The Plant Journal - 68 (4-6), 2011

The Plant Journal - 68 (4), 2011


Contents:


FEATURED ARTICLE


Gibberellin partly mediates LANCEOLATE activity in tomato (pages 571–582)

Osnat Yanai, Eilon Shani, Dor Russ and Naomi Ori


ORIGINAL ARTICLES


An EAR-motif-containing ERF transcription factor affects herbivore-induced signaling, defense and resistance in rice (pages 583–596)

Jing Lu, Hongping Ju, Guoxin Zhou, Chuanshu Zhu, Matthias Erb, Xiaopeng Wang, Peng Wang and Yonggen Lou


A cellular expression map of the Arabidopsis AUXIN RESPONSE FACTOR gene family (pages 597–606)

Eike H. Rademacher, Barbara Möller, Annemarie S. Lokerse, Cristina I. Llavata-Peris, Willy van den Berg and Dolf Weijers


Detailed characterization of mechanical properties and molecular mobility within dry seed glasses: relevance to the physiology of dry biological systems (pages 607–619)

Daniel Ballesteros and Christina Walters


Arabidopsis thaliana GEX1 has dual functions in gametophyte development and early embryogenesis (pages 620–632)

Monica Alandete-Saez, Mily Ron, Samuel Leiboff and Sheila McCormick


DRD1-Pol V-dependent self-silencing of an exogenous silencer restricts the non-cell autonomous silencing of an endogenous target gene (pages 633–645)

Li Dong, Meng Liu, Yuan-Yuan Fang, Jian-Hua Zhao, Xiang-Feng He, Xiao-Bao Ying, Yi-Yue Zhang, Qi Xie, Nam-Hai Chua and Hui-Shan Guo


The E2F transcription factor family regulates CENH3 expression in Arabidopsis thaliana (pages 646–656)

Stefan Heckmann, Inna Lermontova, Barbara Berckmans, Lieven De Veylder, Helmut Bäumlein and Ingo Schubert


The Arabidopsis MERISTEM DISORGANIZATION 1 gene is required for the maintenance of stem cells through the reduction of DNA damage (pages 657–669)

Yuma Hashimura and Chiharu Ueguchi


Barley mildew and its elicitor chitosan promote closed stomata by stimulating guard-cell S-type anion channels (pages 670–680)

Sandra Koers, Aysin Guzel-Deger, Irene Marten and M. Rob G. Roelfsema


LATE, a C2H2 zinc-finger protein that acts as floral repressor (pages 681–692)

Magdalena Weingartner, Christa Subert and Norbert Sauer


Arabidopsis ARP endonuclease functions in a branched base excision DNA repair pathway completed by LIG1 (pages 693–702)

Dolores Córdoba-Canero, Teresa Roldán-Arjona and Rafael R. Ariza


Characterization of Linaria KNOX genes suggests a role in petal-spur development (pages 703–714)

Mathew S. Box, Steven Dodsworth, Paula J. Rudall, Richard M. Bateman and Beverley J. Glover


Combined activity of LACS1 and LACS4 is required for proper pollen coat formation in Arabidopsis (pages 715–726)

Dirk Jessen, Andrea Olbrich, Jessica Knüfer, Antje Krüger, Michael Hoppert, Andrea Polle and Martin Fulda


Arabidopsis MAP kinase phosphatase 1 and its target MAP kinases 3 and 6 antagonistically determine UV-B stress tolerance, independent of the UVR8 photoreceptor pathway (pages 727–737)

Marina A. González Besteiro, Sebastian Bartels, Andreas Albert and Roman Ulm


Arabidopsis RUGOSA2 encodes an mTERF family member required for mitochondrion, chloroplast and leaf development (pages 738–753)

Víctor Quesada, Raquel Sarmiento-Manús, Rebeca González-Bayón, Andrea Hricová, Rubén Pérez-Marcos, Eva Graciá-Martínez, Laura Medina-Ruiz, Eduardo Leyva-Díaz, María Rosa Ponce and José Luis Micol


+++++++++++++++

The Plant Journal - 68 (5), 2011


Contents:

FEATURED ARTICLE


Functional anatomy of the Arabidopsis cytokinesis-specific syntaxin KNOLLE (pages 755–764)

Sonja Touihri, Christian Knöll, York-Dieter Stierhof, Isabel Müller, Ulrike Mayer and Gerd Jürgens


ORIGINAL ARTICLES


Chitinase III in pomegranate seeds (Punica granatum Linn.): a high-capacity calcium-binding protein in amyloplasts (pages 765–776)

Haixia Yang, Tuo Zhang, Taro Masuda, Chenyan Lv, Lei Sun, Guiqin Qu and Guanghua Zhao


Rice 14-3-3 protein (GF14e) negatively affects cell death and disease resistance (pages 777–787)

Patricia M. Manosalva, Myron Bruce and Jan E. Leach


ANGUSTIFOLIA, a plant homolog of CtBP/BARS, functions outside the nucleus (pages 788–799)

Naoko Minamisawa, Mayuko Sato, Kiu-Hyung Cho, Hanako Ueno, Katsuaki Takechi, Masataka Kajikawa, Katsuyuki T. Yamato, Kanji Ohyama, Kiminori Toyooka, Gyung-Tae Kim, Gorou Horiguchi, Hiroyoshi Takano, Takashi Ueda and Hirokazu Tsukaya


Sulfinylated azadecalins act as functional mimics of a pollen germination stimulant in Arabidopsis pistils (pages 800–815)

Yuan Qin, Ronald J. Wysocki, Arpad Somogyi, Yelena Feinstein, Jessica Y. Franco, Tatsuya Tsukamoto, Damayanthi Dunatunga, Clara Levy, Steven Smith, Robert Simpson, David Gang, Mark A. Johnson and Ravishankar Palanivelu


SPATULA and ALCATRAZ, are partially redundant, functionally diverging bHLH genes required for Arabidopsis gynoecium and fruit development (pages 816–829)

Michael Groszmann, Teodora Paicu, John P. Alvarez, Steve M. Swain and David R. Smyth


NIMA-related kinase NEK6 affects plant growth and stress response in Arabidopsis (pages 830–843)

Bo Zhang, Hao-Wei Chen, Rui-Ling Mu, Wang-Ke Zhang, Ming-Yu Zhao, Wei Wei, Fang Wang, Hui Yu, Gang Lei, Hong-Feng Zou, Biao Ma, Shou-Yi Chen and Jin-Song Zhang


The role of the transmembrane domain in determining the targeting of membrane proteins to either the inner envelope or thylakoid membrane (pages 844–856)

John E. Froehlich and Kenneth Keegstra


TaMYB13 is a transcriptional activator of fructosyltransferase genes involved in ß-2,6-linked fructan synthesis in wheat (pages 857–870)

Gang-Ping Xue, Maarten Kooiker, Janneke Drenth and C. Lynne McIntyre


System responses to long-term drought and re-watering of two contrasting alfalfa varieties (pages 871–889)

Yun Kang, Yuanhong Han, Ivone Torres-Jerez, Mingyi Wang, Yuhong Tang, Maria Monteros and Michael Udvardi


A member of the mitogen-activated protein 3-kinase family is involved in the regulation of plant vacuolar glucose uptake (pages 890–900)

Karina Wingenter, Oliver Trentmann, Irina Winschuh, Imke I. Hörmiller, Arnd G. Heyer, Jörg Reinders, Alexander Schulz, Dietmar Geiger, Rainer Hedrich and H. Ekkehard Neuhaus


Induction and detoxification of maize 1,4-benzoxazin-3-ones by insect herbivores (pages 901–911)

Gaétan Glauser, Guillaume Marti, Neil Villard, Gwladys A. Doyen, Jean-Luc Wolfender, Ted C.J. Turlings and Matthias Erb


Two high linolenic mutants of Arabidopsis thaliana contain megabase-scale genome duplications encompassing the FAD3 locus (pages 912–918)

Carmel M. O’Neill, David Baker, Gawain Bennett, Jonathan Clarke and Ian Bancroft


Repression of shade-avoidance reactions by sunfleck induction of HY5 expression in Arabidopsis (pages 919–928)

Romina Sellaro, Marcelo J. Yanovsky and Jorge J. Casal


TECHNICAL ADVANCE


Localized egg-cell expression of effector proteins for targeted modification of the Arabidopsis genome (pages 929–937)

Liron Even-Faitelson, Aviva Samach, Cathy Melamed-Bessudo, Naomi Avivi-Ragolsky and Avraham A. Levy


Correction


+++++++++++++++

The Plant Journal - 68 (6), 2011


Contents:

EDITORIAL


The future is bright for The Plant Journal, now in its 20th year (pages 939–940)

Christoph Benning


FEATURED ARTICLE


Cellulose synthesis via the FEI2 RLK/SOS5 pathway and CELLULOSE SYNTHASE 5 is required for the structure of seed coat mucilage in Arabidopsis (pages 941–953)

Smadar Harpaz-Saad, Heather E. McFarlane, Shouling Xu, Uday K. Divi, Bronwen Forward, Tamara L. Western and Joseph J. Kieber


ORIGINAL ARTICLES


Medicago truncatula mtpt4 mutants reveal a role for nitrogen in the regulation of arbuscule degeneration in arbuscular mycorrhizal symbiosis (pages 954–965)

Hélene Javot, R. Varma Penmetsa, Florence Breuillin, Kishor K. Bhattarai, Roslyn D. Noar, S. Karen Gomez, Quan Zhang, Douglas R. Cook and Maria J. Harrison


Cyclic electron flow around photosystem I via chloroplast NAD(P)H dehydrogenase (NDH) complex performs a significant physiological role during photosynthesis and plant growth at low temperature in rice (pages 966–976)

Wataru Yamori, Naoki Sakata, Yuji Suzuki, Toshiharu Shikanai and Amane Makino


Functional HAK/KUP/KT-like potassium transporter encoded by chlorella viruses (pages 977–986)

Timo Greiner, José Ramos, Maria C. Alvarez, James R. Gurnon, Ming Kang, James L. Van Etten, Anna Moroni and Gerhard Thiel


Glucose and ethylene signalling pathways converge to regulate trans-differentiation of epidermal transfer cells in Vicia narbonensis cotyledons (pages 987–998)

Felicity A. Andriunas, Hui-Ming Zhang, Hans Weber, David W. McCurdy, Christina E. Offler and John W. Patrick


Combined transcription factor profiling, microarray analysis and metabolite profiling reveals the transcriptional control of metabolic shifts occurring during tomato fruit development (pages 999–1013)

Johannes Rohrmann, Takayuki Tohge, Rob Alba, Sonia Osorio, Camila Caldana, Ryan McQuinn, Samuel Arvidsson, Margaretha J. van der Merwe, Diego Mauricio Riano-Pachón, Bernd Mueller-Roeber, Zhangjun Fei, Adriano Nunes Nesi, James J. Giovannoni and Alisdair R. Fernie


Comparative deep transcriptional profiling of four developing oilseeds (pages 1014–1027)

Manuel A. Troncoso-Ponce, Aruna Kilaru, Xia Cao, Timothy P. Durrett, Jilian Fan, Jacob K. Jensen, Nick A. Thrower, Markus Pauly, Curtis Wilkerson and John B. Ohlrogge


Sequence divergence and loss-of-function phenotypes of S locus F-box brothers genes are consistent with non-self recognition by multiple pollen determinants in self-incompatibility of Japanese pear (Pyrus pyrifolia) (pages 1028–1038)

Hiroyuki Kakui, Masaki Kato, Koichiro Ushijima, Miyoko Kitaguchi, Shu Kato and Hidenori Sassa


A plastid protein NUS1 is essential for build-up of the genetic system for early chloroplast development under cold stress conditions (pages 1039–1050)

Kensuke Kusumi, Chikako Sakata, Takahiro Nakamura, Shinji Kawasaki, Atsushi Yoshimura and Koh Iba


Domain loss has independently occurred multiple times in plant terpene synthase evolution (pages 1051–1060)

Matthew L. Hillwig, Meimei Xu, Tomonobu Toyomasu, Mollie S. Tiernan, Gao Wei, Guanghong Cui, Luqi Huang and Reuben J. Peters


An Al-inducible MATE gene is involved in external detoxification of Al in rice (pages 1061–1069)

Kengo Yokosho, Naoki Yamaji and Jian Feng Ma


The pyruvate, orthophosphate dikinase regulatory proteins of Arabidopsis are both bifunctional and interact with the catalytic and nucleotide-binding domains of pyruvate, orthophosphate dikinase (pages 1070–1080)

Holly M. Astley, Kate Parsley, Sylvain Aubry, Chris J. Chastain, Jim N. Burnell, Michael E. Webb and Julian M. Hibberd


