Current Status and Potential for Algal Biofuels Production
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Analysis of Land Suitable for Algae Production State of Hawaii
Analysis of Land Suitable for Algae Production State of Hawaii Prepared for the U.S. Department of Energy Office of Electricity Delivery and Energy Reliability Under Award No. DE-FC26-06NT42847 Hawai‘i Distributed Energy Resource Technologies for Energy Security Subtask 12.1 Deliverable (item 1) Report on Bioenergy Analyses By the Hawai‘i Natural Energy Institute School of Ocean and Earth Science and Technology University of Hawai‘i August 2011 Acknowledgement: This material is based upon work supported by the United States Department of Energy under Award Number DE-FC-06NT42847. Disclaimer: This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference here in to any specific commercial product, process, or service by tradename, trademark, manufacturer, or otherwise does not necessarily constitute or imply its endorsement, recommendation, or favoring by the United States Government or any agency thereof. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof. ii Analysis of Land Suitable for Algae Production State of Hawaii Prepared by Mele Chillingworth Scott Q. Turn Hawaii Natural Energy Institute School of Ocean and Earth Sciences and Technology University of Hawaii at Manoa August 2011 Executive Summary Algae are considered to be a viable crop for biofuel production because of their projected high productivity rates, their ability to grow in a wide range of water qualities, and their potential for cultivation on land unsuitable for food production. -
Ecology of Oceanic Coccolithophores. I. Nutritional Preferences of the Two Stages in the Life Cycle of Coccolithus Braarudii and Calcidiscus Leptoporus
AQUATIC MICROBIAL ECOLOGY Vol. 44: 291–301, 2006 Published October 10 Aquat Microb Ecol Ecology of oceanic coccolithophores. I. Nutritional preferences of the two stages in the life cycle of Coccolithus braarudii and Calcidiscus leptoporus Aude Houdan, Ian Probert, Céline Zatylny, Benoît Véron*, Chantal Billard Laboratoire de Biologie et Biotechnologies Marines, Université de Caen Basse-Normandie, Esplanade de la Paix, 14032 Caen Cedex, France ABSTRACT: Coccolithus braarudii and Calcidiscus leptoporus are 2 coccolithophores (Prymnesio- phyceae: Haptophyta) known to possess a complex heteromorphic life cycle, with alternation between a motile holococcolith-bearing haploid stage and a non-motile heterococcolith-bearing diploid stage. The ecological implications of this type of life cycle in coccolithophores are currently poorly known. The nutritional preferences of each stage of both species, and their growth response to conditions of turbulence were investigated by varying their growth conditions. Of the different cul- ture media tested, only the synthetic seawater medium did not support the growth of both stages of C. braarudii and C. leptoporus. With natural seawater-based media, the growth rate of the haploid phase of both coccolithophores was stimulated by the addition of soil extract (K/2: 0.23 ± 0.02 d–1 and K/2 with soil extract 0.35 ± 0.01 d–1 for the C. braarudii haploid stage), while the diploid phase was not, indicating that the motile stage is capable of utilizing compounds present in soil extract or ingest- ing bacteria that are activated in enriched media. The addition of sodium acetate to the medium also stimulated the haploid phase of C. -
A New Dawn for Industrial Photosynthesis
A New Dawn for Industrial Photosynthesis The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citation Robertson, Dan E., Stuart A. Jacobson, Frederick Morgan, David Berry, George M. Church, and Noubar B. Afeyan. 