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1 tern for oceanic diatom diversity across the Cenozoic.
2 faunal turnover of the first 15 m.y. of the Cenozoic.
3 o form diverse assemblages once again in the Cenozoic.
4 imately 0.15% every million years during the Cenozoic.
5 , during one of the warmest intervals of the Cenozoic.
6 ust experienced strong shortening during the Cenozoic.
7 l complexity and alpha diversity in the Meso-Cenozoic.
8 e size of marine pelagic diatoms through the Cenozoic.
9 ed marine planktonic diatom species over the Cenozoic.
10 genian, Late Ordovician, late Paleozoic, and Cenozoic.
11 ed temperatures in the latter portion of the Cenozoic.
12 system toward a glacial tipping point in the Cenozoic.
13 gen content over short time intervals in the Cenozoic.
14 c, and remained comparatively high until the Cenozoic.
15 hanging Southern Ocean conditions during the Cenozoic.
16 h at least the first 24 million years of the Cenozoic.
17 rtial pressure of atmospheric CO2 during the Cenozoic.
18 h periods of global warmth such as the Early Cenozoic.
19 nstruct mantle structure at the start of the Cenozoic.
20 s Australia became more arid during the late Cenozoic.
21 while major genera diversified near the mid Cenozoic.
22 d global average temperature trends over the Cenozoic.
23 g the Cretaceous and, at a smaller size, the Cenozoic.
24 North American terrestrial mammals over the Cenozoic.
25 attern of fauna replacement in SA during the Cenozoic.
26 e Northern or Southern Hemisphere during the Cenozoic.
27 r five typical geological periods during the Cenozoic.
28 ic era and survived to the beginnings of the Cenozoic.
29 inated the world's terrestrial biotas in the Cenozoic.
30 ntly rose dramatically in the Cretaceous and Cenozoic (145 million years ago-present), indicating tha
31 y over water from South America in the early Cenozoic (47-29 million years ago, Mya), is more likely.
32 Using this proxy, we reconstruct LAI for the Cenozoic (49 million to 11 million years ago) of middle-
34 square meter, three times greater than mean Cenozoic and Early Cretaceous-Late Jurassic dipole momen
35 ale pattern of plate tectonic motions during Cenozoic and late Mesozoic time, provided that subducted
36 tle convection constrained by the history of Cenozoic and Mesozoic plate motions explain some deep-ma
37 olution of seeds and cones at least over the Cenozoic and perhaps over much of the later Mesozoic.
38 ally weaker than it is today for most of the Cenozoic and the robust modern LDG of North American mam
39 as a major driver of global tectonics in the Cenozoic and, we argue, of atmospheric CO(2) concentrati
40 ethyan Ocean during the Cretaceous and early Cenozoic, and identifies an eastward movement of ancestr
41 ase in (87)Sr/(86)Sr in seawater through the Cenozoic apparently had no effect on central Pacific dee
42 e for a burst of fern diversification in the Cenozoic, apparently driven by the evolution of epiphyti
44 ing from 3.0-3.5 kilometres during the early Cenozoic (approximately 55 million years ago) to 4.6 kil
45 ex ecosystems are far more common among Meso-Cenozoic assemblages than among the Paleozoic assemblage
46 se in marine animal biodiversity through the Cenozoic at the genus level has been attributed to a sam
47 t accommodates both the long-term decline of Cenozoic atmospheric CO(2) levels and the effects of orb
49 rpretation of bioalteration trace fossils in Cenozoic basalt glasses and their putative equivalents i
50 -habitat diversity measure Fisher's alpha of Cenozoic benthic foraminifera from the temperate Central
51 al losses of tropical rainforests during the Cenozoic, but not to the cumulative area of tropical rai
55 r obstacle in understanding the evolution of Cenozoic climate has been the lack of well dated terrest
57 omparative phylogenetic methods to infer how Cenozoic climatic change shaped the morphological and ph
60 aves have the potential to help resolve late Cenozoic climatic, speleologic, and tectonic questions.
