Electra devinensis

Overview

Scientific Name: Electra devinensis

Phylum: Bryozoa

Class: Gymnolaemata

Order: Cheilostomatida

Family: Electridae

Genus: Electra

Species:

devinensis [Describe here as A. iricolor]

Native Distribution

Origin Realm:

Temperate Northern Pacific, Central Indo-Pacific, Western Indo-Pacific

Native Region:

Origin Location:

Temperate Northern Pacific [China] North coast of China (North and South of Yangtse River) (Tseng and Huang 1987) STATUS NOT STATED Central Indo-Pacific [China] South coast of China (South of Yangtse River) and Hong Kong (Tseng and Huang 1987) STATUS NOT STATED Ngubat Island, east coast of Mindanao, Philippine. (Canu & Bassler 1929) STATUS NOT STATED Western Indo-Pacific Orissa coast at the mouth of Devi River, Bay of Bengal. (Robertson 1921) STATUS NOT STATED

Geographic Range:

[Western Pacific] North and South coast of China (Tseng and Huang 1987) Ngubat Island, east coast of Mindanao: 9°43'N, 125°48'15"E. (Canu & Bassler 1929)

General Diversity:

NF

Non-native Distribution

Invasion History:

No records of invasion (Global Invasive Species Database 2016)

Non-native Region:

Not applicable

Invasion Propens:

Not applicable

Status Date Non-native:

Not applicable

Vectors and Spread

Initial Vector:

NF

Second Vector:

NF

Vector Details:

NF

Spread Rate:

NF

Date First Observed in Japan:

NF

Date First Observed on West coast North America:

NF

Impacts

Impact in Japan:

NF

Global Impact:

NF

Tolerences

Native Temperature Regime:

Cool temperate, Mild temperate, Warm temperate, Subtropical, Tropical

Native Temperature Range:

[China] Quingdao: max 27.0ºC in summer and min 2.1ºC in winter. (Clark et al. 2003) [China] Hong Kong: max 28.5ºC in summer and min 18.1ºC in winter. (Clark et al. 2003) Cool temperate, Mild temperate, Warm temperate, Subtropical, Tropical (M. Otani, pers. comm.)

Non-native Temperature Regime:

Not applicable

Non-native Temperature Range:

Not applicable

Native Salinity Regime:

Mesohaline, Polyhaline, Euhaline

Native Salinity Range:

[China] Quingdao: max 32.6psu in dry period and min 31.6psu in wet period. (Clark et al. 2003) [China] Hong Kong: max 34.0psu in dry period and min 10.0psu in wet period. (Clark et al. 2003)

Non-native Salinity Regime:

Not applicable

Temperature Regime Survival:

See details

Temperature Range Survival:

RELATED: [Electra spp.] 3.446 - 24.203 ºC (OBIS 2016)

Temperature Regime Reproduction:

NF

Temperature Range Reproduction:

NF

Salinity Regime Survival:

See details

Salinity Range Survival:

RELATED: [Electra spp.] 6.180 - 38.444 PPS (OBIS 2016)

Salintiy Regime Reproduction:

Polyhaline, Euhaline

Salinity Range Reproduction:

NF

Depth Regime:

Shallow subtidal, Deep subtidal

Depth Range:

Nagubat Island, east coast Mindanao, Philippine: 44 fms. (Cnu & Bassler 1929) Devi River, Bay of Bengal: 23-25 fms. (Rbertson 1921) Shallow subtidal (M. Otani, pers. comm.)

Non-native Salinity Range:

Native Abundance:

NF

Reproduction

Fertilization Mode:

See details

Reproduction Mode:

Hermaphrodite/monoecious

Spawning Type:

NA

Development Mode:

Planktotrophic planktonic larva (feeding)

Asexual Reproduction:

Budding/fragmentation (Splitting into unequal parts. Buds may form on the body of the “parent”)

Reproduction Details:

