MORPHOLOGY AND TAXONOMY OF MERISTIELLA GEN. NOV. (SOLIERIACEAE,RHODOPHYTA) 1

Eucheuma acanthocladum (Harvey) J. Agardh, E. gelidium (J Agardh) J. Agardh, E. echinocarpum Areschoug and E. schrammii(P. et H. Crouan) J. Agardh from the tropical and warm temperate waters of the western Atlantic Ocean and Caribbean Sea are transferred to a new genus, Meristiella. Meristiella exhibits the following Unique combination of characters among genera in the Solieriaceae: (1) rotated periaxial cells, (2) a loosely filamentous medulla. (3) an auxiliary cell complex, (4) Single and twin connecting filaments and (5) spinose cystocarps composed of a central, small-celled placentum, based on its reproductive features, Meristiella. is assigned to the tribe Agardhielleae. Culture experiments and herbarium studies provide evidence that E, gelidium and E. acantghocladum are conspecific. Lectotypes are designated for the included species.     

MORPHOLOGY AND SYSTEMATICS OF SCIUROTHAMNION STEGENGAE GEN. ET SP. NOV. (CERAMIACEAE,RHODOPHYTA) FROM THE INDO‐PACIFIC1

A new ceramiaceous alga, Sciurothamnion stegengae De Clerck et Kraft, gen. et sp. nov., is described from the western Indian Ocean and the Philippines. Sciurothamnion appears related to the tribe Callithamnieae on the basis of the position and composition of its procarps and by the majority of post‐fertilization events. It differs, however, from all current members of the tribe by the presence of two periaxial cells bearing determinate laterals per axial cell. Additionally, unlike any present representative of the subfamily Callithamnioideae, no intercalary foot cell is formed after diploidization of the paired auxiliary cells. The genus is characterized by a terminal foot cell (“disposal cell”), which segregates the haploid nuclei of the diploidized auxiliary cell from the diploid zygote nucleus. The nature of three types of foot cells reported in the Ceramiaceae (intercalary foot cells containing only haploid nuclei, intercalary foot cells containing haploid nuclei and a diploid nucleus, and terminal foot cells containing only haploid nuclei) is discussed.     

ACROSYMPHYTON FIRMUM SP. NOV. (RHODOPHYTA,CRYPTONEMIALES), A NEW SUBTIDAL RED ALGA FROM NEW ZEALAND; DEVELOPMENTAL MORPHOLOGY AND DISTRIBUTION OF THE GAMETOPHYTE1

Acrosymphyton firmum sp. nov., is described from the northeastern coast of North 1., New Zealand. Gametophytes are spring–summer annuals which grow subtidally on cobbles. Thalli are uniaxial; each axial cell bears a whorl of four indeterminate and one determinate branchlets. Indeterminate branchlets are alternately arranged giving the thallus a distichous and feather-like appearance. Numerous corticating rhizoidal filaments are produced from the periaxial and lower whorl branchlet cells. These rhizoids entwine and obscure the main axis as the thallus develops until in the mature plant the axes have a firm consistency and lubricous texture. The carpogonial branch bearing short lateral filaments and auxiliary cell branch with terminal auxiliary cell place this new species in the genus Acrosymphyton Sjöstedt. Of the three described species in the genus, A. firmum is most similar to A. taylori. This is the first report of the genus Acrosymphyton and the only confirmed report of the family Dumontiaceae in New Zealand waters.     

DUDRESNAYA PUERTORICENSIS SP. NOV. (DUMONTIACEAE,GIGARTINALES, RHODOPHYTA)1

A new species of Dudresnaya is described from Puerto Rico and Georgia. Gametophytes have cylindrical axes, exserted apical cells, rectangular to hexagonal crystals in the axial cells, ellipsoidal outer assimilatory cells, spermatangial mother cells which are terminal or subterminal cells of the subdichotomously branched outer assimilatory branches and auxiliary cells which are indistinguishable in appearance from adjacent, large, deeply staining cells of the auxiliary cell branch. Tetrasporophytes are unknown.     

