Age Determination of Lingcod (Ophiodon elongatus) Using Dorsal Fin Rays and Scales

1977 ◽  
Vol 34 (9) ◽  
pp. 1305-1313 ◽  
Author(s):  
Richard J. Beamish ◽  
D. Chilton

Cross sections of the 4th–8th fin rays from the second dorsal fin provided reliable ages of lingcod (Ophiodon elongatus), although there was some difficulty interpreting the ages of 1- and 2-yr-old fish. Length was an acceptable indicator of age 1- and 2-yr-old fish. After a scale age of 5 or 6 yr, the scale annulus became difficult to identify. After age 7 or about 75–85 cm, fin-ray ages were older than scale ages. Some of the oldest fish averaged 8 yr older by the fin-ray method.Mature females attained much larger mean sizes than males of similar age, and there was considerable variation in size of similar-aged older fish. Key words: Age determination, fin rays, scales, Ophiodon elongatus, ageing errors.

1969 ◽  
Vol 26 (5) ◽  
pp. 1199-1203 ◽  
Author(s):  
H. T. Bilton ◽  
D. W. Jenkinson

Ages of adult sockeye and chum salmon were estimated from examination of the second anterior pectoral fin ray, and were compared with estimates from their scales or otoliths. For sockeye, only the ocean age could be estimated. Freshwater annual rings could not be distinguished on their fin rays even though they were present on their scales or otoliths. In general, the three methods provided the same estimates of ocean age. Agreement of estimates of ocean age by one to five readers ranged from 78.9 to 98.8%. For chum salmon, the scale and fin ray methods generally provided the same estimates of total age. Agreement of estimates of total age by one or two readers ranged from 73.8 to 99.3%.


1986 ◽  
Vol 43 (8) ◽  
pp. 1588-1594 ◽  
Author(s):  
D. E. Chilton ◽  
H. T. Bilton

Age of spawning chinook salmon (Oncorhynchus tshawytscha) was estimated using a combination of thin cross-sections from the dorsal fin rays and scales. The latter were used when freshwater growth could not be interpreted from fin rays. Fish of known age were used when available. Results were compared with ages obtained from scales only. Due to scale resorption a significant proportion of the older fish ages was undetected using only scales. Determinations of freshwater age from fin rays and from scales were in agreement 88.5 ± 8.7 to 92.3 ± 7.2% at the 95% confidence level. Thus, the fin ray method provided virtually the same freshwater age as did the scale method. Also, fin rays provided quite acceptable estimation of ocean age. It is recommended that managers use a combination of scales and fin rays to estimate the total age of spawning chinook salmon.


2018 ◽  
Vol 82 (3) ◽  
pp. 169
Author(s):  
Ronald Fricke ◽  
Daniel Golani ◽  
Brenda Appelbaum-Golani ◽  
Uwe Zajonz

The scorpionfish Scorpaena decemradiata n. sp. is described from off the coast of Israel in the Gulf of Aqaba, northern Red Sea. The new species is similar to S. porcus Linnaeus, 1758, but is characterized by dorsal fin spines XII, soft dorsal fin rays 10 (the last divided at base); pectoral fin rays 16, uppermost branched pectoral fin ray is the second; lacrimal with 2 spines over maxilla that point at nearly right angle from each other, the posterior pointing ventrally and slightly anteriorly; occipital pit well developed; anteriormost mandibular lateral-line pores small, separated; scales ctenoid; 59-62 scale rows in longitudinal series; scales absent on chest and pectoral fin base; and cirri developed over entire head and body, but no cirri on lower jaw. An updated checklist of the species of the genus Scorpaena Linnaeus, 1758 and a key to the species of the eastern Atlantic, Mediterranean Sea and Red Sea are presented.


Zootaxa ◽  
2019 ◽  
Vol 4551 (3) ◽  
pp. 275 ◽  
Author(s):  
KYOJI FUJIWARA ◽  
HIROYUKI MOTOMURA

