Floral structure and development and systematic aspects of some 'lower' Asparagales

 Floral structure and development of representatives of Asteliaceae, Blandfordiaceae, Boryaceae, Doryanthaceae, and Hypoxidaceae, all members of the `lower' Asparagales, were studied comparatively. The results are discussed in the light of new molecular systematic studies, but also with regard to established morphological characters in related groups. Stamen shape varies considerably within and between taxa: the shape of anthers is from X-shaped, sagittate to non-sagittate, they are either latrorse or introrse, basifixed, centrifixed or dorsifixed. Gynoecia are syncarpous up to the stigmatic region in all taxa. Ovaries of Doryanthaceae and Hypoxidaceae are inferior, but they are superior in Asteliaceae, Blandfordiaceae and Boryaceae. All ovaries have at least a short synascidiate zone. With the exception of Astelia alpina (Asteliaceae), the ovaries are trilocular. Ovaries of Asteliaceae contain mucilage, which is secreted from trichomes on the funicle and on the placenta. Although flowers are polysymmetric at anthesis, they are monosymmetric in earliest stages with a developmental gradient from adaxial to abaxial. Perianth organs arise individually from either a concave (taxa with inferior ovary) or convex (taxa with superior ovary) apex. Hypoxidaceae have pollen flowers with free stamens. One species, Curculigo capitulata, has Solanum-type flowers with postgenitally united stamens. It is most probably pollinated by buzzing bees. All other taxa have nectariferous flowers with internal or external septal nectaries. Received February 5, 2001 Accepted June 20, 2001     

Floral morphology of Maloideae (Rosaceae) and its systematic relevance

Flowers of 169 species of Rosaceae subfamily Maloideae, which were chosen to represent the taxonomic and geographic diversity of the group, were studied to ascertain their morphological variation and its systematic relevance. We describe and illustrate variation in size, indumentum, color, and macroscopic structural features. Most maloid species have syncarpous flowers with two to five carpels in which the ovary is at least three-quarters inferior, whereas species of other Rosaceae subfamilies have apocarpous or unicarpellate flowers with superior ovaries. However, maloid flowers show significant variation in the degree of carpel connation and of ovary adnation to the hypanthium. Cotoneaster, Heteromeles, and Pyracantha are completely apocarpous, and Dichotomanthes is perigynous with a completely superior ovary. Thus, no one floral character is sufficient to separate the Maloideae from other subfamilies of Rosaceae. Differences among their flowers support our recognition of Malus, Pyrus, and Sorbus as separate genera. Further, we argue for removal of Docyniopsis and Eriolobus from Malus, division of Sorbus into several genera, and union of Aronia, Photinia, and Stranvaesia. No floral characters support the traditional dichotomy of the subfamily into tribes Crataegeae and Sorbeae.     

Floral development and morphology of Vochysiaceae. I. The structure of the gynoecium

Vochysiaceae are divided into two tribes on the basis of ovary structure (superior trilocular or inferior unilocular). The superior trilocular ovary has been considered basal in the family, and the term "pseudomonomerous" was used to indicate the presumed evolutionary derivation of the unilocular condition from the trilocular. However, recent evidence that Vochysiaceae are Myrtalean suggests that the superior ovary may be secondarily derived. In addition, published figures cast doubt on the interpretation of the putatively unilocular ovaries. To understand these features, floral ontogeny and anatomy were examined using scanning electron microscopy and serial sectioning. In all taxa examined, the ovary develops in an epigynous fashion, on a concave floral apex, supporting the hypothesis that the superior ovary is secondarily derived. Subsequent to initiation of the ovary, differential growth results in ovaries that are superior, inferior, or partly inferior in different genera. Sections of floral buds of the two unilocular genera, Erisma and Erismadelphus, show aborted locules in the latter but not in the former. The application of the term "pseudomonomerous" to both genera obscures this significant difference. The position of the placenta in the truly unilocular genus varies among species, suggesting a character transformation series from multilocular through intermediates to truly unilocular.     

