Distribution, Age and Growth, and Sexual Maturity of Witch Flounder (Glyptocephalus cynoglossus) in Newfoundland Waters

1976 ◽  
Vol 33 (7) ◽  
pp. 1574-1584 ◽  
Author(s):  
W. R. Bowering

Witch flounder (Glyptocephalus cynoglossus) were caught from the Hawke Channel to the southern edge of the Grand Bank and west to the Scotian Shelf and the Gulf of St. Lawrence. Although the largest catches were taken at 2–6 C and 185–370 m, witch flounder were found at temperatures ranging from −1 to 10 C and depths of 20–870 m. Witch flounder of the Northeast Newfoundland Shelf were largest and those of the Gulf of St. Lawrence smallest at comparable ages, with growth rates for the east coast of Newfoundland being faster than most other areas. Age and length at 50% sexual maturity ranged from 4.20 to 5.59 yr and 25 to 30 cm for males, and from 8.42 to 10.21 yr and 40 to 50 cm for females.

2018 ◽  
Vol 31 (2) ◽  
pp. 429-441
Author(s):  
Arsalan ◽  
Muhammad Faheem Siddiqui ◽  
Moinuddin Ahmed ◽  
Syed Shahid Shaukat ◽  
Alamdar Hussain

2012 ◽  
Vol 9 (3) ◽  
pp. 1253-1265 ◽  
Author(s):  
P. Sabatier ◽  
J.-L. Reyss ◽  
J. M. Hall-Spencer ◽  
C. Colin ◽  
N. Frank ◽  
...  

Abstract. Here we show the use of the 210Pb-226Ra excess method to determine the growth rate of two corals from the world's largest known cold-water coral reef, Røst Reef, north of the Arctic circle off Norway. Colonies of each of the two species that build the reef, Lophelia pertusa and Madrepora oculata, were collected alive at 350 m depth using a submersible. Pb and Ra isotopes were measured along the major growth axis of both specimens using low level alpha and gamma spectrometry and trace element compositions were studied. 210Pb and 226Ra differ in the way they are incorporated into coral skeletons. Hence, to assess growth rates, we considered the exponential decrease of initially incorporated 210Pb, as well as the increase in 210Pb from the decay of 226Ra and contamination with 210Pb associated with Mn-Fe coatings that we were unable to remove completely from the oldest parts of the skeletons. 226Ra activity was similar in both coral species, so, assuming constant uptake of 210Pb through time, we used the 210Pb-226Ra chronology to calculate growth rates. The 45.5 cm long branch of M. oculata was 31 yr with an average linear growth rate of 14.4 ± 1.1 mm yr−1 (2.6 polyps per year). Despite cleaning, a correction for Mn-Fe oxide contamination was required for the oldest part of the colony; this correction corroborated our radiocarbon date of 40 yr and a mean growth rate of 2 polyps yr−1. This rate is similar to the one obtained in aquarium experiments under optimal growth conditions. For the 80 cm-long L. pertusa colony, metal-oxide contamination remained in both the middle and basal part of the coral skeleton despite cleaning, inhibiting similar age and growth rate estimates. The youngest part of the colony was free of metal oxides and this 15 cm section had an estimated a growth rate of 8 mm yr−1, with high uncertainty (~1 polyp every two to three years). We are less certain of this 210Pb growth rate estimate which is within the lowermost ranges of previous growth rate estimates. We show that 210Pb-226Ra dating can be successfully applied to determine the age and growth rate of framework-forming cold-water corals if Mn-Fe oxide deposits can be removed. Where metal oxides can be removed, large M. oculata and L. pertusa skeletons provide archives for studies of intermediate water masses with an up to annual time resolution and spanning over many decades.


