Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Marine and Freshwater Research Marine and Freshwater Research Society
Advances in the aquatic sciences
RESEARCH ARTICLE

The life history of weedy seadragons, Phyllopteryx taeniolatus (Teleostei : Syngnathidae)

Kristy L. Forsgren A and Christopher G. Lowe B
+ Author Affiliations
- Author Affiliations

A University of Washington, School of Aquatic and Fishery Sciences, 1122 NE Boat Street, Seattle, WA 98195, USA.

B California State University, Long Beach, Department of Biological Sciences, 1250 Bellflower Blvd, Long Beach, CA 90840, USA.

C Corresponding author. Email: klforsg@u.washington.edu

Marine and Freshwater Research 57(3) 313-322 https://doi.org/10.1071/MF05094
Submitted: 24 May 2005  Accepted: 8 February 2006   Published: 27 April 2006

Abstract

The aim of this study was to provide a detailed description of the life history of weedy seadragons, Phyllopteryx taeniolatus. Weedy seadragon development was described based on morphological characters and categorised into four periods: incubation, larval, juvenile and sub-adult. Hatching occurred 35–42 days post-fertilisation, most hatchlings exhibited juvenile characteristics upon hatching or shortly thereafter. The von Bertalanffy growth parameters generated from weedy seadragon length-at-age data were L = 285 ± 3 mm standard length (SL; mean ± s.e.) and k = 2.20 ± 0.05 year−1. Females possessed a higher gonosomatic index (GSI; 1.25 ± 1.18%; mean ± s.d.) than males (0.34 ± 0.20%), which increased substantially for females over 230 mm in length. Mature female weedy seadragons (290 ± 32 mm SL) ovulated 110 ± 27 eggs per female per spawning. Additionally, three females produced more than one clutch per season. Male weedy seadragons (319 ± 9 mm SL) successfully incubated 91 ± 40 eggs per spawning event. In addition to improving our understanding of the life history of weedy seadragons, this information can be used to estimate population demography and develop management strategies.

Extra keywords: Australia, development, growth, reproduction, syngnathid.


Acknowledgments

We thank the Aquarium of the Pacific for support and access to their weedy seadragon collection. Special thanks go to C. Forsgren, K. Koons, P. Hampton, P. Branshaw and T. Demas, for their assistance with data collection, and K. Goldman, B. Eldon, K. Young, W. Smith and G. Cailliet for their assistance with the preparation of this manuscript. We also thank G. Goodmanlowe for the early life history drawings. The Aquarium of the Pacific, Sigma Xi Grants-in-Aid of Research, and Boeing-CNSM Graduate Scholarship provided funding for this project.


References

Australian Government Geoscience Australia (2000). Compute sunrise, sunset and twilight times. Available online at: www.ga.gov.au/geodesy/astro/sunrise.jsp [verified April 2006].

Baum, J. , Meeuwing, J. , and Vincent, A. (2003). Bycatch of lined seahorses (Hippocampus erectus) in a Gulf of Mexico shrimp trawl fishery. Fishery Bulletin 101, 721–731.
Cailliet G. , Love M. , and Ebeling A. (1986). ‘Fishes: A Field and Laboratory Manual on their Structure, Identification, and Natural History.’ (Waveland Press: Prospect Heights, IL.)

Carcupino, M. , Baldacci, A. , Mazzini, M. , and Franzoi, P. (1997). Morphological organization of the male brood pouch epithelium of Syngnathus abaster Risso (Teleostea, Syngnathidae) before, during, and after egg incubation. Tissue & Cell 29, 21–30.
Crossref | GoogleScholarGoogle Scholar | Dawson C. (1985). ‘Indo-Pacific Pipefishes (Red Sea to the Americas).’ (The Gulf Coast Research Laboratory: Ocean Springs, MI.)

Fabens, A. (1965). Properties and fitting the von Bertalanffy growth curve. Growth 29, 265–289.
PubMed | Fuiman L. , and Werner R. (2002). Special consideration of fish eggs and larvae. In ‘FisheryScience: The Unique Contributions of Early Life Stages’. (Eds L. Fuiman and R. Werner.) pp. 1–33. (Blackwell Science Ltd.: Oxford, UK.)

Herald, E. (1959). From pipefish to seahorse – a study of phylogenetic relationships. Proceedings of the California Academy of Sciences 13, 465–473.
Hutchins B. , and Swainston R. (1986). ‘Sea Fishes of Southern Australia.’ (Swainston: Perth.)

IUCN (2004). The 2002 IUCN Red List of Threatened Species. Available online at: www.redlist.org/ [verified February 2006].

Kanou, K. , and Kohno, H. (2001). Early life history of a seahorse, Hippocampus mohnikei, in Tokyo Bay, Japan. Ichthyological Research 48, 361–368.
Crossref | GoogleScholarGoogle Scholar | Kuiter R. (2003). ‘Seahorses, Pipefishes and their Relatives.’ Revised edn. (TMC Publishing: Chorleywood, UK.)

Moreau, M. , and Vincent, A. (2004). Social structure and space use in a wild population of the Australian short-headed seahorse Hippocampus breviceps Peters, 1869. Marine and Freshwater Research 55, 231–239.
Crossref | GoogleScholarGoogle Scholar | Pogonoski J. , Pollard D. , and Paxton J. (2002). ‘Conservation Overview and Action Plan for Australian Threatened and Potentially Threatened Marine and Estuarine Fishes.’ (Environment Australia: Canberra.)

Presnell J. , and Schreibman M. (1997). ‘Humason’s Animal Tissue Techniques.’ 5th edn. (The John Hopkins University Press: Baltimore, MD.)

Rasband W. (2000). Scion Image for Windows. Version 4.0.2. National Institutes for Health, Bethesda, MD.

Salin, K. , Yohannan, T. , and Mohanakumaran Nair, C. (2005). Fisheries and trade of seahorses, Hippocampus spp., in southern India. Fisheries Management and Ecology 12, 269–273.
Crossref | GoogleScholarGoogle Scholar | Vincent A. (1996). Phyllopteryx taeniolatus. In ‘IUCN 2004. 2004 IUCN Red List of Threatened Species’. Available online at: www.redlist.org/ [verified February 2006].

von Bertalanffy, L. (1938). A quantitative theory of organic growth (inquiries on growth laws II). Human Biology 10, 181–213.