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    The Problem with Siphocypraea

    By MikeR

    For millennia, humankind has been fascinated by the hard-external shell of the organisms classified within the Phylum Mollusca.   Consumed first as food, their empty shells have served multiple functions in the past; as tools in many ancient cultures, in religious ceremonies by the Aztecs, and money by Pacific Islanders. During the Age of Discovery, sailors could supplement their meager incomes by selling exotic seashells to wealthy gentlemen for their Cabinets of Curiosity.  Today many people first become enchanted with seashells by picking up worn beached shells during a vacation to the shore.  If fortunate to live by the ocean, a newbie might branch off into the live collection of shallow water mollusks while those more land bound might start by purchasing foreign, deep-water or rare specimens.  Because of the shear abundance of marine mollusk species, the more advanced collector will begin to concentrate on a single or small number of molluscan families, acquiring as many of those species as possible, spending major capital for the rarest.  Among the gastropods, one of the most popular families to collect due to its beauty are species of the family Cypraeidae commonly known as the cowries.  Members of this family are known for their egg shaped, brightly colored shells with a narrow slit-like aperture and most notably a porcelain-like glossy shell that is produced by the animal’s soft mantle which when fully extended, covers and polishes the external shell.  Cowries are common worldwide across tropical and subtropical seas even with a few temperate species tolerant of colder water.  Because of their popularity as a biologic collectible, the desire to create new species with minute differences or found at diverse localities have resulted in a large amount of species splitting.  Fabio Moretzson (2014) termed this as taxonomic ‘noise’, much of it from non-peer reviewed amateur publications with new species descriptions based mostly on shell characteristics.  Moretzsohn and the editorial board of the World Register of Marine Species (WoRMS) have attempted to clean up much of the ‘noise’ through review of molecular and anatomical data reducing over 1000 different names to 245 species and 166 subspecies (2013).
    Paleontology is not immune to the proclivities of the cowrie collector.  Going back to at least the Cretaceous, fossil Cypraeidae are also sought and commercially sold with notable species found in the Eocene and Oligocene of Europe, the Miocene of Indonesia, and the Oligocene and Miocene of Australia.  In general, fossil cowries are rare with the notable exception of the genus Siphocypraea from the Upper Pliocene of the Southeastern United States.  Unlike other cowries which have a distinct spire in their immature bulla stage, Siphocypraea has a depression over the apex resulting in either an open or spiral apical sulcus in adults.  Anyone who has collected from the Plio-Pleistocene shell pits of South Florida has encountered these shells in abundance with a staggering amount of variation in characteristics.  In this post, I will review the publication history of Siphocypraea and in doing so describe the different interpretations of its speciation.
    T.A. Conrad (1841) described one of the first fossil cowries found in the United States from a specimen discovered at a sink hole in Duplin County, North Carolina.  This species that he named Cypraea carolinensis, was listed from Miocene deposits now considered as Upper Pliocene Duplin Formation.  Later in 1886 Angelo Heilprin in his paleontological explorations of South Florida described a cowrie found within Pliocene (now considered Lower Pleistocene) marl deposits uncovered in canal construction along the Caloosahatchee River.  Due to its unusual comma-shaped apical sulcus, he named it Cypraea (Siphocypraea) problematica.  At this point in time, no other Neogene cowries were described for almost 50 years.  The Florida development boom began in the early 20th Century and during the construction of the Tamiami Trail connecting Florida’s west and east coasts, draglines encountered a molluscan rich sand near the Monroe-Dade County line.  Among the endemic Miocene (today Pliocene) fauna were large cowries which W.C. Mansfield noticed were very similar to the species found in North Carolina.  Mansfield (1931) named it Cypraea carolinensis floridana differing from the type by being more elongated and having a rounder ventral area.  The following year Mansfield described a near perfect specimen of C. carolinensis carolinensis from what is now called the Jackson Bluff Formation thereby extending its range to the Florida Panhandle.  The German malacologist F.A. Schilder (1932) noting similarities between Cypraea mus, a recent Venezuelan species and Heilprin’s Cypraea (Siphocypraea) problematica assigned C. mus to the subgenera Siphocypraea.  Woodring (1959) would disagree with placing C. mus into Siphocypraea instead, he created a new subgenera Muracypraea for C. mus and its associated fossil species.  Disregarding a similar bulla stage apical depression with C. carolinensis, Julia Gardner (1948) in her monograph of the Miocene and Pliocene molluscan fauna of North Carolina and Virginia, proposed a new section name, Akleistostoma for C. carolinensis and C. mus.  
    One of the more seminal works in Florida biostratigraphy and paleontology in the 1960s was by Alex Olsson and Richard Petit (1964).  In Part 1 Olsson clarified the stratigraphy and associated fossils that were being exposed in shell pits, new canals, and the channelization of the Kissimmee River, by dividing the Neogene of Florida into four units: The Tamimi Limestone in Unit D, the Pinecrest in Unit C, the Caloosahatchee in Unit B and an unnamed Unit A which would later be known as the Bermont Formation and allied these units to their Mid-Atlantic counterparts.  In Part 2, Olsson and Petit named new species and correlated known species into their corresponding unit.  In the process they raised Siphocypraea to genus level noting the extreme variation seen in the genus particularly in the Kissimmee River area.  They questioned how many of these variants should be named but did find two forms that were numerous enough to assign as subspecies of S. carolinensis; S. carolinensis hughesi a very broad elliptical form and S. carolinensis transitoria which shows characteristics transitional between S. carolinensis and S. floridana.  Later Olsson and Petit (1968) expanded upon their views on Siphocypraea by assigning Cypraea mus as Siphocypraea (Muracypraea) mus and reassigning Cypraea chilona found in the Miocene Chipola Formation as Siphocypraea chilona.
    No other United States Siphocypraea were described until the work of Ed Petuch began in the late 1970s first with the description of a new extant species within the Caribbean.  Petuch worked in the Florida Neogene at a time when many pits and construction projects were exposing sediments containing species new to science.  One of these exposures was in a housing project west of Miami in which the digging of a lake exposed a fossil shell deposit with mollusks having close affinities to the Upper Pliocene of the Mid-Atlantic region.  Among the new species was a Cypraea in which Petuch (1986) named C. lindae.  Also found were a diminutive cowrie which he associated with Cypraea pilsbryi an obscure species named by Ingram (1939) from the Cape Fear River in North Carolina.  Petuch (1994) would later reassign both to Siphocypraea.  During this era, Petuch was not the only researcher naming new Siphocypraea species.  In 1988 Juan Parodiz of the Carnegie named a species with similarities in between S. carolinensis and S. problematica naming it S. trippeana.  Within the same paper Parodiz elevated Olsson and Petit’s subspecies S. transitoria and S. hughesi to species level.  In 1991, Petuch named three additional Siphocypraea; S. mulepenensis, S. griffini and S. herweckorum, however it was with the release of his Atlas of Florida Fossil Shells in which the naming of species really began to exponentially increase.  Without going through each individual name, Petuch (1994) named 12 new Siphocypraea species, followed by his 1996 publication creating a new genera Calusacypraea for those Siphocypraea which exhibit neotenic (juvenile traits in adult form) moving his S. sarasotaensis into this generic assignment and naming three new species.  Before the 20th Century concluded, a German researcher, Dirk Fehse (1997) named two additional Siphocypraea species from the Caloosahatchee Formation.
    The number of Siphocypraea species were artificially reduced by Petuch (2004) when he resurrected Gardner’s Akleistostoma as a genus for all Siphocypraea having a simple anterior sulcus with a widely opening posterior aperture and a new genus, Pseudadusta for those species with a comma shaped anterior sulcus and a narrow posterior aperture.  In addition, and without going into much detail here, within the same publication he created a new subgenus within Calusacypraea called Myakkacypraea and two new subgenera within Siphocypraea; Okeechobea and Pahayokea.  Within this entire Siphocypraea complex he named nine new species.  In his book on the Geology of the Everglades, Petuch (2007) pictured two internal casts, one Akleistostoma and the other Calusacypraea from the Lower Pliocene Peace River Formation which if accurate fills in a large gap between the Chipola species S. chilona and the Upper Pliocene S. carolinensis.  Naming of new species continued in Petuch’s unpublished book Compendium of Florida fossil shells (2011).  He gave a name to the Akleistostoma internal cast and named four new subgenera to Akleistostoma and 13 new Pliocene species.  For Siphocypraea he created three new subgenera and 11 species while upgrading his two Siphocypraea subgerera from 2003 to genus level.  Thus, genus Pahayokea has two new subgenera and six new species and genus Okeechobea one new subgenus and eight new species.  For Calusacypraea, the Miocene cast, one new subgenus and one new Pliocene species were named.  Lastly with his genus Pseudadusta Petuch named two new subgenera and 11 new species.  In all 52 new species of the Siphocypraea complex were named in this one work.  Just last year Petuch (2018) published his latest book concentrating solely on the fossil Cypraeidae of South Florida.  I have yet to acquire this book, however it advertises the description of over 100 species, so there must be additional new species that would add to this total, three that I know of for sure.     WoRMS has tried to cleanup some of this taxonomic splitting by failing to recognize any of Petuch’s genera instead accepting only Siphocypraea and Akleistostoma.  Also, they have upgraded the Caribbean fossil and extant species classified under Siphocypraea (Muracypraea) to full genus recognition as Muracypraea.  Under this interpretation, Siphocypraea/Akleistostoma were restricted to the flooded Southeastern United States and became extinct with S. problematica in the Lower Pleistocene.  WoRMS did not challenge the 90-species listed prior to 2018 as it is a register for extant species however its acceptance of Akleistostoma has caused some problems with the systematics of Siphocypraea.  As defined by Gardner, Cypraea carolinensis would be Akleistostoma carolinensis and as defined by Petuch any Cypraeidae with a simple anterior sulcus.  Heilprin’s definition of Siphocypraea could therefore be interpreted broadly as any Cypraeidae with a comma shaped anterior sulcus.  There are many workers of Florida molluscan paleontology that except this believing that there are only two species; carolinensis and problematica.  However, to accept that viewpoint is to ignore the transitional forms and variation that was occurring in South Florida during the Upper Pliocene.  Accepting Olsson & Petit’s view that Gardner created an unnecessary classification with Akleistostoma and that the depressed apex in the Bulla stage is the defining characteristic in Siphocypraea would clarify the inconsistencies with the evolution of S. carolinensis/floridana to the endpoint S. problematica.  It is why I have chosen to use only Siphocypraea in my collection.
