Luffa Sponge Gourd Production Practices for Temperate Climates

Total Page:16

File Type:pdf, Size:1020Kb

Luffa Sponge Gourd Production Practices for Temperate Climates HORTSCIENCE 29(4):263–266. 1994, and distillate flowers, which are followed by solitary distillate flowers at the uppermost nodes (Omini and Hossain, 1987). Increasing Luffa Sponge Gourd Production the number of distillate flowers would in- crease yield potential (Omini and Hossain, Practices for Temperate Climates 1987) and hasten maturity-important factors for a tropical plant grown in a temperate cli- Jeanine M. Davis1 mate. Two greenhouse studies in 1989 and Department of Horticultural Science, North Carolina State University, Mountain 1990 indicated that removing the first four to six lateral shoots would hasten distillate flower Horticultural Crops Research and Extension Center, 2016 Fanning Bridge development (J.M.D., unpublished). In con- Road, Fletcher, NC 28732 trast, preliminary research in Missouri indi- Additional index words. loofa, loofah, Luffa aegyptiaca, Luffa cylindrica, cultural practices, cated that most fruit is set on lateral and sublateral shoots and that pinching out the flowering, yields main stem encouraged early fruit set (C.D. Abstract. The objective of 2 years of field studies was to begin development of a luffa sponge DeCourley, personal communication). gourd (Luffa aegyptiaca Mill.) production system for a cool, temperate climate by studying My objective was to begin development of the effects of planting date, planting method, in-row spacing (30.5, 61, and 91 cm), and a luffa production system for a cool, temperate pruning techniques on yield and quality of luffa sponge gourds. High yields of mature climate by studying the effects of planting gourds were obtained when transplants were field-set as soon as the danger of frost had date, planting method, in-row spacing, and past. Highest marketable yields were obtained when plants were spaced 30.5 cm apart in pruning techniques on yield and quality of the row and the first four lateral shoots were removed. Plants spaced 91 cm apart produced luffa sponge gourds. gourds with the largest diameter, whereas plants with 30.5-cm in-row spacing produced the highest yields of gourds with bath sponge diameters (5.1-7.6 cm). Plants spaced 91 cm Materials and Methods apart and topped at node six obtained high fiber density, strong fibers, and excellent visual appeal, but low yields. Yields were competitive with yields obtained in warmer climates. Two studies were conducted in Fletcher, N.C., on a submountain plateau with an eleva- tion of »631m at lat. 35°26'N, long. 82°34'W. Luffa sponge gourds are tropical and sub- Ample information on growing luffa sponge This region has an average of 188 frost-free tropical members of the Cucurbitaceae and gourds is available for home gardeners days, a mean annual daily temperature of 13C, have been cultivated for centuries in the Middle (Johnson, 1984; Stephens, 1988; Whitaker, and an average annual rainfall of 1470 mm East and India, China, Japan, and Malaysia 1977), but the recommended practices are not (Byrd, 1988). (Porterfield, 1955). The plant is an annual vine necessarily appropriate for commercial pro- In 1989, the influence of three planting with tendrils and large, cylindrica pepo (berry) ducers. Most research relevant to commercial dates (29 May, 12 June, and 26 June) and two fruit that are edible when young (Okusanya et luffa production has been conducted in the planting methods (direct seeding vs. trans- al., 1981). The mature, dry fruit consists of a tropical and subtropical climates of West Af- planting) were examined as a factorial in a hard shell surrounding a stiff, dense network rica and India (Dubey, 1983; Okusanya, 1978, randomized complete-block design with four of cellulose fibers (sponge), adapted for sup- 1983a, 1983b; Okusanya et al., 1981, 1988; replications. Plots consisted of three 6-m rows port and dispersal of hundreds of flat, smooth, Okusanya and Lakanmi, 1985; Omini and spaced 1.5 m apart, center to center. Data were black seeds (Shah et al., 1980). Hossain, 1987; Singh et al., 1976). Only a few collected from the center rows; outer rows Using luffa sponges for personal hygiene studies have been conducted in temperate cli- served as guard rows. and household cleaning is common in many mates (Bai et al., 1985; Ko et al., 1978). Seeds from high-quality luffa sponges were countries. In the United States, the demand for Okusanya (1978) suggested that the natural obtained from China through J.A. Ayers (Earth luffa sponge products for skin care is increas- absence of luffa outside tropical and subtropi- Products, Lapeer, Mich.). Transplants were ing. Currently, most luffa sponge gourds are cal regions was due, in part, to poor germina- produced in the greenhouse in plastic flats produced in tropical or semitropical environ- tion at low temperatures and a need for high with 5 × 5-cm cells. Seed were soaked in