PATTERNS OF GENICULAR DEVELOPMENT IN AMPHIROA (CORALLINACEAE)

Two types of genicular development (designated Types I and II) are present in South African species of Amphiroa. Genicula of both types originate when medullary tissue near branch endings softens by decalcification. In Type I decalcification does not progress to the branch surface and the joint therefore does not become flexible until the cortex, which remains calcified, cracks and partly sloughs. This type occurs in all species of Amphiroa in South Africa except one, and possibly occurs in those in the rest of the world as well. In Type II decalcification continues centrifugally to the surface of the branch; this results in a geniculum comprising medullary and cortical tissue. As far as is known this type occurs only in Amphiroa ephedraea. Type I appears to be more primitive than Type II.     

A COMPARATIVE STUDY OF SEXUAL REPRODUCTION IN FOUR SPECIES OF CHLAMYDOMONAS

Trainor , Francis R. (U. Connecticut, Storrs.) A comparative study of sexual reproduction in four species of Chlamydomonas. Amer. Jour. Bot. 46(2) : 65-70. 1959.—This paper reports results of comparative experiments on some factors affecting sexual reproduction in 4 species of Chlamydomonas. Sexuality can be controlled in 3 of these species (C. chlamydogama, C. eugametos and C. reinhardti) by the level of ammonium nitrate in the harvesting medium. It was demonstrated that periodicity of illumination was of importance for high zygospore yields with C. chlamydogama and C. eugametos. Other variables, e.g., various aspects of nitrogen level, illumination and inter-fertility, were investigated and the results summarized in tabular form.     

SEXUAL DIMORPHISM IN THE APERTURAL NOTCH OF A NEW SPECIES OF GEMMULA (GASTROPODA: TURRIDAE)

The presence of a ‘tertiary’ apertural ‘notch’has been recorded in some species of Gemmula (subfamily Turrinae)and in Aforia circinata (Turriculinae). Studies of a large seriesof the new species Gemmula lordhoweensis confirms the presenceof the notch in adult females. The presence of the notch maybe connected with the processes of fertilization or oviposition. (Received 23 March 1990; accepted 25 June 1990)     

THE EVOLUTION OF REVERSED SEXUAL DIMORPHISM IN SIZE IN MONOGAMOUS SPECIES OF BIRDS

Reversed sexual dimorphism in size (RSD) occurs in most species of several taxonomic groups of birds. The hypotheses proposed to explain this phenomenon are examined theoretically, using inequalities to state selection in the most rigorous possible terms. The most pertinent empirical evidence is also examined critically. Proponents of hypotheses on the evolution of RSD have failed to consider the genetic constraints on the evolution of dimorphism. Selection for dimorphism can act on only that small portion of the genetic determination of body size that is sex limited. In general, selection for body size is much more likely to lead to a similar change (e.g. larger) in both sexes than to dimorphism. The most popular hypotheses involve selection for size-related differences in foraging ability. It is unlikely that there is variation in size-related foraging differences available for selection in a monomorphic, ancestral population. Foraging differences between the sexes cannot lead to the evolution of RSD; evolution of large and small morphs of both sexes is a more likely outcome. Selection for sex-role differentiation factors (e.g. large females lay larger eggs, small males are more agile in flight) can lead to the evolution of RSD, but only if the magnitudes of opposing selection for small males and for large females are equal. Combining selection for size-related foraging differences with selection for sex-role differentiation factors hinders the evolution of RSD until the sexes differ in size by 3 s.d . Empirical evidence supports this assertion: statistically significant differences between the sexes in the size of prey taken are found only in highly dimorphic species. The sex-role differentiation factors that have been proposed appear unlikely to provide the equal selection necessary for the evolution of RSD. Several authors have proposed that small size in males is selected for foraging ability and large size in females for some sex-role differentiation factor. Males cannot be more efficient foragers without females being less efficient and efficiency cannot be a factor only when the male is feeding his family. RSD cannot evolve in monogamous species if large females survive less well than small males. RSD might evolve as the result of sexual selection for small size in males and constraints on the reduction of size in females because of some factor associated with reproduction. Examination of seven studies indicating a relationship between female size and reproductive success shows very little unequivocal evidence for small size in females allowing breeding earlier in the season. Large size in females allows females to breed at a younger age in the sparrowhawk and pairs to form more rapidly in three species of sandpipers. Both of these may be the result of sexual selection. There are fewer theoretical problems with sexual selection as a cause for the evolution of RSD than with the other hypotheses. Empirical evidence for sexual selection is scarce but better than that for the other hypotheses. Evidence is contradictory for the selection of small size in males for agility in aerial displays for courtship or defence of territory. Large size in females does not appear to be the result of selection for competitive ability to obtain mates. Facilitation of female dominance and hence of the formation and maintenance of a pair bond is the most viable explanation of the evolution of RSD. It is most likely that all dimorphism (normal or reversed) is the result of sexual selection. RSD is correlated with birds in the diet in the Falconiformes and this is a central theme in the foraging hypotheses. This correlation may be because birds are abundant and available in a continuum of sizes, thus permitting but not causing the evolution of RSD or because species that prey upon birds are better equipped physically (and perhaps more likely behaviourally) to inflict damaging attacks on conspecifics and the greater RSD increases female dominance and the ease of pair formation.     