67 en isotope records indicates that changes in Cenozoic deep-water circulation patterns were the conseq
68 ture thermochronometry reveals regional Late Cenozoic denudation in Fiordland, New Zealand, consisten
72 The history of the Arctic Ocean during the Cenozoic era (0-65 million years ago) is largely unknown
73 position events have occurred during the mid-Cenozoic era (34 to 7 million years ago) in the northern
75 c carbon dioxide concentrations in the early Cenozoic era (about 60 Myr ago) are widely believed to h
76 during the warmest climatic interval of the Cenozoic era (approximately 65 to 40 million years (Myr)
77 s in global ocean circulation throughout the Cenozoic era (from about 65 million years ago to the pre
78 ttributable to anagenesis is <19% during the Cenozoic era (last 65 Myr) and <10% during the Neogene p
80 lored these responses during portions of the Cenozoic era (the most recent 65.5 million years (Myr) o
81 d dramatic instance of global warming in the Cenozoic era and has been proposed to be a geologic anal
83 Here, using the exceptional fossil record of Cenozoic Era macroperforate planktonic foraminifera, we
84 from other eudicots at the beginning of the Cenozoic era of the Earth (60 Mya), major diversificatio
86 wever, the effect of cooling during the Late Cenozoic era, including the onset of Pliocene-Pleistocen
96 damental to our understanding of the role of Cenozoic-era climate change in the development of topogr
97 ock cooling ages signifies much reduced late Cenozoic erosion despite dominantly glacial conditions h
98 ith independent geologic constraints for the Cenozoic evolution of the central Andes, as well as vari
99 ft system is the result of late Mesozoic and Cenozoic extension between East and West Antarctica, and
100 In contrast to northern continents, the Cenozoic faunal history of SA was characterized by a lon
103 as and insect faunas that are known, but its Cenozoic fossil record of insects and insect herbivory i
104 agree with most early (Palaeozoic) and late (Cenozoic) fossil-based times, but indicate major gaps in
106 arity stratigraphy at Gran Barranca with the Cenozoic geomagnetic polarity time scale indicate that B
109 edicts that enhanced erosion related to late Cenozoic global cooling can act as a first-order influen
112 ging climate and habitat loss throughout the Cenozoic have had strong impacts on the phylogenetic str
116 occurred between the late Mesozoic and early Cenozoic, identifying this period as the "Second Age of
117 nstructions of biomes and climate to examine Cenozoic imprints on the phylogenetic structure of regio
118 the Recent thus accounts for only 5% of the Cenozoic increase in bivalve diversity, a major componen
121 onty) in herbivorous mammals during the late Cenozoic is classically regarded as an adaptive response
122 in amber exclusively from the Cretaceous and Cenozoic is widely regarded to be a result of the produc
123 house-gas-driven global warming event of the Cenozoic-is central to drawing inferences for future cli
124 theses have been put forward to explain the 'Cenozoic isotope-weathering paradox', and the evolution
127 it is clear that in both the Cretaceous and Cenozoic, leptosporangiate ferns were adept at exploitin
128 Using the unparalleled fossil record of Cenozoic macroperforate planktonic foraminifera, we demo
129 cular, the model matches the encroachment of Cenozoic magmatism from the margins towards the plateau
130 al Bayesian survival model of North American Cenozoic mammal species durations in relation to species
131 the duration of bivalve species in the early Cenozoic marine fossil record of the eastern United Stat
134 tions of entire assemblages in more than 500 Cenozoic marine sediment samples, including more than 1
135 radiation associated with global warming and Cenozoic maximum global temperatures, (ii) moderately an
136 further decrease in maximum size during the Cenozoic may relate to the evolution of bats, the Cretac
137 unct plant communities associated with early Cenozoic mesophytic forests and a boreotropical history.
141 emperature increase to the highest prolonged Cenozoic ocean temperature and a similarly distinctive c
142 likely relictual mammals from earlier in the Cenozoic of SA and Antarctica, Necrolestes demonstrates
144 below Lesser Himalayan rocks at the onset of Cenozoic orogenesis are flawed, and that some metamorphi
146 d global analysis was undertaken of earliest Cenozoic (Paleocene) neogastropods and this does indeed
147 nvironmental parameters and comparisons with Cenozoic paleoproxy data show a consistently positive co
149 -mantle slab penetration events by comparing Cenozoic plate motions at the Earth's main subduction zo
151 e under the Indian Ocean at the start of the Cenozoic presents a challenge for connecting the event t
155 China (Xinjiang Province) that is the first Cenozoic record of this clade and renders Deltatheroida
156 nizations of biogenic silica burial over the Cenozoic reduced marine authigenic clay formation, contr
157 eau lithosphere over 35-40 Myr following mid-Cenozoic removal of the Farallon plate from beneath Nort
159 These results enable us to calculate mid-Cenozoic rotation parameters for East and West Antarctic
160 al corrosion textures in volcanic glass from Cenozoic seafloor basalts and the corresponding titanite
161 vince and Rio Grande rift province underwent Cenozoic shortening followed by extension, the plateau e
162 O2 partial pressure and the evolution of the Cenozoic sulphur cycle, and could be accounted for by ge
163 paleoceanographic model that predicts Early Cenozoic surface currents periodically conducive to raft
164 s a tectonic setting for several significant Cenozoic tectonic events in the Ross Sea embayment inclu
165 ecies (<100 million years ago) suggests that Cenozoic tectonic history and oceanic circulation patter
167 ons are more subject to invasion; the latest Cenozoic temperate zones evidently received more invader
169 st 65 My, using 27,903 fossil occurrences of Cenozoic terrestrial mammals from western North America
170 tential solution for mismatches between late Cenozoic terrestrial sedimentation and marine geochemist
171 Fe isotopic composition of seawater over the Cenozoic that reflect the influence of several, distinct
173 ine bivalves shows, in three successive late Cenozoic time slices, that most clades (operationally he
176 er increase in specific lineages towards the Cenozoic to reach, in the most recently derived lineages
177 long-term geological record reveals an early Cenozoic warm climate that supported smaller polar ecosy
179 st size of planktic foraminifera through the Cenozoic was an adaptive response to intensifying surfac
180 All such groups arose in parallel during the Cenozoic, when army ants diversified into modern genera
181 eawater sulfate sulfur isotope curve for the Cenozoic with a resolution of approximately 1 million ye
182 at originated in the tropics during the late Cenozoic, with the contrarian gradient strength at both
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