ライフサイエンスコーパス: leaf

1 ct an integrated WUE(i) over the life of the leaf.

2 t removed relatively little tissue from each leaf.

3 ide the other organs like leaves or the flag leaf.

4 icus root hairs and in Nicotiana benthamiana leaves.

5 but is dispensable for midvein formation in leaves.

6 reaction in wild-type and engineered tobacco leaves.

7 ely, within 90 min after infection of pepper leaves.

8 last cell cultures, and Arabidopsis thaliana leaves.

9 ected trees before symptom development among leaves.

10 ntent and the antioxidant potential of olive leaves.

11 derably lower (76.1-205.2 mg.kg(-1)) than in leaves (1477.7-8709.0 mg.kg(-1)).

12 The fast drying of solvent at liquid surface leaves 3D-like perovskites which surprisingly templates

13 This ask1 mutant produces twisted rosette leaves, a reduced number of petals, fewer viable pollen

14 leaf area scales with leaf mass and how such leaf allometry, under the control of these QTLs, varies

15 that determine developmental trajectories of leaf allometry, whose expression is contingent heavily u

16 mical aglycones in edible African nightshade leaves, an underutilized food resource in the sub-Sahara

17 by C(4) engineering programmes, the simpler leaf anatomical requirements make C(2) engineering a fea

18 ume Medicago truncatula, we identified SMALL LEAF AND BUSHY1 (SLB1), which is required for the contro

19 ional traits are widely used to characterize leaf and canopy properties that drive ecosystem processe

20 This analysis unifies leaf and ecosystem observations in a common theoretical

21 Analysis of the expression of ANK genes in leaf and pepper fruits suggested that the ANKs have spec

22 We investigated the extent to which leaf and plant morphology, gas exchange, leaf and stem h

23 energy flux parameters of photosynthesis and leaf and root anatomy, up-regulation of Si channel and t

24 metophyte defect and also revealed defective leaf and root growth.

25 olved in the phenylpropanoid biosynthesis in leaf and root tissues respectively.

26 ich leaf and plant morphology, gas exchange, leaf and stem hydraulics and growth rates have evolved i

27 exhibit decreased rates of cell division in leaf and vascular primordia.

28 processes across plant organs (chloroplast, leaf and whole plant) and is a first-step towards repres

29 relations between nutrient concentrations of leaves and edible parts than annuals.

30 there is a prompt accumulation of proline in leaves and effective protection of chlorophyll during pe

31 BIA metabolism, occurring primarily in young leaves and embryos of sacred lotus.

32 ure perception on plastid metabolism in both leaves and fruit, specifically on the accumulation of is

33 Fungal challenge assays on leaves and fruits showed that the transgenic lines were

34 d PULSE to control immune responses in plant leaves and generated Arabidopsis transgenic plants.

35 tte leaves and systemically infected cauline leaves and inflorescence.

36 ance to drought such as small sclerophyllous leaves and lower percent loss of hydraulic conductivity.

37 A wave of green leaves and multi-colored flowers advances from low to hi

38 ce is common in seeds and spores but rare in leaves and other vegetative green tissues.

39 spersal) act on fungal community assembly in leaves and roots early in host development and when sorg

40 obtained for mechanically inoculated rosette leaves and systemically infected cauline leaves and infl

41 to controlling the movement of toxic ions to leaves and, therefore, can be seen as a mechanism to cop

42 tionship in a C(4) plant between delta(13) C(leaf) and WUE(plant) under well watered and water-limite

43 (tuber), Brassica oleracea var. capitata L. (leaf), and Bixa orellana L. (seed) had the highest nutri

44 the water pathways between the soil and the leaf, and root radial conductivity is itself defined by

45 ynthesis efficiency and growth rate, smaller leaves, and lower grain yields than wild-type (WT) plant

46 om mature, developing, and germinated seeds, leaves, and roots exposed to different abiotic stresses.

47 conducted a global evaluation of SOX against leaf- and ecosystem-level observations.

48 ed a weak positive correlation between basal leaf angle and pathogenicity level in Johnsongrass.

49 When basal leaf angle distribution data were correlated with pathog

50 this interaction facilitates RH1 function in leaf anthocyanin marking formation.

51 hotosynthetic CO(2) assimilation per unit of leaf area (A) has the potential to increase yield.