ASCOCARPIC CENTRUM ONTOGENY OF SPECIES OF HYPODERMATACEAE OF CONIFERS

Studies on the morphology of the ascocarps of 39 species of Hypodermataceae revealed several previously unknown cytological features. Two basic and one intermediate type of centrum ontogeny are discussed. Ascal initiation within Type I centrum occurs in the basal cells of the pseudoparaphyses and involves anastomoses, while ascal initiation within Type II occurs in cells of a plectenchymatous centrum, with no visible anastomosing in the ascocarp. There is frequent anastomosing between vegetative hyphae well in advance of initiation of the ascocarp. Ascal initiation in the intermediate type has ontogenetic sequences similar to those in Types I and II.     

树鼩(Tupaia belangeri chinensis)生长发育的初步观察

本文对39只树鼩的个体生长发育作了描述。新生幼仔生长发育迅速,在出生后头一个月内,体重可增长3—6倍,其体重的增长与饮奶量有关。出生后4个月性成熟,7个月龄时可繁殖产仔。性器官的重量有明显的季节性变化,1—6月间睾丸、子宫、卵巢重量最大,性行为活跃,其余月份重量下降,性功能出现渐进性衰退。辜丸重和体重的比值小于0.01,表明树鼩是单雄交配繁殖。乳齿的萌发为下颚先于上颚,门齿最先萌发,其次是犬齿,前臼齿,最后是臼齿。与Lyon(1913)和Shigehara(1980)提出的恒齿萌发次序不同。     

SEXUAL REPRODUCTION IN STEPHANODISCUS NIAGARAE (BACILLARIOPHYTA)1

We observed sexual reproduction in a clonal culture of Stephanodiscus niagarae Ehrenb. and used light and scanning electron microscopy to absent flagellated male cells, auxospore growth, initial valve structure and production, and subsequent daughter cell division. Free auxospores were spherical and nonsiliceous throughout growth, producing hemispherical initial valves devoid of spines and with nonfasciculate striae. Pregametangial cells averaged 43% of the diameter of the daughter cell population and were 1/9 the biovolume of initial, cells. This paper is the first confirmed report of sexual reproduction in S. niagarae, although it appears that specimens of Actinocyclus niagarae H. L. Smith, described from Lake Erie in 1878, are actually initial valves of S. niagarae.     

RADIOISOTOPIC STUDY OF CALCIFICATION IN THE ARTICULATED CORALLINE ALCA BOSSIELLA ORBIGNIANA1

Calcification in Bossiella orbigniana (Corallinaceae) is characterized by a series of features which, vary according to the age of the segment (intergeniculum). From the youngest segment at the branch tip to older, more basal segments: (1) weight and degree of mineralization increase, while rate of weight gain decreases; (2) rate and stability of calcium-45 labeling decrease; (3) effect of light on calcium-45 labeling rate decreases, while effect of light on stability of label increases; however, for all segments, calcium-45 labeling is more rapid and more stable in the light than in the dark; (4) rate of calcium-45 labeling in killed controls decreases. Comparative studies with the tropical coralline alga Amphiroa yielded similar results. Characteristics of the gradients in calcification and effect of light in these coralline algae are very similar to those found, in a reef-building coral containing symbiotic algae, and the data suggest that organic products of photosynthesis may be of general importance to calcification.     

ASPECTS OF CONE AND OVULE ONTOGENY IN CRYPTOMERIA (TAXODIACEAE)

The axillary complex of female cones of Cryptomeria is initiated as a tangentially extended triangular structure with a rounded apex. It is bilaterally symmetrical. Structures interpreted as prophylls are differentiated first, but they become insignificant in later development. They are succeeded by two successive pairs of lobes, each lobe being the common primordium for an adaxial ovule and a tooth. The ovule initially much exceeds the tooth. The apex of the complex has a diversity of fates and may differentiate as an ovule-tooth pair. A one-to-one relation between teeth and ovules may be lost by abortion of ovules. The initial relation between teeth and ovules is obscured in later development due to extension of tissues at the base of the complex associated with considerable enlargement of the teeth. Histogenesis of the various parts is described, together with the vascular system. There is a vascular supply to the tooth but not the ovule. The results support a direct comparison with the extinct transition conifers Pseudovoltzia and Aethophyllum but do not fully support Florin's generalized model for the arrangement of parts in the axillary complex of conifers.     

