d-Pinitol as a key oviposition stimulant for sulfur butterfly, Colias erate: chemical basis for female acceptance of host- and non-host plants

The sulfur butterfly, Colias erate, utilizes various legumes as host plants. We examined the chemical constituents of its primary host plant, Trifolium repens (white clover), to identify phytochemicals inducing oviposition by C. erate females. Since one of the four aqueous subfractions prepared from a methanolic extract of the plant has previously been shown to be the most responsible for the oviposition-stimulatory activity exerted by the plant, chemical analyses were conducted of the fraction concerned. Activity-directed fractionation of the subfraction by ion-exchange chromatography revealed that the key substance(s) resided in the neutral fraction. Preparative TLC of the neutral fraction and subsequent spectral analyses identified d-(+)-pinitol, glycerin, methyl β-d-glucoside, and myo-inositol as characteristic components together with ubiquitous sugars (e.g., sucrose and glucose). Of these, only pinitol singly evoked significant oviposition responses at concentrations over 0.05%. In dual-choice bioassays, however, females laid significantly more eggs on pinitol solutions admixed with glycerin or methyl β-d-glucoside than on pinitol alone. Two cyanoglucosides, linamarin, and lotaustralin, occurring in the other aqueous subfractions, also synergistically increased the oviposition response in combination with pinitol. The results clearly indicated that pinitol is a crucial oviposition stimulant involved in host recognition, while glycerin, methyl β-d-glucoside, linamarin, and lotaustralin function as synergists. We further examined the oviposition responses of C. erate females to aqueous fractions, along with their chemical compositions, that had been prepared from five other host plants and a non-host plant, Aristolochia debilis (Aristolochiaceae), on which oviposition occasionally took place in an outdoor cage during the experiments. The plant species accepted by ovipositing females were all found to contain pinitol in amounts enough to induce egg laying by the butterfly, thus leading to the conclusion that pinitol serves as the essential mediator in recognizing and accepting potential host plants.     

N-acyl homoserine lactone production by bacteria within the sponge Suberites domuncula (Olivi, 1792) (Porifera, Demospongiae)

Many bacteria live in close association with sponges. Within these consortia, molecules of communication such as quorum-sensing and hormone-like molecules may occur in order to regulate the partnership. Of particular interest, bacterial N-acyl-l-homoserine lactones (AHLs) were screened in supernatants from Suberites domuncula-associated bacteria using an E. coli bioluminescent reporter system. These sponge-associated bacteria were beforehand isolated on several media supplemented or not with a sponge extract to attempt to isolate sponge-specific bacteria. Out of 81 AHL-producing bacteria, three strains requiring sponge extract to grow were selected for AHL characterization. The in vitro produced AHLs, that is, in bacterial culture supernatants, were identified as N-(3-butanoyl)-l-homoserine lactone and N-(3-oxododecanoyl)-l-homoserine lactone and quantified using LC–ESI–MS/MS. The in vivo production of AHLs by sponge-associated bacteria has also been demonstrated in a healthy host for the first time: N-(3-oxododecanoyl)-l-homoserine lactone, N-(3-hexanoyl)-l-homoserine lactone, and N-(3-heptanoyl)-l-homoserine lactone. This AHL production in sponges may suggest a potential role of these molecules between sponge-associated bacteria and/or between sponge-associated bacteria and the sponge.     

Two distinct forms of the chitin-degrading enzyme N-acetyl-β-d-glucosaminidase in the Antarctic krill: specialists in digestion and moult

In the Antarctic krill Euphausia superba two forms of the chitinolytic enzyme N-acetyl-β-d-glucosaminidase (NAGase, EC 3.2.1.52) have been described, previously identified as NAGase B and NAGase C. Here, we demonstrate the organ-specific distribution and physiological relevance of both forms using a polyclonal antibody preparation which allows them to be distinguished immunologically. While NAGase B was localized in the integument and displayed a pattern of activity related to the moult cycle, the activity of NAGase C was independent of the moult cycle and was predominantly found in the gastrointestinal tract. Accordingly, NAGase B played a significant role in chitin degradation during the krill's moult, whereas NAGase C participated in the digestion of chitin-containing dietary components. Chromatographic elution profiles of isolated organs confirmed the immunological results by displaying characteristic organ-specific patterns in NAGase activity. The molecular characteristics of the moulting form, NAGase B, may further indicate a vesicular transport of moulting enzymes from the epidermis into the ecdysial space. Based on our results we develop a hypothesis explaining the concurrent processes of simultaneous chitin degradation and chitin synthesis occurring during moult. Received: 30 December 1998 / Accepted: 23 April 1999     

