David Rabaey

The evolution and function of vessel and pit characters with respect to cavitation resistance across 10 Prunus species

Various structure-function relationships regarding drought-induced cavitation resistance of secondary xylem have been postulated. These hypotheses were tested on wood of 10 Prunus species showing a range in P50 (i.e., the pressure corresponding to 50% loss of hydraulic conductivity) from -3.54 to -6.27 MPa. Hydraulically relevant wood characters were quantified using light and electron microscopy. A phylogenetic tree was constructed to investigate evolutionary correlations using a phylogenetically independent contrast (PIC) analysis. Vessel-grouping characters were found to be most informative in explaining interspecific variation in P50, with cavitation-resistant species showing more solitary vessels than less resistant species. Co-evolution between vessel-grouping indices and P50 was reported. P50 was weakly correlated with the shape of the intervessel pit aperture, but not with the total intervessel pit membrane area per vessel. A negative correlation was found between P50 and intervessel pit membrane thickness, but this relationship was not supported by the PIC analysis. Cavitation resistance has co-evolved with vessel grouping within Prunus and was mainly influenced by the spatial distribution of the vessel network.

Micromorphology and systematic distribution of pit membrane thickenings in oleaceae: tori and pseudo-tori

Recent studies on the functional significance of pit membranes in water conducting cells have renewed general interest in their micromorphology. At least two types of pit membrane thickenings have been described in angiosperm families, i.e. genuine tori and pseudo-tori. This study explores the distribution and morphology of pit membrane thickenings in 69 species and 23 genera within Oleaceae using light and electron microscopy. Torus-bearing pit membranes are confirmed for Osmanthus, and new records are reported for Chionanthus retusa, Picconia azorica, and P. excelsa, but not for the other species studied of Chionanthus. This infrageneric variation suggests that tori represent a plastic feature that has evolved more than once within the family as the result of functional adaptation to efficient and safe water transport. Pseudo-tori are observed in species of Abeliophyllum, Fontanesia, Forsythia, Jasminum, Ligustrum, Menodora, and Syringa. Based on structural differences, we state that tori and pseudo-tori can be distinguished as non-homologous features.

Torus-Bearing pit Membranes in species of Osmanthus

Torus thickenings of pit membranes are found not only in gymnosperms, but also in certain genera of dicotyledons. One such genus is Osmanthus. Wood from 17 species of Osmanthus was searched for tori. Fourteen species from three of the four sections investigated possessed these thickenings. Ten of the species represent new records. Only the three New Caledonian species of Section Notosmanthus lacked tori. This observation in combination with other factors serves to isolate this section from the remainder of the genus.