scholarly journals Metamorphism obscures primary taphonomic pathways in the early Cambrian Sirius Passet Lagerstätte, North Greenland

Geology ◽  
2021 ◽  
Author(s):  
Morten Lunde Nielsen ◽  
Mirinae Lee ◽  
Hong Chin Ng ◽  
Jeremy C. Rushton ◽  
Katharine R. Hendry ◽  
...  

Correct interpretation of soft-bodied fossils relies on a thorough understanding of their taphonomy. While the focus has often been on the primary roles of decay and early diagenesis, the impacts of deeper burial and metamorphism on fossil preservation are less well understood. We document a sequence of late-stage mineral replacements in panarthropod fossils from the Sirius Passet Lagerstätte (North Greenland), an important early Cambrian Burgess Shale–type (BST) biota. Muscle and gut diverticula were initially stabilized by early diagenetic apatite, prior to being pervasively replaced by quartz and then subordinate chlorite, muscovite, and chloritoid during very low- to low-grade metamorphism. Each new mineral replicates the soft tissues with different precision and occurs in particular anatomical regions, imposing strong biases on the biological information retained. Muscovite and chloritoid largely obliterate the tissues’ original detail, suggesting that aluminum-rich protoliths may have least potential for conserving mineralized soft tissues in metamorphism. Overall, the fossils exhibit a marked shift toward mineralogical equilibration with the matrix, obscuring primary taphonomic modes. Sequential replacement of the phosphatized soft tissues released phosphorus to form new accessory monazite (and apatite and xenotime), whose presence in other BST biotas might signal the prior, more widespread, occurrence of this primary mode of preservation. Our results provide critical context for interpreting the Sirius Passet biota and for identifying late-stage overprints in other biotas.

2009 ◽  
Vol 83 (5) ◽  
pp. 820-825 ◽  
Author(s):  
Linda Lagebro ◽  
Martin Stein ◽  
John S. Peel

The Non-Mineralized arthropod described herein is derived from the Sirius Passet fossil conservation deposit of North Greenland (82°47.6,N, 42°13.7ʹW), the oldest locality with exceptional preservation of soft tissues known from the Cambrian of Laurentia (Cambrian Series 2, Stage 3; Nevadella Zone). As such, it is broadly contemporaneous with the Chengjiang fauna of China (Hou et al., 2004) and some 10 million years older than the Burgess Shale fauna of British Columbia. The Sirius Passet fauna was first documented by Conway Morris et al. (1987) and its geological setting is discussed by Babcock and Peel (2007). In addition to the nevadiid trilobite Buenellus higginsi Blaker, 1988, the fauna is dominated by non-mineralized arthropods (Budd, 1993, 1995, 1997, 1999; Williams et al., 1996; Taylor, 2002). Other finds include sponges (Rigby, 1986), a lobopod (Budd and Peel, 1998), the earliest annelids (Conway Morris and Peel, 2008) and articulated halkieriids (Conway Morris and Peel, 1990, 1995), but most of the assemblage awaits description.


2011 ◽  
Vol 48 (8) ◽  
pp. 1259-1281 ◽  
Author(s):  
Jon R. Ineson ◽  
John S. Peel

The Early Cambrian Sirius Passet Lagerstätte of North Greenland occurs in marine mudstones (Buen Formation) deposited in a slope environment along the eroded scarp of a pre-existing carbonate platform. The shallow-water platform is represented by dolostones of the Portfjeld Formation (Neoproterozoic – earliest Cambrian), which record a belt of tide-swept subtidal ooid shoals and microbial patch reefs at the outer edge of the platform. Solution features and meteoric cements attest to exposure of the platform, accompanied by fracturing, mass wastage and erosional retreat of the escarpment producing slope talus, and extensive debris sheets and olistoliths in basinal deposits. The marine mud-dominated siliciclastics of the Buen Formation, deposited in slope and shelf environments, record the transgression and onlap of the degraded platform in the Early Cambrian. The Sirius Passet Lagerstätte has yielded an arthropod-dominated fossil assemblage of over 40 species, many showing exceptional preservation of soft tissues; the finely laminated mudstones hosting this fauna accumulated from suspension in a poorly oxygenated slope sub-environment, such as an erosional embayment or abandoned slope gully. Although taphonomic features suggest that the fauna is mainly parautochthonous, some components (e.g., sponges, worms, the halkieriids and certain sightless arthropods) may be truly autochthonous. Comparison of the Sirius Passet locality with the renowned Middle Cambrian Burgess Shale of western Canada reveals similarities in overall depositional and tectonic setting: both accumulated in deep water adjacent to the steep, eroded margins of carbonate platforms — settings that subsequently sheltered the faunas from tectonic and metamorphic obliteration.


