Phylogeny Seaweed were not generally considered
homologues of
terrestrial plants, but are only very distantly related to plants, and have evolved plant-like structures through
convergent evolution. Where plants have leaves, stems, and reproductive organs, kelp have independently evolved blades, stipes, and
sporangia. With
radiometric dating and the measure Ma "unequivocal minimum constraint for total group
Pinaceae"
vascular plants have been measured as having evolved around 419–454
Ma while the ancestors of Laminariales are much younger at 189 Ma. Although these groups are distantly related as well as different in evolutionary age, there are still comparisons that can be made between the structures of terrestrial plants and kelp but in terms of evolutionary history, most of these similarities come from convergent evolution. Some kelp species including giant kelp, have evolved transport mechanisms for organic as well as
inorganic compounds, similar to mechanisms of transport in
trees and other
vascular plants. In kelp this transportation network uses trumpet-shaped sieve elements (SEs). A 2015 study aimed to evaluate the efficiency of
giant kelp (
Macrocystis pyrifera) transport anatomy looked at 6 different laminariales species to see if they had typical vascular plant allometric relationships (if SEs had a correlation with the size of an organism). Researchers expected to find the kelp's phloem to work similarly to a plant's
xylem and therefore display similar
allometric trends to minimize
pressure gradient. The study found no universal allometric scaling between all tested structures of the laminariales species which implies that the transport network of brown algae is only just beginning to evolve to efficiently fit their current niches. This niche conservatism means that some species of kelp have convergently evolved to share similar niches, as opposed to all species diverging into distinct niches through
adaptive radiation. A 2020 study looked at functional traits (blade mass per area, stiffness, strength, etc.) of 14 species of kelp and found that many of these traits evolved convergently across kelp phylogeny. With different species of kelp filling slightly different environmental niches, specifically along a wave disturbance gradient, many of these convergently evolved traits for structural reinforcement also correlate with distribution along that gradient. The wave disturbance gradient that this study refers to is the environments that this kelp inhabit have a varied level of perturbation from the
tide and waves that pull at the kelp. It can be assumed from these results that niche partitioning along wave disturbance gradients is a key driver of divergence between closely related kelp. Kelp often have similar
morphological features to other species within its own area since the roughness of the wave disturbance regime, but can look fairly different from other members of its own species that are found in different wave disturbance regimes. Plasticity in kelps most often involves blade morphology such as the width, ruffle, and thickness of blades. Just one example is the giant bull kelp
Nereocystis luetkeana, which have evolved to change blade shape in order to increase drag in water and interception of light when exposed to certain environments. Bull kelp are not unique in this adaptation; many kelp species have evolved a genetic plasticity for blade shapes for different water flow habitats. So individuals of the same species will have differences to other individuals of the same species due to what
habitat they grow in. Many species have different
morphologies for different wave disturbance regimes Where many species only have two or three different blade shapes for maximizing efficiency in only two or three habitats. These different blade shapes were found to decrease breakage and increase ability to
photosynthesize. Blade adaptations like these are how kelp have evolved for efficiency in structure in a turbulent ocean environment, to the point where their stability can shape entire habitats. Apart from these structural adaptations, the evolution of dispersal methods relating to structure have been important for the success of kelp as well. Kelp have had to adapt
dispersal methods that can make successful use of
ocean currents.
Buoyancy of certain kelp structures allows for species to disperse with the flow of water. Certain kelp form kelp rafts, which can travel great distances away from the source
population and colonize other areas. The bull kelp genus
Durvillaea includes six species, some that have adapted buoyancy and others that have not. Those that have adapted buoyancy have done so thanks to the evolution of a gas filled structure called the
pneumatocysts which is an adaptation that allows the kelp to float higher towards the surface to photosynthesize and also aids in dispersal by floating kelp rafts. For
Macrocystis pyrifera, adaptation of pneumatocysts and raft forming have made the species dispersal method so successful that the immense spread of coast in which the species can be found has been found to actually be very recently
colonized. This can be observed by the low genetic diversity in the
subantarctic region. Dispersal by rafts from buoyant species also explains some evolutionary history for non-buoyant species of kelp. Since these rafts commonly have hitchhikers of other diverse species, they provide a mechanism for dispersal for species that lack buoyancy. This mechanism has been recently confirmed to be the cause of some dispersal and evolutionary history for kelp species in a study done with
genomic analysis. Studies of kelp structure evolution have helped in the understanding of the adaptations that have allowed for kelp to not only be extremely successful as a group of organisms but also successful as an
ecosystem engineer of
kelp forests, some of the most diverse and dynamic ecosystems on earth.
Prominent species • Bull kelp
Nereocystis luetkeana, a northwestern American species. Used by coastal
indigenous peoples to create
fishing nets. • Giant kelp
Macrocystis pyrifera, the largest seaweed. Found in the
Pacific coast of
North America and
South America, and the Atlantic coast of
South Africa (formerly
Macrocystis angustifolia). •
Kombu Saccharina japonica (formerly
Laminaria japonica) and others, several edible species of kelp found in
Japan. • Golden V kelp
Aureophycus aleuticus of the
Aleutian Islands. Species of
Laminaria in the British Isles; •
Laminaria digitata (Hudson) J.V. Lamouroux (Oarweed; Tangle) •
Laminaria hyperborea (Gunnerus) Foslie (Curvie) •
Laminaria ochroleuca Bachelot de la Pylaie •
Saccharina latissima (Linnaeus) J.V.Lamouroux (sea belt; sugar kelp; sugarwack) Species of
Laminaria worldwide, listing of species at
AlgaeBase: •
Laminaria agardhii (NE.
America) •
Laminaria bongardina Postels et Ruprecht (Bering Sea to
California) •
Laminaria cuneifolia (NE. America) •
Laminaria dentigera Klellm. (California - America) •
Laminaria digitata (NE. America) • Setchell (Sitka, Alaska, to Monterey County, California - America) • Setchell (Santa Cruz, California, to Baja California - America) • (NE. America) • (NE. America) •
Laminaria nigripes (NE. America) •
Laminaria ontermedia (NE. America) •
Laminaria pallida Greville ex J. Agardh (
South Africa) •
Alaria marginata Post. & Rupr. (Alaska and California -
America) • (C.Ag.) Saunders (Japan; Alaska, California - America) • J. Agardh (Australia; New Zealand) •
Ecklonia maxima (Osbeck) Papenfuss (South Africa) •
Ecklonia radiata (C.Agardh) J. Agardh (Australia; Tasmania; New Zealand; South Africa) •
Eisenia arborea Aresch. (Vancouver Island, British Columbia, Montrey, Santa Catalina Island, California - America) •
Egregia menziesii (Turn.) Aresch. • (C.Ag.) Setch (Alaska, California - America) •
Macrocystis pyrifera (Linnaeus, C.Agardh) (Australia; Tasmania and South Africa) •
Pleurophycus gardneri Setch. & Saund. (Alaska, California - America) •
Pterygophora californica Rupr. (Vancouver Island, British Columbia to Bahia del Ropsario, Baja California and California - America) Non-Laminariales species that may be considered as kelp: •
Durvillea antarctica,
Fucales (
New Zealand,
South America, and
Australia) •
Durvillea willana, Fucales (New Zealand) •
Durvillaea potatorum (
Labillardière) Areschoug, Fucales (
Tasmania; Australia) ==Ecology==