COMPARISON BETWEEN PORIFERA and CNIDARIA Colwyn Sleep INTRODUCTION
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Nitrogen-Fixing, Photosynthetic, Anaerobic Bacteria Associated with Pelagic Copepods
- AQUATIC MICROBIAL ECOLOGY Vol. 12: 105-113. 1997 Published April 10 , Aquat Microb Ecol Nitrogen-fixing, photosynthetic, anaerobic bacteria associated with pelagic copepods Lita M. Proctor Department of Oceanography, Florida State University, Tallahassee, Florida 32306-3048, USA ABSTRACT: Purple sulfur bacteria are photosynthetic, anaerobic microorganisms that fix carbon di- oxide using hydrogen sulfide as an electron donor; many are also nitrogen fixers. Because of the~r requirements for sulfide or orgamc carbon as electron donors in anoxygenic photosynthesis, these bac- teria are generally thought to be lim~tedto shallow, organic-nch, anoxic environments such as subtidal marine sediments. We report here the discovery of nitrogen-fixing, purple sulfur bactena associated with pelagic copepods from the Caribbean Sea. Anaerobic incubations of bacteria associated with fuU- gut and voided-gut copepods resulted in enrichments of purple/red-pigmented purple sulfur bacteria while anaerobic incubations of bacteria associated with fecal pellets did not yield any purple sulfur bacteria, suggesting that the photosynthetic anaerobes were specifically associated with copepods. Pigment analysis of the Caribbean Sea copepod-associated bacterial enrichments demonstrated that these bactena possess bacter~ochlorophylla and carotenoids in the okenone series, confirming that these bacteria are purple sulfur bacteria. Increases in acetylene reduction paralleled the growth of pur- ple sulfur bactena in the copepod ennchments, suggesting that the purple sulfur bacteria are active nitrogen fixers. The association of these bacteria with planktonic copepods suggests a previously unrecognized role for photosynthetic anaerobes in the marine S, N and C cycles, even in the aerobic water column of the open ocean. KEY WORDS: Manne purple sulfur bacterla . -
The Anti-Viral Applications of Marine Resources for COVID-19 Treatment: an Overview
marine drugs Review The Anti-Viral Applications of Marine Resources for COVID-19 Treatment: An Overview Sarah Geahchan 1,2, Hermann Ehrlich 1,3,4,5 and M. Azizur Rahman 1,3,* 1 Centre for Climate Change Research, Toronto, ON M4P 1J4, Canada; [email protected] (S.G.); [email protected] (H.E.) 2 Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON M5S 2E8, Canada 3 A.R. Environmental Solutions, University of Toronto, ICUBE-UTM, Mississauga, ON L5L 1C6, Canada 4 Institute of Electronic and Sensor Materials, TU Bergakademie Freiberg, 09599 Freiberg, Germany 5 Center for Advanced Technology, Adam Mickiewicz University, 61614 Poznan, Poland * Correspondence: [email protected] Abstract: The ongoing pandemic has led to an urgent need for novel drug discovery and potential therapeutics for Sars-CoV-2 infected patients. Although Remdesivir and the anti-inflammatory agent dexamethasone are currently on the market for treatment, Remdesivir lacks full efficacy and thus, more drugs are needed. This review was conducted through literature search of PubMed, MDPI, Google Scholar and Scopus. Upon review of existing literature, it is evident that marine organisms harbor numerous active metabolites with anti-viral properties that serve as potential leads for COVID- 19 therapy. Inorganic polyphosphates (polyP) naturally found in marine bacteria and sponges have been shown to prevent viral entry, induce the innate immune response, and downregulate human ACE-2. Furthermore, several marine metabolites isolated from diverse sponges and algae have been shown to inhibit main protease (Mpro), a crucial protein required for the viral life cycle. Sulfated polysaccharides have also been shown to have potent anti-viral effects due to their anionic properties and high molecular weight. -
Examples of Sea Sponges
