Aspects of xylem anatomy and vulnerability to water stress-induced embolism were examined in stems of two droughtdeciduous species, Brachychiton australis (Schott and Endl.) A. Terracc. and Cochlospermum gillivraei Benth., and two evergreen species, Alphitonia excelsa (Fenzal) Benth. and Austromyrtus bidwillii (Benth.) Burret., growing in a seasonally dry rainforest. The deciduous species were more vulnerable to water stress-induced xylem embolism. B. australis and C. gillivraei reached a 50% loss of hydraulic conductivity at Ϫ3.17 MPa and Ϫ1.44 MPa, respectively; a 50% loss of hydraulic conductivity occurred at Ϫ5.56 MPa in A. excelsa and Ϫ5.12 MPa in A. bidwillii. To determine whether pit membrane porosity was responsible for greater vulnerability to embolism (air seeding hypothesis), pit membrane structure was examined. Expected pore sizes were calculated from vulnerability curves; however, the predicted inter-specific variation in pore sizes was not detected using scanning electron microscopy (pores were not visible to a resolution of 20 nm). Suspensions of colloidal gold particles were then perfused through branch sections. These experiments indicated that pit membrane pores were between 5 and 20 nm in diameter in all four species. The results may be explained by three possibilities: (a) the pores of the expected size range were not present, (b) larger pores, within the size range to cause air seeding, were present but were rare enough to avoid detection, or (c) pore sizes in the expected range only develop while the membrane is under mechanical stress (during air seeding) due to stretching/flexing.Xylem cavitation and embolism are recognized as major constraints affecting plants regularly exposed to water stress (Tyree and Sperry, 1989;Milburn, 1993). Water in the xylem is under negative pressure, or tension, i.e. it is held in a metastable state, below its vapor pressure, a condition that increases the likelihood of cavitation occurring (Oertli, 1971;Pickard, 1981). Cavitation is the process whereby a vapor phase is introduced to the xylem water column, creating an embolism. Embolisms are gas bubbles consisting initially of water vapor and later air, which become trapped within xylem conduits. Because of its inability to transmit tension, the vapor phase limits the volume flow of water through the conduit, reducing the plant's capacity to deliver water to the canopy (Meinzer et al., 2001). Plants must minimize this disruption to water transport to avoid effects on leaf water status that may result in limitations on stomatal conductance and photosynthesis.The structure of xylem vessels is seen as an important factor in determining the occurrence of water stress-induced cavitation (Zimmermann, 1983). Xylem vessels are bounded by pit membranes, through which water must pass to move from one vessel to the next. Pit membranes are the degraded primary cell walls and middle lamella of the vessels and are composed of tightly inter-woven cellulose microfibrils in a matrix of hemicellulose and pectin polysaccharide...
Hydraulic conductivity and xylem anatomy were examined in stems of two evergreen species, Alphitonia excelsa (Fenzal) Benth. and Austromyrtus bidwillii (Benth.) Burret., and two drought-deciduous species, Brachychiton australis (Schott and Endl.) A. Terracc. and Cochlospermum gillivraei Benth., from a seasonally dry rainforest in north Queensland, Australia. The deciduous species possessed hydraulic architecture typical of drought-sensitive plants, i.e. low wood density, wider xylem vessels, higher maximal rates of sapwood specific hydraulic conductivity (K s ) and high vulnerability to drought-induced embolism. In contrast, the evergreen species had lower rates of K h and leaf specific conductivity (K L ) but were less susceptible to embolism. The evergreen species experienced leaf water potentials <−4.0 MPa during the dry season, while the deciduous species shed their leaves before leaf water potentials declined below −2.0 MPa. Thus, the hydraulic architecture of the evergreens allows them to withstand the greater xylem pressure gradients required to maintain water transport to the canopy during the dry season. Our results are consistent with observations made in neotropical dry forests and demonstrate that drought-deciduous species with low wood density and high water storage capacity are
Diurnal and seasonal patterns of leaf gas exchange and water relations were examined in tree species of contrasting leaf phenology growing in a seasonally dry tropical rain forest in north-eastern Australia. Two drought-deciduous species, Brachychiton australis (Schott and Endl.) A. Terracc. and Cochlospermum gillivraei Benth., and two evergreen species, Alphitonia excelsa (Fenzal) Benth. and Austromyrtus bidwillii (Benth.) Burret. were studied. The deciduous species had higher specific leaf areas and maximum photosynthetic rates per leaf dry mass in the wet season than the evergreens. During the transition from wet season to dry season, total canopy area was reduced by 70-90% in the deciduous species and stomatal conductance (g(s)) and assimilation rate (A) were markedly lower in the remaining leaves. Deciduous species maintained daytime leaf water potentials (Psi(L)) at close to or above wet season values by a combination of stomatal regulation and reduction in leaf area. Thus, the timing of leaf drop in deciduous species was not associated with large negative values of daytime Psi(L) (greater than -1.6 MPa) or predawn Psi(L) (greater than -1.0 MPa). The deciduous species appeared sensitive to small perturbations in soil and leaf water status that signalled the onset of drought. The evergreen species were less sensitive to the onset of drought and g(s) values were not significantly lower during the transitional period. In the dry season, the evergreen species maintained their canopies despite increasing water-stress; however, unlike Eucalyptus species from northern Australian savannas, A and g(s) were significantly lower than wet season values.
