Search

(IF 1.67; Q2); International audience; An overview is presented of the Non-Indigenous Species (NIS) of algae and invertebrates recorded in the marine and brackish coastal waters of Normandy in France. Out of the 152 NIS found, 86 have been introduced through shipping (ballast waters and fouling) and 66 through aquaculture activities. A total of 95 NIS are linked to a Pacific origin and 32 come from the northwestern region of the Atlantic. Among the 152 NIS identified, only nine show an invasive demography in Normandy waters. The first introductions occurred in the middle of the 19 th century and became frequent by the beginning of the 20 th century. However, over 50% of the NIS so far recorded were found only during the three last decades.

International audience; Colonisation of artificial structures by primary producers is an important determinant for eco-engineering projects. In this context, interactions between the colonisation by microphytobenthic biofilm and macroalgae were explored on 48 samples of marine infrastructures (MI) immersed for one year in the English Channel. Marine infrastructures samples with smooth and rough surface were compared to evaluate the influence of surface micro-scale rugosity. Microphytobenthos biomass (MPB), macroalgal diversity and photosynthetic parameters of both were assessed during colonisation. No significant differences were found as a function of the surface rugosity of MI samples, which was unexpected, but can be explained by biogenic rugosity provided by barnacles. Marine infrastructures were largely colonised by a red encrusting alga, Phymatolithon purpureum, which showed poor photosynthetic capacity compared to the microphytobenthos present next to it. Colonisation by monospecific encrusting algae tended to reduce the primary productivity of hard substrate.

International audience; δ15N of annual (Ulva sp., Porphyra sp.) and perennial intertidal seaweed species (Chondrus crispus, Fucus sp.) collected on 17 sampling points along the French coast of the English Channel in 2012 and 2013 were assessed on their suitability as bioindicators of N pollution in coastal areas. A sine function applied for δ15N time series data showed for all the species the same seasonal trend with lowest δ15N values in April and highest in summer but with no significant interspecific differences of amplitude (α) and phase angle (ϕ). This model provides a useful tool for monitoring the inter-annual changes of N pollution. An interspecific variability of δ15N values was observed, probably due to their tolerance to emersion. An in vitro study for comparing the kinetic acquisition of the isotopic signal and N uptake mechanisms of each species underlined the influence of algal physiology on the δ15N interspecific variability.

Tissue was cultured and protoplasts isolated from the carrageenophyte Chondracanthus acicularis with the aim of developing micropropagation as an alternative to harvesting raw material from natural beds. Both adventitious shoots and filamentous calluses were induced by tissue culture on medium solidified with 0.4–1 % (w/v) agar. Adventitious shoots were mainly produced from discoid bases while filamentous calluses were mainly induced from basal zones and sub-apical explants. A gradient of the regeneration ability was observed from the top to the bottom of the thallus. The discoid base was the most reactive explant and produced the highest number of adventitious shoots compared to basal zones and sub-apical explants, irrespective of the concentration of agar. Protoplasts were isolated enzymatically from the whole thallus using a combination of cellulase R-10 Onozuka, macerozyme R-10, and crude extract of the gland gut of algivorous molluscs. The highest mean yield of protoplasts (1.2 × 106 protoplasts g−1 fresh weight) was obtained after 16 h of digestion with an enzyme mixture containing 2 % (w/v) cellulase R-10, 1 % (w/v) macerozyme R-10 Onozuka, 4 % (v/v) crude extract of gut gland of Haliotis, 0.8 M mannitol, 50 mM sodium citrate, 0.3 % (w/v) bovine serum albumin. Depending on the conditions, mean protoplast yields ranged from 3.14 × 105 to 1.2 × 106 protoplasts g−1 fresh weight. Different factors (storage duration, mannitol, sodium citrate, crude extract of the gland gut of algivorous molluscs) were tested to improve the yield of protoplasts but none has a significantly effect.

