Amphithallia,a genus with four-celled carpogonial branches and connecting filaments in the Corallinales (Rhodophyta)

The South African marine alga Amphithallia crassiuscula, previously subsumed in the widely reported Synarthrophyton patena, is here re-described as a distinct species and genus. Thalli grow as obligate epiphytes on Gelidium capense in the upper sublittoral zone (while S. patena grows on Ballia callitricha). Gametophytes are monoecious with four-celled carpogonial branches and sterile cells are borne on supporting cells (dioecious or hermaphroditic with two or three-celled carpogonial branches and sterile cells borne on hypogynous cells in Synarthrophyton). Postfertilization stages involve a connecting filament linking the carpogonium to several putative auxiliary cells, demonstrating a non-procarpic condition with apparent absence of a fusion cell. Gonimoblast filaments develop at the level of basal cells of carpogonial branches. Spermatangial mother cells remain either unbranched (cutting off spermatangia only) or develop dendroid (branched) filaments with terminal spermatangia (as in Synarthrophyton). Multiporate conceptacles develop straight pore canals lined by non-differentiated cells (conical canals with differentiated pore cells along the base in Synarthrophyton). The here described pre- and post-fertilization characters are new for the order Corallinales motivating the establishment of the new genus Amphithallia.     

Scapania praetervisa Meyl., not S. mucronata Buch in Britain

Abstract

The protonema of Orthotrichum obtusifolium, regenerated from leafy shoots, comprises a dense mass of largely unbranched exclusively upright filaments. All the cells have transverse cross-walls and contain numerous chloroplasts which become larger and discoidal in older filaments. Differentiation into chloro- and caulonema is absent. When upright filaments are transplanted onto an agar surface, they act as the main axes for a further set of upright branches. Buds and side branches are produced symmetrically at right angles to the mother cells. Protonemal morphogenesis hardly changes on nutrientfree medium and spherical brood cells are not produced after prolonged culture or in the presence of abscisic acid. Rhizoids with oblique septa and pigmented walls arise from the base of gametophores. These revert to protonemata when in contact with nutrient agar.

The upright filaments produce terminal and intercalary filamentous gemmae with well defined abscission cells. The latter swell and lose their contents prior to liberation. Cells immediately below the abscission cells produce side branches in acropetal succession. Secondary gemmae arise by percurrent proliferation and gemmae frequently germinate in situ.     

Studies of the Liagoraceae (rhodophyta) of Western Australia: Gloiotrichus fractalis gen. et sp. nov. and Ganonema helminthaxis sp. nov.

Two new taxa of Liagoraceae (Nemaliales) are described from Western Australia. Gloiotrichus fractalis gen. et sp. nov. has been collected from 3–20 m depths at the Houtman Abrolhos, Western Australia. Plants are calcified, extremely lubricous, and grow to 17 cm in length. Carpogonial branches are straight, 6 or 7 cells in length, arise from the basal or lower cells of cortical fascicles, and are occasionally compound. Branched sterile filaments of narrow elongate cells arise on the lower cells of the carpogonial branch prior to gonimoblast initiation, at first on the basal cells, then on progressively more distal cells. Following presumed fertilisation the carpogonium divides transversely, with both cells giving rise to gonimoblast filaments. The distal cells of the carpogonial branch then begin to fuse, with fusion progressing proximally until most of the cells of the carpogonial branch are included. As fusion extends, the filaments on the carpogonial branch are reduced to the basal 2 or 3 cells. The gonimoblast is compact and bears terminal carposporangia. Spermatangial clusters arise on subterminal cells of the cortex, eventually displacing the terminal cells. The sequence of pre- and post-fertilisation events occurring in the new genus separates it from all others included in the Liagoraceae, although it appears to have close affinities with the uncalcified genus Nemalion. Ganonema helminthaxis sp. nov. was collected from 12 m depths at Rottnest Island, Western Australia. Plants are uncalcified and mucilaginous, the axes consisting of a few (< 10) primary medullary filaments, each cell of which gives rise to a cortical fascicle at alternate forks of the pseudodichotomies borne on successive medullary cells. Subsidiary (adventitious) filaments and rhizoids comprise the bulk of the thallus. Carpogonial branches are straight, (3-)4(-6) cells in length, arise on the basal 1–4 cells of the cortical fascicles, and are frequently compound. Carposporophytes develop from the upper of two daughter cells formed by a transverse division of the fertilised carpogonium. Ascending and descending sterile filaments girdle the carpogonial branch cells and arise mostly on the supporting cell prior to fertilisation. Ganonema helminthaxis is the first completely non-calcified member of the genus, and its reproductive and vegetative morphology supports the recognition of Ganonema as a genus independent from Liagora. Liagora codii Womersley is a southern Australian species displaying features of Ganonema, to which it is transferred.     

