GB2610073A

GB2610073A - Methods of in vitro culturing Sphagnum

Info

Publication number: GB2610073A
Application number: GB2214601.3A
Authority: GB
Inventors: Wright Neal
Original assignee: Micropropagation Services EM Ltd
Current assignee: Micropropagation Services EM Ltd
Priority date: 2020-11-24
Filing date: 2020-11-24
Publication date: 2023-02-22
Anticipated expiration: 2040-11-24
Also published as: GB202214601D0; GB2610073B

Abstract

A method for in vitro culturing Sphagnum is provided. The method comprises providing a vegetative fragment of Sphagnum and surface cleaning the fragment with alcohol. The method further comprises initiating the fragment of Sphagnum in a culture medium 104. The method also comprises culturing the fragment of Sphagnum in vitro for at least 8 weeks without pulverising the Sphagnum. The alcohol may be propanol and the surface cleaning may comprise cleaning the fragment with sterile water before the surface cleaning with alcohol. The culture medium may not include sugar. The method may further comprise, after the culturing, transferring the Sphagnum to a second culture medium. The culturing in the second culture medium may comprise supplying carbon dioxide

Description

METHODS OF IN VITRO CULTURING SPHAGNUM

The present disclosure relates to Sphagnum, in particular to methods for in vitro culturing Sphagnum.

Sphagnum is a genus of moss. It is a lower plant, or a non-vascular plant, and is an example of a bryophyte. It is often referred to as peat moss and typically grows in the wild in peatlands or wetlands. Examples of suitable habitats for Sphagnum include bogs, such as raised bogs and blanket bogs, moors, mires, and fens. Sphagnum has a particularly high capacity for maintaining water in its hyaline cells. As such, in its natural environment, Sphagnum typically grows in wet conditions such as in peatlands.

Peatlands around the world are formed when lower layers of Sphagnum decay to form peat, while the upper layer continues to grow on the surface. As a result of this, carbon is stored within the peat while the actively-growing upper Sphagnum continues sequestering carbon dioxide from the atmosphere. Peatlands cover approximately 3% of the land on the Earth's surface, but store over 500 Gigatonnes of carbon -more than all other vegetation types combined. However, due to adverse impacts on the peatlands (e.g. industrial pollution, drainage -particularly for agriculture, and peat harvesting) the actively-growing upper Sphagnum has been eroded (or is now absent) in many peatlands, thereby exposing the peat to the atmosphere. This absence of surface Sphagnum enables carbon to evaporate from the peatland. This is a pressing environmental issue, and damaged peatlands now contribute around 6% of global anthropogenic carbon dioxide emissions. As a result, there is a pressing need for effective peatland restoration and methods of effectively growing Sphagnum for restoration purposes. Conventional methods of peatland restoration typically involve translocating Sphagnum from other sites including peatlands, which is clearly not sustainable.

Recently, efforts have been made to cultivate Sphagnum sustainably, such as through in vitro tissue culture techniques such as micropropagation. This avoids the need for harvesting large amounts of wild Sphagnum for cultivation. Conventional techniques rely on cultivating Sphagnum from spores. However, spore availability is significantly restricted for Sphagnum (worldwide, but especially in the UK) and the time window for spore harvesting is particularly narrow (sometimes only 2 or 3 weeks per year, if spores can be found at all). As such, obtaining spores is particularly difficult, meaning the starting material is not available for in vitro cultivation at a commercial scale.

Moreover, in vitro cultivation of vegetative parts of Sphagnum has been unsuccessful. Sphagnum is known as a particularly difficult plant to sterilise in order to remove contaminants such as bacteria and fungi. This is especially because of the high water content of Sphagnum in its hyaline cells, from which contaminants are difficult to remove. The resultant culture of Sphagnum therefore generally contains many contaminants which dominate the Sphagnum. In the absence of sufficient sterilisation, contaminants will overcome the Sphagnum, restricting growth and potentially killing the Sphagnum, resulting in poor growth rates and a large number of discarded cultures.

Using conventional sterilants has also proved to be ineffective in the culturing of vegetative Sphagnum. Sten!ants that are conventionally used in micropropagation, such as chlorine or bleach, have been found to kill or significantly damage the vegetative Sphagnum.

The present disclosure seeks to address one or more of the above problems.

The invention is defined by the appended independent claims, while optional features are set out in the appended dependent claims.

According to a first aspect of the present disclosure, there is provided a method for in vitro culturing Sphagnum, comprising: providing a vegetative fragment of Sphagnum; surface cleaning the fragment with alcohol; dissecting the fragment to provide a piece of Sphagnum; and initiating the piece of Sphagnum in a culture medium.

Disclosed herein is a method for in vitro culturing Sphagnum, comprising: providing a vegetative fragment of Sphagnum; surface cleaning the fragment with alcohol; and initiating the fragment of Sphagnum in a culture medium.

As used herein, the term "culturing" preferably refers to maintaining the Sphagnum in conditions suitable for growth. In other words, the Sphagnum may be propagated or cultivated. For example, the Sphagnum may be maintained in a live state. Preferably, the culturing comprises growing the Sphagnum.

In vitro culturing refers to culturing Sphagnum under in vitro conditions. This preferably means that the Sphagnum is cultured under controlled laboratory conditions. Preferably, the in vitro culturing comprises clonal propagation of the Sphagnum. Preferably, the in vitro culturing comprises tissue culture of Sphagnum. Preferably, the in vitro culturing comprises micropropagation of the Sphagnum. The term in vitro culturing should be differentiated from in vivo cultivating. In vivo cultivation refers to growing Sphagnum outside of controlled laboratory conditions, such as in a greenhouse or in a field. In contrast, in vitro culturing refers to culturing under controlled laboratory conditions, preferably in a sterile or substantially sterile environment.

As used herein, the term "vegetative fragment" of Sphagnum refers to a part of the adult form of Sphagnum. In one example, the fragment is from a gametophyte of Sphagnum. In one example, the fragment is from a gametophore of Sphagnum. For example, the fragment may include parts of stems, branches, or leaves of Sphagnum. The fragment preferably does not include a spore of Sphagnum. As a fragment is used, vegetative pieces of Sphagnum can be used as the starting material. This avoids the need for using spores, avoiding the problems with lack of availability. Using a fragment also means that the starting material can be selected with more choice as there is more availability. For example, a specific species of Sphagnum and/or a particular location of origin can be selected and vegetative material can be used. This can be particularly important for restoration of peatlands, where a particular species or origin is desired to replace damaged peatlands without impacting on the ecosystem. Moreover, selection of single species allows traits or properties to be selected, such as fast growing species or species suited to particular habitats. This can be useful for Sphagnum farming, such as for producing biomass, for example for growing media. Biodiversity can also be improved by selecting multiple species without relying on collection of spores of each species. The availability of vegetative material compared to spores means that such selection is easier and more widely possible, even in the absence of spores.