Marine macrophytes contain a variety of biologically active compounds, some reported to have antiprotozoal activity in vitro. As a part of a screening program to search for new natural antiprotozoals, we screened hydroalcoholic and ethyl acetate extracts of 20 species of seaweeds from three phyla (Rhodophyta, Heterokontophyta and Chlorophyta), sampled along the Normandy (France) coast. We tested them in vitro against the protozoa responsible for three major endemic parasitic diseases: Plasmodium falciparum, Leishmania donovani and Trypanosoma cruzi. The selectivity of the extracts was also evaluated by testing on a mammalian cell line (L6 cells). Ethyl acetate extracts were more active than hydroalcoholic ones. Activity against T. cruzi and L. donovani was non-existent to average, but almost half the extracts showed good activity against P. falciparum. The ethyl acetate extract of Mastocarpus stellatus showed the best antiplasmodial activity as well as the best selectivity index (IC50 = 2.8 µg/mL; SI > 30). Interestingly, a red algae species, which shares phylogenetic origins with P. falciparum, showed the best antiplasmodial activity. This study is the first to report comparative antiprotozoal activity of French marine algae. Some of the species studied here have not previously been biologically evaluated.

Protoplasts were isolated enzymatically from the carrageenophyte red alga Grateloupia turuturu (Halymeniales, Rhodophyta) that occurs along the coast of the French Channel in Normandy. Effects of the main factors on the protoplast yield were identified to improve the isolation protocol. The optimal enzyme composition for cell wall digestion and protoplast viability consisted of 2% cellulase Onozuka R-10, 0.5% macerozyme R-10, 2% crude extract from viscera of Haliotis tuberculata, 0.8 M mannitol, 20 mM sodium citrate, 0.3% bovine serum albumin at 25°C, and 4-h incubation period. The protoplasts were approximately 5–15 μm in diameter, liberated mainly from the surface cell layers. Maximum yield was 1.5 × 107 protoplasts g-1 fresh tissue. The protoplasts underwent initial division after 14 days with a high density level of 1 × 106 cells mL-1 in culture medium and developed into microthalli of a line of two to six cells.

The regeneration of meristematic tissues from sporophytes of Laminaria digitata was studied by protoplast and tissue culture. Sequential treatment of explants in sterile seawater with 1% Betadine for 5 min, 1% commercial bleach for 1–2 min and 2% antibiotic treatment supplemented with 1 μM GeO2 overnight enabled viable explants as high as 55%. Different morphogenetic responses were observed from tissue culture on media supplemented with plant growth regulators alone or in combination, mainly filamentous calluses up to 50% according to the media. Dark green compact calluses were observed on two combinations: 4 μM Pi + 2 μM N-(2-chloro-4-pyridyl)-N’-phenylurea (CPPU) and 0.04 μM Pi + 0.44 μM 6-benzylaminopurine. Thalloid-like structures comparable to adventitious buds were regenerated on medium supplemented with 4 μM Pi + 0.45 μM zeatin but at low frequency suggesting a strong genotypic effect. Friable calluses were developed from protoplasts in enriched medium with polyamines and containing 0.40 μM CPPU + 0.45 μM 2,4-dichlorophenoxyacetic acid. In order to produce protoplasts, a one-step enzymatic protocol was developed and yields reached 22 × 106 protoplasts per gram of fresh weight.

A fine-scale survey of δ(15)N, δ(13)C, tissue-N in seaweeds was conducted using samples from 17 sampling points at two sites (Grandcamp-Maisy (GM), Courseulles/Mer (COU)) along the French coast of the English Channel in 2012 and 2013. Partial triadic analysis was performed on the parameter data sets and revealed the functioning of three areas: one estuary (EstA) and two rocky areas (GM(∗), COU(∗)). In contrast to oceanic and anthropogenic reference points similar temporal dynamics characterized δ(15)N signatures and N contents at GM(∗) and COU(∗). Nutrient dynamics were similar: the N-concentrations in seawater originated from the River Seine and local coastal rivers while P-concentrations mainly from these local rivers. δ(15)N at GM(∗) were linked to turbidity suggesting inputs of autochthonous organic matter from large-scale summer seaweed beachings made up of a mixture of Rhodophyta, Phaeophyta and Chlorophyta species. This study highlights the coupling between seaweed beachings and nitrogen sources of intertidal macroalgae.

