Reproduction
Hatching probability
If fairy tern eggs are brought from Australia to genetically rescue
tara iti, do you expect the hatching probability of eggs laid from
admixed pairs to be different from those laid by non ad-mixed tara iti
pairs (0.6 ± 0.11 since 2010)? If so, what do you believe that value
will be?

|
Expert
|
Minimum Plausible
|
Most Likely
|
Maximum Plausible
|
Confidence
|
|
FK
|
36.9
|
70.0
|
85
|
90
|
|
HK
|
67.0
|
75.0
|
83
|
100
|
|
IR
|
40.0
|
65.0
|
80
|
95
|
|
JZ
|
30.0
|
50.0
|
70
|
85
|
|
KB
|
50.0
|
70.0
|
80
|
75
|
|
NR
|
0.0
|
54.4
|
65
|
70
|
|
VK
|
30.0
|
80.0
|
100
|
85
|
|
XQ
|
20.0
|
70.0
|
80
|
100
|
Comments
Mixed offspring
-
VK: Given strong evidence of inbreeding depression, admixture
should bring fitness benefits to the offspring by masking deleterious
alleles by increased heterozygosity. Boosting immune genes should be
beneficial too. Given the closest relative is a different species, there
might also be some negative consequences of admixture, e.g. if genetic
incompatibilities have evolved between species. Admixed individuals will
get one copy of the genome from each parental species, so may not be
affected too strongly. On balance, I feel the benefits of admixture may
outweigh the costs, especially if there is evidence of historical gene
flow between these species.
-
XQ: I expect an improvement in the hatching probability of
hybrids because the high inbreeding in tara iti seems likely to be
contributing to low hatching rate (so hybrids will be less inbred) -
albeit I note that there are other less inbred bird species with lower
hatching rates, so inbreeding is a contributor but not a confident
predictor of low hatching success
-
HK: increase in egg hatch rate following genetic rescue reflects
the stage’s high sensitivity to inbreeding depression and the strong
empirical signal from comparable bird case studies. In small, isolated
populations with high long runs of homozygosity, recessive deleterious
alleles accumulate, leading to reduced fertility, increased embryo
mortality, and lower hatch success. Outcrossing introduces new alleles,
masking many of these lethal or sublethal variants and restoring normal
embryonic development. Effect size given is consistent with other bird
species where recovery is particularly strong at the earliest life
stage, where genetic load is expressed most acutely. This stage can
respond rapidly (within the first post-rescue breeding season) once
donor genes enter the reproductive pool.
-
FK: I consider the hatching probability of eggs from admixed
pairs is likely to be higher than the current hatching probability. In
the information presented ~22% of eggs failed to hatch due to
infertility or early embryo death - and I consider there could be an
increase in hatching probability associated with reduction in this cause
of failure of ~10% with alleviation of inbreeding. However, given my
uncertainty around the changes, I have not increased the lowest
plausible value, but I consider there to be a higher upper plausible
value.
Fledging probability
If fairy tern eggs are brought from Australia to genetically rescue
tara iti, do you expect the fledging probability of hatched eggs laid
from admixed pairs to be different from those laid by non-admixed tara
iti pairs (0.58 ± 0.05 since 2010)? If so, what do you believe that
value will be?

|
Expert
|
Minimum Plausible
|
Most Likely
|
Maximum Plausible
|
Confidence
|
|
FK
|
47
|
65
|
85.0
|
90
|
|
HK
|
62
|
70
|
78.0
|
100
|
|
IR
|
40
|
58
|
75.0
|
98
|
|
JZ
|
0
|
25
|
50.0
|
80
|
|
KB
|
50
|
60
|
70.0
|
75
|
|
NR
|
0
|
66
|
70.0
|
70
|
|
VK
|
40
|
75
|
90.0
|
81
|
|
XQ
|
47
|
58
|
68.2
|
86
|
Comments
Mixed offspring
-
VK: Fledging probability in the wild will depend on environmental
stochasticity, parental behavior (and parental quality as a parent) and
balance between the contrasting effects of heterosis and outbreeding
depression during admixture (i.e. quality and compatibility of the
genomes). The former two factors could be managed to some degree through
the breeding program, by reducing environmental stochasticity and
threats.
-
HK: more modest than for hatching but still considerable
gains. Fledging rate reflects both genetic and environmental influences.
While early embryo mortality is driven largely by recessive lethal
alleles, chick survival to fledging can also be affected by
physiological robustness, immune function, and parental care quality,
all of which may be compromised in inbred individuals.
Introducing unrelated genetic material can improve chick condition
through heterosis, enhancing growth rates, thermoregulation, and
resistance to disease etc. The effect would manifest once admixed chicks
begin to fledge and should persist with ongoing introductions that
maintain genetic diversity.
-
XQ: I think fledging probability is predominantly environmentally
driven. This presumes Australian fairy terns brought over as eggs are
fully imprinted by their foster parents and provide the same level of
care of offspring as tara iti parents do
-
FK: I consider the fledging probability of chicks from hatched
eggs is likely to be slightly higher that the current fledging
probability as the chicks may be less subject to disease. However, given
my uncertainty around the changes, I have not increased the lowest
plausible value, but I consider there is a higher upper plausible value.
Clutch size
If fairy tern eggs are brought from Australia to genetically rescue
tara iti, do you expect the clutch size of a female born from admixed
pairs to be different from that of non-admixed tara iti (1.71 ± 0.45
since 2010)? If so, what do you believe that value will be?

