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51. Microbially mediated fossil concretions and their characterization by the latest methodologies: a review.

52. A Class Project for Investigating Possible Future Local Effects of Global Climate Change through Student Analysis of Fossil Faunas.

53. The Oldest Trace Fossils in Association with an Ediacara-Type Biota in the Upper Vendian of the South Urals.

54. Five new malformed trilobites from Cambrian and Ordovician deposits from the Natural History Museum.

55. Environmental and temporal patterns in bioturbation in the Cambrian–Ordovician of Western Newfoundland.

56. Widespread seafloor anoxia during generation of the Ediacaran Shuram carbon isotope excursion.

57. Heterogeneous sulfide reoxidation buffered oxygen release in the Ediacaran Shuram ocean.

58. New Ediacaran biota from the oldest Nama Group, Namibia (Tsaus Mountains), and re-definition of the Nama Assemblage.

59. Redox Conditions of the Late Ediacaran Ocean on the Southern Margin of the North China Craton.

60. A large enigmatic fossil from the early Cambrian (Series 2, Stage 3) Heatherdale Shale of South Australia.

61. A macroscopic free-swimming medusa from the middle Cambrian Burgess Shale.

62. A Great late Ediacaran ice age.

63. Sulphate-reducing bacteria-mediated pyrite formation in the Dachang Tongkeng tin polymetallic deposit, Guangxi, China.

64. The biogeography of extant lungfishes traces the breakup of Gondwana.

65. Exceptional lower Cambrian fossils from a long‐lost locality in Vermont, USA.

66. The role of iron in the formation of Ediacaran 'death masks'.

67. Ediacaran–Cambrian bioturbation did not extensively oxygenate sediments in shallow marine ecosystems.

68. Palaeobiology and taphonomy of the rangeomorph Culmofrons plumosa.

69. The quality of the fossil record across higher taxa: compositional fidelity of phyla and classes in benthic marine associations.

70. Artifacts resembling Ediacaran or Cambrian fossils: how to identify them and avoid their generation.

71. Body plan of Dickinsonia , the oldest mobile animals.

72. Microbial mats as model to decipher climate change effect on microbial communities through a mesocosm study.

73. Landscape-level variability and insect herbivore outbreak captured within modern forests provides a framework for interpreting the fossil record.

74. Deep origin of the long root tuft: the oldest stalk-bearing sponge from the Cambrian Stage 3 black shale of South China.

75. Praecarbo strigoniensis, a new genus and species of Cormorants (Phalacrocoracinae) from the Late Oligocene of Hungary.

76. Salinity variation and hydrographic dynamics in the early Cambrian Nanhua Basin (South China).

77. Metazoan zooplankton in the Bay of Biscay: 16 years of individual sizes and abundances from the ZooScan and ZooCAM imaging systems.

78. Early Permian zircon ages from the P. confluens and P. pseudoreticulata spore-pollen zones in the southern Bonaparte and Canning basins, northwestern Australia.

79. Multivariate mapping of ontogeny, taphonomy and phylogeny to reconstruct problematic fossil taxa.

80. A Systems Approach to Understanding How Plants Transformed Earth's Environment in Deep Time.

81. Triangular-shaped Ediacaran fossil Thectardis avalonensis from the Sonia Sandstone, Jodhpur Group, Marwar Supergroup, western India.

82. The Ediacaran--Cambrian transition in the southern Great Basin, United States.

83. The record of sea water chemistry evolution during the Ediacaran–Cambrian from early marine cements.

84. A Diverse Microfossil Assemblage from the Ediacaran–Cambrian Deep-Water Chert of the Liuchapo Formation in Guizhou Province, South China.

85. Description and systematic affinity of flower and seed fossils of Erica sect. Chlorocodon (Ericaceae) from the early Pleistocene of Madeira Island, Portugal.

86. Giant, swimming mouths: oral dimensions of extant sharks do not accurately predict body size in Dunkleosteus terrelli (Placodermi: Arthrodira).

87. Tonian Low‐Latitude Marine Ecosystems Were Cold Before Snowball Earth.

88. 富碳质地质样品 Re-Os 同位素体系研究进展.

89. Discovery of jaguar from northeastern China middle Pleistocene reveals an intercontinental dispersal event.

90. Did the Late Ordovician mass extinction event trigger the earliest evolution of 'strophodontoid' brachiopods?

91. Model estimates of metazoans' contributions to the biological carbon pump.

92. Stratigraphic and geographic distribution of dinosaur tracks in the UK.

93. Distribution and geochemical significance of trace elements in kerogens from Ediacaran–Lower Cambrian strata in South China.

94. Reconstruction of the Lateral Series of the Late Cambrian and Early Ordovician Active Continental Margin Structures in the Paleozoides of Northern Kazakhstan.

95. Polyplacophoran Feeding Traces on Mediterranean Pliocene Sirenian Bones: Insights on the Role of Grazing Bioeroders in Shallow-Marine Vertebrate Falls.

96. The Main Controlling Factors on the Evolution of the Cambrian Carbonate Platform in the Tarim Basin and Its Implications for the Distribution of Ultra-Deep Dolomite Reservoirs.

97. Skeletal–cement–microbial reefs in the Pennsylvanian: a case study in Guizhou, South China.

98. Fibrous or Prismatic? A Comparison of the Lamello-Fibrillar Nacre in Early Cambrian and Modern Lophotrochozoans.

99. A new stiodermatid (Hexactinellida, Porifera) from the latest Ordovician of Anhui, South China and its significance for searching the missing link between the Cambrian and late Palaeozoic stiodermatid lineage.

100. Origin of organic matter and depositional characteristics of early Cambrian Niutitang Formation from South China: New insights using molecular fossils.

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