52 There were significant increases in all leaf area and biomass markers in response to [CO(2)] wit

53 The relative contribution of the peak leaf area and vegetation stress intensity was highly var

54 ntly reduced the eCO(2) -induced increase in leaf area by 14.3%, mirroring the aboveground biomass re

55 ure in winter and proceeding to moisture and leaf area during the summer.

56 observed net primary productivity (NPP) and leaf area index (LAI) after 100 years and predicted comp

57 ct conditions strongly depended on GDD, MTA, leaf area index (LAI) and the interaction between MTA an

58 We then examined the proportional change in leaf area index (LAI) as one potential biological respon

59 Leaf area index data from satellites along with climate

60 easured grain yield, plant biomass, plant N, leaf area index, harvest index and in-season soil water

61 reatest in the multi-group scenario when its leaf area is significantly larger than each of its indiv

62 ntitative trait loci (QTLs) that mediate how leaf area scales with leaf mass and how such leaf allome

63 significant; however, significant trends in leaf area, branch number and total above-ground biomass

64 Leaf area, the leaf economics spectrum (indexed by LMA a

65 taneously by tall stature and small specific leaf area.

66 models with and without the inclusion of Psi(leaf) as an additional predictor variable influence the

67 ed with pathogenicity test data from excised-leaf assays for three isolates of Colletotrichum subline

68 result in AM initiation only in the axils of leaves at a certain age.

69 We found a positive correlation between Psi(leaf) at 50% loss of K(leaf) (K(leaf) P(50) ) and maximu

70 illary meristems, which are initiated from a leaf axil meristematic cell population originally detach

71 level of specular reflection (gloss) of the leaf background leads to an increase in the survival of

72 trated a causal role of a properly assembled leaf bacterial community in phyllosphere health.

73 ed the obligate partnership between tortoise leaf beetles (Chrysomelidae: Cassidinae) and their pecti

74 rcane (Saccharum officinarum L.) cultivation leaves behind around 20 t ha(-1) of biomass residue afte

75 This is despite the leaves being exposed to water twice during formation and

76 antisense strand does not alter the 'clover leaf' bend and sugar puckers that are critical for ancho

77 net rates of CO(2) assimilation, (ii) on how leaf biochemical and anatomical factors influence g(m) ,

78 N. sylvestris resulted in a range of severe leaf blade distortions, indicating important role in bla

79 Direct measurements of leaves by attenuated total reflectance Fourier-transform

80 Nevertheless, leaf C:N was low for summer- versus spring-collected pla

81 C(4) plants, theoretical models suggest that leaf carbon isotope composition (delta(13) C), when the

82 Alternatively, leaf carbon stable isotope composition (delta(13) C(leaf

83 of polycomb-group proteins, including CURLY LEAF (CLF) and LIKE HETERCHROMATIN PROTEIN 1 (LHP1), for

84 c water-use efficiency (WUE(i) , the rate of leaf CO(2) assimilation relative to water loss via stoma

85 nduction describes the transient increase in leaf CO(2) uptake with an increase in light.

86 beetles were more likely to choose undamaged leaves compared to damaged leaves or those exposed to vo

87 ogenins in 20 differently sourced nightshade leaves, comprising two African species Solanum scabrum a

88 Nonetheless, olive leaves (containing thin branches), which are separated d

89 on, which opens stomatal pores to facilitate leaf cooling.

90 In this work, six olive leaves cultivars, including three wild cultivars, and tw

91 pressorial base(1-4), forcing it through the leaf cuticle where it elongates invasive hyphae in under

92 Specifically, leaf damage inflicted by insect herbivory or mechanical

93 l of bioactive phytochemical, mahanine in MK leaves depending upon geographical location, weather sui

94 llulosic biomasses, the composition of olive leaves depends on cultivar and to know it is essential f

95 hydrates (NSC) model (FORCCHN2) that couples leaf development and phenology to investigate the relati

96 Such advances in our understanding of leaf development have important implications for potenti

97 e2fb mutant and overexpression lines during leaf development in Arabidopsis (Arabidopsis thaliana),

98 The effect of leaf development on mid-infrared (MIR) reflectance, and

99 As leaf development progresses and cells differentiate, the

100 The plant tissue (fruit or leaves) did not influence C. fioriniae repellency effect

101 Multi-hour R(N) measurements following leaf disc exposure to a wide array of primary carbon met

102 found strong bivariate relationships of both leaf dry matter content (LDMC) and leaf osmotic potentia

103 genes and down-regulation of 2,695 genes in leaf during the infection process.

