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1 ype may be sufficient to trigger reversal to hermaphroditism.
2 idisation and transitions between dioecy and hermaphroditism.
3 hy gld-1 is repeatedly recruited to regulate hermaphroditism.
4 hypotheses about the genetic architecture of hermaphroditism.
5 r results for the maintenance of dioecy over hermaphroditism.
6 nate evolution of behavioral dimorphism with hermaphroditism.
7 omosome in gonadal tissue has been linked to hermaphroditism.
8 lization during the evolution of dioecy from hermaphroditism.
9 xual reproduction, particularly simultaneous hermaphroditism.
10 mental sex determination, haplodiploidy, and hermaphroditism.
11 own in flowering plants, yielding functional hermaphroditism.
12 , its symbiosis with anemones and sequential hermaphroditism.
13  have a breeding system intermediate between hermaphroditism and complete separation of the sexes (di
14             Atrazine (> or =0.1 ppb) induced hermaphroditism and demasculinized the larynges of expos
15 ion may be divided into two main categories: hermaphroditism and dioecy (Botany)/gonochorism (Zoology
16                          Transitions between hermaphroditism and dioecy increased, while transitions
17 edicted by models for the transition between hermaphroditism and dioecy.
18 s Mercurialis, transitions between combined (hermaphroditism) and separate sexes (dioecy or androdioe
19  recently evolved gonochorism from ancestral hermaphroditism), and roundworms (Nematoda) which have u
20 ty before gestational day 11, hydrocephalus, hermaphroditism, and cystic ovaries.
21 y to gonochorism, protogyny and simultaneous hermaphroditism are evolutionarily more stable than prot
22 itions between these two forms of sequential hermaphroditism are unlikely to happen.
23 n in the fog-2 locus, thereby reestablishing hermaphroditism as the primary means of reproduction for
24 dioecy from other states were higher than to hermaphroditism, but transitions away from dioecy increa
25  whereas dioecy might evolve from functional hermaphroditism by conferring upon individuals certain b
26 n males and females, while the facts of true hermaphroditism can be viewed as remnants of temperature
27  those most consistent with the simultaneous hermaphroditism can predominate only when a substantial
28  with theoretical expectations, simultaneous hermaphroditism does not evolve directly from gonochoris
29           Furthermore, the condition of true hermaphroditism does not fit into a simple genotype/phen
30 the latter and for transition from dioecy to hermaphroditism during domestication.
31 been shaped by natural selection, perhaps as hermaphroditism evolved.
32 have arisen during evolution of self-fertile hermaphroditism from an ancestral female/male species.
33  briggsae independently evolved self-fertile hermaphroditism from gonochoristic ancestors.
34                                  Compared to hermaphroditism, gynodioecy generally reduces effective
35 stic spatial simulations we demonstrate that hermaphroditism has an even greater advantage when local
36 s in the evolution of this animal group: (i) Hermaphroditism has evolved independently in C. elegans
37 r focusses on self-incompatible simultaneous hermaphroditism in animals.
38 l, in the repeated evolution of self-fertile hermaphroditism in Caenorhabditis nematodes.
39                       Thus, the evolution of hermaphroditism in Caenorhabditis probably required two
40  vinifera ssp. sylvestris (V. sylvestris) to hermaphroditism in cultivated Vitis vinifera ssp. sativa
41 recombination events led to the reversion to hermaphroditism in grapevine.
42 , it is not fully understood what determines hermaphroditism in the domesticated subspecies and male
43 , it is not fully understood what determines hermaphroditism in the domesticated subspecies and male
44 oincides with the occurrence of simultaneous hermaphroditism in the Euthyneura gastropods.
45 des further support for the observation that hermaphroditism is associated with sedentary species, su
46                        It proposes that such hermaphroditism is not stable in sufficiently heterogene
47 he evolution of separate sexes (dioecy) from hermaphroditism is one of the major evolutionary transit
48 ations, suggesting a possible reason for why hermaphroditism is rare among evolved animal species.
49                                              Hermaphroditism is rare and phylogenically in decline am
50 ring, but no hermaphrodites, suggesting that hermaphroditism is recessive to femaleness.
51                                     However, hermaphroditism is widespread across animals and may ent
52                                              Hermaphroditism leads to reduced sexual selection and ca
53    Overall, our results show that sequential hermaphroditism may affect Ne differently over varying t
54 le competition associated with the origin of hermaphroditism may have permitted the global spread of
55 ionary transitions from dioecy to functional hermaphroditism must overcome an inertia of sexual dimor
56 he transition to unisexual reproduction from hermaphroditism or monoecy (a form of functional hermaph
57 horism but can evolve slowly from sequential hermaphroditism, particularly protandry.
58  it descended from a male/female species, so hermaphroditism provides a model for the origin of novel
59 t) and protogynous (female-first) sequential hermaphroditism (sex change).
60 aphroditism or monoecy (a form of functional hermaphroditism); the times when they arose; and the ext
61 ruled out development by parthenogenesis and hermaphroditism, therefore implicating internal fertilis
62 an important but poorly understood path from hermaphroditism to dioecy, and provide an adaptive hypot
63 cific pathways can drive the transition from hermaphroditism to dioecy.
64 tosome pair in association with a shift from hermaphroditism to dioecy.
65  models for the evolutionary transition from hermaphroditism to monoecy, multiple sex determining gen
66        The many independent transitions from hermaphroditism to separate sexes (dioecy) in flowering
67  are consistent with convergent evolution of hermaphroditism, which is marked by considerable develop
68  the latter might constrain the evolution of hermaphroditism, while the non-duality of the embryologi
69  increases or decreases N(en) as compared to hermaphroditism with the same selfing rate of hermaphrod