Verosphacela silvae sp. nov. (Onslowiaceae, Phaeophyceae) from the Mediterranean Sea

We describe Verosphacela silvae sp. nov., from the Mediterranean Sea. It consists of horizontal filaments living on the lower face of the red alga Peyssonnelia rubra (Greville) J. Agardh, from which erect filaments up to 1.5 mm high rise and grow upright after passing through the thallus of the supporting species. There are both horizontal and erect filaments growing by apical cells. In the subapical cells, 1–2 longitudinal divisions occur (more frequently in the erect filaments) but no secondary transverse divisions occur. Erect filaments bear lateral propagules on a stalk of one to three (rarely more) cells. Propagules, with neither apical cells nor arms, consist of seven cells. Zoidangia are borne at the apex of erect laterals. The new species differs from V. ebrachia Henry mainly in habit, propagules and zoidangia. In addition, distinct from V. ebrachia, filaments of V. silvae never penetrate between the cuticle and the cell wall of the supporting alga. Moreover, propagules of V. silvae consist of seven cells, whereas those of V. ebrachia consist of 9–13 cells, and zoidangia are terminal on laterals in V. silvae, whereas in V. ebrachia they are sessile on both axes and laterals.     

Atypical development of Chaetomorpha antennina in culture (Cladophorales,Chlorophyta)

The green seaweed genus Chaetomorpha is characterized by unbranched filaments. Molecular phylogenetic data indicate that Chaetomorpha forms a clade that is nested in a paraphyletic assemblage of branched species (Cladophora). It follows that the unbranched condition is evolutionarily conserved and likely evolved early in the evolution of this clade. In this study we show that under laboratory culture conditions, the filaments of C. antennina frequently produce lateral branches, similar to Cladophora. Our results thus indicate that the unbranched thallus architecture is not entirely genetically constrained, but at least in part subject to morphological plasticity. Additionally, culture observations of C. antennina allowed a detailed study of rhizoidal development, which seems unique among Cladophorales.     

THE ATLANTIC SPECIES OF SOLIERIA (GIGARTINALES,RHODOPHYTA): THEIR MORPHOLOGY,DISTRIBUTION AND AFFINITIES1

Solieria chordalis (C. Agardh) J. Agardh and S. tenera (J. Agardh) Wynne et Taylor exhibit multiaxial growth from a cluster of four to eight obconical apical cells. A single periaxial cell is cut off from each axial cell and successive periaxial cells are rotated 120° in a zig-zag pattern along each axial filament. Periaxial cells produce branched, laterally diverging filaments which form the cortex. The medulla is composed of axial cells, elongate cells of lateral filaments, stretched interconnecting cells, and secondary rhizoids. The two species are nonprocarpic. Carpogonial branches are 3-celled, inwardly directed, with a reflexed trichogyne. The auxiliary cell together with associated darkly-staining inner cortical cells form an association, the auxiliary cell complex, that is recognizable prior to diploidization. A single, unbranched, non-septate connecting filament issues from the fertilized carpogonium and fuses with the inner, lateral side of an auxiliary cell. Production of an involucre from surrounding vegetative cells is stimulated and a gonimoblast initial is cut off toward the interior of the thallus which divides to form a compact cluster of gonimoblast cells. A fusion cell is produced through fusion of inner gonimoblast cells with the auxiliary cell that, in turn, fuses progressively with cells of the lateral file bearing the auxiliary cell. Mature cystocarps have terminal carposporangia cut off from gonimoblast cells at the periphery of the fusion cell and are surrounded by an involucre with a distinct ostiole. Tetrasporangia are cut off laterally from surface cortical cells which then cut off one or two additional derivatives toward the outside. A lectotype is designated for Solieria chordalis, but the lectotypification of S. tenera is questioned. We conclude that Solieria is closely related to Rhabdonia and place the Rhabdoniaceae in synonomy with the Solieriaceae.     

