By Sandro Pignatti
Plants d'Italia è l. a. ristampa di un'opera prestigiosa in tre volumi in step with un totale di oltre 2300 pagine. Raccoglie un'impressionante quantità di informazioni e dati utili a delineare un landscape completo della flowers italiana. Il testo, coordinato dal Prof. Sandro Pignatti, uno dei massimi esperti in materia, si presenta ricchissimo di dettagli e riferimenti desunti dalla esperienza di illustri studiosi che hanno costituito il comitato di redazione dell'opera. Da segnalare l'inserimento di migliaia di disegni a corredo della descrizione essenziale ma completa delle singole specie e l. a. rilegatura dei volumi in tela e oro con cofanetto.
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This quantity is an account of the flowering plant plant life of West Africa south of the Sahara (Gambia-Nigeria inclusive) with the emphasis upon species of ecological or financial value. The vegetative and reproductive morphological characters, pollination and dispersal mechanisms of representatives of 38 households are defined, and those households look within the related order as within the vegetation of West Tropical Africa.
"The current publication is meant as a growth file on artificial method of evolution because it applies to the plant kingdom". With this easy assertion, G. Ledyard Stebbins formulated the ambitions of "Variation and Evolution in Plants", released in 1950, surroundings forth for crops what grew to become often called the "synthetic thought of evolution" or "the sleek synthesis.
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27 kb/μm, the multicolor fiber FISH can be used to measure the physical distance between the DNA sequences (Fig. 1). It bridges the resolution of megabase molecular techniques, such as pulsed-field gel electrophoresis and genome sequence analysis . Fiber FISH was successfully used for the detailed investigation of chromosomal domains in Arabidopsis , rice , tomato , and sugar beet . In repetitive regions of plant chromosomes which cannot be assembled in genome sequencing projects, fiber FISH allows positioning and length measurement of tandem arrays .
Wash the membrane in TN solution for 15 min and then in TNM solution for 2 min. 6. Pour the detection solution containing 75 μL of NBT/BCIP (nitro blue tetrazolium—5-bromo-4-chloro-3-indolyl-phosphate, in 5 mL of TNM solution over the membrane and incubate for 10 min in the dark (see Note 6). 7. The intensity of the resulting color of the labeled probe with the control allows estimation of the quality of the labeling. 2 Post-hybridization Washing 29 1. , colorless polyethylene autoclavable plastic bags).
Cv. Morex) 1. 08 mM (NH4)6Mo7O24·4H2O (10 mg) in deionized water (100 mL). Store at 4 °C. 2.
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