Marine and Fishery Sciences 38 (1): 109-144 (2025)
126
ious authors for dierent regions where the species
is distributed (Table 1).
According to studies conducted by dierent au-
thors, distinct LT50% values have been observed
among dierent study areas. However, dierences
may be attributed to the methods employed in
each estimation, especially maturity scales, the
technique used for stage assignment (macro or
microscopic), and the seasonal coverage of sam-
plings, making comparison challenging. The only
thing that seems evident and is repeated in almost
all studies is that males mature at smaller body
sizes than females. On the other hand, in those
estimations corresponding to the southernmost
American region, it would appear that values of
length at rst maturity on the Atlantic continental
shelf are quite similar to each other and lower
than those corresponding to the Chilean Pacic,
with the exception of those reported by Arana
(2009). They also seem to be distinguishable from
those estimated in the South Georgia Islands area,
where dierences between males and females are
more pronounced. Prenski and Almeida (2000)
mentioned that specimens possibly mature at an
earlier age in the Patagonian region compared to
those from South Georgia Islands due to more
precocious development caused by temperature
eects. However, later estimates in the Argentine
Sea (Pájaro et al. 2009; Ruocco et al. 2017) would
indicate that at least males would mature at larger
lengths compared to records obtained in the South
Georgia Islands.
Parasitic fauna
Parasitic fauna is a useful biological marker and
a widely accepted methodology for discriminating
sh stocks (MacKenzie 2002; Catalano et al. 2014;
Timi and MacKenzie 2015). It has been applied in
various sh species from the Southwest Atlantic,
and it has been observed that both oceanographic
conditions and host characteristics inuence par-
asitic composition and provide insights into stock
dierentiation (Braicovich and Timi 2008; Timi
ering various retention areas on the Patagonian
shelf, Harte (2020) surprisingly postulated that
Burdwood Bank seems to have little to no connec-
tivity with retention areas around Malvinas Islands
or the Patagonian shelf. It is unlikely to contrib-
ute signicantly to the supply or retention of eggs
and larvae of D. eleginoides in the region. Instead,
results from simulations suggest that spawning
areas in southern Chile are likely the most impor-
tant source of reproductive products for Malvinas
Islands shing grounds. When analyzing the poten-
tial processes governing the ontogenetic migration
and recruitment strength of D. eleginoides in the
Patagonian shelf sector around Malvinas Islands,
Lee et al. (2021) also proposed that after spawn-
ing, eggs and larvae are transported to that area by
currents from reproduction areas located south of
Chile and Burdwood Bank. The presence of sea-
sonal mesoscale eddies connecting the subantarctic
Front with Malvinas Current seems to be of para-
mount importance for the survival of eggs and lar-
vae of the species. However, Rubilar et al. (2014)
found that southern Chile has numerous juvenile
rearing and toothsh recruitment areas, suggesting
that many of them have not yet been adequately
identied and valued. This observation contradicts
to some extent the hypothesis that recruitment oc-
curs mainly on the Argentine shelf south and east of
Malvinas Islands, indicating that it also takes place
in Chilean waters. In this area, juveniles are found
in signicant numbers, at least from 47° S and up
to the border with Argentine waters, implying that
the transport of reproductive products, if it occurs,
could be a phenomenon of smaller dimensions than
assumed by Harte (2020) and Lee et al. (2021).
Length at rst sexual maturation
There are dierent estimations of the length at
rst sexual maturation of the Patagonian toothsh
in the southern region of Atlantic, Pacic and Indi-
an oceans and around the southernmost American
region. As a result, this study describes values of
length at rst maturation (LT50%) estimated by var-