Overexpression of Arabidopsis thaliana PTEN caused accumulation of autophagic bodies in pollen tubes by disrupting phosphatidylinositol 3-phosphate dynamics (pages 1081–1092)

Yan Zhang, Sha Li, Liang-Zi Zhou, Emily Fox, James Pao, Wei Sun, Chao Zhou and Sheila McCormick


Chromosomal rearrangements between tomato and Solanum chilense hamper mapping and breeding of the TYLCV resistance gene Ty-1 (pages 1093–1103)

Maarten G. Verlaan, Dóra Szinay, Samuel F. Hutton, Hans de Jong, Richard Kormelink, Richard G.F. Visser, John W. Scott and Yuling Bai


NAC domain function and transcriptional control of a secondary cell wall master switch (pages 1104–1114)

Huanzhong Wang, Qiao Zhao, Fang Chen, Mingyi Wang and Richard A. Dixon


Specific delivery of AtBT1 to mitochondria complements the aberrant growth and sterility phenotype of homozygous Atbt1 Arabidopsis mutants (pages 1115–1121)

Abdellatif Bahaji, Francisco José Munoz, Miroslav Ovecka, Edurne Baroja-Fernández, Manuel Montero, Jun Li, Maite Hidalgo, Goizeder Almagro, María Teresa Sesma, Ignacio Ezquer and Javier Pozueta-Romero


+++++++++++++++

Haworthiad - 25, 2011

Contents:

'High-breds' or wanting weeds
Gerhard Marx

Some Japanese hybrids and cultivars from Fumio Hagiwara
Hiroshi Nakatani

Desserts - Mastodon vs. Mousse or, what's on the menu?
Steve Hammer

Japanese inspirations and California Sunshine
Renny Hosogai

Cocozza Cuttings - domino delights
Joyce L Cocozza

Thoughts on growing haworthias
Mary Parisi

The art and science of hybridisation
George Theodoris

The Silver Bug family and other hybrids
Francois Hoes


+++++++++++++++

Flora of Thailand - 11 (1) - 12 (1), 2011

Flora of Thailand - 11 (1), 2011



Contents:

Cornaceae,
Daphniphyllaceae,
Erythoxylaceae,
Helwingiaceae,
Lentibulariaceae,
Monimiaceae,
Ranunculaceae,
Stemonaceae.

99 p, 8 coloured plates

+++++++++++++++

Flora of Thailand - 12 (1), 2011



Contents:

Orchidaceae (1)

302 p, 24 coloured plates


++++++++++++++

Abies procera 'Glauca' / Jodła szlachetna 'Glauca'

Taxon - 60 (1), 2011

Contents:


Sixty years of Taxon
Mabberley, David J.

Revisiting the wax plants (Hoya, Marsdenieae, Apocynaceae): Phylogenetic tree using the matK gene and psbA-trnH intergenic spacer
Wanntorp, Livia; Gotthardt, Katherina; Muellner, Alexandra N.

Molecular phylogeny and biogeography of three closely related genera, Soroseris, Stebbinsia, and Syncalathium (Asteraceae, Cichorieae), endemic to the Tibetan Plateau, SW China
Zhang, Jian-Wen; Nie, Ze-Long; Wen, Jun; Sun, Hang

Subgeneric classification in Iris re-examined using chloroplast sequence data
Wilson, Carol A.

Neckera and Thamnobryum (Neckeraceae, Bryopsida): Paraphyletic assemblages
Olsson, Sanna; Enroth, Johannes; Buchbender, Volker; Hedenäs, Lars; Huttunen, Sanna; Quandt, Dietmar

Molecular phylogeny of Camphorosmeae (Camphorosmoideae, Chenopodiaceae): Implications for biogeography, evolution of C4-photosynthesis and taxonomy
Kadereit, Gudrun; Freitag, Helmut

Phylogenetic inference in Leucodon Schwägr. subg. Leucodon (Leucodontaceae, Bryophyta) in the North Atlantic region
Stech, Michael; Werner, Olaf; González-Mancebo, Juana María; Patino, Jairo; Sim-Sim, Manuela; Fontinha, Susana; Hildebrandt, Ina; Ros, Rosa M.

Molecular phylogenetics of the Mesoamerican bamboo Olmeca (Poaceae, Bambuseae): Implications for taxonomy
Ruiz-Sanchez, Eduardo; Sosa, Victoria; Mejía-Saules, M. Teresa

Graphis is two genera: A remarkable case of parallel evolution in lichenized Ascomycota
Plata, Eimy Rivas; Hernández M., Jesús E.; Lücking, Robert; Staiger, Bettina; Kalb, Klaus; Cáceres, Marcela E.S.

Extensive gene flow blurs species boundaries among Veronica barrelieri, V. orchidea and V. spicata (Plantaginaceae) in southeastern Europe
Bardy, Katharina E.; Schönswetter, Peter; Schneeweiss, Gerald M.; Fischer, Manfred A.; Albach, Dirk C.

Phylogenetic relationships in the order Cucurbitales and a new classification of the gourd family (Cucurbitaceae)
Schaefer, Hanno; Renner, Susanne S.

Underestimated endemic species diversity in the dry inter-Andean valley of the Río Maranón, northern Peru: An example from Mimosa (Leguminosae, Mimosoideae)
Särkinen, Tiina E.; Marcelo-Pena, José Luis; Yomona, A. Daza; Simon, Marcelo F.; Pennington, R. Toby; Hughes, Colin E.

Taxonomy of Polygonoideae (Polygonaceae): A new tribal classification
Sanchez, Adriana; Schuster, Tanja M.; Burke, Janelle M.; Kron, Kathleen A.

The generic concept of Lotononis (Crotalarieae, Fabaceae): Reinstatement of the genera Euchlora, Leobordea and Listia and the new genus Ezoloba
Boatwright, James S.; Wink, Michael; van Wyk, Ben-Erik

Blastocaulon (Eriocaulaceae), a synonym of Paepalanthus: Morphological and molecular evidence
de Andrade, Maria José Gomes; Giulietti, Ana Maria; Harley, Raymond Mervyn; van den Berg, Cássio

A case study of DNA barcoding in Chinese Grimmiaceae and a moss recorded in China for the first time
Liu, Yan; Ge, Tong Cao; Ge, Xue-Jin

The controversy over the retypification of Acacia Mill. with an Australian type: A pragmatic view
Thiele, Kevin R.; Funk, Vicki A.; Iwatsuki, Kunio; Morat, Philippe; Peng, Ching-I; Raven, Peter H.; Sarukhán, José; Seberg, Ole

Introducing the Draft BioCode (2011)
Hawksworth, David L.

Draft BioCode (2011): Principles and Rules Regulating the Naming of Organisms
Greuter, W.; Garrity, G.; Hawksworth, D.L.; Jahn, R.; Kirk, P.M.; Knapp, S.; McNeill, J.; Michel, E.; Patterson, D.J.; Pyle, R.; Tindall, B.J.

Who amends the International Code of Botanical Nomenclature? A response to Applequist & al. (2010)
Smith, Gideon F.; Figueiredo, Estrela; Moore, Gerry

Typification of Leontodon taraxacum L. (? Taraxacum officinale F.H. Wigg.) and the generic name Taraxacum: A review and a new typification proposal
Kirschner, Jan; Štěpánek, Jan

The nomenclatural status of the genus Tubifera (Myxomycetes)
Lado, Carlos

Report of the Nomenclature Committee for Fungi: 16
Norvell, Lorelei L.

Report of the Nomenclature Committee for Vascular Plants: 62
Brummitt, R.K.

(1989) Proposal to conserve the name Botrytis brongniartii (Beauveria brongniartii) with a conserved type (Ascomycota)
Minnis, Andrew M.; Rehner, Stephen A.; Humber, Richard A.

(1990) Proposal to conserve the name Pteris arachnoidea (Pteridium arachnoideum) against Aspidium brasilianum and Pteris psittacina (Dennstaedtiaceae)
Schwartsburd, Pedro Bond; Prado, Jefferson

(1991) Proposal to conserve the name Pandanus pervilleanus against P. boucheanus (Pandanaceae)
Callmander, Martin W.; Fumeaux, Nicolas

(1992) Proposal to conserve the name Enicosanthum against Monoon (Annonaceae)
Saunders, Richard M.K.; Xue, Bine

(1993) Proposal to conserve the name Alyssum montanum (Cruciferae) with a conserved type
Marhold, Karol; Zozomová-Lihová, Judita; Španiel, Stanislav

(1994) Proposal to conserve the name Codariocalyx (Leguminosae/Fabaceae) with that spelling
Ohashi, Hiroyoshi; Ohashi, Kazuaki

(1995) Proposal to conserve the name Nilssonia with that spelling (fossil Cycadopsida, Nilssoniaceae)
Wang, Qi

(1996) Proposal to conserve the name Carpolithus with that spelling (fossil Spermatopsida)
Wang, Qi

Synopsis of Proposals on Botanical Nomenclature - Melbourne 2011: A review of the proposals concerning the International Code of Botanical Nomenclature submitted to the XVIII International Botanical Congress
McNeill, John; Turland, Nicholas

(6-8) Proposals to add two Tabulae herbarii L. Pierre or the entire set to the “Opera utique oppressa”
van Rijckevorsel, Paul

New Names and Combinations

Thanks to Our Reviewers

Plant Systematics World
Stuessy, Tod F.

One hundred columns later: Confessions of the Taxon “RevNot” editor
Schmid, Rudolf

