Sage, Rowan Frederick
Rowan F Sage onderzoeker
Sage, Rowan F.
VIAF ID: 19849993 (Personal)
Permalink: http://viaf.org/viaf/19849993
Preferred Forms
- 100 0 _ ‡a Rowan F Sage ‡c onderzoeker
- 200 _ | ‡a Sage ‡b Rowan Frederick
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- 100 1 _ ‡a Sage, Rowan Frederick
- 100 1 _ ‡a Sage, Rowan Frederick
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- 100 1 _ ‡a Sage, Rowan Frederick
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- 100 1 _ ‡a Sage, Rowan Frederick
4xx's: Alternate Name Forms (7)
Works
Title | Sources |
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C4 Photosynthesis and Related CO2 Concentrating Mechanisms | |
C₄ plant biology, c1999: | |
Complex evolutionary transitions and the significance of c(3)-c(4) intermediate forms of photosynthesis in Molluginaceae. | |
Dissecting Molecular Evolution in the Highly Diverse Plant Clade Caryophyllales Using Transcriptome Sequencing | |
Diversity of Kranz anatomy and biochemistry in C4 eudicots | |
Evaluating methods for isolating total RNA and predicting the success of sequencing phylogenetically diverse plant transcriptomes | |
Evolution of photorespiration from cyanobacteria to land plants, considering protein phylogenies and acquisition of carbon concentrating mechanisms | |
Evolution of RLSB, a nuclear-encoded S1 domain RNA binding protein associated with post-transcriptional regulation of plastid-encoded rbcL mRNA in vascular plants | |
The Evolutionary Origin of C4 Photosynthesis in the Grass Subtribe Neurachninae | |
Exploiting the engine of C | |
Facultative crassulacean acid metabolism in a C3-C4 intermediate | |
From proto-Kranz to C4 Kranz: building the bridge to C4 photosynthesis. | |
The functional anatomy of rice leaves: implications for refixation of photorespiratory CO2 and efforts to engineer C4 photosynthesis into rice | |
Functional constraints of CAM leaf anatomy: tight cell packing is associated with increased CAM function across a gradient of CAM expression | |
Functional leaf anatomy of plants with crassulacean acid metabolism | |
The functional significance of C3-C4 intermediate traits in Heliotropium L. (Boraginaceae): gas exchange perspectives. | |
Gisekia (Gisekiaceae): phylogenetic relationships, biogeography, and ecophysiology of a poorly known C₄ lineage in the Caryophyllales | |
Global change biology: A primer | |
High-yielding rice Takanari has superior photosynthetic response to a commercial rice Koshihikari under fluctuating light | |
How terrestrial organisms sense, signal, and respond to carbon dioxide. | |
Initial events during the evolution of C4 photosynthesis in C3 species of Flaveria | |
Is C4 photosynthesis less phenotypically plastic than C3 photosynthesis? | |
Kudzu [Pueraria montana (Lour.) Merr. Variety lobata]: A new source of carbohydrate for bioethanol production | |
Leaf anatomy, gas exchange and photosynthetic enzyme activity in Flaveria kochiana | |
Leaf photosynthetic rate and mesophyll cell anatomy changes during ontogenesis in backcrossed indica × japonica rice inbred lines. | |
Lineage-specific gene radiations underlie the evolution of novel betalain pigmentation in Caryophyllales | |
Manipulating photorespiration to increase plant productivity: recent advances and perspectives for crop improvement | |
Mesophyll cells of C4 plants have fewer chloroplasts than those of closely related C3 plants. | |
Mesophyll Chloroplast Investment in C3, C4 and C2 Species of the Genus Flaveria | |
Microsite characteristics of Muhlenbergia richardsonis (Trin.) Rydb., an alpine C4 grass from the White Mountains, California. | |
Molecular phylogenetics of Euploca (Boraginaceae): homoplasy in many characters, including the C4 photosynthetic pathway | |
Molecular Phylogeny ofPectis(Tageteae, Asteraceae), a C4Genus of the Neotropics, and its Sister GenusPorophyllum | |
The occurrence of C(2) photosynthesis in Euphorbia subgenus Chamaesyce (Euphorbiaceae). | |
On the disintegration of Molluginaceae: a new genus and family (Kewa, Kewaceae) segregated from Hypertelis, and placement of Macarthuria in Macarthuriaceae | |
The origins of C4 grasslands: integrating evolutionary and ecosystem science. | |
Passive CO2 concentration in higher plants. | |
Perspectives for a better understanding of the metabolic integration of photorespiration within a complex plant primary metabolism network. | |
Photosynthesis and nitrogen use ... 1986 | |
Photosynthesis: Mining grasses for a better Rubisco. | |
Photosynthetic diversity meets biodiversity: the C4 plant example | |
Photosynthetic efficiency and carbon concentration in terrestrial plants: the C4 and CAM solutions | |
Photosynthetic pathway influences xylem structure and function inFlaveria(Asteraceae) | |
Photosynthetic pathway of grass fossils from the upper Miocene Dove Spring Formation, Mojave Desert, California | |
Phylogeny and photosynthetic pathway distribution in Anticharis Endl. (Scrophulariaceae). | |
Plants and bioenergy | |
Plants increase CO2 uptake by assimilating nitrogen via the photorespiratory pathway. | |
The Population Structure and Floral Biology of Amborella Trichopoda (Amborellaceae) | |
A portrait of the C4photosynthetic family on the 50th anniversary of its discovery: species number, evolutionary lineages, and Hall of Fame | |
Quo vadis C(4)? An ecophysiological perspective on global change and the future of C(4) plants | |
Regulation of photosynthetic electron-transport in Phaseolus vulgaris L., as determined by room-temperature chlorophyll a fluorescence | |
The regulation of Rubisco activity in response to variation in temperature and atmospheric CO2 partial pressure in sweet potato | |
Reproductive heat tolerance in a Mojave Desert annual plant, Trianthema portulacastrum | |
RNA-Seq based phylogeny recapitulates previous phylogeny of the genus Flaveria (Asteraceae) with some modifications | |
Rubisco, Rubisco activase, and global climate change | |
The sensitivity of photosynthesis to O2 and CO2 concentration identifies strong Rubisco control above the thermal optimum. | |
Some like it hot: the physiological ecology of C4 plant evolution | |
Stopping the leaks: new insights into C4 photosynthesis at low light | |
Sub-zero cold tolerance of Spartina pectinata (prairie cordgrass) and Miscanthus × giganteus: candidate bioenergy crops for cool temperate climates | |
The taxonomic distribution of C4 photosynthesis in Amaranthaceae sensu stricto. | |
The temperature response of photosynthesis in tobacco with reduced amounts of Rubisco | |
Thermal acclimation of photosynthesis in black spruce [Picea mariana (Mill.) B.S.P.]. | |
Tolerance of subzero winter cold in kudzu (Pueraria montana var. lobata) | |
Tracking the evolutionary rise of C4 metabolism | |
Variation in leaf anatomical traits relates to the evolution of C4 photosynthesis in Tribuloideae (Zygophyllaceae) | |
Variation in the k(cat) of Rubisco in C(3) and C(4) plants and some implications for photosynthetic performance at high and low temperature | |
Water-use efficiency and nitrogen-use efficiency of C(3) -C(4) intermediate species of Flaveria Juss. (Asteraceae). | |
Why are there no C4 forests? | |
Winter cold tolerance and the geographic range separation ofBromus tectorumandBromus rubens,two severe invasive species in North America | |
Winter cold-tolerance thresholds in field-grown Miscanthus hybrid rhizomes |