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Sequential hermaphroditism

Sequential hermaphroditism is a reproductive strategy observed in various species of animals and plants, in which an individual changes sex during its lifetime, functioning as one sex at a time and producing either male or female gametes sequentially rather than simultaneously.^[1] This form of sexual plasticity allows organisms to optimize reproductive success by adapting to environmental, social, or physiological conditions that favor one sex over the other at different life stages.^[2] It is distinct from simultaneous hermaphroditism, where both sexes are functional concurrently, and from gonochorism, where individuals remain a single sex throughout life.^[3] The two primary types of sequential hermaphroditism are protandry, in which individuals mature first as males and later transition to females, and protogyny, where the sequence is reversed, starting as females and becoming males.^[2] Protandry is particularly common in crustaceans such as shrimp species like Pandalus platyceros, as well as in certain fishes like anemonefishes (Amphiprion spp.), including the clownfish, where the largest individual in a social group becomes the breeding female.^[1]^[4] Protogyny predominates in many teleost fishes, such as wrasses (Labridae) including the bluehead wrasse (Thalassoma bifasciatum) and seabreams (Sparidae), where females change to males upon reaching a larger size or assuming dominance in a group.^[2]^[3] Bidirectional sequential hermaphroditism, allowing sex changes in either direction, occurs less frequently but is documented in gobies like Trimma okinawae and certain coral gobies (Gobiodon and Paragobiodon spp.).^[2] Evolutionarily, sequential hermaphroditism is thought to arise from gonochorism and provides adaptive advantages in habitats with limited mate availability or high competition, such as coral reefs or patchy environments, by maximizing lifetime reproductive output.^[3] The size-advantage hypothesis posits that this strategy is beneficial when reproductive success increases with body size for one sex but decreases for the other, prompting a sex change at an optimal threshold to exploit these differences.^[1] However, phylogenetic analyses indicate that sequential hermaphroditism is relatively unstable, often reverting to gonochorism due to associated physiological costs, with no direct evolutionary transitions observed between protandry and protogyny in groups like seabreams.^[3] In teleost fishes, which exhibit the highest prevalence (across approximately 41 families), sex change is triggered by social cues like the removal of a dominant individual or environmental factors, involving hormonal shifts (e.g., estrogen and testosterone regulation) and changes in gene expression, such as downregulation of cyp19a1a (aromatase).^[5]^[2]^[6] Epigenetic modifications, including DNA methylation, further facilitate these transitions, enabling rapid gonadal reorganization without altering the underlying genome.^[2]

Overview

Definition

Sequential hermaphroditism is a reproductive strategy in which an individual changes from one functional sex to the other at some point during its lifetime, with the transition typically being irreversible. This phenomenon allows organisms to optimize reproductive success by sequentially functioning as male and then female, or vice versa, depending on environmental or physiological cues. The two primary forms are protandry, where individuals mature first as males before transitioning to females, and protogyny, where the sequence is reversed, beginning as females and later becoming males.^[7] In contrast to sequential hermaphroditism, simultaneous hermaphroditism involves individuals possessing both male and female reproductive organs that are functional concurrently, enabling self-fertilization or cross-fertilization within the same breeding period.^[8] Gonochorism, the most common sexual system in animals, features distinct male and female individuals that maintain a single sex throughout their lives, with no capacity for sex change.^[9] Sequential hermaphroditism occurs across diverse taxa, including many species of fish, mollusks such as snails, certain plants, and other invertebrates.^[10] This strategy has evolved independently multiple times, highlighting its adaptive value in various ecological contexts.^[11]