Floral ontogeny of the Afro-Madagascan genus Mitrasacmopsis with comments on the development of superior ovaries in Rubiaceae

BACKGROUND AND AIMS: Members of Rubiaceae are generally characterized by an inferior ovary. However, Mitrasacmopsis is cited in the literature as having a semi-inferior to superior ovary. It has previously been hypothesized that the gynoecial development of Rubiaceae with semi-inferior to superior ovaries takes place in the same way as in Gaertnera, one of the most commonly cited rubiaceous genera with a superior ovary. To test this hypothesis, a floral ontogenetic study of Mitrasacmopsis was carried out with special attention paid to the gynoecial development. METHODS: Floral ontogeny and anatomy of Mitrasacmopsis were examined using scanning electron and light microscopy. KEY RESULTS: At an early developmental stage, a concavity becomes visible in the centre of the floral apex simultaneously with the perianth initiation. A ring primordium surrounding this concavity expands vertically forming the corolla tube (early sympetaly). Stamen primordia develop inside the corolla. From the bicarpellate gynoecium only two carpel tips are visible because the ovary is formed by a gynoecial hypanthium. In the basal part of each carpel, a placenta primordium is initiated. Two septa divide the ovary into two locules. In each locule, the placenta becomes mushroom shaped and distinctly stalked. Eventually, the inferior ovary of Mitrasacmopsis develops into a beaked capsule. Only very late in the fruiting stage, the continuously expanding ovary is raised above the insertion point of the persistent calyx, changing the ovary position of Mitrasacmopsis from basically inferior to secondarily semi-inferior. CONCLUSIONS: Mitrasacmopsis follows an epigynous pattern of floral development. However, the presence of a prominent beak in the fruiting stage gives the whole ovary a semi-inferior appearance. This kind of secondarily semi-inferior ovary is shown to be different from the secondarily superior ovary observed in Gaertnera.     

FLORAL MORPHOLOGY,ORGANOGENESIS AND INTERPRETATION OF THE INFERIOR OVARY IN DOWNINGIA BACIGALUPII

The inflorescence of Downingia bacigalupii (Campanulaceae; Lobelioideae) is an indeterminate spike. Axillary flowers have a long, linear, inferior ovary with parietal placentation, a pentamerous synsepalous calyx, zygomorphic sympetalous corolla, syngenesious stamens, and a bicarpellate, syncarpous gynoecium. On the basis of floral vascular anatomy the inferior ovary is interpreted as appendicular, representing adnation of outer floral whorls to the gynoecium. Floral ontogeny shows that sepals are initiated in an adaxial to abaxial sequence rather than the 2/5 phyllotaxis reported for other members of Lobelioideae. Growth of the common bases of sepal lobes forms a floral cup and initiation of the following floral whorls occurs along the inner margins of the cup. Continued basal growth of the cup-shaped bud results in the formation of the elongated inferior ovary. Earlier evidence for the interpretation of a cup-shaped receptacle during development of epigynous flowers is reexamined and it is concluded that the concave floral bud of D. bacigalupii can also be interpreted as common growth of connate floral whorls, supporting interpretations based on vascular anatomy. Comparison of floral development between Downingia bacigalupii and Pereskia aculeata (Cactaceae) reveals ontogenetic differences between flowers with appendicular and receptacular cups.     

The development of the superior ovary in Tetraplasandra (Araliaceae)

Tetraplasandra is a small Hawaiian genus of seven species with remarkable diversity in ovary position, ranging from inferior to completely superior. Tetraplasandra gymnocarpa is the only member of the Araliaceae with a fully superior ovary. A comparative study of floral anatomy and development in superior and inferior ovary species of Tetraplasandra revealed that the superior ovary in T. gymnocarpa is unusual in that it develops within an epigynous ground plan. During the course of development, the ovary changes from inferior to secondarily superior primarily by an upward expansion of the ovary from the insertion point of the perianth and androecium to the ovary apex. The superior ovary of T. gymnocarpa, evident in late ontogeny, is a modified inferior ovary; thus it is not structurally homologous to a truly superior ovary. The adaptive significance of the switch from inferior to superior ovary is reexamined. A recent phylogeny of Tetraplasandra and the biogeography of the extant species provide evidence that the change in ovary position may be associated with a shift in pollination strategy that may have occurred as recently as 2.6 million years ago.     