The clingfishes Lepadichthys frenatus Waite 1904 and Lepadichthys misakius (Tanaka 1908) are both redescribed as valid species, although the latter has previously been regarded as a junior synonym of the former. Lepadichthys frenatus and L. misakius are easily distinguished from their congeners by the following combination of characters: 14–19 dorsal-fin rays; 12–14 anal-fin rays; disc size moderate, its length 15.1–20.8 % of standard length (SL); and dorsal, anal and caudal fins connected by membranes. Lepadichthys misakius can be distinguished from L. frenatus by having 25–28 (modally 26 or 27) pectoral-fin rays [vs. 27–29 (29) in L. frenatus]; the upper end of the gill membrane level with the 5th to 8th (usually 6th) pectoral-fin ray base in lateral view [vs. 6th to 8th (7th)]; the lower 8th to 11th (9th) pectoral-fin ray base attached to the disc base by membrane [vs. 10th to 12th (11th)]; 7–11 (9) gill rakers on each arch [vs. 11–14 (12)]; anterior, posterior and least interorbital widths 9.0–11.8 (mean 10.7), 13.4–16.9 (15.3) and 3.2–8.8 (6.2) % SL, respectively [vs. 8.4–10.2 (9.4), 12.1–14.7 (13.5) and 2.8–5.9 (4.8) % SL, respectively]; and NC2 (nasal canal pore) usually located between the anterior and posterior margins of the posterior nostril (vs. usually located before the posterior nostril anterior margin). Morphological changes with growth of the two species are described in detail and a lectotype designated for L. frenatus. 


Zootaxa ◽  
2018 ◽  
Vol 4531 (1) ◽  
pp. 95
Author(s):  
HARALD AHNELT ◽  
MICHAEL SAUBERER

Schindleria macrodentata sp. nov., a new species of the paedomorphic gobiid fish genus Schindleria, is described from the Malay Archipelago. The two specimens were collected in 1929 during the “Dana Expedition” in the Molucca Sea between Sulawesi and Halmahera islands (00°29′N, 125°54′E) (Indonesia) and in the Sulu Sea close to Panay Island (11°43’N, 121°43′E) (Philippines). The new species is characterized by a slender body (body depth at pectoral fin base 3.6–3.7 % of SL and at anal fin origin 3.9–4.8 % of SL), a long second dorsal fin (first dorsal fin absent) originating distinctly anterior to the origin of the anal fin (predorsal length 61.8–65.2 % of SL and preanal length 71.7–75.8 % of SL), a short tail (from anus to tip of longest caudal fin ray) (22.1 % of SL), 19–20 dorsal fin rays and 10 anal fin rays, first anal fin ray below 9th dorsal fin ray, few large, widely spaced teeth in the upper and the lower jaws (7 on the premaxilla and 6 on the dentary), an elongated pectoral radial plate (length 3.7–4.5 % of SL) and, in the caudal skeleton, a procurrent ray with an additional spiny process at its base. No distinct urogenital papilla and no pigmentation on body are developed. In this study we present three morphological traits until now not considered as diagnostic characters for Schindleria, the shape of the pectoral radial plate, the shape of the last procurrent caudal spine and the shape of the arch formed by the lower jaw. We also discuss the caudal-fin skeleton of Schindleria, a character developing beyond the larval stages. The record of S. macrodentata is the first of the genus Schindleria for Indonesia and, at more than 100 km distant to the next shore, it is the first offshore record of a Schindler's fish. 


1979 ◽  
Vol 36 (11) ◽  
pp. 1395-1400 ◽  
Author(s):  
Richard J. Beamish

A comparison of ages determined from surfaces of otoliths and from sections of otoliths showed that ages were similar up to a section age of 22–24 yr. The growth pattern observed on thin sections of otoliths and from broken and burned otoliths from the region of the nucleus was interpreted to indicate that Pacific ocean perch probably live much longer than previously thought. Because the criteria used to identify annuli from otoliths sections appeared valid for younger fish, there was no justification to reject the application of these criteria for estimating ages of older fish and thus no reason to reject the possibility that Pacific ocean perch might live to be older than 70 yr. Ages determined from sections of otoliths from other rockfish species found off the west coast of Canada such as Sebastes fiavidus and Sebastes brevispinis have ranged from 30 to 60 yr indicating that many species of rockfish may live longer than previously thought. Key words: age determination, otolith, maximum age, age determination errors, Pacific ocean perch, otolith sections


1971 ◽  
Vol 28 (4) ◽  
pp. 553-558 ◽  
Author(s):  
L. S. Parsons ◽  
V. M. Hodder

Numbers of vertebrae, gill rakers, and of pectoral, anal, and dorsal fin rays of spring- and autumn-spawning Atlantic herring (Clupea harengus harengus Linnaeus) in 10 samples from the coastal waters of southwestern Newfoundland were compared. There was no significant difference (P > 0.05) between mean vertebral numbers of spring and autumn spawners. Mean numbers of gill rakers and of pectoral, anal, and dorsal fin rays were all higher (P < 0.01) for autumn spawners than for spring spawners with gill-raker and pectoral fin-ray numbers exhibiting the greatest degree of difference. It is suggested that the differences in fin-ray numbers between spring and autumn spawners are related to water temperatures during larval development and to differences in developmental rates of spring- and autumn-hatched larvae.


