Age estimation of marine tucuxi dolphins (Sotalia fluviatilis) in south-eastern Brazil

Author(s):  
M.C. de O. Santos ◽  
S. Rosso ◽  
R.M.A. Ramos

This study reports the age estimation of marine tucuxi dolphins (Sotalia fluviatilis) found dead along the south-east coast of Brazil (24°40′S–25°30′S). The investigated specimens were collected from August 1995 to December 1998. Ages were estimated through the number of Growth Layer Groups (GLGs) from decalcified and stained thin sections of teeth. A total of 36 individuals was investigated. Estimated ages of marine tucuxis varied from zero to 29 years. The growth curve was attained from a modification of the von Bertalanffy equation applied to body length and age data. It was possible to estimate the total length of 97·8 cm in newborns, physical maturity was attained at seven years of age, and an asymptotic length of 179·8 cm.

2019 ◽  
Vol 100 (4) ◽  
pp. 1350-1363 ◽  
Author(s):  
Gina L Lonati ◽  
Amber R Howell ◽  
Jeffrey A Hostetler ◽  
Paul Schueller ◽  
Martine de Wit ◽  
...  

AbstractAges of Florida manatees (Trichechus manatus latirostris) can be estimated by counting annual growth layer groups (GLGs) in the periotic dome portion of the tympanoperiotic complex of their earbones. The Florida Fish and Wildlife Conservation Commission manages an archive of more than 8,700 Florida manatee earbones collected from salvaged carcasses from 1989 to 2017. Our goal was to comprehensively evaluate techniques used to estimate age, given this large sample size and changes to processing protocols and earbone readers over time. We developed new standards for estimating ages from earbones, involving two independent readers to obtain measurements of within- and between-reader precision. To quantify accuracy, precision, and error, 111 earbones from manatees with approximately known ages (first known as calves: “KAC”) and 69 earbones from manatees with minimum known ages (“MKA,” based on photo-identification sighting histories) were processed, and their ages were estimated. There was greater precision within readers (coefficient of variation, CV: 2.4–8.5%) than between readers (CV: 13.1–13.3%). The median of age estimates fell within the true age range for 63.1% of KAC cases and was at least the sighting duration for 75.0% of MKA cases. Age estimates were generally unbiased, as indicated by an average raw error ± SD of −0.05 ± 3.05 years for the KAC group. The absolute error (i.e., absolute value of raw error) of the KAC data set averaged 1.75 ± 2.50 years. Accuracy decreased and error increased with increasing known age, especially for animals over 15 years old, whose ages were mostly underestimated due to increasing levels of resorption (the process of bone turnover that obscures GLGs). Understanding the degree of uncertainty in age estimates will help us assess the utility of age data in manatee population models. We emphasize the importance of standardizing and routinely reviewing age estimation and processing protocols to ensure that age data remain consistent and reliable.


2017 ◽  
Vol 10 ◽  
Author(s):  
Nynne H Nielsen ◽  
Gísli A. Víkingsson ◽  
Steen H. Hansen ◽  
Susanne Ditlevsen ◽  
Mads Peter Heide-Jørgensen

The ages of three species of cetaceans were estimated by counting the growth layer groups (GLG) and measuring the aspartic acid racemization rate (kAsp) by what is referred to as the Aspartic Acid Racemization (AAR) technique. Data on kAsp and the D/L ratio of aspartic acid at birth [(D/L)0] in North Atlantic common minke whales (Balaenoptera acutorostrata) are presented along with data on fin whales (B. physalus) and harbour porpoises (Phocoena phocoena) already published by Nielsen et al. (2012). The kAsp specific for minke whales was 1.40 x 10-3 yr-1 (SE ± 0.00005) and the (D/L)0 was 0.0194 (SE ± 0.0012). The correlation of GLG age and D/L ratio for all three species was highly significant; however, the correlation coefficient varied greatly (fin whales: R2 = 0.59, p <0.0001; minke whales: ­R2=0.96, P <0.0001; harbour porpoises: ­R2=0.36, P <0.0001). Asymptotic body length for all three species was estimated by a von Bertalanffy growth model on both the GLG and AAR techniques, and showed no difference.


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.


