The relative contributions of diet and associated microbiota to the accumulation of UV‐absorbing mycosporine‐like amino acids in the freshwater copepod Boeckella antiqua

1. Mycosporine‐like amino acids (MAAs) are ubiquitous compounds in aquatic organisms that are usually considered sunscreens that protect them from harmful ultraviolet radiation. Given that virtually all animals lack the metabolic pathways to synthesise MAAs de novo, they must acquire them either from their diet or from microorganisms living in close association. In freshwater copepods, accumulation of MAAs is stimulated by exposure to ultraviolet and/or visible radiation. 2. A 2 × 2 factorial experiment was performed to assess the contributions of dietary and microbial sources of MAAs in the freshwater copepod Boeckella antiqua. The treatments consisted of two different diets: an MAA‐free diet, including only Chlamydomonas reinhardtii, and an MAA‐rich diet, including both C. reinhardtii and Peridinium inconspicuum, crossed with two antibiotic treatments, with and without chloramphenicol. Treatment with chloramphenicol was intended to inhibit the development of bacteria associated with the copepods. 3. MAA concentration in B. antiqua was affected by the experimental conditions: (i) exposure to artificial PAR + UVR stimulated the accumulation of several MAAs (up to 62% increase in total MAA concentration with respect to the initial concentration); (ii) the presence of chloramphenicol in the culture media reduced the MAA concentration in copepods fed an MAA‐free diet; (iii) in the absence of chloramphenicol, copepods fed the MAA‐rich diet had significantly higher total MAA concentration than those fed the MAA‐deficient diet; but (iv) dietary supplementation with an MAA‐rich algae in the presence of chloramphenicol failed to significantly increase total MAA concentration. 4. Analysis of profiles from denaturing gradient gel electrophoresis (DGGE) showed that the prokaryotic community associated with the copepods was affected by chloramphenicol. Dendograms constructed from digitalised DGGE images consistently grouped the antibiotics treatments separately from the initial samples and the treatments without antibiotics. Two band positions were exclusive to treatments without antibiotics. 5. We conclude that when offered an MAA‐rich diet, B. antiqua may accumulate a proportion of MAAs from diet. However, we suspect that in the absence of an MAA‐rich dietary source (as in its natural habitat), virtually all MAAs present in B. antiqua are produced by copepod‐associated prokaryotes.     

A world monograph of the lichen genus Gyalectidium (Gomphillaceae)

Seventeen new species of Gyalectidium have been discovered in various parts of the world, and those unexpected findings formed the starting point for a survey of the taxonomy and ecogeography of the genus. The following species are described as new in this paper: G. areolatum Ferraro & Lucking (Neotropics), G. atrosquamulatum Lucking & Kalb (Kenya), G . australe Lücking (Australia), G. conchiferum Lücking& Wirth (Chile), G. den-ticulatum Lücking (Costa Rica), G. fantasticum Ferraro & Lücking (Neotropics), G. flabellatum Sérus. (Australasia), G. fuscum Lücking & Sérus. (Africa and Papua New Guinea), G. gahavisukanum Sérus. (Papua New Guinea), G. kenyanum Lücking & Kalb (Kenya). G. laciniatum Lücking (Costa Rica), G. maracae Lücking (Neotropics), G. membranaceum Sérus. & Lücking (Canary Islands), G. minus Sérus (Canary Islands and southern Italy), G. novoguineense Sérus. (Australasia), G. puntilloi Sérus. (south-west Europe), and G. verruculosum Sérus. (Australasia). Calenia microcarpa Vzda [Syn.: Bullatina microcarpa (Vda) Brusse] is included in Gyalectidium as G. microcarpum (Vzda) Lücking, Sérus. & Vzda comb, nov., and G. catenulatum (Cavalc. & A. A. Silva) Ferraro, Lücking & Sérus. is treated as a species different from G. ftlicinum . Gyalectidium corticola Henssen is transferred to Calenia as Calenia corticola (Henssen) Ferraro, Lücking & Sérus. comb. nov. A key to all 29 accepted species of Gyalectidium is provided. The infrageneric phylogeny is constructed by means of a phenotype-based cladistic analysis, and the systematic affinities of the genus are discussed, accompanied by notes on the distribution and ecology of the species. Apothecia are not yet known in several species, including new ones.     

