These aquaculture-
and conservation-oriented
commentaries are not abstracts written by the original authors.
They reflect the opinions of someone else -- usually Roger Doyle. Direct quotations from the papers or
abstracts are marked with inverted commas.
297. News
flash: "supportive breeding" need not increase inbreeding and drift
Genetic effects of
multiple generations of supportive breeding. 2001. Wang, J., and N.
Ryman. Conservation Biology 15 (6):1619-1631.
In 1991 Ryman and Laikre
published a paper which demonstrated that the effective population number
(Ne; Feb 2000 #18, Aug 2001 #212) of an endangered, wild population would actually be decreased by
supplementing it with hatchery stock (1991, Conservation Biology 5:325-329).
This bad news has strongly influenced the thinking of resource managers
and has helped fuel doubts about the wisdom of stock supplementation. The
1991 paper also triggered an interesting, and ultimately helpful, debate
about the relationship between effective number as it affects genetic
drift and effective number as it affects the accumulation of inbreeding.
The 1991 paper dealt with
the first generation of stock supplementation. In this follow-up paper,
Wang and Ryman show, both analytically and by simulation, that the
reduction in effective number (both drift and inbreeding) is quickly
reversed in later generations as long as the census size of the population
is increased by supplementation. (Census size is the actual number of
animals, including those breeding in the hatchery and the wild.) This
proviso will usually be met because supplementation would be pointless if
it doesn't make the population bigger.
The authors also consider
an important practical decision: should hatchery breeders be chosen at
random, or should they be selected from those whose parents bred in the
wild, or should they be selected from those whose parents bred in the
hatchery? The second course is usually recommended and followed, on the
grounds that it helps prevent unwanted adaptation to the hatchery
environment. The third course is one I recommended years ago, more or less
tongue-in-cheek, on the grounds that since we seem to have taken permanent
control of the environment we should accept our responsibilities and help
fish get used to it: Doyle et al. 1995. In Uses and Effects of Cultured
Fishes in Aquatic Ecosystems, edited by H. L. H. Schramm and R. G.
Piper: American Fisheries Society, pp. 205-211.)
Anyway it turns out that
whichever selection procedure is followed the effective population number
will increase. This should be very good news for conservationists. Of course effective population number only measures one of
the problems potentially caused by supplementation -- domestication
selection and ecological problems remain. nils.ryman@popgen.su.se
296. Successful selection for higher growth
rate in shrimp
Selection for
better growth of Penaeus stylirostris in Tahiti and New Caledonia. 2002. Goyard, E., J. Patrois, J.M. Peignon, V. Vanaa, R. Dufour, V.
Viallon, and E. BĂ©dier. Aquaculture 204 (3-4):461-468.
This important paper
shows that a straightforward mass selection program can produce useful
genetic gains in growth rate in shrimp. Selection intensities, which
ranged between 4% and 18%, were not especially high. Furthermore the
strain is known to have lost some diversity during the early years of
domestication and to be rather inbred (June 2000 #71). Despite these
potential disabilities the program produced a 21% increase in growth rate
by the fifth generation, for a realized heritability of about 0.11.
The authors also ran
experiments aimed at determining the correlation between early and late
selection. These experiments involved grading shrimp at various sizes and
ages and using fluorescent elastomer tags. The authors conclude that
selection of fast-growers at an early stage, when all the shrimp are small
(averaging about one gram)
is likely to be effective in increasing the size at harvest. If is
confirmed this is important information. Selection at harvest size is impracticable for commercial shrimp
farmers in Tahiti because of space limitations.
The authors do acknowledge, however, that their
size-at-age experiments were phenotypic and required some
"unnatural" manipulations like artificially holding back the
growth rate of some individuals. The actual selection experiments
which can measure the genetic correlation between early and late
selection are apparently underway. egoyard@ifremer.fr
295. An Indian carp species shows
"reverse domestication"
Growth and
survival of six stocks of rohu (Labeo rohita, Hamilton) in mono and
polyculture production systems.
2002. Reddy, P.V.G.K.,
B. Bjarne Gjerde, S.D. Tripathi, R.J. Jana, K.D. Mahapatra, S.D. Gupta,
J.N. Saha, M. Sahoo, S. Lenka, P. Govindassamy, M. Rye, and T. Gjedrem.
Aquaculture 203 (3-4):239-250.
Growth and survival of a
domestic Rohu stock and five wild stocks were compared in two farm
environments: alone (monoculture) and in polyculture with other Indian
carp species. Polyculture is the usual farm environment in India. The
domestic stock, with a long farming history, performed worse than the five
wild stocks in both environments. The probable explanation, as the authors
say, is the long history of inbreeding and negative domestication
selection in Indian broodstocks.