|
Expert
|
Minimum Plausible
|
Most Likely
|
Maximum Plausible
|
Confidence
|
|
FK
|
0.81
|
1.71
|
2.61
|
100
|
|
HK
|
1.75
|
1.80
|
1.85
|
100
|
|
IR
|
0.70
|
1.80
|
2.75
|
99
|
|
JZ
|
1.00
|
1.00
|
2.00
|
80
|
|
KB
|
1.00
|
2.00
|
3.00
|
75
|
|
NR
|
0.00
|
1.70
|
2.60
|
80
|
|
VK
|
0.50
|
2.00
|
3.00
|
95
|
|
XQ
|
0.81
|
1.71
|
2.61
|
95
|
Comments
Mixed offspring
-
VK: Expecting a slight positive shift towards higher value due to
heterosis, while recognizing that outbreeding depression may
(potentially temporarily) make this number lower. Without knowing the
clutch size for the Australian fairy terns and tara iti before
inbreeding, assuming that clutch size 2 is the norm and 1 and 3 are
rarer.
-
FK: I don’t believe there will be a change in clutch size, as the
information I have seen indicates that Australian fairy terns have a
similar clutch size (i.e. clutch size does not appear to be affected by
inbreeding/ROH)
-
XQ: I think clutch size is likely fairly similar between the two
species and will have similar determinants i.e. some genetic variation
but also resource allocation by the female according to her condition.
-
HK: genetic-rescue effect is likely to be smaller than for
hatchability but could still be meaningful. Reduced clutch size in
inbred females could result from lower body condition, disrupted
endocrine function, or impaired allocation of resources to eggs etc.
effects probably subtler than early embryo mortality. Introducing
genetically diverse individuals could increase mean clutch size through
improved female health and reproductive investment. Given that clutch
size in terns is often constrained by evolutionary life-history strategy
(1–2 eggs), any increase might manifest more in the proportion of
females laying two eggs rather than a large shift in the mean. A
conservative assumption would therefore be a small positive shift
appearing after the first admixed females begin breeding.
Survival
Juvenile survival
If fairy tern eggs are brought from Australia to genetically rescue
tara iti, do you expect juvenile survival from admixed pairs to be
different from that of non-admixed tara iti pairs (0.69 ± 0.07 since
2010)? If so, what do you believe that value will be?

|
Expert
|
Minimum Plausible
|
Most Likely
|
Maximum Plausible
|
Confidence
|
|
FK
|
54.5
|
72.0
|
90.0
|
90
|
|
HK
|
70.0
|
75.0
|
80.0
|
100
|
|
IR
|
44.5
|
68.7
|
85.9
|
95
|
|
JZ
|
20.0
|
40.0
|
70.0
|
85
|
|
KB
|
60.0
|
75.0
|
85.0
|
75
|
|
NR
|
0.0
|
40.0
|
81.7
|
80
|
|
VK
|
40.0
|
85.0
|
100.0
|
95
|
|
XQ
|
54.5
|
75.0
|
82.9
|
88
|
Comments
Mixed offspring
-
VK: Juvenile survival will depends a lot on the level of
inbreeding, as the chick must go through many developmental processes
during its first year, many of which could be impaired by inbreeding,
lowering overall fitness. Still, accepting a possibility that some
genomic incompatibilities may strongly impact some process, and may
strongly limit fitness of some individuals. Overall, expecting benefit
of heterosis to outweigh outbreeding depression.
-
FK: I believe admixed juveniles are likely to experience slightly
higher fitness, although not a substantial increase as they will still
face numerous challenges associated with recent independence and
dispersal. As with the other vital rates, I consider the lower plausible
value remains unchanged but there is a chance there could be a
reasonably large increase in the highest plausible value (to capture my
uncertainty given the current lack of understanding of the extent to
which juvenile survival is constrained by inbreeding depression).
-
HK: life stage that integrates multiple inbreeding-sensitive
traits e.g., growth rate, immune competence, and foraging efficiency
that influence survival through the critical post-fledging period.
inbred juveniles may suffer reduced muscle mass, impaired
thermoregulation, and heightened susceptibility to disease, all of which
can translate into high first-year mortality. genetic rescue is expected
to reduce the expression of deleterious recessives that compromise early
survival. The effect would likely appear from the first generation of
admixed juveniles and persist if periodic introductions maintain genetic
diversity.
-
XQ: Again, I expect an improvement in the juvenile survival
probability of hybrids because the high inbreeding in tara iti seems
likely to be contributing to some loss of juveniles. Because hybrids
will be less inbred, we might expect their survival to be higher.
Immature survival
If fairy tern eggs are brought from Australia to genetically rescue
tara iti, do you expect immature survival from admixed pairs to be
different from that of non-admixed tara iti pairs (0.92 ± 0.06 since
2010)? If so, what do you believe that value will be?