104 ti-nutritive compounds in African nightshade leaves during moist cooking.

105 Given a binary tree [Formula: see text] of n leaves, each leaf labeled by a string of length at most

106 c responses contrary to the direction of the leaf economic spectrum.

107 Leaf area, the leaf economics spectrum (indexed by LMA and N(area) ) an

108 on could increase P use efficiency; however, leaf entry pathways for inorganic phosphate ion (Pi) upt

109 In leaf epidermal cells where a polygonal ER network can be

110 ts (e.g., bird feathers, insect wings, plant leaves, etc.) are superhydrophobic with rough surfaces a

111 ntial to provide breakthrough assessments of leaf evolution and plant phylogenetic diversity at globa

112 A crude extract of Schinus terebinthifolia leaves exhibited 80% inhibition at 256 ug/mL and underwe

113 Here, direct incubation of leaf explants from the non-medicinal plant Arabidopsis t

114 Olive leaves extract (OLE) was spray-dried with maltodextrin (

115 nd components such as trunk (stem and bark), leaf, flower, seed, and root.

116 In this study, the chemical composition of leaves, flowers and stems of jambu cultivated in hydropo

117 of defensive odors secreted from (1) eastern leaf-footed bugs (Leptoglossus phyllopus, Hemiptera), (2

118 The pinnately lobed Aptian leaf fossil Mesodescolea plicata was originally describe

119 surement of electrolyte leakage to determine leaf freezing tolerance and expression analyses of cold-

120 Remarkably, Welwitschiophyllum leaves from Early Cretaceous, Brazil provide the first c

121 exes and epidermal oil cells with angiosperm leaves from the lower Potomac Group.

122 Food choice experiments with leaves from wild-type and SOT1 knockdown trees suggest t

123 and antioxidant capacity associated with the leaves, fruit, and flowers.

124 Plant stomata play a crucial role in leaf function, controlling water transpiration in respon

125 scales using stable carbon isotope analysis, leaf gas exchange and eddy covariance (EC) fluxes.

126 ught release, we found a gradual recovery of leaf gas exchange to 50% to 60% of control values.

127 C(4) photosynthesis in grasses, we examined leaf gas exchange, anatomy and ultrastructure, and tissu

128 omatal and mesophyll development for optimal leaf gas exchange, and that both genetic and physiologic

129 e growth and lower water loss via changes in leaf gas exchange.

130 e quantitatively test model against multiple leaf gas-exchange datasets.

131 xperimental reefs supplemented with mangrove leaves grown away from humans attracted more fish recrui

132 sity of species than reefs supplemented with leaves grown near humans.

133 ort (NCE, photosynthesis minus the C cost of leaf growth and maintenance) as a fitness proxy.

134 hat, even when undamaged, shows JA-dependent leaf growth restriction.

135 Functionally, leaf growth was decoupled from photosynthesis.

136 rbon stable isotope composition (delta(13) C(leaf) ) has been suggested as a potential time-integrate

137 y the discontinuous frost pattern on natural leaves, here we report findings on the condensation fros

138 Clarifying the coordination of leaf hydraulic traits with gas exchange across closely-r

139 may also coincide with new modifications in leaf hydraulics and growth habit during angiosperm diver

140 ticle concluded that the extract substitutes leaves in bread as a product of a high benefit.

141 s: Results from experiments with Arabidopsis leaves in conventional controlled environments are not n

142 acteristics of oilseed rape (Brassica napus) leaves in different growth stages under different K leve

143 ucting transcriptomic analysis of developing leaves in the WT and the three mutants we identified dif

144 temperature, including heat avoidance, where leaves increase water loss to evaporatively cool regardl

145 While thermal treatment of lettuce leaves increases carotenoid availability, resulting in h

146 Hence, we performed RNA-Seq of leaf infected with or without DB to understand the molec

147 we examined the global AS changes in tomato leaves infected with Phytophthora infestans, the infamou

148 However, leaf initiation is slower and there is no change in shoo

149 s allocation, plant and leaf morphology) and leaf ionomic traits.

150 These results demonstrate that delta(13) C(leaf) is genetically linked to WUE(plant) , likely to be

151 rrelation between Psi(leaf) at 50% loss of K(leaf) (K(leaf) P(50) ) and maximum K(leaf) (K(leaf-max)

152 ss of K(leaf) (K(leaf) P(50) ) and maximum K(leaf) (K(leaf-max) ) across species.

