ALBERT

Description: New sedimentological data of facies and diagenesis as well as chronological data including strontium (87Sr/86Sr)-isotope ratios and uranium (U)-series dating, radiocarbon (14C) accelerator mass spectrometry (AMS) dating and biostratigraphy from elevated reef terraces (makatea) in the southern Cook Islands of Mangaia, Rarotonga and Aitutaki contribute to controversial discussions regarding age and sea-level relationships of these occurrences during the Neogene and Quaternary. The oldest limestones of the uplifted makatea island of Mangaia include reef-related facies which are mid-Miocene in age, based on new Sr-isotope and biostratigraphical data. In between these older deposits and the lowest coastal reef terrace of marine isotope stage (MIS) 5e, various older Pleistocene reef-related facies were identified. Based on Sr-isotope ratios, these were deposited during earlier Pleistocene highstands (as old as 2.28 Ma). Rare reef terraces on Rarotonga belong to the Plio-Pleistocene and the late Miocene, according to 87Sr/86Sr ratios. The late Miocene age is enigmatic as it exceeds the age of subaerially exposed volcanic rocks of Rarotonga island. The fossil reef could have formed on an older submarine volcanic high that was later displaced by younger volcanism to its present position, or the Sr-age could be too old due to diagenetic resetting. The Plio-Pleistocene Rarotonga reef terraces are overlain irregularly by Holocene reef deposits that are interpreted as storm rubble. Reef terraces on Aitutaki represent evidence of a higher-than-present (up to 1 m) sea-level during the late Holocene, based on 14C AMS age data. They are very similar to elevated late Holocene reefs of adjacent French Polynesia with regard to composition, elevation and age.

Description: Predicting the implications of ongoing ocean climate warming demands a better understanding of how short-term thermal variability impacts marine ectotherms, particularly at beyond-optimal average conditions during summer heatwaves. Using a globally important model species, the blue mussel Mytilus, in a 5-week-long experiment, we (a) assessed growth performance traits under 12 scenarios, consisting of four thermal averages (18.5, 21, 23.5 and 26℃) imposed as constant or daily fluctuating regimes with amplitudes of 2 or 4℃. Additionally, we conducted a short-term assay using different mussel individuals to (b) test for the species capacity for suppression and recovery of metabolic performance traits (feeding and aerobic respiration) when exposed to a 1-day thermal fluctuation regime (16.8–30.5℃). Using this high-resolution data, we (c) generated short-term thermal metabolic performance curves to predict and explain growth responses observed in the long-term experiment. We found that daily high-amplitude thermal cycles (4℃) improved mussel growth when fluctuations were imposed around an extreme average temperature of 26℃, representing end-of-century heatwaves. In contrast, thermal cycles negatively affected mussel growth at a less extreme average temperature of 23.5℃, resembling current peak summer temperature scenarios. These results suggest that fluctuations ameliorate heat stress impacts only at critically high average temperatures. The short-term assay demonstrated that during the warming phase, animals stopped feeding between 24 and 30℃ while gradually suppressing respiration. In the subsequent cooling phase, feeding and respiration partially and fully recovered to pre-heating rates respectively. Furthermore, nonlinear averaging of short-term feeding responses (upscaling) well-predicted longer term growth responses to fluctuations. Our findings suggest that fluctuations can be beneficial to or detrimental for the long-term performance of ectothermic animals, depending on the fluctuations' average and amplitude. Furthermore, the observed effects can be linked to fluctuation-mediated metabolic suppression and recovery. In a general framework, we propose various hypothetical scenarios of fluctuation impacts on ectotherm performance considering inter- or intra-species variability in heat sensitivity. Our research highlights the need for studying metabolic performance in relation to cyclic abiotic fluctuations to advance the understanding of climate change impacts on aquatic systems. A free Plain Language Summary can be found within the Supporting Information of this article

Description: The present study aims to valorize the apple peels (AP) and grape seeds (GS) by the fortification of the yogurts using their powder. Firstly, the optimization of the extraction parameters for assessing maximum of total phenolic content (TPC) was achieved. Under the optimized conditions, the experimental maximum yields of TPC were 19.33 ± 2.33 and 240.59 ± 4.77 mg Gallic Acid Equivalents (GAE)/100 g Dry Weight (DW) for AP and GS, respectively, which was in close agreement with predicted values (19.32 ± 0.91 and 242.26 ± 11.08 mg GAE/100 g DW for AP and GS, respectively). The antioxidant capacity of GS extract was better with IC50 of 12.22 ± 0.89 and 225.47 ± 7.10 µg/ml in DPPH and phosphomolybdenum assays, respectively. Besides, powder from these by-products was incorporated into yogurt samples. The classification test revealed that the yogurt prepared with GS powder was the preferred one.