Ovary starch reserves and flower development in apricot (Prunus armeniaca)

In histerant species where flowering takes place prior to leaf emergence, a flower lifespan occurs in the absence of new photoassimilates and at the expense of pre-stored reserves either in the plant as a whole or in the flower itself. In the present study, the role that the photoassimilates stored in the flowers might play in flower development from anthesis to fertilization in Prunus armeniaca L. (apricot), a histerant species, was explored. Starch content in individual flowers was measured with the help of an image analysis system. Starch content decreased from its highest value at anthesis and disappeared from the ovary 9 days later. This decrease was inversely related to an increase in ovary size and in cell number in the pericarp, suggesting an intraflower, self-supported development. This process is conserved in both pollinated and nonpollinated flowers and therefore seems to be inherent to the flower at anthesis. The onset of fruiting is preceded by the establishment of large differences among ovaries; while some experience continuous growth, others stop growing and eventually drop. Interestingly, large differences in starch content are found among flowers at anthesis. These results are discussed in terms of the possible implications of pre-stored starch in the flower supporting initial flower development.     

Floral and inflorescence morphology and ontogeny in Beta vulgaris, with special emphasis on the ovary position

Background and Aims

In spite of recent phylogenetic analyses for the Chenopodiaceae–Amaranthaceae complex, some morphological characters are not unambiguously interpreted, which raises homology questions. Therefore, ontogenetic investigations, emphasizing on ‘bracteoles’ in Atripliceae and flowers in Chenopodioideae, were conducted. This first paper presents original ontogenetic observations in Beta vulgaris, which was chosen as a reference species for further comparative investigation because of its unclarified phylogenetic position and its flowers with a (semi-)inferior ovary, whereas all other Chenopodiaceae–Amaranthaceae have hypogynous flowers.

Methods

Inflorescences and flowers were examined using scanning electron microscopy and light microscopy.

Key Results

Floral development starts from an inflorescence unit primordium subtended by a lateral bract. This primordium develops into a determinate axis on which two opposite lateral flowers originate, each subtended by a bracteole. On a flower primordium, first five tepal primordia appear, followed by five opposite stamen primordia. Simultaneously, a convex floral apex appears, which differentiates into an annular ovary primordium with three stigma primordia, surrounding a central, single ovule. A floral tube, which raises the outer floral whorls, envelops the ovary, resulting in a semi-inferior ovary at mature stage. Similarly, a stamen tube is formed, raising the insertion points of the stamens, and forming a staminal ring, which does not contain stomata. During floral development, the calyces of the terminal flower and of one of the lateral flowers often fuse, forming a compound fruit structure.

Conclusions

In Beta vulgaris, the inflorescence is compound, consisting of an indeterminate main axis with many elementary dichasia as inflorescence units, of which the terminal flower and one lateral flower fuse at a later stage. Floral parts develop starting from the outer whorl towards the gynoecium. Because of the formation of an epigynous hypanthium, the ovary becomes semi-inferior in the course of floral development.Key words: Beta vulgaris, Chenopodiaceae, floral ontogeny, gynoecial development, epigynous hypanthium, semi-inferior ovary, inflorescence ontogeny, LM, SEM     

Floral structure and development in Nartheciaceae (Dioscoreales), with special reference to ovary position and septal nectaries