BATRACHOSPERMUM HETEROCORTICUM SP. NOV. AND POLYSIPHONIA SUBTILISSIMA (RHODOPHYTA) FROM FLORIDA SPRING-FED STREAMS1

Polysiphonia subtilissima Mont. Is reported for the first time from a freshwater environment. The presence of four pericentral cells, subdichotomous branching, apical trichoblasts and rhizoids arising from pericentral cells combined with a lack of cortication and reproductive cells is consistent with marine populations of this species. The range of filament length is 1.4–4.7 cm. Branch diameters are 38–76 μm and pericentral cell lengths are 58–125 μm. Batrachospermum heterocorticum sp. nov. is distinguished primarily by a developmental change in cortical filaments from typical cylindrical cells (5.0–7.9 μm diam in initial stages to enlarged, elliptical cells (12.9–24.1 μm diam) in mature axes. Another unique feature of this species is carpogonia with cylindrical, pedicellate trichogynes on stringht carpogonial branches in mid to outer portions of lateral whorls. Other characteristics of B. heterocorticum include the following: olive-green color, 2–6 cm length, dichotomous to trichotomous fascicles in 4–7 tiers, 385–647 μm whorl diameters, 109–198 μm carpospore diameters and relatively small “chantransia” filaments.     

GAYLIELLA GEN. NOV. IN THE TRIBE CERAMIEAE (CERAMIACEAE,RHODOPHYTA) BASED ON MOLECULAR AND MORPHOLOGICAL EVIDENCE1

On the basis of comparative morphology and phylogenetic analyses of rbcL and LSU rDNA sequence data, a new genus, Gayliella gen. nov., is proposed to accommodate the Ceramium flaccidum complex (C. flaccidum, C. byssoideum, C. gracillimum var. byssoideum, and C. taylorii), C. fimbriatum, and a previously undescribed species from Australia. C. transversale is reinstated and recognized as a distinct species. Through this study, G. flaccida (Kützing) comb. nov., G. transversalis (Collins et Hervey) comb. nov., G. fimbriata (Setchell et N. L. Gardner) comb. nov., G. taylorii comb. nov., G. mazoyerae sp. nov., and G. womersleyi sp. nov. are based on detailed comparative morphology. The species referred to as C. flaccidum and C. dawsonii from Brazil also belong to the new genus. Comparison of Gayliella with Ceramium shows that it differs from the latter by having an alternate branching pattern; three cortical initials per periaxial cell, of which the third is directed basipetally and divides horizontally; and unicellular rhizoids produced from periaxial cells. Our phylogenetic analyses of rbcL and LSU rDNA gene sequence data confirm that Gayliella gen. nov. represents a monophyletic clade distinct from most Ceramium species including the type species, C. virgatum. We also transfer C. recticorticum to the new genus Gayliella.     

LIFE HISTORY AND GROWTH OF LAURENCIA BRACHYCLADOS (RHODOPHYTA,CERAMIALES)1

Laurencia brachyclados Pilger from Hawai'i completed a “Polysiphonia-type” tri-phasic life history in 21 weeks in laboratory culture. Tetraspores developed into gametophytes in a nearly 1:1:1 ratio of females: males: non-reproductive. Carpospores were released as early as 21 days after mixing virgin female and male gametophytes. Cultured thalli showed a “guerilla type” growth form. Other Hawaiian Laurencia species in culture had longer maturation times or remained non-reproductive. Variation in life history schedules may influence Laurencia species coexistence and algal community structure.     

MORPHOLOGY AND SYSTEMATICS OF RHODOCALLIS ELEGANS, RHODOCALLIDEAE, TRIB. NOV. (CERAMIACEAE, RHODOPHYTA), FROM SOUTHEASTERN AUSTRALIA