    The ultimate question is how many species of Siphocypraea are there?  That is not the scope of this post and would require a lot of work which would certainly be contested and contentious.  I do believe there are more than five and less than hundred.  I believe all species up to Olsson and Petit.  I believe that some of Petuch’s species are valid, but exactly which ones are hard to say.  His practice of creating subgenera that he later elevates to genus and description of species within depositional beds and those interpreted beds in different geographically regions make it difficult to say which are species and which are synonyms.  What I have tried to do below is to bin different characters and variations of Siphocypraea within my collection from degree of anterior sulcus coiling and the opening of the posterior aperture.   Siphocypraea chilona (Dall, 1890). Lower Miocene (Burdigalian) Chipola Formation, Liberty County, Florida USA.  Shell is nearly round with a high convex dorsum and a narrow aperture uniform throughout.  Even crenulations of both sides of the aperture.  When preserved, the color pattern is of large reddish spots.  Not uncommon at Alum Bluff.  Both WoRMS and Petuch would assign this species to the genus Akleistostoma.   Siphocypraea carolinensis (Conrad, 1841). Upper Pliocene Duplin Formation.  Left: Darlington County, South Carolina USA.  Right: Florence County, South Carolina USA.  The specimen on the left is typical of S. carolinensis, subovate with a simple anterior sulcus, wide posterior aperture, denticles on parietal lip are weak.  The dorsum or top of shell can be variable with some gerontic specimens being relatively high.  The dorsum height of the specimen on the right is closer to S. floridana but all other characteristics are consistent with S. carolinensis.  Also, Akleistostoma.   Siphocypraea pilsbryi (Ingram, 1939). Upper Pliocene Duplin Formation, Bladen County, North Carolina USA.  The best way to describe this species is as a miniature S. carolinensis.  I had this listed as a dwarf form of S. carolinensis until I came upon the paper describing Cypraea pilsbryi in researching this post.  The type locality is the Cape Fear River and I found several examples of this species on a tributary of the Cape Fear.  Little is found online about this species although Petuch has reported it from South Florida.  Also, Akleistostoma.   Siphocypraea carolinensis floridana (Mansfield, 1931).  Upper Pliocene Pinecrest Sand Member of the Tamiami Formation, Sarasota County, Florida USA.  The specimen on the left is a gerontic individual from APAC, on the right typical S. floridana from SMR.  Highly variable much more so than S. carolinensis.  The dorsum tends to be not as high as S. carolinensis and parietal denticles are more strongly expressed but shares the uncoiled anterior sulcus and wide posterior aperture.  This is the common Siphocypraea found in the Sarasota shell pits.  Also, Akleistostoma.   Siphocypraea sarasotaensis Petuch, 1994.  Upper Pliocene Pinecrest Sand Member of the Tamiami Formation, Sarasota County, Florida USA.  First described as a Siphocypraea, Petuch later classified this species with his Calusacypraea genus which is defined by neotenic characteristics such as an undeveloped anterior sulcus and very light weight.  Many researchers feel that this species is merely a variation of S. floridana (Lyle Campbell pers. comm.).  WoRMS classification Akleistostoma while Petuch would call this species Calusacypraea myakka.   Siphocypraea briani (Petuch, 1994).  Upper Pliocene Pinecrest Sand Member of the Tamiami Formation, Sarasota County, Florida USA.  Described as Calusacypraea briani and differentiated from S. sarasotaensis by having a larger and longer shell.  I have placed this shell as S. briani however it could be a gerontic individual of S. sarasotaensis.  Some Cypraeidae demonstrate sexual dimorphism which could explain the larger size as well.  WoRMS classification Akleistostoma, Petuch Calusacypraea.   Siphocypraea lindae (Petuch, 1986).  Upper Pliocene Golden Gate Member of the Tamiami Formation, Collier County, Florida USA.  Very close to S. carolinensis with a high dorsum and simple sulcus but with a narrower posterior aperture and stronger denticles on parietal lip.  Petuch assigns this species in his genus Pseudadusta.   Siphocypraea trippeana Parodiz, 1988.  Upper Pliocene Pinecrest Sand Member of the Tamiami Formation, Sarasota County, Florida USA.  Typically, shell is small and narrow with a high dorsum.  The sulcus has a slight bend more so than the S. carolinensis complex, described as a keyhole appearance and a narrow aperture like S. problematica.   Siphocypraea ketteri Petuch, 1994.  Upper Pliocene Golden Gate Member of the Tamiami Formation, Collier County, Florida USA.  Another form transitional between S. carolinensis and S. problematica.  Differs from S. trippeana by having a wider shell and flattened base with noticeable wrinkles along the base.  Petuch assigns this species in the genus Pseudadusta.   Siphocypraea hughesi Olsson & Petit, 1964.  Upper Pliocene Pinecrest Sand Member of the Tamiami Formation, Highlands County, Florida USA.  Restricted to the Kissimmee River area.  Distinctive shape, wide and squat.  Anterior sulcus approaching that of S. problematica.  Petuch assigns this species to Akleistostoma (Olssonicypraea).   Siphocypraea transitoria Olsson & Petit, 1964.  Upper Pliocene Pinecrest Sand Member of the Tamiami Formation, Sarasota County, Florida USA.  Although common in the Kissimmee River area, this specimen is from APAC in Sarasota where it is much rarer.  Very close to S. problematica with slightly less coiling of the anterior sulcus and a slightly wider posterior aperture.  Petuch would call this Siphocypraea streami.   Siphocypraea mulepenensis Petuch, 1994.  Upper Pliocene Golden Gate Member of the Tamiami Formation, Collier County, Florida USA.  Like S. problematica with a comma shaped anterior sulcus and narrow aperture.  The shell differs in being shorter with a pyriform shape. The shell around the anterior sulcus noticeably protrudes.   Siphocypraea problematica (Heilprin, 1886).  Lower Pleistocene (Calabrian) Caloosahatchee Formation, Martin County, Florida USA.  The shell is long and narrow with a comma-shaped anterior sulcus and narrow posterior aperture.  Well preserved individuals demonstrate a rich golden color.   Siphocypraea swearingeni Petuch & Drolshagen, 2011.  Lower Pleistocene (Calabrian) Caloosahatchee Formation, Martin County, Florida USA.  I found numerous specimens of this form in mixed spoil with the S. problematica pictured above and based on the adhering matrix, it appears that they came from a different layer.  Wider and shorter than S. problematica, this could be an environmental variant of it.  I was hesitant to put a Petuch 2011 name on this population as there could very well be an earlier name that would take precedent, however it does fit very closely to the figures of S. swearingeni in Petuch 2018.   Muracypraea mus (Linnaeus, 1754).  Recent.  Judibana Bay, Venezuela in sea grass beds at 1-3 feet depth.  Also known as the mouse cowrie, this species was once classified as Siphocypraea.  Since M. mus has two obvious nodes on each side of the mantle line on posterior end of the dorsum and the sulcus fills with callous as it matures, it was placed within a separate genus.  Although restricted to Venezuela and Eastern Columbia, its ancestor M. henekeni had a widespread Caribbean distribution in the Miocene.  
    REFERENCES
    Conrad, T. A.   1841.  Appendix to: Observations on the Secondary and Tertiary formations of the southern Atlantic States, by James T. Hodge.  Am. Journ. Sci., vol. xli, 1st ser., pp. 332-348.
    Dirk Fehse.  1997.  Two new fossil Siphocypraea from Florida, U.S.A. - Schriften zur Malakozoologie, Heft 10: 38-44, pl. 12-13, 1 tab.
    Gardner, J. A. 1948. Mollusca from the Miocene and Lower Pliocene of Virginia and North Carolina: Part 2. Scaphopoda and Gastropoda, United States Geological Survey Professional Paper 199-B: iv, pages 179-310, plates 24-38, [iii].
    Heilprin, Angelo.  1887.  Explorations on the west coast of Florida and in the Okeechobee wilderness: with special reference to the geology and zoology of the Floridian peninsula: a narrative of researches undertaken under the auspices of the Wagner Free Institute of Science of Philadelphia.  Transactions of the Wagner Free Institute of Science of Philadelphia v. 1   Ingram, W. M. 1939. A new fossil cowry from North Carolina. The Nautilus 52(4):120-121.
    Mansfield, W.C. 1930. Miocene Gastropods and Scaphopods of the Choctawhatchee Formation of Florida, Florida Geological Survey Bulletin 3, 189 pages.
    Mansfield, W.C. 1931. Some tertiary mollusks from southern Florida. Proceedings of the United States National Museum, v. 79.
    Moretzson, Fabio.  2014.  Cypraeidae: How well-inventoried is the best-known seashell family?  American Malacological Bulletin. 32(2): 278-289.
    Olsson, A.A., and R.E. Petit. 1964. Some Neogene Mollusca from Florida and the Carolinas, Bulletins of American Paleontology 47(217): pages 509-574, plates 77-83
    Olsson, A.A., and R.E. Petit. 1968 (1993 Reprint). Notes on Siphocypraea, Originally - Special Publication 9, The Paleontological Research Institute Special Publication 19: pages 77-88.
    Parodiz, J.J. 1988. A new species of Siphocypraea (Gastropoda, Cypraeidae) from the Neogene of southwest Florida. Annals of the Carnegie Museum 57(3): 91–97.
    Petuch, Edward J. 1979. A New Species of Siphocypraea (Gastropoda: Cypraeidae) from Northern South America with Notes on the Genus in the Caribbean.  Bulletin of Marine Science -Miami- 29(2):216-225.
    Petuch, Edward J. 1986. Cenozoic The Pliocene reefs of Miami: their geomorphological significance in the evolution of the Atlantic Coastal Ridge, southeastern Florida, USA.  Journal of Coastal Research 2(4).
    Petuch, Edward J. 1991, New Gastropods from the Plio-Pleistocene of Southwestern Florida and the Everglades Basin.  W.H. Dall Paleontological Research Center Special Publication Number 1. 
    Petuch, Edward J. 1994. Atlas of Florida Fossil Shells (Pliocene and Pleistocene Marine Gastropods). Chicago Spectrum Press.
    Petuch, Edward J. 1996. Calusacypraea, a new, possibly neotenic genus of cowries from the Pliocene of southern Florida. Nautilus 110(1): 17-21 .
    Petuch, Edward J. 2004. Cenozoic Seas. CRC Press.
    Petuch, Edward J. 2007. The Geology of the Everglades and Adjacent Areas. CRC Press.
    Petuch, Edward J. and Mardie Drolshagen.  2011.  Compendium of Florida Fossil Shells, Vol. 1 Middle Miocene to Late Pleistocene Marine Gastropods: Families Strombidae, Cypraeidae, Ovulidae, Eocypraeidae, Triviidae, Conidae, and Conilithidae [unpublished].
    Petuch, Edward J. David P. Berschauer, Robert F. Myers.  2018.  Jewels of the Everglades: The Fossil Cowries of Southern Florida.  San Diego Shell Club, 256 pp.   Schilder, F.A.  1932.  Fossilium Catalogus, I, Animalia.  Pars 55.  Cypraeacea, 276 pp.
    Woodring, Wendell Phillips.  1957.  Muracypraea, new subgenus of Cypraea: Nautilus, v. 70, no. 3, p. 88–90,
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  • andreas

