Australian New Crops Info 2016
Supported by the Rural Industries Research and Development Corporation

Listing of Interesting Plants of the World:

Nicotiana longiflora

 

 

This species is usually known as:

Nicotiana longiflora

 

This species has also been known as:

Nicotiana longiflora var. acutiflora, Nicotiana longiflora var. breviflora, Nicotiana longiflora var. grandifolia, Nicotiana longiflora var. oligantha, Nicotiana longiflora var. pauciflora

 

Common names:

Longflower Tobacco

 

 

Trends (five databases) 1901-2013:
[Number of papers mentioning Nicotiana longiflora: 122]

 

 

Popularity of Nicotiana longiflora over time
[Left-hand Plot: Plot of numbers of papers mentioning Nicotiana longiflora (histogram and left hand axis scale of left-hand plot) and line of best fit, 1901 to 2013 (equation and % variation accounted for in box); Right-hand Plot: Plot of a proportional micro index, derived from numbers of papers mentioning Nicotiana longiflora as a proportion (scaled by multiplying by one million) of the approximate total number of papers available in databases for that year (frequency polygon and left-hand axis scale of right-hand plot) and line of best fit, 1901 to 2013 (equation and % variation accounted for in box)] 

[For larger charts showing the numbers of papers that have mentioned this species over years, select this link; there are links to come back from there]

 

Keywords

[Total number of keywords included in the papers that mentioned this species: 396]

 

Nicotiana (11), Nicotiana longiflora (6), flavonoids (4), Nicotiana tabacum (4), essential oils (3), fungal diseases of plants (3), gene expression (3), Nicotiana plumbaginifolia (3), UV-B (3), Adaptability (2), Allelopathic agent (2), Andean community London (2), Andean traditional medicine (2), Asteraceae (2), bacteria (2), Bemisia tabaci (2), Bisabolanoids (2), chemical constituents of plants (2), defence <ARROW (2), Defense genes (2), Flourensia campestris (2), Gossypium hirsutum (2), herbivory (2), Internet resource (2), leaves (2), Manduca sexta (2), Nicotiana glauca (2), Phenylpropanoid/flavonoids biosynthetic pathway (2), photosynthesis (2), phytochrome (2), Phytotoxic activity (2), plant health (2), plant pathogenic fungi (2), Plant resistance (2), Polyphagy (2), preference (2), Resilience (2), secondary metabolites (2), Sesquiterpenoids (2), Solanaceae (2), Solanum lycopersicum var. lycopersicum (2), species differences (2), Suppression subtractive hybridization libraries (2), tobacco (2), Urban ethnobotany (2), Volatile organic compounds (2), Volatiles (2), Wheat (2), (−)-Hamanasic acid A (1), (−)-Hamanasic acid A (1), 17-hydroxygeranyllinalool diterpene glycosides (HGL-DTGs) (1), 2-D PAGE (1), agriculture (1), Agrobacterium tumefaciens (1), agronomic traits (1), Air pollution (1), Alatae (1), Aldoximes (1), AllopolyplDOWN>oidy (1), Amélioration génétique (1), amino acids (1), anthocyanins (1), Antioxidant (1), Arabidopsis thaliana (1), Artificial lighting (1), artificial selection (1), Ascorbate peroxidase (1), Atmospheric change (1), auxin (1), Bayoud (1), beneficial plant–microbe interactions - inducing resistance in plants (1), bHLH (1), Biotechnology-derived plant (1), botany (1), Brassica nigra (1), Brassicaceae (1), Breeding for resistance (1), Calcium signaling (1), carbon transport (1), Cardio-circulatory diseases (1)…..

 

[If all keywords are not here (as indicated by .....), they can be accessed from this link; there are links to come back from there]

 

 

Most likely scope for crop use/product (%):
[Please note: When there are only a few papers mentioning a species, care should be taken with the interpretation of these crop use/product results; as well, a mention may relate to the use of a species, or the context in which it grows, rather than a product]

 

boundary (64.27), shade (14.99), genetics (2.97), timber (2.55), honey (2.15), allelopathy (1.63), weed (1.54), fruit (1.50), starch (0.92), poison (0.79)…..