By surface cleaning a fragment with alcohol, the inventors have found that the fragment can be sufficiently sterilised to inhibit contamination, while the alcohol does not kill the Sphagnum, unlike conventional sterilants such as chlorine or bleach. Instead, surface cleaning with alcohol may effectively partially sterilise the Sphagnum. This sufficiently cleans the Sphagnum to restrict or prevent growth of contaminants, without killing the Sphagnum during cleaning.

In one example, the surface cleaning with alcohol may involve placing the fragment into alcohol e.g. submerging the fragment in alcohol for a short period.

By providing a fragment of Sphagnum, rather than an entire strand or plant, a small surface area is provided, reducing the potential for contamination. The water content of the Sphagnum is also reduced, reducing the risk of contamination from contaminants in the water of the hyaline cells. As the fragment is surface cleaned with alcohol, it is particularly beneficial to use a fragment rather than a whole plant. This is because the alcohol will sterilise less powerfully than e.g. chlorine-based sterilants. On the one hand, this means the cleaning step is less toxic and does not kill the Sphagnum, but this also results in a less thorough sterilisation (e.g. compared to chlorine), meaning it is even more important to avoid contaminants in the first place. Providing a fragment allows the potential contaminants to be reduced, reducing the risk of contamination compared to using a whole plant, which would be less well sterilised by the alcohol than the fragment. Providing a fragment results in a more thorough clean when compared to cleaning a whole plant or strand with alcohol.

As used herein, a "gametophyte" preferably refers to the adult form of vegetative material, including stems, branches, and leaves, which may be the haploid stage of the life cycle of Sphagnum. This is to be differentiated from the sporophyte, which may be the diploid stage. Once Sphagnum germinates from a spore, it forms a filament chain of cells called a protonema. This protonema then differentiates into the adult form of vegetative material, sometimes referred to as the gametophore. The gametophore is the adult plant which forms the stems, branches, and leaves. The term "gametophore" thus preferably refers to vegetative material of Sphagnum in its adult form. The term "gametophyte" preferably includes both the protonema and the gametophore.

In vitro cultivation from a vegetative fragment results in genetically-identical progeny. This allows for the axenic cultivation of a single desired species. The resultant material is also clean compared to wild harvested Sphagnum. This provides a more sustainable method for propagation of Sphagnum, and provides more useful material as Sphagnum can be provided without contamination such as seeds, weeds, micro-organisms, bacteria, viruses, or fungi which may be present in wild-harvested material. This has improved biosecurity compared to translocated Sphagnum, avoiding ecological issues in introducing foreign organisms because the material is clean.

Dissecting of the fragment preferably means cutting the fragment to provide a piece of Sphagnum which is smaller than the original fragment. The dissecting is preferably performed by hand as this has been found to be more precise than using a machine. For example, this may involve using a cutting instrument such as a scalpel or a knife. Preferably, the dissecting the fragment is performed after the surface cleaning the fragment with alcohol. Preferably, the dissecting is performed under sterile conditions, such as using a sterile cutting instrument. Preferably, the dissecting is performed on a sterile surface. For example, the dissecting may be performed in a laboratory. Air filtration systems may be used to remove contaminants from the air and optionally provide sterile air.

Dissecting should preferably be differentiated from pulverising or chopping with a machine. Dissecting preferably involves precise cuts by hand, whereas pulverising or chopping with a machine results in imprecise cuts with a lack of control over the size of the resulting pieces. Pulverising Sphagnum in a machine also often breaks the Sphagnum into pieces which are too small, and sometimes damages the Sphagnum. By dissecting the fragment, the size of the resulting piece can be precisely controlled. Furthermore, the dissecting allows a single suitable piece to be selected for initiation.

In some cases, the fragment may be dissected into a plurality of pieces, which means that at least two pieces of Sphagnum are provided from the fragment.

By dissecting the fragment into a smaller piece, the potential for contamination is reduced because a smaller piece is initiated. This reduces the risk that the piece has contaminants on its surface or within water in its hyaline cells.

It is undesirable to provide a small piece before the surface cleaning because that small piece may become damaged by the alcohol. On the other hand, reducing the time of surface cleaning with alcohol may reduce the effectiveness of the cleaning and may leave contaminants, so it is undesirable to reduce the time too much. Therefore, it is preferable to use a fragment for the surface cleaning and then subsequently dissect the fragment into a smaller piece. This provides the advantages of using a small piece in initiation to reduce contamination risk, while ensuring that the Sphagnum is large enough that it is more resistant to the alcohol and has lower risk of becoming damaged or being killed during the cleaning.

As used herein, the term "initiating" should preferably be understood to mean that the piece of Sphagnum is placed into a culture medium for culturing therein. Successful initiation results in the piece of Sphagnum beginning to grow. In particular, new vegetative parts of Sphagnum visibly appear from the initiated piece.

The culture medium is suitable for culturing Sphagnum. In particular, the culture medium provides conditions suitable for growth of the piece of Sphagnum. For example, the culture medium may be sterile. The culture medium may be arranged in a culture vessel, such as a glass or plastic container.

In some examples, the dissecting may provide a plurality of pieces of Sphagnum. In such cases more than one piece may be initiated, for example the plurality of pieces may be initiated. Each piece may be initiated in a separate culture medium in a separate culture vessel.

Preferably, each culture medium contains only a single piece. This reduces the risk of contamination of each culture medium, and allows for better isolation of contamination.

Optionally, the fragment has a length of less than 10 mm. In some examples, the fragment has a length of less than 30 mm or less than 20 mm. The fragment preferably has a length of less than 5 mm. This is beneficial because the smaller the fragment, the less likely it is to contain contamination that cannot be cleaned by the alcohol. The larger the fragment, the more surface area and water contained within the hyaline cells, and therefore the higher the risk that contamination is present. It is therefore important to minimise the length of the fragment to prevent contamination.

In some examples, the fragment has a length of at least 1 mm. This ensures that the fragment is sufficiently resistant to the alcohol that it will not become damaged or be killed by the alcohol. The larger the fragment, the more resistant to the alcohol, but as mentioned above the higher the risk that it will contain contamination. As such, an optimum is desired. The fragment preferably has a length between 1 mm and 10 mm, more preferably between 1 mm and 5 mm. This provides an optimum length which provides resistance to alcohol, while reducing risk of contamination.