Reviews and Notices of Publications
Schmid, Rudolf

===============

New names and combinations appearing in Taxon 60 (1)
Actinostemmateae H. Schaef. & S.S. Renner, stat. nov.
Alleniella S. Olsson, Enroth & D. Quandt, gen. nov.
Alleniella besseri (Lob.) S. Olsson, Enroth & D. Quandt, comb. nov.
Alleniella brownii (Dix.) S. Olsson, Enroth & D. Quandt, comb. nov.
Alleniella chilensis (Schimp. ex Mont.) S. Olsson, Enroth & D. Quandt, comb. nov.
Alleniella complanata (Hedw.) S. Olsson, Enroth & D. Quandt, comb. nov.
Alleniella hymenodonta (Müll. Hal.) S. Olsson, Enroth & D. Quandt, comb. nov.
Alleniella remota (Bruch & Schimp. ex Müll. Hal.) S. Olsson, Enroth & D. Quandt, comb. nov.
Alleniella scabridens (Müll. Hal.) S. Olsson, Enroth & D. Quandt, comb. nov.
Alleniella submacrocarpa (Dix.) S. Olsson, Enroth & D. Quandt, comb. nov.
Alleniella urnigera (Müll. Hal.) S. Olsson, Enroth & D. Quandt, comb. nov.
Alleniella valentiniana (Besch.) S. Olsson, Enroth & D. Quandt, comb. nov.
Ampelosicyos bosseri (Keraudren) H. Schaef. & S.S. Renner, comb. nov.
Ampelosicyos leandrii (Keraudren) H. Schaef. & S.S. Renner, comb. nov.
Apodanthera longipedicellata (Cogn.) H. Schaef. & S.S. Renner, comb. nov.
Baijiania decipiens (C. Jeffrey & W.J. de Wilde) H. Schaef. & S.S. Renner, comb. nov.
Baijiania smitinandii (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Bassia angustifolia (Turcz.) Freitag & G. Kadereit, comb. nov.
Bassia lasiantha Freitag & G. Kadereit, nom. nov.
Bassia littorea (Makino) Freitag & G. Kadereit, comb. nov.
Bassia odontoptera (Schrenk) Freitag & G. Kadereit, comb. nov.
Bassia pilosa (Fisch. & C.A. Mey.) Freitag & G. Kadereit, comb. nov.
Bassia tianschanica (Pavlov) Freitag & G. Kadereit, comb. nov.
Bassia villosissima (Bong. & C.A. Mey.) Freitag & G. Kadereit, comb. nov.
Benincasa fistulosa (Stocks) H. Schaef. & S.S. Renner, comb. nov.
Ctenolepis lucorum (Keraudren) H. Schaef. & S.S. Renner, comb. nov.
Cyclanthera brevisetosa (Steyerm.) H. Schaef. & S.S. Renner, comb. nov.
Cyclanthera carthagenensis (Jacq.) H. Schaef. & S.S. Renner, comb. nov.
Cyclanthera filiformis (Kuntze) H. Schaef. & S.S. Renner, comb. nov.
Cyclanthera glabra (Kuntze) H. Schaef. & S.S. Renner, comb. nov.
Cyclanthera kuntzeana H. Schaef. & S.S. Renner, nom. nov.
Cyclanthera longiflora (Cogn.) H. Schaef. & S.S. Renner, comb. nov.
Cyclanthera longisepala (Cogn.) H. Schaef. & S.S. Renner, comb. nov.
Cyclanthera peruana H. Schaef. & S.S. Renner, nom. nov.
Cyclanthera quadrifida (Ser.) H. Schaef. & S.S. Renner, comb. nov.
Cyclanthera quinqueloba (Kuntze) H. Schaef. & S.S. Renner, comb. nov.
Echinodiopsis S. Olsson, Enroth & D. Quandt, gen. nov.
Echinodiopsis hispida (Hook. f. & Wilson) S. Olsson, Enroth & D. Quandt, comb. nov.
Echinodiopsis umbrosa (Mitt.) S. Olsson, Enroth & D. Quandt, comb. nov.
Echinodiopsis umbrosa var. glaucoviride (Mitt.) S. Olsson, Enroth & D. Quandt, comb. nov.
Echinopepon rosei (Cogn.) H. Schaef. & S.S. Renner, comb. nov.
Eokochia Freitag & G. Kadereit, gen. nov.
Eokochia saxicola (Guss.) Freitag & G. Kadereit, comb. nov.
Exsertotheca S. Olsson, Enroth & D. Quandt, gen. nov.
Exsertotheca crispa (Hedw.) S. Olsson, Enroth & D. Quandt, comb. nov.
Exsertotheca intermedia (Brid.) S. Olsson, Enroth & D. Quandt, comb. nov.
Ezoloba B.-E. van Wyk & Boatwr., gen. nov.
Ezoloba macrocarpa (Eckl. & Zeyh.) B.-E. van Wyk & Boatwr., comb. nov.
Fagopyrum tibeticum (A.J. Li) Adr. Sanchez & Jan. Burke, comb. nov.
Forsstroemia goughiana (Mitt.) S. Olsson, Enroth & D. Quandt, comb. nov.
Forsstroemia yezoana (Besch.) S. Olsson, Enroth & D. Quandt, comb. nov.
Grubovia Freitag & G. Kadereit, gen. nov.
Grubovia dasyphylla (Fisch. & C.A. Mey.) Freitag & G. Kadereit comb. nov.
Grubovia krylovii (Litv.) Freitag & G. Kadereit, comb. nov.
Grubovia melanoptera (Bunge) Freitag & G. Kadereit, comb. nov.
Hanburia caracasana (Ernst) H. Schaef. & S.S. Renner, comb. nov.
Hanburia grisebachii (Cogn.) H. Schaef. & S.S. Renner, comb. nov.
Hanburia oerstedii (Cogn.) H. Schaef. & S.S. Renner, comb. nov.
Hanburia spectabilis (Mart. Crov.) H. Schaef. & S.S. Renner, comb. nov.
Hanburia subcyclanthera (C. Jeffrey) H. Schaef. & S.S. Renner, comb. nov.
Hemsleya cirromitrata (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Hemsleya peekelii (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Herpetospermum darjeelingense (C.B. Clarke) H. Schaef. & S.S. Renner, comb. nov.
Herpetospermum tonglense (Cogn.) H. Schaef. & S.S. Renner, comb. nov.
Indofevilleeae H. Schaef. & S.S. Renner, tr. nov.
Iris subg. Lophiris (Tausch) C.A. Wilson, stat. nov.
Iris subg. Siphonostylis (W. Schulze) C.A. Wilson, comb. et stat. nov.
Leobordea sect. Digitata (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea sect. Leptis (E. Mey. ex Eckl. & Zeyh.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea sect. Lipozygis (E. Mey.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea sect. Synclistus (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea subsect. Bracteolata (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea subsect. Lipozygis (E. Mey.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea acuticarpa (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea adpressa (N.E. Br.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea adpressa (N.E. Br.) B.-E. van Wyk & Boatwr. subsp. leptantha (B.-E. van Wyk) B.-E. van Wyk, comb. nov.
Leobordea anthylloides (Harv.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea arida (Dümmer) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea benthamiana (Dümmer) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea bracteosa (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea bullonii (Emberger & Maire) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea carinata (E. Mey.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea corymbosa (E. Mey.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea decumbens (Thunb.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea decumbens (Thunb.) B.-E. van Wyk & Boatwr. subsp. rehmannii (Dümmer) B.-E. van Wyk, comb. nov.
Leobordea difformis (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea diffusa (Thunb.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea digitata (Harv.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea eriantha (Benth.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea esterhuyseana (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea foliosa (H. Bolus) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea furcata (Merxmüller & Schreiber) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea globulosa (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea grandis (Dümmer & Jennings) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea hirsuta (Schinz) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea lanata (Thunb.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea lanceolata (E. Mey.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea laticeps (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea longicephala (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea longiflora (H. Bolus) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea magnifica (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea maroccana (Ball) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea mirabilis (Dinter) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea mollis (E. Mey.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea mucronata (Conrath) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea newtonii (Dümmer) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea oligocephala (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea pariflora (N.E. Br.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea pentaphylla (E. Mey.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea platycarpa (Viv.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea plicata (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea polycephala (E. Mey.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea procumbens (H. Bolus) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea pulchra (Dümmer) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea pusilla (Dümmer) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea quinata (Thunb.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea schoenfelderi (Dinter ex Merxmüller & Schreiber) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea spicata (Compton) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea stipulosa (Bak. f.) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea stolzii (Harms) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea sutherlandii (Dümmer) B.-E. van Wyk & Boatwr., comb. nov.
Leobordea tapetiformis (Emberger & Maire) B.-E. van Wyk & Boatwr., comb. nov.
Leptodon acuminatus (M. Fleisch.) S. Olsson, Enroth & D. Quandt, comb. nov.
Listia angolensis (Welw. ex Bak.) B.-E. van Wyk & Boatwr., comb. nov.
Listia bainesii (Bak.) B.-E. van Wyk & Boatwr., comb. nov.
Listia marlothii (Engl.) B.-E. van Wyk & Boatwr., comb. nov.
Listia minima (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Listia solitudinis (Dümmer) B.-E. van Wyk & Boatwr., comb. nov.
Listia subulata (B.-E. van Wyk) B.-E. van Wyk & Boatwr., comb. nov.
Melothria campestris (Naudin) H. Schaef. & S.S. Renner, comb. nov.
Melothria sphaerocarpa (Cogn.) H. Schaef. & S.S. Renner, comb. nov.
Mimosa jaenensis T.E. Särkinen, J.L. Marcelo-Pena & C.E. Hughes sp. nov.
Momordiceae H. Schaef. & S.S. Renner, stat. nov.
Olmeca clarkiae (Davidse & R.W. Pohl) Ruiz-Sanchez, Sosa & Mejía-Saulés, comb. nov.
Olmeca fulgor (Soderstr.) Ruiz-Sanchez, Sosa & Mejía-Saulés, comb. nov.
Olmeca zapotecorum Ruiz-Sanchez, Sosa & Mejía-Saulés, sp. nov.
Paepalanthus speleicolus (Silveira) M.J.G. Andrade & Giul. comb. nov.
Papuasicyos arfakensis (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Papuasicyos belensis (Merr. & L.M. Perry) H. Schaef. & S.S. Renner, comb. nov.
Papuasicyos carrii (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Papuasicyos hippocrepicus (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Papuasicyos parviflorus (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Papuasicyos viridis (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Penelopeia sphaerica (Alain) H. Schaef. & S.S. Renner, comb. nov.
Porotrichodendron madagassum (Kiaer ex Besch.) S. Olsson, Enroth & D. Quandt, comb. nov.
Pteropepon acariaeanthus (Harms) H. Schaef. & S.S. Renner, comb. nov.
Sedobassia Freitag & G. Kadereit, gen. nov.
Sedobassia sedoides (Pall.) Freitag & G. Kadereit, comb. nov.
Sicydium synantherum (Dieterle) H. Schaef. & S.S. Renner, comb. nov.
Siraitieae H. Schaef. & S.S. Renner, tr. nov.
Spirobassia Freitag & G. Kadereit, gen. nov.
Spirobassia hirsuta (L.) Freitag & G. Kadereit, comb. nov.
Thamnomalia S. Olsson, Enroth & D. Quandt, gen. nov.
Thamnomalia glabella (Hedw.) S. Olsson, Enroth & D. Quandt, comb. nov.
Thamnomalia tumidicaulis (K.A. Wagner) S. Olsson, Enroth & D. Quandt, comb. nov.
Thladiantheae H. Schaef. & S.S. Renner, stat. nov.
Xerosicyos hirtellus (Humbert) H. Schaef. & S.S. Renner, comb. nov.
Xerosicyos tripartitus (Humbert) H. Schaef. & S.S. Renner, comb. nov.
Zehneria backeri (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Zehneria lancifolia (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Zehneria macrantha (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Zehneria macrosepala (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Zehneria nesophila (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
Zehneria platysperma (W.J. de Wilde & Duyfjes) H. Schaef. & S.S. Renner, comb. nov.
+++++++++++++++

Flora of Thailand - 10 (1-4), 2009-2011

Volume 10(1)/2009:
Dioscoreaceae


Volume 10(2)/2010:
Celastraceae, Hernandiaceae, Leeaceae, Mastrixiaceae, Passifloraceae, Verbenaceae


Volume 10(3):
Anacardiaceae, Convolvulaceae


Volume 10(4):
Cecropiaceae, Moraceae


+++++++++++++++

POLITYKA I NIE TYLKO , PRZEPISY KULINARNE , ULUBIONE KSIĄŻKI , DOWCIPY , GEOGRAFIA , ŚWIEBODZICE , FORUM O RODZAJU HOYA , PEUGEOT , TWOJE CENTRUM FINANSOWE , PiS , PLATFORMA OBYWATELSKA

+++++++++++++++

PLANT - FAMILY - FLOWER - GENERA - JOURNAL - ARTICOLO - PLANTS - PIANTE - ČLÁNEK - ABSTRAKT - STRESZCZENIE - ABSTRAKTNÍ - ABSTRAKT - RÉSUMÉ - RESUMEN - ANOTACIJA - ZUSAMMENFASSUNG - SAMMANFATTNING - PHOTO – FOTOGRAFIA – FOTKA – IMAGE – TAXON - GENUS - ARTÍCULO - ARTIKEL - ARTIGO - CIKKET - NENI - ARTIKULO - ARTIKLA - GR - STRAIPSNIS - PANTS - BOTANIQUE - ROŚLINY - SINONIM - FAMIGLIA - BOTANY - NAUKA - SINONIMO - BOTANICA - WYCIECZKA - TRAVEL - SINÓNIMO - DOCTOR - FRUIT - ARTICOLO - SYNONIEM - CZASOPISMO - SYNONYM - DOKTOR - SYNONYME - SYSTEMATIC - SYSTEMATYKA - SZINONIMA - PROFESOR - RODZINA - ARTYKUŁ - ARTICLE - FLOWER - KWIATY - OWOC - SEEDS - NASIONA - CULTIVATION - USE - WATERING - PROPAGATION - PESTSM - DISEASES - FERTILIZATION - HOUSE - GARDEN - BOWL - KWITNIENIE - FLOWERBED - SOIL - POND - MARSH - SPECIES - HYBRIDS - VEGETABLE GARDEN - UPRAWA - ZASTOSOWANIE - PODLEWANIE - ROZMNAŻANIE - SZKODNIKI - CHOROBY - NAWOŻENIE - ROŚLINY DOMOWE - ROŚLINY BALKONOWE - ROŚLINY TARASOWE - OGRÓD - PRACA NAUKOWA - POJEMNIK - SUBSTRAT - PODŁOŻE - KERAMZYT - GLINA - TORF - DONICA - DONICZKA - ZIEMIA - RABATA - GLEBA - ROŚLINY WODNE - STAW - WODA - ROŚLINY BAGIENNE - OWOCE - WARZYWA - SPRZEDAŻ ROŚLIN - GATUNKI - MIESZAŃCE - CV - KULTYWARY

+++++++++++++++

Plant Growth Regulation - 64 (3), 2011

Contents:


Chilling-induced changes of vacuolar proton pumps in hypocotyls of Vigna unguiculata

Luciana Maia Nogueira de Oliveira, Alana Cecília de Menezes Sobreira, José Hélio Costa, Maria de Lourdes Oliveira Otoch and Masayoshi Maeshima, et al.


Responses of two lines of Medicago ciliaris to Fe deficiency under saline conditions

Wissal M’sehli, Nahida Jellali, Marta Dell’Orto, Chedly Abdelly and Graziano Zocchi, et al.