Types

Sequential hermaphroditism is primarily categorized into two forms based on the sequence of sex change: protandry and protogyny.^[1]^[12] In protandry, individuals mature first as males and subsequently transition to females later in life.^[1]^[3] This form is often associated with growth-related triggers, where smaller or younger individuals function as males, and the switch to female occurs as body size or age increases, enhancing reproductive success since female fecundity typically rises with size.^[13]^[12] Protandry predominates in certain invertebrates, such as crustaceans (e.g., over 59 species of caridean shrimps), and is also observed in some plants through dichogamy, where male floral organs mature before female ones to promote outcrossing; it is noted as the most common form in many fruit crops.^[1]^[14] Protogyny, conversely, involves initial maturation as females followed by a change to males.^[1]^[3] This type is prevalent in species with male-biased operational sex ratios, such as those with harem-based mating systems where larger males gain advantages in mate access.^[3]^[12] Protogyny is far more common than protandry among vertebrates, particularly in teleost fishes, where it accounts for approximately 80% of sequential hermaphrodites (244 out of 305 species documented).^[12]^[15] In plants, protogyny occurs as a form of dichogamy and is frequent in wind-, bee-, and fly-pollinated species.^[16]^[14] Variations within sequential hermaphroditism include serial changes, which involve a single unidirectional switch (the standard for both protandry and protogyny), and rare bidirectional forms allowing multiple reversals between sexes.^[12]^[15] Bidirectional sex change is uncommon, documented in only about 16-22 fish species, often initiated as protogyny and triggered by social factors like population density.^[12]^[15] Sex change triggers can be environmental, such as social cues or resource availability, or genetically predetermined, with the former more typical in socially structured species.^[12]^[3] Overall, protogyny exhibits greater evolutionary stability than protandry across taxa, particularly in fishes, while protandry is more labile and reverts more readily to gonochorism.^[15]

In Animals

Protandry

Protandry refers to a form of sequential hermaphroditism in which individuals initially develop and function as males before undergoing a transition to the female sex later in life. In animals, this pattern is frequently size- or age-dependent, with juveniles or smaller individuals maturing first as males to capitalize on early reproductive opportunities, followed by a switch to the female phase as body size increases, thereby enhancing overall fecundity since female reproductive success often scales positively with size in many species.^[17]^[13] For instance, in teleost fishes, the male phase typically occurs at smaller sizes, allowing for rapid initial reproduction, while the subsequent female phase supports higher egg output in larger adults.^[18] The physiological triggers for protandric sex change in animals commonly involve hormonal shifts that suppress male function and promote ovarian development. In fish such as the black porgy (Acanthopagrus schlegelii), this includes a decline in androgen levels, particularly 11-ketotestosterone, coupled with rising estradiol concentrations, which activate gonadal aromatase and initiate ovarian differentiation around age two.^[19]^[20] Similar mechanisms operate in mollusks, where decreasing testosterone-like androgens and increasing estrogens facilitate the transition, as observed in slipper snails (Crepidula spp.), enabling stacked individuals to shift sexes based on social position and resource access.^[21] These endocrine changes are often environmentally cued, such as by social cues or nutritional status, ensuring timely reversal.^[22] Adaptively, protandry confers advantages in species where small males can secure fertilizations through mechanisms like sperm competition or random mating, without requiring large body size for mate access, while the later female phase maximizes egg production in larger individuals. This is particularly beneficial in low-density or monogamous systems, where early male reproduction boosts lifetime fitness by avoiding the costs of delayed maturity, and the size-fecundity relationship favors females at maturity.^[13]^[23] In contexts with intense sperm competition, such as broadcast-spawning groups, small males invest heavily in gamete output to compete numerically, transitioning to females once size advantages shift reproductive value toward oogenesis.^[24] Protandry predominates among certain animal taxa, including many crustaceans like caridean shrimps (Lysmata spp.), where it is the most common sequential strategy, some teleost fishes across six families, and polychaete worms, in which it represents the prevalent form of sequential hermaphroditism among marine invertebrates.^[1]^[25] This distribution underscores its evolutionary success in environments where initial male allocation optimizes early mating success before reallocating resources to high-yield female reproduction.^[17]

Protogyny

Protogyny is a form of sequential hermaphroditism in which individuals develop as females first and later transition to males, a pattern commonly observed in various animal species, particularly teleost fishes. This sex change typically occurs in species where early reproduction is female-biased due to higher initial fecundity in smaller sizes, but shifts to male function as body size increases, enhancing advantages in territory defense and mate attraction. In such systems, larger males often monopolize access to multiple females, making protogyny adaptive when male reproductive success rises with size more steeply than female success.^[13]^[3] The triggers for protogynous sex change are predominantly social, often initiated by the removal or absence of a dominant male in the group, which releases inhibition on subordinate females and prompts the largest among them to undergo reorganization. In teleost fishes, this leads to rapid gonadal transformation, where ovaries regress and testicular tissue develops, sometimes completing functional sex reversal within days to weeks through proliferation of spermatogonia and restructuring of the gonad. Visual and behavioral cues, such as the presence of a group of females without a terminal-phase male, play key roles in initiating this process, as demonstrated in experimental setups with wrasses where sex change rates increase significantly in isolation from males.^[26]^[27] Protogyny plays a crucial role in social and mating dynamics, especially in species forming harems or territorial groups on coral reefs, where the largest individuals transition to males to control breeding opportunities and defend resources. This strategy is prevalent in over 75% of sequentially hermaphroditic fish species, encompassing 244 out of 305 documented cases, and is favored in stable, polygynous mating systems where male size confers dominance. By aligning sex with optimal size for each role, protogyny maximizes lifetime reproductive output in environments where social hierarchies dictate access to mates.^[12]^[13]

