Marine Flora and Fauna of the Northeastern United States: Erect Bryozoa

Forty-nine species of erect Bryozoa from a broad range of Cyclostome, Ctenostome, and Cheilostome families are described and illustrated, and an artificial dichotomous key is provided for their identification. In general, the marine bryozoan faunas of the northeastern coasts of the United States are poorly known; species records are sparse and voucher collections few, and it is certain that many more species occur in this region than are presently known. The species described here occur in intertidal, coastal or offshore habitats; some are well known and have been recorded on numerous previous occasions, others have been only rarely reported, while a few are known to occur commonly in the north of the region but have yet to be recorded south of Cape Cod. Some of the species described have not been recorded at all on northeastern coasts of the United States, but are widely distributed in North Atlantic continental shelf habitats and perhaps occur in similar parts of the outer shelf of this region. This fauna is thus provisional, but is intended to stimulate further work on the Bryozoa. (PDF file contains 52 pages.)

The effects of infection by Tetracapsuloides bryosalmonae (Myxozoa) and temperature on Fredericella sultana (Bryozoa)

The myxozoan, Tetracapsuloides bryosalmonae, exploits freshwater bryozoans as definitive hosts, occurring as cryptic stages in bryozoan colonies during covert infections and as spore-forming sacs during overt infections. Spores released from sacs are infective to salmonid fish, causing the devastating Proliferative Kidney Disease (PKD). We undertook laboratory studies using mesocosm systems running at 10, 14 and 20 degrees C to determine how infection by T bryosalmonae and water temperature influence fitness of one of its most important bryozoan hosts, Fredericella sultana, over a period of 4 weeks. The effects of infection were context-dependent and often undetectable. Covert infections appear to pose very low energetic costs. Thus, we found that growth of covertly infected F. sultana colonies was similar to that of uninfected colonies regardless of temperature, as was the propensity to produce dormant resting stages (statoblasts). Production of statoblasts, however, was associated with decreased growth. Overt infections imposed greater effects on correlates of host fitness by: (i) reducing growth rates at the two higher temperatures: (ii) increasing mortality rates at the highest temperature: (iii) inhibiting statoblast production. Our results indicate that parasitism should have a relatively small effect on host fitness in the field as the negative effects of infection were mainly expressed in environmentally extreme conditions (20 degrees C for 4 weeks). The generally low virulence of T. bryosalmonae is similar to that recently demonstrated for another myxozoan endoparasite of freshwater bryozoans. The unique opportunity for extensive vertical transmission in these colonial invertebrate hosts couples the reproductive interests of host and parasite and may well give rise to the low virulence that characterises these systems. Our study implies that climate change can be expected to exacerbate PKD outbreaks and increase the geographic range of PKD as a result of the combined responses of T. bryosalmonae and its bryozoan hosts to higher temperatures. Crown Copyright (C) 2009 Published by Elsevier Ltd. All rights reserved.

Ultrastructure of Buddenbrockia allmani n sp (Myxozoa, Malacosporea), a parasite of Lophopus crystallinus (Bryozoa, Phylactolaemata)

Development of a new species of malacosporean myxozoan (Buddenbrockia allmani n. sp.) in the bryozoan Lophopus crystallinus is described. Early stages, represented by isolated cells or small groups, were observed in the host's body wall or body cavity. Multiplication and rearrangement of cells gave an outer cell layer around a central mass. The outer cells made contact by filopodia and established adherens junctions. Sporoplasmosomes were a notable feature of early stages, but these were lost in subsequent development. Typical malacosporean sacs were formed from these groups by attachment of the inner (luminal) cells by a basal lamina to the outer layer (mural cells). Division of luminal cells gave rise to a population of cells that was liberated into the lumen of the sac. Mitotic spindles in open mitosis and prophase stages of meiosis were observed in luminal cells. Centrioles were absent. Detached luminal cells assembled to form spores with four polar capsules and several valve cells surrounding two sporoplasms with secondary cells. Restoration of sporoplasmosomes occurred in primary sporoplasms. A second type of sac was observed with highly irregular mural cells and stellate luminal cells. A radially striated layer and dense granules in the polar capsule wall, and previous data on 18 rDNA sequences enabled assignment of the species to the genus Buddenbrockia, while specific diagnosis relied on the rDNA data and on sac shape and size.

