Browsing by Author "Yeung, Edward C."

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    Glutathione modulation of white spruce somatic embryogenesis
    (2003) Belmonte, Mark Findlay; Yeung, Edward C.
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    In Search of Physical Explanation of Co-development of Plants and Landscape
    (2018-06-11) Ding, Junyan; Johnson, Edward Arnold; Martin, Yvonne E.; Post, John R.; Yeung, Edward C.
    The physical structure of the landscape is the subject of geology and geomorphology based on physical and chemical principles of material and energy movement under climatic and tectonic forces. The biological inhabitants of this physical landscape, area subject rooted in biological, ecological and evolutionary theories, but the primary focus has been on how the physical environment shaped life on land. It is only recently that we begin to recognize the evolution of the abiotic and biotic worlds are intimately intertwined via complex feedback loops of physical hydrological, and biological pathways, and at a range of spatial and temporal scales. In my thesis, I addressed a subset of these complex interactions: the coevolution of the landform organized as hills-valleys and the plants that occupy the different landscape positions. I used an integrated modeling approach that captures the first-order, well recognized, and mechanistic links to explore feedbacks and to shed new lights on the coupled evolution of the landform and the plants. The landscape is a battleground of tectonics (mountain building) vs. denudation (weathering/erosion that destroy the mountains). The landscape structure, e.g. hillslope shape/size and stream density, depends on the relative dominance of diffusive type erosion (e.g., soil creep and shallow landslides) vs. the advective type (e.g., runoff erosion and channel incision). Climate exerts strong regulation on the dominance erosion processes with increasing rainfall intensity resulting in more advective type erosion landform. The result is a landscape evolution model, with three levels of diffusive vs. advective dominances. Diffusion dominated landscapes tend to have wider/longer hillslopes, more rounded hilltops, and fewer streams (i.e., less dissected). This will have consequences to water movement on land and the resulting soil hydrology. These distinct landforms lead to distinct patterns of soil hydrology. A simple and powerful way to characterize soil hydrology is the Topographic Index (TI) a proxy of equilibrium of water table depth, defined for each point in a watershed as the ratio of drainage area above the point (proxy of rain caught upstream) and local slope at the point (proxy for outflow). Using TI, I translated the three landscape structures above into three hydrologic structures. Higher TI occurs in flat valley bottoms with a large slope above it, low TI on ridge tops, and intermediate TI on hillslopes. These patterns will influence the distribution of plants genetically adapted to different soil moisture conditions. Plants have evolved genetic traits to survive and optimize their performance in given environmental niches. Soil hydrology is a powerful discriminator of plants according to their drought and waterlogging tolerance. To a first order watershed, I represented plants in three tolerance curves: hydric (waterlogging tolerant), xeric (drought tolerant), and mesic (moderate moisture tolerance), each with a preferred distribution along the TI index. This allows me to connect hydrology to plant distribution for each tolerance type. Each plant type occupies a distinct hydrologic position in all three landscapes, but more mesic plants are found in diffusive landscapes. Water and nutrients move from soils to roots, stems, shoots, leaves, and to the atmosphere through a series of resistant flow paths. Plant hydraulic traits reflect evolutionary trade-offs between efficiency and safety. For leaves, denser veins, lower stomatal resistance, wider and larger leaves all decrease leaf hydraulic resistance and increase net primary productivity (NPP), but the same traits also increase risks of embolism and leaf death. I developed a leaf NPP optimization model to explore the joint adjustment of several leaf traits to different levels of soil water stress. It offered a theoretical framework to explain leaf traits seen across hydrologic gradients; e.g., narrow-leaved species tend to occupy xeric habitats on hilltops, and species of large and wide leaves occupy hydric habitats in valleys. In this thesis, by using aboveground traits, I provided a mechanistic connection between abundance and distribution of plant functional groups (PFG) on landscape and the geomorphic processes that created it. It sets the foundation for further investigating how landscape composition of PFGs can regulate topography and hillslope hydrology under the regulation of changing climate thus close the feedback cycle. A missing component here is a mechanistic expressing of soil water-root interaction that creates the dynamic rooting structure across landscape. This should be the focus of future study.
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    Past, present, and future land use of Swan River First Nation
    (2011) Dersch, Ave Tressa; Kooyman, Brian P.; Yeung, Edward C.
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    Physiological control of shoot apical meristem formation in brassica napus cv topas
    (1999) Ramesar-Fortner, Nicole S.; Yeung, Edward C.
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    The effects of ascorbic acid on white spruce somatic embryogenesis
    (2001) Stasolla, Claudio; Yeung, Edward C.
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    The orchid seed coat: a developmental and functional perspective
    (2023-09-27) Lee, Yung-I.; Yeung, Edward C.
    Abstract Orchid seeds are 'dust-like.' The seed coat is usually thin, with only one to a few cell layers. It originates from the integuments formed during ovule development. In orchids, the outer integument is primarily responsible for forming a mature seed coat. The inner integument usually fails to develop after fertilization, becomes compressed, and collapses over the expanding embryo. Hence, the seed coat is formed from the funiculus, chalaza, and outer integumentary cells. The outermost layer of the seed coat, the testa, is lignified, usually at the radial and inner tangential walls. The subepidermal thin-walled layer(s), the tegmen, subsequently cold, resulting in seeds having only a single layer of seed coat cells. In some species, cells of the inner integument remain alive with the ability to synthesize and accumulate lipidic and or phenolic compounds in their walls covering the embryo. This cover is called the 'carapace,' a protective shield contributing to the embryo's added protection. A developmental and functional perspective of the integuments and seed coat during seed development and germination is presented in this review.