 

[To see the full list of crop use/product outcomes, from searching abstracts of the papers that have mentioned this species, select this link; details of the analysis process have also been included; there are links to come back from there]

 

 

Recent mentions of this species in the literature:
[since 2012, with links to abstracts; The references from 1901-2013 which have been used for the trend, keyword and crop use/product analyses below, are listed below these references]

 

Santhanam R, Oh Y, Kumar R, Weinhold A, Luu VT, Groten K and Baldwin IT (2017) Specificity of root microbiomes in native-grown Nicotiana attenuata and plant responses to UVB increase Deinococcus colonization. Molecular Ecology, n/a-n/a. http://dx.doi.org/10.1111/mec.14049

Cerrudo I, Caliri-Ortiz ME, Keller MM, Degano ME, Demkura PV and Ballare CL (2016) Exploring growth-defense tradeoffs in Arabidopsis. Phytochrome B inactivation requires JAZ10 to suppress plant immunity but not to trigger shade avoidance responses. Plant, Cell & Environment, n/a-n/a. http://dx.doi.org/10.1111/pce.12877

Cortés LE, Weldegergis BT, Boccalandro HE, Dicke M and Ballaré CL (2016) Trading direct for indirect defense? Phytochrome B inactivation in tomato attenuates direct anti-herbivore defenses whilst enhancing volatile-mediated attraction of predators. New Phytologist 212, 1057-1071. http://dx.doi.org/10.1111/nph.14210

Poltronieri P (2016) Chapter 6 - Tobacco Seed Oil for Biofuels. In Biotransformation of Agricultural Waste and By-Products (Ed.^(Eds  pp. 161-187. (Elsevier). //www.sciencedirect.com/science/article/pii/B9780128036228000069

Salas Gervassio NG, Luna MG, Lee S, Salvo A and Sánchez NE (2016) Trophic web associated with the South American tomato moth Tuta absoluta: implications for its conservation biological control in Argentina. Agricultural and Forest Entomology 18, 137-144. http://dx.doi.org/10.1111/afe.12146

Vanhaelewyn L, Prinsen E, Van Der Straeten D and Vandenbussche F (2016) Hormone-controlled UV-B responses in plants. J. Exp. Bot. 67, 4469-4482. http://jxb.oxfordjournals.org/cgi/content/abstract/67/15/4469

Ferrieri AP, Arce CCM, Machado RAR, Meza-Canales ID, Lima E, Baldwin IT and Erb M (2015) A Nicotiana attenuata cell wall invertase inhibitor (NaCWII) reduces growth and increases secondary metabolite biosynthesis in herbivore-attacked plants. New Phytologist 208, 519-530. http://dx.doi.org/10.1111/nph.13475

Mazza CA and Ballaré CL (2015) Photoreceptors UVR8 and phytochrome B cooperate to optimize plant growth and defense in patchy canopies. New Phytologist 207, 4-9. http://dx.doi.org/10.1111/nph.13332

Rojas H, Floyd B, Morriss SC, Bassham D, MacIntosh GC and Goldraij A (2015) NnSR1, a class III non-S-RNase specifically induced in Nicotiana alata under phosphate deficiency, is localized in endoplasmic reticulum compartments. Plant Science 236, 250-259. //www.sciencedirect.com/science/article/pii/S0168945215001120

Wargent JJ, Nelson BCW, McGhie TK and Barnes PW (2015) Acclimation to UV-B radiation and visible light in Lactuca sativa involves up-regulation of photosynthetic performance and orchestration of metabolome-wide responses. Plant, Cell & Environment 38, 929-940. http://dx.doi.org/10.1111/pce.12392

Xu X-Q, Cheng G, Duan L-L, Jiang R, Pan Q-H, Duan C-Q and Wang J (2015) Effect of training systems on fatty acids and their derived volatiles in Cabernet Sauvignon grapes and wines of the north foot of Mt. Tianshan. Food Chemistry 181, 198-206. //www.sciencedirect.com/science/article/pii/S0308814615002721