    The Columbianus Zone/alaunium 2/ Norium/upper Triassic, In The So Called “Hallstatt Limestone” Of The Northern Calcareous Alps In Austria

    By andreas

    The columbianus Zone/Alaunium 2/ Norium/Upper Triassic in the so called "Hallstatt Limestone" of the Northern Calcareous Alps in Austria Dear Fossil Forum members! This pictured report about the ammonite bearing Triassic Hallstatt limestone will be the first one of a continuous series of reports. Since the beginning of the geological research in the Northern Calcareous Alps of Austria in the 19th century, about 500 species of Triassic ammonites have been described from the Hallstatt limestone by Mojsisovics, Hauer, Diener and other authors. The most important person in the development of the first Alpine Triassic ammonoid biostratigraphy was the Austrian palaeontologist Edmund von Mojsisovics. When viewing his classical monographs one is overwhelmed by the stunning Lithographics created by the artists of the late 19th century. Every recent serious triassic ammonoid researcher includes these old works in the standard literature of triassic ammonoids. Unfortunely his ammonoid bio-chronostratigraphic scale had some mistakes (changed zones) especially the incorrect stratigraphic position of some ammonoid zones in the Norian stage. It was the merit of E.T. Tozer to discover this weakness and to correct it. Hallstatt limestone facies is a type of triassic Ammonitico Rosso facies which also occurs in several other locations all over the world. The Hallstatt Limestone Facies of Austria consists typically of red to grey –coloured, in some parts abundantly fossiliferous limestones locally interbedded with marls. Also strongly condensed successions are common. Fossils mostly do not occur in continuous layers but in so called lenses and fissure fillings. The most common fossils are Ammonoids and Nautiloids, but Crinoids ossicles, Bivalves, Conodonts and Gastropods also occur. In this report I will introduce you to the Triassic ammonoid zone of the Alaunium 2 /Norium/ Upper Triassic of the Hallstatt formation. The stratigraphic level lower Alaunium 1 will be shown in a future report. Fig.1 A very beautiful view of a tectonic border. The Valley in front marks the tectonic border between the mainly Triassic Hallstatt unit und the Tirolikum unit of the Totengebirgs nappe. The highest mountain shown on the picture is the "Loser". The well bedded limestone in the summit area are of Jurassic age. This is in turn resting on Triassic "Dachstein" limestone that ends roughly in the middle of the picture. The name of this stage was chosen by Mojsisovics after the Celtic folk of the Alauns. In historical times this tribe lived in the forelands of the calcareous Alps in the area of the later Roman province Noricum. Zone ammonite of the Alaunium 2, outside of the Tethys realm, is Mesohimavatites columbianus Mc LEARN, well known from the boreal Triassic of British Columbia in Canada. In the Tethys realm the whole Alaunium is split into three subdivisions. Alaunium 1 = Bicrenatus -Zone, Alaunium 2 = (instead Columbianus) Hogarti- Zone, Alaunium 3 = (instead Columbianus) Macer -Zone The subzones I-IV shown in the timescale below were established after bed by bed collections in the well-bedded erratic limestone blocks of Timor by the Austrian geologist Franz Tatzreiter. Fig.2 In the Hallstatt limestone of the northern calcareous Alps, Himavatites sp. occurs very scarcely. It is impossible to use this genus for Stratigraphic aims on new detected locations. A normal collector could use the following rough scheme to insert ammonoids in the right stratigraphic subzone. But notice that strong condensation, fissure filling etc. can blur this schema. For a newbie collector it is much more difficult to find some fossils there at all. To place them into the right ammonoid zone is the easier part of the exercise. Rough scheme, to place ammonoids into the right subzones of the Alaunium 2 in the Hallstatt limestone. Subzone I+II: Distichites (especiallys in II) but no Halorites, Subzone III: Halorites starts, Distichites can be found too, but ends in this subzone, Subzone IV: Halorites frequent, main zone of „catenate Halorites" especially in the later time of this subzone. In the upper sphere of subzone 3 and in the lower sphere of subzone 4 Halorites sp. is a very common faunal element. In locations which expose this time interval Halorites is more common than other leiostraca (=ammonoids without sculpture) ammonoids like Arcestes sp. The often used term Halorites horizon (KRYSTYN, L., 1973) points that out exactly. Representative for the family of the Haloritidae, is shown Halorites ramsaueri (QUENST.),.Sommeraukogel, MOJSISOVICS (Bd. II), Wien 1893, Tafel 71, 76 und 77. Fig.3 The venter views laterally right show the variability of the end living chamber (after pictures by MOJSISOVICS Bd. II, Wien 1893) of Halorites ramsaueri QUENST. The right venter view could also be termed as a Halorites macer. The difference between H. macer and H. ramsaueri is not clear due to the great variability of these two species and is totally questionable in my opinion. Fig.4 Catenohalorites catenatus BUCH form MOJSISOVICS (Bd. II), Wien 1893 To the genus „Catenohalorites" count all species of Halorites, which show the chain like („catenat") arranged nodes of the inner whorls on the phragmocon too. (The inner whorls are more or less catenat by all Halorites sp.) Historical locations Beside the well known historical location of the Sommeraukogel, which exposed all four subzones, there are several other historical locations. For example: Hallein, Hoher Student, Leisling, Pötschenhöhe, Rossmoos and Röthelstein. Years ago I was lucky to find a talus block in an area of such an historical location. Later in this report I will show the ammonoids of this block. Two new faunas shown here in this report came from locations hitherto not yet described. Fauna 1 The first new location is in an area where the normal succession of limestone is penetrated by fractures with fissure filling and reworked horizons. One reworked horizon (not for sure yet, it could also be an untypical fissure filling) shows a Halorites fauna. Two nearby located, clear fissure fillings show a faunal association with Distichites but without Halorites. A shell fragment of a Himavatites sp. in the Distichites fissure may confirm the higher hogarti zone. One highlight of the Halorites location was the discovering of a Bambanagites MOJS. 1896. This is the first evidence of this genus in the Hallstatt realm. So far Bambanagites is yet only known from the Halorites limestone of the Bambanag- succession on Niti- Pass (Himalaya) in India, described by MOJSISOVICS with two species (B. schlagintweiti MOJS. and B. dieneri MOJS) In Dieners work, „Fauna of the Tropites-Limestone of Byans", another species, B. kraffti DIENER, is described. The Venter of B. kraffti is very sharp with only weak waves on the flank. Further research on Bambanagites (member of the family Pinacoceratidae) resulted in no other location/occurrence than the above mentioned location in India. Maybe Bambanagites occurs also in the Triassic of Timor. I haven't found any citation but judging by the frequent occurrence of fauna of alaunian ammonites there, it could be possible to find some. Fig 5 Bambanagites cf. dieneri MOJS. a first evidence in the Hallstatt limestone of the eastern Alps, possibly a worldwide first evidence outside the type locality in India. Fig.6 Bambanagites Dieneri, MOJSISOVICS 1896 .Cephalopoden der oberen Trias des Himalaya Taf. XVIII, Fig. 3 - 6. The impression of the Bambanagites sp. is on the backside of this slab with Halorites cf. macer MOJS.(8cm) on the following picture Fig.7 Halorites cf. macer MOJS. found in the location together with Bambanagites Fig.8 Halorites sp. with very prominent nodes on the venter Fig.9 Washed block from this location, with visible Halorites sp. Several other ammonoid species are also visible on this block which are frequent in the Alaunium 2. Rhacophyllites neojurensis QUENST. , Placites sp,, Halorites div. sp., Arcestes sp., Leislingites sp., Megaphyllites sp., Paracladiscites multilobatus BRONN., Steinmannites hoernesi HAUER, Alloclionites ares MOJS It is further worth a mention about the occurrence of the Ammonite genus. cf. Psamateiceras in this location. Natural picture size is 45cm. Other important ammonoid species of the macer zone A beautiful, conspicuous faunal element of the macer zone is Steinmannites sp. With different species this genus shows its maximum in this zone and was found relatively frequently in this location within the Halorites location. Fig.10 Steinmannites hoernesi (HAUER) from the Halorites-area in compairson with a Fig.11 cf. Eosteinmannites sp. from the Distichites-area of this location. Fig.12 ? cf. Pseudosirenites sp.(3cm) or cf. Mesohimavatites sp. from the Halorites-area Fig.13 Paracladiscites multilobatus BRONN. (5cm) Another frequent faunal element of the Alaunium 2 is Paracladiscites multilobatus BRONN. This species differs from Cladiscites and Hypocladiscites by the absence of the spiral striations. Only fine radial growth lines are visible on the shell. The genus Paracladiscites reaches throughout the whole columbianus- Zone up to the zone of Sagenites reticulatus/Cochloceras/Paracochloceras (Sevat2) Distichites Fig.14 Distichites megacanthus MOJS. from the Distichites area of this location. Fig.15 Venter view of Distichites megacanthus MOJS. Diameter is 19 cm; this is rather the growth limit of this species. Distichites sp. is easy to determine by the two bulges following the venter furrow Fig.16 Distichites cf. kmetyi (8cm) of this location Distichites were found in different species at this location but very scarcely. From 30-40 other ammonite's roughly one piece of Distichites sp. was found. Most common ammonites are Placites and Arcestes. Fig.17 Rhacophyllites neojurensis QUENST. (7cm) from the Distichites-area Rhacophyllites sp. runs up to the Sevat Fauna 2 The second new location comes from another area and is also a reworked horizon. This horizon is associated to a small tectonic fault which strikes through the surrounding normal-bedded limestone at a low angle. This zone of weakness may have already been active at the time of the limestone sedimentation and may have worked as a trap for fossils. The stratigraphic lower part (compared to the surrounding limestone beds) of this horizon bears big Halorites cf. ramsaueri embedded in micritic red limestone which was tectonically stressed. In the stratigraphic younger part of this horizon, compared to the normal-bedded surrounding limestone beds, sparitic fissure filling is given in which abundant small ammonoids and gastropods are embedded. According to the occurrence of scarce Sagenites sp. small catenate Halorites and small Hydrozoans, this sparitic part of the fissure filling dates into the subzone IV (after Tatzreiter). Fig.18 Cross-section of a Rhacophyllites neojurensis QUENST. In situ picture from the white sparitic filled stratigraphic upper part of the fissure. Natural size of the picture ca.30x25cm The left side of the picture shows how unspectacular the weathered rock looks, although the mossy vegetation has been removed before by hand. Fig.19 Gastropoda and Halorites-core (1cm), embedded in white calcite. Fig. 20 Slab with Steinmannites hoernesi HAUER, Paracladiscites multilobatus BRONN, Arcestes sp., Placites sp. und Leislingites sp., within white calcite embedded red limestone lithoclasts of the stratigraphic upper part of the fissure. Slab size is 16cm Fig.21 Visible Halorites sp. end body chamber from the stratigraphic lower part of this fissure. Fig.22 Block from the tectonically stressed area of this fissure. Well visible are the calcitically healed slip movements in this rock which show us a "frozen" moment during the lithification of this limestone. Now to the aforementioned talus block of an historical location. After the first blow of the hammer a Halorites was visible. By finding an Amarassites cf. semiplicatus HAUER I was able to date the fauna of this block into the Subzone III afterTatzreiter. Fig.23 Amarassites cf. semiplicatus HAUER (5cm) from the above mentioned talus block of an historical location. Fig.24 Halorites sp., freshly split talus block. Natural picture size ca.20cm At the end of my report some pictures of another Alaunian 3 Fauna. From this location I have less material. The faunal composition differs a little bit from the above mentioned locations. New to this location is cf. Parajuvavites mercedis MOJS. and cf. ?Acanthothetidites sp. Fig.25 Slab from this Alaunian fissure with cf. ? Acanthothetidites sp, („thorned"Ammonite on top, 3cm) Fig.26 Paracladiscites multilobatus BRONN, Arcestes sp., Parajuvavites cf. mercedis MOJS.(ribbed ammonite) Size of slab ca. 10cm Fig.27 Matrixrock of this location Natural size on picture ca. 35cm I hope you have enjoyed this report about my favourite collecting area. Unfortunly I cannot load up graphics. Maybe it is possible and I only do not know how to do this. Maybe somebody can help me in this case. A special thank is given to Fossil forum member "Ludwigia" for correcting my uncivil kind of English. Best regards Andreas Literature: DIENER, C.: Fauna of the Tropites-limestone of Byans. In: Himalayan Fossils, Palaeontologia Indica,(ser.15) 5/1, 1-201, Calcutta 1906 KRYSTYN, L. Zur Ammoniten und Conodonten-Stratigraphie der Hallstätter Obertrias(Salzkammergut, Österreich), Verh.Geol. B.-A., Wien 1973 KRYSTYN, L., SCHÄFFER, G. & SCHLAGER, W. (1971b): Der Stratotypus des Nor.- Annales Inst. Geol. Publ. Hungar., 54, 2, 607-629, 7 Abb., Budapest MOJSISOVICS, E. 1893: Die Cephalopoden der Hallstätter Kalke, Abhandlungen der Kaiserlich-Königlichen Geologischen Reichsanstalt, II Band, Wien 1893 MOJSISOVICS, E. 1896: Beiträge zur Kenntniss der obertriadischen Cephalopoden Faunen des Himalaya, Denkschriften der Kaiserlichen Akademie der Wissenschaften Mathematisch–naturwissenschaftliche Classe, 63, 575–701. Wien 1896, TATZREITER, F. 1981, Ammonitenfauna und Stratigraphie im höheren Nor(Alaun, Trias) der Tethys aufgrund neuer Untersuchungen in Timor, Denkschr. Österr. Akad. Wiss., math.-naturwiss. KI., 121, Wien 1981, Springer Verlag TATZREITER, F. 1985. Zur Kenntnis der obertriadischen (Nor; Alaun, Sevat) trachyostraken Ammonoideen Jb. Geol. B.-A. ISSN 0016-7800 Band 128 Heft 2 S.219-226 Wien, Oktober 1985, 8 Abbildungen TATZREITER,F. 1984: Bericht über paläontologische Untersuchungen in Hallstätterkalken auf Blatt 76 Wr. Neustadt und 96 Bad Ischl. - Jb. Geol. B.-A., 128/2, Wien 1985 TOZER, E. T. 1994. Canadian Triassic ammonoid faunas. Geological Survey of Canada Bulletin, 467,1–663.
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  • MikeR