Histochemical demonstration of a glycocalyx on the cell surface of Heterosigma akashiwo

In an attempt to clarify the surface structure of Heterosigma akashiwo, the organisms were processed by a series of currently utilized methods for carbohydrate and protein histochemistry of light microscopy. The results indicated that: (1) H. akashiwo cell has previously undetected glycocalyx on the cell surface; (2) this extracellular structure consists of at least two different types of acidic complex carbohydrates, sulfated and non-sulfated, together with a neutral carbohydrate-protein complex with 1,2-glycol groups and -d-mannosyl and -d-glucosyl residues; (3) a particular moiety of acidic complex carbohydrates involved in the glycocalyx is presumably hyaluronic acid or a closely related substance; and (4) the histochemical nature of the glycocalyx on the cell surface of the present species is comparable with that of Chattonella antiqua, excluding a difference in the nature of the neutral carbohydrate-protein complex.     

Location of toxicity within the Mediterranean sponge Crambe crambe (Demospongiae: Poecilosclerida)

Within-specimen location of toxicity in Crambe crambe (Schmidt) has been addressed by complementary procedures on specimens collected in north-east Spain (Western Mediterranean) in winter of 1993. The toxicity of the distal (ectosome) and basal (choanosome) sponge parts have been analysed and the main cellular types present in these two layers have been studied by light and electron microscopy. The toxicity of the three main cell types, separated by the gradient-density method, has also been analysed. Three main fractions, each of them enriched in a different cellular type, were obtained: Fraction 1 (interface between 2 and 5% Ficoll) contained 90±0.9% (mean±SE) of spherulous cells and 10% of different cell types consisting of choanocytes (5±0.54%), and unidentified cells or cell debris (5±0.84%); Fraction 2 (interface between 5 and 8% Ficoll) was enriched in choanocytes (70±0.95%), and also contained spherulous cells (11.8±0.73%), archeocytes (6.2±0.74%) and unidentified sponge cells (12±0.74%); Fraction 3 (interface between 8 and 11% Ficoll) mainly consisted of archeocytes and archeocyte-like cells (75±0.66%), together with spherulous cells (7±0.74%) and other unidentified sponge cells and cell aggregates mainly formed by choanocytes (18±0.41%). Toxicity [measured in toxicity units, TU, using the Microtox^® procedure] was significantly higher in the sponge ectosome (12.45±1.4 TU) than in the choanosome (2.58±0.92 UT). Only the abundance of spherulous cells in the sponge tissues correlated well with the pattern of toxicity observed, and this was corroborated by the toxic behaviour of the three cellular fractions obtained: the one enriched in spherulous cells was highly toxic (9.08 UT), whereas those enriched in choanocytes and in archeocytes were almost inactive (0.48 UT) or totally innocuous, respectively. All these results point to the spherulous cells being responsible for the storage (and possibly production) of the toxic compounds in C. crambe. Toxicity is concentrated in the sponge periphery. Spherulous cells are also concentrated in this area and can also be observed outside the sponge exopinacoderm. These results correlate well with the assumption of a defensive role of toxicity, since encounters with potential epibionts, predators and competitive neighbours take place through this peripheral zone. However, we found two types of spherulous cells (orange and colourless, respectively) coexisting in the same sponge zones as well as in Cell Fraction 1. Thus, we cannot at present determine whether one or both types are responsible for the toxicity encountered, although it is likely that the two correspond to different states of the same cell type.     

