1,920 research outputs found

    Vascular epiphytes in the temperate zones-a review

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    Vascular epiphytes are typically associated with tropical rainforests, whereas their occurrence in temperate forests is little appreciated. This review summarises the available information on epiphytism in the temperate zones (> 23.5 latitude), which has not been reviewed omprehensively for more than a century, and critically analyses the proposed mechanisms behind the observed biogeographical patterns. Although in the temperate zone epiphytic vascular plants are rarely as impressive as in tropical forests, there are noteworthy exceptions. Temperate rain forests of Chile and New Zealand, or montane forests in the Himalayas are comparable to many tropical forests in terms of epiphyte biomass and diversity, but differ in their taxonomic spectrum temperate epiphyte communities are generally dominated by ferns and fern-allies. Other temperate areas are not, however, necessarily barren of epiphytes, as repeatedly implied. Quite in contrast, local populations of epiphytes in a large number of other non-tropical areas in both the southern and the northern hemisphere can be quite conspicuous. The proposed reasons for the latitudinal gradients in epiphyte abundance and diversity (water scarcity or low tempera-tures). are not fully convincing and, moreover, still await experimental verification. Other factors, both historical (e.g., Pleistocene extinctions) and ecological (e.g., prevalence of conifers in the northern hemisphere), should also be taken into consideration to obtain a comprehensive explanation of the extant global distribution of vascular epiphyte

    How prevalent is crassulacean acid metabolism among vascular epiphytes?

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    The occurrence of crassulacean acid metabolism (CAM) in the epiphyte community of a lowland forest of the Atlantic slope of Panama was investigated. I hypothesized that CAM is mostly found in orchids, of which many species are relatively small and/or rare. Thus, the relative proportion of species with CAM should not be a good indicator for the prevalence of this photosynthetic pathway in a community when expressed on an individual or a biomass basis. In 0.4ha of forest, 103species of vascular epiphytes with 13,099individuals were found. As judged from the C isotope ratios and the absence of Kranz anatomy, CAM was detected in 20 species (19.4% of the total), which were members of the families Orchidaceae, Bromeliaceae, and Cactaceae. As predicted, the contribution of CAM epiphytes to the total number of individuals and to total biomass (69.6kg ha-1) was considerably lower (3.6% or 466 individuals and, respectively, 3.0% or 2.1kg ha-1

    Communicating Impacts

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    This article addresses the need to share Extension program impacts with our constituencies and groups that fund our programs. The article reviews the literature surrounding the need for communicating impacts with decision makers. It also identifies two reporting mechanisms used in one state, County Narrative Reports and the Extension Accountability Reporting System (EARS), that are successfully working to share program impacts with county commissioners, legislators, and the general public. The success of these two reporting systems is based on level or increased funding we have received at the county and state level since the implementation of these two systems

    Neither Host-specific nor Random: Vascular Epiphytes on Three Tree Species in a Panamanian Lowland Forest

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    • Background and Aims A possible role of host tree identity in the structuring of vascular epiphyte communities has attracted scientific attention for decades. Specifically, it has been suggested that each host tree species has a specific subset of the local species pool according to its own set of properties, e.g. physicochemical characteristics of the bark, tree architecture, or leaf phenology patterns. • Methods A novel, quantitative approach to this question is presented, taking advantage of a complete census of the vascular epiphyte community in 0·4 ha of undisturbed lowland forest in Panama. For three locally common host-tree species (Socratea exorrhiza, Marila laxiflora, Perebea xanthochyma) null models were created of the expected epiphyte assemblages assuming that epiphyte colonization reflected random distribution of epiphytes in the forest. • Key Results In all three tree species, abundances of the majority of epiphyte species (69-81 %) were indistinguishable from random, while the remaining species were about equally over- or under-represented compared with their occurrence in the entire forest plot. Permutations based on the number of colonized trees (reflecting observed spatial patchiness) yielded similar results. Finally, a third analysis (canonical correspondence analysis) also confirmed host-specific differences in epiphyte assemblages. In spite of pronounced preferences of some epiphytes for particular host trees, no epiphyte species was restricted to a single host. • Conclusions The epiphytes on a given tree species are not simply a random sample of the local species pool, but there are no indications of host specificity eithe

    The Pressure Is On – Epiphyte Water-Relations Altered Under Elevated CO2

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    Vascular epiphytes are a major biomass component of forests across the globe and they contribute to 9% of global vascular plant diversity. To improve our understanding of the whole-plant response of epiphytes to future climate change, we investigated for the first time both individual and combined effects of elevated CO2 (560 ppm) and light on the physiology and growth of two epiphyte species [Tillandsia brachycaulos (CAM) and Phlebodium aureum (C3)] grown for 272 days under controlled conditions. We found that under elevated CO2 the difference in water loss between the light (650 μmol m-2s-1) and shade (130 μmol m-2s-1) treatment was strongly reduced. Stomatal conductance (gs) decreased under elevated CO2, resulting in an approximate 40–45% reduction in water loss over a 24 h day/night period under high light and high CO2 conditions. Under lower light conditions water loss was reduced by approximately 20% for the CAM bromeliad under elevated CO2 and increased by approximately 126% for the C3 fern. Diurnal changes in leaf turgor and water loss rates correlated strong positively under ambient CO2 (400 ppm) and high light conditions. Future predicted increases in atmospheric CO2 are likely to alter plant water-relations in epiphytes, thus reducing the canopy cooling potential of epiphytes to future increases in temperature