Characterization of oxidative and antioxidative events during dehydration and rehydration of resurrection plant Ramonda nathaliae

Živko Jovanović, Tamara Rakić, Branka Stevanović and Svetlana Radović


The effect of root exudates on root architecture in Arabidopsis thaliana

María M. Caffaro, Jorge M. Vivanco, Flavio H. Gutierrez Boem and Gerardo Rubio


Nickel and Al-excess inhibit nitrate reductase but upregulate activities of aminating glutamate dehydrogenase and aminotransferases in growing rice seedlings

Pallavi Mishra and R. S. Dubey


Effect of nitrogen deficiency on antioxidant status and Cd toxicity in rice seedlings

Ya-Lin Lin, Yun-Yang Chao, Wen-Dar Huang and Ching Huei Kao


Evaluation of salinity tolerance in sorghum (Sorghum bicolor L.) using ion accumulation, proline and peroxidase criteria

Vahid Bavei, Behrouz Shiran and Ahmad Arzani


Effects of 5-aminolevulinic acid on growth and amylase activity in the radish taproot

Masakazu Hara, Ikuo Takahashi, Michiyo Yamori, Toru Tanaka and Shigeyuki Funada, et al.


An efficient protocol for stimulating cell development in protoplast culture of Scaevola

Yu Hua Wang


Identification of the tomato ABA-deficient mutant sitiens as a member of the ABA-aldehyde oxidase gene family using genetic and genomic analysis

E. Harrison, A. Burbidge, J. P. Okyere, A. J. Thompson and I. B. Taylor


Theobroxide induces tubers in potato (Solanum tuberosum L.) and flower buds in morning glory (Pharbitis nil) under non-inductive high temperatures

Kyong-Hee Nam and Teruhiko Yoshihara



+++++++++++++++

POLITYKA I NIE TYLKO , PRZEPISY KULINARNE , ULUBIONE KSIĄŻKI , DOWCIPY , GEOGRAFIA , ŚWIEBODZICE , FORUM O RODZAJU HOYA , PEUGEOT , TWOJE CENTRUM FINANSOWE , PiS , PLATFORMA OBYWATELSKA

+++++++++++++++

PLANT - FAMILY - FLOWER - GENERA - JOURNAL - ARTICOLO - PLANTS - PIANTE - ČLÁNEK - ABSTRAKT - STRESZCZENIE - ABSTRAKTNÍ - ABSTRAKT - RÉSUMÉ - RESUMEN - ANOTACIJA - ZUSAMMENFASSUNG - A???????? - SAMMANFATTNING - PHOTO – FOTOGRAFIA – FOTKA – IMAGE – TAXON - GENUS - ARTÍCULO - ARTIKEL - ARTIGO - CIKKET - NENI - ARTIKULO - ARTIKLA - GR - STRAIPSNIS - PANTS - BOTANIQUE - ROŚLINY - SINONIM - FAMIGLIA - BOTANY - NAUKA - SINONIMO - BOTANICA - WYCIECZKA - TRAVEL - SINÓNIMO - DOCTOR - FRUIT - ARTICOLO - SYNONIEM - CZASOPISMO - SYNONYM - DOKTOR - SYNONYME - SYSTEMATIC - SYSTEMATYKA - SZINONIMA - PROFESOR - RODZINA - ARTYKUŁ - ARTICLE - FLOWER - KWIATY - OWOC - SEEDS - NASIONA - CULTIVATION - USE - WATERING - PROPAGATION - PESTSM - DISEASES - FERTILIZATION - HOUSE - GARDEN - BOWL - KWITNIENIE - FLOWERBED - SOIL - POND - MARSH - SPECIES - HYBRIDS - VEGETABLE GARDEN - UPRAWA - ZASTOSOWANIE - PODLEWANIE - ROZMNAŻANIE - SZKODNIKI - CHOROBY - NAWOŻENIE - ROŚLINY DOMOWE - ROŚLINY BALKONOWE - ROŚLINY TARASOWE - OGRÓD - POJEMNIK - SUBSTRAT - PODŁOŻE - KERAMZYT - GLINA - TORF - DONICA - DONICZKA - ZIEMIA - RABATA - GLEBA - ROŚLINY WODNE - STAW - WODA - ROŚLINY BAGIENNE - OWOCE - WARZYWA - SPRZEDAŻ ROŚLIN - GATUNKI - MIESZAŃCE - CV - KULTYWARY

+++++++++++++++

Molecular Biology and Evolution - 28 (4), 2011

Contents:

Review Article

Rafael Sanjuán and Antonio V. Bordería
Interplay between RNA Structure and Protein Evolution in HIV-1


Research Articles

Zi-Feng Jiang, Dean A. Croshaw, Yan Wang, Jody Hey and Carlos A. Machado
Enrichment of mRNA-like Noncoding RNAs in the Divergence of Drosophila Males

Mannis van Oven, Johannes M. Hämmerle, Marja van Schoor, Geoff Kushnick, Petra Pennekamp, Idaman Zega, Oscar Lao, Lea Brown, Ingo Kennerknecht and Manfred Kayser
Unexpected Island Effects at an Extreme: Reduced Y Chromosome and Mitochondrial DNA Diversity in Nias

Aleksandra Shypitsyna, Edward Málaga-Trillo, Alexander Reuter and Claudia A.O. Stuermer
Origin of Nogo-A by Domain Shuffling in an Early Jawed Vertebrate

Nina Stoletzki and Adam Eyre-Walker
The Positive Correlation between dN/dS and dS in Mammals Is Due to Runs of Adjacent Substitutions

Lino Ometto, DeWayne Shoemaker, Kenneth G. Ross and Laurent Keller
Evolution of Gene Expression in Fire Ants: The Effects of Developmental Stage, Caste, and Species

Klaus Schliep, Philippe Lopez, François-Joseph Lapointe and Éric Bapteste
Harvesting Evolutionary Signals in a Forest of Prokaryotic Gene Trees

Zhenguo Lin and Wen-Hsiung Li
The Evolution of Aerobic Fermentation in Schizosaccharomyces pombe Was Associated with Regulatory Reprogramming but not Nucleosome Reorganization

Harold H. Zakon, Manda C. Jost and Ying Lu
Expansion of Voltage-dependent Na+ Channel Gene Family in Early Tetrapods Coincided with the Emergence of Terrestriality and Increased Brain Complexity

Aurora Fraile, Israel Pagán, Germán Anastasio, Elisa Sáez and Fernando García-Arenal
Rapid Genetic Diversification and High Fitness Penalties Associated with Pathogenicity Evolution in a Plant Virus

Hélene Adam, Mélanie Marguerettaz, Rashad Qadri, Bernard Adroher, Frédérique Richaud, Myriam Collin, Anne-Céline Thuillet, Yves Vigouroux, Patrick Laufs, James W. Tregear and Stefan Jouannic
Divergent Expression Patterns of miR164 and CUP-SHAPED COTYLEDON Genes in Palms and Other Monocots: Implication for the Evolution of Meristem Function in Angiosperms

Aines Castro-Prieto, Bettina Wachter and Simone Sommer
Cheetah Paradigm Revisited: MHC Diversity in the World's Largest Free-Ranging Population

Sunju Kim, Tsvetan R. Bachvaroff, Sara M. Handy and Charles F. Delwiche
Dynamics of Actin Evolution in Dinoflagellates

Ofir Cohen, Uri Gophna and Tal Pupko
The Complexity Hypothesis Revisited: Connectivity Rather Than Function Constitutes a Barrier to Horizontal Gene Transfer

Maxim V. Kapralov, David S. Kubien, Inger Andersson, and Dmitry A. Filatov
Changes in Rubisco Kinetics during the Evolution of C4 Photosynthesis in Flaveria (Asteraceae) Are Associated with Positive Selection on Genes Encoding the Enzyme

Pontus Skoglund, Anders Götherström and Mattias Jakobsson
Estimation of Population Divergence Times from Non-Overlapping Genomic Sequences: Examples from Dogs and Wolves

Robert Piskol and Wolfgang Stephan
Selective Constraints in Conserved Folded RNAs of Drosophilid and Hominid Genomes

Pär J. Höglund, Karl J.V. Nordström, Helgi B. Schiöth and Robert Fredriksson
The Solute Carrier Families Have a Remarkably Long Evolutionary History with the Majority of the Human Families Present before Divergence of Bilaterian Species



+++++++++++++++

POLITYKA I NIE TYLKO , PRZEPISY KULINARNE , ULUBIONE KSIĄŻKI , DOWCIPY , GEOGRAFIA , ŚWIEBODZICE , FORUM O RODZAJU HOYA , PEUGEOT , TWOJE CENTRUM FINANSOWE , PiS , PLATFORMA OBYWATELSKA
+++++++++++++++

PLANT - FAMILY - FLOWER - GENERA - JOURNAL - ARTICOLO - PLANTS - PIANTE - BOTANIQUE - ROŚLINY - SINONIM - FAMIGLIA - BOTANY - NAUKA - SINONIMO - BOTANICA - WYCIECZKA - TRAVEL - SINÓNIMO - FRUIT - ARTICOLO - SYNONIEM - CZASOPISMO - SYNONYM - SYNONYME - SYSTEMATIC - SYSTEMATYKA - SZINONIMA - SYSTEMATYKA - RODZINA - ARTYKUŁ - ARTICLE - FLOWER - KWIATY - OWOC - SEEDS - NASIONA - CULTIVATION - USE - WATERING - PROPAGATION - PESTSM - DISEASES - FERTILIZATION - HOUSE - GARDEN - BOWL - KWITNIENIE - FLOWERBED - SOIL - POND - MARSH - SPECIES - HYBRIDS - VEGETABLE GARDEN - UPRAWA - ZASTOSOWANIE - PODLEWANIE - ROZMNAŻANIE - SZKODNIKI - CHOROBY - NAWOŻENIE - ROŚLINY DOMOWE - ROŚLINY BALKONOWE - ROŚLINY TARASOWE - OGRÓD - POJEMNIK - SUBSTRAT - PODŁOŻE - KERAMZYT - GLINA - TORF - DONICA - DONICZKA - ZIEMIA - RABATA - GLEBA - ROŚLINY WODNE - STAW - WODA - ROŚLINY BAGIENNE - OWOCE - WARZYWA - SPRZEDAŻ ROŚLIN - GATUNKI - MIESZAŃCE - CV - KULTYWARY

Molecular Plant Pathology - 12 (3), 2011

Contents:

Pathogen profiles


Tobacco leaf spot and root rot caused by Rhizoctonia solani Kühn (pages 209–216)

MARLENY GONZALEZ, MERARDO PUJOL, JEAN-PIERRE METRAUX, VICENTE GONZALEZ-GARCIA, MELVIN D. BOLTON and ORLANDO BORRÁS-HIDALGO


The cucurbit downy mildew pathogen Pseudoperonospora cubensis (pages 217–226)

ELIZABETH A. SAVORY, LEAH L. GRANKE, LINA M. QUESADA-OCAMPO, MARINA VARBANOVA, MARY K. HAUSBECK and BRAD DAY


Original articles


The rsmA-like gene rsmAXoo of Xanthomonas oryzae pv. oryzae regulates bacterial virulence and production of diffusible signal factor (pages 227–237)

PEI-LIANG ZHU, SHUAI ZHAO, JI-LIANG TANG and JIA-XUN FENG


CYP1, a hypovirus-regulated cyclophilin, is required for virulence in the chestnut blight fungus (pages 239–246)

MIN-MEI CHEN, MINGGUO JIANG, JINJIE SHANG, XIUWAN LAN, FENG YANG, JINGKUAN HUANG, DONALD L. NUSS and BAOSHAN CHEN


Extracellular invertase is involved in the regulation of clubroot disease in Arabidopsis thaliana (pages 247–262)

JOHANNES SIEMENS, MARIA-CRUZ GONZÁLEZ, SEBASTIAN WOLF, CHRISTINA HOFMANN, STEFFEN GREINER, YEJIE DU, THOMAS RAUSCH, THOMAS ROITSCH and JUTTA LUDWIG-MÜLLER


Mechanisms of powdery mildew resistance in the Vitaceae family (pages 263–274)

ANGELA FEECHAN, SAMUELA KABBARA and IAN B. DRY


A polygalacturonase-inhibiting protein with a role in pea defence against the cyst nematode Heterodera goettingiana (pages 275–287)

PASQUA VERONICO, M. TERESA MELILLO, CONCETTA SAPONARO, PAOLA LEONETTI, ERNESTO PICARDI and JOHN T. JONES


Technical advances


RNA-mediated gene silencing in the cereal fungal pathogen Cochliobolus sativus (pages 289–298)