Figs. 1 and 4 in the
paper reveal that there were many changes in rank among stocks when they
were grown in the different environments. The genotype (stock) x
environment interaction was significant (p<.01) and highly significant
(p<.001) in the two year classes studied. Not only was the growth of
the domesticated stock generally worse than the others, but the proportional decrease in polyculture, relative to monoculture, appears greatest for the
domesticated stock. The absolutely worst-growing stock in the whole
experiment was the farm stock growing in the environment to which it had
been habituated for more than thirty years.
Growth x environment
interaction therefore adds support to the idea that domestic evolution has been
messing up in India.
Paternal as well as
maternal half-sib families were generated in the experiment but only the
full-sib data (families with one sire and one dam) were analysed. The
publication of genetic inferences based solely on full-sib data, when
half-sib data are available, is puzzling, especially when the work was
done on carp.
"The substantial and
highly significant full-sib effect [i.e. variation among families] ...
indicate a significant additive genetic variance within the stocks."
"The significant full-sib effects ... suggest [growth as well as
survival] can be improved through selective breeding." "The
interaction between production system and stock on growth and survival was
significant but low, particularly compared to the significant full-sib
effects." And finally, a conclusion so valuable that it may justify
the means of analysis, "Therefore, the development of specialized
varieties for each of the two production systems is not required."
Reddy e-mail: cifa@ori.nic.in
294. How to compare the growth of strains
in aquaculture
Comparison of
growth performances of three French strains of common carp (Cyprinus
carpio) using hemi-isogenic scaly carp as internal control. 2002.
Vandeputte, M., E. Peignon, D. Vallod, P. Haffray, K. Komen, and B.
Chevassus. Aquaculture 205 (1-2):19-36.
This paper is oriented
towards an evaluation of the internal control technique for comparing
strains. No strain differences were actually found. The internal control
is a "reference strain" which is visibly distinguishable from
the test strains and which is included in all the experimental units such
as cages, tanks, ponds etc. The growth of the test strain is compared with
the growth of the reference strain in the same units, which eliminates
much of the environmental variance.
Data were analysed in
various ways by linear statistical models, and a power analysis was also
performed. The discussion of the statistical analyses is particularly
clear and thorough. The authors found that, "The use of the internal
control divides the number of replicates needed to have a good statistical
power by 5 at 5 weeks [of age] and by 8 at 2 summers [of age], when
compared to separate testing without control".
They put this in a
practical context by saying"... this type of design with an internal
control is more efficient than a classical design by blocks. It is also
much more versatile because if we consider that the environment estimation
by the control is correct, this allows the use of designs ''in the field''
without replication in a given location, or even with some strains not
present in all locations, without hampering the possibilities of correctly
estimating environment effects. This would be of special interest when
there is no experimental facility with a large number of standardized
ponds."
There are, of course,
some difficulties and problems which are also well discussed, mainly
concerning the necessity of exactly matching the size and condition of the
control and test lines. mvande@jouy.inra.fr
293. Successful selection for growth rate
in tilapia
Response to within
family selection for body weight in Nile tilapia (Oreochromis niloticus)
using a single-trait animal model. 2002. Bolivar, R.B., and G.F.
Newkirk. Aquaculture 204 (3-4):371-381.
The experiment,
conducted in the Philippines and analysed here after 12 generations, involved within-family
selection, rotational mating, and preliminary, and pre-selection size
grading ("collimation", Aquaculture 57:27-35, 1986) of
the selected stock." A realized heritability estimate of 0.14 was
obtained based on the regression of mean breeding values on cumulative
selection differentials after 12 generations. The inbreeding coefficient
was 6.3% after 12 generations with an average inbreeding of 0.525% per
generation. The family rotational mating used to propagate the families
was effective in keeping the inbreeding rate to a minimum even at high
selection intensities." Within-family selection permitted high
selection intensities of about 2%. The result seems to have been that the
size of the fish aged 16 weeks more than doubled after 12 generations. rbolivar@mozcom.com
292. Fluctuating asymmetry measures
environmental stress, not genetic stress
Relationship
between heterozygosity and asymmetry: a test across the distribution
range. 2001. Kark, S., U.N. Safriel, C. Tabarroni, and E. Randi.
Heredity 86 (2):119-127.
