We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
Each species is subject to various biotic and abiotic factors during growth. This paper formulates a deterministic model with the consideration of various factors regulating population growth such as age-dependent birth and death rates, spatial movements, seasonal variations, intra-specific competition and time-varying maturation simultaneously. The model takes the form of two coupled reaction–diffusion equations with time-dependent delays, which bring novel challenges to the theoretical analysis. Then, the model is analysed when competition among immatures is neglected, in which situation one equation for the adult population density is decoupled. The basic reproduction number
$\mathcal{R}_0$
is defined and shown to determine the global attractivity of either the zero equilibrium (when
$\mathcal{R}_0\leq 1$
) or a positive periodic solution (
$\mathcal{R}_0\gt1$
) by using the dynamical system approach on an appropriate phase space. When the immature intra-specific competition is included and the immature diffusion rate is neglected, the model is neither cooperative nor reducible to a single equation. In this case, the threshold dynamics about the population extinction and uniform persistence are established by using the newly defined basic reproduction number
$\widetilde{\mathcal{R}}_0$
as a threshold index. Furthermore, numerical simulations are implemented on the population growth of two different species for two different cases to validate the analytic results.
The parasitic nematode Anguillicola crassus was recently introduced into populations of the European eel, Anguilla anguilla. We investigated, under experimental conditions, the regulation of A. crassus infrapopulations. We tested the effects of (1) the resource-limited habitat of the parasite and (2) the coexistence of several developmental stages in its niche (the swim-bladder) on the composition of the infrapopulations. The results revealed that the respective effects of these factors differed substantially during the course of the infection. Third-stage larvae (L3s) establishment would not be constrained by the size of the swim-bladder. Their moult to fourth-stage larvae (L4s) would be accelerated as the number of L3s increased. The moulting time of L4s to adults would be reduced by males and would be constrained by the size of the swim-bladder. However, the moult of L4s to adults and their further development would be synchronized with those of the opposite sex. At the time of mating, the number of males and the body weight of adults would depend on the size of the swim-bladder. Soon after the laying of eggs, the developmental constraint on the late L3s would decrease. When adults die, constraints would cease and late larval stages would moult to become adults.
Recommend this
Email your librarian or administrator to recommend adding this to your organisation's collection.