scholarly journals Validation of Age Estimation in the Harp Seal, Phoca groenlandica, Using Dentinal Annuli

1983 ◽  
Vol 40 (9) ◽  
pp. 1430-1441 ◽  
Author(s):  
W. D. Bowen ◽  
D. E. Sergeant ◽  
T. Øritsland

We investigated the validity and accuracy of age estimation in harp seals, Phoca groenlandica, using a sample of 155 known-age teeth from seals age 3 mo to 10 yr. Under transmitted light, transverse sections of harp seal canine teeth showed distinct incremental growth layers (IGLs) in the dentine. The first growth-layer group (GLG), representing Ist-year growth, consists of two IGLs: an outer layer of opaque dentine, bounded by the neonatal line, and an inner layer of translucent dentine. Subsequent GLGs, each representing 1 yr of growth, generally consist of three IGLs: an outer layer of interglobular dentine deposited during the annual molt in April, a middle layer of opaque dentine formed during the northward spring migration (May–June), and an inner layer of translucent dentine formed from July to March. We show that dentinal GLGs can be used to estimate the absolute age of harp seals. The accuracy of the method decreases with age. Only 72.4% of estimates of 0-group seals were correct using only transverse sections. These errors were virtually eliminated (99.0% correct age determination) when the tooth root was examined. Based on a single examination of a transverse section, the probabilities of correctly estimating age are 0.983, 0.889, 0.817, and 0.553 at ages 1, 2, 3, and 4 + yr, respectively, when clearly inaccurate tag-tooth associations are omitted. The respective probabilities are only slightly higher when age is based on the average of five blind readings, being 1.0, 0.889, 0.833, and 0.625. Beyond age 3 yr, existing data are insufficient to estimate reliably the accuracy of age determined by counting GLGs.

1973 ◽  
Vol 30 (7) ◽  
pp. 1009-1011 ◽  
Author(s):  
D. E. Sergeant ◽  
David K. Caldwell ◽  
Melba C. Caldwell

It is confirmed that one growth layer consisting of one opaque and one translucent zone is laid down annually in the dentine of the teeth of bottlenosed dolphin (Tursiops truncatus), allowing absolute age determination, although the seasonal sequence of dentine deposition is not yet clear. On this basis females from northeast Florida were found to mature at about 12 years and males at 13 years, both sexes living to about 25 years of age. Females accumulated up to 14 corpora albicantia in the ovaries, indicating an accumulation rate of about one per annum. Birth occurred at 100-cm length. Males and females matured at about 245- and 235-cm length, respectively, and attained asymptotic lengths of about 270 and 250 cm.


2018 ◽  
Vol 10 ◽  
Author(s):  
Fiona L. Read ◽  
Aleta A. Hohn ◽  
Christina H. Lockyer

This paper presents a critical review of methods for estimating absolute or relative age in marine mammals. Absolute age is achieved by counting growth layer groups (GLGs) in hard structures such as teeth, ear plugs, baleen, bones and claws. Relative age can be obtained by methods such as aspartic acid racemisation, genetic telomeres, bone mineral density, fatty acid signatures and other methods. Each method is discussed in detail. Accuracy and precision, including inter-reader calibration and anomalies, as well as methods of validating GLG deposition rates are also addressed. Each section concludes with methods of age estimation applicable to monodontids, and suggestions on the focus of future age-estimation research.


1999 ◽  
Vol 48 (1) ◽  
pp. 59-72 ◽  
Author(s):  
J Wolkers ◽  
I.C Burkow ◽  
M Monshouwer ◽  
C Lydersen ◽  
S Dahle ◽  
...  