    A Simulation Study on the Importance of Size‐related Changes in Leaf Morphology and Physiology for Carbon Gain in an Epiphytic Bromeliad

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    This study addresses the question of how size‐related changes in leaf morphology and physiology influence light absorption and carbon gain of the epiphytic bromeliad Vriesea sanguinolenta. A geometrically based computer model, Y‐plant, was used for the three‐dimensional reconstruction of entire plants and for calculation of whole plant light interception and carbon gain. Plants of different sizes were reconstructed, and morphological and physiological attributes of young and old leaves, and small and large plants were combined to examine the individual effects of each factor on light absorption and carbon gain of the plant. The influence of phyllotaxis on light absorption was also explored. Departure of measured divergence angles between successive leaves from the ideal 137·5° slightly decreased light absorption. The only morphological parameter that consistently changed with plant size was leaf shape: larger plants produced more slender foliage, which substantially reduced self‐shading. Nevertheless, self‐shading increased with plant size. While the maximum rate of net CO2 uptake of leaves increased linearly with plant size by a factor of two from the smallest to the largest individual, the potential plant carbon gain (based on total foliage area) showed a curvilinear relationship, but with similar numerical variation. We conclude that leaf physiology has a greater impact on plant carbon gain than leaf and plant morphology in this epiphytic bromelia

    Getting a Grip on the Adhesion Mechanism of Epiphytic Orchids – Evidence From Histology and Cryo-Scanning Electron Microscopy

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    Plants and animals evolve different attachment structures and strategies for reversible or permanent adhesion to different substrate types. For vascular epiphytes, having the ability to permanently attach to their host plants is essential for establishment and survival. Unlike mistletoe roots, roots of vascular epiphytes do not penetrate the host tissues but instead achieve attachment by growing in close contact to the surface of the substrate. However, the fundamental understanding of the attachment functions of epiphytic roots remains scarce, where majority of studies focused on the general root morphology, their functional properties and the descriptions of associated microbial endophytes. To date, research on attachment strategies in plants is almost entirely limited to climbers. Therefore, this study aims to fill the knowledge gap and elucidate the attachment functions of roots of epiphytic orchids. With the use of histology and high-resolution cryo-scanning electron microscopy (cryo-SEM) technique with freeze fracturing, the intimate root-bark substrate interface of epiphytic orchid Epidendrum nocturnum Jacq was investigated. Results showed a flattened underside of the root upon contact with the substrate surface, and the velamen layer appeared to behave like a soft foam, closely following the contours of the substrate. Root hairs emerged from the outermost velamen layer and entered into the crevices in the substrate, whenever possible

    The development of a mechanical device to stretch skeletal muscle of young and old rats

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    OBJECTIVE: How much force is needed to stretch skeletal muscle is still unknown. The aim of this study was to develop a device that mechanically stretches rat muscle to compare the force (N) required to stretch the soleus muscle of young and aged rats and the tibio-tarsal angle joint at neutral and stretched positions. METHODS: Twelve female Wistar rats were divided into two groups: a young group (YG, n=6, 311±11 g) of rats 3 months old and an aged group (AG, n=6, 351±43 g) of rats 15 months old. The left soleus muscle was mechanically held in full dorsal flexion and submitted to mechanical passive stretching: 1 bout of 10 repetitions, each repetition lasted 60 seconds with an interval of 45 seconds between repetitions, performed once a day, twice a week, for 1 week. The force required during stretching was measured by a load cell, and the tibio-tarsal angle joint was measured by photometry. RESULTS: The load cell calibration showed excellent reliability, as confirmed by the intraclass correlation coefficient value of 0.93. A decrease in delta force was found in the comparison between YG and AG (0.11±0.03 N vs 0.08±0.02 N, po0.05, repeated measures ANOVA). There was no difference between the YG and the AG in the tibio-tarsal angle at resting position (87.1±3.8o vs 87.1±3.5o , p=0.35, Kruskal Wallis) and at the end of the stretching protocol (43.9±4.4o vs 42.6±3.4o , p=0.57, Kruskal Wallis). CONCLUSION: The device presented in this study is able to monitor the force necessary to stretch hindlimb rat muscles. Aged rats required less force than young rats to stretch the soleus muscle, and there was no difference regarding the tibio-tarsal angle between the two groups
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