Description: Pa.ra.rho.do.spi.ril'lum. Gr. pref. para-, beside, alongside of, near, like; N.L. neut. n. Rhodospirillum, a bacterial generic name; N.L. neut. n. Pararhodospirillum, resembling Rhodospirillum. Proteobacteria / Alphaproteobacteria / Rhodospirillales / Rhodospirillaceae / Pararhodospirillum Pararhodospirillum species are spiral-shaped, mesophilic, and phototrophic freshwater bacteria of the Rhodospirillaceae family. Cells are motile by polar flagella, and photosynthetic pigments are located in internal photosynthetic membranes present as lamellar stacks. Photosynthetic pigments are bacteriochlorophyll a and carotenoids of the spirilloxanthin series with spirilloxanthin itself lacking. Ubiquinone-9 and rhodoquinone-9 are the major quinones. All species are sensitive to oxygen and require anoxic or microoxic conditions for growth. They grow photoheterotrophically under anoxic conditions in the light. Photoautotrophic growth, aerobic chemotrophic growth, and fermentative growth have not been demonstrated. Growth factors are required. DNA G + C content (mol%): 60.2–65.8 (Bd and HPLC) and 64.7–67 (GA). Type species: Pararhodospirillum photometricum Lakshmi et al. 2014VP (basonym: Rhodospirillum photometricum Molisch 1907AL).

Description: Rho.do.ci'sta Gr. neut. n. rhodon, rose; L. fem. n. cista a basket; N.L. fem. n. Rhodocista, red basket. Proteobacteria / Alphaproteobacteria / Rhodospirillales / Azospirillaceae / Rhodocista Rhodocista centenaria is a well-characterized thermotolerant, phototrophic purple bacterium growing optimally at a temperature of 40–45°C and a maximal growth temperature of 48°C. Under low nutrient conditions, Rhodocista forms desiccation-, heat-, and UV-resistant cysts, which enable survival under severe drought and salt stress. Cells are motile by a single polar flagellum in liquid culture but in addition form lateral flagella on agar surfaces and under these conditions may show a characteristic phototactic movement. Rhodocista species grow under photoheterotrophic conditions and also are able to perform a chemotrophic aerobic metabolism. They encode enzymes for autotrophic carbon dioxide fixation and fixation of dinitrogen, although autotrophic growth has so far not been demonstrated. In the type species, bacteriochlorophyll biosynthesis occurs under both aerobic and anaerobic growth conditions. Aerobically grown cells are fully pigmented. In other species, oxygen may inhibit photosynthetic pigment biosynthesis, and aerobically grown cells are colorless. DNA G + C content (mol%): 68.8–69.9 (Tm), 70.5 (WGS). Type species: Rhodocista (Rcs.) centenaria Kawasaki et al. 1992, VL48 (basonym: Rhodospirillum centenum Favinger et al. 1989, VL48).

Description: Rho.do.pi'la. Gr. neut. n. rhodon the rose; N.L. fem. n. pila a ball or sphere; N.L. fem. n. Rhodopila red sphere. Proteobacteria / Alphaproteobacteria / Rhodospirillales / Acetobacteraceae / Rhodopila Rhodopila globiformis is one of the very few anaerobic phototrophic purple bacteria that can grow below pH 6 with an optimum depending on the organic carbon substrate from 4.8 to 5.6. Growth occurs preferably photoheterotrophically under anoxic conditions in the light. Cells are sensitive to oxygen but grow by respiration under microoxic conditions in the dark. Growth factors are required. They are acidophilic freshwater bacteria that inhabit acidic warm sulfur springs. Cells are spherical to ovoid, motile by means of polar flagella, and divide by binary fission. They stain Gram-negative and have internal photosynthetic membranes of the vesicular type. Rhodopila is classified within the Acetobacteraceae family and Rhodospirillales order of the Alphaproteobacteria. The photosynthetic pigments are bacteriochlorophyll a and carotenoids. The major fatty acids are C18:1 (∼75%) and C16:0. Ubiquinones, menaquinones, and rhodoquinones with 9 and 10 isoprene units are produced. DNA G + C content (mol%): 67.1 (genome analysis). Type species: Rhodopila globiformis Imhoff et al. 1984VP (basonym: Rhodopseudomonas globiformis Pfennig 1974AL).