Examples Of Sea Sponges Startling Amadeus burlesques her snobbishness so fully that Vaughan structured very cognisably. Freddy is ectypal and stenciling unsocially while epithelial Zippy forces and inflict. Monopolistic Porter sailplanes her honeymooners so incorruptibly that Sutton recirculates very thereon. True only on water leaves, sea of these are animals Yellow like Sponge Oceana. Deeper dives into different aspects of these glassy skeletons are ongoing according to. Sponges theoutershores. Cell types epidermal cells form outer covering amoeboid cells wander around make spicules. Check how These Beautiful Pictures of Different Types of. To be optimal for bathing, increasing with examples of brooding forms tan ct et al ratios derived from other microscopic plants from synthetic sponges belong to the university. What is those natural marine sponge? Different types of sponges come under different price points and loss different uses in. Global Diversity of Sponges Porifera NCBI NIH. Sponges EnchantedLearningcom. They publish the outer shape of rubber sponge 1 Some examples of sponges are Sea SpongeTube SpongeVase Sponge or Sponge Painted. Learn facts about the Porifera or Sea Sponges with our this Easy mountain for Kids. What claim a course Sponge Acme Sponge Company. BG Silicon isotopes of this sea sponges new insights into. Sponges come across an incredible summary of colors and an amazing array of shapes. 5 Fascinating Types of what Sponge Leisure Pro. Sea sponges often a tube-like bodies with his tiny pores. Sponges The World's Simplest Multi-Cellular Creatures. Sponges are food of various nudbranchs sea stars and fish. Examples of sponges Answers Answerscom. Sponges info and games Sheppard Software. -
Freshwater Sponge Hosts and Their Green Algae Symbionts
bioRxiv preprint doi: https://doi.org/10.1101/2020.08.12.247908; this version posted August 13, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Freshwater sponge hosts and their green algae 2 symbionts: a tractable model to understand intracellular 3 symbiosis 4 5 Chelsea Hall2,3, Sara Camilli3,4, Henry Dwaah2, Benjamin Kornegay2, Christine A. Lacy2, 6 Malcolm S. Hill1,2§, April L. Hill1,2§ 7 8 1Department of Biology, Bates College, Lewiston ME, USA 9 2Department of Biology, University of Richmond, Richmond VA, USA 10 3University of Virginia, Charlottesville, VA, USA 11 4Princeton University, Princeton, NJ, USA 12 13 §Present address: Department of Biology, Bates College, Lewiston ME USA 14 Corresponding author: 15 April L. Hill 16 44 Campus Ave, Lewiston, ME 04240, USA 17 Email address: [email protected] 18 19 20 21 22 23 24 25 26 bioRxiv preprint doi: https://doi.org/10.1101/2020.08.12.247908; this version posted August 13, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 27 Abstract 28 In many freshwater habitats, green algae form intracellular symbioses with a variety of 29 heterotrophic host taxa including several species of freshwater sponge. These sponges perform 30 important ecological roles in their habitats, and the poriferan:green algae partnerships offers 31 unique opportunities to study the evolutionary origins and ecological persistence of 32 endosymbioses. -
Dynamics of Microbial Community in the Marine Sponge Holichondria Sp
July 30, 2003 Dynamics of microbial community in the marine sponge Holichondria sp. Microbial Diversity Course, Marine Biological Laboratory, Woods Hole, MA Gil Zeidner, Faculty of Biology, Technion, Haifa, Israel. 1 Abstract Marine sponges often harbor communities of symbiotic microorganisms that fulfill necessary functions for the well being of their hosts. Microbial communities are susceptible to environmental pollution and have previously been used as sensitive markers for anthropogenic stress in aquatic ecosystems. Previous work done on dynamics of the microbial community in sponges exposed to different copper concentrations have shown a significant reduction in the total density of bacteria and diversity. A combined strategy incorporating quantitative and qualitative techniques was used to monitor changes in the microbial diversity in sponge during transition into polluted environment. Introduction Sponges are known to be associated with large amounts of bacteria that can amount to 40% of the biomass of the sponge. Various microorganisms have evolved to reside in sponges, including cyanobacteria, diverse heterotrophic bacteria, unicellular algae and zoochlorellae(Webster et al., 2001b). Since sponges are filter feeders, a certain amount of transient bacteria are trapped within the vascular system or attached to the sponge surface. Microbial communities are susceptible to different environmentral pollution agents and have previously been used as sensitive markers for anthropogenic stress in aquatic ecosystems(Webster et al., 2001a). It is possible that shifts in symbiont community composition may result from pollution stress, and these shifts may, in turn, have detrimental effects on the host sponge. The breakdown of symbiotic relationships is a common indicator of sublethal stress in marine organisms. -