RELATED: [Electra] Species in the Genus: Electra were described as non-brooding species; in broadcasters, sperm fuses with the oocyte at or near ovulation (while still in the ovary) (Ostrovsky 2013) [Gymnolaemates] Internal fertilization, whether intracoelomic or intraovarian, is obligatory (Temkin 1994 and 1996, cited in Ostrovsky 2013) [Gymnolaemates] Differ from most organisms in that sperm-egg fusion does not stimulate egg activation. Egg activation may not occur until "spawned" outside of maternal zooid (Temkin 1991) [Bryozoans] Non-brooding bryozoans feed during the larval stage, while the larvae of brooding bryozoans do not, since these larvae tend to settle soon after release (Hill 2001) [Bryozoans] While sperm is spawned through pores in lophophore tentacles, eggs are usually harbored inside the body wall, and are internally fertilized by sperm, coming in on lophophore feeding currents (Brusca and Brusca 2003, cited in Rouse 2011; Kozloff 1990, cited in Rouse 2011) [Bryozoans] Colonial hermaphrodites, with testes (spermatogenic tissue) and ovaries developing either within the same zooid (zooidal hermaphroditism) or in different zooids within the same colony (zooidal gonochorism) (Ostrovsky 2013) [Bryozoans] Members of the phylum Bryozoa are hermaphroditic. Both fertilization and egg brooding may either be internal or external (Ruppert et al. 2004) [Bryozoans] The first zooid in a colony is called the ancestrula. It is from this individual that the rest of the colony will grow asexually from the budding (Hill 2001) [Bryozoa] All bryozoan colonies are hermaphroditic. Autozooids may be dioecious; or monoecious, and protandrous or protogynous. (Hayward & Ryland 1998) [Bryozoa] Reproduces asexually by budding. (Mawatari 1976) [Membraniporidea] Shed numerous small eggs directly to the sea (Hayward & Ryland 1998) and fertilize in the sea. (Mawatari 1976) These develop into shelled, planktorophic larvae, termed cyphonautes, which feed and grow during several weeks or months spent in the plankton. (Hayward & Ryland 1998)

Adult Mobility:

Sessile

Adult Mobility Details:

[Bryozoa] The abundance and taxonomic diversity of benthic bryozoan faunas are directly related to substratum. (Hayward & Ryland 1998) [Bryozoa] Bryozoans are a phylum of sessile, colonial suspension feeders found throughout the world in both marine and freshwater environments. (Tilbrook 2012)

Maturity Size:

NF

Maturity Age:

NF

Reproduction Lifespan:

NF

Longevity:

NF

Broods per Year:

NF

Reproduction Cues:

RELATED: [Bryozoans] Experiments often used light as a cue to collect embryos/larvae (Woollacott and Zimmer 1977) [Bryozoa] In coastal species light is an important stimulus to larval release, and many cheilostomates shed larvae during the first few hours of daylight. (Hayward & Ryland 1998) [Bryozoa] In various degrees of intensity according to the species temperature also stimulates sexual reproduction. (Winston 1977)

Reproduction Time:

NF

Fecundity:

NF

Egg Size:

RELATED: [Gymnolaemata] About 200µm (Woollacott and Zimmer 1977)

Egg Duration:

NF

Early Life Growth Rate:

RELATED: [Gymnolaemata] Two phases of larvae metamorphosis: first stage about 20mins; second stage 1-6 days (Woollacott and Zimmer 1977)

Adult Growth Rate:

NF

Population Growth Rate:

NF

Population Variablity:

NF

Habitat

Ecosystem:

Floating plants or macroalgae, Fouling, Other

Habitat Type:

Epibenthic Ephiphytic

Substrate:

Biogenic, Artificial substrate

Exposure:

Semi-exposed, Protected

Habitat Expansion:

NF

Habitat Details:

[China] found on PVC plates. (Tseng & Huang 1987) [Philippine] found on floating algae. (Canu & Bassler 1929) [Bay of Bengal] attached to a fragment of wood. (Robertson 1921) Semi-exposed, protected (M. Otani, pers. comm.)

Trophic Level:

Suspension feeder

Trophic Details:

RELATED: [Bryozoans] Suspension feeder...filter phytoplankton less than 0.045mm in size from the water column. (Hill 2001) [Bryozoa] Many phytoplankton species are cleary unsuitable as food for bryozoans. (Hayward & Ryland 1998) [Cheilostomata] Main food is diatom, protozoans and etc. and unappropriate sized particles are ejected (Mawatari 1976)

Forage Mode:

Generalist

Forage Details:

RELATED: [Bryozoans] Suspension feeder...filter phytoplankton less than 0.045mm in size from the water column. (Hill 2001) [Bryozoa] Many phytoplankton species are cleary unsuitable as food for bryozoans. (Hayward & Ryland 1998) [Cheilostomata] Main food is diatom, protozoans and etc. and unappropriate sized particles are ejected (Mawatari 1976)