Description: Rho.do.pla'nes. Gr. neut. n. rhodon rose; Gr. masc. n. planos a wanderer; N.L. masc. n. Rhodoplanes a red wanderer. Proteobacteria / Alphaproteobacteria / Rhizobiales / Hyphomicrobiaceae / Rhodoplanes The genus Rhodoplanes accommodates species of anoxygenic facultative phototrophic bacteria that grow optimally under anaerobic conditions in the light. They belong to the family Hyphomicrobiaceae of the order Rhizobiales within the class Alphaproteobacteria. Cells are Gram-stain-negative rods and multiply by budding and asymmetric cell division. Motile by means of polar, subpolar, or lateral flagella. Internal photosynthetic membranes are present as lamellar stacks parallel to the cytoplasmic membrane. Photosynthetic pigments are bacteriochlorophyll a and carotenoids of the spirilloxanthin series. Photoorganotrophy with pyruvate and some other organic acids is the best mode of growth. Straight-chain, monounsaturated C18:1 ω7c is the main component of the cellular fatty acids and C16:0 is a second major component. Ubiquinones and rhodoquinones with 10 isoprene units (Q-10 and RQ-10) are present. The main components of polar lipids are phosphatidylethanolamine, phosphatidylcholine, phosphatidylglycerol, and diphosphatidylglycerol. Terrestrial and freshwater bacteria having a preference for mesophilic to moderately thermophilic habitats and neutral pH. DNA G + C content (mol%): 67.2–70.4. Type species: Rhodoplanes roseus Hiraishi and Ueda 1994 (Rhodopseudomonas rosea Janssen and Harfoot 1991).

Description: Rho.do.pi'la. Gr. neut. n. rhodon the rose; N.L. fem. n. pila a ball or sphere; N.L. fem. n. Rhodopila red sphere. Proteobacteria / Alphaproteobacteria / Rhodospirillales / Acetobacteraceae / Rhodopila Rhodopila globiformis is one of the very few anaerobic phototrophic purple bacteria that can grow below pH 6 with an optimum depending on the organic carbon substrate from 4.8 to 5.6. Growth occurs preferably photoheterotrophically under anoxic conditions in the light. Cells are sensitive to oxygen but grow by respiration under microoxic conditions in the dark. Growth factors are required. They are acidophilic freshwater bacteria that inhabit acidic warm sulfur springs. Cells are spherical to ovoid, motile by means of polar flagella, and divide by binary fission. They stain Gram-negative and have internal photosynthetic membranes of the vesicular type. Rhodopila is classified within the Acetobacteraceae family and Rhodospirillales order of the Alphaproteobacteria. The photosynthetic pigments are bacteriochlorophyll a and carotenoids. The major fatty acids are C18:1 (∼75%) and C16:0. Ubiquinones, menaquinones, and rhodoquinones with 9 and 10 isoprene units are produced. DNA G + C content (mol%): 67.1 (genome analysis). Type species: Rhodopila globiformis Imhoff et al. 1984VP (basonym: Rhodopseudomonas globiformis Pfennig 1974AL).

Description: Rho.do.spi.ril'lum. Gr. neut. n. rhodon, the rose; N.L. neut. n. Spirillum, a bacterial genus; N.L. neut. n. Rhodospirillum, the rose Spirillum. Proteobacteria / Alphaproteobacteria / Rhodospirillales / Rhodospirillaceae / Rhodospirillum The genus Rhodospirillum has harbored a diverse set of spiral-shaped phototrophic bacteria, most of which have been reclassified as species of other genera, families, and even orders and phyla since the 1980s. The heterogeneity has been long known, but only the faith into sequence-based information gave strong support for taxonomic rearrangements. Currently, the genus Rhodospirillum contains a single species, which is characterized by spiral-shaped cells, motility by bipolar flagella, and internal membranes as vesicles. It performs anaerobic photosynthesis, which is restricted to anoxic light conditions due to the oxygen-sensitive biosynthesis of bacteriochlorophyll and thus the phototrophic apparatus. It can grow photoheterotrophically as well as photoautotrophically. The key enzyme of autotrophic carbon dioxide fixation in Rhodospirillum rubrum, ribulose bisphosphate carboxylase (RubisCO) type-II, is well characterized and forms a homodimer that is also encoded in some related genera of Rhodospirillaceae. Chemotrophic growth may also occur under microoxic to oxic conditions in the dark and anaerobically by fermentation. The genus comprises mesophilic freshwater bacteria. Ubiquinones and rhodoquinones with 10 isoprene units and fatty acids typical of other Alphaproteobacteria with C18:1, C16:0, and C16:1 as major components are present. DNA G + C content (mol%): 64.6–65.7, type 65.4 (genome analysis), 63.8–65.8 (Bd). Type species: Rhodospirillum (Rsp.) rubrum Molisch 1907AL (basonym: Spirillum rubrum Esmarch 1887).

