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Phylogenetic relationships and the timing of evolutionary events are essential for understanding evolution on longer time scales. Cheilostome bryozoans are a group of ubiquitous, species-rich, marine colonial organisms with an excellent fossil record but lack phylogenetic relationships inferred from molecular data. We present genome-skimmed data for 395 cheilostomes and combine these with 315 published sequences to infer relationships and the timing of key events among c. 500 cheilostome species. We find that named cheilostome genera and species are phylogenetically coherent, rendering fossil or contemporary specimens readily delimited using only skeletal morphology. Our phylogeny shows that parental care in the form of brooding evolved several times independently but was never lost in cheilostomes. Our fossil calibration, robust to varied assumptions, indicates that the cheilostome lineage and parental care therein could have Paleozoic origins, much older than the first known fossil record of cheilostomes in the Late Jurassic.

Background: Understanding the phylogenetic relationships among species is one of the main goals of systematic biology. Simultaneously, credible phylogenetic hypotheses are often the first requirement for unveiling the evolutionary history of traits and for modelling macroevolutionary processes. However, many non-model taxa have not yet been sequenced to an extent such that statistically well-supported molecular phylogenies can be constructed for these purposes. Here, we use a genome-skimming approach to extract sequence information for 15 mitochondrial and 2 ribosomal operon genes from the cheilostome bryozoan family, Adeonidae, Busk, 1884, whose current systematics is based purely on morphological traits. The members of the Adeonidae are, like all cheilostome bryozoans, benthic, colonial, marine organisms. Adeonids are also geographically widely-distributed, often locally common, and are sometimes important habitat-builders., Results: We successfully genome-skimmed 35 adeonid colonies representing 6 genera (Adeona, Adeonellopsis, Bracebridgia, Adeonella, Laminopora and Cucullipora). We also contributed 16 new, circularised mitochondrial genomes to the eight previously published for cheilostome bryozoans. Using the aforementioned mitochondrial and ribosomal genes, we inferred the relationships among these 35 samples. Contrary to some previous suggestions, the Adeonidae is a robustly supported monophyletic clade. However, the genera Adeonella and Laminopora are in need of revision: Adeonella is polyphyletic and Laminopora paraphyletically forms a clade with some Adeonella species. Additionally, we assign a sequence clustering identity using cox1 barcoding region of 99% at the species and 83% at the genus level., Conclusions: We provide sequence data, obtained via genome-skimming, that greatly increases the resolution of the phylogenetic relationships within the adeonids. We present a highly-supported topology based on 17 genes and substantially increase availability of circularised cheilostome mitochondrial genomes, and highlight how we can extend our pipeline to other bryozoans.

Three new species of lanceoporids from the southern Great Barrier Reef are described. Calyptotheca trimandibulata n. sp. is recorded from inter-reefal sites, Stephanotheca bahloo n. sp. is recorded from a coral reef site, and Stephanotheca kutyeri n. sp. is recorded from inter-reefal sites and also Bass Strait and the Great Australian Bight, and is therefore unusual amongst Australian lanceoporids in occurring in both tropical and temperate locations. The known variation in morphological characters is widened for both genera: C. trimandibulata n. sp. is the only known Calyptotheca species typically having three adventitious avicularia per zooid, S. bahloo n. sp. has the most pronounced orifice dimorphism and the most transversely oval primary orifice for the genus, and S. kutyeri n. sp. is distinguished by long, narrow, slit-like pseudopores in the frontal shield. All three species have occasional dimorphic autozooids, distinguished by larger orifices resembling those of the respective ovicellate zooids, and this is documented for the first time for both genera.

The cheilostome bryozoans Calyptotheca wulguru n. sp. and Calyptotheca tilbrooki n. sp. (Lanceoporidae) are described from inter-reefal, sediment-dominated habitats of the Great Barrier Reef, and Calyptotheca churro n. sp. was washed up on a Heron Island beach, with uncertain origin. Calyptotheca wulguru n. sp. and C. churro n. sp. belong to a subgroup of Calyptotheca species with numerous small, oval, marginal adventitious avicularia and suboral nodular thickening or umbones. The vicarious avicularia of C. tilbrooki n. sp. are elongate-oval, unlike those of other known Calyptotheca species, and C. tilbrooki n. sp. has more pronounced orificial dimorphism than in any other known Calyptotheca species. Calyptotheca churro n. sp. has the most pronounced suboral umbo of all known Calyptotheca species. This study increases the known Calyptotheca species of the Great Barrier Reef to ten, and of tropical Australia to 14.