Examples

The clownfish (Amphiprion ocellaris), a protandrous species, lives in social groups within sea anemones where the largest individual is female, the second largest is breeding male, and smaller juveniles are non-breeding males; upon the female's death, the male transitions to female, and the largest juvenile becomes male.^[4] In the slipper snail (Crepidula fornicata), protandry occurs in stacked colonies where top individuals are male, releasing sperm to fertilize eggs of lower females; as the stack grows or position changes, males shift to female function, laying eggs in protective capsules.^[21] The bluehead wrasse (Thalassoma bifasciatum), a protogynous reef fish, starts as female; the largest female changes to male after the dominant male's removal, adopting aggressive territorial behavior and developing bright coloration to attract females in harem systems.^[3] These cases highlight how sequential hermaphroditism adapts to social structures in marine environments, enhancing reproductive success through flexible sex roles.^[13]

Evolutionary Causes

Sequential hermaphroditism evolves primarily through the size-advantage model, which posits that sex change is adaptive when reproductive success increases more rapidly with body size for one sex than the other, allowing individuals to optimize lifetime reproductive output by switching sexes at an intermediate size. In protogynous species, such as many reef fishes, female fecundity often scales with body volume (proportional to size cubed), while male reproductive success may depend more on linear dimensions like gonopodium length or territory size, making larger individuals more competitive as males and favoring female-to-male transitions.^[28] Conversely, in protandrous species like certain shrimp, male success may peak early due to mate availability, with females benefiting more from larger size for egg production.^[29] The mathematical foundation of this model, developed by Charnov, determines the optimal timing of sex change by maximizing lifetime fitness, approximated as L(x) = m(x) + f(x), where x is body size or age at change, m(x) is cumulative male reproductive success before the switch, and f(x) is female success afterward; the optimum occurs where the marginal fitness gains balance, specifically when \frac{f'(x)}{f(x)} = \frac{m'(x)}{m(x)}, ensuring no further gain from delaying or hastening the transition. This framework predicts that sequential hermaphroditism outperforms simultaneous hermaphroditism or gonochorism when fitness gain curves for the sexes diverge with size, as verified in phylogenetic analyses of labrid fishes where stronger male size advantages correlate with protogynous evolution.^[30] In small or isolated populations, sequential hermaphroditism may also evolve to mitigate inbreeding by enabling individuals to function first as one sex (often dispersing or competing broadly) and later as the other, reducing the risk of mating with close relatives in structured habitats like coral reefs or anemone groups.^[31] For instance, in anemonefishes, the dominant individual changes sex upon the death of the opposite-sex mate, maintaining outbreeding in confined family units.^[31] Additional selective pressures include local mate competition (LMC), where high relatedness among offspring in patchy environments favors female-biased initial sex ratios, which sequential hermaphroditism achieves dynamically through delayed sex change, outperforming fixed gonochorism in adjusting to varying group sizes.^[32] Sex ratio dynamics further promote its evolution, as skewed ratios from initial sex dominance self-correct via changes, stabilizing population fitness under fluctuating conditions like density dependence.^[7] Recent genomic studies from the 2020s reveal evolutionary convergence of sequential hermaphroditism across disparate fish lineages, with independent origins in over 30 teleost families linked to shared regulatory genes like dmrt1 and cyp19a1, underscoring the model's robustness in diverse ecological contexts despite repeated transitions from gonochorism.^[33]