Description: Rho.do.ci'sta Gr. neut. n. rhodon, rose; L. fem. n. cista a basket; N.L. fem. n. Rhodocista, red basket. Proteobacteria / Alphaproteobacteria / Rhodospirillales / Azospirillaceae / Rhodocista Rhodocista centenaria is a well-characterized thermotolerant, phototrophic purple bacterium growing optimally at a temperature of 40–45°C and a maximal growth temperature of 48°C. Under low nutrient conditions, Rhodocista forms desiccation-, heat-, and UV-resistant cysts, which enable survival under severe drought and salt stress. Cells are motile by a single polar flagellum in liquid culture but in addition form lateral flagella on agar surfaces and under these conditions may show a characteristic phototactic movement. Rhodocista species grow under photoheterotrophic conditions and also are able to perform a chemotrophic aerobic metabolism. They encode enzymes for autotrophic carbon dioxide fixation and fixation of dinitrogen, although autotrophic growth has so far not been demonstrated. In the type species, bacteriochlorophyll biosynthesis occurs under both aerobic and anaerobic growth conditions. Aerobically grown cells are fully pigmented. In other species, oxygen may inhibit photosynthetic pigment biosynthesis, and aerobically grown cells are colorless. DNA G + C content (mol%): 68.8–69.9 (Tm), 70.5 (WGS). Type species: Rhodocista (Rcs.) centenaria Kawasaki et al. 1992, VL48 (basonym: Rhodospirillum centenum Favinger et al. 1989, VL48).

Description: Rho.do.tha.las.si.a.ce'ae. N.L. neut. n. Rhodothalassium, type genus of the family; suff. -aceae, ending to denote a family; N.L. fem. pl. n. Rhodothalassiaceae, the family of Rhodothalassium. Proteobacteria / Alphaproteobacteria / Rhodothalassiales / Rhodothalassiaceae Cells are vibrioid to spiral shaped, are motile by means of polar flagella, and multiply by binary fission. They belong to the class Alphaproteobacteria and stain Gram-negative. An unusual protein-rich cell wall with only low amounts of peptidoglycan may be present. Internal photosynthetic membranes are present as lamellar stacks lying parallel to the cytoplasmic membrane. The photosynthetic pigments are bacteriochlorophyll a and carotenoids. The major ubiquinone and menaquinone components are Q-10 and MK-10. Growth occurs preferably photoheterotrophically under anoxic conditions in the light but also may be possible under microoxic to oxic conditions in the dark. Obligately halophilic bacteria that require NaCl or sea salt for growth. Habitats are anoxic zones of hypersaline environments such as salterns, salt lakes, and evaporated coastal lagoons that are exposed to light. At present, the family includes a single genus. DNA G + C content of the type species and genus (mol%): 68.5–69.0 (genome analysis), 60.0–62.8 (HPLC analysis). Type genus: Rhodothalassium Imhoff et al. 1998VP.

Description: Phae.o.spi.ril'lum. Gr. masc. adj. phaeos, brown; N.L. neut. n. Spirillum, a bacterial genus; N.L. neut. n. Phaeospirillum, brown Spirillum. Proteobacteria / Alphaproteobacteria / Rhodospirillales / Rhodospirillaceae / Phaeospirillum Phaeospirillum species are vibrioid to spiral shaped and motile Alphaproteobacteria. They are strictly anaerobic and anoxygenic phototrophic bacteria with a reaction center and light-harvesting complexes located in the internal membrane stacks formed at a sharp angle with the cytoplasmic membrane. The photosynthetic pigments are bacteriochlorophyll a esterified with phytol and carotenoids of the spirilloxanthin series, with spirilloxanthin itself lacking. They have a photoheterotrophic metabolism and depend on anoxic conditions for biosynthesis of bacteriochlorophyll and photosynthesis. The preferred carbon substrates are fatty acids including longer chains up to pelargonate. The longer chain fatty acids provide a selective advantage for several of the species. Chemotrophic growth may be possible at controlled and very low oxygen tensions (〈1.5 kPa) in the dark. Ammonia and dinitrogen serve as nitrogen sources. Assimilatory sulfate reduction is present. Growth factors may be required. Phaeospirillum species are mesophilic freshwater bacteria with a preference for neutral pH that live in stagnant and anoxic freshwater habitats. DNA G + C content (mol%): 60.5–65.3 (Bd), 62.1–62.8 (Tm), 61.5–64.7 (WGS). Type species: Phaeospirillum (Phs.) fulvum Imhoff et al. 1998VP (basonym: Rhodospirillum fulvum van Niel 1944AL).

Description: Rho.do.tha.las.si.a'les. N.L. neut. n. Rhodothalassium, type genus of the order; suff. -ales, ending denoting an order; N.L. fem. pl. n. Rhodothalassiales, the Rhodothalassium order. Proteobacteria / Alphaproteobacteria / Rhodothalassiales The order currently comprises a single family and genus, which is characterized by halophilic anoxygenic phototrophic bacteria having spiral-shaped cells and containing lamellar photosynthetic membranes. The properties of the order are determined by the characteristics of the Rhodothalassiaceae family.