2011. A new dawn for industrial photosynthesis. Photosynthesis Research 107(3): 269-277. Published Version doi://10.1007/s11120-011-9631-7 Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:5130453 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA Photosynth Res (2011) 107:269–277 DOI 10.1007/s11120-011-9631-7 REGULAR PAPER A new dawn for industrial photosynthesis Dan E. Robertson • Stuart A. Jacobson • Frederick Morgan • David Berry • George M. Church • Noubar B. Afeyan Received: 5 October 2010 / Accepted: 26 January 2011 / Published online: 13 February 2011 Ó The Author(s) 2011. This article is published with open access at Springerlink.com Abstract Several emerging technologies are aiming to conversion. This analysis addresses solar capture and meet renewable fuel standards, mitigate greenhouse gas conversion efficiencies and introduces a unique systems emissions, and provide viable alternatives to fossil fuels. approach, enabled by advances in strain engineering, Direct conversion of solar energy into fungible liquid fuel photobioreactor design, and a process that contradicts is a particularly attractive option, though conversion of that prejudicial opinions about the viability of industrial pho- energy on an industrial scale depends on the efficiency of tosynthesis. -
Indiana Aquatic Nuisance Species (ANS) Management Plan
Indiana Aquatic Nuisance Species (ANS) Management Plan Aruana caught by angler in Lake George, Lake County, Indiana Photo credit: Brian Breidert, IDNR Indiana Department of Natural Resources Funded by: Division of Fish and Wildlife Edited by: Phil Seng and Gwen White, D.J. Case & Associates, Mishawaka, Indiana October 1, 2003 Indiana Aquatic Nuisance Species (ANS) Management Plan Table of Contents Page Executive summary 3 Introduction 6 Why should we be concerned? 6 Why are we hearing about more nuisance exotics? 6 Are all exotic species causing problems? 7 Why do some of these species become nuisances? 7 What principles should guide invasive species management in Indiana? 8 Which species are top priorities for management in Indiana? 8 Table 1. Aquatic nuisance species on the watch list and detected 9 Nuisance fish 10 Nuisance insects and crustaceans 13 Nuisance mussels and snails 14 Diseases, pathogens and parasites 15 Aquarium pets caught from Indiana waters 17 Nuisance plants 20 Which programs are engaged in management of invasive species? 23 What regulatory authorities control management of exotic species? 29 Federal role 30 Regional role 32 State role 33 Designing an integrated comprehensive regulatory approach 33 What can Hoosiers do to prevent and control the impacts of ANS? 40 Index to the strategic management plan 41 Description of strategic management plan 44 How will we know if we succeed? 58 Literature cited 60 Glossary of terms 63 List of agency and organization acronyms 64 Appendix A. List of introduced fish and crayfish 65 Appendix B. List of invasive aquatic plants 67 Appendix C. Priority list of ANS in the Great Lakes basin 69 Appendix D. -
Aquatic Species Program Review Proceedings of the March 1985 Principal Investigators Meeting
NOTICE This report was prepared as an account of work sponsored by the United States Government. Neither the United States nor the United States Department of Energy, nor any of their employees, nor any of their contractors, subcontractors, or their employees, makes any warranty, expressed or implied, or assumes any legai liability or responsibility for the accuracy, completeness or usefulness of any information, apparatus, product or process disclosed, or represents that its use would not infringe privately owned rights. Printed in the United States of America Available from: National Technical Information Service U.S. Departmenr of Commerce 5285 Port Royal Road Springfield, VA 221 61 Price: Microfiche A01 Printed Copy A1 6 Codes are ~sedfor pricing ail publications. The code is determined by the number of pages in the publication. lnformation pertaining to the pricing codes can be found in the current issue of the following publications, which are generally available in most tibraries; Energy Research Abstracts. (ERA); Government Reports Announcements and Index (GRA and I); Scientific and Technical Abstract Reports (STAR;; and publication. NTIS-PR-360 available from NT1S at the above address. SER IICP-231-2700 UC Category: 61c DE85Ol2137 Aquatic Species Program Review Proceedings of the March 1985 Principal Investigators Meeting 20 - 21 March 1985 Golden, CO June 1985 Prepared under Task No. 4513.10 FTP No. 513 Solar Energy Research Institute A Division of Midwest Research Institute 1617 Cole Boulevard Golden, Colorado 80401 Prepared for the U.S. Department of Energy Contract No. DE-AC02-83CH10093 PREFACE This volume contains progress reports presented by the Aquatic Species Program subcontractors and SERl researchers at the SERl Aquatic Species Review held at SERI, March 20 and 2 1, 1985. -
