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Florissant Lake Beds
BIOFILMS MEDIATE THE PRESERVATION OF LEAF ADPRESSION FOSSILS BY CLAYS
Freshwater molluscan fauna from the Florissant Formation, Colorado: paleohydrologic reconstruction of a latest Eocene lake
Determining the paleoclimate and elevation of the late Eocene Florissant flora: support from the coexistence approach
THE CONTROLS ON THE PRESERVATION OF STRUCTURAL COLOR IN FOSSIL INSECTS
DEPOSITIONAL SETTING AND FOSSIL INSECT PRESERVATION: A STUDY OF THE LATE EOCENE FLORISSANT FORMATION, COLORADO
Paleontological studies at Florissant have been ongoing for more than 13 decades. As the focus of these studies has shifted through this time, the site has provided important insights into the evolution of paleontology as a science from its beginnings in the nineteenth century through its subsequent development. Early studies focused on the description of new taxa from collections that were being made by the early scientific surveys of the American West, particularly the Hayden Survey during the early 1870s and an expedition from Princeton in 1877. The first studies and descriptions of these fossils were by Leo Lesquereux on the fossil plants, S.H. Scudder on the fossil insects, and E.D. Cope on the fossil vertebrates. At the beginning of the twentieth century, T.D.A. Cockerell conducted field expeditions in 1906–1908, and subsequently published ∼130 papers on fossil plants, insects, and mollusks. Work by these early researchers was the first to consider the implications of the Florissant fossils for evolution, extinction, biogeography, and paleoclimate. Even greater emphasis on these broader implications began when H.D. MacGinitie made excavations during 1936–1937 and published a comprehensive monograph on the fossil flora in 1953, including numerous taxonomic revisions and detailed interpretations of stratigraphic context, paleoecology, paleoclimate, paleoelevation, biogeography, and taphonomy. Other workers during the late 1900s initiated the first studies on pollen, dicotyledonous woods, and multiple organ reconstructions of extinct plant genera, and developed more quantified methods for determining paleoelevation and paleoclimate. Current work emphasizes plant-insect interactions, the use of diatoms as fresh-water paleoen-vironmental indicators and as agents in macrofossil taphonomy, and the use of insects as terrestrial environmental indicators.
Scanning electron microscopy (SEM) of insect and plant fossils in the lacustrine shales of the Eocene Florissant Formation of Florissant, Colorado, was used to investigate the mechanisms of fossil preservation. The fossiliferous Florissant “paper shales” are composed of thin laminae of diatomite that form couplets with alternating smectitic clay laminae. The millimeter-scale sedimentary couplets may preserve an episodic record of sedimentation and are interbedded with less frequent, coarser volcaniclastic layers. The insect and plant fossils are associated with biofilms of extracellular polymeric substances (EPS) secreted by diatoms. The preserved organisms are entangled in the diatom aggregates coated with the EPS biofilm. We suggest that decomposition of the organisms was arrested during sedimentation and burial by the protective nature of the mucus covering, the properties of which limited the actions of bacteria and grazers and may have enhanced fossilization. A novel contribution of the study is a demonstration that this mechanism of exceptional preservation is also common at other similar lacustrine fossil sites, as supported by a further SEM analysis of insect and plant fossils from other Cenozoic lake deposits formed in environments comparable to the Floris-sant Formation. The deposits include the Oligocene shale at Canyon Ferry, Montana; the Miocene Savage Canyon Formation, Stewart Valley, Nevada; and the Miocene Shanwang Beds of Shandong Province in northeast China. In addition, cultures of diatomaceous biofilms, grown in the laboratory display morphological features identical to those of the fossil diatomaceous biofilms. Our contribution indicates the significance of biofilms in fossil preservation at Florissant and other deposits.