153 y tree [Formula: see text] of n leaves, each leaf labeled by a string of length at most k, and a bina

154 esults concerning ranked genealogies without leaf labels unlock opportunities in the analysis of evol

155 uencing platform and performed the L. camara leaf (LCL) and root (LCR) de novo transcriptome analyses

156 tigated how the choice of four commonly used leaf-level g(s) models with and without the inclusion of

157 ning, we find spatially uniform increases in leaf-level intercellular CO(2) and intrinsic water use e

158 us, faster photosynthetic rates, and shorter leaf life span compared to non-wetland plants.

159 The husk-the leaf-like outer covering of maize ear-has multiple funct

160 ch organoids comprised of a highly compacted leaf-like part connected to the adipose tissue that can

161 ticulum and the chloroplast to lower 16:0 in leaf lipids of fab1 plants.

162 We conducted a moss transplant and leaf litter manipulation experiment at three sites with

163 dators) in field mesocosms replicated in the leaf-litter community of Iberian beech forests that diff

164 highest beta-glucuronidase expression in the leaf, male and female flowers, stem, and root tissues.

165 hesis activator that specifically determines leaf marking formation depending on its C-terminal activ

166 alogs RH1 and RH2 in determining anthocyanin leaf markings in M. truncatula, providing a multidimensi

167 QTLs) that mediate how leaf area scales with leaf mass and how such leaf allometry, under the control

168 nitrogen and phosphorus concentrations, and leaf mass per area) and performance proxies (aboveground

169 s observed in non-wetland plants, with lower leaf mass per area, higher leaf nitrogen and phosphorus,

170 ommonly employed traits like wood density or leaf mass per area, yield the power to predict growth.

171 ted using six chloroplast DNA sequences from leaf material from across the BI and the native range.

172 eaf) (K(leaf) P(50) ) and maximum K(leaf) (K(leaf-max) ) across species.

173 dose increases, the bioimpedance of a plant leaf measured at a frequency of 1 kHz linearly decreases

174 We measured functional traits reflecting leaf metabolism and associated with growth (respiration

175 d Whiteman shows that herbivory reshapes the leaf microbiome and increases susceptibility to potentia

176 and inconsistent pleiotropic effects on the leaf microbiome in maize.

177 Bacterial and fungal leaf microbiomes of the resulting near-isogenic lines we

178 For leaf microbiomes, these results were supported by the ob

179 Maule staining of stalk and leaf midrib sections from SbF5H overexpression lines ind

180 r modularity with fertiliser addition, while leaf miner-parasitoid networks showed a rise in generali

181 lots had a significantly higher abundance of leaf miners and parasitoids and a significantly lower ab

182 in particular, as well as gall-inducing and leaf-mining insects, manipulate plant development to for

183 centrate (PC) from Moringa Oleifera defatted leaves (MODL) by enzymatic extraction using Viscozyme L

184 we use longitudinal data from wild Phayre's leaf monkeys to test the hypothesis that fluctuations in

185 crease in absolute triacylglycerol levels in leaves, more than 4-fold higher than in wild-type plants

186 nd a considerable range of fruit quality and leaf morphological traits.

187 ological (growth, mass allocation, plant and leaf morphology) and leaf ionomic traits.

188 wn seedlings, correlating with reductions in leaf N and chlorophyll concentrations.

189 lants, with lower leaf mass per area, higher leaf nitrogen and phosphorus, faster photosynthetic rate

190 limation to dimming that gradually increased leaf nitrogen concentration.

191 empirical relationships with proxies such as leaf nitrogen/chlorophyll content or hyperspectral refle

192 ess of carbon uptake; or heat failure, where leaves non-adaptively lose water also regardless of carb

193 We quantify vein networks for leaves of 260 southeast Asian tree species in samples of

194 ttime O(2) consumption rate (R(N)) in mature leaves of Arabidopsis (Arabidopsis thaliana).

195 assess potential pathways for water entry in leaves of beech, a widely distributed tree species from

196 genes showed similar expression patterns in leaves of both desiccation-tolerant and -sensitive speci

197 Microscopic examination of the Cg-challenged leaves of chilli-CgCOM1i lines revealed highly suppresse

198 roots and A. thaliana roots compared to the leaves of each respective species.