In some examples, the providing the vegetative fragment of Sphagnum comprises providing vegetative Sphagnum and dissecting the Sphagnum in order to provide the fragment. For example, a vegetative part (such as a capitulum) of Sphagnum may be provided and dissected to provide a fragment for surface cleaning. The dissecting may be performed in a similar way to the dissecting of the fragment to provide the piece of Sphagnum following the surface cleaning.

The dissecting may be performed by using a cutting instrument such as a scalpel or a knife.

Preferably, the dissecting is performed under sterile conditions or substantially sterile conditions, using a sterile cutting instrument. Although the fragment will be subsequently surface cleaned, it is preferable to not introduce more contamination at this stage, and therefore this may be performed under sterile conditions. Preferably, the dissecting is performed on a sterile surface. For example, the dissecting may be performed in a laboratory. Air filtration systems may be used to remove contaminants from the air and optionally provide sterile air.

In some examples, the fragment is from a gametophore of Sphagnum. In some examples, the fragment comprises part of a stem, a branch, or a leaf of Sphagnum. It is preferable that the fragment does not comprise a whole stem, branch, or leaf, and instead refers to a part thereof.

This provides a small fragment, which reduces the risk of contamination.

Optionally, the fragment is from a capitulum of Sphagnum. The fragment may comprise a part of a capitulum. The capitulum is the top part of a strand of Sphagnum which contains a terminal bud with a cluster of compact juvenile branches, from where the Sphagnum predominantly grows. The capitulum is the most actively growing part of the Sphagnum, and has been found to be the most effective for initiation as the resulting culture contains fast growing branches. In other examples, the fragment may be from mature Sphagnum. For example, mature Sphagnum may be regarded as stems, leaves, or branches further down the strand of Sphagnum, which are typically slower growing but may be more resistant to alcohol.

In some examples, the Sphagnum is in vivo Sphagnum. This means the Sphagnum has previously been cultivated in vivo. In other words, the Sphagnum may be cultivated out of in vitro conditions, such as in a greenhouse or in a field. By growing Sphagnum out of laboratory conditions, the Sphagnum can become hardier and more resistant to environmental factors. Therefore, it is preferable to use in vivo Sphagnum as the starting fragment, rather than in vitro material. This also ensures the Sphagnum can grow well in vivo, which is important as the progeny of the in vitro culturing will be genetically identical. A fragment of the in vivo Sphagnum can then be provided for surface cleaning. Preferably, the Sphagnum is grown indoors in a greenhouse. This reduces the risk of the Sphagnum containing contaminants compared to growing in a field or in the wild on a peatland. In some cases, the Sphagnum may be grown outdoors in a field. This provides a tougher and more robust fragment which is more resistant to the alcohol, but will likely be less clean.

Optionally, the piece of Sphagnum has a length of less than 1 mm. In other words, the dissecting may comprise dissecting the fragment to provide the piece of Sphagnum having a length of less than 1 mm. This reduces the potential for contaminants on the piece of Sphagnum, thereby increasing the growth potential of the culture when initiated. Preferably, the piece of Sphagnum has a length of less than 0.5 mm, more preferably less than 0.3 mm. The fragment may be dissected to provide a piece as small as possible as seen with the naked eye. It is preferable that the piece is not too small that it inhibits differentiation into a gametophore (vegetative material). Conventionally, sometimes pulverisation using a machine is used for protoplast production, where cultivation is inhibited by repeatedly pulverising the Sphagnum to prevent formation of new shoots (i.e. gametophores). It has been found to be desirable to avoid this, and ensure the piece of Sphagnum differentiates into a gametophore as quickly as possible. As such, it is preferable that the piece of Sphagnum has a length of at least 0.05 mm, preferably at least 0.1 mm. In some examples, the piece of Sphagnum has a length of between 0.1 mm and 1 mm, preferably between 0.1 mm and 0.5 mm. Most preferably, the piece of Sphagnum has a length of between 0.1 mm and 0.3 mm. For example, in cases where the fragment has a length of around 1 mm, in one example the fragment is dissected to provide three pieces so that each piece has a typical length of around 0.3 mm. As the dissecting may be performed by hand, great control over the size of the fragment can be achieved, which cannot be achieved by using a chopping machine.

Optionally, the surface cleaning the fragment with alcohol is performed for less than 30 seconds. In some examples, the surface cleaning the fragment with alcohol is performed for less than one minute. By exposing the fragment to alcohol for a short period, the risk of damaging the tissue or killing the Sphagnum is reduced. It has been found that surface cleaning with alcohol for less than 30 seconds provides optimum cleaning without damaging the Sphagnum. Above 30 seconds can potentially damage the Sphagnum, especially if the fragment is too small. It is preferable to provide a fragment having a length of less than 10 mm in combination with surface cleaning with alcohol for less than 30 seconds. This is particularly synergistic because, for fragments of less than 10 mm (especially sized around 1 mm), more than 30 seconds can potentially damage the Sphagnum. For larger pieces which are more resistant, the time can be increased without damage, but that can be more difficult to remove contaminants from.

Surface cleaning for at least 10 seconds ensures that the fragment is sufficiently clean for initiation, more preferably at least 15 second. Surface cleaning for between 10 and 30 seconds is particularly preferred with providing a small fragment (e.g. less than 10 mm) because this ensures the fragment is sufficiently cleaned without killing the Sphagnum.

Optionally, the alcohol comprises between 50 % and 80 % alcohol by volume (abv). In some examples, the alcohol comprises at least 50 % abv. In some examples, the alcohol comprises between 65 % and 75 % abv. Preferably, the alcohol comprises about 70 % abv. In such cases, the remaining component may comprise (or consist of) water, such as sterile or distilled water. This provides a high enough concentration of alcohol which ensures sufficient sterilisation. 100 % alcohol may be used, but providing some water can improve the cleaning process by wetting the tissue. 70 % abv has been found to be the most effective alcohol, especially when using propanol. 70 % abv alcohol is widely available and is cheaper than higher purity alcohols.

Optionally, the alcohol comprises propanol. In particular, the propanol may be propan-2-ol, often referred to as 2-propanol, isopropanol, or isopropyl alcohol. This is widely available and is sometimes referred to as rubbing alcohol. In other cases, the alcohol may comprise ethanol. It is preferable to use propanol in commercial settings as it is easier to procure than ethanol and is less expensive. Other alcohols may be used in other embodiments. For example, the alcohol may comprise methanol.