Physiological Mechanisms

In animals, sequential hermaphroditism involves complex physiological processes triggered by social, environmental, or age-related cues, leading to gonadal reorganization through hormonal, genetic, and epigenetic pathways. In teleost fishes, the dominant form, sex change is often socially mediated; for protogyny, removal of a dominant male reduces inhibitory signals, prompting elevated androgen levels like 11-ketotestosterone to promote testicular development while suppressing estrogen via downregulation of cytochrome P450 aromatase (cyp19a1a), which converts androgens to estrogens.^[5] In protandry, such as in anemonefishes, rising estradiol and decreased androgens facilitate ovarian differentiation.^[34] Genes like dmrt1 (drives male fate) and amh (anti-Müllerian hormone, inhibits female development) are upregulated during transitions to maleness, while foxl2 and cyp19a1a support femaleness; these form antagonistic networks responsive to endocrine shifts.^[35] Epigenetic modifications, including DNA methylation of promoter regions (e.g., hypermethylation silencing cyp19a1a in protogyny), enable rapid, reversible changes without genomic alterations, as shown in wrasses where methylation patterns correlate with gonadal stages.^[2] In invertebrates like crustaceans and mollusks, similar hormonal axes operate; in protandrous shrimp (Lysmata spp.), serotonin and vertebrate-like steroids trigger female phase, while nutritional status influences timing via vitellogenesis. Environmental factors, such as temperature or photoperiod, modulate these via the brain-pituitary-gonad axis, ensuring alignment with optimal reproductive conditions. Recent studies (as of 2023) highlight conserved pathways across taxa, with transcriptomic shifts in steroidogenesis genes during transitions.^[36]

Genetic Consequences

Sequential hermaphroditism in animals often involves a polygenic genetic basis, where multiple loci contribute to sex determination, frequently integrated with environmental sex determination (ESD) mechanisms rather than relying on strict sex chromosomes. This polygenic architecture allows for flexible responses to environmental cues that trigger sex change, as seen in many teleost fishes. For instance, the dmrt1 gene serves as a key regulator of male gonadal function and testis differentiation across various vertebrate species, including those capable of sequential sex reversal.^[37]^[38]^[39] Inheritance patterns in sequential hermaphrodites can lead to biased offspring sex ratios influenced by the parental reproductive phase, potentially altering transmission dynamics of sex-related alleles. In protogynous species, for example, initial female phases may result in female-biased progeny production, skewing population sex ratios toward the first sex and reducing effective population size compared to gonochoristic counterparts. This bias arises because individuals often reproduce primarily as one sex before changing, affecting the relative contributions of male and female gametes to the next generation.^[7]^[40] At the population level, sequential hermaphroditism can mitigate genetic load by enabling flexible sex allocation, which enhances mating opportunities and reduces inbreeding depression in variable environments. By allowing individuals to function as both sexes over their lifetime, it promotes broader gene flow and dilutes the accumulation of deleterious alleles. However, maladaptive sex changes—triggered by unsuitable environmental conditions—may exacerbate inbreeding risks through persistent sex ratio imbalances, limiting genetic diversity in small or fragmented populations.^[41]^[7] Population genetic modeling of sequential hermaphroditism reveals deviations from Hardy-Weinberg equilibrium due to non-random mating patterns linked to phased reproduction, where individuals mate predominantly as one sex at a time. These deviations stem from violations of equilibrium assumptions, such as altered allele frequencies from sex-specific selection pressures. Simulations of polygenic sex determination systems demonstrate that such dynamics can sustain stable polymorphisms in sex allocation loci, allowing populations to adapt to fluctuating selective regimes without fixation of a single sex-determining mechanism.^[42]^[43] Recent genomic sequencing efforts in 2024 have uncovered conserved genetic pathways underlying sequential hermaphroditism across phyla, including core networks involving dmrt1, sox9, and amh genes that orchestrate gonadal differentiation. These findings, derived from transcriptomic meta-analyses and comparative genomics, highlight a hierarchical structure in sex determination with conserved hubs amid species-specific variability, updating prior views that emphasized rigid genetic determinism in favor of a more plastic, evolvable framework.^[44]^[45]

