Hormosira is a genus of
seaweed in the family
Hormosiraceae. It is
monotypic, with a single species, Hormosira banksii, also known as Neptune's necklace, Neptune's pearls, sea grapes, or bubbleweed[2] it is native to Australia and New Zealand.[1][3]
Distribution
Hormosira is native to southeastern Australia (including Tasmania,
Lord Howe Island and
Norfolk Island) and New Zealand.[1][2][3][4][5][6][7] Despite substantial morphological variation across its range, the species represents a single species and the genus Hormosira is monotypic.[5] Genetic analyses of
mitochondrialCOI and
microsatellite DNA sequence data have indicated that there is low genetic variation across the range of the species in Australia.[5][6]
Description
Hormosira is a perennial[4] species of seaweed (brown algae, Fucales).[3] It is abundant on low-energy rocky reefs within the
intertidal zone, where it outcompetes other algal species due to its high tolerance to
desiccation. Plants vary significantly in morphology.[5] The thallus (or frond) of the species is made up of strings of olive-brown, spherical, gas-filled
pneumatocysts (or beads), which taper towards a small
holdfast.[2] While the holdfast attaches strongly to a substrate, it can be easily dislodged by human trampling.[4] The spheres are buoyant and rise to the surface of the water during high tide, allowing plants to move with the flow of the current and obtain more sunlight.[8]Hormosira also produces a slime layer to reduce desiccation,[8] and plants often grows in high densities,[4][7] which reduces their surface area exposed to the sun and further reduce dehydration.[8] Due to the buoyant thallus, Hormosira plants can drift out to sea over considerable distances, and floating plants can remain fertile for several weeks.[5]
Hormosira seaweed
High densities of Hormosira on a broad rocky platform in
Kaikōura, New Zealand
High densities of Hormosira at
Long Reef, Sydney, Australia
Hormosira growing alongside a petrified log at
Curio Bay, Otago, New Zealand
Reproduction
Hormosira reproduces sexually and is
monoecious. The sex organs (
conceptacles) are on the surface of the beads, and are visible to the naked eye as rough-looking dimples.[9]Hormosira produces eggs throughout the year, but its peak reproduction is often confined to July–October (at least in northern New Zealand) when the sea temperature is around 14 °C, as the viability of the eggs can be low in high sea temperatures such as 17–22 °C.[10] At high tide, the eggs are released directly into the surrounding water. The eggs are negatively buoyant they sink to the substrate to develop for several days before becoming attached.[5] All individuals release at the same time, maximising fertilisation. The species can also reproduce asexually from broken and dislodged fragments.
Hormosira is regarded as an
ecosystem engineer[6] or habitat former[7] that occurs in large patches and outcompetes other algal species due to its high tolerance to
desiccation. Hormosira is a food source for
sea urchins, many small
crustaceans, and some juvenile fish.[8] Young crustaceans and molluscs often rely on the dense canopies of Hormosira for niche space, protection from predators, and avoid desiccation at low tide.[8]Hormosira provides a substrate for
sessile organisms to attach onto, including sea urchins and a wide range of
facultative and
obligate algal
epiphytes such as Notheia anomala.[7] This is beneficial to many organisms as competition for habitat space is a primary limiting factor in the intertidal environment.
Uses
Due to the species high iodine content, Tasmanian schoolchildren were once urged to eat a bead a day to keep the
goitres away.[11]
^
abcdSchiel, D.R.; Taylor, D.I. (1999). "Effects of trampling on a rocky intertidal algal assemblage in southern New Zealand". Journal of Experimental Marine Biology and Ecology. 235 (2): 213–235.
doi:
10.1016/S0022-0981(98)00170-1.
^
abcdefMueller, Rebecca; Wright, Jeffrey T.; Bolch, Christopher J.S. (2018). "Historical demography and colonization pathways of the widespread intertidal seaweed Hormosira banksii (Phaeophyceae) in southeastern Australia". Journal of Phycology. 54: 56–65.
doi:
10.1111/jpy.12599.
^
abcBellgrove, Alecia; van Rooyen, Anthony; Weeks, Andrew R.; Clark, Jennifer S.; Doblin, Martina A.; Miller, Adam D. (2017). "New resource for population genetics studies on the Australasian intertidal brown alga, Hormosira banksii: isolation and characterization of 15 polymorphic microsatellite loci through next generation DNA sequencing". Journal of Applied Phycology. 29: 1721–1727.
doi:
10.1007/s10811-016-1015-0.
^
abcdThomsen, M.S.; Metcalfe, I.; South, P.; Schiel, D.R. (2016). "A host-specific habitat former controls biodiversity across ecological transitions in a rocky intertidal facilitation cascade". Marine and Freshwater Research. 67 (1): 144–152.
doi:
10.1071/MF14152.
^Begum, M.; Taylor, F.J. (1991). "Seasonal egg liberation and potential output of Hormosira banksii". Pakistan Journal of Botany. 23: 145–151.
^Edgar, Graham (2012). Australian marine life : the plants and animals of temperate waters (2nd ed.). Chatswood, N.S.W.: Reed New Holland. p. 40.
ISBN9781921517174.
