A Simple Fish Tag Suitable for Long-Term Marking Experiments

1972 ◽  
Vol 29 (3) ◽  
pp. 339-341 ◽  
Author(s):  
W. J. White ◽  
R. J. Beamish

A simple, inexpensive fish tag that allows for growth of the fish is described. Growth rates of smallmouth bass were not significantly affected by tagging. The rate of retention on smallmouth bass was much higher than that for a tag described by Fraser but rates of retention of the two tags on largemouth bass were not significantly different. Estimated rates of tag loss were 15% after 1 year for smallmouth bass and 17% after 3 years for largemouth bass. Observed tag losses from white suckers over 3 years were only 0.6%.Using this method, two or three persons can conveniently tag fish at a rate of approximately 30 per hour.

1973 ◽  
Vol 30 (2) ◽  
pp. 195-199 ◽  
Author(s):  
Terry A. Haines

The value of RNA–DNA ratio as a measure of long-term growth of fish populations under semi-natural conditions and when subjected to environmental manipulations was determined. Populations of carp and smallmouth bass of known age distribution were established in artificial ponds maintained at two fertility levels. After 15 months, population growth rates (as percent increase in weight) and RNA–DNA ratios of muscle tissue from selected fish were measured. Each species exhibited a range of population growth rates. The relation between population growth rate and individual fish RNA–DNA ratio for each species was significant. When reproduction occurred, the relation was not significant unless young-of-the-year fish were excluded from population growth rate calculations. Age of fish was also found to have an important effect on RNA–DNA ratio, with the ratio being higher in younger fish.RNA–DNA ratio can be a reliable indicator of long-term population growth in fish when population age structure is known and recruitment is controlled. The method has potential for use in detecting response to environmental changes before growth rate changes become severe.


<em>Abstract</em>.—Long-term studies in Ontario, Canada on Largemouth Bass <em>Micropterus salmoides</em> and Smallmouth Bass <em>M. dolomieu</em> have demonstrated that angling nesting males (both catch and harvest and catch and release) can have negative impacts on the reproductive success for the captured individual. They have also demonstrated that within a population, the male bass that provide the best and longest parental care for their offspring are the most capable of having the greatest relative contribution to the year-class. Furthermore, those males are also the most aggressive toward potential brood predators and, hence, the most vulnerable to angling. Based on those relationships, we postulated that angling in general, and especially angling for nesting bass, results in selection against aggressive individuals in a population, and as a result, the angled population evolves to become less aggressive, containing males with diminished parental care attributes, an example of fisheries-induced evolution (FIE). We recognize, however, that some change towards less aggressive behaviors may also result from learning and phenotypic plasticity. Controlled, long-term selective breeding experiments over 30+ years have, however, documented the heritability of vulnerability of bass to angling and, hence, the potential for selection to act on that trait. Reproductive competition experiments further demonstrated that the highly vulnerable strain of bass produced in those selective breeding experiments indeed had greater reproductive success than the less vulnerable strain. Because angling for Largemouth Bass has been occurring for decades, we also postulated that there should be some evidence in the wild of this FIE. In fact, we did find that the level of vulnerability to angling of nesting male Largemouth Bass in lakes that have had little to no exploitation was significantly greater than that observed for nesting males in moderately and heavily angled populations.


2018 ◽  
Vol 75 (5) ◽  
pp. 733-745 ◽  
Author(s):  
Eric J. Pedersen ◽  
Daisuke Goto ◽  
Jereme W. Gaeta ◽  
Gretchen J.A. Hansen ◽  
Greg G. Sass ◽  
...  

Walleye (Sander vitreus) populations are declining in Wisconsin and neighboring regions, motivating broader interest in walleye biology amidst ecological change. In fishes, growth integrates variation in ecological drivers and provides a signal of changing ecological conditions. We used a 23-year data set of length-at-age from 353 walleye populations across Wisconsin to test whether walleye growth rates changed over time and what ecological factors best predicted these changes. Using hierarchical models, we tested whether spatiotemporal variation in walleye growth was related to adult walleye density (density-dependent effects), water temperature, and largemouth bass (Micropterus salmoides) catch per unit effort (CPUE; predator or competitor effects). The average length of young walleye increased over time, and as a result, time to reach harvestable size declined significantly. In contrast, average lengths of older walleye have remained relatively constant over time. Juvenile walleye length-at-age was positively correlated with largemouth bass CPUE and surface water temperatures, but negatively correlated with adult walleye density. Our finding of widespread and long-term changes in walleye growth rates provides additional insights into how inland fisheries are responding to environmental change.