    The End Of My Pliocene Project

    By MikeR

    When I began this blog late in 2010, my intention was to report on recent field trips however, with the exception of one excursion each into the Upper Miocene, Lower Pliocene and the Calabrian Pleistocene, all of my posts have concentrated on the Upper Pliocene of the US Atlantic and Gulf coastal plains. I already had an extensive collection of Florida Upper Pliocene invertebrates that I had collected while a resident of the state in the late 80s and early 90s. The fossils from these beds are contemporaneous with the Zone 2 Yorktown beds of Virginia and North Carolina that I began collecting in the early 2000s, the Duplin Formation that I collected in 2010 and several trips to Jackson Bluff localities in the Florida panhandle in 2011. These more recent collecting endeavors required a reassessment of the identification of my Florida collection due to a better recognition on my part of modern thoughts on speciation and from working with paleontologists who research these deposits. Also I began rejecting non-peer reviewed books and guides geared toward amateurs which exhibited sloppy and unsubstantiated research. In an effort to free display space I began cross-referencing species from different formations to compile at least what I believe is very accurate species identifications and to place the best example of each species regardless of formation within my display cabinets (fig. 1 & 2). Figure 1. Upper Pliocene (Piacenzian) Bivalvia Eastern United States. Figure 2. Upper Pliocene (Piacenzian) Gastropoda Eastern United States. The attached species list represents the completion of my Pliocene project. Unlike my previous lists which concentrated on the mollusks from particular sites and formations, the 16 page document below is a compilation of all Eastern United States Piacenzian fossils in my collection both vertebrate and invertebrate. The ability to observe different species geographically has led to changes that can be seen if comparing mollusks in the list below to those noted from my previous posts. I have eliminated species which were obviously the same but named differently based upon the regional description of the molluscan fauna by earlier research. The list is not meant to be comprehensive of these deposits, but more of a guide of what can be found. Although my collection is strong in Sarasota area Pinecrest, Jackson Bluff Formation and Zone 2 Yorktown, it is very weak in Pinecrest fauna from the coral reef facies near Miami and the Kissimmee River area, weak in the Duplin Formation (only two localities sampled), and almost absent other than a few trades from early Piacenzian faunas from the Raysor and Goose Creek Formations of the Carolinas. For a more extensive list of species from this period of time I would refer those interested in mollusks to Campbell (1993) and for Florida vertebrates to Hulbert (2001). Piacenzian Fauna List_Reagin.pdf The systematics of the specimens listed are by those fields that I find the most useful in query searches within my Access database and for the most part are as follows: Phylum, Class, Order, Family, Genus, Species, and Subspecies. In stating the distribution of each species, only the formation is noted not the individual members of the Yorktown and Tamiami Formations. Abbreviations used are Yorktown (Y), Duplin (D), Jackson Bluff (J), Tamiami (T) Chowan River (C ), Goose Creek (G) and Raysor (R ). For those taxa which are near to another cf. (similar to) was used. Less specific affinity (aff.) as well as species undetermined (sp.) are designated. The reasoning behind classification I used is addressed in the notes section below. NOTES Algae. A single species of calcareous algae was found in the limestone facies (Ochopee) of the Tamiami Formation which could not be identified to genus or species. Bryozoa. The identification of bryozoa is highly specialized requiring microscopic identification of various feeding structures. Due to a lack of references and interest I identified most as bryozoa species. Anthozoa. Eleven species of coral were collected; almost all of which are from the Pinecrest. The exception is the ubiquitous Septastrea marylandica which led a commensal lifestyle by growing on hermit crab inhabited gastropod shells. The other coral outside the Pinecrest was Septastrea crassa found near Williamsburg, Virginia which I obtained with a collection of Zone 2 Yorktown fossils in a trade from the 80s. Since I did not collect it personally and have not found this particular species at any of the numerous Zone 2 sites that I have collected over the past decade I have designated it as questionable from the Yorktown (Y?). Brachiopoda. Only a single Upper Pliocene brachiopod is listed. Discinisca lugrubris is a geologically wide ranging species found from the Lower Miocene to the Upper Pliocene colder water Bed 11 of the Pinecrest Member of the Tamiami Formation and the Jackson Bluff Formation. Mollusca. Since Piacenzian deposits are known world wide for their shell beds, it stands to reason that mollusks should dominate. The list contains 244 species and subspecies of bivalves, 370 of gastropods and 6 scaphopods. In general, the warmer the water, the higher is gastropod diversity. The list shows that bivalves are wide ranging and less so with gastropods where many more were found only in the warmer water Tamiami Formation. Aragonitic shells do not preserve well in carbonate environments and are often difficult to identify to species. Those shells from the Ochopee Member of the Tamiami Formation that were preserved as internal casts that I felt were probably represented in Pinecrest were not listed separately (i.e. Ficus sp. Internal cast from the Ochopee is probably Ficus jacksonensis from the Pinecrest). I followed the systematics of Turgeon et. al. (1998) which Roger Portell Director, Division of Invertebrate Paleontology of the Florida Museum of Natural History uses for the mollusks in the Florida Paleontology Society publications. This has led to some interesting changes in classification of gastropods within my collection. In a previous post to the forum, I had mentioned that at some point the subgenera of the family Turritellidae had been reclassified to genera. As stated by Turgeon concerning several recent species that were reclassified in this manner “We do not know the source of this reclassification nor have we seen evidence of subsequent acceptance...” therefore I reclassified all genera in Turritellidae back to Turritella with the exception of valid Vermicularia. The most drastic change in classification had to be with members from the families Turridae, Drillidae, and Conidae. I originally classified all turrids in Turridae by older systematics based solely on shell characteristics. I have known for awhile that at some point the family had been split based upon internal structure of the animal itself and DNA studies. What I did not know was that some of those species had been reclassified as Conidae. Turgeon noted that the study was controversial but was supported by anatomical and radular data and also stated that the affected subfamilies would be better suited in their own family. It was difficult for me to classify genera Glyptostoma and Cythara as Conidae, but I did so since I committed to using Turgeon. Cirripedia. Barnacles were more diverse in the Eastern US Upper Pliocene than today but much like bryozoa their specific identification is difficult. Factors for species id include the tubular structure of the outer wall and the internal plates that protect the animal. I feel that most of my identifications are correct however some are based upon morphological features of the outer shell and geographical range and thus might not be accurate. Decapoda. Crabs are a common component of shell beds, however due to the formation of the beds by winnowing, crabs are rarely preserved intact. The majority of crab finds are as isolated legs, claws, and occasional carapaces. Very little study has been made of Pliocene crabs, but most notable are publications by Rathbun (1935) who identified a wide geographical range of species and those of Florida by Portell and coauthors (2002, 2004). The crabs of the Yorktown Formation are not characterized and in many cases at generic level I used similar to reference (Cf.) which like Cirripedia does not follow proper identification rules. Echinoids. Much like crabs, disarticulated echinoid remains can be common in shell beds. In limestone however, because of their calcitic tests and gentle conditions in carbonate environments, echinoids can be preserved intact. I have not collected in the Raysor and Goose Creek Formations but I did receive echinoids from these deposits in trades from the 90s. At one point both of these units were considered members of the Duplin Formation. This has led to designation in the list (D/R) meaning that the original label listed Duplin Formation but due to the attached calcareous matrix, I believe that the specimens are from the Raysor. Vertebrates. Those collectors who have been fortunate to collect at the PCS/Lee Creek Mine are well aware of the rich vertebrate fauna found in the Yorktown Formation. The Yorktown however is divided into two different units—Zone 1 Lower Pliocene (Zanclean) and Zone 2 Upper Pliocene (Piacenzian). One of the distinguish features of these two zones is the richness of vertebrates in Zone 1 compared to their very sparse nature in Zone 2. Vertebrates during this interval are only common in Pinecrest Beds 4 and 11 and a bone layer in Bed 3 consisting of a mass die off of cormorants during a red tide which I never collected. Marine vertebrates can also be found within the Jackson Bluff Formation but not as plentiful as the previously described beds. Redeposited vertebrate remains are found in the Upper Pliocene of the Carolinas and Virginia and are not included in my list. These include teeth of the Cretaceous sharks Squalicorax kaupi and Scapanorhynchus texanus that I have found in the Duplin Formation and vertebrates from the lag deposit found at the contact between the Upper Cretaceous Black Creek Group and Zone 2 Yorktown Formation at my locality 1012 which probably represented concentrated bones and teeth from the Lower Pliocene and Upper Miocene. Upper Pliocene vertebrate remains besides bony fish, shark and ray in my collection include one marine turtle, one land tortoise, a capybara, a walrus, and a dugong. I classified large whale remains as Mysticeti and smaller remains as Odontoceti dolphin although there could be crossover. REFERENCES Numerous references were used and I have them listed according to those for identification or taxonomy and those that I used in writing about the geology or ecology of the deposits described within my blog. In addition to the below publications, I found Greta Polites Fossil Muricidae Website (http://glpolites.us/murex/index.htm) to be invaluable in eliminating synonymous species. My only deviation from her list was with Ecphora which I only recognized two species, E. quadricostata and bradlyae. Identification Campbell, Lyle. 1975. Check List of Marine Pliocene Mollusks of Eastern North America in Plio-Pleistocene Faunas of the Central Carolina Coastal Plain. Geologic Notes (South Carolina Division of Geology) Vol. 19, No. 3. Campbell, Lyle. 1993. Pliocene Molluscs from the Yorktown and Chowan River Formations in Virginia. Virginia Division of Mineral Resources Publication 127. Dall W.H. 1890-1903. Contributions to the Tertiary Fauna of Florida, with Especial Reference to the Miocene Silex-Beds of Tampa and the Pliocene Beds of the Caloosahatchie River, Part I: Pulmonate, Opisthobranchiate and Orthodont Gastropods, Transactions of the Wagner Free Institute of Science of Philadelphia 3(1-VI). Gardner, J. A. 1944. Mollusca from the Miocene and Lower Pliocene of Virginia and North Carolina: Part 1. Pelecypoda, United States Geological Survey Professional Paper 199-A: iv, pages 1-178, plates 1-23 Gardner, J. A. 1948. Mollusca from the Miocene and Lower Pliocene of Virginia and North Carolina: Part 2. Scaphopoda and Gastropoda, United States Geological Survey Professional Paper 199-B: iv, pages 179-310, plates 24-38, [iii] Gardner, J. A. and T.H. Aldrich. 1919. Mollusca from the Upper Miocene of South Carolina: with Descriptions of New Species. Proceedings of the Academy of Natural Sciences of Philadelphia 71: pages 17-53. Gibson, Thomas G. 1987. Miocene and Pliocene Pectinidae (Bivalvia) from the Lee Creek Mine and Adjacent Areas in Geology and Paleontology of the Lee Creek Mine, North Carolina, II. Smithsonian Contributions to Paleobiology No. 61. Hendricks, Jonathan. 2008. The genus Conus (Mollusca: Neogastropoda) in the Plio-Pleistocene of the southeastern United States, Bulletins of American Paleontology 375. Kohno, Naoki and Ray, Clayton E. 2008. Pliocene Walruses from the Yorktown Formation of Virginia and North Carolina, and a Systematic Revision of the North Atlantic Pliocene Walruses in The Geology and Paleontology of the Lee Creek Mine, North Carolina, IV. Virginia Museum of Natural History Special Publication No. 14. Mansfield, W.C. 1930. Miocene Gastropods and Scaphopods of the Choctawhatchee Formation of Florida, Florida Geological Survey Bulletin 3, 189 pages. Mansfield, W.C. 1931. Some tertiary mollusks from southern Florida. Proceedings of the United States National Museum, v. 79. Mansfield, W.C. 1931. Pliocene Fossils from Limestone in Southern Florida in Shorter Contributions to General Geology, USGS Professional Paper 170, 11 pages. Mansfield, W.C. 1932. Miocene Pelecypods of the Choctawhatchee Formation of Florida, Florida Geological Survey Bulletin 8, 233 pages. Mansfield, W.C. 1936. Stratigraphic Significance of Miocene, Pliocene, and Pleistocene Pectinidae in the Southeastern United States, Journal of Paleontology, Vol 10, No. 3, 24 pages. Mansfield, W.C. 1939. Notes on the Upper Tertiary and Pleistocene Mollusks of Peninsular Florida, Florida Geological Survey Bulletin 18, 128 pages. Mansfield, W.C., 1943 [1944]. Stratigraphy of the Miocene of Virginia and the Miocene and Pliocene of North Carolina in Gardner, Julia ed. Mollusca from the Miocene and Lower Pliocene of Virginia and North Carolina. USGS Professional Paper 199A, p. 1-19. Hollister, S.C. 1971. New Vasum Species of the Subgenus Hystrivasum. Bulletins of American Paleontology 262. Olsson, A.A. 1967 (1993 Reprint). Some Tertiary Mollusks from South Florida and the Caribbean, Originally - Bulletins of American Paleontology 54(242), The Paleontological Research Institute Special Publication 19: pages 11-75, 9 plates Olsson, A.A., and A. Harbison. 1953 (1990 Reprint). Pliocene Mollusca of Southern Florida with Special Reference to Those from North Saint Petersburg, with special chapters on Turridae by W.G. Fargo and Vitinellidae and Fresh-water Mollusks by H.A. Pilsbry, The Academy of Natural Sciences of Philadelphia Monographs 8, The Shell Museum and Educational Foundation, 457 pages, 65 plates Olsson, A.A., and R.E. Petit. 1964. Some Neogene Mollusca from Florida and the Carolinas, Bulletins of American Paleontology 47(217): pages 509-574, plates 77-83 Olsson, A.A., and R.E. Petit. 1968 (1993 Reprint). Notes on Siphocypraea, Originally - Special Publication 9, The Paleontological Research Institute Special Publication 19: pages 77-88. Petuch, Edward J. 1994. Atlas of Florida Fossil Shells (Pliocene and Pleistocene Marine Gastropods). Chicago Spectrum Press. Portell, Roger W. and Craig W. Oyen. June 2002. Pliocene and Pleistocene Echinoids. Florida Fossil Invertebrates Part 3, 30pp. Portell, Roger W. and Jeffery G. Agnew. February 2004. Pliocene and Pleistocene Decapod Crustaceans. Florida Fossil Invertebrates Part 4, 29 pp. Portell, Roger W. November 2004. Eocene, Oligocene and Miocene Decapod Crustaceans. Florida Fossil Invertebrates Part 4, 29 pp. Portell, Roger W. and B. Alex Kittle. December 2010. Mollusca, Bermont Formation (Middle Pleistocene). Florida Fossil Invertebrates Part 13, 40 pp. Rathbun, Mary J. 1935. Fossil Crustacea of the Atlantic and Gulf coastal plain. Geological Society of America. Special papers; no. 2. Tucker, H.I. and Druid Wilson. 1932. Some new or otherwise interesting fossils from the Florida Tertiary. Bulletins of American paleontology; v. 18: no. 65. Tucker, H.I. and Druid Wilson. 1933. A second contribution to the Neogene paleontology of South Florida. Bulletins of American paleontology; v. 18: no. 66. Tuomey, M., and F.S. Holmes. 1855-1856 (1974 Reprint). Pleiocene Fossils of South-Carolina: Containing Descriptions and Figures of the Polyparia, Echinodermata and Mollusca, Original pages 1-30 and plates 1-12 published in 1855, Original pages 31-152 and plates 13-30 published in 1856, The Paleontological Research Institution Special Publication 12: xvi, 152 pages, 30 plates, [addendum] Ward L.W. and Blackwelder, B.W. 1975. Chesapecten, a New “Genus of Pectinidae (Mollusca: Bivalvia) from the Miocene and Pliocene of Eastern North America. USGS Professional Paper 861. Whitmore, Frank C. Jr and Kaltenbach, James A. 2008. Neogene Cetacea of the Lee Creek Phosphate Mine, North Carolina in The Geology and Paleontology of the Lee Creek Mine, North Carolina, IV. Virginia Museum of Natural History Special Publication No. 14. Weisbord, Norman E. 1966. Some late Cenozoic cirripeds from Venezuela and Florida. Bull. Amer. Paleont., vol. 50, no. 225, pp. 1-145, pls. 1-12. Weisbord, Norman E. 1974. Late Cenozoic Corals of South Florida. Bulletins of American Paleontology vol. 66, no. 285. 544 pp. Zullo, Victor A., 1992. Revision of the balanid barnacle genus Concavus Newman. Supplement to Journal of Paleontology, v. 66, no. 6, pt. II. Zullo, Victor A. and Portell, Roger W. 1993. Paleobiogeography of the Late Cenozoic Barnacle Fauna of Florida in The Neogene of Florida and Adjacent Regions, Florida Geological Survey Special Publication No. 37. Paleoecology Allmon, Warren D. 1992. Whence Southern Florida’s Plio-Pleistocene shell beds? Plio-Pleistocene Stratigraphy and Paleontology of Southern Florida, Florida Geological Survey Special Publication No. 36. Allmon, Warren D; Rosenberg, Gary; Portell, Roger W.; and Schindler, Kevin S. 1993. Diversity of Atlantic Coastal Plain Mollusks since the Pliocene. Science, vol. 260:1626-1629. Allmon, Warren D; Spizuco, Mathew P. and Jones, Douglas S. 1995. Taphonomy and paleoenvironment of two turritellid-gastropod-rich beds, Pliocene of Florida. Lethaia, vol. 28:75-83. Allmon, Warren D; Emslie, Steven D.; Jones, Douglas S.; and Morgan, Gary S. 1996. Late Neogene Oceanographic change along Florida’s West Coast: Evidence and mechanisms. The Journal of Geology, vol. 104:143-162. Christie, Max. 2009. Ecological Interactions Across a Plio-Pleistocene Interval of Faunal Turnover: Naticid Cannibalism North and South of Cape Hatteras, North Carolina. Departmental Honors in Interdisciplinary Studies Thesis, The College of William and Mary. Geary, Dana H. and Allmon, Warren D. 1990. Biological and Physical Contributions to the Accumulation of Strombid Gastropods in a Pliocene Shell Bed. Palaios vol. 5:259-272. Jones, Douglas S and Allmon, Warren D. 1999. Pliocene marine temperatures on the West Coast of Florida: Estimates from mollusk shell stable isotopes In J.H. Wrenn, J.-P. Suc, and S.A.G. Leroy, eds., The Pliocene: Time of Change. American Association of Stratigraphic Palynologists Foundation, Dallas, Texas, pp. 241-250. Molnar, Peter. 2008. Closing of the Central American Seaway and the Ice Age: A critical review. Paleoceanography Volume 21. Petuch, Edward J. 2004. Cenozoic Seas. CRC Press. Petuch, Edward J. 2007. The Geology of the Everglades and Adjacent Areas. CRC Press. Schmidt, D. N., 2007. The closure history of the Panama Isthmus: Evidence from isotopes and fossils to models and molecules. In: Williams, M., Haywood, A. M., Gregory, J. F., and Schmidt, D. N. Eds.), Deep time perspectives on climate change - marrying the signal from computer models and biological proxies. Geological Society of London, London. Biostratigraphy Campbell, Kenneth M. 1985. Alum Bluff Liberty County, Florida. Florida Geological Survey Open File Report 9. Ketcher, Kathleen. 1992. Stratigraphy and Environment of Bed 11 of the "Pinecrest" Beds at Sarasota, Florida in Plio-Pleistocene Stratigraphy and Paleontology of Southern Florida, Florida Geological Survey Special Publication No. 36. Means, Harley. 2002. Introduction to the Geology of the Upper Apalachicola River Basin in Geologic Exposures Along the Upper Apalachicola River. Southeastern Geological Society Field Trip Guidebook 42. Missimer, Thomas M. 1992. Stratigraphic relationships of sediment facies within the Tamiami Formation of Southwest Florida: Proposed intraformational correlations. Plio-Pleistocene Stratigraphy and Paleontology of Southern Florida, Florida Geological Survey Special Publication No. 36. Petuch, E.J. 1982. Notes on the molluscan paleontology of the Pinecrest Beds at Sarasota, Florida with the description of Pyruella, a stratigraphically important new genus: Proceedings of the Academy of Natural Sciences of Philadelphia, v. 134, p. 12–30. Ward, Lauck W. 1992. Tertiary Molluscan Assemblages from the Salisbury Embayment of Virginia. Virginia Journal of Science, Volume 43, no. 1B. Ward, Lauck W. 1992. Diagnostic Mollusks from the APAC Pit, Sarasota, Florida in Plio-Pleistocene Stratigraphy and Paleontology of Southern Florida, Florida Geological Survey Special Publication No. 36. Ward, Lauck W. 1993. Pliocene Stratigraphy and Biostratigraphy, Virginia to Florida in The Neogene of Florida and Adjacent Regions, Florida Geological Survey Special Publication No. 37. Ward, Lauck W. 2008. Synthesis of Paleontological and Stratigraphic Investigations at the Lee Creek Mine, Aurora, NC (1958-2007) in The Geology and Paleontology of the Lee Creek Mine, North Carolina, IV. Virginia Museum of Natural History Special Publication No. 14. Yon, J. William. 1965. Adventures in geology at Jackson Bluff. Florida Geological Survey: Special publication 14. Systematics Hulbert, Richard C. (ed.). 2001. The Fossils Vertebrates of Florida. University Press of Florida. Turgeon, D.D. et al. 1998. Common and scientific names of aquatic invertebrates from the United States and Canada: mollusks. Second edition. American Fisheries Society Special Publication. No. 26. 526 pp.
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  • JohnJ