Description: Rho.do.tha.las'si.um. Gr. neut. n. rhodon, the rose; Gr. masc. adj. thalassios, belonging to the sea; N.L. neut. n. Rhodothalassium, the rose belonging to the sea. Proteobacteria / Alphaproteobacteria / Rhodothalassiales / Rhodothalassiaceae / Rhodothalassium The genus Rhodothalassium is represented by a single species and is the only genus of the Rhodothalassiaceae family and Rhodothalassiales order. It is characterized by vibrioid- to spiral-shaped cells which multiply by binary fission and are motile by means of flagella. Internal photosynthetic membranes are present as lamellar stacks lying parallel to the cytoplasmic membrane. Photosynthetic pigments are bacteriochlorophyll a and carotenoids of the spirilloxanthin series. Ubiquinones and menaquinones with 10 isoprene units (Q-10 and MK-10) are present. Growth occurs preferably photoheterotrophically under anoxic conditions in the light. Most strains also grow chemoorganotrophically under oxic conditions in the dark. Rhodothalassium species are obligately halophilic, require NaCl or sea salt for growth, and live in anoxic zones of hypersaline environments such as salterns, salt lakes, and evaporated coastal lagoons that are exposed to the light. DNA G + C content (mol%): 68.5–69.0 (WGS), 60.0–62.8 (HPLC). Type species: Rhodothalassium salexigens Imhoff et al. 1998VP (basonym: Rhodospirillum salexigens Drews 1981, VL9).

Description: Rho.do.pla'nes. Gr. neut. n. rhodon rose; Gr. masc. n. planos a wanderer; N.L. masc. n. Rhodoplanes a red wanderer. Proteobacteria / Alphaproteobacteria / Rhizobiales / Hyphomicrobiaceae / Rhodoplanes The genus Rhodoplanes accommodates species of anoxygenic facultative phototrophic bacteria that grow optimally under anaerobic conditions in the light. They belong to the family Hyphomicrobiaceae of the order Rhizobiales within the class Alphaproteobacteria. Cells are Gram-stain-negative rods and multiply by budding and asymmetric cell division. Motile by means of polar, subpolar, or lateral flagella. Internal photosynthetic membranes are present as lamellar stacks parallel to the cytoplasmic membrane. Photosynthetic pigments are bacteriochlorophyll a and carotenoids of the spirilloxanthin series. Photoorganotrophy with pyruvate and some other organic acids is the best mode of growth. Straight-chain, monounsaturated C18:1 ω7c is the main component of the cellular fatty acids and C16:0 is a second major component. Ubiquinones and rhodoquinones with 10 isoprene units (Q-10 and RQ-10) are present. The main components of polar lipids are phosphatidylethanolamine, phosphatidylcholine, phosphatidylglycerol, and diphosphatidylglycerol. Terrestrial and freshwater bacteria having a preference for mesophilic to moderately thermophilic habitats and neutral pH. DNA G + C content (mol%): 67.2–70.4. Type species: Rhodoplanes roseus Hiraishi and Ueda 1994 (Rhodopseudomonas rosea Janssen and Harfoot 1991).

Description: Pa.ra.rho.do.spi.ril'lum. Gr. pref. para-, beside, alongside of, near, like; N.L. neut. n. Rhodospirillum, a bacterial generic name; N.L. neut. n. Pararhodospirillum, resembling Rhodospirillum. Proteobacteria / Alphaproteobacteria / Rhodospirillales / Rhodospirillaceae / Pararhodospirillum Pararhodospirillum species are spiral-shaped, mesophilic, and phototrophic freshwater bacteria of the Rhodospirillaceae family. Cells are motile by polar flagella, and photosynthetic pigments are located in internal photosynthetic membranes present as lamellar stacks. Photosynthetic pigments are bacteriochlorophyll a and carotenoids of the spirilloxanthin series with spirilloxanthin itself lacking. Ubiquinone-9 and rhodoquinone-9 are the major quinones. All species are sensitive to oxygen and require anoxic or microoxic conditions for growth. They grow photoheterotrophically under anoxic conditions in the light. Photoautotrophic growth, aerobic chemotrophic growth, and fermentative growth have not been demonstrated. Growth factors are required. DNA G + C content (mol%): 60.2–65.8 (Bd and HPLC) and 64.7–67 (GA). Type species: Pararhodospirillum photometricum Lakshmi et al. 2014VP (basonym: Rhodospirillum photometricum Molisch 1907AL).