Fluctuating asymmetry
(FA: random developmental differences between the left and right sides of
an organism) may be induced by genetic stress such as inbreeding and/or
lack of genetic diversity, or environmental stress such as high
temperature. In either case FA is, potentially, a useful indication that
something is going wrong in a hatchery or conserved population (see brief
explanation in the June 2000 list #70). Recent papers reviewed here have
shown FA is not related to fitness components in Drosophila (June 2000
#70), is
related to inbreeding in ungulates (July 2000 #82) and not itself a
heritable trait in Chinook salmon (February 2001 #167).
This work describes the
relationship between the FA of a morphological trait and allozyme
heterozygosity in a species of partridge "across a sharp climatic
gradient in Israel from the arid periphery, through the Mediterranean–desert
ecotone towards the Mediterranean areas located further away from the
range boundaries. Genetic diversity, as estimated using both observed and
expected heterozygosity, was not associated with asymmetry at either the
population or at the individual level. We argue that whereas asymmetry may
serve as a useful tool for estimating changes in environmental stress, it
may not be widely applicable for estimating genetic stress." salit@stanford.edu
291. Hybrids between locally-adapted
populations are not always unfit
High larval
performance of leopard frog hybrids: effects of environment-dependent
selection. 2001. Parris, M.J. Ecology 82 (11):3001-3009.
Are natural hybrids unfit
in nature? The theoretical answer depends on a number of factors including
the degree of genetic differentiation between species, environmental
specificity of adaptations, habitat variation, genetic architecture of
isolating mechanisms, genetic architecture of the trait itself (e.g.
compatabilities, dominance) ... and the list goes on. Thus
carefully-collected, empirical evidence is very useful.
In this experiment two
frog species and their F1 hybrids were grown in experimental enclosures in
three habitats characteristic of the parental species and their
naturally-occurring hybrids in central Missouri. "There was no
evidence of reduced F1 hybrid larval performance in any environment....
Thus, hybrid genotypes performed equivalently to or better than their
parental species in three aquatic habitat types. Transplant experiments
such as these are critical for directly measuring genotype-by-environment
interactions and for assessing the role of ecological factors in
determining the adaptive potential of natural hybridization."
One should note that the
risk that hybridization poses to the genetic purity of the parental
species also depends on the nature of pre-zygotic isolating mechanisms, if
any, and on the degree of fitness decrease (if any) in F2 and backcross
generations. Risks may also be hiding in the genetics of correlated
fitness traits which were not studied. mparris@memphis.edu
290. Success (but potential problem)
selecting shrimp for growth and survival
Selective breeding
of Pacific white shrimp (Litopenaeus vannamei) for growth and resistance
to Taura Syndrome Virus. 2002. Argue, B.J., S.M. Arce, J.M. Lotz, and
S.M. Moss. Aquaculture 204 (3-4):447-460.
Two vannamei lines
selected at the Oceanic Institute have produced very interesting results.
The growth rate of the line selected for growth increased dramatically in
one generation (21%, giving a realized heritability of 1.0!). The survival
of the line selected mainly for survival increased by 7 percentage points
(18% of the initial value), but the growth rate of this line declined by
about 5%. Similarly, survival in the line selected for growth was slightly,
but non-significantly, lower than the control.
This experiment certainly
gives additional scientific weight to anecdotal evidence that growth and
survival (to TSV challenge) respond well to selection, but that there is
some sort of negative genetic correlation between these traits. Genetic
correlations are notoriously difficult to estimate precisely because of
error variances which are intrinsically large. (Also see #289, below.)
The splitting of a
selected broodstock into two lines with different selection criteria is a
good way to estimate realized correlations but may not be the best way
to increase overall economic value in a commercial broodstock. For that
purpose, properly weighted selection of both traits in a single line is
usually recommended. argueb001@hawaii.rr.com
289. Life-history trade-offs were not
found, although looked for very carefully
Testing
life-history pleiotropy in Caenorhabditis elegans. 2001. Knight, C.G.,
R.B.R. Azevedo, and A.M. Leroi. Evolution 55 (9):1795-1804.
Managers of captive
populations maintained for aquacultural or genetic conservation purposes
are concerned about the practical effects of "trade-offs" among
traits affecting fitness. One type of tradeoff is caused by pleiotropic
genes, i.e. genes that directly affect two or more different components of
fitness (maternal body size and fertility in this study; growth and
survival in other studies such as #290, above). There are other types of tradeoffs too, such
as environmental tradeoffs involving genes which diminish aggression and
may confer greater fitness in captive environments while reducing fitness
in nature.
It is the first sort of trade-off, genes which affect two
components of fitness in opposite directions, that is the focus of this
experimental study.
Attempts to actually find
such genes are so rare that this work on the model organisms C. elegans (a
nematode) should be of considerable interest to population managers who
are interested in long-term effects of captivity and selection. Especially
since the results were negative.