Author(s):  
Gejing Li ◽  
D. R. Peacor ◽  
D. S. Coombs ◽  
Y. Kawachi

Recent advances in transmission electron microscopy (TEM) and analytical electron microscopy (AEM) have led to many new insights into the structural and chemical characteristics of very finegrained, optically homogeneous mineral aggregates in sedimentary and very low-grade metamorphic rocks. Chemical compositions obtained by electron microprobe analysis (EMPA) on such materials have been shown by TEM/AEM to result from beam overlap on contaminant phases on a scale below resolution of EMPA, which in turn can lead to errors in interpretation and determination of formation conditions. Here we present an in-depth analysis of the relation between AEM and EMPA data, which leads also to the definition of new mineral phases, and demonstrate the resolution power of AEM relative to EMPA in investigations of very fine-grained mineral aggregates in sedimentary and very low-grade metamorphic rocks.Celadonite, having end-member composition KMgFe3+Si4O10(OH)2, and with minor substitution of Fe2+ for Mg and Al for Fe3+ on octahedral sites, is a fine-grained mica widespread in volcanic rocks and volcaniclastic sediments which have undergone low-temperature alteration in the oceanic crust and in burial metamorphic sequences.


Author(s):  
Jon R. Ineson ◽  
John S. Peel

NOTE: This article was published in a former series of GEUS Bulletin. Please use the original series name when citing this article, for example: Ineson, J. R., & Peel, J. S. (1997). Cambrian shelf stratigraphy of North Greenland. Geology of Greenland Survey Bulletin, 173, 1-120. https://doi.org/10.34194/ggub.v173.5024 _______________ The Lower Palaeozoic Franklinian Basin is extensively exposed in northern Greenland and the Canadian Arctic Islands. For much of the early Palaeozoic, the basin consisted of a southern shelf, bordering the craton, and a northern deep-water trough; the boundary between the shelf and the trough shifted southwards with time. In North Greenland, the evolution of the shelf during the Cambrian is recorded by the Skagen Group, the Portfjeld and Buen Formations and the Brønlund Fjord, Tavsens Iskappe and Ryder Gletscher Groups; the lithostratigraphy of these last three groups forms the main focus of this paper. The Skagen Group, a mixed carbonate-siliciclastic shelf succession of earliest Cambrian age was deposited prior to the development of a deep-water trough. The succeeding Portfjeld Formation represents an extensive shallow-water carbonate platform that covered much of the shelf; marked differentiation of the shelf and trough occurred at this time. Following exposure and karstification of this platform, the shelf was progressively transgressed and the siliciclastics of the Buen Formation were deposited. From the late Early Cambrian to the Early Ordovician, the shelf showed a terraced profile, with a flat-topped shallow-water carbonate platform in the south passing northwards via a carbonate slope apron into a deeper-water outer shelf region. The evolution of this platform and outer shelf system is recorded by the Brønlund Fjord, Tavsens Iskappe and Ryder Gletscher Groups. The dolomites, limestones and subordinate siliciclastics of the Brønlund Fjord and Tavsens Iskappe Groups represent platform margin to deep outer shelf environments. These groups are recognised in three discrete outcrop belts - the southern, northern and eastern outcrop belts. In the southern outcrop belt, from Warming Land to south-east Peary Land, the Brønlund Fjord Group (Lower-Middle Cambrian) is subdivided into eight formations while the Tavsens Iskappe Group (Middle Cambrian - lowermost Ordovician) comprises six formations. In the northern outcrop belt, from northern Nyeboe Land to north-west Peary Land, the Brønlund Fjord Group consists of two formations both defined in the southern outcrop belt, whereas a single formation makes up the Tavsens Iskappe Group. In the eastern outcrop area, a highly faulted terrane in north-east Peary Land, a dolomite-sandstone succession is referred to two formations of the Brønlund Fjord Group. The Ryder Gletscher