SEXUAL REPRODUCTION OF PERIDINIUM WILLEI (DINOPHYCEAE)1

Sexual reproduction was induced in the dinoflagellate Peridinium willei Huitfeld-Kass when exponentially growing cells were inoculated into nitrogen deficient medium. Small, naked vegetative cells produced by division of thecate cells acted as gametes. The zygote remained motile 13–14 days, during which time it enlarged and the theca formed became warty. Fourteen to 15 days following plasmogamy the zygote was nonmotile with the protoplast contracted. A large red oil droplet appeared and the wall thickened, becoming chitinized. Hypnozygotes with 4 nuclei were observed 7–8 wk following formation. Meiosis was inferred. The hypnozygote germinated, within 8 wk producing one post-zygotic cell retaining the red oil droplet. This cell divided within 24 h into 2 daughter cells each with a prominent red oil droplet. These daughter cells divided after 2 to 3 days into ordinary vegetative cells. Attempts to induce sexual reproduction by inoculation of cells into media deficient in a number of basic elements were unsuccessful.     

A POLYPLOID SPECIES COMPLEX OF SPIROGYRA COMMUNIS (CHLOROPHYTA) OCCURRING IN NATURE 1

Investigations were conducted to determine whether ploidal changes found in laboratory cultures of Spirogyra also occur in nature. In an earlier study filament types identifiable as three different species (Spirogyra singu-laris Nordstedt, S. communis (Hassall)Kütz., S. fragilis Jao) arose from an original clonal culture through vegetative growth and sexual reproduction. These three “species” or filament groups differed in filament width, chloroplast number, zygospore size, and chromosome number. The differences in chromosome number represented a polyploid series of diploid (S. communis), triploid (S. fragilis), and tetraploid (S. singularis) forms in which width increased with ploidal level. The three width groups constituted a “species complex.” Five years after isolation of the original strain in this species complex, filaments corresponding to two of the width groups (S. singularis and S. communis) were found at the original collection site in the Santa Catalina Mountains in southern Arizona. The two field-collected groups were indistinguishable from the laboratory species complex in morphology and chromosome number. Homothallic conjugation within the two field width groups yielded progeny similar to those from homothallic conjugation of groups in the laboratory species complex. Filament widths of progeny were generally within the width limits of respective parental groups. The four possible intergroup crosses between the two laboratory and two field width groups yielded progeny similar to the wider parent (S. singularis) or the parent of intermediate width (S. fragilis). Progeny characteristics were determined by the width groups of parents, regardless of whether parents came from the laboratory or field. The similarities in morphology, chromosome numbers, and reproductive behavior of laboratory and field width groups imply that the laboratory species complex of S. communis has a natural counterpart in the field.     

STRUCTURE AND ONTOGENY OF LATICIFERS IN CICHORIUM INTYBUS (COMPOSITAE)

The branched anastomosed laticifer system in the primary body of Cichorium intybus L. originates in embryos from files of laticiferous members at the boundary between phloic procambium and ground meristem. Upon seed germination, laticiferous members develop perforations in the end walls which become entirely resorbed. Perforations also develop in the longitudinal walls of contiguous laticiferous members and from lateral connections between developing laticifer branches. Additional laticiferous members originate as procambium differentiation proceeds, and their differentiation follows a continuous acropetal sequence in leaf primordia of the plumule. In roots, laticifers closely associated with sieve tubes in the secondary phloem originate from derivatives of fusiform initials in the vascular cambium. These laticifers develop wall perforations and in a mature condition resemble laticifers in the primary body. As the girth of the root increases, laticifers toward the periphery, unlike associated sieve tubes, resist crushing and obliteration. Laticifers vary in width from about 4 to 22 μm; the widest ones occur in involucral bracts and the narrowest ones in florets. There was no evidence that intrusive growth occurs during development of the laticifer system, although such growth may occur during development of occasional branches which extend through ground tissue independent of phloem and terminate in contact with the epidermis. Presence of amorphous callose deposits is related to aging of laticifers and mechanical injury.     

ASCOCARPIC CENTRUM ONTOGENY OF SPECIES OF HYPODERMATACEAE OF CONIFERS. II

Ascocarpic studies of the ontogeny of Lophodermium nitens disclosed a type of development unlike that of all other species of Hypodermataceae occurring on conifer needles. For this reason the centrum of L. nitens is designated as Type III and is compared with Type I (Gordon, 1966). Because L. nitens produces its ascocarp in several tissues of various species of pine, the ontogeny of ascocarps in different locations is discussed and illustrated. The most significant ontogenetic feature of the ascocarp of L. nitens is a layer of hyaline cells in the primordium; this layer is meristematic and gives rise to all subsequent structures of the centrum.     