199 es for differential expression of genes from leaves of ecologically well-characterized ecotypes of tu

200 ransiently expressed with these effectors in leaves of Nicotiana glutinosa.

201 xidant activity were analyzed in berries and leaves of nine cultivars of sea buckthorn (Hippophae rha

202 , which is 16.9 times higher than that of MK-leaves of north-eastern part of India (which measured as

203 Whereas leaves of rice (Oryza sativa) cultivar Nipponbare predom

204 quantitative analysis data comprised that MK-leaves of southern part of India contains highest amount

205 Larvae damaged many leaves on a plant but removed relatively little tissue f

206 st-step towards representing mechanistically leaf ontogenetic processes into physiological and ecosys

207 photosynthesis beside the other organs like leaves or the flag leaf.

208 choose undamaged leaves compared to damaged leaves or those exposed to volatile cues of damage.

209 s of both leaf dry matter content (LDMC) and leaf osmotic potential Psi(osm) with S(spp) .

210 limate warming is currently advancing spring leaf-out of temperate and boreal trees, enhancing net pr

211 ately predicted reductions in the advance of leaf-out.

212 eritable (H(2) = 0.85), as was mid-pod lower leaf P concentrations under normal P conditions (H(2) =

213 between Psi(leaf) at 50% loss of K(leaf) (K(leaf) P(50) ) and maximum K(leaf) (K(leaf-max) ) across

214 We provide evidence that leaf papillae function as specialized structures for Na(

215 and requires the loading of sucrose into the leaf phloem and, at the sink end, its import into the gr

216 Previous studies provide evidence that non-leaf photosynthesis could be an unexploited potential ta

217 n for TLA, N addition significantly enhanced leaf photosynthetic rate per area (A(area) , +12.6%), st

218 fluence and blue light-dependent changes in leaf positioning and morphology.

219 3 (WOX3) homolog expressed at the margins of leaf primordia, and is required for mediolateral outgrow

220 Acute SARS-CoV-2 infection leaves protracted beneficial (ie, activation of T cells)

221 Ala as the most potent stimulators of plant leaf R(N) Using metabolite combinations, we discovered m

222 The fungal-induced change in leaf reflectance may have altered visual cues used by th

223 Leaf removal (LR), shoot thinning (ST) and their combina

224 The impact of crop level and leaf removal on Istrian Malvasia (Vitis vinifera L.) whi

225 ect has often been interpreted as a shift in leaf respiratory metabolism and thus used widely to meas

226 We also found that TARK1 OE in leaves resulted in increased susceptibility to bacterial

227 les of these MADS-box genes were analyzed in leaves, roots, stem sections and after hormones treatmen

228 The wheat leaf rust fungus, Puccinia triticina, is found in the ma

229 RNA-seq profiling was done on leaf samples collected at 0, 1, 3, and 8 days post inocu

230 ce images recorded on cross sections of rice leaf samples.

231 amined transcriptome changes during seasonal leaf senescence in Populus trichocarpa Nisqually-1, the

232 Leaf senescence is driven by the expression of senescenc

233 on regulates the expression of SAGs and thus leaf senescence remain elusive.

234 o better understand the molecular control of leaf senescence, we examined transcriptome changes durin

235 of promoter sequence motifs associated with leaf senescence.

236 ver, comprehensive intraspecific analyses of leaf shape variation across variable environments is sur

237 We showed that extensive leaf shape variation exists within I. batatas, and ident

238 Leaf shape, a spectacularly diverse plant trait, varies

239 ter activity was observed in roots, ligules, leaves, sheaths, pollen grains, and surrounding the vasc

240 Source leaves, sink leaves, stems and storage roots were harves

241 stems and decreased apical height growth and leaf size.

242 n of RNA synthesis is fully retracted, which leaves space in the active-site cavity for RNA elongatio

243 Leaf spectral measurements were paired with a number of

244 iral life cycles, the structures of cucumber leaf spot virus (CLSV; genus Aureusvirus) and red clover

245 microscopy (cryo-EM) structures of cucumber leaf spot virus and red clover necrotic mosaic virus.

246 several agro-morphological traits related to leaves, stems and roots with high heritability.

247 Source leaves, sink leaves, stems and storage roots were harvested during st

248 C(3) species, g(m) is influenced by diverse leaf structural and anatomical traits; however, little i

249 salt-sensitive Panicoid crops with analogous leaf structures.