    Ancient Hunters

    By JohnJ

    June 5, 2010 Barry held his camera barely two feet away from the back of an Agkistrodon piscivorus. Although a small snake, it was still very dangerous and he positioned his camera based on years of experience with these reptiles. Known more commonly as a Cottonmouth or Water Moccasin, the twelve inch juvenile snake had coloration similar to the closely related Copperhead. However, its patterns were muted by late afternoon shadows in a remote location that was not favorable to an easy medical evacuation. So, we slowly moved away and eased our paddles back in the water to complete an adventure which began long before daylight.     Almost twelve hours earlier my friend and I had packed our gear, food, and water into my eighteen foot canoe. Soon after, our paddles fell into a synchronous rhythm that allowed us to quietly experience an aquatic wilderness. We were searching in Texas - hunting in alluvial debris and Pleistocene terraces for the slightest hint of extinct creatures. Our unrushed pace allowed us the time to get a feel for the local geology. Occasionally, groundwater from the surrounding area made its way to the base of the Pleistocene gravels and created springs which emerged just above older impermeable shale. The cool water supported rich vegetation that resisted the summer sun. It was also a visual key to the strata we were trying to find.     A little later, we found an area where the gravel spilled onto a ledge just above the water. Almost immediately I spotted a gravel encrusted bone fragment. I looked over to see Barry higher up on the river terrace. Still scanning the area, I hollered, “Hey, I found some mineralized bone over here. Uhhh…wait, here’s another one.” I noticed the second piece was gnarly and pitted while Barry made his way down to inspect my finds.   “What do you think of the encrusted bone?” I asked.  He replied, “Not sure; but there’s no doubt it’s old. Which bone do you think it is?”   I tried to imagine the fossil without the encrusting gravel, “Looks like it could be the ‘joint’ end of a scapula…I’m not sure about the second one, though.”   Before and after cleaning – proximal scapula & unknown fragment   I headed back to the canoe to pack away my finds while Barry searched further down the ledge. It wasn’t long before he yelled he had found more bone, and after I paddled the boat over to him, he grinned and asked me to find the camouflaged fossil. The fragment was difficult to spot amid the varied textures of rock and silt. We were off to a good start.   Barry's mineralized bone fragment   In Texas, June temperatures can quickly reach the upper 90’s. We maintained a regular fluid intake and an occasional soak in the water. Proper hydration and cooling were essential for us to enjoy an amazing adventure versus a headache pounding endurance test. Since we still had more than a dozen miles to travel, the hot conditions could not be ignored.     A few miles later a short rocky ledge barely emerged from the water. It looked like a good spot to check and take a break. What I really did not expect was to step a few feet from the boat and see a broken stone dart point. I looked at it with a little skepticism; the area seemed like a place fisherman would use to access the water and I wondered if someone had passed the time trying to replicate an ancient weapon. But the patina on a few nearby flakes confirmed the find was old.   Barry searched the rocky debris fan on the downstream end of the ledge. I let him know to keep an eye out for more than bone and kept scanning the ground. Before me was an area the size of two cars where the water had peeled away part of an upper bank which had slipped into the water. I stopped. There, in the gravel and weeds, were more flakes…and another dart point! As I reached for my camera, I saw another broken point by my knee…a cool moment. Then things started to get comical - in an amazing sort of way - because as I took the photo of the first point, I spotted a third one just beyond it…an incredible moment!     Still kneeling in the same spot, I yelled to Barry, “Hey, you’re not going to believe this, but I’ve found…hang on….” I shook my head in disbelief at the fourth late Archaic projectile point tucked in the gravel. “You have to come over here, now,” I smiled. I tried to explain to him what had just happened – pointing out each of the finds. He was as awestruck as I, but we both almost lost composure when, within seconds of ‘show and tell’, another light colored point met my eye a few inches from where I laid the paddle. I edged backward to get a good camera angle. Then, I just looked up at Barry in stunned silence and back down again beside my other knee at a small gray-purple dart point. That is when we both erupted with the excitement of two kids.     “I’m now walking away. There have to be more here; so you find them,” I jokingly announced as I headed upstream to survey the ledge. Savoring an unbelievable fifteen minutes of discovery included the analytical questions forced by the finds. Often people have asked, “Where did these artifacts come from?” Sometimes the answer is simple because the ‘site’ still exists. Other times, I will touch two fingers together in front of me, representing a point in space, because similar coordinates may be all that remain of ancient eroded camps. My quick recon of the area seemed to confirm a similar origin for these artifacts. Our timing had offered us the chance to experience something that would have been erased by the next flood.   My six dart points fill Barry’s hand   Barry’s voice carried down the bank, “I found one!” I saw him gently scratching the sand and gravel in the weeds. I took in the view of the area because I wanted to remember this place and time. Barry called out again, “Hey, you should see this large white base I found!” By the time I made it back to him, he had found another dart! While he pointed out his finds, I felt like we were functioning in a mild state of shock – still trying to wrap our minds around what was happening. After a few more broken finds and photos, we cooled off in the water. In all we found 19 pieces; some were complete and some were fragments.     Dream-like remnants of the artifact discoveries stayed with us for miles. I told Barry I was not sure I would have believed the event if I had not been part of it. Roughly thirteen hundred years earlier, someone made the weapons we found. Handling them was like touching an old pocket knife owned by your great grandfather or holding an old wooden spoon used by your great grandmother - except, they were much older and no one remembered the owners anymore. We could not know what the circumstances were during the last moments someone held these artifacts, but we were the next men to hold them and imagine those days.   We found a few pieces of fossil bone over the next couple of hours and it really began to get hot. To get relief from the temperature, we paddled closer to the shady banks. On few occasions we startled beavers from their dens. Not many things can get your attention quicker than a forty pound animal hurtling into the water on the edge of your vision. My only regret was that the camera had not recorded our comical reactions.   Then, as we rounded a large bend, a huge gravel bar came into view. In the distance, I could see something big lying on the rocks. “Barry, what’s that?”   “I don’t know….” He shaded his eyes and leaned forward, then exploded, “IT’S A HUGE GAR!” He spun to face me, “Can I have the SKULL?!” He spun back, “It’s HUGE! You’ve got to let me have it, please!”   He sounded like a ten year old begging for his favorite birthday present. It was hilarious. But my smile was temporarily gagged when I caught a whiff of the almost dry carcass. “If you can separate the skull from the rest, you can have it…but it stays on your end of the canoe,” I winced.     The smell matched the size of the alligator gar – it was a monster. I was fascinated to see such a large specimen up close. Barry finally separated his prize from its ragged remains. Then, he placed it in the canoe under his seat and we continued to search the bar.     The multi-colored gravel camouflaged many pieces of petrified wood and the new ‘gar skull owner’ took advantage of the canoe’s carrying capacity. We left shore a little heavier and smellier. Unfortunately for me, the prevailing wind came from the bow of the boat. I joked with him about the odor coming from his direction, but he firmly insisted he was unaware of any stench.   On another bar, the gravel teased us with more bits of bone; then Barry spotted a large brown lump. He called me over to take some photos. Whose bone he had found was not immediately obvious; but it had some size. Only after he freed it from the sand were the features of a large vertebra confirmed. Likely from a mammoth, it had suffered the erosive effects of time and water. Yet, Barry grinned. He had accomplished one of the goals we had for the trip – find mammoth bone.         The heat was relentless, but we kept cooling off and drinking. Even the butterflies were frequently tapping moisture and minerals in the damp sand. Eventually, we reached an area where the channel narrowed and we took advantage of the shade. I was looking for beaver dens when Barry cried, “Snake! Back there by the large stump!”     We buried the paddles in a series of strong back strokes to reverse our direction. I finally spotted the handsome reptile crawling into a small pile of logs. I could tell he wanted to catch it, when he almost whispered, “Elaphe obsoleta lindheimeri.” After three seconds of heat affected thinking, I realized he had not issued curses to move faster, but had just named the scientific classification for a Texas Rat Snake – the name that had passed through my mind 5 seconds earlier….  Barry scrambled up the bank and had the snake in hand within two minutes. He slowly manipulated it while I took photos. I have always enjoyed my encounters with these non-poisonous reptiles. They can be very aggressive and strike repeatedly, or try to intimidate any threats with their loud hiss and vibrating tail. He left on the log where we found it.     About a half hour downstream we were exposed again to the late afternoon sun. It reflected from the water and the barren high bluffs beside us. We paddled and scanned both water and banks. Through the salty sweat in my eyes, I saw something out of place halfway up one of the bluffs.   “OK, that can’t be what I think it is, can it Barry?” A bowling ball sized dome contrasted sharply with the surrounding tan soil. We slowed the canoe to a stop. I remembered the “dome” of a four foot mammoth humerus I had found almost a year earlier…. My heart rate increased.     Barry insisted, “John, that shape is too perfect; it has to be a bone.” The closer we got the boat, the more my pulse quickened. From fifteen feet below it, I still had to get closer to allow myself to acknowledge the obvious…it was a bone!     We positioned the canoe as close as possible to the vertical bank. The water was not moving fast there, but it was deep. In a tricky move that involved me stepping on the tip of the stern and stabbing my rock hammer into the soil of the steep ledge above, I pulled myself up to a spot where I could rest. Our access point was a little downstream of the “dome”, so I had to dig footholds to make my way to the find. It was impressive when I could finally rest beside it. “Hey Barry, it’s bone!” I grinned.   After a difficult time staging a few digging tools, we started to excavate. I carefully determined the perimeter of the fossil and had some vivid flashbacks to last year’s humerus find. However, the deeper we dug, the more it became apparent that the rest of the bone was not attached. We tested the ‘ball’ for movement and it popped free of the matrix below. In the soil below, we did not find any more evidence of bone.     Initially it seemed there was a large scavenging scar across the surface, but after cleaning, the mark appeared to be an eroded part of the internal vascular structure. Other old gouges and marks may have been due to ancient scavenging. Shape and size suggested I had found my first mammoth ‘femur ball’ or the head of the femur. Regardless of the number of mammoth fossils I have found, they never cease to spark my imagination.   Mammoth femur head – approx. 7 inches in diameter     Scars and vascular structures   The shadows had begun to lengthen by the time we loaded the femur ball and started back downstream. Temperatures had dropped a few degrees which energized us for the next few miles. In a large eddy, we saw another snake crossing the water and sped up to see it. Both of us recognized the juvenile Water Moccasin as it paused and floated on the water. Barry pulled out his camera and I positioned the canoe to assist him. All was going well until the young snake thought the boat would make a good rest stop. The most important result of the next few moments was that no one entered the water, and nothing entered the canoe. I repositioned us to allow the little pit viper to reach the bank. It seemed to respond to the security of solid ground and assumed the confident demeanor of the species.     We reached the take-out after twelve hours on the water. Tired, but feeling the satisfaction of an incredible adventure, we completed a relatively short shuttle run back upstream. The trip had so many layers – so many memories. We hunted and found what we sought. And somewhere between our imaginations, the water, willows, cottonwood, and stone, we caught a reflective glimpse of the ancient hunters.
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Our community blogs

