scholarly journals Were the First Trace Fossils Really Burrows or Could They Have Been Made by Sediment-Displacive Chemosymbiotic Organisms?

Author(s):  
Duncan McIlroy

This review asks some hard questions about what the enigmatic graphoglyptid trace fossils are, documents some of their early fossil record from the Ediacaran-Cambrian transition and explores the idea that they may not have been fossils at all. Most researchers have considered the Graphoglyptida to have had a microbial-farming mode of life similar to that proposed for the fractal Ediacaran Rangeomorpha. This begs the question “What are the Graphoglyptida if not the Rangeomorpha persevering” and if so then “What if…?”. This provocative idea has at its roots some fundamental questions about how to distinguish burrows sensu-stricto from the external molds of endobenthic sediment displacive organisms.

2021 ◽  
Vol 4 (1) ◽  
pp. 001-014
Author(s):  
MATHIAS JASCHHOF

Twenty-four fossil gall midges (Cecidomyiidae) described from 1917–2020 from Mesozoic deposits, mostly ambers, are reviewed. Information from the original publications is used as the basis for reinterpretation, when such is regarded as appropriate here. As a result, the fossil record of cecidomyiids from the Mesozoic comprises representatives of the following subfamilies and tribes, all mycophagous (numbers in parentheses refer to species described): Catotrichinae (1); Micromyinae: Catochini (2), Amediini (1), Campylomyzini (1), Micromyini (2) and Aprionini (1); Winnertziinae: Heteropezini (2), Diallactiini (4) and Winnertziini (1); Porricondylinae: Dicerurini (1). Other Winnertziinae (3) and Micromyinae (5) cannot be classified to tribe because information on critical morphological structures is unavailable; they are thus considered incertae sedis. Members of the Lestremiinae sensu stricto are unrecorded from the Mesozoic, as are any Cecidomyiinae (the only subfamily containing phytophages and predators). Commonly occurring reasons for misinterpretation of amber fossils are the non-recognition of artefacts and the unfamiliarity with group-specific literature regarding prevailing taxonomic concepts and the morphological diversity found in Cecidomyiidae. These causes as well as obvious differences between neontological and paleontological taxonomic practices are discussed. Amediini trib. nov. Jaschhof, 2021 is introduced as a new tribe of the Micromyinae, to absorb the genera Amedia Jaschhof, 1997 (extant, North America, type genus), Amediella Jaschhof, 2003 (extant, New Zealand) and Eltxo Arillo & Nel, 2000 (extinct, Alava amber). A diagnosis of the new tribe is given. Krassiloviolini Fedotova & Perkovsky, 2017 is a new junior synonym of Heteropezini Schiner, 1868. Amediini Plakidas, 2017 and Zarqacecidomyius singularis Kaddumi, 2007 are nomina nuda.


2018 ◽  
Vol 115 (21) ◽  
pp. 5323-5331 ◽  
Author(s):  
Allison C. Daley ◽  
Jonathan B. Antcliffe ◽  
Harriet B. Drage ◽  
Stephen Pates

Euarthropoda is one of the best-preserved fossil animal groups and has been the most diverse animal phylum for over 500 million years. Fossil Konservat-Lagerstätten, such as Burgess Shale-type deposits (BSTs), show the evolution of the euarthropod stem lineage during the Cambrian from 518 million years ago (Ma). The stem lineage includes nonbiomineralized groups, such as Radiodonta (e.g., Anomalocaris) that provide insight into the step-by-step construction of euarthropod morphology, including the exoskeleton, biramous limbs, segmentation, and cephalic structures. Trilobites are crown group euarthropods that appear in the fossil record at 521 Ma, before the stem lineage fossils, implying a ghost lineage that needs to be constrained. These constraints come from the trace fossil record, which show the first evidence for total group Euarthropoda (e.g., Cruziana, Rusophycus) at around 537 Ma. A deep Precambrian root to the euarthropod evolutionary lineage is disproven by a comparison of Ediacaran and Cambrian lagerstätten. BSTs from the latest Ediacaran Period (e.g., Miaohe biota, 550 Ma) are abundantly fossiliferous with algae but completely lack animals, which are also missing from other Ediacaran windows, such as phosphate deposits (e.g., Doushantuo, 560 Ma). This constrains the appearance of the euarthropod stem lineage to no older than 550 Ma. While each of the major types of fossil evidence (BSTs, trace fossils, and biomineralized preservation) have their limitations and are incomplete in different ways, when taken together they allow a coherent picture to emerge of the origin and subsequent radiation of total group Euarthropoda during the Cambrian.