Plumatella geimermassardi, a newly recognized freshwater bryozoan from Britain, Ireland, and continental Europe (Bryozoa : Phylactolaemata)

Plumatella geimermassardi is a newly recognized species of phylactolaemate bryozoan. Its known range extends from Ireland east through southern Norway and south into Italy. Colonies grow close to the substrate with little free branching; the body wall is mostly transparent and without an obvious raphe. Floatoblasts are broadly oval and relatively small, with distinctively large dorsal fenestra and uniformly narrow ventral annulus. The sessoblast basal valve is low and dish-shaped; the annulus bears tubercles which vary in their prominence. This species brings to 14 the number of phylactolaemate bryozoans known in the region.

New and little-known cheilostomatous Bryozoa from the south and southeastern Brazilian continental shelf and slope

The present paper reports on 22 species collected by the Brazilian Program of Living Resources in the Exclusive Economic Zone (REVIZEE). A new genus and species of Cribrilinidae, Corbuliporina crepida n. gen. et sp., is described, along with seventeen other new species: Chaperia brasiliensis n. sp., Amastigia aviculifera n. sp., Isosecuriflustra pinniformis n. sp., Cellaria subtropicalis n. sp., Melicerita brasiliensis n. sp., Arachnopusia haywardi n. sp., Smittina migottoi n. sp., Hippomenella amaralae n. sp., Rogicka joannae n. sp., Malakosaria atlantica n. sp., Turbicellepora winstonae n. sp., Rhynchozoon coalitum n. sp., Stephanollona angusta n. sp., Stephanollona arborescens n. sp., Aulopocella americana n. sp., Conescharellina cookae n. sp. and Conescharellina bocki n. sp. Chorizopora brongniartii (Audouin, 1826) is recorded for the first time in Brazilian waters and a new combination for Rhynchozoon arborescens Canu & Bassler, 1928 is established. New illustrations and taxonomic remarks are included for two little-known species from Brazil, Rogicka scopae (Canu & Bassler, 1928) and Fenestrulina ampla Canu & Bassler, 1928. A compilation of species recorded from deeper waters of the Brazilian coast is included.

A review of Australian Siphonicytara Busk (Bryozoa : Cheilostomatida)

Until recently, species of the deep-water ascophoran genus Siphonicytara have been recorded from only two areas, nearly 10,000 km apart. Three species were known from the East Indies and one from the southwest Indian Ocean. A hitherto unrecognized species is now known from the southern-most Philippine region, and six new species have recently been described from New Caledonia. A further new species from relatively shallow water, S. occidentalis, is described here from Western Australia. Examination of fossil specimens from the Tertiary of Victoria and South Australia has shown that specimens attributed to Parina clypeata Waters have a close relationship with Siphonicytara, and the species is referred here to this genus, as is Mucronella airensis Maplestone. Another Tertiary species with a similar distribution, 'Eschara elevata' Waters not Tenison Woods, is assigned to Siphonicytara irregularis (Maplestone). The stratigraphic range for the family extends from the Late Eocene to Recent. Eschara elevata Tenison Woods sensu stricto is the type species of the genus Tubitrabecularia Bassler, and a discussion of the nature and status of this genus is included. A key to the species described is given.

Calescharidae, a new family for the Tertiary to Recent Genera Caleschara MacGillivray and Tretosina Canu and Bassler (Bryozoa: Cheilostomata)

A new family of Cheilostomata, the Calescharidae, is introduced for the genus Caleschara MacGillivray and its Recent Australian typespecies, C. denticulata(MacGillivray), which is redefined from type and other material. The Australian Tertiary genus Tretosina Canu & Bassler and its type species,T. arcifera Canu & Bassler, are closely related,and are also assigned to the Calescharidae. The history and significance of family attributions of both genera are outlined, and RecentC. denticulata from Australian and other localities is distinguished from the Late Tertiary Victorian species C. parva Maplestone. Caleschara lithconis, sp. nov., from the Late Eocene of Victoria is one of the earliest known species: its morphology closely resembles a Recent form from the Philippines, C. junctifera Canu & Bassler. Another Recent species, Caleschara minuta (Maplestone) from the GilbertIslands, is a senior synonym of three other Indo-Pacific species,C. levinseni Harmer, C. laxa Canu & Bassler and Floridinella arculifera Canu & Bassler, and resembles the European Paleocene C. squamosa. Three other related species are briefly discussed. Close relationships to other families are problematic and are discussed; divergence in the early history of the cheilostomes is inferred.

Revision of tertiary species of Anaskopora Wass (Bryozoa: Cribrimorpha)

The subgenus Anaskopora Wass, 1975 is raised to generic rank, separated from the genus Corbulipora, and redefined. The type species, Cribrilina elevata MacGillivray, 1895, is a Tertiary fossil from Victoria with small globular colonies formed principally by a special kind of interzooidal frontal budding. Other Tertiary fossil species with a similar colony structure, here assigned to Anaskopora, are Cribrilma cornuta MacGIllIvray, 1895 and Lepralia rotundata MacGillivray, 1895. Two further new Tertiary species, A. simplex and A. mesa, from Victoria and South Australia have small encrusting colonies. A key to species is given.