Natural Control:

RELATED: PREDATION [Predation] [Bryozoa] Browsers and grazers, including sea urchins, fish, crabs and some prosobranchs, are known to include bryozoans in their diet. (Hayward & Ryland 1998) [Predation] [Bryozoa] Bryozoans are also the prey of very many small, selective predators, some of which may be adapted to a very narrow spectrum of prey species. Among them opisthobranch predators of bryozoans are well known. (Hayward & Ryland 1998) [Predation] [Bryozoa] Other than opisthobranchs as a predator, amphipods, isopods, mites and pycnogonids have all been recorded preying on bryozoan colonies. (Hayward & Ryland 1998) EPIBIONTS [Epibionts] [Cheilostomata] It is frequently observed in Japan that several species of hydroids flourish on Cheilostomata cause damages to them. (Mawatari 1976)

Associated Species:

NF

References and Notes

References:

Canu F & Bassler RS (1929) Contributions to the biology of the Philippine Archipelago and adjacent regions. Bryozoa of the Philippine region. Smithsonian Institutuion United States National Museum Bulletin 100: 1-685. Clarke C, Hillard R, Junqueira AOR, Neto ACL, Polglaze J, Raaymakers S (2003) Ballast water risk assessment, Port of Sepetiba, Fedral Republic of Brazil. GloBallast Monograph Series 14: 1-63 + 7 Appendices. Global Invasive Species Database. http://www.iucngisd.org/gisd/ Access Date: 8-Mar-2016. Hayward PF & Ryland JS (1998) Cheilostomatous Bryozoa part I. Aeteoidea - Cribrilinoidea. Synopses of the British Fauna (New Series). Barnes RSK & Crothers JH (eds.) No. 10 (Second Edition). The Linnean Society of London and The Estuarine and Coastal Sciences Association by Field Studies Council: 366pp. Hill, K. (2001) Smithsonian Marine Station at Fort Pierce. Retrieved from http://www.sms.si.edu/irlspec/IntroBryozoa.htm Mawatari S (1976) Bryozoa (Ectoprocta). In: Animal systematics. Uchida T (ed.) Nakayama-shoten Co. Ltd., Tokyo: 35-229. (in Japanese) OBIS. Ocean Biogeographic Information System. http://iobis.org/mapper Access date: 10-09-2016 *Note: genus level data Ostrovsky, A. N. (2013). Evolution of Sexual Reproduction in Marine Invertebrates – Example of gymnolaemate bryozoans. Dordrectht: Springer Netherlands. Doi: 10.1007/978-94-007-7146-8 Robertson A (1921) Report on a collection of Bryozoa from the Bay of Bengal. Records of the Indian Museum 22: 33-65. http://www.biodiversitylibrary.org/item/41901#page/89/mode/1up Rouse, S. (2011). Aetea anguina. Bryozoa of the British Isles. Retrieved from http://britishbryozoans.myspecies.info/content/aetea-anguina-linnaeus-1758 Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology: A functional evolutionary approach. Ann Arbor, MN: Thomson Brooks/Cole. Temkin, M. H. (1991). Fertilization in the Gymnolaemate Bryozoa (Doctoral dissertation). Retrieved from ProQuest Dissertations and Theses database. (DP23819). Tilbrook KJ (2012) Cheilostomata: first records of two invasive species in Australia and the northerly range extension for a third. Check List 8: 181-183. http://www.checklist.org.br/getpdf?NGD192-11 Tseng, W. Y., & Huang, Z. K. (1987). Marine Biofouling and Fisheries. Kagoshima University Research Center of the South Pacific. Occasional Papers 13. 42-55. http://ir.kagoshima-u.ac.jp/bitstream/10232/16226/1/AN10030752_v13_p42-55.pdf Winston JE (1977). Distribution and ecology of estuarine ectoprocts: A critical review. Chesapeake Science, 18: 34‐57. doi:10.2307/1350363. https://fau.digital.flvc.org/islandora/object/fau%3A6214/datastream/OBJ/view/Distribution_and_ecology_of_estuarine_ectoprocts__A_critical_review.pdf Woollacott, R. M., & Zimmer, R. L. (Eds.). (1977). Biology of Bryozoans. New York, NY: Academic Press

Literature:

Little or no information; expert opinion based on general knowledge

Notes:

NA