Two new species of Stephanotheca are described from the southeast Gulf of Carpentaria, northern Australia, providing the first tropical records of this genus. Stephanotheca ipsum n. sp. is provisionally placed in the genus on the basis of a low ridge of calcification around the edge of the ooecium, which differs from the fully pseudoporous ooecium of Calyptotheca (Lanceoporidae) and resembles the 'crowned' ooecium of Stephanotheca, with a central porous area surrounded by a nodular imperforate area. Stephanotheca ipsum and Stephanotheca romajoyae n. sp. are the only species in the genus with more than one avicularium on some zooids. The latter species is distinguished by high variability in avicularium size, shape, position and orientation; it also shares dimorphic avicularia with S. ochracea (Hincks) and is the only species in which they sometimes occur together on the same zooid. This study increases the number of Australian Stephanotheca species to four. The Australian species all have smaller primary orifices and variations in ovicell morphology compared with other, all European, species. In S. ipsum n. sp. the ooecia are ridged, those of S. victoriensis Reverter-Gil et al. have a single row of pseudopores forming an arch, and those of S. ambita (Waters) and S. romajoyae n. sp. have a relatively large pseudoporous area and smaller, lower nodular imperforate area. None of the Australian species have vicarious avicularia, which are known only from the type species, S. barrosoi Reverter-Gil et al.

Onychatrium gen. nov. is described, with five included species: Onychatrium forceps sp. nov., the type species and Onychatrium torosus sp. nov., both from the Great Barrier Reef; Onychatrium entale (Nordenstam, 1946) comb. nov., from Tapateuen (= Tabiteue Island), Gilbert Islands; Onychatrium thomasi (Bolstad & Kensley, 1999) comb. nov., from Madang, Papua New Guinea; and Onychatrium echiurum (Nobili, 1906) comb. nov., and species inquirenda from the Tumaotu Islands, Eastern French Polynesia. The primary distinguishing characters for Onychatrium gen. nov. are a trapezoid pseudosrostrum, the male pereopod 1 with elongate dactylus (4.7-7.3 as long as proximal width), propodus with strongly produced and acute lobe, carpus with a distally acute, flat, ventrally directed process (except O. torosus sp. nov., which has a short and truncate process) and the merus with a distally directed inferodistal lobe. The genus is known only from the southern Pacific, from the Tuamotus (eastern French Polynesia) to the Great Barrier Reef and northern Papua New Guinea.

A new diagnosis is presented for Calyptotheca Harmer, 1957 and six species are described from the Gulf of Carpentaria: C. wasinensis (Waters, 1913) (type species), C. australis (Haswell, 1880), C. conica Cook, 1965 (with a redescription of the holotype), C. tenuata Harmer, 1957, C. triquetra (Harmer, 1957) and C. lardil n. sp. These are the first records of Bryozoa from the Gulf of Carpentaria, and the first Australian records for C. wasinensis, C. tenuata and C. triquetra. The limit of distribution of three species is extended east to the Gulf of Carpentaria, from Kenya for C. wasinensis, from China for C. tenuata, and from northwestern Australia for C. conica. The number of tropical Calyptotheca species in Australian territorial waters is increased from seven to eleven.

Infection with the Hepatitis C virus (HCV) has been aetiologically linked with the lymphoproliferative disorder mixed cryoglobulinaemia and more recently with certain subgroups of B cell non-Hodgkin's lymphoma (NHL). Many of the studies which have documented the association with NHL have originated from Italy, where the background prevalence of infection with the virus is relatively high. We have performed a study, based in the West of Scotland, to determine the prevalence of infection with HCV in an unselected group of 110 individuals with lymphoproliferative disorders (72 with NHL, and 38 with chronic lymphocytic leukaemia). None of our cohort (both NHL and CLL) had evidence of infection with the virus. Our study suggests that whilst HCV may be important in the aetiology of certain subgroups of NHL, this effect may be regional and dependent upon the background prevalence of the virus in the community.