Zavala JA, Mazza CA, Dillon FM, Chludil HD and BallarÉ CL (2015) Soybean resistance to stink bugs (Nezara viridula and Piezodorus guildinii) increases with exposure to solar UV-B radiation and correlates with isoflavonoid content in pods under field conditions. Plant, Cell & Environment 38, 920-928. http://dx.doi.org/10.1111/pce.12368

Cargnel MD, Demkura PV and Ballaré CL (2014) Linking phytochrome to plant immunity: low red : far-red ratios increase Arabidopsis susceptibility to Botrytis cinerea by reducing the biosynthesis of indolic glucosinolates and camalexin. New Phytologist 204, 342-354. http://dx.doi.org/10.1111/nph.13032

Leone M, Keller MM, Cerrudo I and Ballaré CL (2014) To grow or defend? Low red : far-red ratios reduce jasmonate sensitivity in Arabidopsis seedlings by promoting DELLA degradation and increasing JAZ10 stability. New Phytologist 204, 355-367. http://dx.doi.org/10.1111/nph.12971

Mourelos CA, Malbrán I, Balatti PA, Ghiringhelli PD and Lori GA (2014) Gramineous and non-gramineous weed species as alternative hosts of Fusarium graminearum, causal agent of Fusarium head blight of wheat, in Argentina. Crop Protection 65, 100-104. //www.sciencedirect.com/science/article/pii/S0261219414002336

de Wit M, Spoel SH, Sanchez-Perez GF, Gommers CMM, Pieterse CMJ, Voesenek LACJ and Pierik R (2013) Perception of low red:far-red ratio compromises both salicylic acid- and jasmonic acid-dependent pathogen defences in Arabidopsis. The Plant Journal 75, 90-103. http://dx.doi.org/10.1111/tpj.12203

ĐInh ST, GÁLis I and Baldwin IT (2013) UVB radiation and 17-hydroxygeranyllinalool diterpene glycosides provide durable resistance against mirid (Tupiocoris notatus) attack in field-grown Nicotiana attenuata plants. Plant, Cell & Environment 36, 590-606. http://dx.doi.org/10.1111/j.1365-3040.2012.02598.x

Eberle CA, Anderson NO, Clasen BM, Hegeman AD and Smith AG (2013) PELPIII: the class III pistil-specific extensin-like Nicotiana tabacum proteins are essential for interspecific incompatibility. The Plant Journal 74, 805-814. http://dx.doi.org/10.1111/tpj.12163

Ferrieri AP, Agtuca B, Appel HM, Ferrieri RA and Schultz JC (2013) Temporal Changes in Allocation and Partitioning of New Carbon as 11C Elicited by Simulated Herbivory Suggest that Roots Shape Aboveground Responses in Arabidopsis. Plant Physiology 161, 692-704. http://www.plantphysiol.org/cgi/content/abstract/161/2/692

Fukaya M, Uesugi R, Ohashi H, Sakai Y, Sudo M, Kasai A, Kishimoto H and Osakabe M (2013) Tolerance to Solar Ultraviolet-B Radiation in the Citrus Red Mite, An Upper Surface User of Host Plant Leaves. Photochemistry and Photobiology 89, 424-431. http://dx.doi.org/10.1111/php.12001

Jimenez-Duran K, McClure B, Garcia-Campusano F, Rodriguez-Sotres R, Cisneros J, Busot G and Cruz-Garcia F (2013) NaStEP: A Proteinase Inhibitor Essential to Self-Incompatibility and a Positive Regulator of HT-B Stability in Nicotiana alata Pollen Tubes. Plant Physiology 161, 97-107. http://www.plantphysiol.org/cgi/content/abstract/161/1/97

Kegge W, Weldegergis BT, Soler R, Eijk MV-V, Dicke M, Voesenek LACJ and Pierik R (2013) Canopy light cues affect emission of constitutive and methyl jasmonate-induced volatile organic compounds in Arabidopsis thaliana. New Phytologist 200, 861-874. http://dx.doi.org/10.1111/nph.12407

Mazza CA, Giménez PI, Kantolic AG and Ballaré CL (2013) Beneficial effects of solar UV-B radiation on soybean yield mediated by reduced insect herbivory under field conditions. Physiologia Plantarum 147, 307-315. http://dx.doi.org/10.1111/j.1399-3054.2012.01661.x