Optionally, the method further comprises surface cleaning the fragment with sterile water before the surface cleaning with alcohol. For example, the surface cleaning with sterile water may involve placing the fragment into water e.g. submerging the fragment in water. For example, the sterile water may be distilled water, reverse osmosis water, or other substantially pure water, that has preferably been treated to sterilise it. This washes off any large contaminants adhering to the surface of the fragment. To some degree, this can also partially replace the water within the hyaline cells with sterile water, removing unwanted contaminants. Wetting the surface of the Sphagnum also improves the effectiveness of the cleaning with alcohol.

Optionally, the method further comprises surface cleaning the fragment with sterile water after the surface cleaning with alcohol. For example, the surface cleaning with sterile water may involve placing the fragment into water e.g. submerging the fragment in water. For example, the sterile water may be distilled water, reverse osmosis water, or other substantially pure water, that has preferably been treated to sterilise it. This avoids the alcohol being in contact with the Sphagnum for a long period of time, even after the surface cleaning has finished. Alcohol may pass into hyaline cells during the surface cleaning, so cleaning with sterile water afterwards allows the sterile water to replace the alcohol, preventing damage caused by prolonged exposure. This avoids residual alcohol eventually causing damage to the Sphagnum. This can allow the alcohol to act for the desired amount of time, and then washing with water can remove the alcohol.

In some examples, the surface cleaning with sterile water after the surface cleaning with alcohol is performed for at least one minute. This gives enough time for the water to remove any alcohol remaining on the Sphagnum or in the hyaline cells.

Optionally, the method further comprises placing the piece of Sphagnum onto a sterile absorption surface before initiating. This step preferably occurs after the surface cleaning with alcohol and before the initiating, more preferably after the surface cleaning with water following the surface cleaning with alcohol. The absorption surface is configured to absorb moisture from the Sphagnum, and to absorb any residual water or alcohol. In some examples, this may at least partially dry the Sphagnum, although it may be preferable to prevent completely drying and killing the Sphagnum. The absorption surface is sterile so that contamination is not introduced at this stage. Preferably, the absorption surface comprises paper or card. This is a cheap and effective surface which can easily be sterilised and is naturally absorbent. After drying, the piece of Sphagnum can then be placed onto the culture medium for initiation.

Optionally, the surface cleaning does not comprise using a chlorine-based sterilant. In other words, the method preferably does not comprise using a chlorine-based sterilant to sterilise the fragment. Conventionally, chlorine-based sterilants are used to sterilise spores, but these have been found to kill vegetative parts of Sphagnum. Therefore, it is preferable to use alcohol instead, and it is desirable to clean the fragment without using a chlorine-based sterilant. Examples of conventional chlorine-based sterilants include sodium hypochlorite, calcium hypochlorite, and sodium dichloroisocyanurate.

Optionally, the surface cleaning does not comprise using a detergent. In other words, the method preferably does not comprise using a detergent to sterilise the fragment. Conventionally, detergents are used to sterilise spores, but these have been found to kill vegetative parts of Sphagnum. Therefore, it is preferable to use alcohol instead, and it is desirable to clean the fragment without using a detergent. Examples of conventional detergents include Tween (i.e. polysorbate).

Optionally, the culture medium does not comprise sugar. Sugar is often conventionally used during in vitro culturing of Sphagnum to provide a carbon source for photosynthesis, promoting growth. Sugar is generally provided in the form of glucose or sucrose added to the culture medium. However, providing sugar results in ideal growth conditions for contaminants, which then tend to dominate and out-compete Sphagnum. This effect is particularly significant for Sphagnum because Sphagnum is adapted to grow in harsh conditions. However, where an abundance of sugar is supplied during cultivation of Sphagnum, it has been found to promote unwanted growth of contaminants, which can then out-compete the Sphagnum. As such, it has been found that providing a culture medium without sugar is advantageous as the effects of contamination can be reduced. This is particularly important as the Sphagnum is initiated from a vegetative piece which is cleaned with alcohol, and there is a higher risk of contamination than if a stronger sterilant such as chlorine were used. As such, it is particularly advantageous to use a culture medium without sugar where the Sphagnum has been surface cleaned with alcohol.

In some examples, the culture medium comprises nutrients.

In some examples, the culture medium comprises nutrients comprising nitrogen, phosphorus, potassium, calcium, magnesium, sodium, manganese, copper, zinc, sulfur, boron, iron, molybdenum, and/or chlorine. In some examples, the culture medium comprises nutrients comprising nitrogen, phosphorus, potassium, calcium, magnesium, sodium, manganese, copper, zinc, sulfur, boron, iron, molybdenum, chlorine, cobalt, and/or iodine.

Optionally, the culture medium may comprise nitrogen, phosphorus, potassium, calcium, magnesium, sodium, manganese, copper, zinc, sulfur, boron, iron, molybdenum, chlorine, cobalt, and iodine.

In some examples, the culture medium comprises at least 18.05 mg per L of nitrogen. In some examples, the culture medium comprises between 18.05 mg and 103.98 mg per L of nitrogen.

Preferably, the culture medium comprises at least 40 mg per L of nitrogen. More preferably, the culture medium comprises between 40 mg and 55 mg per L of nitrogen. In some examples, the culture medium comprises less than 103.98 mg per L of nitrogen. For example, nitrogen may be present in nitrite, nitrate, and/or ammonium form. For example, nitrogen may be provided by (e.g. disodium) EDTA, (e.g. ferrous sodium) DTPA, ammonium nitrate (NH4NO3) , and/or calcium nitrate (Ca(NO3)2.H20).

In some examples, the culture medium comprises at least 9.12 mg per L of phosphorus. In some examples, the culture medium comprises at least 10.99 mg per L of phosphorus. In some examples, the culture medium comprises between 10.99 mg and 54.02 mg per L of phosphorus. Preferably, the culture medium comprises at least 5 mg per L of phosphorus. More preferably, the culture medium comprises between 5 mg and 15 mg per L of phosphorus. For example, phosphorus may be provided by potassium (dihydrogen) phosphate (KH2PO4).

In some examples, the culture medium comprises at least 66.84 mg per L of potassium. In some examples, the culture medium comprises between 66.84 mg and 151.10 mg per L of potassium. Preferably, the culture medium comprises at least 120 mg per L of potassium. More preferably, the culture medium comprises between 120 mg and 130 mg per L of potassium. For example, potassium may be provided by potassium (dihydrogen) phosphate (KH2PO4), potassium sulfate (K2SO4), and/or potassium iodide (KI).

In some examples, the culture medium comprises at least 1.17 mg per L of calcium. In some examples, the culture medium comprises between 1.17 mg and 36.96 mg per L of calcium. Preferably, the culture medium comprises at least 25 mg per L of calcium. More preferably, the culture medium comprises between 25 mg and 35 mg per L of calcium. For example, calcium may be provided by calcium nitrate (Ca(NO3)2.H20) and/or calcium chloride dihydrate (CaCl2.2H20).