Revision of the multiphased genus Corbulipora MacGillivray (Bryozoa: Cribrimorpha)

Corbulipora MacGillivray is redefined to include only species which occur in successive growth phases. The fossil type species, Corbulipora ornata MacGillivray, occurs in an encrusting ancestrulate phase, an erect quadriserial, ovicellate phase, and a frontally-budded partially kenozooidal phase. The encrusting ancestrulate phase of the Recent species, C tubulifera (Hincks), is the type species of the genus Acanthocella Canu and Bassler, which is a junior synonym of Corbulipora. The succeeding, ovicellate, flustrine phase, known as Watersia militaris (Waters), is the type species of Watersia, another junior synonym of Corbulipora. It produces a third bilaminar phase known as C. oriparma, a synonym of C. tubulifera. This has rhizoids and develops further flustrine phases. Fossil specimens assigned to Acanthocella tubulifera in the past are here considered to be the primary encrusting phase of a bilaminar phase, known as Corbuhpora suggerens (Waters). from which it has become separated. A thinly calcified intervening erect phase similar to the flustrine phase of C. tubulifera IS inferred to have existed but not to have been preserved as a fossil. Some species previously referred to Watersia are assigned to Klugeflustra Moyano which, like Neoflustra Lopez Gappa, has flustrine colomes with large, hyperstomial ovicells, unlike those of the family Flustridae sensu stricto. A key to species of Corbulipora and their various phases is given.

First fossil finds of some Australian Bryozoa (Cheilostomata)

The abundant fossil record of well-preserved Bryozoa in samples from the Tertiary of Victoria and South Australia includes some 'first fossil finds' which are recorded here. Several are of species known from the Recent of the Australian or Indo-West-Pacific regions, but some represent genera with a much wider temporal and geographical range. Of the 11 species illustrated, six are known, or may be inferred, to have inhabited 'sand fauna' environments. Specimens of one species are complete enough to allow its formal description as Chlidoniopsis inopina sp. nov.

Dimorphic brooding zooids in the genus Adeona Lamouroux from Australia (Bryozoa: Cheilostomata)

The genus Adeona is a characteristic and common part of the Australian shelf fauna, extending to the tropical Indo-West Pacific. The genus first appears in the fossil record of the Miocene of south-eastern Australia. Zooid dimorphism has been recognised initially from subtle differences in the external appearance, which have not been described previously. Detailed examination has shown enlarged brooding zooids with marked differences from autozooids in the internal structure of the peristomes and in the occurrence of a primary calcified orifice.

A review of Australian Conescharellinidae (Bryozoa : Cheilostomata)

The family Conescharellinidae Levinsen is defined and is regarded as comprising seven cheilostome genera (Conescharellina, Bipora, Trochosodon, Flabellopora, Zeuglopora, Crucescharellina and Ptoboroa). The astogeny of colonies, that consists of frontally budded zooids with "reversed" orientation, is briefly described and compared between genera. The morphology of zooids and heterozooids is defined and keys to genera and Australian species are provided. Taxa that were first described from Australia or from reliable subsequent records are redescribed and illustrated where possible. Australian specimens that have been identified as non-Australian species, have generally been found to be distinct and are here redescribed as new species. Some non-Australian records of specimens previously assigned to Australian species have also been re-examined. These are described and sometimes referred to other taxa. Altogether, eight previously described species that have not been found in the present material are discussed and 27 taxa are described from collections, principally from the eastern and southern coasts of Australia and from the Tertiary of Victoria. Eighteen of these are considered to be new species. Where possible, type or at least topotype material of previously described species has been examined. Colonies from the collections of Museum Victoria (NMV) and the Natural History Museum, London (BMNH), have been examined. New species from Australia described here are: Conescharellina cognata, C. ecstasis, C. diffusa, C. obscura, C. stellata, C. plana, C. perculta, C. pustulosa, C. ocellata, C. macgillivrayi, C. humerus; Trochosodon fecundus, T. asymmetricus, T. diommatus, T. aster, T. anomalus, T. praecox and Crucescharellina australis. In addition, the New Zealand bryozoan Trochosodon multiarmatus (Gordon, 1989) (not Bipora multiarmata Maplestone, 1909) is described as Trochosodon gordoni sp. nov.