In Plants

Dichogamy

Dichogamy in plants is defined as the temporal separation of male and female reproductive functions, specifically the sequential presentation of pollen release from stamens and stigma receptivity in pistils, which primarily functions to prevent self-pollination and promote outcrossing in hermaphroditic flowers.^[46] This mechanism addresses potential interference between pollen export and receipt within the same flower or plant, enhancing both male and female reproductive success by reducing geitonogamy and autogamy.^[46] As the plant analog to sequential hermaphroditism, dichogamy operates at the floral or inflorescence level rather than involving a wholesale sex reversal in the organism, distinguishing it from the gonad-level transitions typical in certain animal species. The two primary types of dichogamy are protandry, in which stamens mature and pollen is dispersed before the stigmas become receptive, and protogyny, in which stigmas are receptive prior to pollen release.^[46] These types can manifest intrafleurally, within a single flower through changes in anther dehiscence and stigma maturity, or interfleurally, across multiple flowers on the same plant via phased blooming sequences.^[46] Protandry tends to predominate in biotically pollinated species, while protogyny is more frequent in wind-pollinated ones, reflecting adaptations to specific pollination vectors and environmental conditions.^[46] Dichogamy is a widespread adaptation in angiosperms, occurring in many hermaphroditic species as a core strategy for avoiding self-fertilization. This prevalence underscores its evolutionary significance in maintaining genetic diversity, particularly in outcrossing populations where selfing would otherwise compromise fitness.

Examples

In the genus Arisaema, commonly known as jack-in-the-pulpit, plants exhibit size-dependent sequential hermaphroditism where smaller individuals typically produce male inflorescences, while larger plants produce female or monoecious ones, allowing for protandrous transitions that optimize reproductive success based on resource availability.^[47] This pattern is influenced by nutrient levels, with stressed or young plants favoring male function to conserve energy for growth before shifting to costlier female reproduction in subsequent seasons.^[48] The striped maple (Acer pensylvanicum) demonstrates protandry through temporal separation in flowering, where male-phase flowers mature early to facilitate pollen dispersal, followed by female-phase flowers on the same individuals, promoting outcrossing in forest understories.^[49] This sequential expression within inflorescences enhances genetic diversity in populations where synchronous hermaphroditism could lead to self-pollination.^[50] Certain Opuntia cacti species, such as Opuntia robusta, exhibit mixed sexual systems with hermaphroditic and unisexual individuals coexisting, providing reproductive flexibility in arid environments.^[51] In papaya (Carica papaya), size-dependent sex transitions occur, particularly from male to hermaphroditic forms as plants grow larger and accumulate resources, though primarily genetically controlled; environmental stresses like drought can trigger reversals, altering the trioecious system (males, females, hermaphrodites).^[52] These shifts are documented in cultivation, where nutrient-rich conditions promote hermaphroditic fruit production over male sterility.^[53] Such examples illustrate how sequential hermaphroditism in plants promotes outcrossing and adaptability in variable environments, with timing of sex expression potentially disrupted by climate change through altered resource cues and phenological mismatches.^[54]

Evolutionary Aspects

Sequential hermaphroditism in plants, manifested as dichogamy, likely evolved from cosexual ancestors as a mechanism to promote outcrossing by temporally separating male and female reproductive functions, thereby reducing the risk of self-pollination.^[16]^[55] This adaptation is particularly evident in the correlation between dichogamy and self-incompatibility systems, where phylogenetic analyses indicate that dichogamy facilitates genetic diversity by minimizing inbreeding depression.^[56] In basal angiosperms, protogyny—where female function precedes male—is considered the ancestral form of dichogamy, occurring widely in primitive lineages to enhance cross-pollination efficiency.^[57] Recent genomic studies, such as the 2024 Amborella genome analysis, provide insights into the origins of sex determination in basal angiosperms, highlighting the evolutionary pathways from hermaphroditism to more specialized systems including sequential strategies.^[58] The primary evolutionary advantages of dichogamy include the reduction of geitonogamy, or self-pollen transfer within the same plant, which conserves resources and boosts pollen export to outcross partners.^[55] By prioritizing male function in protandrous species or female in protogynous ones, dichogamy minimizes sexual interference, leading to higher male fitness through improved siring success and overall reproductive assurance in pollinator-limited environments.^[55] In mixed-mating systems, such as those in the genus Collinsia, the presence of dichogamy strongly correlates with higher outcrossing rates, while its loss defines selfing syndromes that favor autonomous self-fertilization.^[59] Genetic models suggest that dichogamy arose through mutations altering the timing of floral organ maturation, building on foundational frameworks like the ABC model of flower development, which governs organ identity and could extend to phase separations via regulatory changes in MADS-box genes.^[60] These modifications lead to dichogamous polymorphisms that balance male and female functions, often in conjunction with self-incompatibility loci.^[56] Recent phylogenetic studies, incorporating phylogenomic data, reveal multiple independent evolutions of dichogamy across angiosperm clades, with distinct patterns in monocots (favoring protogyny) versus eudicots (showing more transitions to protandry), challenging earlier views of a uniform evolutionary trajectory.^[56] This polyphyletic origin underscores dichogamy's adaptive flexibility in response to diverse pollination ecologies.^[56]