In some examples, the culture medium comprises at least 0.33 mg per L of magnesium. In some examples, the culture medium comprises between 0.33 mg and 13.17 mg per L of magnesium. Preferably, the culture medium comprises at least 5 mg per L of magnesium. More preferably, the culture medium comprises between 5 mg and 15 mg per L of magnesium. For example, magnesium may be provided by magnesium sulfate (MgSO4.7H20) In some examples, the culture medium comprises at least 1.32 mg per L of sodium. In some examples, the culture medium comprises at least 2.51 mg per L of sodium. In some examples, the culture medium comprises between 2.51 mg and 53.47 mg per L of sodium. In some examples, the culture medium comprises at least 0.1 mg per L of sodium. Preferably, the culture medium comprises at least 1 mg per L of sodium. More preferably, the culture medium comprises between 1 mg and 10 mg per L of sodium. For example, sodium may be provided by disodium EDTA, (e.g. ferrous) sodium DTPA, and/or sodium molybdate (Na2Mo04.2H20).

In some examples, the culture medium comprises at least 3 mg per L of manganese. In some examples, the culture medium comprises at least 5.49 mg per L of manganese. In some examples, the culture medium comprises at least 0.21 mg per L of manganese. In some examples, the culture medium comprises between 0.21 mg and 1.94 mg per L of manganese. Preferably, the culture medium comprises at least 1 mg per L of manganese. More preferably, the culture medium comprises between 1 mg and 10 mg per L of manganese. For example, manganese may be provided by manganese sulfate (MnSO4.4H20).

In some examples, the culture medium comprises at least 0.01 mg per L of copper. In some examples, the culture medium comprises at least 0.09 mg per L of copper. In some examples, the culture medium comprises between 0.09 mg and 0.25 mg per L of copper. Preferably, the culture medium comprises at least 0.01 mg per L of copper. More preferably, the culture medium comprises between 0.01 mg and 0.25 mg per L of copper. For example, copper may be provided by copper sulfate (CuSO4.5H20).

In some examples, the culture medium comprises at least 0.37 mg per L of zinc. In some examples, the culture medium comprises between 0.37 mg and 1.56 mg per L of zinc. Preferably, the culture medium comprises at least 1 mg per L of zinc. More preferably, the culture medium comprises between 1 mg and 2 mg per L of zinc. For example, zinc may be provided by zinc sulfate (ZnSO4.7H20).

In some examples, the culture medium comprises at least 4.30 mg per L of sulfur. In some examples, the culture medium comprises between 4.30 mg and 65.59 mg per L of sulfur. In some examples, the culture medium comprises at least 40 mg per L of sulfur. Preferably, the culture medium comprises at least 60 mg per L of sulfur. More preferably, the culture medium comprises between 60 mg and 70 mg per L of sulfur. For example, sulfur may be provided by zinc sulfate (ZnSO4.7H20).

In some examples, the culture medium comprises at least 0.14 mg per L of boron. In some examples, the culture medium comprises between 0.14 mg and 1.02 mg per L of boron. In some examples, the culture medium comprises at least 0.5 mg per L of boron. Preferably, the culture medium comprises at least 0.6 mg per L of boron. More preferably, the culture medium comprises between 0.6 mg and 1.5 mg per L of boron. For example, boron may be provided by boric acid (H3B03).

In some examples, the culture medium comprises at least 0.31 mg per L of iron. In some examples, the culture medium comprises between 0.31 mg and 9.15 mg per L of iron. In some examples, the culture medium comprises at least 3 mg per L of iron. Preferably, the culture medium comprises at least 1 mg per L of iron. More preferably, the culture medium comprises between 1 mg and 10 mg per L of iron. For example, iron may be provided by ferrous sulfate (FeSO4.7H20) and/or ferrous (e.g. sodium) DTPA.

In some examples, the culture medium comprises at least 0.01 mg per L of molybdenum. In some examples, the culture medium comprises between 0.01 mg and 0.15 mg per L of molybdenum. Preferably, the culture medium comprises at least 0.1 mg per L of molybdenum. More preferably, the culture medium comprises between 0.1 mg and 0.15 mg per L of molybdenum. For example, molybdenum may be provided by sodium molybdate (Na2Mo04.2H20).

In some examples, the culture medium comprises at least 0.16 mg per L of chlorine. In some examples, the culture medium comprises between 0.16 mg and 97.64 mg per L of chlorine. Preferably, the culture medium comprises at least 10 mg per L of chlorine. More preferably, the culture medium comprises between 10 mg and 25 mg per L of chlorine. For example, chlorine may be provided by calcium chloride dihydrate (CaC12.2H20) and/or cobalt chloride (CoCl2.6H20).

In some examples, the culture medium comprises at least 0.006 mg per L of cobalt. In some examples, the culture medium comprises at least 0.001 mg per L of cobalt. For example, chlorine may be provided by cobalt chloride (CoCl2.6H20).

In some examples, the culture medium comprises at least 0.64 mg per L of iodine. In some examples, the culture medium comprises at least 0.10 mg per L of iodine. For example, chlorine may be provided by potassium iodide (KI).

In some examples, the culture medium comprises: a) at least 18.05 mg per L of nitrogen; b) at least 10.99 mg per L of phosphorus; c) at least 66.84 mg per L of potassium; d) at least 1.17 mg per L of calcium; e) at least 0.33 mg per L of magnesium; f) at least 2.51 mg per L of sodium; g) at least 0.21 mg per L of manganese; h) at least 0.09 mg per L of copper; i) at least 0.37 mg per L of zinc; j) at least 4.30 mg per L of sulfur; k) at least 0.14 mg per L of boron; I) at least 0.31 mg per L of iron; m) at least 0.01 mg per L of molybdenum; and/or n) at least 0.16 mg per L of chlorine.

The culture medium may further comprise at least 0.006 mg per L of cobalt and/or at least 0.64 mg per L of iodine.

In a preferred example, the culture medium comprises: a) at least 40 mg per L of nitrogen; b) at least 5 mg per L of phosphorus; c) at least 120 mg per L of potassium; d) at least 25 mg per L of calcium; e) at least 5 mg per L of magnesium; f) at least 1 mg per L of sodium; g) at least 1 mg per L of manganese; h) at least 0.01 mg per L of copper; i) at least 1 mg per L of zinc; j) at least 60 mg per L of sulfur; k) at least 0.6 mg per L of boron; I) at least 1 mg per L of iron; m) at least 0.1 mg per L of molybdenum; and/or n) at least 10 mg per L of chlorine.