water ments such as Taiwan, Korea, El Salvador, light intensity and temperature for optimum for 24 h and sown, two seeds per cell, in a Guatemala, and Colombia (Davis and plant growth. soilless peat–bark mix on 28 Apr., 11 May, DeCourley, 1993). Wholesale prices of $0.40 Luffa sponge gourd plants are similar in and 24 May. Plants were watered daily with to $0.50 per sponge (Davis and DeCourley, growth habit to cucumbers (Cucumis sativus 100 mg N/liter as 20N–4.4P–16.6K. 1993; D. Brinker, personal communication) L.). Substantial yield increases can be ob- The experiment was conducted on a coupled with the rising demand for luffa prod- tained by training cucumbers to a vertical Delanco loam (fine loamy, mixed, mesic, Aquic ucts and a desire for new, high-value crops trellis rather than growing them on the ground Hapludults). Okusanya (1983b) suggested that have stimulated interest among some North (Hanna et al., 1987; Russo et al., 1991). If luffa L. aegyptiaca grew best in a neutral pH soil American growers. gourds contact the ground, fruit rot, discolored with high fertility, particularly N and P. There- sponges, and misshaped gourds may result; fore, on 19 May, 84N–291P–134K (in kg·ha-1) Received for publication 12 July 1993. Accepted for thus, luffa plants also benefit from being trained and 1121 kg lime/ha (for a pH of 6.5) were publication 3 Nov. 1993. This research 7695-7643 to trellises (Porterfield, 1955; Sinnott and broadcast-applied to the soil and incorporated. was supported in part by North Carolina Agricul- Bloch, 1943). Results from three on-farm tests Beds were shaped to 15 cm high × 1 m wide, tural Research Service, Raleigh, and the U.S. Dept. in western North Carolina in 1989 demon- and a black polyethylene mulch (0.08 mm of Agriculture Special Grant P.L. 89-106. I grate- strated the benefits of using black polyethyl- thick) and drip-irrigation tape (Ro-Drip, 46- fully acknowledge materials supplied by Roberts ene mulch and drip irrigation for luffa gourd cm emitter spacing; Roberts Irrigation, San Irrigation Products, seeds supplied by John Ayres, production (J.M.D., unpublished). Marcos, Calif.) were applied in a single opera- and technical assistance from George Cox. Use of Most luffa cultigens are monoecious. Stami- tion. Holes were punched 46 cm apart in the trade names does not imply endorsement of the nate flowers develop in an inflorescence, polyethylene mulch using a bulb planter. On products named nor criticism of similar ones not named. The cost of publishing this paper was de- whereas distillate flowers develop singly or in each planting date, seed (that had been soaked frayed in part by the payment of page charges, Under association with a staminate inflorescence in water for 24 h) were sown two per hole (25 postal regulations, this paper therefore must be (Takahashi, 1980). As with most monoecious mm deep) or 4-week-old transplants were set hereby marked advertisement solely to indicate this cucurbits, the lower nodes of luffa usually bear out. A 1.5-m-tall vertical trellis system was fact. only staminate inflorescences, followed by constructed of 10 × 10-cm wood posts with a 1Assistant Professor. nodes having both staminate inflorescences 2.5-cm-diameter steel pipe as the horizontal HORTSCIENCE, VOL. 29(4), APRIL 1994 263 I CROP PRODUCTION I top wire. Individual strings were suspended pulled apart. Visual appeal was rated on a scale did not develop on the lower portion of the over each plant to help train plants to the top of of 1 to 5 (1 = poor with loose, broken, uneven plant (Omini and Hossain, 1987; Takahashi et the trellis. Direct-seeded plants were thinned fibers; 3 = good with fairly close woven, even al., 1980), in this study, there were a few to one plant per hole 3 weeks after planting. fibers; 5 = excellent with close woven, even pistillate flowers (one or two per plot) present The first four lateral shoots were pruned from fibers and a smooth finish). Data were ana- on the lower plant nodes (nodes 5 and 6; data all plants, and plants were trained to the strings lyzed by an analysis of variance and protected not shown). By 18 July, flowers and fruit were as needed. A hive of honey bees was posi- least significant difference (MSTAT-C, Michi- present on all plants that had been transplanted, tioned near the field at first bloom. Pest prob- gan State Univ.). but only on direct-seeded plants that were lems were minimal; fungicides and insecti- sown on 29 May (Table 1). The largest number cides registered for gourds were applied as Results and Discussion of fruit was present on plants transplanted on needed for powdery mildew (Erysiphe spp.) the two earliest planting dates. and cucumber beetle [spotted, Diabrotica In 1989, using transplants resulted in a Dried gourds harvested immediately after undecimpunctata howardi Barber and striped, better plant stand than did direct-seeded plants the first killing frost were the highest quality Acalymma vittata (Fabricius)] control.