And Macro-Algae: Utility for Industrial Applications
MICRO- AND MACRO-ALGAE: UTILITY FOR INDUSTRIAL APPLICATIONS Outputs from the EPOBIO project September 2007 Prepared by Anders S Carlsson, Jan B van Beilen, Ralf Möller and David Clayton Editor: Dianna Bowles cplpressScience Publishers EPOBIO: Realising the Economic Potential of Sustainable Resources - Bioproducts from Non-food Crops © September 2007, CNAP, University of York EPOBIO is supported by the European Commission under the Sixth RTD Framework Programme Specific Support Action SSPE-CT-2005-022681 together with the United States Department of Agriculture. Legal notice: Neither the University of York nor the European Commission nor any person acting on their behalf may be held responsible for the use to which information contained in this publication may be put, nor for any errors that may appear despite careful preparation and checking. The opinions expressed do not necessarily reflect the views of the University of York, nor the European Commission. Non-commercial reproduction is authorized, provided the source is acknowledged. Published by: CPL Press, Tall Gables, The Sydings, Speen, Newbury, Berks RG14 1RZ, UK Tel: +44 1635 292443 Fax: +44 1635 862131 Email: [email protected] Website: www.cplbookshop.com ISBN 13: 978-1-872691-29-9 Printed in the UK by Antony Rowe Ltd, Chippenham CONTENTS 1 INTRODUCTION 1 2 HABITATS AND PRODUCTION SYSTEMS 4 2.1 Definition of terms 4 2.2 Macro-algae 5 2.2.1 Habitats for red, green and brown macro-algae 5 2.2.2 Production systems 6 2.3 Micro-algae 9 2.3.1 Applications of micro-algae 9 2.3.2 Production -
Literature Review of the Microalga Prymnesium Parvum and Its Associated Toxicity
Literature Review of the Microalga Prymnesium parvum and its Associated Toxicity Sean Watson, Texas Parks and Wildlife Department, August 2001 Introduction Recent large-scale fish kills associated with the golden-alga, Prymnesium parvum, have imposed monetary and ecological losses on the state of Texas. This phytoflagellate has been implicated in fish kills around the world since the 1930’s (Reichenbach-Klinke 1973). Kills due to P. parvum blooms are normally accompanied by water with a golden-yellow coloration that foams in riffles (Rhodes and Hubbs 1992). The factors responsible for the appearance of toxic P. parvum blooms have yet to be determined. The purpose of this paper is to present a review of the work by those around the globe whom have worked with Prymnesium parvum in an attempt to better understand the biology and ecology of this organism as well as its associated toxicity. I will concentrate on the relevant biology important in the ecology and identification of this organism, its occurrence, nutritional requirements, factors governing its toxicity, and methods used to control toxic blooms with which it is associated. Background Biology and Diagnostic Features Prymnesium parvum is a microalga in the class Prymnesiophyceae, order Prymnesiales and family Prymnesiaceae, and is a common member of the marine phytoplankton (Bold and Wynne 1985, Larsen 1999, Lee 1980). It is a uninucleate, unicellular flagellate with an ellipsoid or narrowly oval cell shape (Lee 1980, Prescott 1968). Green, Hibberd and Pienaar (1982) reported that the cells range from 8-11 micrometers long and 4-6 micrometers wide. The authors also noted that the cells are PWD RP T3200-1158 (8/01) 2 Lit. -
PRYMNESIUM FAVEOLATUM SP. NOV. (PRYMNESIOPHYCEAE), a NEW TOXIC SPECIES from the MEDITERRANEAN SEA J Fresnel, I