In a more preferred example, the culture medium comprises: a) between 40 mg and 55 mg per L of nitrogen; b) between 5 mg and 15 mg per L of phosphorus; c) between 120 mg and 130 mg per L of potassium; d) between 25 mg and 35 mg per L of calcium; e) between 5 mg and 15 mg per L of magnesium; f) between 1 mg and 10 mg per L of sodium; g) between 1 mg and 10 mg per L of manganese; h) between 0.01 mg and 0.25 mg per L of copper; i) between 1 mg and 2 mg per L of zinc; j) between 60 mg and 70 mg per L of sulfur; k) between 0.6 mg and 1.5 mg per L of boron; I) between 1 mg and 10 mg per L of iron; m) between 0.1 mg and 0.15 mg per L of molybdenum; and/or n) between 10 mg and 25 mg per L of chlorine.

Because the fragment is surface cleaned with alcohol and the fragment is dissected into a smaller piece of Sphagnum, a culture medium with relatively high nutrient content can be used. By mitigating contamination risk by using alcohol and keeping the piece of Sphagnum small, higher nutrient levels can be used, which permits faster growth. In the absence of sufficient sterilisation, this would result in worse growth rates as the high levels of nutrients would cause contaminants to thrive and out-compete the Sphagnum. It is particularly advantageous to clean a small fragment of Sphagnum (e.g. between 1 mm and 10 mm) with alcohol and initiate a small piece (e.g. less than 1 mm), and subsequently use a culture medium with high nutrient levels, because this can lead to improved growth without leading to increased contamination. It has also been found that when Sphagnum can be grown substantially axenically, high nutrient levels promote growth. Conventional methods provide little or no nutrients to Sphagnum as it is widely understood that Sphagnum grows in environments with little or no nutrient supply.

However, by surface cleaning with alcohol to remove contamination, growth of Sphagnum can be improved by supplying with high levels of nutrients.

It will be appreciated that the above nutrients may be provided in a nutrient composition for in vitro cultivation of Sphagnum independently from the method of the first aspect.

In some examples, the culture medium does not comprise plant hormones.

Optionally, the culture medium is a solid culture medium. For example, the culture medium may contain a solidifying agent such as agar to solidify the medium. In other examples, the culture medium is a liquid culture medium. It is preferable to initiate the fragment on a solid medium because this allows for better isolation of contaminants. This allows for easier identification of contamination and allows non-contaminated portions of the Sphagnum to be removed. In a liquid culture medium, if contamination were left, it would spread, and the entire culture vessel and all the Sphagnum would be contaminated.

The culture medium may be arranged in a culture vessel. For example, the culture vessel may be in the form of a jar, such as a glass jar. Glass jars are often used in tissue culture, and can easily be sterilised such as by autoclaving. For example, the culture vessel may have a volume of around 300 ml. In other examples, culture vessels of other materials may be used, such as plastic. The culture vessel may have a lid for inserting and removing the culture medium and the Sphagnum.

Optionally, the method further comprises culturing the piece of Sphagnum in the culture medium. Preferably, the culturing comprises growing the Sphagnum. Once initiated, the Sphagnum can be cultured to begin to form a shoot and grow. By culturing the Sphagnum, the Sphagnum can be left to grow. Culturing may involve supplying light for growth of the Sphagnum. For example, light may be provided by white fluorescent tubes or LEDs. Preferably, a light source provides at least 50 pmol m-2 s-1 photosynthetically active radiation (PAR) (i.e. wavelength of 400 to 700 nm), and more preferably between 50 pmol m-2 s-1 PAR and 110 pmol m-2 s-i PAR.

Optionally, the culturing is performed for at least 8 weeks. This provides enough time to ensure that a new shoot will grow, and that the Sphagnum will grow into a differentiated adult form. For example, during this time the Sphagnum may be left in the culture medium. The culture medium therefore preferably contains enough nutrient supply for around 8 weeks. In some examples, the culturing is performed for at least 1 week, preferably at least 2 weeks, more preferably at least 4 weeks, even more preferably at least 6 weeks, most preferably at least 8 weeks. In some examples, the culturing may be performed for several months to ensure sufficient growth and to establish that the culture is clean.

Optionally, the culturing is performed to form a gametophore. In other words, the culturing may be performed until a gametophore is formed. For example, this may be in the form of a new shoot. In other words, the initiated piece of Sphagnum is cultured until the adult vegetative form is provided. The gametophore should preferably be distinguished from the protonema. For example, the culturing may be performed until new stems, branches, or leaves are formed. In some examples, the culturing is performed continuously until the formation of a gametophore.

This means that culturing does not cease, and that the Sphagnum is left in the culture medium until formation of a gametophore and/or for at least 8 weeks. Preferably, the Sphagnum is not chopped or pulverised after initiation until formation of a gametophore and/or for at least 8 weeks. In some examples, the culturing comprises culturing the fragment in the same culture medium until formation of the gametophore and/or for at least 8 weeks.

Optionally, the culturing is performed without pulverising the Sphagnum. Pulverising Sphagnum using a machine is sometimes conventionally used to maintain Sphagnum in the protonema stage or for production of protoplasts. Pulverising prevents the differentiation into the gametophore. This is used to build up density of protonema, but delays differentiation. It has been found to be preferable that the Sphagnum is not maintained in the protonema stage, and that differentiation into gametophore occurs rapidly. Therefore, it is desirable to avoid pulverisation. In other words, the initiated Sphagnum is preferably cultured until a gametophore is formed, without pulverising the Sphagnum. Preferably, culturing is performed for at least 8 weeks, without pulverising the Sphagnum.

Optionally, the method further comprises, after the culturing, transferring the Sphagnum to a second culture medium. For example, the second culture medium may be arranged in a second culture vessel. The second culture vessel may be separate to the first culture vessel (i.e. the culture vessel in which the Sphagnum was initiated). The second culture vessel may be the similar to the first culture vessel. For example, the second culture medium may be a container such as a glass jar.

Transferring the Sphagnum to a second culture medium allows the nutrient supply to be replenished. Preferably, the culturing is performed for around 8 to 12 weeks after initiation, and then the Sphagnum is transferred to a second culture medium. This provides an ideal time for transfer after substantial growth has occurred and when the nutrient supply is beginning to deplete. After this time, it is also possible to observe any visual signs of contamination. Therefore, it can be ensured that the culture is clean before transfer into a liquid medium, for example.

In some examples, the method further comprises determining if visible contamination is present, and if contamination is not visible, then transferring the Sphagnum to the second culture medium. Contamination may be visible in the culture medium or on the Sphagnum at this stage (preferably around 8 to 12 weeks). If the Sphagnum appears clean, it can be transferred to a second culture medium. This can be done under sterile conditions.

