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1 ing details of the pores in the margo of the pit membrane.
2  of the pits in the case of margo-torus type pit membrane.
3 mber, and a modified primary wall called the pit membrane.
4  unique torus-margo structure of the conifer pit membrane.
5 hrough the pores present in the margo of the pit membrane.
6  tracheid-bearing plants with more permeable pit membranes.
7 e connected to one another via intertracheid pit membranes.
8 y digested regions in the cell wall known as pit membranes.
9 te gradients to determine whether damages to pit membranes accumulate as the xylem ages.
10 ypical angiosperm conduit with a homogeneous pit membrane and a typical gymnosperm conduit with a tor
11 tional, a result of air entering through the pit membrane and nucleating cavitation in the water colu
12 and central projections of fibers within the pit membrane and the LTTD became visible.
13  electron microscopy in pores of intervessel pit membranes and deposited on vessel wall surfaces.
14 cles may contribute to the disruption of the pit membranes and facilitate systemic virus transport.
15         Embolism-resistant species had thick pit membranes and narrow vessels.
16 d pits, suggesting that microchannels in the pit membranes are altered by the swelling and deswelling
17 ng in angiosperm xylem occurs via mesoporous pit membranes between vessels.
18  that electrokinetic effects in the bordered pit membrane (BPM) contribute to this response.
19           The modelled constriction sizes in pit membranes decreased with increasing membrane thickne
20      For conduits with torus-margo type pits pit membrane deflection was also modeled and pit aspirat
21 ening of the cellulosic mesh of interconduit pit membranes during the water stress and cavitation tre
22 ion and always for conduits with homogeneous pit membranes, embolism growth is more rapid but still m
23                                          The pit membrane facilitates transport of solutions between
24                                  Only vessel pit membrane fraction was positively correlated to embol
25                                              Pit membranes have been well studied in woody plants, bu
26 esting the presence of accumulated damage to pit membranes impairing water transport.
27 s pressures (3.8 MPa) compared with bordered pit membranes in vessels located in older annular rings
28 ch revealed a morphological partition of the pit membrane into three well-defined sensory areas with
29 tigate how the size of pore constrictions in pit membranes is related to pit membrane thickness and e
30 ead and confirm that air seeding through the pit membranes is the principle mechanism of embolism spr
31  pits, particularly through the pores in the pit membrane, is not well understood, but is critical fo
32 ressure required to push gas across bordered pit membranes of current year xylem did not vary with di
33 V in xylem involves chelation of Ca(2+) from pit membranes of infected cells, thereby stabilizing the
34                   We found that the bordered pit membranes of vessels located in current year xylem c
35 ockdown of MAP20 causes bigger pits, thinner pit membranes, perturbed vasculature development, lower
36                                          The pit membrane (PM) is a primary cell wall barrier that se
37 ding enzymes (CWDEs) to break up intervessel pit membranes (PMs) and spread through the vessel system
38  low values when concentrated as they are in pit membrane pores.
39 es on how air-seeding occurs at the level of pit membranes, raising the question of whether capillary
40 in plant conductive systems, such as conduit pit membrane resistance, should scale in exact harmony w
41     We propose that the partial digestion of pit membranes resulting from programmed cell death may p
42 essure required to force air across bordered pit membranes separating individual xylem vessels.
43  are coupled with additional data concerning pit membrane structure and function and are discussed in
44 ypical gymnosperm conduit with a torus-margo pit membrane structure.
45 nd EGFR is incorporated into clathrin-coated pits--membrane structures containing clathrin and other
46 glucans and anti-RYMV antibodies over vessel pit membranes suggests a pathway for virus migration bet
47 ited in the regularly spaced paired-pits and pit membranes that hydraulically connect neighboring xyl
48 l pit area (A(p) ), inversely related to the pit membrane thickness (T(PM) ) and driven by a pressure
49 ssel diameter (D(h) ) and tested its link to pit membrane thickness (T(PM) ) and specific conductivit
50 constrictions in pit membranes is related to pit membrane thickness and embolism resistance.
51 explaining the measured relationship between pit membrane thickness and embolism resistance.
52 delled as multiple layers to investigate how pit membrane thickness and the number of intervessel pit
53 ns provide a mechanistic explanation for why pit membrane thickness determines embolism resistance, w
54 rought adaptation by modulating pit size and pit membrane thickness in metaxylem.
55 mations were complemented by measurements of pit membrane thickness, embolism resistance, and number
56  size and embolism resistance much less than pit membrane thickness.
57 und in species vulnerability to embolism and pit membrane thickness.
58  and pit aspiration, the displacement of the pit membrane to the low pressure side of the pit chamber
59   In addition, displacement of the Ca2+ from pit membranes to virus particles may contribute to the d
60                                              Pit membranes were modelled as multiple layers to invest
61 izes, angiosperms are unlikely to have leaky pit membranes, which enables tensile transport of water.
62 r, but convex due to flow across intervessel pit membranes, which represent mesoporous media within m