**The title, authors, and abstract for this completion
report are provided below. For a copy of
the completion report, please contact the GLFC via e-mail or via telephone at 734-662-3209**
Development of a stable isotope marking technique for early life stages of lake sturgeon
Gregory W. Whitledge1
and Kurt T. Smith1
1Fisheries and Illinois Aquaculture Center, Southern
Illinois University, Carbondale, IL 62901-6511 USA
December 2009
ABSTRACT:
Lake sturgeon, like many other North
American sturgeon species, is listed as endangered, threatened, or as a species
of conservation concern by several management agencies. Assessments of habitat
use and dispersal for early life stages, evaluation of the most suitable life
stages for stocking, and methods for differentiating stocked from wild fish are
important research needs to support rehabilitation of populations of lake
sturgeon and other imperiled species. Tracking fish dispersal and evaluating
stocking success require appropriate tagging methods, but conventional tagging
methods are limited in their applicability to early life stages or do not
provide the possibility for multiple differentiating marks. A recently
developed technique for mass marking fish otoliths using stable isotopes offers
the potential to produce multiple chemical marks that are distinct from one
another and from stable isotope ratios of wild fish. However, examination of
otoliths for chemical marks requires sacrificing fish. Naturally occurring
trace element signatures in pectoral fin rays have recently been demonstrated to
provide valuable new insights into environmental history of fishes, including
sturgeons. However, whether techniques developed for marking otoliths with
unique stable isotope ratios are also applicable to marking pectoral fin rays
has not been evaluated. The objectives of this study were to develop a
technique for marking age-0 lake sturgeon pectoral fin rays with stable
strontium isotope ratios (88Sr/86Sr) and to evaluate retention of stable
isotopic marks. Groups of lake sturgeon were reared in water spiked with
different concentrations of 86SrCO3 (0, 25, 50, or 100 μg/L)
for 10-24 d. Following the labeling period, fish from each treatment group were
retained for up to 120 d to assess mark retention. Stable isotope labeling
produced 88Sr/86Sr marks in pectoral fin rays that were distinct from fin ray 88Sr/86Sr
of control fish reared in ambient laboratory water, with the 100 μg/L 86SrCO3 treatments consistently yielding the
highest rate of marking success. Stable isotopic marks applied to fin rays were
retained for 120 d post-labeling and may persist longer. Production of multiple
unique batch marks in fin rays of early life stages of fish using stable
isotopes will enable researchers to distinguish among different groups of
stocked fish from a single source and between stocked and wild fish without
having to sacrifice fish to check for marks. The ability to differentiate
multiple groups of stocked fish from a single source will facilitate evaluation
of factors affecting stocking success, such as stocking location and timing and
fish size, as well as assessment of dispersal,
habitat use, and survival of marked and released fish when fish may become
interspersed following stocking.