We present a comparative study of the floral structure and development of Nartheciaceae, a small dioscorealean family consisting of five genera (Aletris, Lophiola, Metanarthecium, Narthecium, and Nietneria). A noticeable diversity existed in nine floral characters. Analyses of their respective character states in the light of a phylogenetic context revealed that the flowers of Nartheciaceae, whose plesiomorphies occur in Aletris and Metanarthecium, have evolved toward in all or part of Lophiola, Narthecium, and Nietneria: (1) loss of a perianth tube; (2) stamen insertion at the perianth base; (3) congenital carpel fusion; (4) loss of the septal nectaries; (5) unilocular style; (6) unfused lateral carpellary margins in the style; (7) flower with the median outer tepal on the abaxial side; (8) flower with moniliform hairs; and (9) flower with weak monosymmetry. We further found that, as the flowers developed, the ovary shifted its position from inferior to superior. As a whole, their structure changes suggest that the Nartheciaceae flowers have evolved in close association with pollination and seed dispersal. By considering inferior ovaries and the presence of septal nectaries as plesiomorphies of Nartheciaceae, we discussed evolution of the ovary position and septal nectaries in all the monocots.     

Ontogenetic shift in buoyancy and habitat in the Antarctic toothfish, <Emphasis Type="Italic">Dissostichus mawsoni</Emphasis> (Perciformes: Nototheniidae)

Buoyancy measurements and depth of capture were taken on 70 individuals of Dissostichus mawsoni collected from the Southern Scotia Arc and McMurdo Sound, Antarctica, to examine the effect of age on buoyancy and habitat use. Standard lengths (SL) ranged from 10.4 to 138.0 cm. Juveniles were not buoyant (heavy in water), whereas adults were neutrally buoyant. The slope of the relationship between buoyancy and SL was significantly negative for juveniles (individuals less than 81 cm SL), but there was no significant relationship for adults (individuals greater than 81 cm SL). These results demonstrate an ontogenetic shift in buoyancy. For juveniles, depth of capture and SL had a significantly positive relationship. As individuals reach adulthood they achieve neutral buoyancy and appear to use deeper water habitats. This interpretation is supported by a significant positive correlation between buoyancy and depth of capture for juveniles. Changes in buoyancy with maturation of juveniles may also be associated with a shift in habitat use. Juveniles appear to exploit benthic habitats, whereas adults use the entire water column over deeper water. Given the differences in prey species available in these habitats and based on our results, we predict that diets of juveniles and adults should differ significantly. We also hypothesize that accumulation of lipid deposits from the diet during maturation of juveniles may account for the ontogenetic shift in buoyancy and allow neutral buoyancy to be achieved in adulthood.     

澜沧舞花姜繁殖生物学特性及其进化意义探讨

 舞花姜属（Globba）植物具有多样的繁殖策略。分布于西双版纳的澜沧舞花姜（Globba lancangensis）自然条件下既能结实,同时又能在花序下部产生珠芽。通过对澜沧舞花姜的花部性状、花粉活力、传粉昆虫的访花行为、结实状况、珠芽产量等多方面的观测,初步了解了澜沧舞花姜的繁殖生物学特性。结果表明,澜沧舞花姜具有雄花及两性花同株的性表达特征。雄花及两性花的花粉在中午12∶00以前活力很高,之后雄花的花粉活力急剧下降,而两性花的花粉到16∶00仍有萌发能力。澜沧舞花姜在花序上产生雄花及两性花,每个花序每天仅开少量的花,其中50%的时间仅开雄花或两性花,在整个种群中形成了一定程度的暂时性的雄花两性花异株现象,从而增加了异交的可能性。澜沧舞花姜雄花的存在为P/O低的两性花提供了花粉补贴,这使得它可以通过调节雄花与两性花比例来调节种群的P/O,从而保证一定的结实能力。人工自交与异交下结果率没有差异,但自交结实率显著低于异交结实率,表明澜沧舞花姜有明显的自交不亲和现象。排蜂（Megapis dorstata）和黄绿彩带蜂（Nomia strigata）是澜沧舞花姜的主要访花昆虫,其中排蜂是它的有效传粉昆虫。澜沧舞花姜可能通过雄花两性花同株与自交不亲和相结合来促进异交。     