|
Expert
|
Minimum Plausible
|
Most Likely
|
Maximum Plausible
|
Confidence
|
|
FK
|
79.6
|
92.2
|
99.0
|
100
|
|
HK
|
90.0
|
93.0
|
96.0
|
100
|
|
IR
|
76.6
|
92.2
|
99.0
|
96
|
|
JZ
|
60.0
|
80.0
|
90.0
|
80
|
|
KB
|
85.0
|
95.0
|
98.0
|
100
|
|
NR
|
79.7
|
88.0
|
96.2
|
100
|
|
VK
|
79.6
|
95.0
|
100.0
|
100
|
|
XQ
|
79.6
|
92.2
|
99.0
|
100
|
Comments
Mixed offspring
-
HK: probably only show modest gains from genetic rescue. By this
stage, many strongly deleterious recessives that drive early mortality
have already been “filtered out” in the egg–chick–juvenile stages.
baseline immature survival is already high, so probably a ceiling effect
(less room for improvement). Any gains would come from heterosis in
sub-lethal traits (better body condition, immune function etc).
-
FK: Immature survival probability is already high (most likely
value) and the current upper plausible value captures what I consider
would be the upper plausible value with admixture.
-
VK: Not expecting a strong effect here, but still some overall
positive effect of admixture (based on empirical examples from other
systems)
-
XQ: This value is already very high for tara iti. It suggests
that individuals who have made it this far are not carrying a strong
deleterious inbreeding load - those individuals may have been lost at
previous life stages. This survival rate is likely in the majority
environmentally driven, and so would not differ between hybrid and
non-admixed offspring
Adult survival
If fairy tern eggs are brought from Australia to genetically rescue
tara iti, do you expect adult survival from admixed pairs to be
different from that of non-admixed tara iti pairs (0.9 ± 0.03 since
2010)? If so, what do you believe that value will be?
The same plot but truncated to survival >70%

|
Expert
|
Minimum Plausible
|
Most Likely
|
Maximum Plausible
|
Confidence
|
|
FK
|
84.3
|
92.0
|
98.0
|
100
|
|
HK
|
90.0
|
92.0
|
94.0
|
100
|
|
IR
|
74.3
|
89.5
|
94.7
|
95
|
|
JZ
|
70.0
|
85.0
|
90.0
|
80
|
|
KB
|
88.0
|
92.0
|
95.0
|
75
|
|
NR
|
0.0
|
89.7
|
92.8
|
80
|
|
VK
|
84.3
|
95.0
|
99.0
|
95
|
|
XQ
|
84.3
|
85.0
|
94.7
|
88
|
Comments
Mixed offspring
-
VK: Expecting shift due to heterosis, improvement of immune
system and masking deleterious variation that may have lowered fitenss
-
FK: Based on analyses I have undertaken for other species, I
consider there could be a slight increase in adult survival in admixed
birds. This is reflected in both the most likely value and the highest
plausible value. I have left the lowest plausible value unchanged, as I
also consider it feasible that there will be no increase compared to
survival rates in the existing population.
-
HK: probably the least responsive life stage to genetic rescue
in long-lived species. By the time individuals reach adulthood, they
have already passed multiple survival filters, so those carrying severe
inbreeding-related defects are less likely to be present in the breeding
population.
That said, high inbreeding can still depress adult survival through
reduced physiological resilience, impaired immune function, and lower
tolerance to environmental stressors (e.g., food shortages etc).
Outcrossing can mitigate these effects by increasing heterozygosity,
which may improve overall health, stress recovery, body condition etc.
For tara iti, there is a high starting baseline and limited scope for
improvement, but even small gains would have significant impact on
long-term population persistence .
-
XQ: As with my previous answer, I believe adult survival is
mostly environmentally rather than genetically driven. Having said that,
there may be some innate behavioural differences between the Australian
fairy tern and tara iti that mean the Australian fairy tern don’t make
the ‘best’ decisions for their survival. So, there may be a slightly
lower survival rate of these hybrid adults carrying genetics from both
subspecies.