Recent collections of Rhodocallis elegans Kützing from southeastern Australia have permitted detailed observations of vegetative and reproductive structures that reveal features not exhibited by any existing tribe of Ceramiaceae. As a consequence, we establish the new tribe Rhodocallideae based on the unispecific genus Rhodocallis. Defining characters include: 1) four periaxial cells cut off in an alternating (rhodomelaceous) sequence; 2) determinate branchlets of two types: a) persistent lateral branchlets produced from the first-formed periaxial cells, and b) deciduous transverse branchlets produced from the second and third periaxial cells, with cortical filaments issuing from all four periaxial cells; 3) first- and second-order determinate branchlets terminated by thick-walled spines; 4) indeterminate branches formed at the tips of directly converted determinate branchlets; 5) axial cells of indeterminate branches heavily corticated by a cylinder of descending rhizoidal filaments; 6) spermatangial parent cells borne directly on unmodified outer cortical cells; 7) carpogonial branches borne in series on second and third periaxial cells of modified indeterminate axes; 8) procarps lacking sterile-cell groups; 9) a single derivative of the zygote nucleus transferred from the carpogonium to the auxiliary cell directly through a tube rather than by means of a connecting cell; 10) gonimoblasts surrounded by a network of rhizoidal filaments through which the gonimolobes protrude, the carposporophyte subtended by an investment of determinate branchlets; and 11) tetrasporangia tetrahedrally divided, borne on surface cortical cells of special determinate branchlets and protruding outside the cuticular layer.     

VEGETATIVE AND REPRODUCTIVE MORPHOLOGY OF EUCHEUMA ISIFORME (SOLIERIACEAE,GIGARTINALES, RHODOPHYTA)1

Eucheuma isiforme (C. Agardh) J. Agardh exhibits a combination of vegetative and reproductive features that distinguish it from other critically studied genera in the Solieriaceae. The development of the multiaxial thallus, emphasizing the arrangement of periaxial cells around each axial file; presence of reproductive nemathecia that contain carpogonial branches and auxiliary cells; and post-diploidization stages, including gonimoblast and pericarp initiation, stages of fusion cell formation, and carposporophyte development are described and illustrated for the first time in this species. The vegetative and reproductive features observed in E. isiforme are not diagnostic of any of the recently erected tribes in the Solieriaceae. Eucheuma appears most closely related to the Indian Ocean genus, Sarconema.     

MORPHOLOGY AND DEVELOPMENT OF AHNFELTIA PLICATA (RHODOPHYTA): PROPOSAL OF AHNFELTIALES ORD. NOV.1

Ahnfeltia plicata (Hudson) Fries, the type species of Ahnfeltia Fries, is currently assigned to the Phyllophoraceae (Gigartinales). Several morphological and biochemical characters distance A. plicata from the Phyllophoraceae but, because sexual reproduction has never been demonstrated, an alternative placement has not been possible. A. plicata now is shown to have a heteromorphic sexual life history. Erect branched gametophytes are dioecious. In male sori, spermatangia are cut off transversely from spermatangial mother cells. Female sori form numerous terminal sessile carpogonia. Following fertilization, several zygotes in each sorus fuse facultatively with undifferentiated intercalary cells of the female sorus and cut off gonimoblast initials obliquely outwards. These initials give rise to branching gonimoblast filaments that fuse with apical and intercalary female sorus cells and with each other, then grow radially outward in the compound external carposporophyte and terminate in carposporangia. Carpospores develop in culture into crustose tetrasporophytes identical to Porphyrodiscus simulans Batters. Field-collected P. simulans tetraspores grew into erect A. plicata axes. Tetrasporangia are formed by division and enlargement of crust apical cells followed by sequential enlargement and maturation of tetrasporocytes in an erosive process. Monosporangia are formed in sori on male gametophytes. Pit plugs of both gametophyte and tetrasporophyte phases consist of naked plug cores without cap layers of membranes. Gametophytes exhibit both cell fusions and secondary pit connections whereas tetrasporophytes form cell fusions but lack secondary pit connections. On the basis of the unique female and postfertilization reproductive development and in conjunction with the pit plug structure which is unique among florideophytes, the order Ahnfeltiales, containing the family Ahnfeltiaceae, is proposed.     