The culturable microbial community of the Great Barrier Reef sponge Rhopaloeides odorabile is dominated by an α-Proteobacterium

The microbial community cultured from the marine sponge Rhopaloeides odorabile Thompson et al. is dominated by a single bacterium, designated strain NW001. Sequence analysis of 1212 bp of the16S rRNA gene of strain NW001 indicates that it is a member of the α-subgroup of the class Proteobacteria. The association between this bacterium and its host sponge was observed in healthy R. odorabile collected from six different reefs in the Great Barrier Reef representing a geographic distance of 460 km, and in four collections in different seasons in 1997–1998 at Davies Reef (18°49.6′S; 147°34.49′E). The proportion of colonies of strain NW001 in samples from R. odorabile, expressed as a percentage of the total heterotrophic bacterial colony count, showed no significant spatial (range: 81–98%) or temporal differences (range: 81–99%), although colony counts of strain NW001 varied by up to two orders of magnitude between reef sites and sampling periods. The location of strain NW001 within the sponge mesohyl was visualized by in situ hybridization, using fluorescently labeled probes based on the 16S rRNA gene sequence of this strain. Cells of strain NW001 surround the choanocyte chambers, suggesting that these bacteria may play a role in nutrient uptake by the sponge. The absence of strain NW001 from corresponding seawater samples indicates that it has a specific, intimate relationship with R. odorabile and is not being utilized as a food source. A unique cyanobacterium related to the genera Leptolyngbya and Plectonema was also isolated from R. odorabile and characterized by 16S rRNA gene sequencing. Received: 19 May 2000 / Accepted: 18 November 2000     

Alloimmune memory for glycoproteid recognition molecules in sea anemones competing for space

A highly specific recognition system, capable of distinguishing between allogeneic (non-clonemates) and syngeneic (clonemates) conspecifics, exists in Anemonia sulcata (Coelenterata: Anthozoa). During a competitive interaction between allogeneic individuals, specialized structures (acrorhagi) are exposed and used to sting opponents. This complex behavior is called the acrorhagial response. In order to quantify this behavior we measured the acrorhagial response time (period from first contact with opponent to full expansion of acrorhagi). More than 320 reciprocal histoincompatibility responses were recorded. These histoincompatibility (H) markers are free components of the sea anemone mucus: they were characterized as glyco-proteins of a molecular weight <18 KD (Kilo-Dalton) containing terminal -d-glucose and/or -d-mannose. In alloimmune memory testing experiments, the memory trace in A. sulcata was found to persist for 5 d.     

Evidence for a symbiosis between bacteria of the genus Rhodobacter and the marine sponge Halichondria panicea : harbor also for putatively toxic bacteria?

Halichondria panicea (Pallas) is a marine sponge, abundantly occurring in the Adriatic Sea, North Sea, and Baltic Sea. It was the aim of the present study to investigate if this sponge species harbors bacteria. Cross sections through H. panicea were taken and inspected by electron microscopy. The micrographs showed that this sponge species is colonized by bacteria in its mesohyl compartment. To identify the bacteria, polymerase chain reaction (PCR) analysis of the 16S rRNA gene segment, typical for bacteria, was performed. DNA was isolated from sponge material that had been collected near Rovinj (Adriatic Sea), Helgoland (North Sea), and Kiel (Baltic Sea) and was amplified with bacterial primers by PCR. The data gathered indicate that in all samples bacteria belonging to the genus Rhodobacter (Proteobacteria, subdivision α) are dominant, suggesting that these bacteria live in symbiotic relationship with the sponge. In addition, the results show that the different samples taken contain further bacterial species, some of them belonging to the same genus even though found in sponges from different locations. The possibility of the presence of toxic bacteria was supported by the finding that organic extracts prepared from sponge samples displayed toxicity, when analyzed in vitro using leukemia cells. Received: 7 March 1997 / Accepted: 2 October 1997     

Effect of host and larval frass volatiles on behavioural response of the old house borer,Hylotrupes bajulus (L.) (Coleoptera: Cerambycidae), in a wind tunnel bioassay