We used higher taxonomic composition of 241 modern forest plots from across the New World to identify the closest modern analog of the Florissant fossil flora and to infer late Eocene paleotemperature for Florissant. Nonmetric multidimensional scaling (NMS) based on both genus and family presence-absence placed Florissant in a no-analog taxonomic space surrounded by North American warm temperate broad-leaved forests, Mexican humid pine-oak forests, and subtropical moist forests from Florida, Mexico, and Argentina. The site most similar to Florissant, as indicated by the mean of Euclidean distances in genus and family NMS space, was a subtropical moist forest in southern Florida, followed by the humid pine-oak forests of central and northeastern Mexico, and the broad-leaved deciduous forests of eastern North America. Weighted-averaging partial least-squares regression (WAPLS) based on genus composition predicted a mean annual temperature (MAT) for Florissant of 14.7 ± 2.2 °C. WAPLS based on family composition predicted a MAT of 15.6 ± 2.5 °C. Our estimates fall between the relatively cool temperatures predicted by leaf physiognomy and the higher temperatures predicted by the nearest living relative method. Although this study demonstrates the feasibility of using higher taxa for paleoclimate reconstruction and analog analysis, its methods are subject to many of the same biases and assumptions as other biological proxy techniques. Furthermore, interpretation of differences between results obtained using different taxonomic levels remains unclear. Some of these limitations may be resolved by employing methods based on phylogenies rather than taxonomic ranks.
The biogeographic affinities of the Florissant flora are in need of reevaluation. We give a critical review, based on megafossil and pollen records representing genera whose affinities we accept as well founded. The Florissant assemblage includes taxa of diverse modern geographic distribution. The flora is composed mainly of Laurasian elements, some of which are now confined to Asia ( Ailanthus , Dipteronia , Eucommia , Platycarya , Pteroceltis ) and a wide number co-occurring in the eastern United States and Asia. Others are now confined to western North America ( Sequoia , Cercocarpus , Sarcobatus ) and many occur in Mexico. The major geographic affinities of the Florissant genera discussed here are broad and include the present-day warm temperate and subtropical floras of Mexico, central and southern China, and the southeastern United States. Many taxa appear to have been shared between North America and Asia by Eocene time. The Rocky Mountain flora was distinct from that of the southeastern United States, probably because of the barrier represented by the Cannonball epeiric sea that traversed the Midcontinent in the Paleocene. Similarity of Florissant taxa to the South American flora is low. The deterioration of climate after the time of Florissant deposition represents one of the most significant decreases in temperature of the entire Tertiary. Following the warm interval of the latest Eocene, a few Florissant genera were locally extirpated, a few became extinct, some were already at or dispersed to lower-elevation regions, and others persisted in the southern Rocky Mountains. Over longer geologic time spans, some taxa seem to have persisted on the West Coast of North America through the Miocene, and in a few cases even up to the present. Many deciduous taxa have persisted in the summer-wet climate area of the eastern United States.
Magnetic stratigraphy of the Eocene-Oligocene floral transition in western North America
Eocene and Oligocene floras of the western United States show a climatic deterioration from warmer conditions to much cooler and drier conditions. Recent 40 Ar/ 39 Ar dates and magnetic stratigraphy have greatly improved their correlation. In this study, the uppermost Eocene Antero Formation, Colorado, is entirely reversed in polarity, and is correlated with late Chron C13r, based on 40 Ar/ 39 Ar dates of 33.77–33.89 Ma. The early Oligocene Pitch-Pinnacle flora of Colorado is within rocks of normal polarity, and best correlated with Chron C12n (30.5–31.0 Ma), based on 40 Ar/ 39 Ar dates of 32.9–29.0 Ma (although correlation with Chron C11n is also possible). The late Oligocene ( 40 Ar/ 39 Ar dated 26.26–26.92 Ma) Creede flora of southwestern Colorado is correlated with Chron C8r. The early Oligocene ( 40 Ar/ 39 Ar dated at 31.5 Ma) Granger Canyon flora in the Warner Mountains, near Cedarville, northeastern California, is correlated with Chron C12r. These results are compiled with previously published dates and magnetic stratigraphy of the Eugene-Fisher floral sequence in western Oregon, the Bridge Creek floras in central Oregon, other floras in the Warner Mountains of northeast California, and the Florissant flora of central Colorado. In Colorado, the climatic change seems to have occurred between the Florissant and Antero floras, and is dated between 33.89 and 34.07 Ma, or latest Eocene in age, although the Pitch-Pinnacle flora suggests that the deterioration was less severe and took place in the early Oligocene. In northeast California, the dating is not as precise, so the climatic change could have occurred between 31.5 and 34.0 Ma (probably early Oligocene). In western Oregon (Eugene and Fisher Formations), the change occurs between the early Oligocene Goshen flora (33.4 Ma) and the early Oligocene Rujada flora (31.5 Ma). In the John Day region of Oregon, it occurs before the oldest Bridge Creek flora, dated at 33.62 Ma (right after the Eocene-Oligocene boundary). Thus, only two of these four floral sequences (Eugene, Oregon, and Cedarville, California) clearly show the early Oligocene climatic change consistent with that documented in the global marine record, whereas the climatic change was seemingly abrupt in the late Eocene in Colorado between 33.89 and 34.07 Ma, and also sometime during the late Eocene (before 33.62 Ma) in central Oregon.