Geomorphological observations show no detectable uplift (i.e. falling relative sea level) of Amery Oasis since the establishment of relatively stable sea level during the mid-Holocene. The observations around the basin of Beaver Lake include an absence of raised shoreline features, the presence down to the present tidal limit of in situ ventifacts and residual landforms, the cliffed southern shoreline and adjacent shallow subhorizontal floor of Beaver Lake, and the composition of recent moraines on the basin's north eastern edge. This lack of Holocene uplift is consistent with low uplift rates observed from coastal oases of East Antarctica and suggests minor, rather than major, changes to the Antarctic ice sheet during the most recent Quaternary glacial cycle. The formation of Beaver basin is attributed to late Cenozoic glacial excavation by south flowing ice of the palaeo-Nemesis Glacier, initially eroding when relative sea level was higher than it is today. The basin containing Radok Lake was excavated by the palaeo-Battye Glacier probably when most effective during the numerous long cold periods of the late Cenozoic. The field evidence from landforms and the presence of marine fossil deposits suggests Amery Oasis was not overrun by erosive ice since at least the Pliocene, major ice streams such as Lambert Glacier flowing then, as now, around the oasis.
Debate concerning the environmental impact of human arrival in Australia has continued for more than a century. Here we review the evidence for human impact and the mechanisms by which humans may have affected the environment of tropical Australia. We limit our review to tropical Australia because, over three decades ago, it was proposed that the imposition of an anthropogenic fire regime upon human occupation of the Australian continent may have resulted in profound changes in regional vegetation and climate across this region. We conclude that ecological processes and vegetation-fire-climate-human feedbacks do exist that could have driven a significant shift in boundary conditions and ecosystem state at the sub-continental scale through the sustained imposition of an anthropogenic fire regime over tens of millennia. These potential feedbacks operate through the inhibition of forest expansion both directly, by targeted burning at established forest edges and newly irrupted forest patches, and indirectly, through lengthening of the dry season because of changes to the timing of burning. However, the impact of any such anthropogenic forcing may have been entirely overshadowed by the effects of natural climate change and variability, as well as the generally low nutrient status of Australian soils. A robust assessment of the degree to which the environment of tropical Australia at the large scale has been modified from its 'natural' state because of human occupation will require new, coordinated collaborations between indigenous traditional landowners, archaeologists, anthropologists, geochronologists, geoscientists, ecologists, climatologists and modellers.
Pollen and diatom analyses of organic sediments from Three-Quarter Mile Lake, a perched lake on Cape York Peninsula, north Queensland, indicate that significant changes in vegetation and hydrology occurred during the Holocene. Early Holocene grass-dominated landscapes were replaced in mid-Holocene times by increasingly woody vegetation comprising tropical heathlands, savanna and rainforest. Early-Holocene lake levels fluctuated widely. From mid-Holocene times, lake levels stabilized and water became increasingly acidic as a mature swamp forest developed adjacent to the lake and contributed tannins to the lake water. The timing and character of changes are consistent with those described from the Atherton Tableland in wet tropical Queensland. Holocene dry phases described from the Northern Territory and the western shores of Cape York cannot be identified from Three-Quarter Mile Lake. Rainforest is currently close to its greatest Holocene extent, suggesting that the rainforest-dependent endemic fauna of northern Cape York have been isolated from rainforest blocks to the south throughout the last 10 000 years and, by inference, throughout at least the 120 000 years beyond that.
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