Aluminium balance studies were carried out on eight patients with various immunological disorders who were receiving plasma exchange with albumin solutions known to be contaminated with aluminium. Four patients with impaired renal function (creatinine clearance less than 50 ml/min) retained between 60% and 74% of the aluminium infused during a single plasma exchange. Transiliac bone biopsy specimens from three patients in this group had a high content of aluminium and showed histological evidence of current or previous bone disease related to aluminium. Two of these patients suffered intermittent bone pain. The main route of excretion of injected aluminium was in urine, only a small proportion of the total input being removed in the "plasma bag" during plasma exchange. The extent of aluminium retention and bone deposition was not reflected by the plasma aluminium concentration before or after plasma exchange. Treatment of five patients with intravenous desferrioxamine increased the plasma aluminium concentration and urinary output of aluminium in those with evidence of aluminium retention. These studies show that patients with poor renal function receiving treatment with albumin contaminated with aluminium retain the metal and deposit it in bone, where it may eventually cause aluminium bone disease. Plasma exchange should be used with caution in patients with renal impairment.

A 39 year old man who presented with classical Henoch-Schönlein purpura was shown to have mediastinal nodular sclerosing Hodgkin's lymphoma. The Henoch-Schönlein purpura resolved after treatment of the lymphoma.

Studies of iron metabolism were made in 24 patients following surgery under general anaesthesia. No postoperative complications occurred. There was a marked fall in serum iron in all patients on the first postoperative day (P less than 0.001) which remained significantly depressed even at the seventh postoperative day. The total iron binding capacity fell progressively to reach the lowest levels on the third postoperative day, returning to normal levels by the end of the study. Serum ferritin concentration rose significantly in a reciprocal pattern to the changes in serum iron. This study highlights the limitation of iron studies in peripheral blood in postoperative patients.

Hairy cell leukaemia affecting primarily the spleen is a very rare feature of this disease at presentation. Splenectomy in such cases would seem to provide a cure. We report a case of primary splenic hairy cell leukaemia in which clinical and haematological remission were achieved after splenectomy, and we review the literature.

An association linking multiple myeloma with a higher incidence of carcinomatous tumours has been reported. The following case report describes a man diagnosed as having bronchogenic carcinoma found also to have myelomatosis. Aspects of this association are discussed.

1. The mechanism of the stimulation of ferritin synthesis by iron in vivo has been studied in rat liver. Ferritin synthesis and turnover was measured by [(14)C]leucine incorporation. 2. Actinomycin D had no inhibitory effect, after administration of iron, on [(14)C]leucine incorporation into ferritin but appeared to augment the effect of iron on ferritin synthesis. 3. Cycloheximide completely abolished the stimulation by iron of [(14)C]leucine into ferritin and was subsequently utilized to show that iron acts in vivo by translational induction of apoferritin synthesis, rather than by stabilization of apoferritin or its precursors. 4. This conclusion was confirmed by showing that 2 days after acute bleeding, when iron was in the process of being removed from hepatic ferritin stores, ferritin synthesis was decreased whereas breakdown rates were unchanged.

1. Ferritin was isolated from human and horse spleen and liver, and apoferritin prepared therefrom. 2. The electrophoretic mobilities of the four apoferritins were determined on polyacrylamide gels and on cellulose acetate strips, and all found to be equal. 3. Homologous ferritins share reactions of identity in immunodiffusion experiments, whereas heterologous ferritins show only partial identity. 4. The subunit molecular weight of each of the apoferritins was determined by polyacrylamide-gel electrophoresis in sodium dodecyl sulphate and by chromatography on agarose columns in 6m-guanidine-HCl. A value of approx. 18500 was found in all cases. The proteins all had sedimentation coefficients of 17-18S. It thus seems that they have identical quaternary structures. 5. The amino acid compositions of the proteins revealed distinct differences both between organs and between species. This was confirmed by analysis of the tryptic peptide patterns, where it was found that about one-third of the peptides were common to the four proteins and the other two-thirds varied from protein to protein. 6. It is concluded that the apoferritins present in the liver and spleen of human and horse are both organ- and species-specific. 7. The apoferritin isolated from the liver of a patient with idiopathic haemochromatosis was identical with normal human liver apoferritin by the criteria described above.