1992 ◽  
Vol 5 ◽  
pp. 105-120 ◽  
Author(s):  
H. Allen Curran

Tracemaking organisms are common and diverse components of the fauna and flora of tropical, shallow-marine and coastal carbonate environments. In the shallow subtidal zone, the burrowing activity of callianassid shrimp commonly is the dominant process in the modification of original depositional fabrics (Tudhope and Scoffin, 1984; Tedesco and Wanless, 1991). Both borers and burrowers have great potential to leave their mark in tropical carbonate sediments and rocks and to become part of the fossil record.


Paleobiology ◽  
2007 ◽  
Vol 33 (3) ◽  
pp. 469-493 ◽  
Author(s):  
Geerat J. Vermeij

AbstractMost evolutionary innovations—power-enhancing phenotypes previously absent in a lineage—have arisen multiple times within major clades. This repetition permits a comparative approach to ask how, where, when, in which clades, and under which circumstances adaptive innovations are acquired and secondarily lost. I use new and literature-based data on the phylogeny, functional morphology, and fossil record of gastropods to explore the acquisition and loss of the siphonal canal and its variations in gastropods. The siphonal indentation, canal, notch, or tube at the front end of the shell is associated in living gastropods with organs that detect chemical signals directionally and at a distance in an anteriorly restricted inhalant stream of water.Conservative estimates indicate that the siphonate condition arose 23 times and was secondarily lost 17 times. Four siphonate clades have undergone prodigious diversification. All siphonate gastropods have a shell whose axis of coiling lies at a low angle above the plane of the aperture (retroaxial condition). In early gastropods, the siphonal canal was short and more or less confined to the apertural plane. Later (mainly Cretaceous and Cenozoic) variations include a dorsally deflected canal, a long canal, and a closed canal. The closed siphonal canal, in which the edges join to form a tube, arose 15 times, all in the adult stages of caenogastropods with determinate growth.Gastropods in which the siphonate condition arose were mobile, bottom-dwelling, microphagous animals. Active predaceous habits became associated with the siphonate condition in the Mesozoic and Cenozoic Purpurinidae-Latrogastropoda clade. Loss of the siphonate condition is associated with nonmarine habits, miniaturization, and especially with a sedentary or slow-moving mode of life.The siphonate condition arose seven times each during the early to middle Paleozoic, the late Paleozoic, and the early to middle Mesozoic, and only once each during the Late Cretaceous and Cenozoic. Well-adapted incumbents prevented most post-Jurassic clades from evolving a siphonal indentation and its associated organs. Dorsally deflected, long, and closed canals are known only from Cretaceous and Cenozoic marine gastropods, and represent improvements in sensation and passive armor.In a discussion of contrasting ecologies of clades that gained and lost the siphonate condition, I argue that macroevolutionary trends in the comings and goings of innovations and clades must incorporate ecological and functional data. Acquisitions of energy-intensive, complex innovations that yield greater power have a greater effect on ecosystems, communities, and their resident clades than do reversals, which generally reflect energy savings.


Author(s):  
Reinhard Förster

ABSTRACTThe fossil record of unquestionable decapod remains dates back to Permo Triassic times. Evaluation of all available data from the fossil record, trace fossils and facies reveals various trends within the evolution of Mesozoic decapods, and its relation to their ecology. One of these trends is the protection of the long vulnerable abdomen. The most successful method, gradual reduction and inflection of the abdomen against the ventral cephalothorax, led to the Brachyura. Brachyurans exhibit the broadest spectrum of habitat adaptions.


2016 ◽  
Vol 90 (4) ◽  
pp. 721-733 ◽  
Author(s):  
Zain Belaústegui ◽  
Allan A. Ekdale ◽  
Rosa Domènech ◽  
Jordi Martinell

AbstractA well-preserved omission surface (sedimentary discontinuity) in an outcrop near Alcoi in southeastern Spain displays trace fossils and body fossils that reflect a dynamic benthic community during the Miocene (Langhian–Tortonian). This outcrop, besides being the type locality of Spongeliomorpha iberica Saporta, 1887, exhibits other abundant trace fossils, such as Glossifungites saxicava Łomnicki, 1886 and Gastrochaenolites ornatus Kelly and Bromley, 1984. These trace fossils are restricted to a single stratigraphic horizon and constitute a typical firmground ichnoassemblage of the Glossifungites ichnofacies. The interiors of some of the Glossifungites and Spongeliomorpha burrows were occupied by encrusting balanomorph barnacles (Actinobalanus dolosus Darwin, 1854). This paper is the first report of cryptic barnacles colonizing the interior of open burrows that constitute a typical firmground ichnocoenose in the fossil record. Detailed ichnologic study demonstrates that the ichnospecies Glossifungites saxicava stands as a valid ichnotaxon and is not a synonym of the ichnogenus Rhizocorallium, as has been suggested by some previous workers.


