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1 iation and inventory relative to P since the Proterozoic.
2 arine sulphate concentrations throughout the Proterozoic.
3 a build-up of atmospheric oxygen before the Proterozoic.
4 the fossil record may be pushed back to the Proterozoic.
5 eaking the long-term static state of the mid-Proterozoic.
6 onate could have been relevant since the mid-Proterozoic.
7 gical and geochemical conditions in the late Proterozoic.
8 for the rise of metazoans at the end of the Proterozoic.
9 on of Earth's surface environment during the Proterozoic.
10 deposits formed during the Archean and early Proterozoic.
11 nental stabilization at the beginning of the Proterozoic.
14 he most abundant type of fossil found in the Proterozoic (2,500 to 590 Myr ago), but they then declin
15 mats in benthic environments for most of the Proterozoic (2,500-542 Mya), marine planktonic cyanobact
17 coincident with a major regime change in the Proterozoic acritarch record, including: (i) disappearan
18 cean environmental conditions earlier in the Proterozoic adverse to nitrogen-fixers and their evoluti
20 exture, and structure of fluvial deposits in Proterozoic-age Torridonian Group, Scotland-a type-examp
22 (Synechococcus sp. PCC 7002), an engineered Proterozoic analog lacking a CO(2)-concentrating mechani
23 a from rocks formed near the boundary of the Proterozoic and Archaean eons, some 2.5 Gyr ago, show ma
26 oth anomalous climatic stasis during the mid-Proterozoic and extreme climate perturbation during the
30 periods of lithospheric thinning during the Proterozoic and Phanerozoic eons, the lithosphere beneat
31 and mean temperature of cold periods within Proterozoic and Quaternary climates, and recent climate
32 the microbially dominated ecosystems of the Proterozoic and the Cambrian emergence of the modern bio
33 ains in the sandstone are Permian, Devonian, Proterozoic, and Archean in age and, with the exception
34 la trace their diversity to the Archaean and Proterozoic, and bacterial families prior to the Phanero
35 approach to geological observations from the Proterozoic, and provide the first quantitative constrai
36 ulphide in injected sands extend back to the Proterozoic, and show that injected sand complexes have
37 organic-walled microfossils extracted from a Proterozoic ( approximately 1.4-gigayear-old) shale in N
39 r-filled structures common in early- and mid-Proterozoic ( approximately 2,500-750 million years ago,
40 oncentrations and rates of Fe cycling in the Proterozoic are the largest differences from modern oxyg
41 We propose that the root formed during the Proterozoic assembly of interior East Antarctica (possib
42 was abundant in the late Archaean and early Proterozoic atmosphere and that methane was probably sca
44 r highlight that deep chemical weathering of Proterozoic bedrock and denudation associated with the G
46 served crustal thickness across the Archaean/Proterozoic boundary, these data are consistent with a m
47 nts phosphorus and nickel across the Archean-Proterozoic boundary, which might have helped trigger th
48 obialites were common and diverse during the Proterozoic, but declined in abundance and morphological
49 gered by environmental perturbation near the Proterozoic-Cambrian boundary and subsequently amplified
52 ed to estimate the impact this would have on Proterozoic carbon cycling and global atmospheric compos
53 -cyanobacterium is fully consistent with the Proterozoic carbon isotope record, suggesting that cyano
55 g events, by a Paleozoic silicic fluid and a Proterozoic carbonatitic fluid, are also encapsulated in
57 Here we use a simple box model of a generic Proterozoic coastal upwelling zone to show how these fee
59 is implies not only that cyanobacteria built Proterozoic conical stromatolites but also that fossil b
60 at microaerophilic levels throughout the Mid-Proterozoic, consistent with the prevalence of some clad
61 overt assembly of Rodinia from thickened mid-Proterozoic continental crust via two-sided subduction c
63 ion beneath Venetia from the Archaean to the Proterozoic.Dating of inclusions within diamonds is used
64 d that the metal enrichment record implies a Proterozoic deep ocean characterized by pervasive anoxia
74 2.3 billion years ago, Gyr ago) and the late Proterozoic eon (about 0.8 Gyr ago), with the latter imp
75 orus cycle may have occurred during the late Proterozoic eon (between 800 and 635 million years ago),
77 decay of Earth's dynamo strength through the Proterozoic Eon and could challenge the hypothesis of a
78 and diversification of the eukaryotes in the Proterozoic Eon as viewed through fossils, organic bioma
79 e record of marine carbon indicates that the Proterozoic Eon began and ended with extreme fluctuation
80 surface redox conditions evolved through the Proterozoic Eon is fundamental to understanding how biog
81 low gradient, single-threaded rivers in the Proterozoic eon, at a time well before the evolution and
82 ed Earth's surface and atmosphere during the Proterozoic Eon, pushing it away from the more reducing
83 ich environments in the late Archean Eon and Proterozoic Eon, respectively, by the spread of arsM gen
84 ies a unique ocean chemistry for much of the Proterozoic eon, which would have been neither completel
92 ty in anoxic seawater during the Archean and Proterozoic eons (4.0-0.541 billion years ago) would hav
93 wth of landmass in the late Archean to early Proterozoic Eons could have reorganized biogeochemical c
94 of Eucarya occurred in the late Archaean or Proterozoic Eons when atmospheric oxygen levels were low
96 however, extend into the Archaean and early Proterozoic eons, in the form of impact spherule beds: g
97 iment was widespread during the Archaean and Proterozoic Eons, playing an important role in global bi
100 ets may have reached the Equator in the late Proterozoic era (600-800 Myr ago), according to geologic
113 spheric oxygen concentration during the late Proterozoic has been inferred from multiple indirect pro
114 idence for such low O2 concentrations in the Proterozoic helps explain the late emergence and diversi
116 Our temporal framework for the terminal Proterozoic is a critical step for testing hypotheses re
119 lly to the base of the much thinner adjacent Proterozoic lithosphere creates a zone of highly concent
120 d thickness differences between Archaean and Proterozoic lithosphere on deep-carbon fluxes remains un
121 the Sierran batholith formed on preexisting Proterozoic lithosphere, most of the original lithospher
125 ve anoxia in the subsurface ocean during the Proterozoic may have allowed large fluxes of biogenic CH
126 /188Os ratios (0.1193 to 0.1273), which give Proterozoic model ages of 820 to 1230 million years ago.