Morales LO, Brosche M, et al. (2013) Multiple Roles for UV RESISTANCE LOCUS8 in Regulating Gene Expression and Metabolite Accumulation in Arabidopsis under Solar Ultraviolet Radiation. Plant Physiology 161, 744-759. http://www.plantphysiol.org/cgi/content/abstract/161/2/744

Potter KA and Woods HA (2013) Immobile and tough versus mobile and weak: effects of ultraviolet B radiation on eggs and larvae of Manduca sexta. Physiological Entomology 38, 246-252. http://dx.doi.org/10.1111/phen.12030

Somavilla NS, Cosenza GP, Fagg CW and Brandão MGL (2013) Morpho-anatomy and chemical profi le of native species used as substitutes of quina (Cinchona spp.) in Brazilian traditional medicine. Part I: Polyouratea hexasperma. Revista Brasileira de Farmacognosia 23, 592-599. //www.sciencedirect.com/science/article/pii/S0102695X13700747

Wargent JJ and Jordan BR (2013) From ozone depletion to agriculture: understanding the role of UV radiation in sustainable crop production. New Phytologist 197, 1058-1076. http://dx.doi.org/10.1111/nph.12132

Alon M, Elbaz M, Ben-Zvi MM, Feldmesser E, Vainstein A and Morin S (2012) Insights into the transcriptomics of polyphagy: Bemisia tabaci adaptability to phenylpropanoids involves coordinated expression of defense and metabolic genes. Insect Biochemistry and Molecular Biology 42, 251-263. http://www.sciencedirect.com/science/article/pii/S0965174811002207

Ballare CL, Mazza CA, Austin AT and Pierik R (2012) Canopy Light and Plant Health. Plant Physiology 160, 145-155. http://www.plantphysiol.org

Burrows GE and Tyrl RJ (2012) Solanaceae Juss. In Toxic Plants of North America (Ed.^(Eds  pp. 1130-1176. (Wiley-Blackwell). http://dx.doi.org/10.1002/9781118413425.ch69

Cerrudo I, Keller MM, Cargnel MD, Demkura PV, de Wit M, Patitucci MS, Pierik R, Pieterse CMJ and Ballare CL (2012) Low Red/Far-Red Ratios Reduce Arabidopsis Resistance to Botrytis cinerea and Jasmonate Responses via a COI1-JAZ10-Dependent, Salicylic Acid-Independent Mechanism. Plant Physiology 158, 2042-2052. http://www.plantphysiol.org/cgi/content/abstract/158/4/2042

Demkura PV and Ballare CL (2012) UVR8 Mediates UV-B-Induced Arabidopsis Defense Responses against Botrytis cinerea by Controlling Sinapate Accumulation. Mol Plant, sss025. http://mplant.oxfordjournals.org/cgi/content/abstract/sss025v1

ĐInh ST, GÁLis I and Baldwin IT (2012) UVB radiation and 17-hydroxygeranyllinalool diterpene glycosides provide durable resistance against mirid (Tupiocoris notatus) attack in field-grown Nicotiana attenuata plants. Plant, Cell & Environment, no-no. http://dx.doi.org/10.1111/j.1365-3040.2012.02598.x

Foyer CH, Neukermans J, Queval G, Noctor G and Harbinson J (2012) Photosynthetic control of electron transport and the regulation of gene expression. J. Exp. Bot. 63, 1637-1661. http://jxb.oxfordjournals.org/cgi/content/abstract/63/4/1637

Fukaya M, Uesugi R, Ohashi H, Sakai Y, Sudo M, Kasai A, Kishimoto H and Osakabe M (2012) Tolerance to Solar Ultraviolet-B Radiation in the Citrus Red Mite, An Upper Surface User of Host Plant Leaves. Photochemistry and Photobiology, n/a-n/a. http://dx.doi.org/10.1111/php.12001

Jansen MAK and Bornman JF (2012) UV-B radiation: from generic stressor to specific regulator. Physiologia Plantarum 145, 501-504. http://dx.doi.org/10.1111/j.1399-3054.2012.01656.x