PRYMNESIUM FAVEOLATUM SP. NOV. (PRYMNESIOPHYCEAE), A NEW TOXIC SPECIES FROM THE MEDITERRANEAN SEA J Fresnel, I. Probert, C. Billard To cite this version: J Fresnel, I. Probert, C. Billard. PRYMNESIUM FAVEOLATUM SP. NOV. (PRYMNESIO- PHYCEAE), A NEW TOXIC SPECIES FROM THE MEDITERRANEAN SEA. Vie et Milieu / Life & Environment, Observatoire Océanologique - Laboratoire Arago, 2001, pp.89-97. hal-03192104 HAL Id: hal-03192104 https://hal.sorbonne-universite.fr/hal-03192104 Submitted on 7 Apr 2021 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. VIE ET MILIEU, 2001, 51 (1-2) : 89-97 PRYMNESIUM FAVEOLATUM SP. NOV. (PRYMNESIOPHYCEAE), A NEW TOXIC SPECIES FROM THE MEDITERRANEAN SEA /. FRESNEL, I. PROBERT, C. BILLARD Laboratoire de Biologie et Biotechnologies Marines, Université de Caen, Esplanade de la Paix, 14032 Caen Cedex, France PRYMNESIUM FAVEOLATUM SP. NOV. ABSTRACT. - A new marine species of Prymnesium is described based on cultu- PRYMNESIOPHYCEAE red material originating from a sublittoral sample collected on the eastern French SCALES Mediterranean coast. Prymnesium faveolatum sp. nov. exhibits typical generic cha- ULTRASTRUCTURE TOXICITY racters in terms of cell morphometry, swimming mode and organelle arrangement. MEDITERRANEAN Organic body scales, présent in several proximal layers, have a narrow inflexed rim and are ornamented with a variably developed cross. -
Emerging Interaction Patterns in the Emiliania Huxleyi-Ehv System
viruses Article Emerging Interaction Patterns in the Emiliania huxleyi-EhV System Eliana Ruiz 1,*, Monique Oosterhof 1,2, Ruth-Anne Sandaa 1, Aud Larsen 1,3 and António Pagarete 1 1 Department of Biology, University of Bergen, Bergen 5006, Norway; [email protected] (R.-A.S.); [email protected] (A.P.) 2 NRL for fish, Shellfish and Crustacean Diseases, Central Veterinary Institute of Wageningen UR, Lelystad 8221 RA, The Nederlands; [email protected] 3 Uni Research Environment, Nygårdsgaten 112, Bergen 5008, Norway; [email protected] * Correspondence: [email protected]; Tel.: +47-5558-8194 Academic Editors: Mathias Middelboe and Corina Brussaard Received: 30 January 2017; Accepted: 16 March 2017; Published: 22 March 2017 Abstract: Viruses are thought to be fundamental in driving microbial diversity in the oceanic planktonic realm. That role and associated emerging infection patterns remain particularly elusive for eukaryotic phytoplankton and their viruses. Here we used a vast number of strains from the model system Emiliania huxleyi/Emiliania huxleyi Virus to quantify parameters such as growth rate (µ), resistance (R), and viral production (Vp) capacities. Algal and viral abundances were monitored by flow cytometry during 72-h incubation experiments. The results pointed out higher viral production capacity in generalist EhV strains, and the virus-host infection network showed a strong co-evolution pattern between E. huxleyi and EhV populations. The existence of a trade-off between resistance and growth capacities was not confirmed. Keywords: Phycodnaviridae; Coccolithovirus; Coccolithophore; Haptophyta; Killing-the-winner; cost of resistance; infectivity trade-offs; algae virus; marine viral ecology; viral-host interactions 1. -
John Benemann Institute for Environmental Management, Inc
IEA Bioenergy ExCo64, Liege, Belgium,, 1/10/20091/10/2009 Algae – The Future for Bioenergy? Algae Biofuels: Challenges in Scale-up, Productivity and Harvesting (and Economics too!) John R. Benemann Benemann Associates Walnut Creek [email protected] 1 The Energy Journal, Vol. 1, No.1, 1980 Challenges to Algae Biofuels Development Microalgae are currently cultivated commercially (>100 mt/y) mainly in open shallow ponds, mostly in raceway-type, paddle wheel mixed ponds, for high value nutritional supplements, ~10,000 t/yr produced, with typical plant gate cost >$10,000/t. The biofuels challenge: producing millions of tons at <$1,000/t Microalgae are very small, grow as very dilute (<1 g/l) cultures in suspension, have very low standing biomass (<100 g/m2), require daily harvesting from large volumes of liquid, with the harvested biomass at <10% solids, must immediately process. Microalgae cultures requires a source of CO2, either purchased or “free” (power plant flue gases, biogas or ethanol plants, etc.) Not often there were we want. CO2 use is a need not a virtue! Microalgae require good climate – for a long cultivation season. For biofuels these must be produced at very high productivity And expand the number of species cultivated from four to more. 2 OUTLINE OF TALK 1. Historical development of microalgae technology 2. Current commercial reality of microalgae production 3. Scale-up: closed photobioreactors vs. open ponds 4. Harvesting: wastewater treatment by microalgae 5. Productivity: reality, fantasy and genetic engineering 6. Economics: projections for microalgae biofuels 7. Conclusions: just a few more R&D challenges First algal mass culture Inoculum Tubes project (for Chlorella) Plastic bag-type photobioreactors (PBRs) Roof of MIT Building~ 1950 3 Jack Bessel Myers Kok 2006, Austin, TX 1956, Stanford 40 hectare design based on MIT Rooftop pilot plant Fisher (1956), A.D. -