YUEQIANG LENG, CHENGXIANG WU, ZHAOHUI LIU, TIMOTHY L. FRIESEN, JACK B. RASMUSSEN and SHAOBIN ZHONG


The reliability of virus-induced gene silencing experiments using tobacco rattle virus in tomato is influenced by the size of the vector control (pages 299–305)

CHENGJUN WU, LINGLING JIA and FIONA GOGGIN


+++++++++++++++

PLANT - FAMILY - FLOWER - GENERA - JOURNAL - ARTICOLO - PLANTS - PIANTE - BOTANIQUE - ROŚLINY - SINONIM - FAMIGLIA - BOTANY - NAUKA - SINONIMO - BOTANICA - WYCIECZKA - TRAVEL - SINÓNIMO - FRUIT - ARTICOLO - SYNONIEM - CZASOPISMO - SYNONYM - SYNONYME - SYSTEMATIC - SYSTEMATYKA - SZINONIMA - SYSTEMATYKA - RODZINA - ARTYKUŁ - ARTICLE - FLOWER - KWIATY - OWOC - SEEDS - NASIONA - CULTIVATION - USE - WATERING - PROPAGATION - PESTSM - DISEASES - FERTILIZATION - HOUSE - GARDEN - BOWL - KWITNIENIE - FLOWERBED - SOIL - POND - MARSH - SPECIES - HYBRIDS - VEGETABLE GARDEN - UPRAWA - ZASTOSOWANIE - PODLEWANIE - ROZMNAŻANIE - SZKODNIKI - CHOROBY - NAWOŻENIE - ROŚLINY DOMOWE - ROŚLINY BALKONOWE - ROŚLINY TARASOWE - OGRÓD - POJEMNIK - SUBSTRAT - PODŁOŻE - KERAMZYT - GLINA - TORF - DONICA - DONICZKA - ZIEMIA - RABATA - GLEBA - ROŚLINY WODNE - STAW - WODA - ROŚLINY BAGIENNE - OWOCE - WARZYWA - SPRZEDAŻ ROŚLIN - GATUNKI - MIESZAŃCE - CV - KULTYWARY

+++++++++++++++

POLITYKA I NIE TYLKO , PRZEPISY KULINARNE , ULUBIONE KSIĄŻKI , DOWCIPY , GEOGRAFIA , ŚWIEBODZICE , FORUM O RODZAJU HOYA , PEUGEOT , TWOJE CENTRUM FINANSOWE , PiS , PLATFORMA OBYWATELSKA

+++++++++++++++

Rodzaj Rosa (róża) - ciekawsze odmiany uprawne

A
Rosa ‘Abbeyfield Rose’
Rosa ‘Abigaile’
Rosa ‘Abraham Darby’
Rosa ‘Acropolis’
Rosa ‘Adélaïde d`Orléans’
Rosa ‘Adele Crofton’
Rosa ‘Aenne Burda’
Rosa ‘Agatha Christie’
Rosa ‘Agnes’
Rosa ‘Aicha’
Rosa ‘Akito’
Rosa ‘Alain’
Rosa x alba 'Alba Maxima'
Rosa x alba 'Alba Semiplena’
Rosa ‘Albèric Barbier’
Rosa ‘Albertine’
Rosa ‘Alchymist’
Rosa ‘Alexande`r’
Rosa ‘Alexandra’
Rosa ‘Alexandre Girault’
Rosa ‘Alida Lovett’
Rosa ‘Alinka’
Rosa ‘Allgold’
Rosa ‘Allgold Climbing’
Rosa ‘Aloha’ ®
Rosa ‘Alpine Sunset’
Rosa ‘Altissimo’
Rosa ‘Amadeus’ ®
Rosa ‘Amber Queen’
Rosa ‘Ambroise Paré’
Rosa ‘American Beauty’
Rosa ‘Americana’
Rosa ‘American Pillar’
Rosa ‘Andalusien’
Rosa ‘Angela’
Rosa ‘Angela Rippon’
Rosa ‘Anna Ford’
Rosa ‘Anna Livia’
Rosa ‘Anne Cocker’
Rosa ‘Anne de Bretagne’
Rosa ‘Anne Harkness’
Rosa ‘Antique Silk’
Rosa ‘Apricot Sunblaze’
Rosa ‘Arndt’
Rosa ‘Artemis’
Rosa ‘Arthur Bell’
Rosa ‘Ascot’
Rosa ‘Autumnalis’
Rosa ‘Ave Maria’
Rosa ‘Avon’

B
Rosa ‘Baby Masquerade’
Rosa ‘Ballerina’
Rosa ‘Balzac’
Rosa banksiae ‘Lutea’
Rosa ‘Bantry Bay’
Rosa ‘Barkarole’ ®
Rosa ‘Baron Girod de l’Ain’
Rosa ‘Baronne Prévost’
Rosa ‘Belle de Crécy’
Rosa ‘Benson and Hedges Special’
Rosa ‘Benvenuto’
Rosa ‘Bicolor’
Rosa ‘Big Purple’
Rosa ‘Black Lady’
Rosa ‘Blairii Number Two’
Rosa ‘Blanche Double de Coubert’
Rosa ‘Blanche Moreau’
Rosa ‘Blaze Improved’
Rosa ‘Blessings’
Rosa ‘Blue Moon’
Rosa ‘Bob Hope’
Rosa ‘Bobbie James’
Rosa ‘Bonfire Night’
Rosa ‘Bonica’
Rosa ‘Boule de Neige’
Rosa ‘Boys` Brigade’
Rosa ‘Brandy’
Rosa ‘Bright Smile’
Rosa ‘Bucks Fizz’
Rosa ‘Buff Beauty’
Rosa ‘Burgund 81’
Rosa ‘Bush Baby’
Rosa ‘Buttons’
Rosa ‘By Appointment’

C
Rosa californica ‘Plena’
Rosa ‘Camaïeux’
Rosa ‘Campanille’
Rosa ‘Canary Bird’
Rosa canina ‘Kiese’
Rosa ‘Capitaine John Ingram’
Rosa ‘Caprice de Festival’
Rosa ‘Caprice de Meilland’
Rosa ‘Caramella’
Rosa ‘Cardinal de Richelieu’
Rosa ‘Carina’
Rosa ‘Carmenetta’
Rosa ‘Cécile Brunner’
Rosa ‘Celeste’
Rosa ‘Céline Forestier’
Rosa ‘Centenaire de Lourdes’
Rosa x centifolia 'Cristata'
Rosa x centifolia 'Muscosa'
Rosa x chinensis ‘Mutabilis’
Rosa ‘Champagne Cocktail’
Rosa ‘Champs Elysees’
Rosa ‘Chanele’
Rosa ‘Chapeau de Napoléon’
Rosa ‘Charles Austin’
Rosa ‘Charles de Mills’
Rosa ‘Cherry Brandy’
Rosa ‘Cheshire Life’
Rosa ‘Chicago Peace’
Rosa ‘Chinatown’
Rosa ‘Chippendale’
Rosa ‘Chopin’
Rosa ‘Christian Dior’
Rosa ‘Chrysler Imperial’
Rosa ‘Cider Cup’
Rosa ‘Cinderella’
Rosa ‘City of London’
Rosa ‘Clair Matin’
Rosa ‘Climbing Crimson Glory’
Rosa ‘Climbing Grand – mire Jenny’
Rosa ‘Climbing Rosa’
Rosa ‘Colette’
Rosa ‘Common Moss’
Rosa ‘Compassion’
Rosa ‘Comte de Chambord’
Rosa ‘Comtes de Champagne’
Rosa ‘Concerto 94’
Rosa ‘Concerto’
Rosa ‘Concerto’
Rosa ‘Condesa de Sçstago’
Rosa ‘Congratulations’
Rosa ‘Constance Spry’
Rosa ‘Coral Satin’
Rosa ‘Cornelia’
Rosa ‘Coronado’
Rosa ‘Crepe de Chine’
Rosa ‘Crested Moss’
Rosa ‘Crimson Duke’
Rosa ‘Crimson Shower’
Rosa ‘Cristata’
Rosa ‘Cuisse de Nymphe’

D
Rosa ‘Dacapo’
Rosa ‘Dame de Coeur’
Rosa ‘Dame Wendy’
Rosa ‘Darling Flame’
Rosa ‘Dawn Chorus’
Rosa ‘De Meaux’
Rosa ‘De Rescht’
Rosa ‘Dicbar’
Rosa ‘Dirigent’
Rosa ‘Display’
Rosa ‘Divine’
Rosa ‘Doctor McAlpine’
Rosa ‘Don Juan’
Rosa ‘Doreen’
Rosa ‘Dornroschen’
Rosa ‘Dortmund’
Rosa ‘Double Delight’
Rosa ‘Dream Girl’
Rosa ‘Dreaming Spires’
Rosa ‘Dronningen av Danmark’
Rosa ‘Drummer Boy’
Rosa ‘Du Maître d`Ecole’
Rosa ‘Dublin Bay’
Rosa ‘Duc de Guiche’
Rosa ‘Duchesse de Montebello’
Rosa ‘Duchess of Portland’
Rosa ‘Duftfestival’
Rosa ‘Duftrausch’
Rosa ‘Duplex’
Rosa ‘Dupontii’
Rosa ‘Dutch Gold’

E
Rosa ‘Eagle’
Rosa ‘Easter Morning’
Rosa ecae ‘Helen Knight’
Rosa ‘Eddies Crimson’
Rosa ‘Eden Rose 85’ ®
Rosa ‘Eden Rose’ ®
Rosa ‘Eglantyne’
Rosa ‘E.H. Morse’
Rosa ‘Edith Holden’
Rosa ‘Eiffel Tower’
Rosa ‘Elfe’
Rosa ‘Elina’
Rosa ‘Elizabeth Harkness’
Rosa ‘Elizabeth of Glamis’
Rosa ‘Elmshorn’
Rosa ‘Emelie’
Rosa ‘Emily Gray’
Rosa ‘Empress Josephine’
Rosa ‘Ena Harkness’
Rosa ‘English Garden’
Rosa ‘English Miss’
Rosa ‘Ernest H. Morse’
Rosa ‘Enric Palau’
Rosa ‘Erotika’ ®
Rosa ‘Escapade’
Rosa ‘Esmeralda – Kordes Rose Esmeralda’ ®
Rosa ‘Essex’
Rosa ‘Europeana’
Rosa ‘Evelyn’
Rosa ‘Evening Star’
Rosa ‘Excelsa’
Rosa ‘Eye Paint’

F
Rosa ‘F.E. Lester’
Rosa ‘F.J. Grootendorst’
Rosa ‘Falstaff’
Rosa ‘Fantasia Mondiale’ ®
Rosa ‘Fantin Latour’
Rosa ‘Fashion’
Rosa ‘Felicia’
Rosa ‘Félicité Parmentier’
Rosa ‘Félicité Perpétue’
Rosa ‘Ferdy’
Rosa ‘Festival’
Rosa ‘Feudor’
Rosa ‘Feuerwerk’
Rosa ‘Fimbriata’
Rosa ‘First Lady’
Rosa ‘Fisherman’
Rosa ‘Flammentanz’
Rosa ‘Flora Danica’
Rosa ‘Flora Romantica’
Rosa ‘Flower Carpet’
Rosa foetida ‘Bicolor’
Rosa foetida 'Parkfeuer'
Rosa ‘Followship”
Rosa ‘Fountain’
Rosa ‘Fragrant Cloud’
Rosa ‘Fragrant Delight’
Rosa ‘Fragrant Dream’
Rosa ‘Francesca’
Rosa ‘Francine Austin’
Rosa ‘Francis E. Lester’
Rosa ‘François Juranville’
Rosa ‘Frau Karl Druschki’
Rosa ‘Fred Cramphorn’
Rosa ‘Fred Loads’
Rosa ‘Frederic Mistral’
Rosa ‘Freedom’
Rosa ‘Friesia’
Rosa ‘Fritz Nobis’
Rosa ‘Fru Dagmar Hastrup’
Rosa ‘Fruite’
Rosa ‘Frühlingsgold’
Rosa ‘Frühlingsmorgen’