Kaczorowski RL, Seliger AR, Gaskett AC, Wigsten SK and Raguso RA (2012) Corolla shape vs. size in flower choice by a nocturnal hawkmoth pollinator. Functional Ecology 26, 577-587. http://dx.doi.org/10.1111/j.1365-2435.2012.01982.x

Mahajan M, Joshi R, Gulati A and Yadav SK (2012) Increase in flavan-3-ols by silencing flavonol synthase mRNA affects the transcript expression and activity levels of antioxidant enzymes in tobacco. Plant Biology 14, 725-733. http://dx.doi.org/10.1111/j.1438-8677.2011.00550.x

Mazza CA, Giménez PI, Kantolic AG and Ballaré CL (2012) Beneficial effects of solar UV-B radiation on soybean yield mediated by reduced insect herbivory under field conditions. Physiologia Plantarum, n/a-n/a. http://dx.doi.org/10.1111/j.1399-3054.2012.01661.x

Mewis I, Schreiner M, Nguyen CN, Krumbein A, Ulrichs C, Lohse M and Zrenner R (2012) UV-B Irradiation Changes Specifically the Secondary Metabolite Profile in Broccoli Sprouts: Induced Signaling Overlaps with Defense Response to Biotic Stressors. Plant Cell Physiol. 53, 1546-1560. http://pcp.oxfordjournals.org/cgi/content/abstract/53/9/1546

Natalis LC and Wesselingh RA (2012) Post-pollination barriers and their role in asymmetric hybridization in Rhinanthus (Orobanchaceae). Am. J. Botany 99, 1847-1856. http://www.amjbot.org/cgi/content/abstract/99/11/1847

Onkokesung N, Gaquerel E, Kotkar H, Kaur H, Baldwin IT and Galis I (2012) MYB8 Controls Inducible Phenolamide Levels by Activating Three Novel Hydroxycinnamoyl-Coenzyme A:Polyamine Transferases in Nicotiana attenuata. Plant Physiology 158, 389-407. http://www.plantphysiol.org/cgi/content/abstract/158/1/389

Ruberti I, Sessa G, Ciolfi A, Possenti M, Carabelli M and Morelli G (2012) Plant adaptation to dynamically changing environment: The shade avoidance response. Biotechnology Advances 30, 1047-1058. //www.sciencedirect.com/science/article/pii/S0734975011001467

Runquist RDB (2012) Pollinator-mediated competition between two congeners, Limnanthes douglasii subsp. rosea and L. alba (Limnanthaceae). Am. J. Botany 99, 1125-1132. http://www.amjbot.org/cgi/content/abstract/99/7/1125

Silva MP, Piazza LA, López D, López Rivilli MJ, Turco MD, Cantero JJ, Tourn MG and Scopel AL (2012) Phytotoxic activity in Flourensia campestris and isolation of (−)-hamanasic acid A as its active principle compound. Phytochemistry 77, 140-148. http://www.sciencedirect.com/science/article/pii/S0031942211005942

 

 

References 1901-2013 (and links to abstracts):
[Number of papers mentioning Nicotiana longiflora: 122; Any undated papers have been included at the end]

 

Ferrieri AP, Agtuca B, Appel HM, Ferrieri RA and Schultz JC (2013) Temporal Changes in Allocation and Partitioning of New Carbon as 11C Elicited by Simulated Herbivory Suggest that Roots Shape Aboveground Responses in Arabidopsis. Plant Physiology 161, 692-704.  http://www.plantphysiol.org/cgi/content/abstract/161/2/692

Jimenez-Duran K, McClure B, Garcia-Campusano F, Rodriguez-Sotres R, Cisneros J, Busot G and Cruz-Garcia F (2013) NaStEP: A Proteinase Inhibitor Essential to Self-Incompatibility and a Positive Regulator of HT-B Stability in Nicotiana alata Pollen Tubes. Plant Physiology 161, 97-107.  http://www.plantphysiol.org/cgi/content/abstract/161/1/97