Protoplasts were isolated enzymatically from meristematic tissues of the brown algae, Fucus serratus, using a combination of 2% cellulase R-10 Onozuka, 0.5% macerozyme and 1% crude extract of gland gut of Aplysiavaccaria. The main factors affecting protoplast yield were identified. Protoplasts were produced in large quantities from apical region of thallus and from plantlets compared to mature explants. Yields were greatly improved by the addition of sodium citrate and bovine serum albumin in the enzymatic solution and could reach 5.8 × 106 protoplasts per gram of fresh wt. The applicability of these optimal parameters to other species Fucus vesiculosus was shown.

A continuous micropropagation was established from protoplasts of thegreen alga Enteromorpha intestinalis. The effects of two differentcrude enzymes and the osmolarity at different concentrations of the enzymesolution on algal protoplast yields were tested. The optimal enzymecomposition for cell wall digestion and protoplast viability was 2%cellulase R 10 Onozuka and 2% Aplysie with 0.5 m mannitol. Largenumbers of Enteromorpha protoplasts were released (10.0 × 106protoplasts from 1 g fresh thalli) and settled on a rangeof substrata. Regeneration of the protoplasts followed the normal patternfor this species. Conditions for pure cultures and efficient systems offloating supports with nets were determined to optimise the product qualityof plantlets of Enteromorpha. A promising storage process has beendeveloped which involves including protoplasts in beads of alginic acid gel.Plants regenerated from protoplasts may also be used as seedstock tofacilitate propagation for macroalgal culture.

In multicellular eukaryotes, the zygote, a single cell, gives rise to the different cell types of the organism. The study of the mechanisms involved is a key point of developmental biology. Generally, the first stages are characterized by an orderly sequence of asymmetrical divisions resulting from an initial developmental polarity. The establishment of this initial polarity has been the subject of numerous studies in animals, but not in higher plants since the zygote is encased in several layers of tissues that prevent experimental approaches. Moreover, plant development is characterized by two successive ontogenetic steps: the construction of the embryonic apico-basal axis and the establishment of meristems in charge of organogenesis. Members of the Fucophyceae provide good models for the investigation of these processes. Any inferred homology of mechanisms must take into account the polyphyletic nature of the algae. This paper is a tentative review of two case studies: fucoid zygotes and Sphacelaria apical cells, and deals respectively with the two successive ontogenetic steps characteristic of higher plant development. The first part concerns development of the fucoid zygotes. Fucoid zygotes, including those of different species, are considered as model systems in plants for studying the establishment of the polarity axis because, at the moment of fertilization, they do not have any morphological or biochemical polarity. This report concerns progress in the identification of some cellular or molecular mechanisms involved in the settlement and/or stabilization of the polarity axis, and the consequence of this polar organisation for the control of asymmetrical divisions and the building of a functional embryo. The second part concerns the apical cell of Sphacelaria as a model for establishing and maintaining a meristematic cell. The apical cell exhibits a permanent polarized organisation throughout repetitive asymmetric divisions and can be comparatively analysed in situ and isolated as a protoplast. This allowed us to investigate the evolution of the cytoplasmic cytoskeleton, centrosomes and the mitotic apparatus during the cell cycle in relation to the cell polarity; particularly the interactions between the cytoskeleton and cell wall. For the two models, the results are compared with mechanisms involved in the development of other multicellular organisms, and their value in gaining an insight into higher plant ontogenesis is assessed.

The apical cell ofSphacelaria, a tip-growing filamentous brown alga, and its protoplast constitute a model for the investigation of the consequences of cell wall removal on microtubular cytoskeletal organization and cell polarity. In the apical cell, the microtubular cytoskeleton is strongly polarized and, in most cases, extends from two centrosomes to the cortex where it constitutes a fine meshwork. Observations of microtubule dynamics throughout the cell cycle emphasize the coincidence between orientation of the mitotic axis and cell polarity. Just after protoplast isolation, dramatic alterations of initial polarity are observed, whatever the mitotic stage. In particular, the coincidence between cytoplasmic polarity and polarity of the system nucleus-centrosomes is lost in most cases. 12–24 h after protoplast isolation, the cell shows a more symmetrical organization while a dense cortical microtubular network spreads out concomitantly with wall reformation. Our discussion emphasizes the possible relationship between cell polarity and cell totipotency, and the relevance of such a model for higher plant studies.