2015 ◽  
Author(s):  
Walter G. Joyce ◽  
Márton Rabi

Background. Over the course of the last decades, much effort has gone into unraveling the biogeographic history of turtles, but while much progress has been achieved in resolving post- Jurassic dispersal events, traditional phylogenetic hypotheses have yielded incongruous results in regards to the early history of the group. Methods. We re-evaluate the fossil record of turtles in context of recent phylogenetic analyses and fossil finds, including the extensive record of fragmentary but diagnostic remains. Given that near-coastal and marine turtles readily disperse across aquatic barriers, a broad set of neritic to pelagic groups were disregarded from consideration. Significant disagreement still exists among current phylogenetic hypotheses and we therefore place much effort into tracing the fossil record of unambiguously monophyletic groups. We finally employed molecular backbone constraints, given that the molecular phylogenies are more consistent with the fossil record than current, morphological phylogenies. Results. Among derived, aquatic turtles, we recognize four clades that can be traced back to discrete biogeographic centers: Paracryptodira in North America and Europe, Pan- Cryptodira in Asia, Pan-Pelomedusoides in northern Gondwanan landmasses and Pan- Chelidae in southern Gondwanan landmasses. This pattern is partially mirrored by three clades of primarily terrestrial, basal turtles: Solemydidae in North American and Europe, Sichuanchelyidae in Asia, and Meiolaniformes sensu stricto in southern Gondwanan landmasses. Although the exact interrelationships of these clades remain unclear, most can be traced back to the Middle Jurassic. Discussion. The conclusion that the two primary lineages of pleurodires and paracryptodires can be traced back to mutually exclusive land masses is not novel, but the realization that the early history of pan-cryptodires is restricted to Asia has not been realized previously, because traditional phylogenies implied an early, global presence of pan-cryptodires. The timing of the origin of the three primary clades of derived turtles (i.e., Pan-Pleurodira, Pan-Cryptodira, and Paracryptodira) correlates with the opening of the central Atlantic and the formation of the Turgai Strait in the Middle Jurassic, somewhat later than predicted by molecular calibration studies. The primary diversity of extant turtles therefore appears to have been driven by vicariance. A similar hypothesis could also be formulated for the three clades of basal turtles that survive at least into the Late Cretaceous, but given that their combined monophyly remains uncertain, it is unclear if their diversity was also driven by vicariance, or if they emulate a vicariance-like pattern. Although most groups remained within their primary geographic range throughout their evolutionary history, the dominant vicariance signal was thoroughly obfuscated by rich dispersal from littoral to marine turtles and crown cryptodires.


Geosciences ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 397
Author(s):  
Przemysław Sztajner

The paper is an attempt to reconstruct the mode of life of Pholadomya bivalves, very common in the fossil record, particularly that of the Jurassic. The only extant representative of the genus is extremely rare and very poorly known. Materials from the Polish Jurassic deposits (Bajocian–Kimmeridgian; Western Pomerania and Polish Jura) and literature data were used for the reconstruction. Specifically, observations on the anatomy, taphonomy, and diagenesis of the specimens examined as well as lithology of the deposits housing the specimens were used. Shell anatomy characteristics are known for their particular utility in mode of life reconstructions, although the extremely thin-shelled and coarsely sculpted bivalves, such as the Pholadomya examined, have not been studied so far. The reconstruction suggest a diversity of the mode of life, coincident with the morphological differences between the Pholadomya species. At least the adults of anteriorly flattened species are inferred to have lived extremely deeply buried in the sediment, and were hardly mobile. The smaller, more oval in shape, species were more mobile, and some of them are thought to have preferred life in shelters, should those be available. In addition, the function of the cruciform muscle, other than that considered so far, is suggested.


2002 ◽  
Vol 76 (5) ◽  
pp. 906-909 ◽  
Author(s):  
Robert A. Henderson ◽  
E. Donald McKenzie

The late Albian marine fossil record from eastern Australia derives from the sedimentary succession of the Great Artesian Basin deposited in a vast epicontinental sea which then covered much of the continent (see Frakes et al., 1987). Ammonites of this age are common but their generic diversity is low. Heteromorph assemblages almost exclusively comprise the taxa Myloceras, Labeceras sensu stricto and Labeceras (Appurdiceras) of the Family Labeceratidae that were widely distributed in higher latitudes of the Southern Hemisphere during Late Albian time (see Aguirre Urreta and Riccardi, 1988; Klinger, 1989). Some 19 endemic species of these genera are recorded from the Great Artesian Basin in the present literature (Etheridge, 1892; Whitehouse, 1926; Reyment, 1964) and there are additional undescribed species (Henderson and McKenzie, unpublished data). The Australian Late Albian epicontinental sea was clearly a site of significant speciation for Labeceras and Myloceras and it has been argued that the Great Artesian Basin represents the evolutionary center for these genera (Henderson, 1990).


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