Morales LO, Brosche M, et al. (2013) Multiple Roles for UV RESISTANCE LOCUS8 in Regulating Gene Expression and Metabolite Accumulation in Arabidopsis under Solar Ultraviolet Radiation. Plant Physiology 161, 744-759.  http://www.plantphysiol.org/cgi/content/abstract/161/2/744

Alon M, Elbaz M, Ben-Zvi MM, Feldmesser E, Vainstein A and Morin S (2012) Insights into the transcriptomics of polyphagy: Bemisia tabaci adaptability to phenylpropanoids involves coordinated expression of defense and metabolic genes. Insect Biochemistry and Molecular Biology 42, 251-263.  http://www.sciencedirect.com/science/article/pii/S0965174811002207

Ballare CL, Mazza CA, Austin AT and Pierik R (2012) Canopy Light and Plant Health. Plant Physiology 160, 145-155.  http://www.plantphysiol.org

Cerrudo I, Keller MM, Cargnel MD, Demkura PV, de Wit M, Patitucci MS, Pierik R, Pieterse CMJ and Ballare CL (2012) Low Red/Far-Red Ratios Reduce Arabidopsis Resistance to Botrytis cinerea and Jasmonate Responses via a COI1-JAZ10-Dependent, Salicylic Acid-Independent Mechanism. Plant Physiology 158, 2042-2052.  http://www.plantphysiol.org/cgi/content/abstract/158/4/2042

Demkura PV and Ballare CL (2012) UVR8 Mediates UV-B-Induced Arabidopsis Defense Responses against Botrytis cinerea by Controlling Sinapate Accumulation. Mol Plant, sss025.  http://mplant.oxfordjournals.org/cgi/content/abstract/sss025v1

Demkura PV and Ballare CL (2012) UVR8 Mediates UV-B-Induced Arabidopsis Defense Responses against Botrytis cinerea by Controlling Sinapate Accumulation. Mol Plant 5, 642-652.  http://mplant.oxfordjournals.org/cgi/content/abstract/5/3/642

ĐInh ST, GÁLis I and Baldwin IT (2012) UVB radiation and 17-hydroxygeranyllinalool diterpene glycosides provide durable resistance against mirid (Tupiocoris notatus) attack in field-grown Nicotiana attenuata plants. Plant, Cell & Environment, no-no.  http://dx.doi.org/10.1111/j.1365-3040.2012.02598.x

Foyer CH, Neukermans J, Queval G, Noctor G and Harbinson J (2012) Photosynthetic control of electron transport and the regulation of gene expression. J. Exp. Bot. 63, 1637-1661.  http://jxb.oxfordjournals.org/cgi/content/abstract/63/4/1637

Fukaya M, Uesugi R, Ohashi H, Sakai Y, Sudo M, Kasai A, Kishimoto H and Osakabe M (2012) Tolerance to Solar Ultraviolet-B Radiation in the Citrus Red Mite, An Upper Surface User of Host Plant Leaves. Photochemistry and Photobiology, n/a-n/a.  http://dx.doi.org/10.1111/php.12001

Jansen MAK and Bornman JF (2012) UV-B radiation: from generic stressor to specific regulator. Physiologia Plantarum 145, 501-504.  http://dx.doi.org/10.1111/j.1399-3054.2012.01656.x

Kaczorowski RL, Seliger AR, Gaskett AC, Wigsten SK and Raguso RA (2012) Corolla shape vs. size in flower choice by a nocturnal hawkmoth pollinator. Functional Ecology 26, 577-587.  http://dx.doi.org/10.1111/j.1365-2435.2012.01982.x

Mahajan M, Joshi R, Gulati A and Yadav SK (2012) Increase in flavan-3-ols by silencing flavonol synthase mRNA affects the transcript expression and activity levels of antioxidant enzymes in tobacco. Plant Biology 14, 725-733.  http://dx.doi.org/10.1111/j.1438-8677.2011.00550.x

Mazza CA, Giménez PI, Kantolic AG and Ballaré CL (2012) Beneficial effects of solar UV-B radiation on soybean yield mediated by reduced insect herbivory under field conditions. Physiologia Plantarum, n/a-n/a.  http://dx.doi.org/10.1111/j.1399-3054.2012.01661.x