Description: Ro.se.o.spi'ra. L. masc. adj. roseus, rosy; Gr. fem. n. spira, the spiral; N.L. fem. n. Roseospira the rosy spiral. Proteobacteria / Alphaproteobacteria / Rhodospirillales / Rhodospirillaceae / Roseospira Roseospira species are vibrioid to spiral shaped, anoxygenic, and phototrophic bacteria of the Rhodospirillaceae family that live in various types of marine and slightly saline habitats all over the world. The photosynthetic pigments are bacteriochlorophyll a and carotenoids of the spirilloxanthin series, and internal photosynthetic membranes are present as vesicles. They perform a phototrophic way of life using organic substrates (photoheterotrophic growth) or inorganic reduced sulfur compounds (photoautotrophic growth) as electron donors for photosynthesis. Bacteriochlorophyll biosynthesis depends on anoxic to microoxic conditions, and chemotrophic growth is possible under microoxic to oxic conditions in the light. Nitrogenase and ribulose bisphosphate carboxylase may be present. Vitamins or yeast extracts are required as growth factors. The G + C content of the DNA is 67.8–71.2 (GA), and the genome size ranges from 4.19 to 4.61 Mb. DNA G + C content (mol%): 67.8–71.2 (GA) (type species 66.6 Tm). Type species: Roseospira mediosalina Imhoff et al. 1998VP (synonym: “Rhodospirillum mediosalinum” Kompantseva and Gorlenko 1984).

Description: It is generally assumed that seismic activity at volcanoes is closely connected to degassing processes. Intuitively, one would therefore expect a good correlation between degassing rates and seismic amplitude. However, both examples and counterexamples of such a correlation exist. In this study on Villarrica volcano (Chile), we pursued a different approach to relate gas flux and volcanic seismicity using 3 months of SO$_2$ flux rate measurements and 12 days of seismic recordings from early 2012.〈br /> We analyzed the statistical distributions of interevent times between transient seismic waveforms commonly associated with explosions and between peaks in the degassing time series.〈br /> Both event types showed a periodic recurrence with a mode of 20-25 s and around 1 h for transients and degassing, respectively. The normalized interevent times were fitted by almost identical log-normal distributions. Given the actually very different time scales, this similarity potentially indicates a scale-invariant phenomenon. We could reproduce these empirical findings by modelling the occurrence of transients as a renewal process from which the degassing events were derived recursively with increasing probability since the previous degassing event. In this model, the seismic transients could be either produced by degassing processes within the conduit or by gas release at the lava lake surface while the longer intervals of the degassing events may be explained by accumulation of gas either in the magma column or in the juvenile gas plume.〈br /> Additionally, we analyzed volcano-tectonic events, which behaved very differently from the transients. They showed the clustered occurrence of tectonic earthquakes.

Description: Proteobacteria Alphaproteobacteria Rhizobiales Hyphomicrobiaceae Blas.to.chlo'ris. Gr. masc. n. blastos bud shoot; Gr. masc. adj. chloros green; N.L. fem. n. Blastochloris green bud shoot. Proteobacteria / Alphaproteobacteria / Rhizobiales / Hyphomicrobiaceae / Blastochloris Blastochloris species are anoxygenic phototrophic Alphaproteobacteria that have bacteriochlorophyll b in their photosynthetic reaction centers. Crystals of the photosynthetic reaction centers of Blastochloris viridis were the first that have been studied in high‐resolution structure analysis at 3 Å resolution. Internal photosynthetic membranes are present as lamellae underlying and parallel to the cytoplasmic membrane. Cells are rod shaped to ovoid and exhibit polar growth, budding, and asymmetric cell division and form rosette‐like cell aggregates. They are motile by means of subpolar flagella and stain Gram‐negative. Straight‐chain monounsaturated C18:1 is the predominant component of cellular fatty acids. Ubiquinones and menaquinones are present, and the lipopolysaccharides are characterized by a 2,3‐diamino‐2,3‐deoxy‐d‐glucose (DAG)‐containing, phosphate‐free lipid A with amide‐bound C14:0 3OH. DNA G + C content (mol%): 63.8–68.3. Type species: Blastochloris viridis (Drews and Giesbrecht 1966) Hiraishi 1997 (Rhodopseudomonas viridis Drews and Giesbrecht 1966).

Description: Keypoints This contribution is a reply on a comment submitted by A. Argnani. The alternate interpretation of the wide-angle seismic model is discussed. The Alfeo Fault system is proposed to be the current location of STEP fault. Abstract Andrea Argnani in his comment on Dellong et al., 2020 (Geometry of the deep Calabrian subduction (Central Mediterranean Sea) from wide‐angle seismic data and 3D gravity modeling), proposes an alternate interpretation of the wide-angle seismic velocity models presented by Dellong et al., 2018 and Dellong et al., 2020 and proposes a correction of the literature citations in these paper. In this reply, we discuss in detail all points raised by Andrea Argnani.