Group is a thick succession of shallow-water, platform interior carbonates and siliciclastics that extends throughout North Greenland and ranges in age from latest Early Cambrian to Middle Ordovician. The Cambrian portion of this group between Warming Land and south-west Peary Land is formally subdivided into four formations.The Lower Palaeozoic Franklinian Basin is extensively exposed in northern Greenland and the Canadian Arctic Islands. For much of the early Palaeozoic, the basin consisted of a southern shelf, bordering the craton, and a northern deep-water trough; the boundary between the shelf and the trough shifted southwards with time. In North Greenland, the evolution of the shelf during the Cambrian is recorded by the Skagen Group, the Portfjeld and Buen Formations and the Brønlund Fjord, Tavsens Iskappe and Ryder Gletscher Groups; the lithostratigraphy of these last three groups forms the main focus of this paper. The Skagen Group, a mixed carbonate-siliciclastic shelf succession of earliest Cambrian age was deposited prior to the development of a deep-water trough. The succeeding Portfjeld Formation represents an extensive shallow-water carbonate platform that covered much of the shelf; marked differentiation of the shelf and trough occurred at this time. Following exposure and karstification of this platform, the shelf was progressively transgressed and the siliciclastics of the Buen Formation were deposited. From the late Early Cambrian to the Early Ordovician, the shelf showed a terraced profile, with a flat-topped shallow-water carbonate platform in the south passing northwards via a carbonate slope apron into a deeper-water outer shelf region. The evolution of this platform and outer shelf system is recorded by the Brønlund Fjord, Tavsens Iskappe and Ryder Gletscher Groups. The dolomites, limestones and subordinate siliciclastics of the Brønlund Fjord and Tavsens Iskappe Groups represent platform margin to deep outer shelf environments. These groups are recognised in three discrete outcrop belts - the southern, northern and eastern outcrop belts. In the southern outcrop belt, from Warming Land to south-east Peary Land, the Brønlund Fjord Group (Lower-Middle Cambrian) is subdivided into eight formations while the Tavsens Iskappe Group (Middle Cambrian - lowermost Ordovician) comprises six formations. In the northern outcrop belt, from northern Nyeboe Land to north-west Peary Land, the Brønlund Fjord Group consists of two formations both defined in the southern outcrop belt, whereas a single formation makes up the Tavsens Iskappe Group. In the eastern outcrop area, a highly faulted terrane in north-east Peary Land, a dolomite-sandstone succession is referred to two formations of the Brønlund Fjord Group. The Ryder Gletscher Group is a thick succession of shallow-water, platform interior carbonates and siliciclastics that extends throughout North Greenland and ranges in age from latest Early Cambrian to Middle Ordovician. The Cambrian portion of this group between Warming Land and south-west Peary Land is formally subdivided into four formations.


1987 ◽  
Vol 119 (1) ◽  
pp. 103-103
Author(s):  
S. Koponen ◽  
M.S. Wasbauer

Anoplius tenuicornis (Tournier) is a holarctic species with a broad distribution both in Europe (Wolf 1967) and North America (Wasbauer and Kimsey 1985). Despite the widespread occurrence of the species, individuals are not frequently encountered, so it is not surprising that biological information on it has not been available for North America and very little for Europe. Richards and Hamm (1939) gave two fragmentary reports of some significance on A. tenuicornis in England, reported as A. piliventris (Morawitz). In one case, cocoons of the wasp were found in dead thistle stems. In the other, an old burrow of Ectemnius continuus (Fabricius) (Sphecidae) (reported as Solenius) in rotten wood contained a series of wasp cocoons and fragments of clubionid spiders, the presumed prey.


2017 ◽  
Vol 10 (2) ◽  
pp. 479-484 ◽  
Author(s):  
Masato Saito ◽  
Kazumasa Nishimoto ◽  
Robert Nakayama ◽  
Kazutaka Kikuta ◽  
Masaya Nakamura ◽  
...  