Mewis I, Schreiner M, Nguyen CN, Krumbein A, Ulrichs C, Lohse M and Zrenner R (2012) UV-B Irradiation Changes Specifically the Secondary Metabolite Profile in Broccoli Sprouts: Induced Signaling Overlaps with Defense Response to Biotic Stressors. Plant Cell Physiol. 53, 1546-1560.  http://pcp.oxfordjournals.org/cgi/content/abstract/53/9/1546

Natalis LC and Wesselingh RA (2012) Post-pollination barriers and their role in asymmetric hybridization in Rhinanthus (Orobanchaceae). Am. J. Botany 99, 1847-1856.  http://www.amjbot.org/cgi/content/abstract/99/11/1847

Onkokesung N, Gaquerel E, Kotkar H, Kaur H, Baldwin IT and Galis I (2012) MYB8 Controls Inducible Phenolamide Levels by Activating Three Novel Hydroxycinnamoyl-Coenzyme A:Polyamine Transferases in Nicotiana attenuata. Plant Physiology 158, 389-407.  http://www.plantphysiol.org/cgi/content/abstract/158/1/389

Runquist RDB (2012) Pollinator-mediated competition between two congeners, Limnanthes douglasii subsp. rosea and L. alba (Limnanthaceae). Am. J. Botany 99, 1125-1132.  http://www.amjbot.org/cgi/content/abstract/99/7/1125

Silva MP, Piazza LA, López D, López Rivilli MJ, Turco MD, Cantero JJ, Tourn MG and Scopel AL (2012) Phytotoxic activity in Flourensia campestris and isolation of (−)-hamanasic acid A as its active principle compound. Phytochemistry 77, 140-148.  http://www.sciencedirect.com/science/article/pii/S0031942211005942

Ceuterick M, Vandebroek I and Pieroni A (2011) Resilience of Andean urban ethnobotanies: A comparison of medicinal plant use among Bolivian and Peruvian migrants in the United Kingdom and in their countries of origin. Journal of Ethnopharmacology 136, 27-54.  http://www.sciencedirect.com/science/article/pii/S0378874111001899

Fisher AJ and Franklin KA (2011) Chromatin remodelling in plant light signalling. Physiologia Plantarum 142, 305-313.  http://dx.doi.org/10.1111/j.1399-3054.2011.01476.x

Kazan K and Manners JM (2011) The interplay between light and jasmonate signalling during defence and development. J. Exp. Bot. 62, 4087-4100.  http://jxb.oxfordjournals.org/cgi/content/abstract/62/12/4087

Wargent JJ, Elfadly EM, Moore JP and Paul ND (2011) Increased exposure to UV-B radiation during early development leads to enhanced photoprotection and improved long-term performance in Lactuca sativa. Plant, Cell & Environment 34, 1401-1413.  http://dx.doi.org/10.1111/j.1365-3040.2011.02342.x

Bilgin DD, Zavala JA, Zhu JIN, Clough SJ, Ort DR and DeLucia EH (2010) Biotic stress globally downregulates photosynthesis genes. Plant, Cell & Environment 33, 1597-1613.  http://dx.doi.org/10.1111/j.1365-3040.2010.02167.x

Broekgaarden C, Poelman EH, Voorrips RE, Dicke M and Vosman B (2010) Intraspecific variation in herbivore community composition and transcriptional profiles in field-grown Brassica oleracea cultivars. J. Exp. Bot. 61, 807-819.  http://jxb.oxfordjournals.org/cgi/content/abstract/61/3/807

Demkura PV, Abdala G, Baldwin IT and Ballare CL (2010) Jasmonate-Dependent and -Independent Pathways Mediate Specific Effects of Solar Ultraviolet B Radiation on Leaf Phenolics and Antiherbivore Defense. Plant Physiology 152, 1084-1095.  http://www.plantphysiol.org/cgi/content/abstract/152/2/1084

Gómez S, Ferrieri RA, Schueller M and Orians CM (2010) Methyl jasmonate elicits rapid changes in carbon and nitrogen dynamics in tomato. New Phytologist 188, 835-844.  http://dx.doi.org/10.1111/j.1469-8137.2010.03414.x