Description: Seamounts are ubiquitous on the oceanic plate; those situated near convergent margins will eventually undergo subduction. Using six prestack depth migrated MCS profiles transecting the Aleutian Trench, we investigate deeply buried seamounts offshore Kodiak Island, within 145–155°W and 55–58°N. A distinct sedimentary horizon exists in all six seismic profiles, at or above the average height of seamounts, which appears to be the preferred structural detachment zone. Where drilled, this horizon contains gravel‐sized debris interpreted to be ice rafted and marks the onset of intensification of Northern Hemisphere glaciation at ~2.7 Ma. Beneath this horizon, sediments prior to the Surveyor Fan development were deposited, all or the majority of these sediments will eventually be subducted. Despite the subducted seamounts being deeply buried, these features cause enhanced surface slope of the accretionary prism. Our observations lead us to propose a model for the stages of subduction for deeply buried seamounts. These stages include the following: (1) Prior to subduction, the protothrust zone undergoes enhanced shortening, (2) frontal thrust steepening and enhanced backthrusting occurs during subduction with a potential décollement step down seaward and a steeping outward of the deformation front to the limit of the protothrust zone, and (3) further subduction results in a pattern of uplift farther into the wedge resulting in enhanced out‐of‐sequence thrusting and persistence of the more seaward deformation front position. This pattern is distinct from the dominance of embayments and effective removal of prism material during seamount subduction described along margins with less deeply buried edifices.

Description: A coordinated regional climate model (RCM) evaluation and intercomparison project based on observations from a July–October 2014 trans‐Arctic Ocean field experiment (ACSE‐Arctic Clouds during Summer Experiment) is presented. Six state‐of‐the‐art RCMs were constrained with common reanalysis lateral boundary forcing and upper troposphere nudging techniques to explore how the RCMs represented the evolution of the surface energy budget (SEB) components and their relation to cloud properties. We find that the main reasons for the modeled differences in the SEB components are a direct consequence of the RCM treatment of cloud and cloud‐radiative interactions. The RCMs could be separated into groups by their overestimation or underestimation of cloud liquid. While radiative and turbulent heat flux errors were relatively large, they often invoke compensating errors. In addition, having the surface sea‐ice concentrations constrained by the reanalysis or satellite observations limited how errors in the modeled radiative fluxes could affect the SEB and ultimately the surface evolution and its coupling with lower tropospheric mixing and cloud properties. Many of these results are consistent with RCM biases reported in studies over a decade ago. One of the six models was a fully coupled ocean‐ice‐atmosphere model. Despite the biases in overestimating cloud liquid, and associated SEB errors due to too optically thick clouds, its simulations were useful in understanding how the fully coupled system is forced by, and responds to, the SEB evolution. Moving forward, we suggest that development of RCM studies need to consider the fully coupled climate system.

Description: Green sulfur bacteria, the Chlorobiaceae, have gained much attention because of unique structures of the photosynthetic apparatus and the presence of chlorosomes as very powerful light antenna that can capture minute amounts of light. This has important ecological consequences, because the efficient light‐harvesting determines the ecological niche of these bacteria at the lowermost part of stratified environments where the least of light is available. The oxidation of sulfide as their outmost important photosynthetic electron donor involves the deposition of elemental sulfur globules outside the cells and separates the process of sulfide oxidation to sulfate into two parts. This is the basis for stable syntrophic associations between green sulfur bacteria and sulfur‐ and sulfate‐reducing bacteria in which the sulfur compounds are recycled. The green sulfur bacteria are distantly related to other bacteria and systematically members of the Chlorobiaceae family with Chlorobium, Chlorobaculum, Prosthecochloris and Chloroherpeton as representative genera. Green sulfur bacteria depend on light for life due to their obligate phototrophic metabolism. Green sulfur bacteria are most efficient in photosynthesis due to the presence of light‐harvesting organelles, the chlorosomes, which are filled with bacteriochlorophyll molecules. Green sulfur bacteria are offsprings of one of the most ancient bacterial lineages performing biosynthesis of bacteriochlorophyll and photosynthesis. Green sulfur bacteria inhabit the lowermost light‐receiving part of the chemocline in the stratified environment due to their high sensitivity to oxygen, high tolerance to the toxic sulfide and highly efficient light capture. Green sulfur bacteria are important drivers of oxidation of reduced sulfur compounds in the stratified, sulfide‐containing environment receiving low irradiation.