PARASITIC INTERACTIONS AND VEGETATIVE ULTRASTRUCTURE OF CHOREOAEMA THURETII (CORALLINALES,RHODOPHYTA)1

The monotypic coralline red alga, Choreonema thuretii (Bornet) Schmitz (Choreonematoideae), grows endophytically within three geniculate genera of the Corallinoideae. Although the thallus of Choreonema is reduced, lacks differentiated plastids, and is endophytic except for its conceptacles, its status as a parasite has been questioned because cellular connections to the host had not been ob served. Transmission electron microscopy, however, disclosed a previously undescribed type of parasitic interaction in which Choreonema interacts with its host through specialized cells known as lenticular cells. These small, lens-shaped cells are produced from the single file of host-penetrating vegetative cells. Pit plug morphology between vegetative and lenticular cells is polarized. Plug caps facing the vegetative cell have normal coralline morphology, while those facing the lenticular cell are composed of three layers. Regions of lenticular cells near host cells protrude toward the host cell; upon encountering the host cell wall, the prolrusion produces numerous finger-like fimbriate processes that make cellular connections with the host cell. Lenticular cells may extend several protrusions toward a host cell or penetrate more than one host cell; two or more lenticular cells may also penetrate the same host cell. The lack of secondary pit connections, cell fusions, and passage of parasitic nuclei suggest that this parasitic relationship may be evolutionarily older than previously reported cases of parasitism in red algae.     

COMPARATIVE MORPHOLOGY AND TAXONOMIC STATUS OF GRACILARIOPSIS (GRACILARIALES,RHODOPHYTA)1

The vegetative organization and reproductive development of Gracilariopsis lemaneiformis (Bory) Dawson, Acleto et Foldvik [including Gracilaria sjoestedtii Kylin] were investigated. Our observations on spermatangial development and post-fertilization features establish that Gracilariopsis Dawson is distinct at the generic level from Gracilaria Greville, and ice propose the resurrection of Gracilariopsis Dawson as a result. Spermatangial parent cells of Gracilariopsis are superficial, initiated in pairs or groups of three by concavo-convex longitudinal and transverse divisions. Each spermatangial parent cell cuts off a single, colorless spermatangium distally by a transverse division. The female reproductive apparatus consists of a supporting cell that bears a two-celled carpogonial branch flanked by two sterile branches, as in Gracilaria. Likewise, up to six sterile cells fuse with the carpogonium after fertilization to produce a primary fusion cell that generates the gonimoblasts; however, a secondary fusion cell is absent. Inner gonimoblast cells unite with cytologically modified cells of the inner pericarp by means of secondary pit-connections. Tubular nutritive cells are absent. The gonimoblast consists of a central sterile tissue interconnected throughout by secondary pit-connections surmounted by a fertile layer composed of carposporangia aligned in straight chains. The distribution of Gracilariopsis is extended to Western Europe.     

A MORPHOLOGICAL STUDY OF HOMMERSANDIA MAXIMICARPA GEN. ET SP. NOV. (KALLYMENIACEAE,RHODOPHYTA) FROM THE NORTH PACIFIC1

A new foliose red alga, common subtidally from British Columbia to the Aleutian Islands, is described and given the name Hommersandia maximicarpa. The lobed perennial thallus, which can reach a height of 23 cm, is distinguished by its vegetative structure and by its unique pattern of nonprocarpic carposporophyte development. In transverse section, the blades consist of a narrow filamentous medullary layer sandwiched on either side by large ellipsoidal subcortical cells and a thin outer cortex. The monocarpogonial branch and auxiliary cell systems of the female plants are typical of many members of the Kallymeniaceae. However, after the carpogonialfusion cell forms, a distinctive developmental pattern begins. The connecting filaments radiate outward into the surrounding tissue, branch abundantly, and become septate. They then contact, in addition to auxiliary cells, many small moniliform accessory branches. These branches appear to act as initiation points for the gonimoblast filaments. The large diffuse carposporophytes produced are unknown in any other member of the Cryptonemiales. The vegetative and reproductive anatomy of Hommersandia is compared to other Kallymeniaceae, and similar patterns of postfertilization development are examined in the Rhodophyta.     

NORTH CAROLINA MARINE ALGAE. IX. ONSLOWIA ENDOPHYTICA GEN. ET SP. NOV. (PHAEOPHYTA,SPHACELARIALES) AND NOTES ON OTHER NEW RECORDS FOR NORTH CAROLINA1

Four benthic algae are reported here for the first time in the North Carolina flora. The new brown algal genus and species, Onslowia endophytica Searles, is described as an endophyte of Halymenia floridana from the North Carolina continental shelf. New records of Boodleopsis pusilla and Naccaria corymbosa from North Carolina constitute range extensions of these tropical species on the American coast north from Florida. Blastophysa rhizopus, an endophyte and epiphyte known from the North Atlantic coast of Europe and America as well as the Caribbean is reported from North Carolina for the first time and in a new host, Predaea feldmannii.     