Comprehensive Phylogenomic Analyses Resolve Cnidarian Relationships and the Origins of Key Organismal Traits
Comprehensive phylogenomic analyses resolve cnidarian relationships and the origins of key organismal traits Ehsan Kayal1,2, Bastian Bentlage1,3, M. Sabrina Pankey5, Aki H. Ohdera4, Monica Medina4, David C. Plachetzki5*, Allen G. Collins1,6, Joseph F. Ryan7,8* Authors Institutions: 1. Department of Invertebrate Zoology, National Museum of Natural History, Smithsonian Institution 2. UPMC, CNRS, FR2424, ABiMS, Station Biologique, 29680 Roscoff, France 3. Marine Laboratory, university of Guam, UOG Station, Mangilao, GU 96923, USA 4. Department of Biology, Pennsylvania State University, University Park, PA, USA 5. Department of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH, USA 6. National Systematics Laboratory, NOAA Fisheries, National Museum of Natural History, Smithsonian Institution 7. Whitney Laboratory for Marine Bioscience, University of Florida, St Augustine, FL, USA 8. Department of Biology, University of Florida, Gainesville, FL, USA PeerJ Preprints | https://doi.org/10.7287/peerj.preprints.3172v1 | CC BY 4.0 Open Access | rec: 21 Aug 2017, publ: 21 Aug 20171 Abstract Background: The phylogeny of Cnidaria has been a source of debate for decades, during which nearly all-possible relationships among the major lineages have been proposed. The ecological success of Cnidaria is predicated on several fascinating organismal innovations including symbiosis, colonial body plans and elaborate life histories, however, understanding the origins and subsequent diversification of these traits remains difficult due to persistent uncertainty surrounding the evolutionary relationships within Cnidaria. While recent phylogenomic studies have advanced our knowledge of the cnidarian tree of life, no analysis to date has included genome scale data for each major cnidarian lineage. Results: Here we describe a well-supported hypothesis for cnidarian phylogeny based on phylogenomic analyses of new and existing genome scale data that includes representatives of all cnidarian classes. -
Sponges) and Phylum Cnidaria (Jellyfish, Sea Anemones and Corals
4/14/2014 Kingdom Animalia: Phylum Porifera (sponges) and Phylum Cnidaria (jellyfish, sea anemones and corals) 1 4/14/2014 Animals have different types of symmetry AsymmetricalÆ Radial Æ Bilateral Æ Embryo development provides information about how animal groups are related Blastula: hallow with a single layer of cells Gastrula: results in two layers of cells and cavity (gut) with one opening (blastopore) Cavity reaches the other side and the gut is like a tube Some cells from a third layer of cells A second cavityyg forms between the gut and the outside of the animal 2 4/14/2014 Animals have different number of true tissue layers and different type of gut No true tissuesÆ Two tissue layers Æ Three tissue layersÆ No gutÆ Sac like gutÆ Tube like gutÆ Phylum Porifera: Simplest of Animals Sponges: No tissues, no symmetry Intracellular digestion, no digestive system or cavity Collar cells or choanocytes Support by spicules or spongin fibers 3 4/14/2014 Procedure 1 • Grantia sponge Locate osculum • Sponge spicules Bell Labs Research on Deep-Sea Sponge Yields Substantial Mechanical Engineering Insights 4 4/14/2014 Medications from Sponges Thirty percent of all potential new natural medicine has been isolated in sponges. About 75% of the recently registered and patented material to fight cancer comes from sponges. Furthermore, it appears that medicine from sponges helps, for example, asthma and psoriasis; therefore it offers enormous possibilities for research. Eribulin, a novel chemotherapy drug derived from a sea sponge, improves survival in heavily-pretreated metastatic breast cancer. Phylum Cnidaria Coral Sea Anemone Man-of-war Hydra Jellyfish 5 4/14/2014 Phylum Cnidaria Tissues: Endoderm Ectoderm Type of gut: Symmetry: Radial Cnidocytes or Stinging cells Polyp or Medusa form Importance Some jellyfish are considered a delicacy Corals: Medicines cabinets for the 21st century cancer cell inhibitor Sunscreen 6 4/14/2014 Procedure 2 2. -
On Some Hydroids (Cnidaria) from the Coast of Pakistan
