Using genetic pedigree reconstruction to estimate effective spawner abundance from redd surveys: an example involving Pacific lamprey (Entosphenus tridentatus)

2017 ◽  
Vol 74 (10) ◽  
pp. 1646-1653 ◽  
Author(s):  
S.L. Whitlock ◽  
L.D. Schultz ◽  
C.B. Schreck ◽  
J.E. Hess

Redd surveys are a commonly used technique for indexing the abundance of sexually mature fish in streams; however, substantial effort is often required to link redd counts to actual spawner abundance. In this study, we describe how genetic pedigree reconstruction can be used to estimate effective spawner abundance in a stream reach, using Pacific lamprey (Entosphenus tridentatus) as an example. Lamprey embryos were sampled from redds within a 2.5 km reach of the Luckiamute River, Oregon, USA. Embryos were found in only 20 of the 48 redds sampled (suggesting 58% false redds); however, multiple sets of parents were detected in 44% of the true redds. Estimates from pedigree reconstruction suggested that there were 0.48 (95% CI: 0.29–0.88) effective spawners per redd and revealed that individual lamprey contributed gametes to a minimum of between one and six redds, and in one case, spawned in patches that were separated by over 800 m. Our findings demonstrate the utility of pedigree reconstruction techniques for both inferring spawning-ground behaviors and providing useful information for refining lamprey redd survey methodologies.

2020 ◽  
Vol 97 (3) ◽  
pp. 804-816
Author(s):  
Timothy A. Whitesel ◽  
Michelle McGree ◽  
Gregory S. Silver

1980 ◽  
Vol 58 (6) ◽  
pp. 957-966 ◽  
Author(s):  
Murray D. Wiegand ◽  
R. E. Peter

Female goldfish were held under conditions of 12 °C and a 12 h light: 12 h dark photoperiod during three phases of the sexual cycle. A pretreatment blood sample was taken after 2 weeks of acclimation. Comparison of pretreatment levels of plasma lipids from the three experiments revealed that the concentration of triglycerides (TG) increased and total cholesterol (TC) decreased with increasing ovarian size. Plasma lipid phosphorus (LP) levels were slightly higher in sexually mature fish than in sexually regressed fish. Two weeks after the pretreatment blood sample, the fish were injected intraperitoneally with salmon gonadotrophin (SG-G100) or control solution for 3 days, after which a posttreatment blood sample was taken. In sexually maturing fish injection of SG-G100 caused increased plasma TG levels (compared with pretreatment) in fish with small ovaries, changing to decreased levels in fish with larger ovaries. A similar effect was also seen in maturing fish with plasma TC; these effects were abolished by castration or by keeping fish at 21 °C. SG-G100 had little effect on plasma LP. The results suggest that gonadotrophin causes a net mobilization of lipid in fish with small ovaries (presumably via sex steroids) and accelerated ovarian uptake of lipid in fish with larger ovaries.


1956 ◽  
Vol 13 (4) ◽  
pp. 467-487 ◽  
Author(s):  
Wilfred Templeman ◽  
H. J. Squires

Haddock otolith lengths decline from over 5% of the total length of the fish at 14 to 17 cm. to almost 3% at 74 to 77 cm. The otolith lengths of slow-growing haddock decline less rapidly than those of fast-growing haddock. Little difference was found between otolith lengths in male and female haddock of the same length.Slow-growing haddock both from the Grand Bank and from St. Pierre Bank have heavier otoliths than fast-growing haddock at the same fish lengths. This is true not only for fish of different year-classes in the same year but also for fish of the same year-class in different years.The otoliths of male haddock of the Grand Bank exceed progressively in weight the otoliths of females of the same length after the males become sexually mature. The relative increase in otolith weight of the male fish is attributed to a probably slower growth rate after sexual maturity, which occurs earlier than in females. Similarly, the heavier otoliths of mature fish in sizes overlapping with immature fish are due to a greater age of the mature fish at these sizes. Otolith weight relative to fish weight decreased considerably with increase in fish size, and no distinct differences were apparent between otolith weights as a percentage of fish weights in slow-growing and fast-growing fish of the same length.


2019 ◽  
Vol 29 (4) ◽  
pp. 767-788 ◽  
Author(s):  
Benjamin J. Clemens ◽  
Laurie Weitkamp ◽  
Kevin Siwicke ◽  
Joy Wade ◽  
Julianne Harris ◽  
...  

2006 ◽  
Vol 63 (1) ◽  
pp. 200-211 ◽  
Author(s):  
Christian Jørgensen ◽  
Bruno Ernande ◽  
Øyvind Fiksen ◽  
Ulf Dieckmann

That sexually mature fish skip reproduction, especially in response to poor condition, has been documented in many species. We present results from an energy-allocation life history model that shed light on the underlying logic of skipped spawning, based on the Northeast Arctic stock of Atlantic cod (Gadus morhua). The model predicts that skipped spawning is a regular phenomenon, with up to 30% of the sexually mature biomass skipping spawning. Spawning should be skipped if the expected future gain in reproductive output, discounted by survival, more than balances the expected reproductive success the current year. Skipped spawning was most common (i) among potential second-time spawners and (ii) early in life, (iii) when fishing mortality at the spawning grounds was high, (iv) when fishing mortality at the feeding grounds was low, (v) when natural mortality was low, and (vi) when the energetic and mortality costs associated with migration and spawning were high. Cod skipped spawning more often when food availability was both increased (opportunities for better growth) and decreased (too little energy for gonad development), and this pattern interacted with mortality rate. We conclude that skipped spawning may be more widespread than appreciated and highlight potential consequences for the understanding of stock–recruitment relationships.


2005 ◽  
Vol 52 (3) ◽  
pp. 297-301 ◽  
Author(s):  
Yuji Yamazaki ◽  
Norio Fukutomi ◽  
Norio Oda ◽  
Koichi Shibukawa ◽  
Yasuo Niimura ◽  
...  

2016 ◽  
Vol 35 (8) ◽  
pp. 2092-2102 ◽  
Author(s):  
Julia R. Unrein ◽  
Jeffrey M. Morris ◽  
Rob S. Chitwood ◽  
Joshua Lipton ◽  
Jennifer Peers ◽  
...  

2011 ◽  
Vol 93 (2) ◽  
pp. 245-254 ◽  
Author(s):  
Benjamin J. Clemens ◽  
Matthew G. Mesa ◽  
Robert J. Magie ◽  
Douglas A. Young ◽  
Carl B. Schreck

PLoS ONE ◽  
2017 ◽  
Vol 12 (1) ◽  
pp. e0169334 ◽  
Author(s):  
Kellie J. Carim ◽  
J. Caleb Dysthe ◽  
Michael K. Young ◽  
Kevin S. McKelvey ◽  
Michael K. Schwartz

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