STRUCTURE AND REPRODUCTION OF AMANSIA AND MELANAMANSIA GEN. NOV. (RHODOPHYTA,RHODOMELACEAE) ON THE SOUTHEASTERN AFRICAN COAST1

Four species of Amansia Lamouroux were initially found in Natal. More Complete studies on these species revealed a new genus, Melanamansia, Which is described on the basis of presence of two dorsal pseudopericentral cells in two new species from Natal (M. seagriefii sp. nov. & M. fimbrifolia sp. nov.) in addition to other structural characters and features of pigmentation and reproduction. Pseudopericentral cells are not present in the type species of Amansia, A. multifida Lamouroux. The other two species of Amansia occurring in Natal, A. glomerata C. Agardh & A. loriformis sp. nov., have characters similar to the type species. Comparison of species from other regions of the world has shown that eight additional species, previously assigned to Amansia, belong to the new genus.     

ULTRASTRUCTURE OF VEGETATIVE ORGANIZATION AND CELL DIVISION IN THE UNICELLULAR RED ALGA DIXONIELLA GRISEA GEN. NOV. (RHODOPHYTA) AND A CONSIDERATION OF THE GENUS RHODELLA1

This study suggests that the genus Rhodella be restricted to that set of features currently observed only in Rhodella maculata Evans and Rhodella violacea (Korn-mann) Wehrmeyer, that a new genus Dixoniella be established to accommodate the unicellular red alga, Rhodella grisea (Geitler) Fresnel, Billard, Hindák et Pekár-ková, and that Rhodella cyanea Billard et Fresnel be further studied for probable reclassification. These conclusions are based on ultrastructural comparisons of Dixoniella grisea with published information on the genus Rhodella. The presence of thylakoids in the pyrenoid, a peripheral encircling thylakoid in the chloroplast, a dictyosome/nuclear envelope association, and the lack of a specialized pyrenoid/nucleus association in D. grisea separate this alga from the genus Rhodella. Cell division in D. grisea is not demonstrably different from that in Rhodella, although the unusually well-defined material of the presumptive microtubule organizing center (MTOC) made it possible to follow the development and behavior of the MTOC to a greater degree than in previously studied red algal cells. The surprising amount of conformity in cell division characters between D. grisea and the genus Rhodella prompted a comparison of cell division characteristics in all red algal unicells studied to date. All unicells show a remarkable degree of similarity except for differences in interzonal spindle length, dissimilarities in size of the nucleus-associated organelle (NAO), and the unusual NAO of Porphyridium purpureum (Bory) Drew et Ross.     

MARIPELTA ATLANTICA SP. NOV. (RHODOPHYTA,RHODYMENIALES) A NEW DEEP-WATER ALGA FROM FLORIDA1

A red alga with a cylindrical stipe bearing a single deciduous blade was collected in deep water off the east coast of Florida. It is described as Maripelta atlantica sp. nov., differing from M. rotata (Dawson) Dawson (the type of the genus, from deep water off California and Baja California) chiefly by having an annular tetrasporangial nemathecium on the lower surface of the blade rather than scattered nemathecia on the upper surface. Both species are vegetatively and reproductively distinct from M. thivyae Dawson, which is transferred to Halichrysis. New information is given regarding the reproduction and distribution of M. rotata.     

COMPARATIVE DEVELOPMENT OF THE RED ALGAL PARASITES BOSTRYCHIOCOLAX AUSTRALIS GEN. ET SP. NOV. AND DAWSONIOCOLAX BOSTRYCHIAE (CHOREOCOLACACEAE,RHODOPHYTA)1

