Relations Among Net Reproductive Rate and Life History Parameters for Lake Whitefish (Coregonus clupeaformis)

1985 ◽  
Vol 42 (1) ◽  
pp. 164-168 ◽  
Author(s):  
A. L. Jensen

An equation is derived that relates net reproductive rate to six life history parameters; the equation is applied to determine changes in the net reproductive rate of lake whitefish (Coregonus clupeaformis) that result from variation in these life history parameters. Changes in age at maturity and survival of immature fish are the only parameters that have a large effect on the net reproductive rate. Age at maturity occurs near the inflection of the growth curve, and this implies a relationship between age at maturity, length at maturity, the growth coefficient, and asymptotic length.

1997 ◽  
Vol 54 (5) ◽  
pp. 987-989 ◽  
Author(s):  
A L Jensen

Four patterns occur in growth and mortality parameters across species of fish. Three of these relations, Mxm = 1.65, M = 1.50K, and L(xm) = 0.66Linf where M is natural mortality, xm is age at maturity, L(xm) is length at maturity, and Linf is asymptotic length, were previously shown to result from optimization of the age at maturity. In this study the fourth relation, that between asymptotic size and the growth coefficient, Linf = CK-h, was obtained from a bioenergetic growth equation. A numerical value of h = 0.33 was predicted, and this agrees with the observed value. The relation between the growth coefficient K and size Linf results from the limited amount of assimilated food that must be used both for growth and body functions, and the body functions are a function of body size. The four Beverton and Holt invariants, together with the net reproductive rate, relate many life history parameters to a metabolic parameter and mortality.


PLoS ONE ◽  
2021 ◽  
Vol 16 (3) ◽  
pp. e0248819
Author(s):  
Yujeong Park ◽  
Young-gyun Park ◽  
Joon-Ho Lee

Bemisia tabaci Mediterranean (Gennadius) (Hemiptera: Aleyrodidae) is an economically important insect pest worldwide. Previously, we have reported that most B. tabaci Mediterranean (MED) populations occurring in greenhouse tomatoes in Korea have been displaced from well-differentiated two genetic clusters (C1 and C2) to one (C2) during one-year period. To elucidate factors responsible for this phenomenon, we compared life history parameters of these two different genetic clusters through single and cross mating experiments on two different host plants, cucumber and tobacco, at 26°C. Intrinsic rate of increase (r), finite rate of increase (λ), and net reproductive rate (Ro) were significantly higher in the dominating cluster (C2) (0.247, 1.280, and 192.402, respectively on cucumber; 0.226, 1.253, and 133.792, respectively on tobacco) than in the other cluster (C1) (0.149, 1.161, and 50.539, respectively on cucumber; 0.145, 1.156, and 53.332, respectively on tobacco). Overall performances of cross mating groups, C2fC1m (C2 female × C1 male) and C1fC2m (C1 female × C2 male), were in-between those of C2 and C1, with C2fC1m performing better than C1fC2m. Thus, maternal inheritance appeared to be significantly associated with their life history parameters, with partial involvement of paternal inheritance. Our results demonstrated that the rapid displacement of genetic clusters of B. tabaci MED populations was clearly associated with differences in their life history parameters.


1965 ◽  
Vol 22 (5) ◽  
pp. 1229-1259 ◽  
Author(s):  
P. McCart

A comparison is made of the growth, morphometry, age at maturity, food, and depth distribution of pygmy whitefish (Prosopium coulteri) in four British Columbia lakes. In Tacheeda and Cluculz Lakes where the species is of the usual dwarfed variety, the fish exists sympatrically with two other whitefishes, the mountain whitefish (Prosopium williamsoni) and the lake whitefish (Coregonus clupeaformis). These slow-growing pygmy whitefish differ markedly in morphometry and depth distribution from the "giant" pygmy whitefish of McLeese and Maclure Lakes which live in the absence of other whitefishes. The possibility that differences in the populations might be due to interspecific competition is discussed.


2019 ◽  
Vol 112 (5) ◽  
pp. 2116-2120
Author(s):  
M Amin Jalali ◽  
M Reza Mehrnejad ◽  
Peter C Ellsworth

Abstract Aspects of the nutritional ecology and life histories of five predatory coccinellids (Coleoptera: Coccinellidae)—two arboreal predator species, Oenopia conglobata contaminata (Menetries) and Adalia bipunctata (Linnaeus), and three herbaceous dwelling predator species, Coccinella undecimpunctata aegyptica (Reiche), Exochomus nigripennis (Erichson), and Hippodamia variegata (Goeze) (Coleoptera: Coccinellidae)—were compared when fed either Agonoscena pistaciae Burckhardt and Lauterer (Hemiptera: Aphalaridae), the key psylla pest of pistachio trees, or Aphis gossypii Glover (Hemiptera: Aphididae), a common aphid on herbaceous plants in pistachio orchards. The putative habitat preferences of four of the five coccinellids studied were consistent with their performance on the major herbivore present in those two habitats in terms of net reproductive rate. Oenopia conglobata contaminata and Ad. bipunctata showed higher net reproductive rates when fed on pistachio psylla prey, whereas C. undecimpunctata aegyptiaca and E. nigripennis had better reproductive output on aphid prey. Moreover, E. nigripennis was the most specialized of these generalist predators, eating more and reproducing better when fed aphids. Hippodamia variegata was relatively unaffected by the diet offered, suggesting greater ability to switch among herbivore prey and perhaps better potential as a biocontrol agent with abilities to exploit Ag. pistaciae without large life history tradeoffs.