International audience; The cell wall fine structure of the red alga Palmaria palmata has been analysed extensively in recent years, but cell wall biosynthesis has not. The glycosidic composition of the cell walls of gametophytic and sporophytic fronds revealed no differences between the two stages. Spores were isolated from mature sporophytes and cultivated in vitro. Spore settlement, germination and first stages of germling development were described in terms of glycoside composition. Isolated spores were surrounded by a cell wall composed of xylose, galactose and glucose. During germination and germling development, the xylose content increased to the level of glycosides found in erect fronds, concurrently with starch degradation. Spores isolated from Palmaria palmata appeared to be good candidates for studying cell wall biosynthesis.

International audience; Pilot scale studies were carried out to develop a methodology for the cultivation of fresh young fronds of Palmaria palmata to supply abalone hatcheries. This is the first report of cultivation of P. palmata in land-based tanks using isolated spores as seedstocks. Spores were released from fieldcollected tetrasporphytic fronds. A phenological study determined that tetrasporophytic fronds were fertile during the winter along the coast of northern France. This paper describes techniques for the induction of sporulation, for spore settlement and for incubation of germlings in 1.5-m-diameter tanks in semi-controlled conditions. The yield of released spores was in the range of 5000 to 25,000 gÀ 1 of fertile sections. Mean spore density on substrate placed in hatching tanks was 500 spores cmÀ 2. Spore germination occurred 3 days after inoculation and at this stage survival rate was high (80%). A few days after spore inoculation, both male and female gametophytes had germinated and a male to female ratio of approximately 1:1 was observed. Female gametophytic discs remained microscopic whereas males developed gametophytic fronds. Growth of plantlets was well correlated with the concentration of medium supplements. After 3 months of cultivation in tanks, survival rate was 35% and some plantlets measured more than 2 cm. At this stage, substrates covered with soft young fronds were transferred to an abalone hatchery to feed abalone juveniles.

International audience; Confocal laser scanning microscopy was used to investigate the three-dimensional organisation of the microtubular cytoskeleton of protoplasts isolated from the cortex and medulla of the red alga Palmaria palmata. Immunofluorescence labelling revealed the presence of abundant microtubules in interphase cells. Cortexderived and medulla-derived protoplasts each exhibited a distinctive arrangement of microtubules. In cortexderived protoplasts, a continuous network of cytoplasmic microtubules connected the peripheral array to the array which surrounded the single nucleus at the centre of the cell. At telophase, the microtubular cytoskeleton was reorganised into a network apparently involved in cytokinesis. In the multi-nucleate medulla-derived protoplasts, each nucleus, located near the plasma membrane, was surrounded by microtubules. A uniformly arranged cortical array of microtubules was observed in both cortex-derived and medulla-derived protoplasts during interphase and we hypothesise that it likely plays a role in the biogenesis of the cell wall in red algal cells.

The natural floridoside (2-O-alpha-d-galactopyranosylglycerol) was isolated from Dilsea carnosa, and its structure has been determined by single-crystal X-ray diffraction analysis. The solved structure is in agreement with the previously solved crystal structure of floridoside [Simon-Colin, C.; Michaud, F.; Léger, J.-M.; Deslandes E. Carbohydr. Res.2003, 338, 2413-2416] and demonstrates for the first time the presence of floridoside in the red algae Dilsea carnosa.

The growth of the filamentous brown alga Sphacelaria depends on a large, strongly polarized, apical cell. The protoplast derived from this cell can be distinguished in a heterogeneous suspension by cytological markers, so it is possible to study development of the cytoskeleton during protoplast isolation and the first steps of regeneration. In the initial cell, microtubules show an asymmetric distribution along the axis; they are mainly located at the distal part around the physodes. After protoplast isolation, this polarity initially seems to be maintained; subsequently, the microtubules radiate from the two centrioles and spread out to the plasmalemma. This experimental model is suitable for investigating the development of the polarity of the initial cell, and the sequence of the first morphogenetic events leading to protoplast regeneration.