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Abstract submission deadline - 28 September 2007
Posters will be limited to 30 and so will be subject to a selection
procedure based on submitted abstracts. Please send your abstracts
according to the guidelines below by 28th September 2007. You will
receive an email by 12th October 2007 informing you whether or
not your abstract has been accepted and whether it has been accepted
as a poster or an oral presentation.
Poster abstracts will be published in the symposium program and will
be made available on the symposium website.
Grants
Grant submission deadline - 27 July 2007
We have a number of travel grants available for students and early-stage
career scientists (researchers in their first post-doctoral position)
wishing to attend. Each grant will consist of a free registration
plus a contribution towards travel expenses (Participants from
the UK £50; Europe £100; rest of the world £300 UK
Sterling). If you wish to apply for a grant please accompany your
poster abstract submission with a brief (no more than 200 word) statement
indicating your position (graduate student/postdoc), reasons for
wishing to attend and a supporting statement from a scientist who
has agreed to act as a referee for your application, usually your
group leader (please include their contact details). Decisions will
be notified by the 10 August 2007.
Abstract guidelines
Format
- Abstracts should be no more than 200 words and should fill a space
no larger than half an A4 page
- Single spacing, Arial font, 10 point
- First line: title in bold lower case
- Second line: the author(s)' name(s) in upper case. Underline the
name of the author presenting the work
- Third line: full address of the institution(s) where the work was
carried out, in italic lower case
- Leave a single line space after the address
- Main text: provide concise details of the background and objective(s)
of the investigation, methods used, results and conclusions
| Example abstract:
The origin of Helianthus deserticola: survival
and selection in a desert habitat
GROSS, BRIANA L., KANE, NOLAN C., LEXER, CHRISTIAN & RIESEBERG,
LOREN H.
Department of Biology, Indiana University,
Jordan Hall 142, 1001 East Third Street,
Bloomington, IN 47405, USA
The diploid hybrid species Helianthus deserticola inhabits
an extreme environment relative to its parental species H.
annuus and H. petiolaris. Adaptation to the arid
desert floor may have occurred via the acquisition of novel
phenotypes resulting from transgressive segregation in early
hybrids. We have explored this possibility through a field
experiment designed to test the direction and intensity of
phenotypic selection, using crosses between the parental species
as proxies for the ancestral genotype of the ancient hybrid
species. Helianthus deserticola, H. annuus, H. petiolaris, and
early-generation hybrids between H. annuus and H. petiolaris were
all grown in native H. deserticola habitat, and a
selection analysis revealed that several traits were subject
to strong selective pressures. Several of the traits under
selection were also extreme or transgressive in H. deserticola, and
the range of variation present in BC2 hybrids suggests that
many aspects of the H. deserticola phenotype are easily
recreated. Thus, transgressive segregation may have contributed
to the adaptation of H. deserticola to the desert
habitat.
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Submission
- Abstracts should be formatted as .DOC or .RTF documents and emailed
as an attachment to Helen Pinfield-Wells (newphytsymp@lancaster.ac.uk).
In the subject header of the email write 18th NPS Abstract – followed
by the name of the author presenting the work (e.g. 18th NPS Abstract – H
Slater).
- Receipt of abstracts will be notified by email.
- Decision on abstract will be sent by email by the 12th
October 2007 informing you whether or not your abstract has been
accepted and whether it has been accepted as a poster or an oral
presentation.
Poster guidelines
Posters should be no larger than A0 size, portrait (118 cm high x
84 cm wide)
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Symposium logo Calcium signalling by Sam
Day. Transgenic Arabidopsis plant being chilled, the pseudocolour
represents luminesence from the jellyfish protein aequorin when it reacts
with calcium, courtesy of Marc Knight. Alternative conceptual models for
the circadian regulation of physiology in the extensor (a) and flexor cells
(b–e) of the pulvini of legumes from Webb,
2003. Localization
of calmodulin (CaM) in tobacco cotyledon cells from Snedden
and Fromm, 2001.
Ca2+ fluxes and Ca2+-dependent events in cryptogein-treated
tobacco cells from Lecourieux
et al., 2006. Abscisic acid (ABA)- and hydrogen peroxide (H2O2)-induced changes
in the cytosolic calcium concentration ([Ca2+]i) in the protoplasts of mesophyll
cells from Hu
et al., 2007.
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