Recommended publications
  • 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 .
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • Sponge–Seaweed Associations in Species of Ptilophorae
    Blackwell Publishing AsiaMelbourne, AustraliaPREPhycological Research1322-08292006 Japanese Society of PhycologyJune 2006542140148Original Article Sponge–seaweed associations in species of PtilophoraE. Tronchin et al. Phycological Research 2006; 54: 140–148 Sponge–seaweed associations in species of Ptilophora (Gelidiaceae, Rhodophyta) Enrico Tronchin,1,2* T. Samaai,3 R. J. Anderson4 and J. J. Bolton1 1Department of Botany, University of Cape Town, Private Bag, Rondebosch 7701, Cape Town, 3Council for Scientific and Industrial Research, Environmentek, PO Box 17001, Congella 4013, Durban and 4Seaweed Research Unit, Marine and Coastal Management, Private Bag X2, Roggebaai 8012, South Africa, and 2Phycology Research Group, University of Ghent, 281/S8 Krijgslaan, Ghent 9000, Belgium, 1990). Both are microscopic and filamentous algae SUMMARY that grow embedded in Mycale laxissima Duchassaing and Michelotti (Mycalidae). Some sponge–seaweed Sponge–seaweed associations in the seaweed genus associations form a structural relationship where the Ptilophora are poorly understood; therefore, 94 speci- sponge is epiphytic on a seaweed host. In such cases mens, representing all 17 species of Ptilophora, were the sponge might determine the overall shape of the examined to detail this phenomenon. All but 2 Ptilo- association, for example, in the subtropical western phora species were shown to produce surface prolif- Atlantic Xytopsues osburnensis George and Wilson erations, with 13 species found to have sponge (Phoriospongiidae), which reinforces its skeleton with associations. Evidence for facultative sponge epi- fronds of an articulated coralline alga, Jania capillacea phytism was found with species–specific interactions Harvey (Corallinaceae) (Rützler 1990). In other cases, being unlikely. Results show that surface proliferations the seaweed determines the overall shape of the asso- are not induced by sponge epiphytes, as they often ciation (Scott et al.
    [Show full text]
  • Aplysina Insularis(Yellow Tube Sponge)
    UWI The Online Guide to the Animals of Trinidad and Tobago Ecology Aplysina insularis (Yellow Tube Sponge) Order: Verongida (Spicule-less Sponges) Class: Demospongiae (Common Sponges) Phylum: Porifera (Sponges) Fig. 1. Yellow tube sponge, Aplysina insularis. [http://oceana.org/marine-life/corals-and-other-invertebrates/yellow-tube-sponge, downloaded 26 February 2016] TRAITS. Yellow tube sponges can be found growing in coral reefs, and are native to the Caribbean region. They are characteristically joined at the base and grow in an upwards direction (Fig. 1). They are open at the top and closed at the base, and are immobile (Animals.mom.me, 2016). The length of the tubes are commonly 1m, but the length of the tubes can vary based on the depth of the body of water they inhabit. The organisms are yellowish in colour but sometimes they appear to be iridescent bluish-yellow at deeper depths (D’Aloia, Majoris and Buston, 2011). When exposed to the atmosphere, the sponges turn purple then black and die. The surface of the tubes are finely conulose (with tent-shaped projections) and it does not show the deep set, curving channels of Aplysina lacunosa (Kensley and Heard, 1991). Aplysina insularis was formerly known as A. fistularis (Species-identification.org, 2016). DISTRIBUTION. Yellow tube sponges are indigenous to the Caribbean region and the Gulf of Mexico, from Florida to northern Brazil (Species-identification.org, 2016). They can be found in countries such as Trinidad and Tobago, The Bahamas, and Bermuda. UWI The Online Guide to the Animals of Trinidad and Tobago Ecology HABITAT AND ACTIVITY.