Zootaxa ◽  
2010 ◽  
Vol 2434 (1) ◽  
pp. 60 ◽  
Author(s):  
ADRIANA E. ALMIRÓN ◽  
JORGE R. CASCIOTTA ◽  
MARÍA DE LAS M. AZPELICUETA ◽  
MARCELO LOUREIRO
Keyword(s):  
Fin Ray ◽  

Astyanax stenohalinus Messner, 1962 is redescribed based on type material and new specimens collected in many localities of Argentina and Uruguay. This species is distinguished by a combination of the following characters: possession of hooks in all fins of males, teeth not expanded distally, two or three maxillary teeth, 37–39 perforated scales in the lateral series, 25–30 branched anal-fin rays, and anal-fin origin located before a vertical through last dorsal-fin ray insertions.


1982 ◽  
Vol 39 (12) ◽  
pp. 1664-1685 ◽  
Author(s):  
I-H. Ni

The distribution of Northwest Atlantic beaked redfishes, Sebastes mentella and S. fasciatus, has been confused for the past several decades. Sebastes fasciatus has been reported as having lower meristic counts than S. mentella. Meristic elements of 33 301 vertebrae, 22 622 anal fin ray, and 16 290 dorsal fin ray counts were utilized to examine the yearly, depth, and geographic variation of meristics in beaked redfishes. Data collected from specimens caught off West Greenland, Baffin Island, Labrador, Newfoundland, Quebec, and Nova Scotia were analyzed by 100-m-depth intervals. Temporal and depth variation were examined by the χ2-test of independence on meristic frequencies. Geographic variation was evaluated using the modes and mean values in the meristic frequency histograms. Cluster analysis of meristic frequencies displayed the dendrographic affinities and the distance matrix among division–depth blocks.Temporal variation indicated a mixture of vertebral frequency patterns which varied with depth and area. Depth variation and geographic clines were found for each of these meristic characters; the shallow and southern waters were dominated by counts of 29, 14–13, and 7 for vertebrae, dorsal fin rays, and anal fin rays, respectively, whereas deep and northern waters were dominated by 30, 15–14, and 8–9. These results suggested that S. fasciatus occurs on the Nova Scotian Shelf and Grand Bank whereas S. mentella is largely found in Baffin Bay, Labrador waters, and the Gulf of St. Lawrence. The common names of S. mentella and S. fasciatus are discussed. Additionally, five hypothetical stocks of beaked redfishes based on meristic patterns are proposed for management purposes.Key words: Sebastes mentela, S. fasciatus, redfish, meristic variation, distribution, cluster analysis


2018 ◽  
Vol 36 (2) ◽  
pp. 864 ◽  
Author(s):  
I. Vakalas ◽  
G. Ananiadis ◽  
N. Kontopoulos ◽  
K. K. Stoykova ◽  
A. Zelilidis

The study area is part of the Pindos foreland (Underhill, 1985). Pindos foreland is a tertiary turbiditic foreland basin fill trending parallel to the external Hellenides and occupies Gavrovo and Ionian isopic zones (Aubouin, 1959). The age of Pindos foreland sediments is still a matter of discussion. B.P. (1971) proposed an early Miocene to middle Miocene age, explaining the presence of Oligocene fauna as a product of large scale erosion and reworking of older sediments during Miocene. IGSR&IFP(1966) suggested a late Eocene to early Miocene age for the basin fill while Fleury (1980), Leigh (1991), Wilpshaar (1995), Bellas (1997) assigned an Oligocene age. Avramidis et al (1999) proposes a middle Eocene to early Miocene age assessment, using nannofosil zones from three studied cross sections in the Klematia-Paramythia basin (middle Ionian zone). The determination of the sediment ages was based on the study of calcareous nannofossils, which came from almost 120 samples covering 11 geological cross sections. The nannofosil marker species that were found in the samples were classified using the biozones proposed by Martini in 1971. According to the age assessments arose from the studied samples, clastic sedimentation in the study area began in the Middle Eocene, with small differences among the basin. The end of clastic sedimentation seems to be at different times in different parts of the basin.


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