helpful. I wish I caught his name. He said one lifetime isn’t enough to enjoy all the wonders of this planet — and then there’s space!
13. Milazzo Castle 060913Just before lunch we had the requisite castle visit, this one in Milazzo. The Milazzo Castle suffered some bombing damage in World War II. The Germans and Italians used Milazzo and its port as a supply center for the Afrika Korps, and then later as a communications center for their resistance to the Allied invasion in 1943. The walls we are looking at here were built by the Spanish (Aragonese) in the 15th Century.
14. Messina Strait 060913Finally we passed by the Strait of Messina, with mainland Italy visible through the haze. This narrow body of water is extraordinarily deep and its sides continue to be uplifted by tectonic activity. These waters have wicked currents and have been known as a navigational hazard since antiquity. When we saw this strait we knew we had rounded the corner of Sicily and nearly completed our journey around the entire island.

Thank you again to our University of Catania leaders, especially Antonietta Rosso and Rossana Sanfilippo. Now we have a few hours to rest before the official International Bryozoology Association Conference begins tomorrow morning.

Return to the Pliocene at Altavilla Milicia, Sicily

June 8th, 2013

9. Altavilla Milicia 060813Our last stop of the day on the IBA field trip was to a classic fossil locality on the north coast of Sicily about an hour east of Palermo. These are fine sandstones and marls preserving a diverse array of mollusks from the Pliocene, including the bivalves shown below. Over 130 bryozoan species have been recorded from this site since 1921. The most interesting features to me were the numerous sclerobionts, including shallow worm and barnacle borings and encrusting bryozoans and barnacles.
10. Altavilla Milicia fossils 060813From here it was a long drive to the beautiful and ancient city of Milazzo to prepare for our last day of the field trip.

Pliocene marls white as snow in southern Sicily

June 6th, 2013

6. Pliocene Cliff 060613SCIACCA, SICILY, ITALY–Our last stop of the day on this International Bryozoology Association pre-conference field trip was to a massive outcrop of foraminiferan-rich marls known as the Trubi. A view of the cliffs with the sun setting behind them is above.

7. Hans Arne Pliocene 060613My colleague (and roommate on this trip) Hans Arne Nakrem is serving as a scale to show the regular cyclicity of these marls. Appropriately, he is from snowy northern Norway. These sediments were deposited immediately after the Messinian Salinity Crisis when the entire Mediterranean was reduced to a shallow series of evaporitive ponds. These marls mark the opening of the Strait of Gibraltar which flooded the Mediterranean Basin with normal seawater (the Zanclean Flood) 5.33 million years ago.

8. Pliocene Cliff 060613I wish I had better lighting to show just how brightly white these rocks are. They are now used as the base type section of the Zanclean Stage.

SicilyBeachSandHere is a late addition to this post (June 23, 2013). I collected some sand from the beach in front of these chalky rocks. A close-up image is shown above. Note that the chalk itself is eroded so quickly that it leaves no trace in the sand. We see here mostly rounded quartz grains and shell fragments.

Wooster’s Fossils of the Week: More bryozoan etchings and an African slug surprise

March 3rd, 2013

CheilostomeEtchings2_585This is the inside of a modern cockle shell (Dinocardium vanhyningi) found on a beach in Wilmington, North Carolina. Across the surface is a radiating series of pits, each of which was formed under a zooid of an encrusting cheilostome bryozoan colony, much like Ropalonaria described last week. This etched shell gives me an opportunity to tell a cautionary tale of trace fossils, slugs and taxonomy.
pdt12291This scanning electron microscope image was taken by my friend and colleague Paul Taylor at The Natural History Museum in London. It shows a cheilostome bryozoan etching (the elongated pits) across a shell surface very much like the modern shell at the top of the page. In the lower right is a bit of the cheilostome bryozoan Amphiblestrum. This particular bryozoan did not make the pits themselves (it is oriented in a different direction), but another colony of the same species likely did. This assemblage comes from the Coralline Crag Formation (Pliocene) exposed in Broom Pit, Suffolk, England.

In 1999, Paul Taylor, Richard Bromley and I published a paper in the journal Palaeontology describing these bryozoan etching pits as a new ichnogenus (a category of trace fossil) with a Late Cretaceous to Holocene range. We invented (or so we thought) the name Leptichnus using the Greek roots leptos (‘flimsy, delicate, subtle’) and ichnos (‘track, footprint’). It was a fun little project, and we provided a useful name to embed this fossil in the literature.

This past fall, thirteen years after publication, I decided to write a Fossil of the Week entry on Leptichnus. In my innocence I searched Google for “Leptichnus” and was very surprised to find it has a Wikipedia page — and it was an East African slug! Yes, the beautiful name Leptichnus was preoccupied by a urocyclid terrestrial gastropod, Leptichnus Simroth, 1896, found in Kenya and Tanzania. 1896 is a long time before 1999, so Simroth’s name has priority over ours. The ichnogenus Leptichnus Taylor, Wilson and Bromley, 1999, thus became a junior homonym of the gastropod genus Leptichnus Simroth, 1896. We had to come up with a new name for it.
LeptichnusOriginalDescription_585 copyAbove is the original 1896 description of Leptichnus The Slug by Heinrich Rudolf Simroth (1851-1917). He apparently came up with the name because this shell-less snail left a subtle trail behind it when it slithered. It is the first time I’ve seen the -ichnus suffix used for anything but a trace fossil.
Heinrich_Simroth_1902Herr Doktor Professor Simroth was a German zoologist and malacologist educated at the University of Leipzig. He was a schoolteacher for his whole career, doing prodigious research in his spare time. His speciality was, unsurprisingly, terrestrial slugs. He worked on specimens brought back by scientific expeditions, including one in the short-lived colony of German East Africa. It is from this collected material he described Leptichnus. Simroth’s type collection was long considered lost, but many specimens were recently rediscovered in Berlin (Glaubrecht, 2010). These do not, alas, include any representatives of Leptichnus. The image above is of Simroth in 1902.