Extraskeletal chondroma is defined as a rare, benign, cartilaginous tumor arising from soft tissues such as tendons, tendon sheath synovia, and joint capsules with no continuity to the periosteum or bone cortex. In histopathologic findings, the tumor exhibits many lobular structures and some parts similar to hyaline cartilage. Therefore, it is sometimes difficult to differentiate this tumor from low-grade chondrosarcoma because of their similar histopathologic findings. In order to prevent recurrence, it is necessary to remove the tumor as a whole, including the capsule, so as not to leave any remnants of the tumor. In this article, we report our treatment experience with a case of extraskeletal chondroma in the index finger of a 63-year-old patient.


1992 ◽  
Vol 6 ◽  
pp. 287-287 ◽  
Author(s):  
Paul D. Taylor ◽  
Jonathan A. Todd

Bioimmuration, broadly defined as fossilization by virtue of organic overgrowth, allows preservation of soft-bodied organisms and soft parts of organisms with mineralized skeletons. Sessile organisms attached to hard or firm substrates are routinely overgrown by other organisms competing for living space. If the overgrowing organism has a mineralized skeleton which is likely to be fossilized, then it may carry a high fidelity (sub-micron scale) impression of the overgrown organism on its underside. This is a mould bioimmuration, the simplest mode of preservation. A diagenetic infilling of the mould, commonly by calcite, produces a cast bioimmuration. In addition, the protected microenvironment between the overgrowing organism and the substratum favours early diagenetic permineralization of the soft tissues of the bioimmured organism and the development of more complex preservational styles.In spite of its potential for soft part fossilization, very little research has been undertaken on bioimmuration, with the notable exception of the work of Ehrhard Voigt principally on Maastrichtian sea-grass communities. Research in progress is revealing a great abundance of bioimmured fossils in Mesozoic shallow marine deposits of NW Europe where oysters and serpulids overgrew a variety of other organisms.Bioimmured soft-bodied bryozoans belonging to the Order Ctenostomata are very common and display a range of preservational styles. Minute spines and pores ornamenting the cuticular zooidal walls are sometimes present, as are permineralized pore chambers. The high diversity of stoloniferan and carnosan ctenostomes encrusting hard substrates in the Oxfordian and Kimmeridgian is striking and contrasts with the depauperate fauna of calcified cyclostome bryozoans.Oyster shells in the Kimmeridge Clay are often encrusted by myriads of tiny individuals of the inarticulate brachiopod Discinisca, previously known from comparatively few specimens of this age. Emerging from the fragile commissures are setae several times the length of the delicate phosphatic shells. Setae of neighbouring individuals may be aligned in parallel facing away from the direction of approach of the overgrowing organism.The hemichordate Rhabdopleura is common as a bioimmured fossil in the Oxford Clay. Overgrowth protects the periderm and the black stolons, and colonies are much more intact than previously described examples of this genus from the Jurassic.The Phylum Entoprocta had no unequivocal fossil record before the recent discovery of bioimmured entoprocts in the Kimmeridge Clay. Colonies comprise stolons linking erect zooids which have been pushed flat against the substratum during overgrowth. The existence of thickened sockets at the base of the zooids permits assignment of the fossils to the extant genus Barentsia. Permineralization of the entoproct cuticle has occurred, leaving minute pores apparently once occupied by epithelial microvilli.Pedunculate barnacles are commonly found bioimmured by oysters in the mid-Cretaceous Cambridge Greensand. Normally the cirri are retracted but in one exceptional example their outlines are clearly visible as moulds on the attachment area of an oyster.


2018 ◽  
Vol 93 (1) ◽  
pp. 115-125
Author(s):  
John S. Peel

AbstractPhosphatic sclerites of the problematicTarimspiraYue and Gao, 1992 (Cambrian Series 2) recovered by weak acid maceration of limestones display a unique range of mainly strongly coiled morphologies. They were likely organized into multielement scleritomes, but the nature of these is poorly known; some sclerites may have had a grasping function.Tarimspirasclerites grew by basal accretion in an analogous fashion to younger paraconodonts (Cambrian Series 3–4) but lack a basal cavity. Based on proposed homologies,Tarimspiramay provide an extension of the early vertebrate paraconodont–euconodont clade back into the early Cambrian.Tarimspirais described for the first time from Laurentia (North Greenland), extending its known range from China and Siberia in Cambrian Series 2. In addition to the type species,Tarimspira planaYue and Gao, 1992, the Greenland record ofTarimspiraincludes two morphotypes of a new species,Tarimspira artemi.UUID:http://zoobank.org/c7c536c8-cdaf-49a9-ae1d-77c392f553fc.