  1. Hello Everyone its been way to long since my last entry. I've been sharing on the Facebook page because its so easy to upload from my phone. But I will start back bogging...... I miss it :)

    I found these cephalopods two weeks ago here in middle TN- Leipers Formation from what I'm told. I found it interesting how the shell casing seems to have been peeled back on both......

  2. Lepidodendrons

    blogentry-814-0-25566400-1379333148.jpgblogentry-814-0-31338200-1379333151.jpgblogentry-814-0-57246800-1379333154.jpg

    Lepidophloios laricinus

    blogentry-814-0-70893600-1379333191.jpgblogentry-814-0-93044000-1379333193.jpgblogentry-814-0-34017900-1379333196.jpg

    Seed ferns (Cyclopteris, Neuropteris, Macroneuropteris, Mariopteris, Mixoneura, seed fern rachis impression, seed fern male fructification)

    blogentry-814-0-13507100-1379333231.jpgblogentry-814-0-55645100-1379333233.jpgblogentry-814-0-10792800-1379333237.jpgblogentry-814-0-21294600-1379333240.jpgblogentry-814-0-97433700-1379333243.jpgblogentry-814-0-19723700-1379333246.jpgblogentry-814-0-43683900-1379333249.jpg

    Bothrodendrons

    blogentry-814-0-47100100-1379333594.jpgblogentry-814-0-19844700-1379333597.jpgblogentry-814-0-67461500-1379333600.jpgblogentry-814-0-28806200-1379333603.jpg

    Sigillaria

    blogentry-814-0-43993100-1379333713.jpg

    Calamites (Calamostachys, Macrostachya, Asterophyllites)

    blogentry-814-0-19212400-1379333815.jpgblogentry-814-0-45951800-1379333819.jpgblogentry-814-0-94667800-1379333822.jpg

    Cordaicarpus (Cordaites seed)

    blogentry-814-0-67074000-1379333888.jpg

    Dicranophyllum

    blogentry-814-0-32663200-1379333932.jpg

    Jurassic (Bothonian) petwood

    blogentry-814-0-45801000-1379334110.jpg

    Euproops danae

    blogentry-814-0-48422700-1379333672.jpg

    Trigonia Myophorella

    blogentry-814-0-98021100-1379334050.jpg

    to be continued...

  3. meadow's Blog

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    meadow
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    blog-0928283001370478681.jpgMy dad
  4. Fossil-Hound
    Latest Entry

    These are some of the highlights from a trip to you-Dig in Delta Utah for my undergrad Historical Geology course at BYU-Idaho.

  5. the pterosaurs saw what happened that day

    a second Sun dropped from the sky

    the pressure wave blasted those closest to haze

    and wafted their ashes on high

    then hundreds more pterosaurs lifeless and torn

    took flight in a terrible dance

    broken umbrellas tossed far by the storm

    untethered kites left to mischance

    thousands of pterosaurs fell like dead leaves

    caught up in sudden tumultuous seas

    waves smashed the pterosaurs huddled on land

    waves buried eggs under layers of sand

    the dark with mercy tried to hide these ravages in night

    receding waters banked the once majestic bodies high

    and now at last as all the worlds great forests come alight

    they are transformed

    as cinders reborn

    they take their final flight

  6. Lise MacFadden's Poetry Blog

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    For millions of years and then some

    I've waited for someone to come

    Even though I am dead

    and I'm missing my head

    I still have my pygidium

  7. Carcharodontosaurus' Blog

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    Location: Eden Delta, Earth 2.

    Year: 3400.

    Season: Spring.

    Upon the plains of the terraformed planet, a massive animal roamed. Spinosaurus. It ignored the herd of Deinotherium nearby, as their skin would be too thick to penetrate. Instead, it was heading towards the river. As soon as it got there, it noticed a group of Andrewsarchus nearby. It decided that it would kill these, as they would provide competition for food.

    The dinosaur ran towards the small group, and quickly charged at the oldest male, throwing it against a rock. This killed it instantly. However, the 2 adult females attacked the male spinosaur's leg, but the giant just kicked them aside as if they were stones. One blow from the claws made short work of them. He then headed towards the young Andrewsarchus, and managed to swallow those whole.

    ______________________________________________________________

    Earth 2 is a terraformed planet I made up. It is basically a terraformed planet where most extinct species of the Phanerozoic live. Different creatures have different niches in different places, so competition between groups is greatly reduced.

  8. VisionXray23's Blog

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    I just filmed and posted a new youtube video. I would love to hear what you guys think about it !

  9. Western NY Explorer's Blog

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    Started out visiting 18 mile creek in Hamburg. Found quite a few braciopods. Shale was quite slippery and could not make it to the lake. Site is promising for dryer weather and waders. Headed over to Penn Dixie. The trilobite bed is covered with overburden as the site is not ready for the season. Picked through lots of weathered shale and found tons of horn coral , some partial phacops, lots of brachiopods, and a couple enrolled phacops. My wife took the day with her find. I think its a greenops, but not 100 % sure. Whole greenops are rare at this site. Will start prepping and photographing specimens during the week.

    possible greenops

  10. blogentry-5434-0-01847200-1325705436.jpg

    ---Prologue---

    Milky Way Galaxy

    25,000 years ago

    A spiral galaxy, one of the billions of islands of stars moving across the dark matter that is known as the universe, it rotates like a huge galactic wheel, pulling countless stars within its titanic gravitational pull. This particular galaxy is known as the Milky Way, 100,000 light-years across and 1,000 light-years thick. Like a grain of sand pulled by an ocean current, an asteroid races through the galaxy. The asteroid measures nearly seven miles in diameter, and has been moving through the galaxy since the dawn of time, passing planets and other asteroids. It is now on a collision course with a medium sized planet. The planet is still millions of miles away, but the asteroid is approaching quickly. The planet is warm and tropical, and also has an abundant source of water, oxygen, and life. The asteroid hurdles towards Earth, nothing can stop it. When it impacts, it will cause world-wide destruction and chaos. The countdown to extinction has begun.

  11. Kehbe's Kwips

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    I was surfing the web recently and came across a site whose members collect rocks that have faces in them. Here is a quick link to it… http://www.cst.cmich.edu/users/dietr1rv/mimetoliths/ It’s interesting to me. I turned to my wife and told her, “Wow, I’m gonna have to keep my eyes open for rocks like these and start collecting them!” Well, to put it bluntly, she puts up with my collecting, if I keep them picked up and don’t wash to much mud down her kitchen sink while scrubbing that latest fossil find or those most recent quartz crystals i found, ..... with her toothbrush… ;) but she laughed and nodded in agreement, knowing full well that soon she would start seeing average looking, run of the mill, unimpressive rocks piling up that only a sun beaten, weary and bleary eyed rock and fossil hound, after hours of searching, can see the elusive and mysterious image of ‘Jimi Hendrix’ in one of them and the shadowy profile of ’Mother Theresa’ in another! “What’s that? Where’s ‘Jimi’ you ask? Hmm, right here…if you turn it just right….uh…Well honey, it looked like ‘Jimi Hendrix’ at the time or I wouldn’t have brought it home! I swear! It must have been the way the sun was shining on it!” Anyway, what I am getting to is this, most folks just don’t understand my desire to collect rocks and fossils. Well actually it’s an obsession! I mean, I even had an online roleplaying character named “Eclo Stonehoarder” I can’t explain it exactly, and maybe you can relate in some way! It’s just the way I am and the way I’ve always been. To attempt a better explanation, I wrote this poem about it.

    (This actually happened to me not so long ago!)

    While strolling with a friend one day,

    I spied a glimmer bright.

    It shone like diamond in the sun,

    reflecting all that light!

    I bent down close and got a look,

    a wonder to behold.

    I gently picked it up to see,

    the story to be told!

    I turned it round, and round again,

    while feeling every face.

    Each one so smooth and polished slick,

    it took me to that place!

    A place a million years ago,

    when Earth was just a child.

    A place devoid of human things,

    just raw and wet and wild!

    The time this jewel has spent on Earth,

    my mind can barely think.

    Yet to this gem upon my hand,

    ’twas nothing but a blink!

    Amazed and full of wonder at

    the beauty of this Earth.

    The things it has created

    since the moment of it’s birth!

    I marvel at the symmetry,

    the artistry and grace.

    I hold it up to show my friend,

    I hold it to his face!

    “Just look”, I say, “It’s beautiful”,

    and to my utter shock.

    He only shrugged and said to me,

    “It’s just another rock!”

    Well, needless to say, that floored me. I really didn’t know how to respond so I said nothing but I thought to myself, ”Just another rock? Really? Thats what you think? “Just another rock?” Oh how sad it must be to sleepwalk through life and never appreciate the natural beauty of all of Earths wonders and what inhabited this Earth long before us! I’ve since had time to think about it a bit and I wrote a second part to the poem that says what I should have said that day. It goes like this…

    Contraire my friend, this here is quartz,

    not just another stone.

    Theres minerals and sediments,

    theres igneous and bone!

    Each one unique and on it’s own

    it holds a mystery.

    It tells a tale of life on Earth,

    it’s part of history!

    We study them, we covet them,

    we trade some just like money.

    With Diamonds, Sapphires, Rubies,

    and Amber gold as honey!

    Theres fossils, corals, limestone cliffs,

    diversity abounds.

    A grain of sand that wind can move,

    or one, a million pounds!

    If you my friend are blind to this,

    theres nothing I can say

    to make you stop and look at things

    in quite a different way.

    One day both you and I won’t walk,

    upon this Earthen block.

    A million years will pass and you’ll be,

    “Just another rock!”

    Poetry composed by KehBe

    Related Posts:

  12. Here are the top common species and counts at WB, as per Emerson's book.

    1. Coral - Turbinolia pharetra 1000 (common, ranges from 5mm and up)
    2. Bivalve - Anomia lisbonensis 1000 (fairly large)
    3. Bivalve - Barbatia (Barbatia) uxorispalmeri 1000
    4. Bivalve - Notocorbula texana 1000
    5. Gastropod - Latirus moorei 1000
    6. Gastropod - Polinices aratus 600 (very common snail, as a Naticid, drills holes in prey)
    7. Bivalve - Vokesula smithvillensis petropolitana 500
    8. Gastropod - Buccitriton texanum 500 (very common snail, and a predatory hole driller)
    9. Gastropod - Hesperiturris nodocarinatus 500
    10. Bivalve - Pachecoa (Pachecoa) sabinica 308
    11. Gastropod - Buccitriton sagenum 300 (predatory snail drills holes)
    12. Gastropod - Turritella nasuta 300 (oddly, a filter feeder)
    13. Bryozoa - Lunelites bouei 253
    14. Bryozoa - Schizorthosecos interstitia 253
    15. Gastropod - Mesalia claibornensis 250
    16. Gastropod - Protosurcula gabbii 250
    17. Scaphopoda - Dentalium (Antalis) minutistriatum 244
    18. Gastropod - Michela trabeatoides 240
    19. Gastropod - Pseudoliva vetusta CONRAD FORMA 232
    20. Bivalve - Vokesula smithvillensis smithvillensis 200
    21. Gastropod - Bonellitia parilis 200

    And with additional information added:

    blogentry-2987-0-57452000-1314060962.png

    Emerson's book provides info on the number of specimens in his collection. The rarest species, of which there are many, are represented by only one specimen. The more common specimens range from a few to an unspecified, large number.