Summary. In a wind tunnel bioassay the effect of three concentrations of natural extracts of (1) Scots pine wood, Pinus sylvestris, and (2) larval frass on the behavioural response of unmated females and males of the old house borer, Hylotrupes bajulus, was tested and compared to the behavioural effects of the male-produced sex pheromone (3R)-3-hydroxy-2-hexanone. The influence on the behaviour of both sexes was found to be equally significant for the two higher concentrated hexane extracts of wood and larval frass. Therefore several synthetic monoterpenes present in the extracts and ethanol were tested at the two higher concentrations (1:100, 1:1000 vol/vol). Among the higher concentrated monoterpenoid hydrocarbons [(+)-α-pinene, (+)-β-pinene, (+)-limonene], only α-pinene increased the activity, orientation towards scent source and interest towards conspecifics. The tests with higher concentrated ethanol and the oxygenated monoterpenes [(-)-verbenone, (-)-trans-pinocarveol, (+)-terpinen-4-ol, (+)-α-terpineol, (-)-myrtenol] revealed that verbenone is the most effective stimulant for the females, followed by trans-pinocarveol, terpinen-4-ol and α-terpineol. For males, terpinen-4-ol was the only mediator significantly inducing attraction and orientation towards the scent source combined with an interest in conspecifics apparent by fighting or courtship behaviour. Males did not respond to verbenone which is a main compound of larval frass. Myrtenol and ethanol were ineffective in both sexes. In fact behavioural observations suggest that the beetles were repelled by the high dose of myrtenol. Using the ten-fold lower dose of the synthetic monoterpenes (1:1000 vol/vol), all semiochemicals except myrtenol lost activity. Myrtenol, however, induced behavioural responses, like increased activity and orientation towards scent source, only at the low concentration. Based on the results, primary attraction of unmated old house borer is probably mediated by monoterpenes of coniferous wood, while secondary attraction to infested wood would occur in response to volatiles of larval frass. Received 5 May 1999; accepted 30 September 1999     

Asexual reproduction in homoscleromorph sponges (Porifera; Homoscleromorpha)

Asexual reproduction by external budding in Homoscleromorpha is reported for the first time. Two Mediterranean sponge species were studied, Oscarella lobularis and O. tuberculata. Buds are formed in the marginal basal part of sponge. Budding takes from 1 to 4 days and is defined in three budding stages. First, small irregular protuberances, consisting of external parental tissue, are formed. Second, they elongate and acquire more regular, nipple-like shape. These protuberances are tube like, their internal cavity derived from parental exhalant canal. The wall consists of three layers: (a) external layer is flagellated exopinacoderm, (b) internal one is flagellated endopinacoderm and (c) intermediate one is a thin layer of mesohyl. Third, a spherical bud with a large central cavity is formed. During budding, we did not observe cell proliferation or transdifferentiation either in budding zone or in any special mitotically active region. The bud attached to the substrate is similar to the rhagon developing after larva metamorphosis, it has a syconoid organization. Morphogenetically, budding in Oscarella differes from that in other sponges. Occurring by epithelial morphogenesis, it is similar to morphallaxis during regeneration. The presence in Homoscleromorpha of an epithelial morphogenesis is unique among sponges. This feature is shared by Homoscleromorpha and Eumetazoa.     

Assessment of estrogenic chemicals using an estrogen receptor α (ERα)- and ERβ-mediated reporter gene assay in fish

In vitro reporter gene assays using vertebrate cell lines or yeast have been used for assessment of the estrogenic chemicals. However, estrogen receptor α (ERα)- and ERβ-mediated reporter gene system in fish has yet to be developed. In the present study, we developed an ERα- and ERβ-mediated reporter gene assay in fish and estimated estrogenic activities of 17β-estradiol (E2), p-nonylphenol (NP), bisphenol A (BPA), p,p′-DDE, and genistein (Gen) using the in vitro reporter assay. The activity was intensely induced by transfection with either ERα or ERβ expression plasmid under E2 or Gen administration, whereas it was significantly induced by transfection with ERα expression plasmid, but not with ERβ expression plasmid under NP administration. On the other hand, the activity was induced more intensely by transfection with ERα expression plasmid than ERβ expression plasmid under BPA or p,p′-DDE administration. These results indicate that there are obvious differences in the activity through ERα and ERβ among the estrogenic chemicals examined in vitro. Thus, the in vitro reporter assay provides an excellent system for elucidating the action mechanism of estrogenic chemicals in fishes. Physical and Chemical Impacts on Marine Organisms, a Bilateral Seminar Italy–Japan held in November 2004     

