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    <title>UTas ePrints - Light response characteristics of a morphologically diverse group of southern hemisphere conifers as measured by chlorophyll fluorescence</title>
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    <meta content="Brodribb, Tim J." name="eprints.creators_name" />
<meta content="Hill, Robert S." name="eprints.creators_name" />
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<meta content="2007-12-10 21:28:06" name="eprints.datestamp" />
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<meta content="Light response characteristics of a morphologically diverse group
of southern hemisphere conifers as measured
by chlorophyll fluorescence" name="eprints.title" />
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<meta content="chlorophyll fluorescence; light response; leaf morphology; shade adaptation; conifers " name="eprints.keywords" />
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<meta content="Unlike northern hemisphere conifer families, the southern family, Podocarpaceae, produces a great variety of foliage forms ranging from functionally broad-, to needle-leaved. The production of broad photosynthetic surfaces in podocarps has been linked qualitatively to low-light-environments, and we undertook to assess the validity of this assumption by measuring the light response of a morphologically diverse group of podocarps. The light response, as apparent photochemical electron transport rate (ETR), was measured by modulated fluorescence in ten species of this family and six associated species (including five Cupressaceae and one functionally needle-leaved angiosperm) all grown under identical glasshouse conditions. In all species, ETR was found to increase as light intensity increased, reaching a peak value (ETR(max)) at saturating quantum flux (PPFDsat), and decreasing thereafter. ETR(max) ranged from 217 mu mol electrons . m(-2). s(-1) at a PPFDsat of 1725 mu mol photons . m(-2). s(-1) in Actinostrobus acuminatus to an ETR of 60 mu mol electrons . m(-2). s(-1) at a PPFDsat of 745 mu mol electrons . m(-2). s(-1) in Podocarpus dispermis. Good correlations were observed between ETR(max) and both PPFDsat and maximum assimilation rate measured by gas-exchange analysis. The effective quantum yield at light saturation remained constant in all species with an average value of 0.278 +/- 0.0035 determined for all 16 species. Differences in the shapes of light response curves were related to differences in the response of non-photochemical quenching (q(n)), with q(n) saturating faster in species with low PPFDsat. Amongst the species of Podocarpaceae, the log of average shoot width was well correlated with PPFDsat, wider leaves saturating at lower light intensities. This suggests that broadly flattened shoots in the Podocarpaceae are an adaptation to low light intensity. " name="eprints.abstract" />
<meta content="1997" name="eprints.date" />
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<meta content="Oecologia" name="eprints.publication" />
<meta content="110" name="eprints.volume" />
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<meta content="10-17" name="eprints.pagerange" />
<meta content="10.1007/s004420050127" name="eprints.id_number" />
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<meta content="http://dx.doi.org/10.1007/s004420050127" name="eprints.official_url" />
<meta content="Bilger W, Schreiber U, Brock M (1995) Determination of the
quantum efficiency of photosystem II and of non-p
quenching of chlorophyll ¯uorescence in the ®eld. Oecologia
102: 425±432
BjoÈrkman O, Demmig B (1987) Photon yield of O2 evolution and
chlorophyll ¯uorescence characteristics at 77 K among vascular
plants of diverse origins. Planta 170: 489±504
Bond WJ (1989) The tortoise and the hare: ecology of angiosperm
dominance and gymnosperm persistence. Biol J Linn Soc 36:
227±249
Bordman N (1977) Comparative photosynthesis of sun and shade
plants. Annu Rev Plant Physiol 28: 355±377
Brodribb T (1996) Dynamics of changing intercellular CO2 concentration
during drought and determination of minimum
functional ci. Plant Physiol 111: 179±185
Carter GA, Smith WK (1985) In¯uence of shoot structure on light
interception and photosynthesis in conifers. Plant Physiol 79:
1038±1043
Demmig-Adams B, Adams W, Logan B, Verhoeven A (1995)
Xanthophyll cycle dependant energy dissipation and ¯exible
photosystem II efficiency in plants acclimated to light stress.