Kuhlmann F and Müller C (2010) UV-B impact on aphid performance mediated by plant quality and plant changes induced by aphids. Plant Biology 12, 676-684.  http://dx.doi.org/10.1111/j.1438-8677.2009.00257.x

Mazza CA, Izaguirre MM, Curiale J and Ballare CL (2010) A look into the invisible: ultraviolet-B sensitivity in an insect (Caliothrips phaseoli) revealed through a behavioural action spectrum. Proc R Soc B 277, 367-373.  http://rspb.royalsocietypublishing.org/cgi/content/abstract/277/1680/367

Misra P, Pandey A, et al. (2010) Modulation of Transcriptome and Metabolome of Tobacco by Arabidopsis Transcription Factor, AtMYB12, Leads to Insect Resistance. Plant Physiology 152, 2258-2268.  http://www.plantphysiol.org/cgi/content/abstract/152/4/2258

Montgomery BR, Soper DM and Delph LF (2010) Asymmetrical conspecific seed-siring advantage between Silene latifolia and S. dioica. Ann. Bot. 105, 595-605.  http://aob.oxfordjournals.org/cgi/content/abstract/105/4/595

Morales LO, Tegelberg R, Brosche M, Keinanen M, Lindfors A and Aphalo PJ (2010) Effects of solar UV-A and UV-B radiation on gene expression and phenolic accumulation in Betula pendula leaves. Tree Physiol 30, 923-934.  http://treephys.oxfordjournals.org/cgi/content/abstract/30/7/923

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Morales LO, Tegelberg R, Brosche M, Keinanen M, Lindfors A and Aphalo PJ Effects of solar UV-A and UV-B radiation on gene expression and phenolic accumulation in Betula pendula leaves. Tree Physiol 30, 923-934.  http://treephys.oxfordjournals.org/cgi/content/abstract/30/7/923

Onkokesung N, Gaquerel E, Kotkar H, Kaur H, Baldwin IT and Galis I MYB8 Controls Inducible Phenolamide Levels by Activating Three Novel Hydroxycinnamoyl-Coenzyme A:Polyamine Transferases in Nicotiana attenuata. Plant Physiology 158, 389-407.  http://www.plantphysiol.org/cgi/content/abstract/158/1/389

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Silva MP, Piazza LA, LÓpez D, LÓpez Rivilli MJ, Turco MD, Cantero JJ, Tourn MnG and Scopel AL Phytotoxic activity in Flourensia campestris and isolation of (−)-hamanasic acid A as its active principle compound. Phytochemistry 77, 140-148.  http://www.sciencedirect.com/science/article/pii/S0031942211005942

 


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Grateful acknowledgment is made to the following: for plant names: Australian Plant Name Index, Australian National Herbarium http://www.anbg.gov.au/cpbr/databases/apni-search-full.html; ; The International Plant Names Index, Royal Botanic Gardens, Kew/Harvard University Herbaria/Australian National Herbarium http://www.ipni.org/index.html; Plants Database, United States Department of Agriculture, National Resources Conservation Service http://plants.usda.gov/;DJ Mabberley (1997) The Plant Book, Cambridge University Press (Second Edition); JH Wiersma and B Leon (1999) World Economic Plants, CRC Press; RJ Hnatiuk (1990) Census of Australian Vascular Plants, Australian Government Publishing Service; for information: Science Direct http://www.sciencedirect.com/; Wiley Online Library http://onlinelibrary.wiley.com/advanced/search; High Wire http://highwire.stanford.edu/cgi/search; Oxford Journals http://services.oxfordjournals.org/search.dtl; USDA National Agricultural Library http://agricola.nal.usda.gov/booleancube/booleancube_search_cit.html; for synonyms: The Plant List http://www.theplantlist.org/; for common names: http://en.wikipedia.org/wiki/Main_Page; etc.


All information is included in good faith but this website does not warrant or guarantee the accuracy of any information on these pages, nor does the website accept responsibility for any loss arising from the use of this information.  Views and opinions are those of the authors themselves.  Every effort has been made to respect copyright owners' rights. 


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