2014 ◽  
Vol 8 ◽  
Author(s):  
Christina H Lockyer ◽  
Gill T Braulik

The South Asian river dolphins (Platanista gangetica minor and P. g. gangetica) are endangered, geographically isolated, freshwater cetaceans. Accurate age estimation of individuals is an important aspect of population biology as it is used for calculating parameters such as age at maturity and reproduction, longevity, and growth and survival rates. However this has never been comprehensively studied for this endangered cetacean family. A sample of 41 teeth from 29 skulls stored in museum collections was available. We compared two different aging methods to select the most appropriate. This involved decalcification and freeze-sectioning of teeth at variable thicknesses (10–25 micron), and staining with 1) Toluidine Blue, or 2) Ehrlichs Acid Haematoxylin. Stains were then compared for readability of Growth Layer Groups (GLG). The optimum section was found at 20 micron using Erhlichs Acid Haematoxylin. Both dentinal and cemental GLG were readable and comparable, but cemental GLG were generally easier to interpret because they were better defined. Ages varied from newborn / young of year (with none or only a neonatal line present) to a maximum age of 30 GLG. There is currently no validation available for GLG deposition rate, but it is likely annual because of the extreme seasonal changes in the river habitat. 


1982 ◽  
Vol 60 (11) ◽  
pp. 2557-2567 ◽  
Author(s):  
V. de Buffrenil

Sharply defined growth lines are revealed by hematoxylin staining of thin sections of mandibular periosteal bone of the harbour porpoise, Phocoena phocoena (L.). The comparison of these lines to dentinal growth layer groups (GLG) suggests that they are deposited at the rate of one per annum. In this species, bone growth lines allow more reliable and much more complete age determinations than do dentinal GLG's. The actual longevity of the harbour porpoise, as determined by growth lines in bone, is at least 21 years.


2016 ◽  
Vol 8 ◽  
Author(s):  
Katherine Brill ◽  
Miriam Marmontel ◽  
Meghan Bolen-Richardson ◽  
Robert EA Stewart

Manatees are routinely aged by counting Growth Layer Groups (GLGs) in periotic bones (earbones). Manatee carcasses recovered in Florida between 1974 and 2010 provided age-estimation material for three readers and formed the base for a retrospective analysis of aging precision (repeatability). All readers were in good agreement (high precision) with the greatest apparent source of variation being the result of earbone remodelling with increasing manatee age. Over the same period, methods of sample preparation and of determining a final age estimate changed. We examined the effects of altering methods on ease of reading GLGs and found no statistical differences. Accurate age estimates are an important component for effective management of the species and for better models of population trends and we summarize the currently recommended methods for estimating manatee ages using earbones. 


2004 ◽  
Vol 31 (2) ◽  
pp. 177 ◽  
Author(s):  
S. Childerhouse ◽  
G. Dickie ◽  
G. Hessel

Live New Zealand sea lions (Phocarctos hookeri) were aged from growth layer groups (GLGs) in the cementum of a lower first post-canine tooth. A single post-canine (PC1) was removed from individuals of known-age (n = 74) between 1997 and 2001 while under a full anaesthetic. Teeth were decalcified, sectioned on a cryostat, stained and then mounted on glass slides. Age was estimated by counting GLGs in the cementum multiple times. Age estimates were calibrated with known-aged individuals and confirmed the annual formation of cementum annuli in PC1 tooth. While there is some variation in assigning exact age to individuals, it was possible to age 94% of teeth to the exact year or to within 1 year of actual age. There was no significant difference in the slope of regression lines associated with actual and estimated age using this technique (t-test, t = 0.309, d.f. = 144, P < 0.05). Accuracy in ageing was improved by discarding sets of readings with low precision and re-reading the tooth until a precise set of estimates was made. GLGs in the cementum were more accurate and robust for age estimation than using GLGs in the dentine. This paper describes a reliable method for the preparation and ageing of the first post-canine tooth (PC1) from live New Zealand sea lions.


1969 ◽  
Vol 26 (11) ◽  
pp. 3069-3072 ◽  
Author(s):  
William Knight

The author contends that the parameters of any growth curve should be a direct description of the graphical appearance of the data. For growth that is even approximately linear this is not true of the von Bertalanffy curve in its usual form (von Bertalanffy, Human Biol. 10: 181–213, 1938). On the above grounds, an alternate form of the von Bertalanffy curve for use in such instances is proposed.


1987 ◽  
Vol 3 (1) ◽  
pp. 14-21 ◽  
Author(s):  
Arthur D. Goren ◽  
Paul F. Brodie ◽  
Stephen Spotte ◽  
G. Carleton Ray ◽  
H. W. Kaufman ◽  
...  

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