Abscisic Acid Alters the Metabolism of Indole-3-Acetic Acid in Senescing Flowers of Cucumis melo L

Experiments were conducted to investigate indole-3-acetic acid (IAA) and abscisic acid (ABA) metabolism associated with postanthesis senescence of ovaries from nonpollinated muskmelon (Cucumis melo L.) flowers. Flowers attached to the vine were allowed to senesce for 4 days after anthesis or were harvested at full anthesis and aged for the same time interval with or without access to water. The IAA ester, amide-linked forms of IAA, free ABA, and ABA esters increased in senescent ovaries from flowers left attached to the vine. Detaching flowers from the vine resulted in an accumulation of free and amide-linked IAA in the senescing ovary but suppressed accumulation of ester IAA. Free ABA failed to increase in ovaries detached from the vine. Subjecting detached flowers to water stress had no effect on the endogenous level of free ABA but resulted in the accumulation of ABA ester and suppression of any increase in free IAA. However, detached flowers treated with 0.1 millimolar ABA accumulated 75% less free IAA and initiated the synthesis of ester IAA. Detached flowers treated with ABA also accumulated high levels of ester ABA. These results suggest that the metabolism of free IAA in muskmelon ovary tissue is regulated in situ and not the consequence of external synthesis and importation. ABA appears to be transported into the senescing ovary from an external source and alters the IAA metabolism in such a manner as to suppress the level of free IAA while stimulating accumulation of the ester IAA.     

Dynamic Changes of Endogenous Phytohormones During the Development of Embryos Derived from Wheat Crossed with Zea mays and Tripsacum dactyloides

The embryos derived from intergeneric crosses between Triticum aestivum L. (2n = 6x= 42) and Zea mays L. (2n= 20), Tripsacum dactyloides L. (2n= 4x= 72), as results of the elimination of paternal chromosome and having no endosperm as normal, are difficult to develop completely in vivo. Hormonal analyses in such intergeneric hybridized ovaries have been carried out including indole-3-acetic acid (IAA), zeatin (Z) and zeatin riboside (ZR), and abscisic acid (ABA) during different developmental stages of embryo. The results indicated that IAA level in hybridized ovaries was much lower than that in self-pollinated ovaries. Moreover, the active changes of Z+ZR and ABA contents were also different between the above two types of ovary. Nevertheless, the ratio changes of IAA/(Z+ZR) and IAA/ABA were similar between the two types of ovary, the same was true in the ratio changs of IAA, Z+ZR, and ABA to the sum of these three types of endogenous hormones. But the three types of ratios in hybridized ovaries were varied far more greater than those in self-pollinated ones. It suggested the importance to maintain dynamic equilibrium of multiple hormones and sequential regulation during the embryo development. That the distantly hybridized embryos failed to mature successfully was probably associated with a deviation from the normal changes of endogenous hormones levels and balance system of multiple hormones in addition to the lack of endosperm nourishment.     

南瓜两性花的形态与结构研究

对南瓜的两性花进行外部形态及结构的研究,结果表明：南瓜的两性花可有子房上位花、子房半下位花和子房下位花三种类型：花萼、花冠均为５,合瓣;雄蕊３,其中有两枚各由两个雄蕊合生而成,分离和部分联合,花药结构特殊,花粉发育正常;雌蕊具有单个或两个柱头及花柱。子房壁结构正常。上方的子房壁表皮发育完好,具气孔器。胚珠在外形上也发育正常。两性花与单性花同生长在一个植株上,可以连续多代稳定地遗传,萌生当代植株的种子来源于上一代雌花。这对探讨被子植物的系统进化关系有着重要的意义     

Diversity of floral visitors to sympatric Lithophragma species differing in floral morphology