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.     

NEW ENDOLITHIC CYANOPHYTES FROM THE NORTH ATLANTIC OCEAN. III. HYELLA PYXIS LUKAS & HOFFMAN SP. NOV.1

A new species of marine endolithic cyanophyte, Hyella pyxis Lukas and Hoffman (Order: Pleurocapsales), differs from other species of Hyella in its cell and filament dimensions, the manner in which its branches are initiated and the presence of gloeocapsin in the sheaths of colonies from the intertidal zone. Hyella pyxis colonies consist of a small cluster of coccoid cells located at the substrate surface and long, conspicuously branched filaments composed of cells that are longer than they are wide. Branches are initiated by the reorientation of the distal end of a filament cell or by the elongation of a filament cell, usually at one of its distal corners. Chromatic adaptation was not observed perhaps accounting for the relatively shallow depth limit of this species. Hyella pyxis was found within mollusk shells from the continental margin of eastern Florida to a depth of 50 m and carbonate rocks in the intertidal zone on Bermuda.     

MORPHOLOGY AND TAXONOMY OF HIMANTOTHALLUS (INCLUDING PHAEOGLOSSUM AND PHYLLOGIGAS), AN ANTARCTIC MEMBER OF THE DESMARESTIALES (PHAEOPHYCEAE)1

The sporophyte of Himantothallus develops according to a closed pattern in which the number and position of the blades is determined by the location of trichothallic meristems in a filamentous germling. Expansion of the miniature juvenile to the massive adult thallus is accomplished by diffuse secondary growth and involves a change from filamentous rhizoids to a hapteroid holdfast, flattening of the stipe, and enormous increases in length, breadth, and thickness of both stipe and blade. The axis usually bears 1–8 lateral blades, often paired, and terminates in a flattened stub. Phaeoglossum is interpreted as a growth form of Himantothallus in which a terminal blade develops to the exclusion of lateral blades, the latter being represented by a single spine. Phyllogigas clearly falls within the morphological spectrum of Himantothallus, the lack of twisting being related to physical factors in the environment. Sporangia, interspersed with an equal or somewhat larger number of two-celled paraphyses, are borne in slightly elevated sori scattered over both surfaces of the blade. Zoospore germination was not observed, nor were gametophytes, either in culture or in the field. Haptera apparently originate from the meristoderm in the lower part of the maturing stipe and lack a filamentous medulla. The mature stipe and the mature blade are anatomically similar, being composed of a superficial meristoderm, a cortex of parenchyma-like cells, and a filamentous medulla. The meristoderm is usually a single layer of plastid-containing cells that divide anticlinally to accommodate (or effect) expansion and periclinally to produce cortical tissue inward. Cortical cells are in radial files and increase in diameter towards the interior. They usually are densely packed with physodes. The medulla is uniquely distinguished by the presence of sheathed trumpet hyphae. Cells of the trumpet hyphae have perforate end walls with callose deposits and probably function in conduction as do the sieve filaments in Laminariales. Sheathing cells are filled with plastids. Sheathing filaments form connections among themselves and with nearby unsheathed filaments. The sheathed trumpet hyphae and their matrix of unsheathed filaments form a plexus, which in the mature blade is flattened and may be stripped intact from the other tissues. Development of the embryonic sporophyte is very similar to that in Desmarestia, as is the anatomy of the adult thallus and the sporangia. From these considerations, Himantothallus is assigned to the Desmarestiaceae (Desmarestiales).     

