rijen – -Translation – Keybot Dictionary

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  Monocotylen  
Bladeren van monocotyle planten (eenzaadlobbigen) zijn parallelnervig en zijn meestal pijl- tot lintvormig. De huidmondjes liggen bijna altijd in lange parallelle rijen, net als de epidermiscellen. Deze kenmerken vind je terug in onderstaande foto's van bladeren van mais, papyrus en yucca.
Monocotyledonous leaves show a parallel venation and mostly are arrow or band-shaped. Stomata and other epidermal cells are almost always arranged in parallel arrays. These characterics are depicted in the photographs below of maize, papyrus and yucca. How monocotyle leaves develop is further explained in the section on monocot leaf formation.
  Xeromorf  
Tot de xeromorfe soorten behoren niet alleen sommige Angiospermen (zie twee bovenstaande voorbeelden, maar ook de naalddragende Gymnospermen (naaktzadigen) (Voorbeeld hieronder: de grove den, Pinus sylvestris, naalden en kegels hier links). Net zoals bij de bladeren van monocotylen (behorende tot de angiospermen - bedektzadigen - bloemplanten - anthophyta) liggen bij de dennennaalden de huidmondjes in rijen.
; habitus here left) and privy (privet)) belong to the xeromorphic plants, but also needle-bearing Gymnosperms (Example below: pine tree, Pinus sylvestris; needles and cones here left). Like in the leaves of monocots (belonging to the angiosperms - anthophyta or flowering plants) the stomata are arranged in long arrays in pine needles.
  Aanleg blad  
Alleen aan de basis van het blad blijft een zone waar nog delingen plaats kunnen vinden (6), en wel bijna uitsluitend evenwijdig aan de bladbasis. Daardoor ontstaan de typische lange rijen epidermiscellen en de parallelnervige structuur van het monocotyle (eenzaadlobbige) blad.
In monocots the initial bulge further elongates by mitotic cell divisions until a certain size is reached (1-4). Then, overal cell division stops (5). Only cells in a small region at the base of the leaf further divide (6), i.e. nearly exclusively in parallel to the leaf base. This is how the typical longitudinal arrays of epidermal cells and the parallel venation of monocot leaves arise. Below this division zone a sheath is formed that surrounds the stem. A leaf stalk is absent. The opposite side develops into the leaf blade. Leaf growth may continue without limitation as long as this meristem exists (7). As a result, grasses can resume growth after mowing or grazing. This behavior is common to all monocots, also to the aquatic plants belonging to this group, like
  Kurkcambium  
Kurkcambium cellen delen alleen periclinaal waardoor de typische rijen dochtercellen ontstaan: er worden voornamelijk kurkcellen (= felleem) aangemaakt en wel naar buiten toe en in veel mindere mate (soms zelfs helemaal niet) kurkparenchym (= felloderm), naar binnen toe.
Cork originates from a layer of cambium (=phellogen) that itself is formed as a secondary meristem from a layer of collenchyma or parenchyma immediately beneath the epidermis. In contrast to sclerenchyma cells, collenchyma cells are alive and they have retained the potency to de-differentiate. Cork cambium cells only divide periclinally so that the typical rows of daughter cells arise: cork cells (=phellem) are mainly generated toward the outside. In a lesser extent also cork parenchyma (=phelloderm) is made toward the inside. Cork cambium, cork cells and cork parenchyma together are also named periderm. Mature cork cells are dead; their cell walls contain suberine, a fatty substance that repels water. The layer of cork provides protection against desiccation, but it also isolates tissues in the inner parts of the stem or trunk so thoroughly that exchange of gas with the outer world is impeded. 'Breathing' is yet achieved by so-called lenticels. The cork cambium starts to generate numerous parenchyma cells toward the surface, in most cases at the level of a stoma. These thin-walled parenchyma cells, which eventually degenerate, force an interruption of the sealing created by the cork layer and focus an opening for gas-exchange.