G
Rosa ‘Gaiety’
Rosa ‘Gail Borden’
Rosa ‘Galileo’
Rosa gallica 'Officinalis'
Rosa gallica 'Splendens'
Rosa gallica ‘Tour de Malakoff’
Rosa gallica ‘Versicolor’
Rosa gallica ‘Violacea’
Rosa galica var. officinalis ‘Complicata’
Rosa galica var. officinalis ‘Versicolor’
Rosa ‘Galway Bay’
Rosa ‘Gartenträume’
Rosa ‘Gaujard’
Rosa ‘Gay Paris’
Rosa ‘Gefylt’
Rosa ‘Gentle Touch’
Rosa ‘Geranium’
Rosa ‘Gertrude Jekyll’
Rosa ‘Ghislaine de Féligonde’
Rosa ‘Giardina’
Rosa ‘Gingernut’
Rosa ‘Gipsy Boy’
Rosa ‘Glamis Castle’
Rosa “Glenfiddich’
Rosa ‘Gletscherfee’
Rosa ‘Gloire de Dijon’
Rosa ‘Gloire des Mousseuses’
Rosa ‘Gloria Dei’
Rosa ‘Goldbush’
Rosa ‘Golden Celebration’
Rosa ‘Golden Dawn’
Rosa ‘Golden Eye’
Rosa ‘Golden Gate’
Rosa ‘Golden Jubilee’
Rosa ‘Golden Masterpiece’
Rosa ‘Golden Showers’
Rosa ‘Golden Spray’
Rosa ‘Golden Wedding’
Rosa ‘Golden Wings’
Rosa ‘Golden Years’
Rosa ‘Goldfinch’
Rosa ‘Grace’
Rosa ‘Gräfin von Hardenberg’
Rosa ‘Graham Thomas’
Rosa ‘Granat’
Rosa ‘Grand Amore’
Rosa ‘Grand Castle’
Rosa ‘Grandpa Dickson’
Rosa ‘Gratitude’
Rosa ‘Great Maiden`s Blush’
Rosa ‘Green Ice’
Rosa ‘Green Rose’
Rosa ‘Greenall`s Glory’
Rosa ‘Gruß an Aachen’
Rosa ‘Gruss an Coburg’
Rosa ‘Guinée’
Rosa ‘Gypsy Boy’

H
Rosa ‘Hagoramo’
Rosa ‘Halloween’
Rosa ‘Hampshire’
Rosa ‘Handel’
Rosa ‘Hannah Gordon’
Rosa ‘Hanne’
Rosa ‘Hansa’
Rosa ‘Hanseat’
Rosa ‘Hansestadt Bremen’
Rosa harisonii ‘Harison`s Yellow’
Rosa ‘Harlekin’
Rosa ‘Harry Wheatcroft’
Rosa ‘Harvest Fayre’
Rosa ‘Heidelberg’
Rosa helenae ‘Semiplena’
Rosa ‘Helen Knight’
Rosa ‘Henri Martin’
Rosa ‘Heritage’
Rosa ‘Herkules’
Rosa ‘Hertfordshire’
Rosa ‘Highdownensis’
Rosa ‘Highfield’
Rosa ‘High Hopes’
Rosa ‘History’
Rosa ‘Hocus Pokus’
Rosa ‘Honey Bunch’
Rosa ‘Honeymoon’
Rosa ‘Honore de Balzac’
Rosa ‘Honorine de Brabant’
Rosa ‘Hurdalsrose’

I
Rosa ‘Iceberg’
Rosa ‘Ice Cream’
Rosa ‘Ice Lady’
Rosa ‘Iced Ginger’
Rosa ‘Ingrid Bergman’
Rosa ‘Invincible’
Rosa ‘Irena’
Rosa ‘Irène Watts’
Rosa ‘Isabel de Ortiz’
Rosa ‘Ispahan’

J
Rosa ‘Jacqueline’
Rosa ‘Jacqueline du Pré’
Rosa ‘Jacques Cartier’
Rosa ‘James Galway’
Rosa ‘Jane Asher’
Rosa ‘Jan Speck’
Rosa ‘Jardins de Bagatelle’
Rosa ‘Jasmina’ ®
Rosa ‘Jiminy Cricket’
Rosa ‘John F. Kennedy’
Rosa ‘Joseph Clemens’
Rosa ‘Joseph`s Coat’
Rosa ‘Jubile de Prince de Monaco’
Rosa ‘Judy Fischer’
Rosa ‘Julia`s Rose’
Rosa ‘Julischka’
Rosa ‘Just Joey’

K
Rosa ‘Kalinka’
Rosa ‘Keepsake’
Rosa ‘Kent’
Rosa ‘Kimono’
Rosa ‘King’s Ransom’
Rosa ‘Kismet’
Rosa ‘Knirps’
Rosa ‘Königin von Dänemark’
Rosa ‘Konigsberg’
Rosa ‘Konrad Adenauer’
Rosa kordesii ‘Sympathie’
Rosa ‘Kordes Brillant’
Rosa ‘Kordes Perfecta’
Rosa ‘Korresia’
Rosa ‘Kristall
Rosa ‘Kronerbourg’

L
Rosa ‘La Jolla’
Rosa ‘La Parisienne’
Rosa ‘La Reine Victoria’
Rosa ‘La Sevillana’
Rosa ‘Lady Hllington’
Rosa ‘Lady Gay’
Rosa ‘Lady Rose’
Rosa ‘Lafayette’
Rosa ‘Lagerfeuer’
Rosa ‘Landora’ ®
Rosa ‘Laura Ashley’
Rosa ‘Laura Ford’
Rosa ‘Lavender Dream’
Rosa ‘Lavender Lassie’
Rosa ‘Lawinia’
Rosa ‘La France’
Rosa ‘La Ville de Bruxelles’
Rosa ‘Lavinia’
Rosa ‘Le Rouge et le Noir’
Rosa ‘Leander’
Rosa ‘Leaping Salmon’
Rosa ‘Leo Ferré’ ®
Rosa ‘Leonardo da Vinci’
Rosa ‘Leonidas’
Rosa ‘Leverkusen’
Rosa ‘Lichtkönigin Lucia’
Rosa ‘Lilac Charm’
Rosa ‘Lilli Marlene’
Rosa ‘Little Bo-Peep’
Rosa ‘Little Buckaroo’
Rosa ‘Little White Pet’
Rosa ‘L`Oréal Trophy’
Rosa ‘Lolita’
Rosa ‘Louise Odier’
Rosa ‘Lovely Lady’
Rosa ‘Loving Memory’
Rosa ‘Lucie Marie’
Rosa ‘Lykkefund’
Rosa ‘L. D. Braithwaite’

M
Rosa ‘Madame Alfred Carrière’
Rosa ‘Madame Butterfly’
Rosa ‘Madame G. Forest – Colcombet’
Rosa ‘Madame Hardy’
Rosa ‘Madame Herbert’
Rosa ‘Madame Isaac Pereire’
Rosa ‘Madame Knorr’
Rosa ‘Madame Ph. Plantamour’
Rosa ‘Madame Pierre Oger’
Rosa ‘Madame Plantier’
Rosa ‘Macrexy’
Rosa macrophylla ‘Master Hugh’
Rosa ‘Magic Carrousel’
Rosa ‘Magitta’
Rosa ‘Magnifica’
Rosa ‘Maiden’s Blush’
Rosa ‘Maigold’
Rosa ‘Mainzer Fastnacht’ ®
Rosa ‘Maltese Rose’
Rosa ‘Marco Polo’
Rosa ‘Marguerite Hilling’
Rosa ‘Mariandel’
Rosa ‘Maria Lisa’
Rosa ‘Marie Curie’
Rosa ‘Marinette’
Rosa ‘Maritim’
Rosa ‘Martha’
Rosa ‘Mary Rose’
Rosa ‘Maurice Chevalier’
Rosa ‘Mazowsze’
Rosa ‘Mercedes Mendoza’
Rosa ‘Merle Blanc’
Rosa ‘Mezzoforte’
Rosa ‘Millie Perkins’
Rosa ‘Miranda’
Rosa ‘Molineux’
Rosa ‘Morgengruss’
Rosa ‘Mount Shasta’
Rosa ‘Mozart’
Rosa ‘Mrs F.F.Prentiss’
Rosa ‘Mrs. John Laing’
Rosa ‘Mutabilis’
Rosa ‘My Fair Lady’
Rosa ‘My Girl’
Rosa ‘Mysterium’

N
Rosa ‘National Nypels’
Rosa ‘National Trust’
Rosa ‘N.I. Kichunov’
Rosa ‘Neue Revue’
Rosa ‘Nevada’
Rosa ‘New Daily Mail’
Rosa ‘New Dawn’
Rosa ‘Night Light’
Rosa ‘Nobilo`s Chardonnay’
Rosa ‘Nordia’
Rosa ‘Nostalgia’
Rosa ‘Nostalgie’
Rosa ‘Nozomi’

O
Rosa ‘Olala’
Rosa ‘Opera’
Rosa ‘Ophelia’
Rosa ‘Oriental Charm’

P
Rosa ‘Palette’
Rosa ‘Parade’
Rosa ‘Parole’ ®
Rosa ‘Pas de Deux’
Rosa ‘Pat Austin’
Rosa ‘Patricia’
Rosa ‘Paulii’
Rosa ‘Paul`s Himalayan Musk’
Rosa ‘Peace’
Rosa pendulina 'Harstad'
Rosa ‘Perennial Blue’ ®
Rosa ‘Persian Yellow’
Rosa ‘Petite de Hollande’
Rosa ‘Pharao’
Rosa ‘Phare’
Rosa ‘Piano’
Rosa ‘Pilgrim’
Rosa ‘Pinata’
Rosa ‘Pink Cloud’
Rosa ‘Pink Star’
Rosa ‘Piroshka’
Rosa pomifera 'Karpatia'
Rosa ‘Prairie Yourth’
Rosa ‘Praise of Jiro’
Rosa ‘President Dr. Schroder’
Rosa ‘President Jac. Smits’
Rosa ‘Prickly Red’
Rosa ‘Prima Ballerina’

Q
Rosa ‘Queen Elizabeth’

R
Rosa ‘Raubritter’
Rosa ‘Red Eden Rose’ ®
Rosa ‘Red Leonardo da Vinci’
Rosa ‘Red Rock’
Rosa ‘Reine des Violettes
Rosa ‘Rhapsody in Blue’
Rosa ‘Rheinaupark’
Rosa ‘Robin Hood’
Rosa ‘Robusta’
Rosa ‘Roelof Buisman’
Rosa ‘Rose de Resht’
Rosa ‘Rose de Restch’
Rosa ‘Rose Guajard’
Rosa ‘Rose Romantic’
Rosa ‘Rosemary Harkness’
Rosa ‘Rosenrot’
Rosa ‘Rosy Cushion’
Rosa ‘Rote Pharisaer’
Rosa ‘Rotes Meer’
Rosa ‘Royal Gold’
Rosa ‘Royal Scarlet’
Rosa ‘Rubaiyat’
Rosa rubrifolia 'Nova'
Rosa rugosa ‘Abelzieds’
Rosa rugosa ‘Adam Chodun’
Rosa rugosa ‘Agnes’
Rosa rugosa ‘Alba’
Rosa rugosa ‘Amdo’
Rosa rugosa ‘Amelie Gravereaux’
Rosa rugosa ‘Blanc Double de Coubert’
Rosa rugosa ‘Carmen’
Rosa rugosa ‘Dagmar Hastrup’
Rosa rugosa ‘F.J. Grootendorf’
Rosa rugosa ‘F.J. Grootendorst’
Rosa rugosa ‘Grootendorst Supreme’
Rosa rugosa ‘Guna’
Rosa rugosa ‘Hansa’
Rosa rugosa ‘Kaiserin des Nordens’
Rosa rugosa ‘Koza’
Rosa rugosa ‘Kórnik’
Rosa rugosa ‘La Melusine’
Rosa rugosa ‘Le Cid’
Rosa rugosa ‘Minisa’
Rosa rugosa ‘Moje Hammarberg’
Rosa rugosa ‘Parsla’
Rosa rugosa ‘Pink Grootendorst’
Rosa rugosa ‘Red Dagmar’
Rosa rugosa ‘Regelliana’
Rosa rugosa ‘Ritausma’
Rosa rugosa ‘Scabrosa’
Rosa rugosa ‘White Hedge’
Rosa rugosa ‘Zaiga’
Rosa ‘Rumba’