1977 ◽  
Vol 34 (7) ◽  
pp. 942-953 ◽  
Author(s):  
Graham Bell ◽  
Paul Handford ◽  
Carl Dietz

The life history of the exploited lake whitefish (Coregonus clupeaformis) population of Lesser Slave Lake, Alberta, is described. Mean age is high, having increased under continued exploitation during the last 30 yr. A method of estimating the population age structure is described. The apparent annual rate of survival of adult fish has fluctuated markedly, but on average seems to lie in the interval 0.40–0.50; the annual rate of natural survival is estimated to be 0.53. Juveniles survive better than adults. Rate of survival during the 1st yr of life was estimated to be about 0.0002. Maturity was late, the median age at first reproduction being 6–61/2 yr. The regressions of fecundity on age and length are described; length now contributes almost all the attributable variance to maturity and fecundity. The sex ratio fluctuates in time; this is caused by the fluctuations in age structure, since sex ratio varies with age. The relationship between sex ratio and age is used to calculate the relative rates of survival of male and female fish.These data are used to construct a life table and to compute population parameters. It is inferred that the ability of the population to respond to exploitation has been eroded during the last 30 yr. In some respects, the life history of the Lesser Slave Lake stock appears to be unusual.After about 30 yr of large-amplitude oscillation the whitefish population collapsed in 1965. This does not seem to have been caused by chronic overfishing. In the first place, the rate of fishing mortality is no more than moderate. Secondly, a multiple regression equation describing whitefish catch in 48 other Alberta lakes in which there has been no overall decline in catch successfully predicts the observed mean catch at Lesser Slave Lake. The oscillations in catch are claimed to reflect a limit cycle in the abundance of the whitefish, driven by a lagged relationship between a predator (the fishermen) and its prey (the whitefish). Whether or not this cycle was deterministically stable, such behavior will inevitably put the population in risk of extinction during troughs in the cycle. We suggest that current management policies may encourage the destabilization of whitefish populations, and we propose a remedy. Key words: population dynamics, population regulation, life history, exploitation, survival, fecundity, Coregonus clupeaformis


1982 ◽  
Vol 60 (11) ◽  
pp. 2841-2851 ◽  
Author(s):  
Carl M. Way ◽  
Thomas E. Wissing

The pisidiid clams, Pisidium variabile (Prime) and Pisidium compressum (Prime), from permanent ponds in southwestern Ohio are iteroparous, bivoltine, and have approximate longevities of 1 year. Intrapopulation differences in life history characteristics are discussed in relation to environmental heterogeneity. For the P. variabile population, only age at first reproduction (110 and 226 days for the spring and fall generations, respectively) is different for both annual generations. This is due to differences in environmental variables (temperature, dissolved oxygen levels, food availability) which set physiological limits on growth, reproduction, and maintenance functions. The spring and fall generations of P. compressum show differences in several life history characteristics: age at first reproductive (122 and 270 days, respectively), net reproductive rate (8.7 and 3.7, respectively), r (0.005 and 0.003, respectively), and the number of broods per year (2 and 1, respectively). The results of this study tend to question the validity of using current theories (e.g, r- and K-selection, bet-hedging) which attempt to predict the set of demographic characteristics that should be found in populations under varying environmental circumstances.


Author(s):  
Jayme Magalhães Santangelo ◽  
Bruno Nascimento Soares ◽  
Thecia Paes ◽  
Paulina Maia-Barbosa ◽  
Ralph Tollrian ◽  
...  

Cladocerans serve as prey for several aquatic predators like fish and Chaoborus larvae. However, because different predators consume different sized prey, cladocerans may display differing life-history responses depending on predator type. Although most studies use the genus Daphnia to evaluate phenotypic plasticity in cladocerans, other genera might also respond to predator infochemicals. In this study, we compared life-history responses of Daphnia similis and Moina macrocopa to infochemicals released by a vertebrate (fish) and an invertebrate (Chaoborus) predator. As expected, some life-history parameters were altered depending on the type of predator. Overall, fish infochemicals increased the size at primipara, clutch size, net reproductive rate and longevity in both cladocerans. We argue that increased body lengths in the presence of fish promote bigger clutch sizes. Conversely, responses to Chaoborus were weaker, affecting only the net reproductive rates and longevity. Non-daphniid cladocerans may display similar responses to Daphnia when exposed to predators. However, as Daphnia is usually underrepresented in tropical lakes, studying other genera might offer new insights into predator-prey relationships and food webs in lake ecosystems.


2018 ◽  
Vol 75 (3) ◽  
pp. 953-963 ◽  
Author(s):  
Sebastián A Pardo ◽  
Andrew B Cooper ◽  
John D Reynolds ◽  
Nicholas K Dulvy

Abstract Sensitivity to overfishing is often estimated using simple models that depend upon life history parameters, especially for species lacking detailed biological information. Yet, there has been little exploration of how uncertainty in life history parameters can influence demographic parameter estimates and therefore fisheries management options. We estimate the maximum intrinsic rate of population increase (rmax) for ten coastal carcharhiniform shark populations using an unstructured life history model that explicitly accounts for uncertainty in life history parameters. We evaluate how the two directly estimated parameters, age at maturity αmat and annual reproductive output b, most influenced rmax estimates. Uncertainty in age at maturity values was low, but resulted in moderate uncertainty in rmax estimates. The model was sensitive to uncertainty in annual reproductive output for the least fecund species with fewer than 5 female offspring per year, which is not unusual for large elasmobranchs, marine mammals, and seabirds. Managers and policy makers should be careful to restrict mortality on species with very low annual reproductive output <2 females per year. We recommend elasmobranch biologists to measure frequency distributions of litter sizes (rather than just a range) as well as improving estimates of natural mortality of data-poor elasmobranchs.


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