Aust J Plant Physiol 22: 249±260
Edwards GE, Baker NR (1993) Can assimilation in maize leaves be
predicted accurately from chlorophyll ¯uorescence analysis?
Photosynth Res 37: 89±102
Enright NJ, Hill RS (eds) (1995) Ecology of the southern conifers.
Melbourne University Press, Melbourne
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990: 87±92
Hill RS (1995) Conifer origin, evolution and diversi®cation in the
southern hemisphere. In: Enright NJ, Hill RS (eds) Ecology of
the southern conifers. Melbourne University Press, Melbourne
pp 10±29
Hill RS, Carpenter RJ (1991) Evolution of Acmopyle and Dacrycarpus
(Podocarpaceae) foliage as inferred from macrofossils in
south-eastern Australia. Aust Sys Bot 4: 449±479
Hill RS, Pole MS (1992) Leaf and shoot morphology of extant
Afrocarpus, Nageia and Retrophyllum (Podocarpaceae) species,
and species with similar leaf arrangement from Tertiary sediments
in Australasia. Aust Syst Bot 5: 337±358
Hill RS, Scriven LJ (1995) The angiosperm-dominated woody
vegetation of Antarctica: a review. Rev of Palaeobot Palynol
86: 175±198
Leverenz JW (1995) Shade shoot structure of conifers and the
photosynthetic response to light at two CO2 partial pressures.
Funct Ecol 9: 413±421
Loreto F, Domenico T, Di Marco G (1995) On the relationship
between electron transport rate and photosynthesis in leaves of
the C4 plant Sorghum bicolor exposed to water stress, temperature
changes and carbon metabolism inhibition. Aust J Plant
Physiol 22: 885±892
KoÈniger M, Harris GC, Virgo A, Winter K (1995) Xanthophyllcycle
pigments and photosynthetic capacity in tropical forest
species: a comparative ®eld study on canopy gap and understorey
plants. Oecologia 104: 280±290
McKiernan M, Baker NR (1992) A method for the rapid monitoring
of photosynthetic shade adaptation in leaves. Funct Ecol
6: 405±410
16
Schreiber U, Bilger W (1992) Progress in chlorophyll ¯uorescence
research: major developments during the past years in retrospect.
Prog Bot 54: 151±173
Schreiber U, Schlewa U, Bilger W (1986) Continuous recording of
photochemical and non±photochemical chlorophyll ¯uorescence
quenching with a new type of modulation ¯uorometer.
Photosynth Res 10: 51±62
Schreiber U, Bilger W, Neubauer C (1994) Chlorophyll ¯uorescence
as a non-intrusive indicator for rapid assessment of in
vivo photosynthesis. In: Schulze ED, Caldwell MM (eds) Ecophysiology
of photosynthesis. Springer, Berlin Heidelberg New
york, pp 49±70
Sorrensen-Cothern KA, Ford ED, Sprugel DG (1993) A model of
competition incorporating plasticity through modular foliage
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Taylor G, Truswell EM, McQueen KG, Brown MC (1990) Early
Tertiary palaeogeography, landform evolution and palaeoclimates
of the Southern Monaro, NSW, Australia. Palaeogeogr
Palaeoclimatol Palaeoecol 78: 109±134
Truswell EM (1991) Antarctica: a history of terrestrial vegetation.