Taylor, Wilson and Bromley (2013) proposed the new name Finichnus to replace Leptichnus Taylor, Wilson and Bromley, 1999. To preserve the meaning of the original name, we substituted the Greek finos (‘fine, delicate’) for leptos.

The lesson of this story? Search, search, search for homonyms of new taxonomic names. In our defense, searching wasn’t as easy back in the 90s (Google’s search engine came online in 2000, for example, and Wikipedia began in 2001). At least the adventure introduced us to Heinrich Rudolf Simroth and his slugs!

References:

Glaubrecht, M. 2010. Slug(-gish) science, or an annotated catalogue of the types of tropical vaginulid and agriolimacid pulmonates (Mollusca, Gastropoda), described by Heinrich Simroth (1851–1917), in the Natural History Museum Berlin. Zoosystematics and Evolution 86: 15–335.

Rosso, A. 2008. Leptichnus tortus isp. nov., a new cheilostome etching and comments on other bryozoan-produced trace fossils. Studi Trentini – Acta Geologica 83: 75–85.

Simroth, H. 1896. Über bekannte und neue Urocycliden. Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft 19: 281–312.

Taylor, P.D., Wilson, M.A. and Bromley, R.G. 1999. Leptichnus, a new ichnogenus for etchings made by cheilostome bryozoans into calcareous substrates. Palaeontology 42: 595–604.

Taylor, P.D., Wilson, M.A. and Bromley, R.G. 2013. Finichnus, a new name for the ichnogenus Leptichnus Taylor, Wilson and Bromley, 1999, preoccupied by Leptichnus Simroth, 1896 (Mollusca, Gastropoda). Palaeontology (in press).

Wooster’s Fossil of the Week: A swimming clam from the Pliocene of Cyprus

December 23rd, 2012

In the summer of 1996, I was a co-director of a Keck Geology Consortium project in Cyprus. One of my students was Steve Dornbos (’97), now a professor at the University of Wisconsin, Milwaukee. We had a great time exploring the Nicosia Formation (Pliocene) and its fossils on the Mesaoria Plain near the center of this Mediterranean island. (We published the study — Steve’s Independent Study thesis at Wooster — in 1999.)

One of our most common fossils in the Nicosia Formation is shown above. It is the pectinoid bivalve Amusium cristatum Röding, 1798. It is a remarkably thin and delicate shell that still retains much of its color after over four million years. Note that it is almost completely equilateral, meaning that it is nearly symmetrical. There’s a functional reason for this we’ll get to later.

Amusium is a genus still very much in existence today. They are usually found in abundance on carbonate platforms, often in the deeper portions. They are called “saucer scallops” or “moon shells” by collectors. There are many living species of Amusium, and they are apparently good eating (see below a platter from Thailand).

Both the genus and species of Amusium were named by Peter Friedrich Röding (1767–1846), a German shell specialist from Hamburg. He wrote a 1798 sale catalogue of a mollusk collection, providing the first publication of over 1500 taxonomic names. His descriptions were minimal, but enough to meet the requirements for new taxa, including Amusium cristatum.

Now, what is the functional importance of the symmetry of this particular scallop? Turns out it is one of the best swimmers in the bivalve world. By clapping its valves together with its strong adductor muscle, Amusium can swim at an average of 37-45 cm/second, usually for 8-10 seconds. Symmetry of the shell gives it good control over swimming direction. Features that also enhance the swimming abilities of Amusium include strengthening ribs (visible in our specimen above), a centrally-located adductor muscle, and a mantle that can direct water expulsion during the “clapping” actions of swimming.

We can be certain, then, that Amusium cristatum was a beautiful and unusually active mollusk in those shallow seas that once covered the beautiful island of Cyprus.

References:

Aguirre, J. 2009. Biological concentrations of Amusium cristatum. Journal of Taphonomy 2-3: 263-264.

Dornbos, S.Q. and Wilson, M.A. 1999. Paleoecology of a Pliocene coral reef in Cyprus: Recovery of a marine community from the Messinian Salinity Crisis. Neues Jahrbuch für Geologie und Paläontologie, Abhandlungen 213: 103-118.

Morton, B. 1980. Swimming in Amusium pleuronectes (Bivalvia: Pectinidae). Journal of Zoology 190: 1469-7998.

Röding, P.F. 1798. Museum Boltenianum sive catalogus cimeliorum e tribus regnis naturæ quæ olim collegerat Joa. Fried Bolten, M.D. p. d. per XL. annos proto physicus Hamburgensis. Pars secunda continens conchylia sive testacea univalvia, bivalvia & multivalvia. – pp. [1-3], [1-8], 1-199. Hamburgi, Trapp.

Williams, M.J. and Dredge, M.C.L. 1981. Growth of the saucer scallop, Amusium japonicum balloti Habe, in central eastern Queensland. Australian Journal of Marine and Freshwater Research 32: 657–666.

Next »