If contamination is visible, then the Sphagnum can be discarded if the contamination is significant and covers the whole Sphagnum. If the contamination is visible but does not cover all the Sphagnum, or is limited to a small area of the culture medium, then a small part of the non-contaminated Sphagnum can be taken (e.g. dissected) and used for initiation. In some examples, this may involve performing the surface sterilising steps again. This is why is it particularly useful to use a solid culture medium, because contamination can be easily identified and isolated.

Optionally, the second culture medium does not comprise sugar. As set out above, it is preferable to avoid sugar in the culture medium to avoid growth of contaminants.

Optionally, the second culture medium comprises a liquid culture medium. After the culturing in the first culture medium, any contaminants will generally be visible after that period, allowing for the selection of clean cultures and the discarding of contaminated cultures. As contamination has been identified at this stage, the second culture vessel can contain a liquid culture medium.

Solid media is not required at this stage because any contamination has usually previously been identified. Using a liquid culture medium is advantageous because supply of nutrients can be increased by supplying over the entire surface area of the Sphagnum, whereas nutrient supply is limited with solid media. This can lead to improved growth rates for the culture period after transfer to the second culture vessel with liquid media. The improved growth rates are also more significant now that the Sphagnum is a larger size, as the effect on growth rate in the initial culture phase would be far less significant as the initiated piece is so small.

In some examples, the second culture medium comprises nutrients. The nutrients of the second culture medium may be the same as the first culture medium as set out above.

Optionally, the second culture medium comprises nutrients comprising nitrogen, phosphorus, potassium, calcium, magnesium, sodium, manganese, copper, zinc, sulfur, boron, iron, molybdenum, chlorine, cobalt, and iodine.

In some examples, the second culture medium contain the same composition as the first culture medium, but is preferably liquid instead of solid. For example, the second culture medium may contain the same nutrients, and optionally the same levels of those nutrients. In other examples, the second culture medium may contain other nutrients or different levels of nutrients to the first culture medium in which the fragment is initiated.

Optionally, the method further comprises culturing the Sphagnum in the second culture medium. For example, the Sphagnum may be cultured in a similar way as the culturing in the first culture medium. Culturing may involve supplying light for growth of the Sphagnum. For example, light may be provided by white fluorescent tubes or LEDs. Preferably, a light source provides at least 50 pmol m-2 s-1 photosynthetically active radiation (PAR) (i.e. wavelength of 400 to 700 nm), and more preferably between 50 pmol m-2 s-1 PAR and 110 pmol m-2 s-PAR.

Optionally, the culturing the gametophore in the second culture medium comprises supplying carbon dioxide. Carbon dioxide can be provided as a carbon source for photosynthesis. It is preferable to supply carbon dioxide instead of sugar because of the risk of encouraging contaminant growth. Typically, carbon dioxide is not required during the first culture in the first culture medium because the piece of Sphagnum is so small. After transfer to the second culture medium, it is beneficial to supply carbon dioxide for faster growth. This is particularly synergistic with using alcohol as a surface cleaner because where alcohol is used it is undesirable to use sugar because contaminant growth is encouraged. Using carbon dioxide provides a supply of carbon without encouraging contaminant growth.

In some examples, the second culture vessel comprises a tube permeable to carbon dioxide arranged to loop into and out of holes in the second culture vessel. The second culture vessel is therefore sealed with a section of permeable tube passing through the airspace above the liquid culture media. For example, the tube may be made from silicone rubber. Carbon dioxide (e.g. at least 1 % carbon dioxide by volume, preferably at least 50 %, more preferably at least 90 %) may be delivered through the tube from a source of carbon dioxide, which can diffuse through the wall of the permeable tube and into the second culture vessel. This allows supply of carbon dioxide while the permeable tube provides a barrier to prevent ingress of contamination. For example, the tube may be permeable to carbon dioxide but impermeable to larger particles such as contaminants. In cases where the second culture vessel contains a liquid culture medium, carbon dioxide levels in the airspace above the liquid culture medium can rise, and carbon dioxide can diffuse into the liquid medium and supply the Sphagnum. The liquid culture medium can be stirred to improve uptake, such as by a heat source to provide a convection current. For example, a light source, such as a fluorescent tube, may provide such a stirring effect.

In some examples, the Sphagnum may be transferred to a third culture medium. For example, the Sphagnum may be sub-divided and split up into a plurality of culture vessels. This also allows for the bulking up of Sphagnum. This avoids limitations on the growth of Sphagnum, and encourages new growth for the Sphagnum in each culture medium, which is particularly beneficial in a commercial growing situation. The Sphagnum may be cultured in the second culture medium for around 8 to 12 weeks and then transferred to a third culture medium. In 8 to 12 weeks, the Sphagnum typically increases weight by around four times compared to the initial Sphagnum in the culture vessel. For example, after 8 to 12 weeks Sphagnum in a 2 L culture vessel may be sub-divided into four 2 L culture vessels and the process may be repeated. After a further 8 to 12 weeks, the Sphagnum may be sub-divided again and so on.

During sub-dividing, the Sphagnum can be broken up or torn, preferably under sterile conditions. This not only permits the bulking up of Sphagnum, but also breaks stems to generate new growing points, leading to faster growth. For example, the Sphagnum may be chopped. This allows the growth rate of the Sphagnum to be improved because it can be chopped into a plurality of fragments. When Sphagnum grows as a strand, the top of the strand forms a capitulum which is the primary growing point of the Sphagnum. In vitro Sphagnum typically grows as a long strand without significant branches. However, when the strand is broken up into a plurality of fragments, each fragment will then form a growing point at the tip.

Each of these fragments therefore provides an individual growing point, resulting in faster growth than the original single strand.

According to a second aspect of the present disclosure, there is provided Sphagnum obtainable by the method as disclosed herein.

According to a third aspect of the present disclosure, there is provided a nutrient composition for in vitro cultivation of Sphagnum comprising nutrients. For example, the nutrients may comprise the nutrients disclosed herein.

In some examples, the nutrient composition comprises nitrogen, phosphorus, potassium, calcium, magnesium, sodium, manganese, copper, zinc, sulfur, boron, iron, molybdenum, and/or chlorine.

In some examples, the nutrient composition comprises nitrogen, phosphorus, potassium, calcium, magnesium, sodium, manganese, copper, zinc, sulfur, boron, iron, molybdenum, chlorine, cobalt, and/or iodine.