2008 ◽  
pp. 94-109 ◽  
Author(s):  
D. Sorokin

The problem of the Russian economy’s growth rates is considered in the article in the context of Russia’s backwardness regarding GDP per capita in comparison with the developed countries. The author stresses the urgency of modernization of the real sector of the economy and the recovery of the country’s human capital. For reaching these goals short- or mid-term programs are not sufficient. Economic policy needs a long-term (15-20 years) strategy, otherwise Russia will be condemned to economic inertia and multiplying structural disproportions.


2003 ◽  
Vol 132 (6) ◽  
pp. 1065-1075 ◽  
Author(s):  
Marosh Furimsky ◽  
Steven J. Cooke ◽  
Cory D. Suski ◽  
Yuxiang Wang ◽  
Bruce L. Tufts

1999 ◽  
Vol 34 (2) ◽  
pp. 109-115 ◽  
Author(s):  
J.-L. Mouget ◽  
G. Tremblin ◽  
A. Morant-Manceau ◽  
M. Morançais ◽  
J.-M. Robert
Keyword(s):  

2018 ◽  
Vol 48 (7) ◽  
pp. 809-820 ◽  
Author(s):  
Neil P. Thompson ◽  
Kathy J. Lewis ◽  
Lisa M. Poirier

Drought tolerance of trees may be affected by competition, but most studies quantifying the relationship do not consider the effect of stem clustering. Trees are often clustered in interior Douglas-fir (Pseudotsuga menziesii var. glauca (Mayr) Franco) forests near the grassland interface in central British Columbia due to past harvesting practices or habitat management for mule deer (Odocoileus hemionus hemionus (Rafinesque, 1817)). Climate change projections indicate continued increases in temperature, an outcome that would stress trees growing in dry environments. Trees placed in different states of competition by mechanical harvesting in the 1970s were sampled to provide a 40-year comparison of three levels of competition during 1–2 year droughts. Tree-ring analysis was used to assess the reduction in growth during drought years and resumption of growth in subsequent years. A clear separation of growth rates was evident between open-growing trees, trees on the edge of harvesting trails, and trees within the unharvested interior. Edge trees had intermediate growth rates but no differences were found in the long-term climate–growth relationship compared with open-growing trees. Both Edge and Open classes showed less relative growth reduction during droughts than Interior trees growing between harvest trails. Precipitation throughfall rates and competition for resources are likely driving short-term drought tolerance in combination with other factors.


Author(s):  
J.A. Baars ◽  
G.J. Goold ◽  
M.F. Hawke ◽  
P.J. Kilgarriff ◽  
M.D. Rolm

Patterns of pasture growth were measured on 3 farms in the Bay of Plenty (BOP) and at No2 Dairy (Ruakura Agricultural Centre) in the Waikato from 1989 to 199 1. A standardised trim technique with cages and 4-weekly cutting under grazing was used. Long-term seasonal growth patterns, using a predictive pasture model, were also simulated. Simulated pasture growth from long-term climatic data shows that pasture growth rates are higher in winter, early spring and late autumn in the BOP than the Waikato. However, the actual measurements over the 2 years show that pasture growth over the latter periods is lower at the BOP sites than at the Waikato site. In the BOP the spring peak is much later than in the Waikato while an early summer peak, with higher growth rates than in the Waikato, occurred in the BOP. No such summer peak was evident in the Waikato. The difference between the two regions is caused by the large contribution of subtropical grasses to sward production in summer and autumn, The prolific summer growth of subtropical grasses may explain the low ryegrass content and low pasture production in winter. The lower than expected autumn, winter, spring production may also becaused by low clover content, possibly a result of competition from subtropical grasses and a sulphur deficiency. The apparent low amount of nitrogen fixed by clover may explain the low rates of pasture production over the cooler season. Applications of nitrogen fertiliser may substantially increase dry matter production from April to September. Keywords pasture,simulation,subtropical grasses, Paspalum, Digitaria sanguinalis, growth rates


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