PeerJ ◽  
2015 ◽  
Vol 3 ◽  
pp. e1392
Author(s):  
Juan C. Levesque

Ladyfish (Elopssp) are a common and economically valuable coastal nearshore species found along coastal beaches, bays, and estuaries of the southeastern United States, and subtropical and tropical regions worldwide. Previously, ladyfish were a substantial bycatch in Florida’s commercial fisheries, but changes in regulations significantly reduced commercial landings. Today, ladyfish are still taken in commercial fisheries in Florida, but many are also taken by recreational anglers. Life-history information and research interest in ladyfish is almost non-existent, especially information on age and growth. Thus, the overarching purpose of this study was to expand our understanding of ladyfish age and growth characteristics. The specific objectives were to describe, for the first time, age, growth, and recruitment patterns of juvenile ladyfish from the east coast of Florida (USA). In the Indian River Lagoon (IRL), annual monthly length-frequency distributions were confounded because a few small individuals recruited throughout the year; monthly length-frequency data generally demonstrated a cyclical pattern. The smallest were collected in September and the largest in May. Post-hoc analysis showed no significant difference in length between August and May, or among the other months. In Volusia County (VC), annual monthly length-frequency distribution demonstrated growth generally occurred from late-winter and spring to summer. The smallest ladyfish were collected in February and the largest in August. On average, the absolute growth rate in the IRL was 36.3 mm in 60 days or 0.605 mm day−1. Cohort-specific daily growth rates, elevations, and coincidentals were similar among sampling years. Cohort-specific growth rates ranged from 1.807 in 1993 to 1.811 mm day−1in 1994. Overall, growth was best (i.e., goodness of fit) described by exponential regression. On average, the absolute growth rate in VC was 28 mm in 150 days or 0.1866 mm day−1. Cohort-specific daily growth rates were significantly different among sampling years; however, the elevations and coincidentals were similar. Cohort-specific growth rates ranged from 1.741 in 1994 to 1.933 mm day−1in 1993. Mean ladyfish growth was best described by linear regression; however, natural growth was explained better by exponential regression. In the IRL, the corrected exponential growth equation yielded a size-at-age 1 of 156.0 mm SL, which corresponded to an estimated growth rate of 0.4356 mm day−1. In VC, the corrected exponential growth equation yielded a size-at-age 1 of 80 mm SL corresponding to an estimated growth rate of 0.2361 mm day−1.


2019 ◽  
Vol 33 (4) ◽  
pp. 549-566 ◽  
Author(s):  
Michael Weinstein ◽  
Melissa N. Liotta ◽  
Aaron Solitt ◽  
Adam Hunt ◽  
Jessica K. Abbott ◽  
...  

Author(s):  
G. A. Steven

The first serious attempt to determine the age and growth rate of the common mackerel (Scomber scombrus L.) appears to have been made by Captain Atwood in 1856 (quoted by Brown Goode, 1884, p. 116) in the Massachusetts Bay area of northern North America. Small fish caught by Atwood in October of that year measuring 6½–7 in. in length (16.5–17.5 cm.) he believed to be the young of the year (i.e. they belonged to the O-group). Mackerel belonging to this group he calls ‘spikes’. ‘Blinks', ‘tinkers’ and ‘second size’ fish he assigns to the I-, II- and III-year age groups respectively, but unfortunately gives no data as to the sizes of those categories, merely stating that everyone well acquainted with mackerel makes the same groupings ‘as there seems to be a line of demarkation between the different kinds which stands out prominently’. Sixteen years later, on 27 July 1872, Malm (1877, p. 409) observed large numbers of small mackerel close inshore in the Gullmarfjord near Christineberg. Several tons of those mackerel were enclosed in a seine, but only ten specimens were retained as all the others escaped through the meshes. These ten fish ranged in length from 67 to 100 mm. and Malm surmised their age to be 13 months. Collett (1880, p. 18) stated that on the coast of Norway I-year-old mackerel are ‘fingerlang’. To fish of 20 cm., taken at the end of August, he ascribed (without supporting data) an age of 2 years, with sexual maturity supervening at 3 years at an unspecified length.