The development of two red algal parasites was examined in laboratory culture. The red algal parasite Bostrychiocolax australis gen. et sp. nov., from Australia, originally misidentified as Dawsoniocolax bostrychiae (Joly et Yamaguishi-Tomita) Joly et Yamaguishi-Tomita, completes its life history in 6 weeks on its host Bostrychia radicans (Montagne) Montagne. Initially the spores divide to form a small lenticular cell, and then a germ tube grows from the opposite pole. Upon contact with the host cuticle, the germ tube penetrates the host cell wall. The tip of the germ tube expands, and the spore cytoplasm moves into this expanded tip. The expanded germ tube tip becomes the first endophytic cell from which a parasite cell is cut off that fuses with a host tier cell. The nuclei of this infected host cell enlarge. As parasite development continues, other host-parasite cell fusions are formed, transferring more parasite nuclei into host cells. The erumpent colorless multicellular parasite develops externally on the host, and reproductive structures are visible within 2 weeks. Tetrasporangia are superficial and cruciately or tetra-hedrally divided. Spermatia are formed in clusters. The carpogonial branches are four-celled, and the carpogonium fuses directly with the auxiliary (support) cell. The mature carposporophyte has a large central fusion cell and sympodially branched gonimoblast filaments. Early stages of development differ markedly in Dawsoniocolax bostrychiae from Brazil. Upon contact with the host, the spore undergoes a nearly equal division, and a germ tube elongates from the more basal of the two spore cells, penetrates the host cell wall, and fuses with a host tier cell. Subsequent development involves enlargement of the original spore body and division to form a multicellular cushion, from which descending rhizoidal filaments form that fuse with underlying host cells. This radically different development is in marked contrast to the final reproductive morphology, which is similar to B. australis and has lead to taxonomic confusion between these two entities. The different spore germination patterns and early germ-ling development of B. australis and D. bostrychiae warrant the formation of a new genus for the Australian parasite.     

BIODIVERSITY OF CORALLINE ALGAE IN THE NORTHEASTERN ATLANTIC INCLUDING CORALLINA CAESPITOSA SP. NOV. (CORALLINOIDEAE,RHODOPHYTA)1

The Corallinoideae (Corallinaceae) is represented in the northeastern Atlantic by Corallina officinalis L.; Corallina elongata J. Ellis et Sol.; Haliptilon squamatum (L.) H. W. Johans., L. M. Irvine et A. M. Webster; and Jania rubens (L.) J. V. Lamour. The delimitation of these geniculate coralline red algae is based primarily on morphological characters. Molecular analysis based on cox1 and 18S rRNA gene phylogenies supported the division of the Corallinoideae into the tribes Janieae and Corallineae. Within the Janieae, a sequence difference of 46–48 bp (8.6%–8.9%) between specimens of H. squamatum and J. rubens in the cox1 phylogeny leads us to conclude that they are congeneric. J. rubens var. rubens and J. rubens var. corniculata (L.) Yendo clustered together in both phylogenies, suggesting that for those genes, there was no genetic basis for the morphological variation. Within the Corallineae, it appears that in some regions, the name C. elongata has been misapplied. C. officinalis samples formed two clusters that differed by 45–54 bp (8.4%–10.0%), indicating species‐level divergence, and morphological differences were sufficient to define two species. One of these clusters was consistent with the morphology of the type specimen of C. officinalis (LINN 1293.9). The other species cluster is therefore described here as Corallina caespitosa sp. nov. This study has demonstrated that there is a clear need for a revision of the genus Corallina to determine the extent of “pseudocryptic” diversity in this group of red algae.     

WATER MOTION AND MORPHOLOGY IN CHONDRUS CRISPUS (RHODOPHYTA)1

Morphological variability of intertidal Chondrus crispus Stackh. fronds along a small open rocky coast was related to wave exposure and emersion. Cluster analysis revealed two well-defined morphologies: filiform and planiform, named the N morphotype and B morphotype, respectively. We propose a rapid method of classifying fronds based on the morphology of the cross section at half the height on the thallus. The N morphotype is characterized by fewer dichotomies per unit length, a circular cross section with a large inner cortex, and narrow fronds. It is abundant at low intertidal and exposed sites. The B morphotype is characterized by more dichotomies, smaller sizes, a subelliptical or flattened cross section, and broad fronds. It is abundant at high intertidal sites in sheltered areas. Regression analysis revealed a major effect of water movements on frond morphology with respect to tidal level, which was more evident at high intertidal levels. No relationships were observed between morphology and life history phases.