Microbial diversity in the marine sponge Aplysina cavernicola (formerly Verongia cavernicola) analyzed by fluorescence in situ hybridization (FISH)

We have employed electronmicroscopical methods (SEM, TEM) to document the microbial community associated with the marine sponge Aplysina cavernicola (formerly Verongia cavernicola, class Demospongiae). Five dominant bacterial types were identified, three of which resemble the morphotypes originally described by Vacelet (1975). One bacterial type possesses morphological properties that are characteristic of the genus Planctomyces. In addition, morphologically uniform bacteria which reside inside the nuclei of host cells were observed. Using in situ hybridization with fluorescently labelled rRNA probes directed against known bacterial groups, the phylogenetic affiliation of the mesohyl bacteria was assessed. It could be shown that the vast majority of mesohyl bacteria belongs to the domain Bacteria with a low GC content. Among the Bacteria, the delta-Proteobacteria were most abundant, followed by the gamma-Proteobacteria and representatives of the Bacteroides cluster. Clusters of Gram-positive bacteria with a high GC content were also found consistently in low amounts. No hybridization signal was obtained with probes specific to the domain Archaea, to the alpha- and beta-Proteobacteria and to the Cytophaga/Flavobacterium cluster. This study describes for the first time the application of the “top-to-bottom approach” using 16S rRNA probes and in situ hybridization to assess the microbial diversity in Aplysina sponges. Received: 18 December 1998 / Accepted: 12 March 1999     

Ultrastructural aspects of the symbiosis between two species of the genus Aphanocapsa (Cyanophyceae) and Ircinia variabilis (Demospongiae)

The association between two species of the genus Aphanocapsa (Cyanophyceae) and the sponge Ircinia variabilis has been studied by electron microscopy. A. feldmanni is localized in the mesohyl or inside the cells of the sponge, while the larger A. raspaigellae is located only in an extracellular position inside cavities of the mesohyl. Both algae differ from other symbiotic Cyanophyceae in having a normal cell wall. They are able to reproduce in symbiotic condition, but also undergo, in their various extracellular and intracellular positions, a massive process of disintegration. A large amount of algal material is dispersed in the sponge tissues, which is a confirmation, at the ultrastructural level, of trophic relationships in the symbiosis Aphanocapsa-Ircinia.     

Electrophysiological responses of Dendroctonus armandi (Coleoptera: Curculionidae: Scolytinae) to volatiles of Chinese white pine as well as to pure enantiomers and racemates of some monoterpenes

To better understand the attractiveness of host tree, Chinese white pines (Pinus armandi Fr.) to Chinese white pine beetle (Dendroctonus armandi Tsai and Li), the antennal responses of D. armandi to the host volatile, as well as the pure enantiomers and racemates of some monoterpenes, were examined using an electroantennogram (EAG). EAG responses of male and female D. armandi to blended volatiles extracted from the host and some synthetic terpenes (α-phellandrene, (−)-β-pinene, (+)-α-pinene, (−)-α-pinene, (−)-camphene, β-myrcene, (S)-(−)-limonene, (+)-camphene and (R)-(+)-limonene) showed significant variation due to different compound concentrations and sex of the beetles. EAG responses to extracted blended volatiles were significantly greater in females than in males, but the EAG response was not always proportional to the volatile concentration. At lower concentrations, females responded strongly to α-phellandrene and males to (−)-β-pinene, while at higher concentrations, females responded most strongly to α-phellandrene and males to (+)-α-pinene. Females were significantly responsive to (−)-α-pinene, α-phellandrene and (−)-camphene, while males were more responsive to (S)-(−)-limonene, (+)-α-pinene and (R)-(+)-limonene. The EAG responses of the female D. armandi to the volatile oil were significantly higher than that of the males, and the infested pine volatiles could evoke higher EAG response. Most of the test compounds elicited similar responses, which suggested that several of the compounds may be used in combination by D. armandi in habitat and/or host community location at the Qinling forest ecosystem.     