2014 ◽  
Vol 22 (2) ◽  
pp. 145-150
Author(s):  
Bożena Szczepkowska ◽  
Mirosław Szczepkowski ◽  
Iwona Piotrowska

Abstract Vendace, Coregonus albula L., was reared to commercial size in a recirculating system. Three different feed rations were applied during the ten-month-long experiment. The feed rations impacted fish growth rates, and fish in the different groups achieved body weights of 26.6 g to 57.5 g. The final survival in all groups was similar from 44.3% among the fish fed the smallest feed ration to 53.2% in the group receiving the largest feed ration. No differences were noted in the share of viscera, peritoneal fat, or in the hepatosomatic indexes, but there were differences in the gonadosomatic indexes. After thermal stimulation, only males achieved sexual maturity. The number of mature fish was similar in all groups and ranged from 17.8 to 21.3% of all fish. The results of the present study indicated that vendace can achieve commercial size in an intensive rearing period of ten months in RAS.


1970 ◽  
Vol 27 (12) ◽  
pp. 2155-2158 ◽  
Author(s):  
G. P. Ennis

In Newfoundland waters, shorthorn sculpins, Myoxocephalus scorpius (L.), live to age 15 and attain a maximum size of just over 50 cm. The growth rates of males and females are little different below age 4, but above age 4 the females grow faster than the males, and the difference between average length-at-age for males and females gets progressively larger with age. Males mature at a younger age and at a smaller size than females. In any age-group where there are mature and immature individuals the mature ones are larger.


Author(s):  
J. D. Gage

Recoveries of tetracycline-labelled specimens of the sea urchin Echinus esculentus (Echinodermata: Echinoidea) from a wild population marked two years previously indicate very low skeletal growth rates in large adults. The post-tag growth in the test of a smaller specimen showed two clear growth zones in the middle layer of the plates, this conforming to the expectation of a single growth band each year. Merging of the spinochrome pigment bands present in the outer layer near the plate edge in older urchins will probably result in underestimation of age based on counts of these bands.The large literature on growth banding in the European sea urchin Echinus esculentus L. and other echinoids is reviewed by Pearse & Pearse (1975), Smith (1980) and Gage (1991). Moore (1935) utilised spinochrome pigment banding in the genital (apical) plates of E. esculentus from the Isle of Man (Irish Sea) and Firth of Clyde (western Scotland) in one of the first studies utilising growth bands to interpret the age structure and growth rates of sea urchins. A single band was assumed to be formed each year. Counts of spinochrome bands have been used to obtain nearly all subsequently published age data for this species (Sime, 1982; Nichols et al., 1985; Sime & Cranmer, 1985; Comely & Ansell, 1988).The present study was aimed at helping to resolve differing interpretations of age and growth rates in Echinus esculentus provided by these studies. This was undertaken by time marking the skeletal plates of a large sample of a wild population accessible by scuba diving on a submerged rock reef at 10–15 m depth off the islet of Eilean Mor near the Dunstaffnage Laboratory.


1991 ◽  
Vol 12 (1) ◽  
pp. 81-102 ◽  
Author(s):  
Jacques Castanet ◽  
Marcos Baez

AbstractQualitative and quantitative comparisons of histological data recorded from growing bone from seven extant and extinct taxa of Gallotia show that these lizards do not have the same longevity, reach sexual maturity at various ages and probably have different growth rates which are in reverse proportion to the specific size of individuals in each taxon. In term of relative growth, the highest rate is seen in the smallest taxon (G. atlantica) and the lowest in the largest taxon (G. goliath). It appears that differences between the maximum size reached, irrespective of the size of hatchlings, are only the consequence of changes in longevity allowing a more or less protracted growth; they are not due to differences in growth rates. On the basis of these data we discuss some points relating to adaptive strategies and evolutionary features of these lizards.


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