Description: Rho.do.mi.cro' bi.um. Gr. neut. n. rhodon the rose; Gr. masc. adj. micros small; Gr. masc. n. bios life; N.L. neut. n. Rhodomicrobium red microbe. Proteobacteria / Alphaproteobacteria / Rhizobiales / Hyphomicrobiaceae / Rhodomicrobium Most characteristic for Rhodomicrobium species is the polar cell growth and the characteristic vegetative growth cycle which includes the formation of peritrichously flagellated swarmer cells and nonmotile “mother cells,” which form prosthecae from one to several times the length of the mother cell. Daughter cells originate as spherical buds at the end of the prosthecae and may undergo differentiation in various ways. They are Gram-negative ovoid to elongate-ovoid bacteria belonging to the Alphaproteobacteria. Internal photosynthetic membranes are of the lamellar type. Photosynthetic pigments are bacteriochlorophyll a and carotenoids of the spirilloxanthin series. The predominant cellular fatty acid is C18:1, which comprises more than 80% of the membrane-bound fatty acids. Ubiquinone and rhodoquinone with 10 isoprene units are present, and the lipopolysaccharides are characterized by a glucosamine-containing, phosphate-free lipid A with amide-bound C16:0 3 OH. DNA G + C content (mol%): 61.8–63.8. Type species: Rhodomicrobium vannielii Duchow and Douglas 1949.

Description: Proteobacteria Alphaproteobacteria Rhizobiales Hyphomicrobiaceae Blas.to.chlo'ris. Gr. masc. n. blastos bud shoot; Gr. masc. adj. chloros green; N.L. fem. n. Blastochloris green bud shoot. Proteobacteria / Alphaproteobacteria / Rhizobiales / Hyphomicrobiaceae / Blastochloris Blastochloris species are anoxygenic phototrophic Alphaproteobacteria that have bacteriochlorophyll b in their photosynthetic reaction centers. Crystals of the photosynthetic reaction centers of Blastochloris viridis were the first that have been studied in high-resolution structure analysis at 3 Å resolution. Internal photosynthetic membranes are present as lamellae underlying and parallel to the cytoplasmic membrane. Cells are rod shaped to ovoid and exhibit polar growth, budding, and asymmetric cell division and form rosette-like cell aggregates. They are motile by means of subpolar flagella and stain Gram-negative. Straight-chain monounsaturated C18:1 is the predominant component of cellular fatty acids. Ubiquinones and menaquinones are present, and the lipopolysaccharides are characterized by a 2,3-diamino-2,3-deoxy-d-glucose (DAG)-containing, phosphate-free lipid A with amide-bound C14:0 3OH. DNA G + C content (mol%): 63.8–68.3. Type species: Blastochloris viridis (Drews and Giesbrecht 1966) Hiraishi 1997 (Rhodopseudomonas viridis Drews and Giesbrecht 1966).

Description: Rho.do.mi.cro' bi.um. Gr. neut. n. rhodon the rose; Gr. masc. adj. micros small; Gr. masc. n. bios life; N.L. neut. n. Rhodomicrobium red microbe. Proteobacteria / Alphaproteobacteria / Rhizobiales / Hyphomicrobiaceae / Rhodomicrobium Most characteristic for Rhodomicrobium species is the polar cell growth and the characteristic vegetative growth cycle which includes the formation of peritrichously flagellated swarmer cells and nonmotile “mother cells,” which form prosthecae from one to several times the length of the mother cell. Daughter cells originate as spherical buds at the end of the prosthecae and may undergo differentiation in various ways. They are Gram‐negative ovoid to elongate‐ovoid bacteria belonging to the Alphaproteobacteria. Internal photosynthetic membranes are of the lamellar type. Photosynthetic pigments are bacteriochlorophyll a and carotenoids of the spirilloxanthin series. The predominant cellular fatty acid is C18:1, which comprises more than 80% of the membrane‐bound fatty acids. Ubiquinone and rhodoquinone with 10 isoprene units are present, and the lipopolysaccharides are characterized by a glucosamine‐containing, phosphate‐free lipid A with amide‐bound C16:0 3 OH. DNA G + C content (mol%): 61.8–63.8. Type species: Rhodomicrobium vannielii Duchow and Douglas 1949.

Description: The availability of dissolved iron (dFe) exerts an important control on primary production. Recent ocean observation programs have provided information on dFe in many parts of the ocean, but knowledge is still limited concerning the rates of processes that control the concentrations and cycling of dFe in the ocean and hence the role of dFe as a determinant of global primary production. We constructed a three-dimensional gridded dataset of oceanic dFe concentrations by using both observations and a simple model of the iron cycle, and estimated the difference of processes among the ocean basins in controlling the dFe distributions. A Green's function approach was used to integrate the observations and the model. The reproduced three-dimensional dFe distribution indicated that iron influx from aeolian dust and from shelf sediment were 7.6 Gmol yr and 4.4 Gmol yr in the Atlantic Ocean and 0.4 Gmol yr and 4.1 Gmol yr in the Pacific Ocean. The residence times were estimated to be 12.2 years in the Atlantic and 80.4 years in the Pacific. These estimates imply large differences in the cycling of dFe between the two ocean basins that would need to be taken into consideration when projecting future iron biogeochemical cycling under different climate change scenarios. Although there is some uncertainty in our estimates, global estimates of iron cycle characteristics based on this approach can be expected to enhance our understanding of the material cycle and hence of the current and future rates of marine primary production.