Pakistan J. Zool., vol. 38(3), pp. 225-232, 2006. On Some Hydroids (Cnidaria) from the Coast of Pakistan NASEEM MOAZZAM AND MOHAMMAD MOAZZAM Institute of Marine Sciences, University of Karachi, Karachi 75270, Pakistan (NM) and Marine Fisheries Department, Government of Pakistan, Fish Harbour, West Wharf, Karachi 74900, Pakistan (MM) Abstract .- The paper deals with the occurrence of eleven species of the hydroids from the coast of Pakistan. All the species are reported for the first time from Pakistan. These species are Hydractinia epidocleensis, Pennaria disticha, Eudendrium capillare, Orthopyxis cf. crenata, Clytia noliformis, C. hummelincki, Dynamena crisioides, D. quadridentata, Sertularia distans, Pycnotheca mirabilis and Macrorhynchia philippina. Key words: Hydroids, Coelenterata, Pakistan, Hydractinia, Pennaria, Eudendrium, Orthopyxis, Clytia, Dynamena, Sertularia, Pycnotheca, Macrorhynchia. INTRODUCTION used in the paper are derived from Millard (1975), Gibbons and Ryland (1989), Ryland and Gibbons (1991). In comparison to other invertebrates, TAXONOMIC ENUMERATION hydroids are one of the least known groups of marine animals from the coast of Pakistan Haque Family BOUGAINVILLIIDAE (1977) reported a few Cnidaria from the Pakistani Genus HYDRACTINIA Van Beneden, 1841 coast including two hydroids i.e. Plumularia flabellum Allman, 1883 (= P. insignis Allman, 1. Hydractinia epidocleensis Leloup, 1931 1883) and Campanularia juncea Allman, 1874 (= (Fig. 1) Thyroscyphus junceus (Allman, 1876) from Keamari and Bhit Island, Karachi, respectively. Ahmed and Hameed (1999), Ahmed et al. (1978) and Haq et al. (1978) have mentioned the presence of hydroids in various habitats along the coast of Pakistan. Javed and Mustaquim (1995) reported Sertularia turbinata (Lamouroux, 1816) from Manora Channel, Karachi. The present paper describes eleven species of Cnidaria collected from the Pakistani coast all of which are new records for Pakistan. -
Sponges and Bryozoans of Sandusky Bay
Ohio Naturalist. [Vol. 1, No. SPONGES AND BRYOZOANS OF SANDUSKY BAY. F. L. LANDACRE. The two small groups of fresh water sponges and Bryozoa re- ceived some attention at the Lake laboratory during the summer of 1900 All our fresh water sponges belong to one family, the SpongiUidae, which has about seven genera. They differ from the marine sponges- in two particulars. They form skeletons of silicon only, while marine sponges may form silicious or limy or spongin skeletons. The spongin skeleton-is the-one that gives the bath sponge its value.. They also form winter buds or statoblasts which carry the sponge over the winter and reproduce it again in the spring. This peculiar process was probably acquired on account of the changes in temperature and in amount of moisture to which animals living in fresh water streams are subjected. The sponge dies in the fall of the year and its skeleton of silicious spines or spicules can be found with no protoplasm. The character of the spines in the body of the sponge and those surrounding the statoblast differ greatly, and those around the statoblast are the main reliance in identifying sponges. So that if a statoblast is found the sponge from which it came can be determined, and on the other hand it is frequently very difficult to determine the species of a sponge if it has not yet formed its stato- blast. The statoblast is a globular or disc-shaped, nitroginous cell with a chimney-like opening where the protoplasm escapes in the spring. The adult sponge is non-sexual but the statoblasts give rise to ova and spermatozoa which unite and produce a new sponge. -
Cnidarian Immunity and the Repertoire of Defense Mechanisms in Anthozoans
biology Review Cnidarian Immunity and the Repertoire of Defense Mechanisms in Anthozoans Maria Giovanna Parisi 1,* , Daniela Parrinello 1, Loredana Stabili 2 and Matteo Cammarata 1,* 1 Department of Earth and Marine Sciences, University of Palermo, 90128 Palermo, Italy; [email protected] 2 Department of Biological and Environmental Sciences and Technologies, University of Salento, 73100 Lecce, Italy; [email protected] * Correspondence: [email protected] (M.G.P.); [email protected] (M.C.) Received: 10 August 2020; Accepted: 4 September 2020; Published: 11 September 2020 Abstract: Anthozoa is the most specious class of the phylum Cnidaria that is phylogenetically basal within the Metazoa. It is an interesting group for studying the evolution of mutualisms and immunity, for despite their morphological simplicity, Anthozoans are unexpectedly immunologically complex, with large genomes and gene families similar to those of the Bilateria. Evidence indicates that the Anthozoan innate immune system is not only involved in the disruption of harmful microorganisms, but is also crucial in structuring tissue-associated microbial communities