250 situ hybridization assays of maize embryonic leaves suggested that maize ANT1 (ZmANT1) regulates vasc

251 taxonomic shifts were detected in the tomato leaf surface (phylloplane).

252 an approach to understand how Pi crosses the leaf surface and assimilates to meet plant nutrient dema

253 rowth is intimately related to the effective leaf surface area (ELSA), identifying genes controlling

254 that 72% of empty trichomes refilled during leaf surface wetting and microscopic investigations reve

255 er and tomato fruit surfaces, but not tomato leaf surfaces, increased significantly and remained elev

256 ften accompanied by rain that results in wet leaf surfaces.

257 n respiration for a 10 degrees C increase in leaf temperature).

258 ndent stomatal closure, leading to increased leaf temperature, lower photosynthetic carbon assimilati

259 efine the ease of flow of the gas within the leaf, termed mesophyll conductance.

260 nd UBP13 were downregulated produced smaller leaves that contained fewer and smaller cells.

261 We show here that ISOW leaves the boundary and spreads into the interior toward

262 enes also contribute to cell division in the leaf, the gynoecium and the ovules in A. fimbriata.

263 interface with ATP-bound HSP70 dimers, which leaves them intact and thereby eliminates an inhibitory

264 Leaves themselves decreased the quality of the bread, wh

265 r the formation of both planar and nonplanar leaves through adaxial-abaxial domains of gene activity

266 ent post-harvest drying techniques for betel leaves through the quantitative analysis of unambiguousl

267 l chemotactic transport of bacteria within a leaf tissue in response to photosynthesis occurring with

268 osynthesis were down-regulated in the yellow leaf tissue.

269 nd toward photosynthetic products within the leaf tissue.

270 dophytic phyllosphere microbiota and display leaf-tissue damage associated with dysbiosis.

271 In presenescent leaf tissues, PP2A-B'gamma is also required to negativel

272 ucrose from photosynthetically active source leaves to seed sinks.

273 ls in coordinating the response of different leaves to stress.

274 of carboxylation (V(cmax) ) is an essential leaf trait determining the photosynthetic capacity of pl

275 Several publications have examined leaf-trait and carbon-cycling shifts along an Amazon-And

276 show coordinated relationships between plant leaf traits and their capacity to predict ecosystem func

277 Variation in leaf traits due to VPC are likely to provide distinct be

278 However, how leaf traits will change within species and whether inter

279 ronger predictors of fungal communities than leaf traits.

280 Leaf trichomes on soybeans were not found to be responsi

281 d the role of nonstructural carbohydrates in leaf turgor maintenance.

282 models including mycorrhizal association and leaf venation, suggesting substantial modifications in f

283 t on hexyl glucoside, which releases a green leaf volatile with a grassy aroma when hydrolyzed, but n

284 m C(4) to C(4) -CAM hybrid photosynthesis in leaves was strictly under environmental control.

285 dry continuum depending on how they regulate leaf water potential (Psi(L) ).

286 functioning despite diurnal fluctuations in leaf water potential and the role of nonstructural carbo

287 essed trees experiencing significantly lower leaf water potentials, and higher, but variable, levels

288 de that is widely used for controlling broad leaf weeds.

289 Brassicaceae leaves were also moderate dietary sources of Se, Ni, Zn

290 rall, unfermented and fermented P. pellucida leaves were best dried with microwaving and freeze dryin

291 es regardless of fertilization rate, whereas leaves were effective only against HeLa cell line.

292 uantitative trait loci (QTL) for delta(13) C(leaf) were found and co-localized with transpiration, bi

293 we measured the effects of diffuse light and leaf wetting on photosynthesis in canopy species from a

294 21- and 22-nt) were detected in non-treated leaves, which indicates endogenous processing and transp

295 We show that the decrease in apple leaf width with increasing altitude is controlled by a b

296 hk5 and hk6 single mutants, the root growth, leaf width, inflorescence architecture and/or floral dev

297 intensify, tall trees with drought-sensitive leaves will be most vulnerable to immediate and longer-t

298 icits that coincide with flowering result in leaf wilting, necrosis, tassel browning, and sterility,

299 lant shares the presence of gum ducts inside leaves with its presumed extant relative the gnetalean W

300 Repeated pregnancy leaves young mothers nutritionally deprived which may in