IAWA Journal ◽  
2005 ◽  
Vol 26 (2) ◽  
pp. 161-174 ◽  
Author(s):  
Hisashi Abe ◽  
Ryo Funada

We examined the orientation of cellulose microfibrils (Mfs) in the cell walls of tracheids in some conifer species by field emission-scanning electron microscopy (FE-SEM) and developed a model on the basis of our observations. Mfs depositing on the primary walls in differentiating tracheids were not well-ordered. The predominant orientation of the Mfs changed from longitudinal to transverse, as the differentiation of tracheids proceeded. The first Mfs to be deposited in the outer layer of the secondary wall (S1 layer) were arranged as an S-helix. Then the orientation of Mfs changed gradually, with rotation in the clockwise direction as viewed from the lumen side of tracheids, from the outermost to the innermost S1 layer. Mfs in the middle layer of the secondary wall (S2 layer) were oriented in a steep Z-helix with a deviation of less than 15° within the layer. The orientation of Mfs in the inner layer of the secondary wall (S3 layer) changed, with rotation in a counterclockwise direction as viewed from the lumen side, from the outermost to the innermost S3 layer. The angle of orientation of Mfs that were deposited on the innermost S3 layer varied among tracheids from 40° in a Z-helix to 20° in an S-helix.


1995 ◽  
Vol 14 (3) ◽  
pp. 335-338
Author(s):  
Erling Sverre Nordøy
Keyword(s):  

1984 ◽  
Vol 41 (12) ◽  
pp. 1843-1847 ◽  
Author(s):  
Jay Barlow

Estimates of mortality rates from age distributions are biased by imprecision in age estimation, even if age estimates are unbiased. I have derived a method for predicting the magnitude of this bias from information on the precision of age determination. Monte Carlo simulations show that bias can be accurately predicted. The commonly used Chapman–Robson mortality estimator is shown to be robust to imprecision in age determination if all age-classes are included. Errors are likely, however, if one or more age-classes are excluded or if other mortality estimators are used. Biases can be corrected if the distribution of age-estimation errors is known.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Mi-Sun Hur ◽  
Seunggyu Lee ◽  
Tong Mook Kang ◽  
Chang-Seok Oh

AbstractThis study was conducted to determine the muscular arrangement of the human pyloric sphincter using a comprehensive approach that involved microdissection, histology, and microcomputed tomography (micro‐CT). The stomachs of 80 embalmed Korean adult cadavers were obtained. In all specimens, loose muscular tissue of the innermost aspect of the sphincter wall ran aborally, forming the newly found inner longitudinal muscle bundles, entered the duodenum, and connected with the nearby circular bundles. In all specimens, approximately one-third of the outer longitudinal layer of the sphincter entered its inner circular layer, divided the circular layer into several parts, and finally connected with the circular bundles. Anatomical findings around the sphincter were confirmed in micro-CT images. The sphincter wall comprised three layers: an inner layer of longitudinal bundles, a middle layer of major circular and minor longitudinal bundles, and an outer layer of longitudinal bundles. The stomach outer longitudinal bundles were connected to the sphincter circular bundles. The inner longitudinal bundles of the sphincter were connected to the adjacent circular bundles of the duodenum.


2000 ◽  
Vol 2 ◽  
pp. 29 ◽  
Author(s):  
Tore Haug ◽  
Kjell T Nilssen ◽  
Lotta Lindblom

Data were collected from harp seal (Phoca groenlandica) and hooded seal (Cystophora cristata) pups belonging to the Greenland Sea (or "West Ice") stocks in 1995-1997. Pups of both species were observed to feed independently shortly after weaning, and their first food was almost exclusively crustaceans. Parathemisto sp., particularly P. libellula, dominated the diet of both the harp and the hooded seal pups, but the diet also contained sympagic amphipods of the genus Gammarus. Krill (Thysanoessa sp.) was of minor importance as food for seal pups in 1995, but occurred more frequentlyin the diet of both species in 1996 and 1997. Considerable niche overlap may suggest some interspecific competition between harp and hooded seal pups in the West Ice.


1963 ◽  
Vol s3-104 (65) ◽  
pp. 141-144
Author(s):  
E. H. SIDDIQUI

The structure of the cuticle of the cysticerci of 3 species of Taenia was studied by means of optical and electron microscopy. In all 3 species the cuticle is composed of 3 layers and covered with hair-like processes. The middle layer, which comprises the bulk of the cuticle, varies in thickness from head to bladder, but there are no differences in thickness between the species studied. The hairs are composed of a core representing an extension of the middle layer and are covered by a continuation of the outer layer. The arrangement of these hairs varies in the species studied.


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