    Most of the time, he provides an exact count. Example: 232. Often, he provides a minimum value, such as 250, meaning that there were at least 250 specimens in the collection. Other times, he omits a number, but states the species is very common. These latter specimens are noted above as the number 1000.

  13. Alright, in 2003 it was the second year of my dad and my trip to big brook. this time, we brought my older sister and her friend. we dug in the pit for hours (they sat on logs, how helpful :rolleyes: ) we found a decent amount. suddenly, my dad finds a fish tooth (now remembering it was probably a good puny goblin). he gave it to the girls to look at. u wont believe it. THEY DROPPED IT! :o my dad was so ##### and dug desperatly in the spot of the brook were the tooth was dropped. in the first sift, we didnt find the tooth, but he says things not allowed to be said on this forum without my account being banned! :D in his hand, he held a tooth 1.5 in down and 1in across, fully complete with two HUGE cusps and all enamel and root. So he thanked my sister and stupid friend. i guess bad luck makes good fortune. i will get pics later, but it looks like an otodus or a goblin that is hugenous.

  14. It's been 3 months since the secret PABLI was assembled. They are currently still recruiting members.

    Charles Darwin scratched his head. "A message for you, father." says Darwin's daughter. "Oh, another one of those scrabbled hate messages, I suppose." "Oh no father, not at all. This time it's completely different. Please, take a look." his daughter said as she handed him a message with a golden stamp in the back. Darwin tilted his head with a frown, and flipped the message open. folded neatly inside, was a message written in cursive from something called "PABLI".

    Dear Sir Darwin,

    It's a great pleasure to meet you. I am Jameson C. Rowley, the president of the secret PABLI group, consisting of top evolutionists, paleontologists, anthropologists and biologists. I have read your newly published book, titled "On The Origin Of Species". Marvelous content. Despite the number of people who abuse your view of creation, we think it's the work of a god. We would be jubilant to have you be a member of our society. Please reply this message as soon as you can, for we have a very serious matter to discuss. It would be great if you can come the day after tomorrow in London, Pennington Square, Block #24. Thank you for your time, and I sincerely hope you can come.

    Truly Yours,

    Jameson C. Rowley

    President of PABLI

    Darwin looked at the letter for another minute or so, then set it down and rubbed his eyes. "My dear, can you please fetch me a piece of paper, an envelope and a pen?" "Yes, father." within a minute, Darwin started writing back.

    "Dear Sir Rowley,

    It's great to hear a few praises for my hard work. I am more than happy to join the secret PABLI society. As for the visit, I will be there. May I ask, what's the big hurry? (the letter continues)"

  15. Piranha Blog

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    Charles Darwin with his elegant theory,

    Met the burden of proof with those sneery,

    One-hundred-fifty years later,

    There is no idea greater,

    In advance he would have felt cheery !!

     

    Trilobites appeared with complexity,

    Still viewed to this day with perplexity,

    They are fun at this forum,

    And deserve our decorum,

    Tens of thousands of species collectively !!

     

    Tiktaalik arose from the sea,

    Stood so tall spectacularly,

    Fins like our hands,

    To conquer the lands,

    A fantastical family tree !!

     

    While Ida was swinging in trees,

    Never thought of being marquee,

    Now hotly debated,

    The evidence weighted,

    Awaiting her next show for TeeVee !!

     

    Fossil shark teeth are quite the rage,

    From Paleozoic to Pleistocene Age,

    The forms are so graceful,

    This forum is faithful,

    All others are always upstaged !!

     

    T.rex had a monstrous bite,

    Gave all the Trikes a big fright,

    Although taking a horn,

    Would be quite a thorn,

    Like any smart bird he took flight !!

     

    Fossil limericks are always such fun,

    No way I would only make one,

    A vast inventory,

    Treasures mined in a quarry,

    The magnificent tales are all spun !!

     

     

  16. emmytee
    Latest Entry

    That's right, I'm back. I'm sorry I didn't update as much as I should have. I was very busy with exams and essays (but it paid off, I made the Dean's List woo!) and then on break I just wanted to chillax and never write again.

    So... where did we leave off?

    I went on a field trip with my class to Portland Point. It was very rewarding. I found tons of brachiopods and some crinoid and trilobite material. My finds include a small, orange colored crinoid, and a near complete trilobite that's partially rolled. I wish I could include pictures but the fossils are currently at home.

    The internship continued as usual no new developments really, and I got an A in my fossil prep class. I wish I could go back and continue working on the fish but the prep lab is closed because it will be renovated starting February.

    So where does that leave me? I received an offer from the Volunteer Coordinator to serve as an intern to the Museum Operations and Programs Coordinator. In this job I would serve as a tour guide as well as assist the Coordinator in organizing programs and events. I accepted because I feel that I would gain more experience than just doing busy work in collections which is important because I am considering working at a museum in the future. And, I can still appreciate the museum's specimens as a docent. I will still update the blog with fun facts I learn from tour guide training and with my experiences serving as an intern. I have found out how to get college credit for the internship so although it's too late to get credit for last semester, this semester I can focus more on my internship by not taking as many classes.

    I'm already thinking about summer and whereI should work. I found a dream job out west for which I am adequately qualified but it's way too far away for my first summer in college. There's always next year! Instead, I am hoping to work at my local conservation center and museum but I would need to find and apply for a grant to get paid. I can't survive sophomore year unless I get a summer job! If all else fails, I can be a camp counselor again. Fun, but not relevant to my scientific interests.

    This semester I am taking Evolution and Diversity, Ecology and the Environment, Evolution of the Earth and Life, and Statistics.

    I'm sorry I left unannounced! I'll try not to let it happen again. I start next week :)

    Until then,

    Emily

  17. As many say, good things come to those who wait. Well, fruition at last!

    While working for an elderly couple last Saturday, cleaning up various parts of the lawn for cash, I learned that this couple once traveled the world, collecting fossils and stones along the way. The next day at church, I was greeted with a very pleasant surprise, a slab of rock literally overflowing with crinoid stems!

    While many may say that it isn't that big of a deal, as an amatuer fossil hunter, and one with no luck to his name, it was a great thrill to see so many wonderfully preserved fossils (see pictures in album, beware, pictures are blurry as I was forced to use the computer webcam.)

    And yet another surprise, the more I worked, the more fossils I will be able to have, including shark teeth. Which is always a great motivator!

    And on another note, while working on a science fair project for my chemistry class, I created a project on the most efficent way of preparing fossils using household items. The judges seemed very impressed by the rarity of such a project and how well it was done, and by the more amazing ways of cleaning fossils. I hope to see great results tomorrow.

    Overall, it's been a very good week.

  18. trilobite guy's Blog

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    well i just got back from the museum and got lotsa stuff :P all invertabrates except some shark teeth. it was a great time, though i didnt have time to see all the galleries..well here are some pictures,

    first the museum

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    now the fossils

    bryozoans and corals

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    belemnites

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    crinoid stem peice

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    ammonites

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    gastropod

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    and then some shark teeth-i think its 3 tigers and 1 bull

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  19. Fossilefinder's Blog

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    I was at work in Newport RI this morning..surfing ..not working.....found this site..since I grew up in Newindsor NY, Mysef and close friends hunted and explored on foot a 50 mile radius from ages 10 to 17. I was always the amature geologist & fossile hunter. I made one discovery 25 30 years ago, I never knew who to tell...maby you.

    While hunting off RT218 in Cornwall walking all day..which I hunted since 10....most of my hunting turned in exploring the mountain sides and tops between Cornwall & West Point, finding insignificint primative sites a stray arrow head..yadayada..

    So after morning hunting I took about a 5 or 6 hour stroll/climb to the very top on one those mount tops (not Butterhill). At the top there was a large "bear stone table top" flat area...couple hundred yards square....with vegetation clumps & grassy patches across & interspursed. There was a set of tracks depressed in the stone for at least 50 to maby 150 feet or more before dissapearing under the earthin cover...they ran in a line under the grassy patches and re emerged on each side of the large patch work of grassy spots. I saw and walked with 20 -30 consistant "walking" tracks.

    Long time ago..no camera, I went back with a camera few years back but only had couple hours to look and didn't find the spot...Probebly need a weekend to find it again..maby google earth??? Maby not..

    The impressions were about a foot long, 2- 4 inches deep, about three inches wide at "heel" widened to 7-9 or 10 inchea at "toe end", some puddled with water, the track strides were three or five feet distance right track to right track, about four feet separated right track form left track, as I recall. Sadly I dont remember the tracks as the traditional V shape, but more oblong depressions & wider at front. Duck like...

    Not sure if this is of interest to anyone, but I love the Hudson Valley, so here's some eyewitness lore that maby no one knows about.

  20. HeritageFossils' Blog

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    After picking up a rather interesting amber-in-matrix specimen, I decided to look into the geological history surrounding the deposition of Dominican Amber.

    Mentally I had always pictured Dominican amber forming as sap oozed out of trees and deposited on the forest floor; resulting in burial in forest detritus.

    The more interesting reality is that the ooze from the Hymenaea tree would get washed out to coastal sedimentary basins; such as coastal lagoons. Here the sap would settle and get fossilized into amber in siltstone. This is why large masses of amber, as can be seen in the picture, are present all as one layer while the rest of the rock is all siltstone; large storm events would wash the ooze out.

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    http://historical.ha.com/common/view_item.php?Sale_No=810091&Lot_No=81055&type=yinan-fossilforum

    Usually the miners of this material remove the amber for easy transportation, which makes matrix pieces hard to come by. Rarely are pieces big enough to see the depositional layering effect.

    -YvW

  21. Hunt'n 'odonts!

    Acryzona
    Latest Entry

    Today I started dissolving samples of Rochester Fm (Silurian) from upstate NY, Jacksonburg Limestone (Ordovician) from a quarry near Bethlehem, PA and finally the Whitewater Limestone (Ordovician) from Indiana.

  22. JohnJ
    Latest Entry

    June 5, 2010

    Barry held his camera barely two feet away from the back of an Agkistrodon piscivorus. Although a small snake, it was still very dangerous and he positioned his camera based on years of experience with these reptiles. Known more commonly as a Cottonmouth or Water Moccasin, the twelve inch juvenile snake had coloration similar to the closely related Copperhead. However, its patterns were muted by late afternoon shadows in a remote location that was not favorable to an easy medical evacuation. So, we slowly moved away and eased our paddles back in the water to complete an adventure which began long before daylight.

     

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    Almost twelve hours earlier my friend and I had packed our gear, food, and water into my eighteen foot canoe. Soon after, our paddles fell into a synchronous rhythm that allowed us to quietly experience an aquatic wilderness. We were searching in Texas - hunting in alluvial debris and Pleistocene terraces for the slightest hint of extinct creatures.

    Our unrushed pace allowed us the time to get a feel for the local geology. Occasionally, groundwater from the surrounding area made its way to the base of the Pleistocene gravels and created springs which emerged just above older impermeable shale. The cool water supported rich vegetation that resisted the summer sun. It was also a visual key to the strata we were trying to find.

     
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    A little later, we found an area where the gravel spilled onto a ledge just above the water. Almost immediately I spotted a gravel encrusted bone fragment. I looked over to see Barry higher up on the river terrace. Still scanning the area, I hollered, “Hey, I found some mineralized bone over here. Uhhh…wait, here’s another one.” I noticed the second piece was gnarly and pitted while Barry made his way down to inspect my finds.

     

    “What do you think of the encrusted bone?” I asked.  He replied, “Not sure; but there’s no doubt it’s old. Which bone do you think it is?”

     

    I tried to imagine the fossil without the encrusting gravel, “Looks like it could be the ‘joint’ end of a scapula…I’m not sure about the second one, though.”

     

    Before and after cleaning – proximal scapula & unknown fragment

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    I headed back to the canoe to pack away my finds while Barry searched further down the ledge. It wasn’t long before he yelled he had found more bone, and after I paddled the boat over to him, he grinned and asked me to find the camouflaged fossil. The fragment was difficult to spot amid the varied textures of rock and silt. We were off to a good start.

     

    Barry's mineralized bone fragment

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    In Texas, June temperatures can quickly reach the upper 90’s. We maintained a regular fluid intake and an occasional soak in the water. Proper hydration and cooling were essential for us to enjoy an amazing adventure versus a headache pounding endurance test. Since we still had more than a dozen miles to travel, the hot conditions could not be ignored.

     

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    A few miles later a short rocky ledge barely emerged from the water. It looked like a good spot to check and take a break. What I really did not expect was to step a few feet from the boat and see a broken stone dart point. I looked at it with a little skepticism; the area seemed like a place fisherman would use to access the water and I wondered if someone had passed the time trying to replicate an ancient weapon. But the patina on a few nearby flakes confirmed the find was old.