Most coevolving relationships between pairs of species are embedded in a broader multispecific interaction network. The mutualistic interaction between Lithophragma parviflorum (Saxifragaceae) and its pollinating floral parasite Greya politella (Lepidoptera, Prodoxidae) occurs in some communities as a pairwise set apart from most other interactions in those communities. In other communities, however, this pair of species occurs with congeners and with other floral visitors to Lithophragma. We analyzed local and geographic differences in the network formed by interactions between Lithophragma plants and Greya moths in communities containing two Lithophragma species, two Greya species, and floral visitors other than Greya that visit Lithophragma flowers. Our goal was to evaluate if non-Greya visitors were common, if visitor assembly differs between Lithophragma species and populations and if these visitors act as effective pollinators. Sympatric populations of L. heterophyllum and L. parviflorum differ in floral traits that may affect assemblies of floral visitors. Visitation rates by non-Greya floral visitors were low, and the asymptotic number of visitor species was less than 20 species in all populations. Lithophragma species shared some of the visitors, with visitor assemblages differing between sites more for L. heterophyllum than for L. parviflorum. Pollination efficacy experiments showed that most visitors were poor pollinators. Single visits to flowers by this assemblage of species resulted in significantly higher seed set in Lithophragma heterophyllum (30.6 ± 3.9 SE) than in L. parviflorum (4.7 ± 3.4 SE). This difference was consistent between sites, suggesting that these visitors provide a better fit to the floral morphology of L. heterophyllum. Overall, none of the non-Greya visitors appears to be either sufficiently common or efficient as a pollinator to impose strong selection on any of these four Lithophragma populations in comparison with Greya, which occurs within almost all populations of these species throughout their geographic ranges.     

FLORAL STRUCTURE AND EVOLUTION IN LOPEZIEAE (ONAGRACEAE)

The Lopezieae present an interesting mixture of ancestral and derived characters: some members of the tribe retain the basic onagraceous chromosome number (n = 11), but the flowers are advanced in that they are mostly zygomorphic and always have a two-merous androecium. Species differ in the position of the nectaries, also in the way in which floral parts are united above the inferior ovary. These differences, when analyzed with information from a new monograph of the Lopezieae, provide the basis for a phylogenetic tree. It is inferred that ancestral Lopezieae were bird-pollinated woody perennials with regular flowers, two fertile stamens, and no floral tube distal to the ovary. Evolutionary events accompanying the emergence of modern taxa included abortion of the abaxial stamen (all surviving Lopezieae except Lopezia lopezioides), development of an epigynous floral tube (L. riesenbachia, L. semeiandra), decrease in floral symmetry without conversion to insect pollination (in two independent lines), and decrease in floral symmetry with conversion to insect pollination (in at least two independent lines). The prominent tubercles on upper petals of certain insect-pollinated species apparently evolved from the less prominent swollen areas still present in some of the bird-pollinated species. The tubercles and an associated snapping mechanism arose in response to increasing selection for fly pollination. Densely staining areas in some specimens may be osmophores; if so, scent plays a supplementary role in the orienting of insects to the upper petals. Interstaminal nectaries and the absence of a floral tube link the Lopezieae to Ludwigia; the relationship of these two taxa to Epilobium is presently unclear. Fossil records indicate that the Onagraceae had evolved by the beginning of the Tertiary Period and that the Ludwigia line is very old. The family's ancestral features are retained to a greater degree in Fuchsia, however, than in Ludwigia.     

Fossil floral and fruit evidence for the evolution of unusual developmental characters in Fagales