A comparison of plant-insect associations in the middle Eocene Green River Formation and the Upper Eocene Florissant Formation and their climatic implications
The fossil plants found in the Eocene Florissant Formation and Green River Formation are preserved with a level of detail that allows one to closely examine traces of insect feeding damage. Levels (amounts) and patterns (abundance of various types) of fossilized insect feeding damage from Florissant and the middle Eocene Green River Formation were compared. This allowed for a detailed examination of feeding damage and provided an opportunity to examine long-term patterns of change in insect herbivory during a period of climate fluctuation. Samples including 624 fossil leaves from Florissant and 584 fossil leaves from the Green River Formation were examined to document overall damage levels, the presence/absence of specific feeding guilds (i.e., hole-feeding, skeletonization, leaf-mining), and host-specific damage types. Florissant insects show host specificity in their feeding preferences as evidenced through the distribution of feeding damage on plants and through the presence of identifiable host-specific interactions. Some of these interactions appear to be long lasting as they are also apparent on the same, or closely related, leaf species found in the Green River Formation. Insect damage levels declined from the middle to late Eocene. This decline is correlated with a cooling event during this time interval and is in concurrence with the findings of other authors who have examined fossilized herbivory and climate change patterns. There is also an increase in the abundance of galls during this same interval, which also may be related to climate change.
Using available shape characters we conducted an outline morphometric analysis to make family-level identifications of fossil spiders from the Florissant Formation in Colorado. In this analysis we used carapace shape because it is a character that can be observed on most fossil spiders, and we also used linear leg characters. All measurements were first made on 202 modern spiders from eight families found in localities similar to the fossil lake environment. A multiple discriminant analysis (MDA) of the eigenshape axes was used to predict family placement among the modern data set to test the accuracy of the predictions. The modern spider families that were predicted correctly most often were the Salticidae (91.2%), Linyphiidae (80%), Dictynidae (76.5%), Tetragnathidae (68.2%), Clubionidae (66.7%), and Araneidae (65.5%). Families that produced less successful results were the Agelenidae (46.7%) and the Lycosidae (39.1%). Forty-three fossil spiders from Florissant were then added to the model to determine their family placement. All fossils were placed into modern families with varying degrees of accuracy. Only 42% of our identifications agree with those made by previous authors, but it is likely that these specimens were originally misidentified. With the addition of more taxa and characters, we believe that an outline morphometric approach shows great promise for helping to identify fossil taxa that are lacking traditional taxonomic characters.
The Chadronian mammalian fauna of the Florissant Formation, Florissant Fossil Beds National Monument, Colorado
During the past five years, renewed prospecting and collecting of mammalian fossils in the Florissant Formation within Florissant Fossil Beds National Monument in central Colorado has nearly tripled the known diversity of fossil mammals from this rock unit. Taxa first recorded here from the Florissant Formation include the eomyid rodent Paradjidaumo trilophus , the lagomorph Palaeolagus , and the rare artiodactyl Pseudoprotoceras longinaris . We also describe an isolated deciduous premolar of a protoceratid. We update the mammalian faunal list of the Florissant Formation, which includes some 16 species in 13 families and 6 orders. The mammalian fauna corroborates the Chadronian (latest Eocene) age determined by others. Geographic ranges of Pelycomys , Palaeolagus , and Paradjidaumo trilophus are extended slightly southwest from northeastern Colorado, and the range of Pseudoprotoceras longinaris is extended southwest from Wyoming and Nebraska. Based upon comparison with nearest living relatives and plausible analogs, the mammalian taxa represented in the Florissant Formation seem to be consistent with the moist, warm temperate, relatively high elevation wetland and woodland habitats that have been inferred by others for the area in and around late Eocene Lake Florissant.