S
Rosa ‘S`Agaro’
Rosa ‘Sahara’
Rosa ‘Santana’ ®
Rosa ‘Schneewalzer’ ®
Rosa ‘Schneewittchen’
Rosa ‘Sebastian Kneipp’ ®
Rosa ‘Sekel’
Rosa ‘Senteur Royale’
Rosa sericea ‘Chrysocarpa’
Rosa sericea ‘Pteracantha’
Rosa ‘Showbiz’
Rosa ‘Shropshire Lass’
Rosa ‘Smarty’
Rosa ‘Snow Ballett’
Rosa ‘Snow Goose’
Rosa ‘South Seas’
Rosa ‘Souvenir de la Malmaison’
Rosa ‘Sparrieshoop’
Rosa ‘Speths Jubileum’
Rosa spinosissima ‘Red Nelly’
Rosa spinosissima ‘Schloss Seutlitz’
Rosa spinosissima ‘White Scotch’
Rosa ‘Srebra’
Rosa ‘Stadt Rom’
Rosa ‘Stanwell Perpetual’
Rosa ‘Star Profusion’
Rosa ‘Starina’
Rosa ‘Suffolk’
Rosa ‘Suma’
Rosa ‘Sun Valley’
Rosa ‘Sunbright’
Rosa ‘Sundowner’
Rosa ‘Sunlicht Romantika’
Rosa ‘Sunny Sky’ ®
Rosa ‘Super Dorothy’
Rosa ‘Surrey’
Rosa ‘Sympathie’

Ś
Rosa ‘Święta Tereska’

T
Rosa ‘Taboo’
Rosa ‘Tahiti’
Rosa ‘Tall Story’
Rosa ‘Tango’
Rosa ‘Tatjana’
Rosa ‘Teasing Georgia’
Rosa ‘Terracota’
Rosa ‘The Alamo’
Rosa ‘The Fairy’
Rosa ‘The Herbalist’
Rosa ‘The New Dawn’
Rosa ‘The Pilgrim’
Rosa ‘The Prince’
Rosa ‘Thérese Bugnet’
Rosa ‘Thisbe’
Rosa ‘Topsi’
Rosa ‘Torch Song’
Rosa ‘Tornado’
Rosa ‘Tradescant’
Rosa ‘Trier’
Rosa ‘Troika’
Rosa ‘Tropique’
Rosa ‘Tschaikowski’
Rosa ‘Tuscany Superb’
Rosa ‘Tuscany’
Rosa ‘Twist’

V
Rosa ‘Valencia’
Rosa ‘Valiant’
Rosa ‘Varlon’
Rosa ‘Veilchenblau’
Rosa ‘Victor Verdier’
Rosa ‘Vidal Sassoon’
Rosa ‘Vltawa’
Rosa ‘Vogelpark Walsrode’

W
Rosa ‘Waltz Time‘
Rosa ‘Warm Welcome’
Rosa ‘Wee Jock’
Rosa ‘Whisky Mac’
Rosa ‘White Bath’
Rosa ‘White New Dawn’
Rosa ‘William Shakespeare’
Rosa ‘Winchester Cathedral’

Y
Rosa ‘Yankee Doodle’
Rosa ‘Yellow Garnish’
Rosa ‘Yellow Hammer’
Rosa ‘Yellow Star’
Rosa ‘Yolande d`Aragon’

Z
Rosa ‘Zéphirine Drouhin’
Rosa ‘Zigeunerknabe’
Rosa ‘Zwergkünig’


© Mark 2011




====================
plant - family - flower - genera - journal - articolo - plants - piante - botanique - rośliny - sinonim - famiglia - botany - nauka - sinonimo - botanica - wycieczka - travel - sinónimo - fruit - sinônimo - articolo - synoniem - czasopismo - synonym - synonyme - systematic - systematyka - szinonima - systematyka - rodzina - artykuł - article - flower - kwiaty - owoc - seeds - nasiona
====================
POLITYKA I NIE TYLKO , PRZEPISY KULINARNE , ULUBIONE KSIĄŻKI , DOWCIPY , GEOGRAFIA , ŚWIEBODZICE , FORUM O RODZAJU HOYA , PEUGEOT , TWOJE CENTRUM FINANSOWE , PiS , PLATFORMA OBYWATELSKA

Rodzaj Rosa (róża) - gatunki botaniczne

>> Rosa (róża)
>>>>>>>>>> Rosa abietina
>>>>>>>>>> Rosa abyssinica
>>>>>>>>>> Rosa acicularis (róża igiełkowata)
>>>>>>>>>> Rosa agrestis (róża eliptyczna, róża polna)
>>>>>>>>>> Rosa albertii
>>>>>>>>>> Rosa amblyotis
>>>>>>>>>> Rosa arkansana
>>>>>>>>>> Rosa arvensis
>>>>>>>>>> Rosa baltica
>>>>>>>>>> Rosa banksiae
>>>>>>>>>> Rosa banksiopsis
>>>>>>>>>> Rosa beggeriana
>>>>>>>>>> Rosa bella
>>>>>>>>>> Rosa blanda (róża labradorska)
>>>>>>>>>> Rosa bracteata
>>>>>>>>>> Rosa brunonii
>>>>>>>>>> Rosa cabulica
>>>>>>>>>> Rosa californica
>>>>>>>>>> Rosa canina (róża dzika)
>>>>>>>>>> Rosa carolina (róża karolińska)
>>>>>>>>>> Rosa caudata
>>>>>>>>>> Rosa centifolia (róża stulistna)
>>>>>>>>>> Rosa cerasocarpa
>>>>>>>>>> Rosa chinensis (róża chińska)
>>>>>>>>>> Rosa clinophylla
>>>>>>>>>> Rosa coriifolia
>>>>>>>>>> Rosa corymbifera
>>>>>>>>>> Rosa corymbulosa
>>>>>>>>>> Rosa cymosa
>>>>>>>>>> Rosa damascena (róża damasceńska)
>>>>>>>>>> Rosa davidii
>>>>>>>>>> Rosa davurica (róża dahurska)
>>>>>>>>>> Rosa doluchanovii
>>>>>>>>>> Rosa dumalis (róża sina)
>>>>>>>>>> Rosa ecae
>>>>>>>>>> Rosa elegantula
>>>>>>>>>> Rosa elliptica
>>>>>>>>>> Rosa fedtschenkoana
>>>>>>>>>> Rosa filipes
>>>>>>>>>> Rosa foetida (róża żółta)
>>>>>>>>>> Rosa foliolosa
>>>>>>>>>> Rosa forrestiana
>>>>>>>>>> Rosa gallica (róża francuska)
>>>>>>>>>> Rosa gentiliana
>>>>>>>>>> Rosa giraldii
>>>>>>>>>> Rosa glauca (róża czerwonawa)
>>>>>>>>>> Rosa glomerata
>>>>>>>>>> Rosa gorenkensis (róża rosyjska)
>>>>>>>>>> Rosa graciliflora
>>>>>>>>>> Rosa gymnocarpa
>>>>>>>>>> Rosa helenae
>>>>>>>>>> Rosa hemisphaerica
>>>>>>>>>> Rosa hemsleyana
>>>>>>>>>> Rosa henryi
>>>>>>>>>> Rosa iberica
>>>>>>>>>> Rosa jundzillii (róża Jundziłła)
>>>>>>>>>> Rosa kokanica
>>>>>>>>>> Rosa laevigata
>>>>>>>>>> Rosa laxa
>>>>>>>>>> Rosa leschenaultiana
>>>>>>>>>> Rosa longicuspis
>>>>>>>>>> Rosa luciae
>>>>>>>>>> Rosa macrophylla
>>>>>>>>>> Rosa mairei
>>>>>>>>>> Rosa majalis (róża girlandowa)
>>>>>>>>>> Rosa manca
>>>>>>>>>> Rosa maracandica
>>>>>>>>>> Rosa marretii
>>>>>>>>>> Rosa marschalliana
>>>>>>>>>> Rosa maximowicziana
>>>>>>>>>> Rosa micrantha (róża drobnokwiatowa)
>>>>>>>>>> Rosa microcarpa
>>>>>>>>>> Rosa minutifolia
>>>>>>>>>> Rosa miyoshii
>>>>>>>>>> Rosa mollis (róża jabłkowata)
>>>>>>>>>> Rosa montana
>>>>>>>>>> Rosa moschata (róża piżmowa)
>>>>>>>>>> Rosa moyesii
>>>>>>>>>> Rosa multibracteata
>>>>>>>>>> Rosa multiflora (róża wielokwiatowa)
>>>>>>>>>> Rosa murielae
>>>>>>>>>> Rosa nanothamnus
>>>>>>>>>> Rosa nitida (róża błyszcząca)
>>>>>>>>>> Rosa nitidula
>>>>>>>>>> Rosa nutkana
>>>>>>>>>> Rosa palustris (róża błotna)
>>>>>>>>>> Rosa pendulina (róża alpejska)
>>>>>>>>>> Rosa persetosa
>>>>>>>>>> Rosa persica
>>>>>>>>>> Rosa phoenicia
>>>>>>>>>> Rosa pisocarpa
>>>>>>>>>> Rosa platyacantha
>>>>>>>>>> Rosa pouzinii
>>>>>>>>>> Rosa prattii
>>>>>>>>>> Rosa pulverulenta
>>>>>>>>>> Rosa roxburghii
>>>>>>>>>> Rosa rubiginosa (róża rdzawa)
>>>>>>>>>> Rosa rubus
>>>>>>>>>> Rosa rugosa (róża pomarszczona)
>>>>>>>>>> Rosa sabini
>>>>>>>>>> Rosa sambucina
>>>>>>>>>> Rosa saturata
>>>>>>>>>> Rosa schrenkiana
>>>>>>>>>> Rosa sempervirens
>>>>>>>>>> Rosa serafinii
>>>>>>>>>> Rosa sericea
>>>>>>>>>> Rosa sertata
>>>>>>>>>> Rosa setigera
>>>>>>>>>> Rosa setipoda
>>>>>>>>>> Rosa sherardii (róża zapoznana)
>>>>>>>>>> Rosa sicula
>>>>>>>>>> Rosa sikangensis
>>>>>>>>>> Rosa sinowilsonii
>>>>>>>>>> Rosa soulieana
>>>>>>>>>> Rosa spinosissima (róża gęstokolczasta)
>>>>>>>>>> Rosa squarrosa
>>>>>>>>>> Rosa stellata
>>>>>>>>>> Rosa suffulta
>>>>>>>>>> Rosa sweginzowii
>>>>>>>>>> Rosa tomentosa (róża kutnerowata)
>>>>>>>>>> Rosa turcica
>>>>>>>>>> Rosa turkestanica
>>>>>>>>>> Rosa tuschetica
>>>>>>>>>> Rosa villosa (róża jabłkowata)
>>>>>>>>>> Rosa virginiana (róża wirgińska)
>>>>>>>>>> Rosa webbiana
>>>>>>>>>> Rosa wichuraiana (róża Wichury)
>>>>>>>>>> Rosa willmottiae
>>>>>>>>>> Rosa woodsii
>>>>>>>>>> Rosa xanthina
>>>>>>>>>> Rosa zagrabiensis
>>>>>>>>>> Rosa zalana (róża węgierska)

=============================

++++++++++++++++++++++

plant - family - flower - genera - journal - articolo - plants - piante - botanique - rośliny - sinonim - famiglia - botany - nauka - sinonimo - botanica - wycieczka - travel - sinónimo - fruit - sinônimo - articolo - synoniem - czasopismo - synonym - synonyme - systematic - systematyka - szinonima - systematyka - rodzina - artykuł - article - flower - kwiaty - owoc - seeds - nasiona - flora - przyroda - siedlisko

++++++++++++++++++++++

POLITYKA I NIE TYLKO , PRZEPISY KULINARNE , ULUBIONE KSIĄŻKI , DOWCIPY , GEOGRAFIA , ŚWIEBODZICE , FORUM O RODZAJU HOYA , ŚWIEBODZICE - FORUM

_________________

African Journal of Plant Science - 4 (9), 2010

Contents:



Research Articles



Adeduntan Sunday Adeniyi

Effects of slash and burning on soil microbial diversity and abundance in the tropical rainforest ecosystem, Ondo State, Nigeria


Huiping Bi, Mahender Aileni and Peng Zhang

Evaluation of cassava varieties for cassava mosaic disease resistance jointly by agro-inoculation screening and molecular markers


Ali Zakaria Babiker, Mohammad Ehsan Dulloo, M. A. Mustafa El Balla and El Tahir Ibrahim

Effects of low cost drying methods on seed quality of Sorghum bicolor (L.) Monech


Waseem Shahri, Inayatullah Tahir, Sheikh Tajamul Islam and Mushtaq Ahmad

Response of some ornamental flowers of family Ranunculaceae to sucrose feeding


Amelework Kassa, Ricardo Alía, Wubalem Tadesse, Valentin Pando and Felipe Bravo

Seed germination and viability in two African Acacia species growing under different water stress levels


S. Ravan

Ecological distribution and feeding preferences of Iran termites


E. Nepolo, P. M. Chimwamurombe, C. A. Cullis and M. A. Kandawa-Schulz

Determining genetic diversity based on ribosomal intergenic spacer length variation in Marama bean (Tylosema esculentum) from the Omipanda area, Eastern Namibia