In: Tingey RJ (ed) The geology of Antarctica. Clarendon, Oxford.
pp 499±537
Yun JI, Taylor SE (1986) Adaptive implications of leaf thickness
for sun- and shade-grown Abutilon theophrasti. Ecology 67:
1314±131" name="eprints.referencetext" />
<meta content="Brodribb, Tim J. and Hill, Robert S. (1997) Light response characteristics of a morphologically diverse group of southern hemisphere conifers as measured by chlorophyll fluorescence. Oecologia, 110 (1). pp. 10-17. ISSN 0029-8549" name="eprints.citation" />
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of southern hemisphere conifers as measured
by chlorophyll fluorescence" name="DC.title" />
<meta content="Brodribb, Tim J." name="DC.creator" />
<meta content="Hill, Robert S." name="DC.creator" />
<meta content="270402 Plant Physiology" name="DC.subject" />
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<meta content="Unlike northern hemisphere conifer families, the southern family, Podocarpaceae, produces a great variety of foliage forms ranging from functionally broad-, to needle-leaved. The production of broad photosynthetic surfaces in podocarps has been linked qualitatively to low-light-environments, and we undertook to assess the validity of this assumption by measuring the light response of a morphologically diverse group of podocarps. The light response, as apparent photochemical electron transport rate (ETR), was measured by modulated fluorescence in ten species of this family and six associated species (including five Cupressaceae and one functionally needle-leaved angiosperm) all grown under identical glasshouse conditions. In all species, ETR was found to increase as light intensity increased, reaching a peak value (ETR(max)) at saturating quantum flux (PPFDsat), and decreasing thereafter. ETR(max) ranged from 217 mu mol electrons . m(-2). s(-1) at a PPFDsat of 1725 mu mol photons . m(-2). s(-1) in Actinostrobus acuminatus to an ETR of 60 mu mol electrons . m(-2). s(-1) at a PPFDsat of 745 mu mol electrons . m(-2). s(-1) in Podocarpus dispermis. Good correlations were observed between ETR(max) and both PPFDsat and maximum assimilation rate measured by gas-exchange analysis. The effective quantum yield at light saturation remained constant in all species with an average value of 0.278 +/- 0.0035 determined for all 16 species. Differences in the shapes of light response curves were related to differences in the response of non-photochemical quenching (q(n)), with q(n) saturating faster in species with low PPFDsat. Amongst the species of Podocarpaceae, the log of average shoot width was well correlated with PPFDsat, wider leaves saturating at lower light intensities. This suggests that broadly flattened shoots in the Podocarpaceae are an adaptation to low light intensity. " name="DC.description" />
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    <h1 class="ep_tm_pagetitle">Light response characteristics of a morphologically diverse group of southern hemisphere conifers as measured by chlorophyll fluorescence</h1>
    <p style="margin-bottom: 1em" class="not_ep_block"><span class="person_name">Brodribb, Tim J.</span> and <span class="person_name">Hill, Robert S.</span> (1997) <xhtml:em>Light response characteristics of a morphologically diverse group of southern hemisphere conifers as measured by chlorophyll fluorescence.</xhtml:em> Oecologia, 110 (1). pp. 10-17. ISSN 0029-8549</p><p style="margin-bottom: 1em" class="not_ep_block"></p><table style="margin-bottom: 1em" class="not_ep_block"><tr><td valign="top" style="text-align:center"><a href="http://eprints.utas.edu.au/2648/1/Oecol__conifer__light.pdf"><img alt="[img]" src="http://eprints.utas.edu.au/style/images/fileicons/application_pdf.png" class="ep_doc_icon" border="0" /></a></td><td valign="top"><a href="http://eprints.utas.edu.au/2648/1/Oecol__conifer__light.pdf"><span class="ep_document_citation">PDF</span></a> - Full text restricted - Requires a PDF viewer<br />419Kb</td><td><form method="get" accept-charset="utf-8" action="http://eprints.utas.edu.au/cgi/request_doc"><input accept-charset="utf-8" value="3471" name="docid" type="hidden" /><div class=""><input value="Request