Gracilaria corallicola and G. multipartita (Gracilariales,Rhodophyta), two related flattened European species

Two European species of Gracilaria possess flattened blades borne on cylindrical axes, namely, G. multipartita, known primarily from the Atlantic coast, and G. corallicola from the Mediterranean Sea. They are sister species that cluster with G. armata, G. bursa-pastoris and G. longa in rbcL analyses with strong bootstrap support. Blades of G. multipartita taper towards the tips, whereas those of G. corallicolla have broadly rounded tips. Spermatangia of G. corallicola are borne in shallow conceptacles (textorii-type) and data from the literature indicate that the same is true of G. multipartita. Cystocarp morphology is similar, with the gonimoblast filaments initially elongated, narrow and densely filled with cytoplasm, and with tubular nutritive cells issuing initially from lower gonimoblast cells and fusing with cells in the lowermost regions of the outer pericarp. Tetrasporangia are initiated terminally and displaced laterally with the production of side branches from the subterminal cell. The diagnostic characters of the Gracilariaceae are reviewed from a developmental perspective.     

Sorellocolax stellaris gen. et sp. nov., a hemiparasitic alga (Delesseriaceae, Rhodophyta) from the east coast of Honshu, Japan

A hemiparasitic alga, Sorellocotax stellaris sp. nov. is described growing on plants of Sorella repens collected from Onagawa, Miyagi Prefecture, east coast of Honshu, Japan. The thallus is small, up to 2 mm high, once or twice branched from the margin. The growing apex has a transversely dividing apical cell, and intercalary cell divisions occur in the cells of first-order rows. Tetrasporangia are cut off from the cells of the inner cortex, The procarp is composed of a supporting cell, one group of sterile cells and two carpogonial branches. Carposporangia are borne in short chains.     

Dasya adela sp. nov. (Rhodophyta,Ceramiales), an enigmatic new Dasya from a landlocked fjord in southwest Norway

We here report a new Dasya species found in a landlocked fjord or poll in southwestern Norway; Dasya adela sp. nov. The thallus of this species is small (1–3 cm), normally sparsely branched, and its axes are completely covered with cortex cells. The species is set with long (3–4 mm) and flaccid monosiphonous pseudolaterals, and during autumn it showed high growth of adventitious monosiphonous branches. Only a few individuals with tetrasporangia have been recorded, and no sexual reproductive structures have been observed in field collections. In culture stichidia readily developed on the pseudolaterals, with four tetrasporangia per section. The spores showed high mortality. A few sporelings survived in culture, and developed into small and loosely organized filaments with no upright axes. After 2 years in culture a few plants bearing spermatangial branches were observed, but no individuals with carpogonia. The monosiphonous branches are readily shed in culture, attach themselves by rhizoids and rapidly develop into new thalli, some of which have produced tetrasporangial stichidia. Sequences analyses of partial COI and the rbc L gene showed that the new taxon belongs within Dasyoideae. However, no close relationship was found with other European species of Dasya. The new taxon was compared to other Dasya taxa with which it shared a number of selected characters, but none of these taxa shared all characters of the new Dasya.     

AUGOPHYLLUM,A NEW GENUS OF THE DELESSERIACEAE (RHODOPHYTA) BASED ON rbcL SEQUENCE ANALYSIS AND CYSTOCARP DEVELOPMENT1

A new genus, Augophyllum Lin, Fredericq et Hommersand gen. nov. related to Nitophyllum, tribe Nitophylleae, subfam. Nitophylloideae of the Delesseriaceae, is established to contain the type species Augophyllum wysorii Lin, Fredericq et Hommersand sp. nov. from Caribbean Panama; Augophyllum kentingii Lin, Fredericq et Hommersand sp. nov. from Taiwan; Augophyllum marginifructum (R. E. Norris et Wynne) Lin, Fredericq et Hommersand comb. nov. (Myriogramme marginifructa R. E. Norris et Wynne 1987) from South Africa, Tanzania, and the Sultanate of Oman; and Augophyllum delicatum (Millar) Lin, Fredericq et Hommersand comb. nov. (Nitophyllum delicatum Millar 1990 ) from southeastern Australia. Like Nitophyllum, Augophyllum is characterized by a diffuse meristematic region, the absence of macro‐ and microscopic veins, procarps consisting of a supporting cell bearing a slightly curved four‐celled carpogonial branch flanked laterally by a cover cell and a sterile cell, a branched multicellular sterile group after fertilization, absence of cell fusions between gonimoblast cells, and tetrasporangia transformed from multinucleate surface cells. Augophyllum differs from Nitophyllum by the blades becoming polystromatic inside the margins, often with a stipitate cylindrical base, the possession of aggregated discoid plastids neither linked by fine strands nor forming bead‐like branched chains, spermatangia and procarps initiated at the margins of blades, not diffuse, and a cystocarp composed of densely branched gonimoblast filaments borne on a conspicuous persistent auxiliary cell with an enlarged nucleus. Analyses of the rbcL gene support the separation of Augophyllum from Nitophyllum. An investigation of species attributed to Nitophyllum around the world is expected to reveal other taxa referable to Augophyllum.     