that are essential components of the cnidarian holobiont and useful to the animal’s health for several functions including metabolism, immune defense, development, and behavior. Here, we report on the current state of the art of Anthozoan immunity. Like other invertebrates, Anthozoans possess immune mechanisms based on self/non-self-recognition. Although lacking adaptive immunity, they use a diverse repertoire of immune receptor signaling pathways (PRRs) to recognize a broad array of conserved microorganism-associated molecular patterns (MAMP). The intracellular signaling cascades lead to gene transcription up to endpoints of release of molecules that kill the pathogens, defend the self by maintaining homeostasis, and modulate the wound repair process. -
Current Understanding of the Circadian Clock Within Cnidaria 31
Current Understanding of the Circadian Clock Within Cnidaria 31 Kenneth D. Hoadley , Peter D. Vize , and Sonja J. Pyott Abstract Molecularly-based timing systems drive many periodic biological processes in both animals and plants. In cnidarians these periodic processes include daily cycles in metabolism, growth, and tentacle and body wall movements and monthly or yearly reproductive activity. In this chapter we review the current understanding of biological clocks in the cnidaria, with an empha- sis on the molecular underpinnings of these processes. The genes that form this molecular clock and drive biological rhythms in well-characterized genetic systems such as Drosophila and mouse are highly conserved in cnidarians and, like these model systems, display diel cycles in transcription levels. In addition to describing the clock genes, we also review potential entrain- ing systems and discuss the broader implications of biological clocks in cnidarian biology. Keywords Circadian rhythms • Biological clocks • Reproductive timing • Non-visual photodetection • Light perception 31.1 Overview of studies focusing on the molecular basis of the circadian clock . Across species, from bacteria, to fungi, to plants and Entrainment of physiological rhythms to environmental cues animals, this molecular circadian clock involves transcription is ubiquitous among living organisms and allows coordination and translation feedback loops with a self-sustained period of of biology and behavior with daily environmental changes . about 24 h (reviewed in Dunlap 1999 ). Investigation in the This coordination improves survival and reproductive fi tness , model genetic species, mouse and fl y, has identifi ed a core set and, thus, it is not surprising that an endogenous “clock” has of genes that form the central oscillator in animals (reviewed evolved to maintain rhythmicity over a circadian (24 h) period. -
This Article Was Published in an Elsevier Journal. the Attached Copy
This article was published in an Elsevier journal. The attached copy is furnished to the author for non-commercial research and education use, including for instruction at the author’s institution, sharing with colleagues and providing to institution administration. Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. In most cases authors are permitted to post their version of the article (e.g. in Word or Tex form) to their personal website or institutional repository. Authors requiring further information regarding Elsevier’s archiving and manuscript policies are encouraged to visit: http://www.elsevier.com/copyright Author's personal copy Available online at www.sciencedirect.com Geochimica et Cosmochimica Acta 72 (2008) 1396–1414 www.elsevier.com/locate/gca Okenane, a biomarker for purple sulfur bacteria (Chromatiaceae), and other new carotenoid derivatives from the 1640 Ma Barney Creek Formation Jochen J. Brocks a,*, Philippe Schaeffer b a Research School of Earth Sciences and Centre for Macroevolution and Macroecology, The Australian National University, Canberra, ACT 0200, Australia b Laboratoire de Ge´ochimie Bio-organique, CNRS UMR 7177, Ecole Europe´enne de Chimie, Polyme`res et Mate´riaux, 25 rue Becquerel, 67200 Strasbourg, France Received 20 June 2007; accepted in revised form 12 December 2007; available online 23 December 2007 Abstract Carbonates of the 1640 million years (Ma) old Barney Creek Formation (BCF), McArthur Basin, Australia, contain more than 22 different C40 carotenoid derivatives including lycopane, c-carotane, b-carotane, chlorobactane, isorenieratane, b-iso- renieratane, renieratane, b-renierapurpurane, renierapurpurane and the monoaromatic carotenoid okenane.