The offspring are haploids and they're sterile.
"The Lani People" by J. F. Bone
Each of these divides again by mitosis (the chromosomes splitting lengthwise), the half or haploid number remaining.
"Taboo and Genetics" by Melvin Moses Knight, Iva Lowther Peters, and Phyllis Mary Blanchard
The egg nucleus, now known as the female pronucleus, and each body contain the reduced or haploid number of chromosomes.
"Being Well-Born" by Michael F. Guyer
***
Each genome has a unique signature of network links between its complementary parental haploid genomes.
A Developmental Network Theory of Gynandromorphs, Sexual Dimorphism and Species Formation
All the genomes are identical except for their distinct inter-haploid network linkages.
A Developmental Network Theory of Gynandromorphs, Sexual Dimorphism and Species Formation
The model by Kirpatrick [145] is a haploid sexual model, i.e. each individual has one set of chromosomes.
Biological Evolution and Statistical Physics
This haploid model was chosen for its analytical tractability, although it is not very realistic.
Biological Evolution and Statistical Physics
The recombination event is initiated by a double strand break in the mating locus by the HO endonulease in haploid yeasts.
Epigenetic Chromatin Silencing: Bistability and Front Propagation
Consider a population of N haploid individuals (players).
Evolutionary game dynamics in phenotype space
M¨ohle, M. (2001) Forward and backward diffusion approximations for haploid exchangeable population models.
Coalescent approximation for structured populations in a stationary random environment
The haploid selection is based on a ﬁtness function on the space of types and the mutation is type-dependent.
Duality for spatially interacting Fleming-Viot processes with mutation and selection
This paper is an extension of previous work on the sub ject, which considered the case of haploid genomes.
Semiconservative quasispecies equations for polysomic genomes: The general case
Interestingly, with an appropriate classiﬁcation of population fractions, we obtain a system of equations that is formally identical to the haploid case.
Semiconservative quasispecies equations for polysomic genomes: The general case
As with the work for haploid genomes, we consider both random and immortal DNA strand chromosome segregation mechanisms.
Semiconservative quasispecies equations for polysomic genomes: The general case
However, in contrast to the haploid case, we have found that an analytical solution for the mean ﬁtness is considerably more diﬃcult to obtain for the polyploid case.
Semiconservative quasispecies equations for polysomic genomes: The general case
Howa rate characterized by a genome-dependent ﬁrst-order ever, the work on polysomic genomes only considered growth rate constant κ ˆσ . haploid genomes.
Semiconservative quasispecies equations for polysomic genomes: The general case
It is interesting to note that even when we do not assume that the genomes are necessarily haploid, it still follows that it is possible to derive an ordered strand-pair formulation of the dynamics that is identical to the haploid case .
Semiconservative quasispecies equations for polysomic genomes: The general case
At this point, the random and immortal strand segregation equations for arbitrary genomes become formally identical to the equations for haploid genomes.
Semiconservative quasispecies equations for polysomic genomes: The general case
***