127 s after about 1,800 Myr ago maintained a mid-Proterozoic molybdenum reservoir below 20 per cent of th
128 oxygen generated during Archean and earliest Proterozoic non-Snowball glacial intervals could have dr
133 nktonic productivity, various models for mid-Proterozoic ocean chemistry imply different effects on t
134 e to show how these feedbacks caused the mid-Proterozoic ocean to exhibit a spatial/temporal separati
135 Here, we link geologic information about the Proterozoic ocean to microbial processes in modern low-o
136 y the major primary producers in the pelagic Proterozoic ocean, despite atmospheric CO(2) levels up t
137 diverse palaeogeographic settings in the mid-Proterozoic ocean, inviting new models for the temporal
139 much dissolved oxygen was present in the mid-Proterozoic oceans between 1.8 and 1.0 billion years ago
141 Thus, a redox structure similar to those in Proterozoic oceans may have persisted or returned in the
142 suggest that subsurface water masses in mid-Proterozoic oceans were predominantly anoxic and ferrugi
144 modern oxygen minimum zones as an analog for Proterozoic oceans, we explore the effect of low oxygen
147 ation of organic sulfur cycling from the Mid-Proterozoic onwards, with implications for climate regul
152 s C) and show evidence for heating and yield Proterozoic Os model ages, whereas the deeper portions (
154 state of the oceans, generated by the early Proterozoic oxygen revolution and terminated by the envi
160 the divergence of living agnathans, near the Proterozoic/Phanerozoic boundary (approximately 550Mya).
161 rovide the first quantitative constraints on Proterozoic plate velocities that substantiate the postu
162 modern DOC is (13)C-enriched relative to the Proterozoic, possibly because of changing autotrophic ca
163 from weak to strong in the Paleozoic and the Proterozoic present challenges in identifying the onset
165 f western North America some younger (middle Proterozoic) regions have remained stable, whereas some
167 yanobacterial sheaths routinely preserved in Proterozoic rocks, this assemblage includes multicellula
172 ally continuous suites of samples from Upper Proterozoic sedimentary successions of East Greenland, S
174 f chromium (Cr) isotope data from a suite of Proterozoic sediments from China, Australia, and North A
175 ere we show that hydrocarbons extracted from Proterozoic sediments in several locations worldwide are
177 g-distance correlation between fossiliferous Proterozoic strata of Mexico and the United States.
178 entary changes, including the replacement of Proterozoic-style microbial matgrounds by Phanerozoic-st
179 alt, the HIMU source formed as Archean-early Proterozoic subduction-related carbonatite-metasomatized
181 rom sulfur isotope data for Archean to early Proterozoic surface material in the deep HIMU mantle sou
184 n hydrated and probably weakened much of the Proterozoic tectospheric mantle beneath the Colorado pla
185 ability of the evolution of Ecdysozoa in the Proterozoic, the otherwise prolific fossil record of the
186 n of animal life on Earth for much of Middle Proterozoic time ( approximately 1.8-0.8 billion years a
187 reviving the faint young Sun paradox during Proterozoic time and challenging existing models for the
192 nently oxygenated atmosphere at the Archaean-Proterozoic transition (approximately 2.5 billion years
193 lar oxygen (O(2)) shortly after the Archaean-Proterozoic transition 2.5 billion years ago was more co
194 Earth's atmosphere shortly after the Archean-Proterozoic transition during the 'Great Oxidation Event
196 , the assumption of elevated pCH4 during the Proterozoic underlies most models for both anomalous cli
198 wn, but it is generally assumed that the mid-Proterozoic was home to a globally sulphidic (euxinic) d
199 tionary trajectories and highlight the early Proterozoic, which encompasses the Great Oxidation Event
200 significant non-arc magmatism during the mid-Proterozoic, while fewer occurrences of many other miner
202 show that higher mantle temperatures in the Proterozoic would have resulted in a larger proportion o