Chromosome numbers and meiotic studies in species of Senecio (Asteraceae) from Argentina

Meiotic chromosome counts, chromosomal behaviour and meiotic configurations of ten taxa of Senecio from Argentina were examined. Most counts are original: S. crepidifolius DC., S. francisci Phil. and S. octolepis Griseb. var. saltensis (Hicken) Cabrera & Zardini have 2 n  = 40, and S. chrysolepis Phil., 2 n  = 80 + 8B. We confirmed previous reports for S. deferens Griseb. (2 n  = 40 + 4B), S. filaginoides DC. var. filaginoides (2 n  = 40), S. hieronymi Griseb. (2 n  = 40 + 7B), S. pampeanus Cabrera (2 n  = 40) and S. rudbeckiifolius Meyen & Walp. (2 n  = 40 + 7B). In S. bracteolatus Hook. & Arn. var. bracteolatus , we found a new number (2 n  = 40) that differs from the one cited previously. In four species, numerical polymorphisms for B-chromosomes were observed. Several of the analysed species presented secondary bivalent association. This phenomenon, together with other evidence, supports x  = 5 as the basic chromosome number. The number of chiasmata and their positions were also surveyed, with the finding that open bivalents were the most frequent meiotic figures and terminal chiasmata the preferential position. These features are related to recombination rate, and the success and persistence of these polyploids. We discuss some systematic and evolutionary aspects in the light of cytogenetic data and conclude that polyploidy is the major force modelling the chromosome evolution within this genus.  © 2005 The Linnean Society of London, Botanical Journal of the Linnean Society , 2005, 148 , 465–474.     

New chromosome reports in the subtribes Diocleinae and Glycininae (Phaseoleae: Papilionoideae: Fabaceae)

The base chromosome number of x = 11 is the most probable in all the subtribes included in tribe Phaseoleae, although some aneuploid reduction is evident in Collaea and Galactia (Diocleinae) and chromosome duplications are seen in Amphicarpaea, Cologania and Glycine (Glycininae). The aims of this study were to improve the cytological knowledge of some species of Collaea and Galactia and to examine the anomalous counts reported for Calopogonium (Glycininae) and verify its taxonomic position. In addition, a molecular phylogeny was constructed using nuclear ribosomal DNA sequences (internal transcribed spacer region), and the chromosome number was optimized on the topology. In this work, the chromosome counts for Galactia lindenii, Galactia decumbens and Collaea cipoensis (all 2n = 20), and Calopogonium sericeum (2n = 22) are reported for the first time. The new reports for Galactia and Collaea species are in agreement with the chromosome number proposed for subtribe Diocleinae. The study rejects the concept of a cytologically anomalous Calopogonium and, based on the phylogenetic analysis, corroborates the position of this genus within subtribe Glycininae. The ancestral basic chromosome number of x = 11 proposed for Phaseoleae is in agreement with the evolutionary pathway of chromosome numbers analysed in this work. © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society, 2008, 158 , 336–341.     

The Effects of Bacterial Endotoxin on the Infection of Mice with Trypanosoma cruzi*

Mice (Rockland strain) infected with Trypanosoma cruzi strain Tulahuén were treated with Escherichia coli endotoxin before, simultaneously with, and after inoculation of the parasites. The peak parasitemias of endotoxin-treated mice were higher than those of nontreated infected animals, regardless of the time of endotoxin administration. Peak parasitemias occurred at the same time in infected nontreated mice as in animals given endotoxin before or simultaneously with the trypanosomes. If endotoxin was administered 24 hr after the infection, a delay in the peak parasitemia was noted. Changes in the survival time were not observed unless endotoxin was given 24 hr postinfection. Infected mice had an increasing susceptibility to the lethal effect of endotoxin. The LD₅₀ of endotoxin decreased from 675 μg for normal mice to 230, 92, and 18 μg for infected animals 1, 3, and 8 days after the infection, respectively. In the infected mice, the endotoxin-detoxifying ability of the spleen was found to be impaired.