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.     

DIAPHORODENDRACEAE,FAM. NOV. (LYCOPSIDA: CARBONIFEROUS): SYSTEMATICS AND EVOLUTIONARY RELATIONSHIPS OF DIAPHORODENDRON AND SYNCHYSIDENDRON,GEN. NOV.

Synchysidendron, gen. nov., is segregated from Diaphorodendron DiMichele emend. Both genera are determinate, rhizomorphic, arborescent lycopsids that share identical reproductive organs but differ radically in growth architecture and consequently in the timing of reproduction. Cones in Synchysidendron (two species) are borne on late-formed crown branches; in Diaphorodendron (three species) cones are borne on deciduous lateral branches, produced over much of the life of the tree. The two genera also differ in several characteristics of the stele and periderm. We hypothesize that Diaphorodendron gave rise to Synchysidendron within their shared Late Carboniferous coal-swamp habitat, by heterochronic suppression of lateral branching during ontogeny. Together, these genera form a highly apomorphic clade, here recognized as the new family Diaphorodendraceae, that is distinguished primarily by siphonostelic axes, a bifacial periderm, distinctive megasporangia, and gulate megaspores.     

Molecular phylogeny and developmental studies of Apoglossum and Paraglossum (Delesseriaceae,Rhodophyta) with a description of Apoglosseae trib. nov.

Our morphological and molecular studies indicate that species from the southern hemisphere previously placed in Delesseria belong in Paraglossum and that Paraglossum and Apoglossum comprise a separate tribe, the Apoglosseae, S.-W. Lin, Fredericq & Hommersand, trib. nov., within the family Delesseriaceae. From a vegetative perspective the Apoglosseae is readily recognized because some or all fourth-order cell rows are formed on the inner sides of third-order cell rows. All fourth-order cell rows grow adaxially in Apoglossum, whereas both adaxial and abaxial cell rows are present in Paraglossum. Periaxial cells do not divide in Apoglossum, whereas they divide transversely in Paraglossum in the same way as in Delesseria. Major branches are formed mainly from the margins of midribs in the Apoglosseae. The procarp consists of a straight carpogonial branch and two sterile cells, with the second formed on the same side as the first. The carpogonium cuts off two connecting cells in tandem from its apical end, the terminal cell being nonfunctional and the subterminal cell typically fusing with the auxiliary cell. Gonimoblast filaments radiate in all directions from the gonimoblast initials and produce carposporangia terminally in branched chains, with pit connections between the inner gonimoblast cells broadening and enlarging. The auxiliary cell, supporting cell, and sterile cells unite into a fusion cell, which remains small in Apoglossum but incorporates the branched inner gonimoblast filaments and cells in the floor of the cystocarp in Paraglossum. Elongated inner cortical cells seen in mature cystocarps in the Delesserieae are absent in the Apoglosseae. Phylogenetic studies based on rbcL (RuBisCO large subunit gene) sequence analyses strongly support the recognition of the Apoglosseae within the subfamily Delesserioideae of the Delesseriaceae, in agreement with our previous observations based primarily on analyses of large subunit ribosomal DNA (LSU).     