Algae's Potential As a Transportation Biofuel
Algae’s Potential as a Transportation Biofuel Kelsi Bracmort Specialist in Agricultural Conservation and Natural Resources Policy April 1, 2013 Congressional Research Service 7-5700 www.crs.gov R42122 CRS Report for Congress Prepared for Members and Committees of Congress Algae’s Potential as a Transportation Biofuel Summary Congress continues to debate the federal role in biofuel research, biofuel tax incentives, and renewable fuel mandates. The debate touches on topics such as fuel imports and security, job creation, and environmental benefits, and is particularly significant for advanced biofuels, such as those produced by algae. Congress established the Renewable Fuel Standard (RFS2)—a mandate requiring that the national fuel supply contain a minimum amount of fuel produced from renewable biomass. The RFS2 is essentially composed of two biofuel mandates—one for unspecified biofuel, which is being met with corn-starch ethanol, and one for advanced biofuels (or non-corn starch ethanol), which may not be met in coming years. Within the advanced biofuels category, the RFS2 requirements for the cellulosic biofuels subcategory (e.g., ethanol from switchgrass) have not been met for the last few years, which could cause alarm, as this subcategory is slated to ramp up from roughly 3% of the standard in 2012 to roughly 44% of the standard in 2022. Limited cellulosic biofuels production has occurred to date. As a result, as allowed under the RFS2, the Environmental Protection Agency (EPA) has lowered the required cellulosic biofuels volume for 2010, 2011, and 2012 and has proposed to do the same for 2013. Currently, algae-based biofuel qualifies as an advanced biofuel under the RFS2, but not as a cellulosic biofuel. -
An Overview on Biodiesel Fuel Production from Algae
ISSN 1907-0500 An overview on biodiesel fuel production from algae Evelyn and Padil Department of Chemical Engineering, University of Riau Kampus Bina Widya Km 12,5 Simpang Panam Pekanbaru 28293 Tel. 0761-632732, email: [email protected] Abstract Biodiesel fuel has emerged as a viable substitute for petroleum diesel and as a component to mitigate greenhouse gas emission. Biodiesel is biodegradable, less CO2 and NOx emissions and can be obtained from renewable sources. The fuel can be made easily from either virgin or waste cooking oil such as palm, soybean, canola, rice bran, sunflower, corn oil, fish oil and chicken fat. Those feedstocks are still estimated compete with the food consumptions in the future. Presently, research is being done on algae as one of alternative feedstock which are particularly rich in oils (up to 60% of their mass) and whose yield per hectare is considerably higher than that of palm (7 to 31 times). The objective of the paper gives a brief overview on biodiesel fuel production from algae to further undertake significant research. It also describes the common method of production which is base- catalyzed transesterification and some requirements of that are needed in order to achieve high-yield algal oil production. Algae require primarily three components to grow: sunlight, CO2 water and Indonesia has appropriate geographical condition that could support the growth and production of algae, therefore it is expected to introduce algae as potential feedstock for biodiesel production. In practice however, while algal oil certainly appears promising, it should be pointed out that lots more aspects need to be analysed and further experimentations to be done before one can be sure of algal oil being a worthy substitute for petro-diesel.