     

    Barry searched the rocky debris fan on the downstream end of the ledge. I let him know to keep an eye out for more than bone and kept scanning the ground. Before me was an area the size of two cars where the water had peeled away part of an upper bank which had slipped into the water. I stopped. There, in the gravel and weeds, were more flakes…and another dart point! As I reached for my camera, I saw another broken point by my knee…a cool moment. Then things started to get comical - in an amazing sort of way - because as I took the photo of the first point, I spotted a third one just beyond it…an incredible moment!

     

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    Still kneeling in the same spot, I yelled to Barry, “Hey, you’re not going to believe this, but I’ve found…hang on….” I shook my head in disbelief at the fourth late Archaic projectile point tucked in the gravel. “You have to come over here, now,” I smiled. I tried to explain to him what had just happened – pointing out each of the finds. He was as awestruck as I, but we both almost lost composure when, within seconds of ‘show and tell’, another light colored point met my eye a few inches from where I laid the paddle. I edged backward to get a good camera angle. Then, I just looked up at Barry in stunned silence and back down again beside my other knee at a small gray-purple dart point. That is when we both erupted with the excitement of two kids.

     

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    “I’m now walking away. There have to be more here; so you find them,” I jokingly announced as I headed upstream to survey the ledge. Savoring an unbelievable fifteen minutes of discovery included the analytical questions forced by the finds. Often people have asked, “Where did these artifacts come from?” Sometimes the answer is simple because the ‘site’ still exists. Other times, I will touch two fingers together in front of me, representing a point in space, because similar coordinates may be all that remain of ancient eroded camps. My quick recon of the area seemed to confirm a similar origin for these artifacts. Our timing had offered us the chance to experience something that would have been erased by the next flood.

     

    My six dart points fill Barry’s hand

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    Barry’s voice carried down the bank, “I found one!” I saw him gently scratching the sand and gravel in the weeds. I took in the view of the area because I wanted to remember this place and time. Barry called out again, “Hey, you should see this large white base I found!” By the time I made it back to him, he had found another dart! While he pointed out his finds, I felt like we were functioning in a mild state of shock – still trying to wrap our minds around what was happening. After a few more broken finds and photos, we cooled off in the water. In all we found 19 pieces; some were complete and some were fragments.

     

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    Dream-like remnants of the artifact discoveries stayed with us for miles. I told Barry I was not sure I would have believed the event if I had not been part of it. Roughly thirteen hundred years earlier, someone made the weapons we found. Handling them was like touching an old pocket knife owned by your great grandfather or holding an old wooden spoon used by your great grandmother - except, they were much older and no one remembered the owners anymore. We could not know what the circumstances were during the last moments someone held these artifacts, but we were the next men to hold them and imagine those days.

     

    We found a few pieces of fossil bone over the next couple of hours and it really began to get hot. To get relief from the temperature, we paddled closer to the shady banks. On few occasions we startled beavers from their dens. Not many things can get your attention quicker than a forty pound animal hurtling into the water on the edge of your vision. My only regret was that the camera had not recorded our comical reactions.

     

    Then, as we rounded a large bend, a huge gravel bar came into view. In the distance, I could see something big lying on the rocks. “Barry, what’s that?”

     

    “I don’t know….” He shaded his eyes and leaned forward, then exploded, “IT’S A HUGE GAR!” He spun to face me, “Can I have the SKULL?!” He spun back, “It’s HUGE! You’ve got to let me have it, please!

     

    He sounded like a ten year old begging for his favorite birthday present. It was hilarious. But my smile was temporarily gagged when I caught a whiff of the almost dry carcass. “If you can separate the skull from the rest, you can have it…but it stays on your end of the canoe,” I winced.

     

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    The smell matched the size of the alligator gar – it was a monster. I was fascinated to see such a large specimen up close. Barry finally separated his prize from its ragged remains. Then, he placed it in the canoe under his seat and we continued to search the bar.

     

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    The multi-colored gravel camouflaged many pieces of petrified wood and the new ‘gar skull owner’ took advantage of the canoe’s carrying capacity. We left shore a little heavier and smellier. Unfortunately for me, the prevailing wind came from the bow of the boat. I joked with him about the odor coming from his direction, but he firmly insisted he was unaware of any stench.

     

    On another bar, the gravel teased us with more bits of bone; then Barry spotted a large brown lump. He called me over to take some photos. Whose bone he had found was not immediately obvious; but it had some size. Only after he freed it from the sand were the features of a large vertebra confirmed. Likely from a mammoth, it had suffered the erosive effects of time and water. Yet, Barry grinned. He had accomplished one of the goals we had for the trip – find mammoth bone.

     

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    The heat was relentless, but we kept cooling off and drinking. Even the butterflies were frequently tapping moisture and minerals in the damp sand. Eventually, we reached an area where the channel narrowed and we took advantage of the shade. I was looking for beaver dens when Barry cried, “Snake! Back there by the large stump!”

     

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    We buried the paddles in a series of strong back strokes to reverse our direction. I finally spotted the handsome reptile crawling into a small pile of logs. I could tell he wanted to catch it, when he almost whispered, “Elaphe obsoleta lindheimeri.” After three seconds of heat affected thinking, I realized he had not issued curses to move faster, but had just named the scientific classification for a Texas Rat Snake – the name that had passed through my mind 5 seconds earlier….  Barry scrambled up the bank and had the snake in hand within two minutes. He slowly manipulated it while I took photos. I have always enjoyed my encounters with these non-poisonous reptiles. They can be very aggressive and strike repeatedly, or try to intimidate any threats with their loud hiss and vibrating tail. He left on the log where we found it.

     

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    About a half hour downstream we were exposed again to the late afternoon sun. It reflected from the water and the barren high bluffs beside us. We paddled and scanned both water and banks. Through the salty sweat in my eyes, I saw something out of place halfway up one of the bluffs.

     

    “OK, that can’t be what I think it is, can it Barry?” A bowling ball sized dome contrasted sharply with the surrounding tan soil. We slowed the canoe to a stop. I remembered the “dome” of a four foot mammoth humerus I had found almost a year earlier…. My heart rate increased.

     

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    Barry insisted, “John, that shape is too perfect; it has to be a bone.” The closer we got the boat, the more my pulse quickened. From fifteen feet below it, I still had to get closer to allow myself to acknowledge the obvious…it was a bone!

     

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    We positioned the canoe as close as possible to the vertical bank. The water was not moving fast there, but it was deep. In a tricky move that involved me stepping on the tip of the stern and stabbing my rock hammer into the soil of the steep ledge above, I pulled myself up to a spot where I could rest. Our access point was a little downstream of the “dome”, so I had to dig footholds to make my way to the find. It was impressive when I could finally rest beside it. “Hey Barry, it’s bone!” I grinned.

     

    After a difficult time staging a few digging tools, we started to excavate. I carefully determined the perimeter of the fossil and had some vivid flashbacks to last year’s humerus find. However, the deeper we dug, the more it became apparent that the rest of the bone was not attached. We tested the ‘ball’ for movement and it popped free of the matrix below. In the soil below, we did not find any more evidence of bone.

     

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    Initially it seemed there was a large scavenging scar across the surface, but after cleaning, the mark appeared to be an eroded part of the internal vascular structure. Other old gouges and marks may have been due to ancient scavenging. Shape and size suggested I had found my first mammoth ‘femur ball’ or the head of the femur. Regardless of the number of mammoth fossils I have found, they never cease to spark my imagination.

     

    Mammoth femur head – approx. 7 inches in diameter

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    Scars and vascular structures

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    The shadows had begun to lengthen by the time we loaded the femur ball and started back downstream. Temperatures had dropped a few degrees which energized us for the next few miles. In a large eddy, we saw another snake crossing the water and sped up to see it. Both of us recognized the juvenile Water Moccasin as it paused and floated on the water. Barry pulled out his camera and I positioned the canoe to assist him. All was going well until the young snake thought the boat would make a good rest stop. The most important result of the next few moments was that no one entered the water, and nothing entered the canoe. I repositioned us to allow the little pit viper to reach the bank. It seemed to respond to the security of solid ground and assumed the confident demeanor of the species.

     

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    We reached the take-out after twelve hours on the water. Tired, but feeling the satisfaction of an incredible adventure, we completed a relatively short shuttle run back upstream. The trip had so many layers – so many memories. We hunted and found what we sought. And somewhere between our imaginations, the water, willows, cottonwood, and stone, we caught a reflective glimpse of the ancient hunters.

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  23. The Fury's Grand Blog

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    Since I just got a blog and need to put "Second Chance" in better description, why not blog it? Well, we left Taylor at about 11:30, and headed to the used to be hated South San Gabriel site. Now that we know how to get down there easily, it was a great trip. My first cool find was a candosa texana. Then we found some oysters and some other stuff. After that we traveled to another part of the South San Gabriel.We didn't find any fossils, but we did find dinosaur footprints (probably pleurocelus/paluxysaurus) and a modern jawbone. The next site was private property, so we couldn't hunt on it. The last site was a decent site, we found a few oysters and inverts. Then we went to my grandparents to show them and my cousins our very nice load.

  24. Digging America

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    Well now I can say that I have been into fossils since the 2010 aurora fossil festival and do not see myself getting out of anytime soon. I am still hunting the infamouns Green Mill Run and a few sites along the Tar and Neuse rivers. Having so much sucess at GMR I do not want to leave, I was once told if a spot is producing dont leave that spot stay in it until it quits, well almost 4 weeks into GMR and its still giving me a few nice size teeth ever so often I am not planning on leaving.

    Yesterday was the best day that I have had, I took both my father in law and brother in law that sift the spoil piles in Aurora alot to GMR for a different kind of hunting the 1st few hours in I dont think that were liking it to much b/c all they were seeing was 1/2 teeth and bones, but then I had an idea. I said lets dig over there, I will dig and you can sift well my 50 year old father in law liked that idea, I think he just wanted to see me work my A$$ off,lol. Well all of a sudden alot of big bone started comeing out of the hole, and I told him usally from my past experiences when you start seeing alot of big bone like that teeth are sure to follow. Well sure enough all of a sudden a perfect 3" meg comes up in the shovel, his exact words and I quote were " snarge let me do some digging, I have never found one that big" Well in my head I was thinking you didnt find it, I did the digging all you did was sift. But I didnt say anything, and he stuck it in his pocket, another 15 min in and out comes another this time the best GW that I have ever seen, a perfecy 2 3/4". I grabbed that sucker and stuck it in my pocket real quick.

    He took over and dug for a little while pulling nice 1 1/2" to 1 5/8" GW and megs out of that hole, when he said that he back was starting to hurt, it was time for him to leave and go to the house along with my brother in law. They left with around 300 teeth ranging from 1" to my nice 3" meg. Well still in discuss that he took my tooth I stayed a little while longer, not finding much and extremly tired of digging since 7 am and its was now 6:30 pm I decided to head back to the truck, I picked up the phone and called the wife to tell here about the day that we had and about my big tooth that I "gave" away, she said "I know my dad has already called and told me that you gave a big tooth" "he said that he was very happy and that he enjoyed his time with you, and wished that my brother would spend time like that with him" Well when she said that I felt bad about thinking bad about the old man, and decided to call him myself, when I did I got so many thank yous and he wanted to know when we were going to go again.

    This made me feel very good inside as the man that I thought hated my guts for the past 9 years actually enjoyed his time with me and wanted to spend more time. So I guess we should all think before we act.

    Matt J.

    "

  25. Deep-Thinker's Blog

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    At over 60 feet in length and weighing over 50 tons, C. megalodon was without a doubt one of the largest and most terrifying predators to ever exist.

    It was literally,

    The Apex Predator, The Top of the Food Chain.

    Megalodon sharks lived from about 25 million years ago to around 1.5 million years ago. Megalodons had enormous teeth that grew up to seven inches in length. These razor sharp teeth were used to attack and devour ancient whales. In general, all shark teeth are highly evolved, being perfectly adapted for the shark's prey. Because Megalodon preyed upon whales, their teeth were massive and sharply serrated like a steak knife - an adaption which allowed them to easily cut through the meat and bones of giant whales.

    A team of scientists led by Stephen Wroe conducted an experiment in 2008 to determine the bite force of the C. megalodon and concluded that very large specimens were capable of exerting a bite force of up to 40,131 pounds per square inch (over 5 times greater than that of T. Rex), arguably making the giant shark one of the most formidable and powerful predators to have ever inhabited the oceans.

    Megalodon teeth were also extremely robust and solid allowing them to bite into whale bone without breaking. During their lives, Megalodons had teeth that were a bright ivory white color just like our teeth. Fossil Meg teeth however come in a variety of beautiful colors. Over millions of years of fossilization, the white enamel becomes mineralized, taking on the characteristic colors of the minerals surrounding it. By far the most common color is a dark grey color typical of teeth found in South Carolina rivers and some other Southern areas of the United States. Rarer colors include Reds, Blues, Greens, Yellows, Oranges, Black and combinations of these colors. Ivory colored Megalodon teeth typically come from phospate deposits, while other colors are usually found in Rivers. The more unusually colored teeth are much rarer and command significantly higher prices than the more common colors. Also, because high quality teeth over six inches in length are both rare and in high demand, these monster teeth command much higher prices than their smaller cousins. In fact Meg teeth over 5 inches in length tend to increase exponentially in price with increasing size.

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