Genetic variation and clonal structure in the scleractinian coral Pocillopora damicornis in the Ryukyu Archipelago, southern Japan

Samples of the scleractinian coral Pocillopora damicornis were collected from six sites located around four islands in the Ryukyu Archipelago, southern Japan, and subjected to allozyme electrophoresis. Seven polymorphic loci were examined for their allelic patterns. The ratio of observed to expected genotypic diversity (0.30 < G _o :G _e  < 0.64), the ratio of the observed number of genotypes to the number of individuals (0.47 < N _g :N _i  < 0.75), and deviations from Hardy–Weinberg equilibrium indicated that asexual reproduction plays a major role in the maintenance of established populations. However, populations were not completely dominated by a single or a few clones, and most clones were represented by only a few individual samples. The high frequency of typhoons in the region suggests that, in P. damicornis, fragmentation caused through occasional exposure to powerful waves is a major mode of asexual reproduction, but asexual production of planulae may also be contributing to the maintenance of populations. A significant genetic differentiation (F ST) was found between the six populations examined (0.027 < F ST < 0.092, average F ST = 0.056). The moderate gene flow is discussed according to characteristics of the larval stage of the species, and to circulation patterns in the region. Received: 7 August 1998 / Accepted: 18 May 1999     

Regulation of spirocyst discharge in the model sea anemone, Nematostella vectensis

Test probes were touched to tentacles to investigate whether discharge of spirocysts likely is regulated by hair bundle mechanoreceptors. Significantly more spirocysts discharge onto test probes in the presence of vibrations at 11–15 Hz as compared to 0 Hz. Adding N-acetylneuraminic acid, NANA, shifts maximal discharge of spirocysts upwards to 36–40 Hz, and possibly to 21–25 Hz. In contrast, NANA shifts maximal discharge of basitrichous isorhiza nematocysts downwards to 1–20 Hz. Thus, discharge of cnidae (‘stinging capsules’) is differentially regulated according to the type of cnida. Furthermore, it appears that chemodetection of N-acetylated sugars is not a prerequisite to capturing prey because, in seawater alone, maximal discharge of cnidae occurs at frequencies overlapping movements of calmly swimming prey. Nevertheless, chemodetection of N-acetylated sugars broadens the range of frequencies stimulating maximal discharge of cnidae and, therefore, likely enhances prey capture.     

Temperature cues gametogenesis and larval release in a tropical sponge

Determining the reproductive processes of benthic invertebrates is central to our understanding of their recruitment and population dynamics. Sexual reproduction of the gonochoric and viviparous Great Barrier Reef sponge, Luffariella variabilis (Poléjaeff 1884) was quantified from histological samples collected over two reproductive seasons (2004 and 2005). Gametogenesis commenced for females at a water temperature of 21°C, the lowest water temperature of the year. Spermatogenesis occurred above 22.5°C with sperm asynchronously developed and released from August or September to October. Oocytes developed asynchronously from July to September, embryos from September to December, and larvae from November to December. Female reproduction terminated in December (after larval release) prior to the highest mean annual water temperature of 30°C in January. There was a significant (35%) decrease in female reproductive output in 2005 compared to 2004, as measured by the reproductive index (0.68 ± 0.12 female reproductive propagules mm⁻² of mesohyl in 2005 compared with 1.05 ± 0.10 mm⁻² in 2004). This corresponded with delayed oogenesis and spermatogenesis, and a shortened larval development cycle corresponding with a delayed minimum temperature (21°C) in August of 2005 compared with July 2004. Accordingly, the maximum percentage of the mesohyl occupied by female reproductive propagules (eggs, embryos and larvae) was also reduced by 60% in 2005 (overall mean of 13.04% in October 2004 compared with 5.35% in October 2005). However, the mean sizes of individual female propagules remained the same from year to year. Males in contrast, showed no overall difference in either reproductive index or percentage occupation of the mesohyl between 2004 and 2005. The lowered reproductive output (∼35%) of females of L. variabilis associated with delayed minimum water temperatures may have important implications for population reproductive success where oogenesis and spermatogenesis and larval release are cued by minimum and maximum water temperatures, respectively.     