    [Show full text]
  • Sponge-Covered Red Algae
    Pictured Key to some common sp red algae of southern Australia with rough, sponge-covered surfaces Fig. 1 cross section of a Thamnoclonium Red Algae. With some 800 species, many of which are dichotomum blade bl og sp endemic (found nowhere else), southern edge: blade Australia is a major centre of diversity for red algae. Classification is based on detailed outgrowths (bl og) reproductive features. Many species unrelated and sponge tissue (sp reproductively have similar vegetative form or t) with glassy, needle shape, making identification very difficult if the technical systematic literature is used. like spicules (sp) This key Fortunately, we can use this apparent problem to advantage - common shapes or morphologies will allow you to sort some algae directly into the level of genus or Family and so shortcut a systematic search through intricate and often unavailable reproductive features. The pictured key below uses this artificial way of starting the search for a name. It’s designed to get you to a possible major group in a hurry. Then you can proceed to the appropriate fact sheets within this website. Scale: the coin used as a scale is 24mm or almost 1” wide. Microscope images of algae are usually blue stained The algae in this key have numerous small outgrowths, a surface layer of sponge or both Fig. 2: Codiophyllum flabelliforme Fig. 3. Codiophyllum flabelliforme: outgrowths and sponge that give the surface a unique detail of branch lobes roughened appearance. Sponge can be recognised from microscopic examination of cross sections. Glassy “needles” – spicules making up the sponge skeleton – can be seen on the algal surface (Fig.
    [Show full text]
  • Sponges by Cindy Grigg
    Sponges By Cindy Grigg 1 Sponges are the simplest multicellular animals. They lack true tissues. They have no muscles, nerves, or internal organs. 2 Sponges live all over the world. Most of them live in oceans, but some can be found in freshwater lakes and rivers. Sponges are attached to hard surfaces underwater. They are well-adapted to their watery life. Moving water currents carry food and oxygen to them and take away the sponges' waste products. 3 Sponges don't look or act like most animals. In fact, they are so different that people used to think they were plants. Like plants, adult sponges stay in one place. But unlike plants, sponges must take food into their bodies to live. They can not make their own food like plants do. This puts them into the same kingdom as animals. These strange animals have been on Earth for about 540 million years. 4 The bodies of most sponges have irregular shapes. Most of them have no symmetry. Although some of their cells do specialized jobs, sponges lack tissues and organs. Hundreds of pores, many of them too small to be seen by the unaided eye, dot the surface of a sponge's body. In fact, the name of the group to which sponges belong-phylum Porifera-means "having pores." 5 Because moving water carries food and removes wastes, it is the key to the sponge's survival. Water enters the small pores throughout the sponge's body. Then it flows into a central cavity. Water leaves the sponge through the osculum, a large opening.
    [Show full text]
  • Symbiosis Between Methane-Oxidizing Bacteria and a Deep-Sea Carnivorous Cladorhizid Sponge
    MARINE ECOLOGY PROGRESS SERIES Published December 31 Mar Ecol Proy Ser Symbiosis between methane-oxidizing bacteria and a deep-sea carnivorous cladorhizid sponge Jean ~acelet'v*,Aline ~iala-~edioni~,C. R. is her^, Nicole Boury-Esnaultl 'Centre d'oceanologie de Marseille, Universite de la Mediterranee - UMR CNRS no. 6540, Station Marine d'Endoume, F-13007 Marseille, France 20bservatoireOceanoloyique. Laboratoire Arayo, F-66650 Banyuls-sur-Mer, France 3Department of Biology, Pennsylvania State University, University Park, Pennsylvania 16802. USA ABSTRACT Dense bush-l~keclumps of several hundred ~nd~vldualsof a new specles of Cladorhiza (Demosponglae, Poeciloscler~da)were observed near methane sources in mud volcanoes 4718 to 4943 m dcep In the Barbddos Trench The sponge tissue contalns 2 maln mo~pholog~caltypes of extra- cellular symbiotic bacteria small rod-shaped cells and larger cocco~dcells with stacked membranes Stdble carbon ~sotopevalues, the presence of methanol dehydrogenase and ultrastructural observa- tlons all lndlcate that at least some of the syrnblonts are methdnotrophic Ultrastructural ev~denceof ~nlracell~~lard~gest~on of thp syn~b~ontsand the stable C and X values suggest that thc sponge obtalns a slgnlflcdnt portion of its nutr~tlonfrom the symbionts Ultrdstructure of the sponqe embryo suggests d~recttransmission throuqh qc.neratlons In brooded embryos The sponge also ma~ntrilnsa carnivorous feed~nghdblt on tin\ swlmmlng prey, as do other cladorhlzlds KEY L\/ORDS. Methanotrophy POI-~fera. Deep-sea . Symbiosis . Cold-seep communities INTRODUCTION although they are sometimes abundant on extinct chimneys (Boury-Esnault & De Vos 1988) or in vent Associations between several phyla of marine inver- peripheral areas.
    [Show full text]