Mineralogy and geochemistry of late Eocene silicified wood from Florissant Fossil Beds National Monument, Colorado
Silicified stumps preserved within a late Eocene lahar deposit have diverse mineralogy, ranging from opal-CT to chalcedony. In specimens that contain both silica polymorphs, the minerals appear to have originated independently, rather than from diagenetic transformation of an opaline parent material. This petrifaction process is unlike the progressive transformation of opal-A→opal-CT→chalcedony that has long been accepted as a general model for wood silicification. At the Florissant fossil forest, petrifaction occurred in several stages, beginning with precipitation of amorphous silica on cell wall surfaces. Cell lumina later became filled with opal-CT and chalcedony. A final phase of silica deposition is evidenced by chalcedony-filled fractures that crosscut permineralized tissues in some specimens. Spaces between adjacent tracheids commonly remain unmineralized, causing the silicified wood to remain permeable to water, and to readily cleave radially and tangentially. To a lesser degree, the fossilized wood is subject to transverse fracturing. This combination of structural characteristics causes Florissant fossil stumps to be susceptible to damage from freeze-thaw weathering.
Silicified stumps at Florissant Fossil Beds National Monument are subject to degradation from a variety of causes, including freeze-thaw weathering. In the past, noninvasive measures have been taken to conserve selected fossils, including use of metal bands for reinforcement and construction of shelters. Our study had two goals. The first was to document the temperature and relative humidity to which petrified stumps are exposed at Florissant. The second was to conduct a preliminary examination of the feasibility of using consolidants and adhesives to reinforce fossil wood and reduce its susceptibility to weathering. Electronic data loggers were used to monitor temperature and relative humidity both internally and externally for one exposed and one sheltered fossil stump, and results indicated that over 289 days of the cold season, there were 119 freeze-thaw events for the surface of the exposed stump and 95 events for the surface of the stump protected by a roof. Temperature and humidity variations were markedly lower for the subsurface sensors. Seven organosilicate formulations were field tested as consolidants on samples of petrified wood. Adhesives used to repair fractures included two polyvinyl butyral (PVB) formulations, two casein adhesives, and one epoxy. After eight months of exposure, fractures repaired with epoxy remained well bonded. Specimens repaired with PVB remained intact, but outer regions were visibly damaged, presumably from UV radiation. Of the two casein products that were tested, one had poor bond strength and the other was difficult to apply because of its low viscosity. Evaluating the effectiveness of organosilicate emulsions as consolidants to reduce weathering rates will require more research. Preliminary results of our field tests have identified goals for future efforts and established performance criteria for adhesives and consolidants used for silicified wood.
A detailed survey of collections and publications for the Florissant fossil beds (Colorado, USA) forms the basis for developing a new relational database and Web site that documents information that had become widely scattered following 130 years of scientific study at Florissant. More than 1700 species that remain valid, mostly of plants, insects, and spiders, had been described in more than 300 publications, and these published specimens had been dispersed among ∼15 museums. Some of these specimens were not well documented in original publications and many of the type specimens had never been illustrated. Catalog data were compiled on-site at museums, specimens were photographed, and all of the publications referring to Florissant specimens were located. Taxonomic classification of the fossils was updated to modern concepts. A relational database incorporates the data into five core tables for specimens, bibliography, references to specimens in publication, taxonomy, and images. The database allows for complex searches to interrelate these categories, enabling new research and facilitating collections management. Examples show that the largest number of scientific publications and new species descriptions appeared from 1890 to 1920 and that most of the originally described insect species, but only about half of the plant species, still remain valid and unrevised. Digital images of the fossils and digital files for pre-1923 publications form an archive that is linked to the data records. A Web site makes the database publicly accessible for technical use, and also provides a less complex application for the layperson as well as a new college-level curriculum.