THE SPORANGIUM OF HORNEOPHYTON LIGNIERI (RHYNIOPHYTINA)

Numerous sporangia of Horneophyton lignieri from the Rhynie Chert locality in Scotland have been studied. The sporangia are branched, with two to four columellate lobes of varying length, and a continuous sporogenous zone or cavity occurs among the lobes. Unbranched sporangia, generally thought to be the typical form for the plant have not been found, and their presence is not established. Although not definitely proven, evidence suggests that the sporangia opened by means of a small apical pore or stoma. An area of thick-walled cells at the apex of each sporangial lobe probably played some role in this opening. Radial, trilete, azonate spores ranging from 39–49 μm in diam, with curvaturae perfectae are produced most commonly in tetrahedral tetrads and occasionally in isobilateral tetrads. Matters of spore preservation and possible ornamentation are discussed. The branched sporangia of this genus are unique among bryophytes and vascular plants and provide some evidence that certain synangia may have arisen from a single sporangium rather than from multiple sporangia borne singly at the tips of ultimate branches.     

Comparative morphology and systematics of Chondrymenia lobata from the Mediterranean Sea and a phylogeny of the Chondrymeniaceae fam. nov. (Rhodophyta) based on rbcL sequence analyses

The Chondrymeniaceae Rodríguez-Prieto, G. Sartoni, S.-M. Lin & Hommersand, fam. nov., is proposed for Chondrymenia lobata. Analyses of rbcL sequences place the new family in a large gigartinalean assemblage that comprises the Cystocloniaceae–Solieriaceae complex. Plants are decumbent and growth takes place by division of multiple apical cells at the margin of the blade. Thalli consist of an outer cortex of subspherical to elongate cortical cells arranged in anticlinal rows, a subcortex of cells cross-linked by lateral arms, and a large central medulla composed of primary medullary filaments intermixed with numerous rhizoidal filaments. Male stages are reported in monoecious individuals. Inactive carpogonial branches consist of a two-celled filament that is directed inwards from the supporting cell. Functional carpogonial branches are oriented outwardly, with the carpogonia and trichogynes pointed towards the thallus surface. After presumed fertilization, the carpogonium fuses with the hypogynous cell and transfers the zygote nucleus. The hypogynous cell, in turn, fuses with the supporting cell which contains many haploid nuclei. The resulting fusion cell functions as an auxiliary cell that cuts off a single gonimoblast initial, which produces the gonimoblast filaments. Gametophytic cells close to the auxiliary cell unite with it to form a placental fusion network of variable size and outline, and a placental fusion cell. Proximal gonimoblast cells fuse with the placental fusion cell, while the distal cells differentiate into branched chains of subspherical carposporangia. The superficial similarity of the outwardly developed osteolate cystocarp is responsible for Kylin's (1956) placement of Chondrymenia in his family Sarcodiaceae; however, the manner in which the placenta is formed is more like that seen in the Cystocloniaceae–Solieriaceae complex.     

PHILLIPOPTERIS GEN. NOV.—ANATOMICALLY PRESERVED SPORANGIAL FRUCTIFICATIONS FROM THE UPPER PENNSYLVANIAN OF THE APPALACHIAN BASIN

The discovery of a new type of sporangial fructification in coal balls from the Upper Pennsylvanian of Ohio provides the basis for describing Phillipopteris globiformis gen. et sp. nov. Sporangia are borne terminally on up to two orders of branching axes. Penultimate axes branch pinnately to produce irregularly branched ultimate axes. Sporangial wall cells are of a single type and show no specialization for dehiscence. Spores are radial and trilete, and reminiscent of the sporae dispersae genus Dictyotriletes. Phillipopteris increases our knowledge of diversity among fernlike plants from the late Paleozoic, and shares several features with Sclerocelyphus Mamay.     

Dasya enomotoi sp. nov. (Dasyaceae,Ceramiales), a new large Dasya from Japan

A new red alga, Dasya enomotoi, is described from Japan. This species is characterized by having a large thallus consisting of an elongated axis and many, radially arranged, polysiphonous branches both of which are heavily corticated and densely covered with numerous, soft monosiphonous filaments. It is distinguished from several similar species by the combination of the following: (i) indistinct pericentral cells in transverse sections except near the apices, (ii) the presence of enlarged, inner cortical cells, (iii) radially arranged adventitious monosiphonous filaments, (iv) three‐celled carpogonial branches, (v) six (sometimes five) tetrasporangia in each fertile segment of the stichidia, and (vi) three tetrasporangial cover cells that are not elongated longitudinally and usually not divided transversely. This species may have been identified as D. villosa Harvey by previous investigators in Japan.