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Welcome to the chapter dedicated to two
 models of brown algae: <i>Saccharina</i> and <i>Ectocarpus</i>.


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These two brown algae belong to different 
orders, <i>Ectocarpus</i> belongs to Ectocarpales


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which usually includes very simple
 algae with very simple morphology, 


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usually filamentous, while <i>Saccharina</i> 
belongs to Laminariales, which includes


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much larger algae - we call them kelp. 
<i>Saccharina </i>and <i>Ectocarpus</i> are close


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 phylogenetically. They diverged 75 mya.
 This duration might look or sound long to


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 you, but actually this is the same that
 separates humans from rodents like mice.


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So let's see if <i>Saccharina</i> and <i>Ectocarpus</i>
 are as different as humans and rodents. 


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Let's start with <i>Ectocarpus</i>.

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<i>Ectocarpus</i> was first described as <i>Conferva</i>
<i> siliculosa</i> by Dillwyn at the beginning of the


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 19th century. It is a tiny, filamentous alga
found in temperate waters in both northern


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and southern hemispheres.

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This wide distribution is not common in 
brown algae, and this might be due to 


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the fact that this alga sticks
 easily to any surface.


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It is a widespread biofouling agent, an issue
 for boats and marine equipment in general.


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Let's see how it develops and reproduces. 
Actually, <i>Ectocarpus</i> develops two generations


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which alternate within the life cycles, 
and this is very common in macroalgae.


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 The 1st generation is a sporophyte and
 it is diploid. It is made of a string of cells


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 like pearls in a necklace. It grows apically,
and reaching a given stage, it branches.


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All the filaments produced then
 are similar to the initial filament. 


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This is a re-iterative development. ﻿


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This produces a prostrate base sticking to
 a solid suface. After about four weeks, the


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 sporophyte resemble a tuft of 
about one centimeter wide, 


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made of many filaments
 attached to each other.


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They can all undulate in the seawater 
because only their base is attached.


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 After a few more days they will differentiate 
reproductive organs, named sporangia,


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 which would produce meiospores.

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These meiospores are haploid, they are 
released in the seawater where they settle


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 to the bottom. They will then germinate
 as haploid gametophytes. This is what is 


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shown in the yellow part of the diagram.

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There are female and male meiospores,
 and they will each produce a distinct 


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gametophyte. Gametophytes are also 
filamentous but they lack the basal part


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seen in the sporophyte so that they float 
more easily. They also produce reproductive


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 organs, this time named gametangia because
 they are the ones producing the gametes. 


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Male and female gametophytes look similar
 morphologically and it is stated that 


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 <i>Ectocarpus</i> has virtually no sexual 
dimorphism. Both types of gametes are


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also released freely in the sea water, where 
they will fuse together to produce the diploid


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sporophytes. The female gamete produces
a pheromone, Ectocarpen, which attracts


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the male gametes. So to summarise about
 this life cycle, we call it a haplodiplontic


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life cycle because it has two
 generations, haploid and diploid.


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It is isomorphic because both the
 gametophyte and the sporophyte look similar.


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 It is dioicous because the sexes are 
carried by two independent organisms,


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 here the female and the male gametophytes.

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And finally it is isogamous because
 both gametes are similar.


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 In nature this generation can be found at 
different locations and at different times,


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 but it all depends on the
 species and the strain.


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And in the lab we usually work with a 
specific strain which is able to reproduce


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 vegetatively, its unfertilised gametes are
able to germinate and to produce a pattern


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of sporophytes and it's very convenient for 
example to produce mutants because it eases


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 the screening of phenotypes.

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<i>Ectocarpus</i> has been a model for academic
 research for at least 15 years. 


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In 2010 its genome has been sequenced.

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It is 214 mega base pairs, it has
 and codes for 17,000 genes.


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Its genome has a peculiar organisation, 
the genes are made of a given number of 


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short exons and they are 
split by pretty large introns.


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Since, several technical tools have been
 developed and I will present some of them


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 in the next chapter.

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Now we will shift to the second 
brown algal model, <i>Saccharina</i>.


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 <i>Saccharina</i> is very different from <i>Ectocarpus</i>. 
It was first described by Linneus in the 


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middle of the 18th century who thought
 it resembled<i> Ulva</i>, and <i>Ulva</i> is the alga 


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responsible for green tides. So
 consequently he first named it 


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<i>Ulva latissima</i>, but since, the name has 
changed several times, first <i>Saccharina</i>


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 at the beginning of the 19 century, then

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<i>Laminaria saccharina</i>, and 200 years 
later, back to <i>Saccharina latissima</i>.


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 In Asia it is just named <i>kombu</i>.

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 The origin of <i>Saccharina</i> can be traced to
 the subarctic waters of the northern Pacific 


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Ocean, then it dispersed to the northern 
Atlantic, but is still absent from the 


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southern hemispheres.

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The life cycle of <i>Saccharina </i>has also 
two generations, but this time the two 


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generations show large differences in size.
 The gametophyte is microscopic as in 


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<i>Ectocarpus</i>, and the sporophyte is much
 bigger. Gametophytes usually live during


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summer and autumn, while the sporophyte
develops during winter and spring.


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As in <i>Ectocarpus</i>, the life cycle is dioicous,
meaning that the two sexes are carried by 


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two independent organisms, here the haploid
male and the haploid female gametophytes.


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However, in contrast to <i>Ectocarpus</i>, the 
gametophyte usually does not develop much.


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 They are filamentous, but immediately get 
fertile so that they don't have time to expand.


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Also in contrast to <i>Ectocarpus</i>, the female 
gametophyte produces eggs, rather big,


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which remain attached to 
the maternal tissue. 


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The sperm cells have to swim to the egg.

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As a result, the embryo remains 
attached to the maternal tissue. 


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Therefore, this life cycle, as in<i> Ectocarpus</i>, 
is haplodiplontic and dioicous.


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But in contrast to <i>Ectocarpus</i>, it is hetero-
morphic because the sporophyte looks


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 different from the gametophyte, and it is 
oogamous because the female gametophyte


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 produces an egg and the male 
gametophyte a sperm cell.


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 The genome of <i>Saccharina japonica </i>
has been sequenced since 2015.


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 It is three times larger than that of <i>Ecto-</i>
<i>carpus </i>with 518 mbp and twice more genes.


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When scientists analysed the genome 
structure, they found that several gene


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 families expanded. The first one is the 
one involved in the metabolism of iodine, 


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and this fits very well with the biology
 of <i>Saccharina</i>, which is the most efficient 


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accumulator of iodine within 
all the living systems.


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They are capable of pumping up to 30k-fold
 the concentration of iodine in the seawater.


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Consequently, they accumulate 
up to 1% of their dry weight.


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The second gene family, which expanded
in the genome of <i>Saccharina </i>is that 


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involved in the biosynthesis of alginate, 
which is this polysaccharide present in


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 the cell wall, and this fits again very
 well with the biology of this alga, 


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 which is a high producer of alginate.
 Up to 34% of its dry weight.


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 So now I hope you have a better idea of 
what <i>Ectocarpus</i> and <i>Saccharina</i> are 


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and how they differ in many aspects.
 In chapter one, you saw how <i>Saccharina</i>


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 is cultivated in the sea.

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In Chapter 4 you will see how it is cultivated 
in the lab to address research topics


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 that you will hear about in Chapter 5.