Physiological Mechanisms

In plants exhibiting sequential hermaphroditism, such as size-dependent sex change in species like Arisaema triphyllum, hormonal signaling plays a central role in regulating the timing and expression of male and female reproductive structures during floral development. Auxins and gibberellins are key hormones that influence the maturation sequence of stamens and pistils, with auxins often promoting feminization by enhancing carpel development and gibberellins favoring masculinization through stamen elongation and pollen production. For instance, in monoecious analogs like Cucumis sativus, exogenous auxin application induces female flower formation, while gibberellins suppress it, suggesting similar mechanisms underlie the temporal shifts in hermaphroditic flowers where stamen maturation precedes or follows pistil development in protandrous or protogynous patterns.^[61]^[62] Ethylene further modulates these processes by promoting the female phase in certain species, delaying male function through inhibition of stamen growth and enhancement of pistil sensitivity to pollinators. In Cucumis melo, ethylene biosynthesis mutants exhibit delayed female organ maturation, confirming its role in synchronizing sex expression with environmental cues during inflorescence development. These hormonal interactions often occur via crosstalk, where auxin transport influences ethylene signaling to fine-tune the sequential activation of reproductive organs, ensuring outcrossing advantages in resource-variable conditions.^[61]^[63] Environmental factors, particularly nutrient availability, exert proximate control over sex allocation in sequential hermaphrodites by modulating plant size and resource status, which in turn trigger hormonal shifts. In protogynous species like Arisaema, low nutrient levels limit growth, favoring initial male function in smaller plants to conserve energy for pollen production, while nutrient-rich conditions enable larger sizes that support costly female reproduction through enhanced gibberellin and auxin activity. Stress from nutrient limitation or habitat disturbance, such as post-fire recovery, delays male maturation and promotes protogynous transitions, as observed in A. triphyllum populations where soil fertility correlates with higher female ratios.^[64]^[47] At the genetic level, MADS-box transcription factors orchestrate the developmental timing of sequential organ maturity by regulating floral identity genes in a phase-specific manner. Genes such as APETALA1 (AP1) integrate hormonal signals to control the transition from vegetative to reproductive phases, ensuring stamens mature before or after pistils in dichogamous flowers; in Arabidopsis thaliana mutants, altered AP1 expression disrupts this sequence, leading to synchronous organ development. These factors form complexes that respond to auxin and gibberellin gradients, directing differential gene expression for male or female dominance during inflorescence growth.^[65]^[66] Experimental evidence from hormone mutants in model plants like Arabidopsis confirms the causality of these mechanisms in sequential sex expression. Gibberellin-deficient ga1 mutants show delayed stamen maturation and enhanced pistil development, mimicking protogyny, while ethylene-insensitive mutants (etr1) exhibit premature male function, underscoring the interplay in timing reproductive phases. Similar studies in Cucumis hormone mutants validate that disrupting auxin-ethylene balance alters the duration of female phases, providing insights into dichogamous control applicable to wild sequential hermaphrodites.^[61]^[62]