2021 ◽  
Vol 12 (4) ◽  
pp. 471-472
Author(s):  
Aida Oulehri ◽  
Sara Elloudi ◽  
Hanane Baybay

Sir, Cutaneous squamous cell carcinoma, a malignant proliferation of the cutaneous epithelium, represents the second most common non-melanoma skin cancer after basal cell carcinoma [1]. Verrucous carcinoma (VC) is a rare, low-grade, well-differentiated squamous cell carcinoma most commonly seen in the mucosa, infrequently reported to occur in the skin, where it is a slow-growing and locally aggressive tumor. It is not uncommon for cutaneous verrucous carcinomas to be mistaken for the more frequent wart (verruca vulgaris) and treated accordingly [2]. The etiopathogenesis of VC is not completely known. One theory mentions the human papillomavirus (HPV) infection; with plantar lesions, the types involved are reported to be 16 and 11 [3]. Histopathological diagnosis is difficult and needs one or more broad and in-depth biopsies. Morbidity results from the local destruction of the skin and soft tissues and, occasionally, from a perineural, muscular, and even bony invasion. Metastasis to regional lymphatic ganglia is rare, found in 5% of cases [4]. VC bears a high risk of local relapse. No matter the treatment employed, the rate of recurrence varies from 30% to 50% and usually is not the result of incomplete surgical interventions. The treatment of choice is complete surgical excision with safety margins [5]. A forty-year-old female patient with no previous history presented herself with a hyperkeratotic lesion on the right foot persistent for two years, which she had been manipulating routinely, which had progressively been increasing in size for the previous year, and which, for the previous three months, had become painful and bleeding. An examination revealed a hyperkeratotic plaque with a hyperpigmented border, hard on palpation, adherent to the deep plane, and with an eroded surface (Fig. 1). Dermoscopy was able to find a papillomatous appearance surrounded by dotted vessels (Fig. 2). This dermoscopic aspect typical of vulgar warts was confusing. Indeed, dermoscopy of the foot wart shows red or black dots in the center of papillomatous structures, which are thrombosed vessels supplying the wart; hence the importance, in our opinion, of the clinical and pathological correlation. For this reason, we performed a skin biopsy; an anatomopathological study found a squamous cell carcinoma of the verrucous type.


2005 ◽  
Vol 8 (4) ◽  
pp. 449-451
Author(s):  
Marcelo A. F. Ribeiro Jr ◽  
Christian Evangelista Garcia ◽  
Telma Eugênio dos Santos ◽  
Adavio de Oliveira e Silva ◽  
Regina Leitão ◽  
...  

Introduction: Epithelioid hemangioendothelioma of liver is a rare, low-grade neoplasm of vascular origin that has an unpredictable malignant potential. It preferentially arises in soft tissues and bones, and seldom in the liver. Biologically, it trends to be multi-focal and often unresectable. Objective: The outcome of a patient submitted to a living-related liver transplant to treat epithelioid hemangioendothelioma of the liver. Case report: The reported case involves a 39-year old female patient with an immense epithelioid hemangioendothelioma of the liver, involving segments III, IV, V, VII, and VIIl. The prognostic to any kind of treatment was considered unfavorable, and the decision of submitting her to a liver transplant was made. It was suggested a living-related liver transplant. The donor was the patient’s 36-year old brother, who donated his right liver lobe (segments V, VI, VII, VIII). The recipient´s original liver was large, presenting very solid consistence and no node evidence. The transplant itself was performed using the conventional living-related liver transplantation technique. The recovery was good, and she was discharged from hospital on the 15th postoperative day using micophenolate mofetil, tacrolimus, and corticoid. Conclusion: Liver transplantation for epithelioid hemangioendothelioma of the liver can be performed with acceptable survival rate. The living related liver transplant opens a great perspective to that group of patients presenting liver tumors and who are unfeasible to wait for an organ on a waiting list.


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