Three QTLs affecting
fertility and two affecting body size were found. None of them had
pleiotropic effects on both traits, One fertility QTL was closely linked
with a body-size QTL, however, so it is easy to imagine a situation in
which a small population selected for one trait would respond in both
traits. The point, though, is that this correlated response is not an
intrinsic property of the genes and is unpredictable; it could be either
positive or negative depending on accidents of sampling and gene frequency
at start-up. a.leroi@ic.ac.uk
288. Host genetic diversity reduces
herbivore and disease damage
Does host genotype
diversity affect the distribution of insect and disease damage in willow
cropping systems? 2001. Peacock, L., T. Hunter, H. Turner, and P.
Brain. Journal of Applied Ecology 38 (5):1070-1081.
The authors planted
willow tree genotypes having different susceptibilities to beetles and
rust fungus in pure monocultures and mixtures. In all cases the damage to
the plants was greater in the monocultures than in the genotype mixtures.
What is especially interesting is the fact that the arrangement (location) of the
genotypes within the mixture also made a big difference to the magnitude
and distribution of damage. lori.peacock@bbsrc.ac.uk
287. Sorting out the origins of mixed
stocks
Admixture analysis
and stocking impact assessment in brown trout (Salmo trutta) estimated
with incomplete baseline data. 2001. Hansen, M.M., E.E. Nielsen, D.
Bekkevold, and K-L.D. Mensberg. Canadian Journal of Fisheries and Aquatic
Sciences 58:1853-1860.
The authors of this
interesting paper try out a Bayesian method of analysing the genetic
contribution of hatchery fish to an artificially stocked trout populations
when there was no information about gene frequencies prior to stocking.
The method (the STRUCTURE program of Pritchard, et al. 2000. Inference of
population structure using multilocus genotype data. Genetics 155:
945-959)
appeared to work well, but, "The results showed almost complete
absence of stocked, domesticated trout in samples of trout from the
[Danish] rivers." Evidently the stocking didn't contribute much to
long-term rehabilitation of the population. See November 2001 #260 for
another paper which comes to the same conclusion. mmh@dfu.min.dk
286. Valuable local adaptation not well
indicated by neutral markers
Local adaptation
across a climatic gradient despite small effective population size in the
rare sapphire rockcress. 2001. McKay, J.K., J.G. Bishop, J-Z. Lin, J.H.
Richards, A. Sala, and T. Mitchell-Olds. Proceedings of the Royal Society
(Ser. B.) 268 (1477):1715-1721.
A lot of controversy and
uncertainty attends the issue of whether on not a population at risk of
extinction is actually worth saving, given that resources are limited and
we can't save everything. Genetic uniqueness and genetic diversity are
often cited as the proper criteria. However, as noted before in these
Genecomp listings, the neutral markers with which genetic diversity and
uniqueness are measured may have no correlation with the quantitative
genetic variation which is the actual basis of adaptation (short term
adaptation anyway; see May 2001 #194, Sept. 2001 #237, Jan. 2002 #281).
The authors of this paper
found that small, peripheral populations of their rare plant are
genetically adapted to local microclimates. "Local adaptation occurs
despite (i) the absence of divergence at almost all marker loci and (ii)
very small effective population sizes, as evidenced by extremely low
levels of allozyme and DNA sequence polymorphism. Our results provide
empirical evidence that setting conservation priorities based exclusively
on molecular marker diversity may lead to the loss of locally adapted
populations."
The authors performed
transplantation (common garden) experiments on plants living at various
altitudes in western Montana. Adaptive traits included water use
efficiency, carbon isotope ratios and root mass ratio. jmackay@selway.umt.edu
285. On-line help with genetics, virology
etc.
National Center for
Biological Information resource for molecular biology information. 2002. URL.
The NCBI has begun to
provide full-text, on-line access to a number of comprehensive standard
genetics texts. The background material needed to understand most of the
population, molecular genetic and bioengineering research papers noted on
this GCL website can be found in these books, which include: Molecular
Biology of the Cell. 3rd ed. B. Alberts et al.(1994); Introduction
to Genetic Analysis. 7th ed. A.J.F. Griffiths et al. (1999); Modern
Genetic Analysis. A.J.F Griffiths et al. (1999); Molecular Cell
Biology. 4th ed. H. Lodish et al (1999).
NOTE: to get information
about a topic you merely enter a word or phrase into the "search
box" at the top of the first page of the NCBI website. The rest of
the website appears to be trying to sell you the books. This URL has been added
to the "Dictionaries" page. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=Books
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