BREEDING SYSTEM OF A HYBRID BETWEEN A SEXUAL AND AN APOMICTIC SPECIES OF AMELANCHIER,SHADBUSH (ROSACEAE,MALOIDEAE)

Amelanchier bartramiana, which has been shown to be sexual and self-incompatible, and A. laevis, in which apospory and self-compatibility occur, grow in a mixed population in western Maine. Also present there is the putative interspecific hybrid, A. × neglecta. Principal components and canonical discriminant analyses of seven morphological characters from 96 parental and putative hybrid individuals substantiate morphological intermediacy of the hybrids. A Nomarski differential interference microscopy study of megasporogenesis and megagametogenesis in five hybrid plants shows a predominantly aposporous mode of reproduction, and controlled pollinations indicate that seed formation between A. bartramiana and A. laevis is possible and that the hybrids are self-compatible. The hybrids, which are tetraploids (n = ca. 34) like both parents in Maine, produce viable pollen and seed, but there is little evidence for backcrossing with either parent.     

SIMILAR UNSTABLE MUTATIONS IN THREE SPECIES OF GRACILARIA (RHODOPHYTA)1

Unstable mutants with similar variegated pigmentation were genetically characterized in the red algae. Gracilaria tikvahiae (McLachlan), G. foliifera (Forsk.) Børg. and. G. sjoestedtii (Kylin). All three mutants were green plants with flecks of red tissue where cells had reverted to wild type. The mutant green phenotypes were all recessive, and their genetic behavior in crosses indicated that each was the result of a single, unstable, nuclear gene. Wild-type revertant tissue was stable one it arose. Revertant plants obtained from spores and revertant fronds taken from variegated plants could not be distinguished from the normal wild type, either phenotypically or genetically. Reversion to wild type occurred during all phases of the life cycle. In crosses between the mutants and wild type, most of the F₁ tetrasporophytes were heterozygous wild-type plants, an observation consistent with the recessive nature of the mutations; however, a low frequency of homozygous unstable-green F₁ tetrasporophytes was also obttained from these crosses. The molecular basis of neither the mutant instability, i.e. the reversion to wild type, nor of the process producing the unstable green F₁ tetrasporophytes can yet be deduced, but the phenotype of the plants and genetic results suggest the involvement of transposable genetic elements.     

MORPHOLOGICAL STUDIES IN A NEW SPECIES OF ACROSYMPHYTON (RHODOPHYCEAE)

Abbott , Isabella A. (Hopkins Marine Sta. of Stanford U., Pacific Grove, Calif.) Morphological studies in a new species of Acrosymphyton (Rhodophyceae). Amer. Jour. Bot. 49(8): 845–849. Illus. 1962.—Acrosymphyton taylori sp. nov. (Dumontiaceae, Cryptonemiales, Rhodophyceae) is shown to have a sexual cycle essentially similar to that of the 2 other species in the genus, but differs in some details of the sexual structures and the vegetative structure. Acrosymphyton taylori, from the Hawaiian Islands, is the only member of the genus from the Pacific. Acrosymphyton is only one of several genera of red algae possessing soft, gelatinous, uniaxial thalli. A study of specimens from various herbaria showed that specimens of Dudresnaya and Calosiphonia have been confused with Acrosymphyton.     

A NEW MEASURE OF GENETIC IDENTITY BETWEEN POPULATIONS OF SEXUAL AND ASEXUAL SPECIES

We define a new genetic identity measure that is especially well suited for asexual polyploid species as it circumvents errors in the estimation of gene frequencies. It also can be applied to sexuals allowing the study of phylogenetic relationships in species complexes consisting of sexuals and asexuals of different ploidy levels. The measure groups genotypes into classes dependent on homozygosity vs heterozygosity and the number of ancestral allele types vs the number of presumed new mutations. Its value is related to evolutionary time since divergence. The application of the method is illustrated by using electrophoretic data on the species group Solenobia triquetrella (Lepidoptera: Psychidae). A high similarity of estimated relationships among the proposed as well as other genetic identity measures is shown in the case of diploid sexual and asexual races of this species group. The phylogenetic relationships within the group are reanalyzed and monophyletic vs polyphyletic origin of parthenogenesis in this species complex is discussed. The genetic identity values found by the proposed procedure are explained by a polyphyletic origin of parthenogenesis, though a monophyletic origin of parthenogenesis in a broader sense cannot be excluded. The explanation of the phylogenetic relationships is based on the assumption of hybridization between related species and the extinction of one ancestral species. Furthermore, the genetic diversity is compared among sexual and parthenogenetic races of the species.