Isolation of Oscillatoria spongeliae,the filamentous cyanobacterial symbiont of the marine sponge Dysidea herbacea

The tropical marine sponge Dysidea herbacea (Keller) (Dictyoceratidae: Dysideidae) is always found associated with the filamentous cyanobacterium (blue-green alga) Oscillatoria spongeliae (Schulze) Hauck (Cyanophyceae: Oscillatoriaceae), which occurs abundantly throughout the sponge mesohyl. Intact, metabolically active, trichomes of O. spongeliae were isolated from the sponge by chopping the sponge tissue with a razor blade and squeezing the trichomes into a seawater-based medium containing polyvinylpyrrolidone, bovine serum albumin, dithiothreitol, glycerol, KCl and Na₂CO₃. The isolated cyanobacteria were concentrated by centrifugation and then washed several times in fresh medium. The isolated O. spongeliae have photosynthetic rates which are similar to the intact sponge-alga association for periods of at least 6 h after isolation. Addition of sponge homogenate to the isolated cyanobacteria causes rapid cell lysis.     

Recurrent disease outbreaks in corneous demosponges of the genus Ircinia: epidemic incidence and defense mechanisms

During 2008 and 2009, an epidemic affected sponges of the genus Ircinia in the Western Mediterranean. Investigations at a site on the European coast (6o43′08.80′′N; 3o43′52.20′′W) and another on the African coast (35o10′51.00′′N; 2o25′33.00′′W) revealed healthier African populations. The disease started with small pustules on the sponge surface, which subsequently coalesced forming larger, extensive lesions. An ultrastructural study suggested that a twisted rod is the etiological agent. It infected the sponges from the outside, initially killing the cells below the ectosome and then penetrating deeper into the body. The sponges responded to the bacterial progression by secreting concentric barriers of collagen and concentrating phagocytic cells at the diseased zones. This primitive immune system successfully resisted the disease in many instances, although mortality reached 27% in the studied populations. Epidemic outbreaks recur each year in September through November, arguably favored by abnormally high seawater temperatures in August.     

Heterotrophic nitrogen fixation (acetylene reduction) during leaf-litter decomposition of two mangrove species from South Florida, USA

Heterotrophic nitrogen-fixation (acetylene reduction) was measured during decomposition (under dark conditions) of Rhizophora mangle L. and Avicennia germinans (L.) Stearn leaf litter. Nitrogen-fixation rates in leaf litter increased following 24 d incubation, then decreased after ≃44 d for both species. Maximum rates of 66.2 and 64.6 nmol C₂H₄ g⁻¹ dry wt h⁻¹ were reached by R. mangle and A. germinans leaf litter, respectively. Higher fixation rates of leaf litter were associated with an increase in water content and sediment particles on leaf surfaces of both species. Rates of nitrogen fixation by diazotrophs attached to sediment particles were not significantly different from zero. With additions of d-glucose, ethylene production rates increased by factors of 625-, 34- and 7-fold for sediment, R. mangle and A.␣germinans leaf litter, respectively, compared to rates prior to enrichment. These organically enhanced rates of nitrogen fixation on leaves could be accounted for by increased activity associated with attached sediment particles and not the leaf material. Total phenolics [reported as tannic acid equivalent (TAE) units] decreased nitrogen-fixation rates when added to d-glucose-enriched sediment at >20 mg TAE l⁻¹. Phenolic compounds could explain the initial lag in rates of nitrogen fixation during leaf-litter decomposition of R. mangle (initial content of 110.8 mg TAE g⁻¹ dry wt), but not of A. germinans (initial content of 23.4 mg TAE g⁻¹ dry wt). The higher phenolic content and reportedly lower carbon substrate of R. mangle did not result in species-specific differences in either the magnitude or temporal pattern of nitrogen fixation compared to A. germinans leaf litter. We conclude that the availability of organic substrates leached from the leaf litter along with colonization by the heterotrophic diazotrophs (as indicated by sediment accumulation) controls nitrogen-fixation rates in a similar manner in the leaf litter of both species. Received: 8 August 1997 / Accepted: 4 December 1997