a copy" name="_action_null" class="ep_form_action_button" onclick="return EPJS_button_pushed( '_action_null' )" type="submit" /> </div></form></td></tr></table><p style="margin-bottom: 1em" class="not_ep_block">Official URL: <a href="http://dx.doi.org/10.1007/s004420050127">http://dx.doi.org/10.1007/s004420050127</a></p><div class="not_ep_block"><h2>Abstract</h2><p style="padding-bottom: 16px; text-align: left; margin: 1em auto 0em auto">Unlike northern hemisphere conifer families, the southern family, Podocarpaceae, produces a great variety of foliage forms ranging from functionally broad-, to needle-leaved. The production of broad photosynthetic surfaces in podocarps has been linked qualitatively to low-light-environments, and we undertook to assess the validity of this assumption by measuring the light response of a morphologically diverse group of podocarps. The light response, as apparent photochemical electron transport rate (ETR), was measured by modulated fluorescence in ten species of this family and six associated species (including five Cupressaceae and one functionally needle-leaved angiosperm) all grown under identical glasshouse conditions. In all species, ETR was found to increase as light intensity increased, reaching a peak value (ETR(max)) at saturating quantum flux (PPFDsat), and decreasing thereafter. ETR(max) ranged from 217 mu mol electrons . m(-2). s(-1) at a PPFDsat of 1725 mu mol photons . m(-2). s(-1) in Actinostrobus acuminatus to an ETR of 60 mu mol electrons . m(-2). s(-1) at a PPFDsat of 745 mu mol electrons . m(-2). s(-1) in Podocarpus dispermis. Good correlations were observed between ETR(max) and both PPFDsat and maximum assimilation rate measured by gas-exchange analysis. The effective quantum yield at light saturation remained constant in all species with an average value of 0.278 +/- 0.0035 determined for all 16 species. Differences in the shapes of light response curves were related to differences in the response of non-photochemical quenching (q(n)), with q(n) saturating faster in species with low PPFDsat. Amongst the species of Podocarpaceae, the log of average shoot width was well correlated with PPFDsat, wider leaves saturating at lower light intensities. This suggests that broadly flattened shoots in the Podocarpaceae are an adaptation to low light intensity. </p></div><table style="margin-bottom: 1em" cellpadding="3" class="not_ep_block" border="0"><tr><th valign="top" class="ep_row">Item Type:</th><td valign="top" class="ep_row">Article</td></tr><tr><th valign="top" class="ep_row">Additional Information:</th><td valign="top" class="ep_row">The original publication is available at www.springerlink.com&#13;
</td></tr><tr><th valign="top" class="ep_row">Keywords:</th><td valign="top" class="ep_row">chlorophyll fluorescence; light response; leaf morphology; shade adaptation; conifers </td></tr><tr><th valign="top" class="ep_row">Subjects:</th><td valign="top" class="ep_row"><a href="http://eprints.utas.edu.au/view/subjects/270402.html">270000 Biological Sciences &gt; 270400 Botany &gt; 270402 Plant Physiology</a><br /><a href="http://eprints.utas.edu.au/view/subjects/270400.html">270000 Biological Sciences &gt; 270400 Botany</a></td></tr><tr><th valign="top" class="ep_row">ID Code:</th><td valign="top" class="ep_row">2648</td></tr><tr><th valign="top" class="ep_row">Deposited By:</th><td valign="top" class="ep_row"><span class="ep_name_citation"><span class="person_name">Scholarly Publications Librarian</span></span></td></tr><tr><th valign="top" class="ep_row">Deposited On:</th><td valign="top" class="ep_row">11 Dec 2007 08:28</td></tr><tr><th valign="top" class="ep_row">Last Modified:</th><td valign="top" class="ep_row">09 Jan 2008 02:30</td></tr><tr><th valign="top" class="ep_row">ePrint Statistics:</th><td valign="top" class="ep_row"><a target="ePrintStats" href="/es/index.php?action=show_detail_eprint;id=2648;">View statistics for this ePrint</a></td></tr></table><p align="right">Repository Staff Only: <a href="http://eprints.utas.edu.au/cgi/users/home?screen=EPrint::View&amp;eprintid=2648">item control page</a></p>
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