Flowers of many living Fagales exhibit unusual developmental characteristics. At anthesis, ovulate flowers have carpels bearing immature orthotropous ovules. After pollination, the ovules increase in size and become anatropous and the ovary enlarges. Simultaneously, the pollen tubes extend from the stigma to the ovules with several phases of growth and quiescence. Finally, after the first fertilization, the remaining ovules abort, resulting in a single‐seeded fruit. Three‐dimensionally preserved potentially fagaceous mesofossil flowers from the Campanian of Massachusetts, USA, provide evidence on the evolution of these characters. The fossils share putative synapomorphies with the Fagales (six tepals, mostly inferior, three‐carpellate ovary with each locule initially containing two pendant ovules, punctate‐rugulate, tricolporate pollen and fruit with a single seed). However, the fossil is bisexual and has nectaries, characters shared with the sister order Cucurbitales, and both lack the fagalean immature orthotropous developmental stage. The fossil shares synapomorphies of an inferior ovary and a single‐seeded indehiscent fruit with both living orders and appears to be transitional. Comparison of ontogenetic changes between the fossil and related fagalean taxa suggests independent stepwise changes in development in which some characters of the modern clades were in place at ～ 75 Myr and others evolved more recently. © 2012 The Linnean Society of London, Botanical Journal of the Linnean Society, 2012, 168 , 353–376.     

MORPHOLOGY AND DEVELOPMENT OF THE FLOWERS OF BOOTTIA CORDATA,OTTELIA ALISMOIDES,AND THEIR SYNTHETIC HYBRID (HYDROCHARITACEAE)

The inferior ovary of Boottia cordata, Ottelia alismoides, and their hybrid is appendicular in nature, the carpels are congenitally only slightly connate, and they are unsealed. All floral organs except the sepals originate from common primordia in the female and bisexual flowers. A flat residual floral apex is pressnt. There is a vestigial superior ovary of three ontogenetically fused carpels in the male flower of Boottia cordata. The hybrid is intermediate in many characteristics and has partially fertile stamens and staminodia. The sequence of development in all flowers is acropetal. These plants appear to be related to the Butomaceae and they show evolutionary tendencies parallel to those in the Nymphaeaceae.     

DEVELOPMENT OF TRISTYLY IN PONTEDERIA CORDATA (PONTEDERIACEAE). I. MATURE FLORAL STRUCTURE AND PATTERNS OF RELATIVE GROWTH OF REPRODUCTIVE ORGANS

Pontederia cordata is a tristylous, self-incompatible emergent aquatic. Measurements of reproductive organs in mature flowers and developing buds and analysis of relative growth rates of the styles, filaments, and floral tube were used to analyze the developmental processes that result in reciprocal positioning of reproductive parts among the style morphs. Flowers are trimerous with two series of three tepals, two series of three stamens, and a tricarpellate ovary with a single ovule. Each flower has stamens of two lengths, but the two lengths correspond to upper vs. lower position in the zygomorphic flowers, not to the two series initiated in the primordium. Morph-dependent variation in stigma height depends on differences in style length, not ovary length. Differences among morphs in anther height result from differences in the position of filament insertion on the floral tube and differences in filament length. Styles of the three morphs develop to different lengths as a result of two distinct processes. Styles of L and M morphs develop at different rates with the L style growing more rapidly than the M style, whereas styles of the S morph have a brief period of rapid growth followed by early inhibition. Stamen growth in the S morph also differs qualitatively from that in the L and M morphs, which are distinguished from each other by quantitative differences in growth rates. Results indicate that the developmental processes that result in the complementary arrangements of organs in different morphs are morph-specific. An attempt is made to integrate the findings of this study with the model for genetic control of tristyly.     

Female reproductive biology of two sympatric incirrate octopod species, <Emphasis Type="Italic">Adelieledone polymorpha</Emphasis> (Robson 1930) and <Emphasis Type="Italic">Pareledone turqueti</Emphasis> (Joubin 1905) (Cephalopoda: Octopodidae), from South Georgia

The reproductive biology of two species of endemic Southern Ocean octopods was investigated around the sub-Antarctic islands of South Georgia and Shag Rocks. The females of both the species produce few, large eggs. This appears to be governed by phylogenetic constraint. No evidence was found for ontogenetic migration or seasonality associated with gonad maturation. Based on oocyte length frequency distributions and observations of oocyte development within the ovary, it is possible that both species could have either a single or multiple-batch spawning strategy. Pareledone turqueti ovaries contained fewer larger oocytes than those of Adelieledone polymorpha, which may help to reduce competition for resources immediately after hatching.