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The hypothesis predicts that reproductive success will increase less with body size for males than for females, eventually promoting sex change in males.Missing: seminal paper
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Ecological and evolutionary consequences of alternative sex ...
Aug 22, 2017 · In protandrous species, populations are composed of many small males and fewer large, highly fecund females. The reproductive mode is often ...
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A COMPARATIVE ANALYSIS OF SEX CHANGE IN LABRIDAE ...
Aug 3, 2010 · The evolution of sequential hermaphroditism in Labridae is significantly correlated with the strength of the male size advantage. We compare a ...
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Evolutionary Perspectives on Hermaphroditism in Fishes
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Information constraints and the precision of adaptation: Sex ratio ...
One of the best-supported areas in the field of sex allocation is Hamilton's theory of local mate competition, which predicts female-biased offspring sex ratios ...Missing: hermaphroditism dynamics
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Switches, stability and reversals in the evolutionary history of sexual ...
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Hormonal interactions and gene regulation can link monoecy and ...
Jun 1, 2013 · Numerous hormones affect floral development including auxin, gibberellin, jasmonates, brassinosteroids, ethylene, and cytokinin. (See Table ...
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The Diversity and Dynamics of Sex Determination in Dioecious Plants
Jan 15, 2021 · ... ethylene appears to be the major player (Boualem et al., 2015). In dioecious species, hormones appear to influence sexual differentiation as ...
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Determinants of gender in Jack-in-the-pulpit: the influence of plant ...
Jack-in-the-pulpit, Arisaema triphyllum, is a perennial forest herb with the ability to change sex. At two sites in upstate New York, plant sex was correla.
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MADS-box genes are involved in floral development and evolution
MADS-box genes encode transcription factors in all eukaryotic organisms thus far studied. Plant MADS-box proteins contain a DNA-binding (M), an intervening ...
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Genome-wide analysis of MADS-box families and their expressions ...
MADS-box genes play crucial roles in plant vegetative and reproductive growth, better development of inflorescences, flower, and fruit.
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Insight into Nephrotoxicity and Processing Mechanism of Arisaema ...
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Polygenic sex determination in vertebrates – is there any such thing?
The initiating signal for SD (genetic, GSD, or environmental, ESD) activates a downstream regulatory network that governs male or female gonad development.
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Decoding Dmrt1: insights into vertebrate sex determination and ...
The Dmrt gene family is characterized by a conserved DM domain, and is crucial to sex determination and sexual differentiation. Dmrt1 is pivotal in testis ...
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Genetic architecture of sex determination in fish - Frontiers
Here, we review the available data on the genetic architecture of sex determination (SD) in fish and how sex ratio is controlled in aquaculture production. We ...
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Sex change and effective population size: implications for ... - Nature
Aug 10, 2016 · In sequentially hermaphroditic (sex-changing) fish, the sex ratio is typically skewed and biased towards the 'first' sex, while reproductive ...<|separator|>
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Sexual antagonism in sequential hermaphrodites - Journals
Nov 22, 2023 · ... sequential hermaphroditism, which has the additional complexities of age-structure. ... protandry (male first), to protogyny (female first) ...
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Polygenic sex determination in vertebrates – is there any such thing?
Polygenic sex determination (PSD) is when multiple genes at different loci determine sex, but documented cases are rare and often transient.
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Polygenic sex determination produces modular sex polymorphism in ...
Apr 5, 2022 · Species with polygenic sex determination (PSD) have multiple interacting sex determination alleles segregating within a single species, allowing ...
[56]
Extraordinary variability in gene activation and repression programs ...
Jan 22, 2024 · We propose viewing vertebrate gonadal sex differentiation as a hierarchical network, with conserved hub genes such as sox9 and amh alongside ...
[57]
Meta‐analysis of gonadal transcriptome provides novel insights into ...
Sep 29, 2024 · Sequential hermaphroditism, a phenomenon in which individuals undergo sex change during their lifetime, has been extensively recognized in ...
[58]
The avoidance of interference between the presentation of pollen ...
Dichogamy is the separation of the presentation of pollen and stigmas in time within a plant. It is a common but neglected feature of outcrossing angiosperms.Missing: prevalence percentage
[59]
Sexual interference of the floral kind | Heredity - Nature
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Do dichogamy and herkogamy reduce sexual interference in a self ...
Oct 13, 2010 · Our results suggest that dichogamy is mostly driven by the advantage to male fitness and herkogamy is chiefly determined by female fitness.Missing: gain | Show results with:gain
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Correlated Evolution of Dichogamy and Self‐Incompatibility
Aug 7, 2025 · Here we reexamined the association between dichogamy and SI in a phylogenetic framework and tested the hypothesis that dichogamy evolved to ...
[62]
Floral ecology of Oreocharis acaulis (Gesneriaceae): An exceptional ...
Phylogenetically, protogyny is apparently the ancestral condition in angiosperms, because almost all basal angiosperms are protogynous (Endress, 2010, ...
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Dichogamy correlates with outcrossing rate and defines the selfing ...
Oct 6, 2011 · Loss of dichogamy defines Collinsia's selfing syndrome. Floral size, longevity and herkogamy also differ significantly between these groups.
[64]
[PDF] An Overview of Dichogamy in Angiosperms - CABI Digital Library
Dichogamy is the maturation of sex organs at different times, with proterandry (male first) and proterogyny (female first) being main types.