Bronwyn May Gillanders

Bronwyn May Gillanders

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Bronwyn May Gillanders

Southern Seas Ecology Laboratories, School of Biological Sciences, University of Adelaide, Adelaide, Australia

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2001 in BioScience
Verified
Journal Article
Open access
PDF file
MBMichael W. Beck
Michael W. Beck
KHKenneth L. Heck
Kenneth L. Heck
KAKenneth W. Able
Kenneth W. Able
DCDaniel Childers
Daniel Childers
DEDavid B. Eggleston
David B. Eggleston
MWMichael P. Weinstein
Michael P. Weinstein
Nearshore estuarine and marine ecosystems—e.g., seagrass meadows, marshes, and mangrove forests—serve many important functions in coastal waters. Most notably,

1 January 2003 in Marine Ecology Progress Series
Verified
Journal Article
Closed access
BGBm Gillanders
Bm Gillanders
KAKw Able
Kw Able
JBJa Brown
Ja Brown
DEDb Eggleston
Db Eggleston
PSPf Sheridan
Pf Sheridan
A critical link missing from our understanding of the nursery role of specific marine habitats is the evidence of connectivity between juvenile and adult habitats. This paper reviews and evaluates evidence of, and spatial scales for, movements from juvenile to adult habitats and it summarises the methods used to study movements. Examples include many fish families but few invertebrate taxa, and most are species of economic importance for USA and Australia. The types of juvenile habitat range from the entire estuary or shallow open coastal waters to specific habitats within estuaries or coastal waters; in some cases juvenile habitats include habitats not traditionally regarded as nursery areas (e.g. the surf zone). The duration of time spent in juvenile habitats averages 13 mo (range 8 d to 5 yr). The majority of organisms move distances of kilometres to hundreds of kilometres from juvenile to adult habitats, although the scale of movements ranged from metres to thousands of kilometres. Changes in abundance among separate habitats and the progression of size classes among separate habitats are the main methods used to infer movement and habitat connectivity. Spatial partitioning of stages of maturity, natural parasites, and a variety of artificial tagging methods have also been used. The latter will become more useful with continued developments in the miniaturisation of artificial tags. More recent studies have used natural tags (e.g. trace elements and stable isotopes) and these methods show great promise for determining movements from juvenile to adult habitats. Few studies provide good evidence for movement from specific juvenile habitats to adult habitats. Future studies need to focus on this movement to supplement data on density, growth and survival of organisms in putative nursery habitats. Such information will allow management and conservation efforts to focus on those habitats that make the greatest contribution to adult populations.Bronwyn M. Gillanders, Kenneth W. Able, Jennifer A. Brown, David B. Eggleston, Peter F. Sherida

24 April 2006 in Marine Ecology Progress Series
Verified
Journal Article
Closed access
CDCp Dahlgren
Cp Dahlgren
GKGt Kellison
Gt Kellison
AAAj Adams
Aj Adams
BGBm Gillanders
Bm Gillanders
MKMs Kendall
Ms Kendall
JSJe Serafy
Je Serafy
Much recent attention has been focused on juvenile fish and invertebrate habitat use, particularly defining and identifying marine nurseries. The most significant advancement in this area has been the development of a standardized framework for assessing the relative importance of juvenile habitats and classifying the most productive as nurseries. Within this framework, a marine nursery is defined as a juvenile habitat for a particular species that contributes a greater than average number of individuals to the adult population on a per-unit-area basis, as compared to other habitats used by juveniles. While the nursery definition and framework provides a powerful approach to identifying habitats for conservation and restoration efforts, it can omit habitats that have a small per-unit-area contribution to adult populations, but may be essential for sustaining adult populations. Here we build on the nursery concept by developing a framework for evaluating juvenile habitats based on their overall contribution to adult populations, and introduce the concept of Effective Juvenile Habitat (EJH) to refer to habitats that make a greater than average overall contribution to adult populations.Craig P. Dahlgren, G. Todd Kellison, Aaron J. Adams, Bronwyn M. Gillanders, Matthew S. Kendall, Craig A. Layman, Janet A. Ley, Ivan Nagelkerken, Joseph E. Seraf

1 May 2016 in Current Biology
Verified
Journal Article
Closed access
ZDZoë A. Doubleday
Zoë A. Doubleday
TPThomas A.A. Prowse
Thomas A.A. Prowse
AAAlexander Arkhipkin
Alexander Arkhipkin
GPGraham John Pierce
Graham John Pierce
JSJayson Semmens
Jayson Semmens
BGBronwyn M. Gillanders
Bronwyn M. Gillanders

1 November 2002 in Canadian Journal of Fisheries and Aquatic Sciences
Verified
Journal Article
Closed access
TETravis S Elsdon
Travis S Elsdon
BGBronwyn M Gillanders
Bronwyn M Gillanders
The concentrations of elements and isotopes in fish otoliths may provide a method of reconstructing movements of fish by differentiating between water bodies of different temperatures and salinities. However, before otoliths can be used to reconstruct environmental histories of fish, it is necessary to assess the effects of seawater temperature and salinity on otolith microchemistry. Using controlled laboratory experiments, juvenile black bream, Acanthopagrus butcheri (family Sparidae), were reared for 50 days in aquaria of varying temperatures and salinities using three experimental designs: temperature × salinity, temperature only, and salinity only. Temperature and salinity interacted to significantly affect the elemental concentration ratios of Sr:Ca and Ba:Ca and the concentrations of isotopes δ13C and δ18O in otoliths. The single-factor experiments showed that temperature significantly affected the concentration ratios of Sr:Ca and Ba:Ca and the concentrations of δ13C and δ18O in otoliths, whereas salinity alone did not affect the concentration ratios of any elements but did affect both isotopes. The concentration ratios of Mg:Ca and Mn:Ca varied considerably among fish within the same treatment level and showed little or no effects due to temperature and (or) salinity. The significant interactive effects of temperature and salinity on otolith microchemistry highlight the need for a multifactorial approach to testing hypotheses regarding the environmental histories of fish.

1 September 2003 in Reviews in Fish Biology and Fisheries
Verified
Journal Article
Closed access
PDF file
TETravis S. Elsdon
Travis S. Elsdon
BGBronwyn M. Gillanders
Bronwyn M. Gillanders