Hormosira is a genus of
seaweed in the family
Hormosiraceae. It is
monotypic, with a single species, Hormosira banksii, also known as Neptune's necklace, Neptune's pearls, sea grapes, or bubbleweed[2] it is native to Australia and New Zealand.[1][3]
Distribution
Hormosira is native to southeastern Australia (including Tasmania,
Lord Howe Island and
Norfolk Island) and New Zealand.[1][2][3][4][5][6][7] Despite substantial morphological variation across its range, the species represents a single species and the genus Hormosira is monotypic.[5] Genetic analyses of
mitochondrialCOI and
microsatellite DNA sequence data have indicated that there is low genetic variation across the range of the species in Australia.[5][6]
Description
Hormosira is a perennial[4] species of seaweed (brown algae, Fucales).[3] It is abundant on low-energy rocky reefs within the
intertidal zone, where it outcompetes other algal species due to its high tolerance to
desiccation. Plants vary significantly in morphology.[5] The thallus (or frond) of the species is made up of strings of olive-brown, spherical, gas-filled
pneumatocysts (or beads), which taper towards a small
holdfast.[2] While the holdfast attaches strongly to a substrate, it can be easily dislodged by human trampling.[4] The spheres are buoyant and rise to the surface of the water during high tide, allowing plants to move with the flow of the current and obtain more sunlight.[8]Hormosira also produces a slime layer to reduce desiccation,[8] and plants often grows in high densities,[4][7] which reduces their surface area exposed to the sun and further reduce dehydration.[8] Due to the buoyant thallus, Hormosira plants can drift out to sea over considerable distances, and floating plants can remain fertile for several weeks.[5]
Hormosira seaweed
High densities of Hormosira on a broad rocky platform in
Kaikōura, New Zealand
High densities of Hormosira at
Long Reef, Sydney, Australia
Hormosira growing alongside a petrified log at
Curio Bay, Otago, New Zealand
Reproduction
Hormosira reproduces sexually and is
monoecious. The sex organs (
conceptacles) are on the surface of the beads, and are visible to the naked eye as rough-looking dimples.[9]Hormosira produces eggs throughout the year, but its peak reproduction is often confined to July–October (at least in northern New Zealand) when the sea temperature is around 14 °C, as the viability of the eggs can be low in high sea temperatures such as 17–22 °C.[10] At high tide, the eggs are released directly into the surrounding water. The eggs are negatively buoyant they sink to the substrate to develop for several days before becoming attached.[5] All individuals release at the same time, maximising fertilisation. The species can also reproduce asexually from broken and dislodged fragments.
Hormosira is regarded as an
ecosystem engineer[6] or habitat former[7] that occurs in large patches and outcompetes other algal species due to its high tolerance to
desiccation. Hormosira is a food source for
sea urchins, many small
crustaceans, and some juvenile fish.[8] Young crustaceans and molluscs often rely on the dense canopies of Hormosira for niche space, protection from predators, and avoid desiccation at low tide.[8]Hormosira provides a substrate for
sessile organisms to attach onto, including sea urchins and a wide range of
facultative and
obligate algal
epiphytes such as Notheia anomala.[7] This is beneficial to many organisms as competition for habitat space is a primary limiting factor in the intertidal environment.
Uses
Due to the species high iodine content, Tasmanian schoolchildren were once urged to eat a bead a day to keep the
goitres away.[11]
^
abcdSchiel, D.R.; Taylor, D.I. (1999). "Effects of trampling on a rocky intertidal algal assemblage in southern New Zealand". Journal of Experimental Marine Biology and Ecology. 235 (2): 213–235.
doi:
10.1016/S0022-0981(98)00170-1.
^
abcdefMueller, Rebecca; Wright, Jeffrey T.; Bolch, Christopher J.S. (2018). "Historical demography and colonization pathways of the widespread intertidal seaweed Hormosira banksii (Phaeophyceae) in southeastern Australia". Journal of Phycology. 54: 56–65.
doi:
10.1111/jpy.12599.
^
abcBellgrove, Alecia; van Rooyen, Anthony; Weeks, Andrew R.; Clark, Jennifer S.; Doblin, Martina A.; Miller, Adam D. (2017). "New resource for population genetics studies on the Australasian intertidal brown alga, Hormosira banksii: isolation and characterization of 15 polymorphic microsatellite loci through next generation DNA sequencing". Journal of Applied Phycology. 29: 1721–1727.
doi:
10.1007/s10811-016-1015-0.
^
abcdThomsen, M.S.; Metcalfe, I.; South, P.; Schiel, D.R. (2016). "A host-specific habitat former controls biodiversity across ecological transitions in a rocky intertidal facilitation cascade". Marine and Freshwater Research. 67 (1): 144–152.
doi:
10.1071/MF14152.
^Begum, M.; Taylor, F.J. (1991). "Seasonal egg liberation and potential output of Hormosira banksii". Pakistan Journal of Botany. 23: 145–151.
^Edgar, Graham (2012). Australian marine life : the plants and animals of temperate waters (2nd ed.). Chatswood, N.S.W.: Reed New Holland. p. 40.
ISBN9781921517174.