++++++++++++++++++++++

plant - family - flower - genera - journal - articolo - plants - piante - botanique - rośliny - sinonim - famiglia - botany - nauka - sinonimo - botanica - wycieczka - travel - sinónimo - fruit - sinônimo - articolo - synoniem - czasopismo - synonym - synonyme - systematic - systematyka - szinonima - systematyka - rodzina - artykuł - article - flower - kwiaty - owoc - seeds - nasiona

++++++++++++++++++++++

POLITYKA I NIE TYLKO , PRZEPISY KULINARNE , ULUBIONE KSIĄŻKI , DOWCIPY , GEOGRAFIA , ŚWIEBODZICE , FORUM O RODZAJU HOYA

_________________

Rodzaje należące do rodziny różowatych (Rosaceae) - alfabetycznie

>>>>>>>> Acaena (acena)
>>>>>>>> Adenostoma
>>>>>>>> Agrimonia (rzepik)
>>>>>>>> Alchemilla (przywrotnik)
>>>>>>>> Amelanchier (świdośliwa)
>>>>>>>> Aremonia
>>>>>>>> Aronia
>>>>>>>> Aruncus (parzydło)
>>>>>>>> Bencomia
>>>>>>>> Cercocarpus
>>>>>>>> Chaenomeles (pigwowiec)
>>>>>>>> Chamaebatia
>>>>>>>> Chamaebatiaria
>>>>>>>> Chamaemeles
>>>>>>>> Chamaerhodos
>>>>>>>> Cliffortia
>>>>>>>> Coleogyne
>>>>>>>> Coluria
>>>>>>>> Comarum (siedmiopalecznik)
>>>>>>>> Cotoneaster (irga)
>>>>>>>> Cowania
>>>>>>>> Crataegus (głóg)
>>>>>>>> Cydonia (pigwa)
>>>>>>>> Dalibarda
>>>>>>>> Dasiphora
>>>>>>>> Dichotomanthes
>>>>>>>> Docynia
>>>>>>>> Dryas (dębik)
>>>>>>>> Drymocallis
>>>>>>>> Duchesnea (poziomkówka, suszotka)
>>>>>>>> Eriobotrya (eriobotria, miszpelnik, nieśplik)
>>>>>>>> Exochorda (egzochorda, obiela)
>>>>>>>> Fallugia
>>>>>>>> Filipendula (wiązówka)
>>>>>>>> Fragaria
>>>>>>>> Geum (kuklik)
>>>>>>>> Gillenia
>>>>>>>> Hagenia
>>>>>>>> Hesperomeles
>>>>>>>> Heteromeles
>>>>>>>> Holodiscus (pustokrężnik)
>>>>>>>> Horkelia
>>>>>>>> Horkeliella
>>>>>>>> Ivesia
>>>>>>>> Kageneckia
>>>>>>>> Kelseya
>>>>>>>> Kerria (złotlin)
>>>>>>>> Leucosidea
>>>>>>>> Lindleya
>>>>>>>> Luetkea
>>>>>>>> Lyonothamnus
>>>>>>>> Maddenia
>>>>>>>> Malacomeles
>>>>>>>> Malus (jabłoń)
>>>>>>>> Margyricarpus
>>>>>>>> Mespilus (nieszpułka)
>>>>>>>> Neillia
>>>>>>>> Neviusia
>>>>>>>> Oemleria
>>>>>>>> Orthurus
>>>>>>>> Osteomeles
>>>>>>>> Peraphyllum
>>>>>>>> Petrophytum
>>>>>>>> Photinia (głogownik)
>>>>>>>> Polylepis
>>>>>>>> Potaninia
>>>>>>>> Potentilla (pięciornik)
>>>>>>>> Poteridium
>>>>>>>> Poterium [=Sanguisorba]
>>>>>>>> Prinsepia
>>>>>>>> Prunus (śliwa – nazwa ogólna)
>>>>>>>> Pseudocydonia
>>>>>>>> Purshia
>>>>>>>> Pyracantha (ognik)
>>>>>>>> Pyrus (grusza)
>>>>>>>> Rhaphiolepis
>>>>>>>> Rhodotypos (różowiec, okółkowiec)
>>>>>>>> Rosa (róża)
>>>>>>>> Rubus
>>>>>>>> Sanguisorba (krwiściąg)
>>>>>>>> Sarcopoterium
>>>>>>>> Sibbaldia (sybaldia)
>>>>>>>> Sibbaldianthe
>>>>>>>> Sibbaldiopsis
>>>>>>>> Sibiraea
>>>>>>>> Sieversia
>>>>>>>> Sorbaria (tawlina)
>>>>>>>> Sorbus (jarząb)
>>>>>>>> Spenceria
>>>>>>>> Spiraea (tawuła)
>>>>>>>> Spiraeanthus
>>>>>>>> Taihangia
>>>>>>>> Tetraglochin
>>>>>>>> Vauquelinia
>>>>>>>> Waldsteinia (pragnia)
>>>>>>>> Xerospiraea
====
>>>>>>>> X Amelasorbus
>>>>>>>> X Crataemespilus [Crataegus × Mespilus]
>>>>>>>> X Fragotentilla (Fragaria chiloensis x Potentilla glandulosa)
>>>>>>>> X Pyracomeles
>>>>>>>> X Pyronia
>>>>>>>> X Sorbaronia
>>>>>>>> X Sorbocotoneaster (jarząboirga)
>>>>>>>> X Sorbocrataegus
>>>>>>>> X Sorbomespilus
>>>>>>>> X Sorbopyrus (jarząbogrusza)
====
>>>>>>>> + Crataegomespilus [Crataegus + Mespilus (chimera)]
>>>>>>>> + Pyrocydonia



POLITYKA I NIE TYLKO , PRZEPISY KULINARNE , ULUBIONE KSIĄŻKI , DOWCIPY , GEOGRAFIA , ŚWIEBODZICE , FORUM O RODZAJU HOYA

Molecular Biology and Evolution - 27 (5), V 2010

(Volume 27, Issue 5, May 2010)

SPIS TREŚCI:

LETTER

Withering Away — 25,000 Years of Genetic Decline Preceded Cave Bear Extinction
Mathias Stiller, Gennady Baryshnikov, Hervé Bocherens, Aurora Grandal d'Anglade, Brigitte Hilpert, Susanne C. Münzel, Ron Pinhasi, Gernot Rabeder, Wilfried Rosendahl, Erik Trinkaus, Michael Hofreiter, Michael Knapp

RESEARCH ARTICLES

Expansion of the miRNA Pathway in the Hemipteran Insect Acyrthosiphon pisum
Stéphanie Jaubert-Possamai, Claude Rispe, Sylvie Tanguy, Karl Gordon, Thomas Walsh, Owain Edwards, Denis Tagu

Evaluating the Relationship between Evolutionary Divergence and Phylogenetic Accuracy in AFLP Data Sets
María Jesús García-Pereira, Armando Caballero, and Humberto Quesada

Demographic histories of four spruce ( Picea ) species of the Qinghai-Tibetan Plateau and neighboring areas inferred from multiple nuclear loci
Yuan Li, Michael Stocks, Sofia Hemmilä, Thomas Källman, Hongtao Zhu, Yongfeng Zhou, Jun Chen, Jianquan Liu, Martin Lascoux

Comparative Testing of DNA Segmentation Algorithms Using Benchmark Simulations
Eran Elhaik, Dan Graur, and Kre š imir Josi ´c

Positions under Positive Selection — Key for Selectivity and Potency of Scorpion a -Toxins
Hagar Weinberger, Yehu Moran, Dalia Gordon, Michael Turkov, Roy Kahn, and Michael Gurevitz

The Increase in the Number of Subunits in Eukaryotic RNA Polymerase III Relative to RNA Polymerase II Is due to the Permanent Recruitment of General Transcription Factors
Robert Carter and Guy Drouin

Using Data-Display Networks for Exploratory Data Analysis in Phylogenetic Studies
David A. Morrison

Evolutionary Expansion and Specialization of the PDZ Domains
O. Sakarya, C. Conaco, S.A. Solla, T.H. Oakley, K.S. Kosik

Permuted tRNA Genes in the Nuclear and Nucleomorph Genomes of Photosynthetic Eukaryotes
Shinichiro Maruyama, Junichi Sugahara, Akio Kanai, and Hisayoshi Nozaki

Timing of Replication Is a Determinant of Neutral Substitution Rates but Does Not Explain Slow Y Chromosome Evolution in Rodents
Catherine J. Pink and Laurence D. Hurst

Evolution of Caenorhabditis Mitochondrial Genome Pseudogenes and Caenorhabditis briggsae Natural Isolates
Michael J. Raboin, Ashley F. Timko, Dana K. Howe, Marie-Anne Félix, and Dee R. Denver

Functional Diversity of Signaling Pathways through G Protein – Coupled Receptor Heterodimerization with a Species-Specific Orphan Receptor Subtype
Tsubasa Sakai, Masato Aoyama, Takehiro Kusakabe, Motoyuki Tsuda, and Honoo Satake

Divergence of the Mitochondrial Genome Structure in the Apicomplexan Parasites, Babesia and Theileria
Kenji Hikosaka, Yoh-ichi Watanabe, Naotoshi Tsuji, Kiyoshi Kita, Hiroe Kishine, Nobuko Arisue, Nirianne Marie Q. Palacpac, Shin-ichiro Kawazu, Hiromi Sawai, Toshihiro Horii, Ikuo Igarashi, Kazuyuki Tanabe

Field, Genetic, and Modeling Approaches Show Strong Positive Selection Acting upon an Insecticide Resistance Mutation in Anopheles gambiae s.s.
Amy Lynd, David Weetman, Susana Barbosa, Alexander Egyir Yawson, Sara Mitchell, Joao Pinto, Ian Hastings, Martin J. Donnelly

Lineage-Specific Patterns of Functional Diversification in the a - and b -Globin Gene Families of Tetrapod Vertebrates
Federico G. Hoffmann, Jay F. Storz, Thomas A. Gorr, and Juan C. Opazo

Homoplasy and Distribution of AFLP Fragments: An Analysis In Silico of the Genome of Different Species
Armando Caballero and Humberto Quesada

A Novel Method to Detect Proteins Evolving at Correlated Rates: Identifying New Functional Relationships between Coevolving Proteins
Nathaniel L. Clark and Charles F. Aquadro

A Continuous-State Coalescent and the Impact of Weak Selection on the Structure of Gene Genealogies
Brendan D. O’Fallon, Jon Seger, and Frederick R. Adler

A Generation Time Effect on the Rate of Molecular Evolution in Invertebrates
Jessica A. Thomas, John J. Welch, Robert Lanfear, and Lindell Bromham

Functionally Compensating, Coevolving Positions Are Neither Homoplasic Nor Conserved in Clades
Gregory B. Gloor, Gaurav Tyagi, Dana M. Abrassart, Andrew J. Kingston, Andrew D. Fernandes, Stanley D. Dunn, Christopher J. Brandl

Degeneration of Olfactory Receptor Gene Repertories in Primates: No Direct Link to Full Trichromatic Vision
Atsushi Matsui, Yasuhiro Go, and Yoshihito Niimura

MIKC* MADS-Box Proteins: Conserved Regulators of the Gametophytic Generation of Land Plants
Oliver Zobell, Wolfram Faigl, Heinz Saedler, and Thomas Münster

Epitope Discovery with Phylogenetic Hidden Markov Models
Miguel Lacerda, Konrad Scheffler, and Cathal Seoighe

______________________

Synonimy rodziny Zygophyllaceae R. Br., nom. cons.:

Balanitaceae M. Roem., nom. cons.
Tribulaceae Trautv.








-----

Jeśli chcesz poczytać o czymś innym to zapraszam na inne blogi:

POLITYKA ORAZ SPORT

PRZEPISY KULINARNE

BOTANIKA na nim właśnie jesteś

ULUBIONE KSIĄŻKI

DOWCIPY

Synonim rodziny Xyridaceae C. Agardh, nom. cons.

Abolbodaceae Nakai

--

Synonim rodziny Tetrameristaceae Hutch.

Pellicieraceae L. Beauvis. ex Bullock


---

Synonim rodziny Schizaeaceae Kaulf.

Mohriaceae C. F. Reed




---

Synonimy rodziny Sarcolaenaceae Caruel, nom. cons.:

.

Rhodolaenaceae Bullock
Schizolaenaceae Barnhart

.

Synonim rodziny Proteaceae Juss., nom. cons.

Lepidocarpaceae Schultz Sch.


-----