In some examples, the nutrient composition comprises at least 0.025 mg per L of sodium, preferably at least 0.1 mg, more preferably at least 1 mg per L of sodium.

In some examples, the nutrient composition comprises at least 0.005 mg per L of copper, preferably at least 0.01 mg per L of copper, more preferably at least 0.015 mg per L of copper.

In some examples, the nutrient composition comprises: a) at least 18.05 mg per L of nitrogen; b) at least 10.99 mg per L of phosphorus; c) at least 66.84 mg per L of potassium; d) at least 1.17 mg per L of calcium; e) at least 0.33 mg per L of magnesium; f) at least 2.51 mg per L of sodium; g) at least 0.21 mg per L of manganese; h) at least 0.09 mg per L of copper; i) at least 0.37 mg per L of zinc; j) at least 4.30 mg per L of sulfur; k) at least 0.14 mg per L of boron; I) at least 0.31 mg per L of iron; m) at least 0.01 mg per L of molybdenum; and/or n) at least 0.16 mg per L of chlorine. 30 In a preferred example, the nutrient composition comprises: a) at least 40 mg per L of nitrogen; b) at least 5 mg per L of phosphorus; c) at least 120 mg per L of potassium; d) at least 25 mg per L of calcium; e) at least 5 mg per L of magnesium; f) at least 1 mg per L of sodium; g) at least 1 mg per L of manganese; h) at least 0.01 mg per L of copper; i) at least 1 mg per L of zinc; j) at least 60 mg per L of sulfur; k) at least 0.6 mg per L of boron; I) at least 1 mg per L of iron; m) at least 0.1 mg per L of molybdenum and/or n) at least 10 mg per L of chlorine.

In a more preferred example, the nutrient composition comprises: a) between 40 mg and 55 mg per L of nitrogen; b) between 5 mg and 15 mg per L of phosphorus; c) between 120 mg and 130 mg per L of potassium; d) between 25 mg and 35 mg per L of calcium; e) between 5 mg and 15 mg per L of magnesium; f) between 1 mg and 10 mg per L of sodium; g) between 1 mg and 10 mg per L of manganese; h) between 0.01 mg and 0.25 mg per L of copper; i) between 1 mg and 2 mg per L of zinc; j) between 60 mg and 70 mg per L of sulfur; k) between 0.6 mg and 1.5 mg per L of boron; I) between 1 mg and 10 mg per L of iron; m) between 0.1 mg and 0.15 mg per L of molybdenum; and/or n) between 10 mg and 25 mf per L of chlorine. 25 In any of the above examples, the nutrient composition may further comprise at least 0.006 mg per L of cobalt and/or at least 0.64 mg per L of iodine.

Sphagnum is conventionally cultured with little or no nutrients. Even in conventional in vitro culturing Sphagnum, it is typical to provide very low nutrient content. The present inventors have surprisingly found that Sphagnum can be cultured in vitro in the presence of a relatively high concentration of nutrients. Growth rates can be improved by supplying such high levels of nutrients. This is particularly beneficial where the culture of Sphagnum is substantially sterile, and contamination has been avoided. Therefore, it is particularly advantageous to use the nutrient composition in combination with surface cleaning with alcohol such as described herein in relation to the first aspect.

According to a fourth aspect of the present disclosure, there is provided a nutrient medium comprising the nutrient composition of the third aspect.

In some examples, the nutrient medium may comprise a liquid medium. In some examples, the nutrient medium may comprise a solid medium. For example, the solid medium may be solidified with a solidifying agent such as agar. Nutrients and levels thereof of the first or third aspect may readily be applied to the fourth aspect.

According to a fifth aspect of the present disclosure, there is provided a method for in vitro culturing Sphagnum, comprising: culturing Sphagnum in the nutrient medium of the fourth aspect. Nutrients and levels thereof of the first or third aspect may readily be applied to the fifth aspect.

Any suitable Sphagnum species (or optionally a combination thereof) may be used in the present disclosure. As different species of Sphagnum may have different growth requirements, the Sphagnum species for use in the present disclosure may be selected depending on the environment.

The Sphagnum may comprise one or more Sphagnum species. Any species could be used, but in one example the present disclosure comprises the use of one or more Sphagnum species selected from the group consisting of: Sphagnum angustifolium, Sphagnum australe, Sphagnum capillifolium, Sphagnum centrale, Sphagnum compactum, Sphagnum cusp/datum, Sphagnum denticulatum, Sphagnum fa/lax, Sphagnum fimbriatum, Sphagnum fuscum, Sphagnum imbricatum (ausfinii), Sphagnum inundatum, Sphagnum magellanicum (medium), Sphagnum palustre, Sphagnum papillosum, Sphagnum pulchrum, Sphagnum russowii, Sphagnum squarrosum, Sphagnum subnitens, Sphagnum tenellum, and Sphagnum cristatum. In one example, the method comprises the use of one or more Sphagnum species selected from the group consisting of: Sphagnum palustre, Sphagnum capillifolium, Sphagnum rubellum, Sphagnum subnitens, Sphagnum denticulatum, Sphagnum squarrosum, Sphagnum fa/lax, Sphagnum fimbriatum, Sphagnum cusp/datum, Sphagnum magellanicum, and Sphagnum papillosum. In one example, the invention comprises the use of one or more Sphagnum species selected from the group consisting of: Sphagnum palustre, Sphagnum capillifolium, Sphagnum capillifolium rubellum, Sphagnum subnitens, Sphagnum squarrosum, Sphagnum magellanicum, and Sphagnum papillosum.

In one example, a Sphagnum species for use in the present disclosure may be one or more selected from the group consisting of: Sphagnum palustre, Sphagnum capillifolium, Sphagnum fallax, Sphagnum magellanicum, Sphagnum papillosum, and Sphagnum squarrosum.

Most preferably the Sphagnum species is Sphagnum palustre. For example, Sphagnum palustre may be preferable for use in a growing medium because of its physical properties.

It is also envisaged that the invention could be applied to any hybrid Sphagnum species.

In some examples, the fragment of Sphagnum comprises at least one of the Sphagnum species disclosed herein. In some examples, the fragment of Sphagnum comprises at least 2, 3, 4, 5 or more Sphagnum species.

Features of one aspect can be readily applied to other aspects. Apparatus features can be readily applied to method features and vice versa.

Embodiments of the disclosure are described below, by way of example only, with reference to the accompanying Figures.

Figure 1 shows a photograph from the side of a culture vessel for in vitro culturing Sphagnum

according to a first embodiment of the disclosure.

Figure 2 shows a photograph from the side of a culture vessel for in vitro culturing Sphagnum of Figure 1, after 6 weeks of growth Figure 3 shows a photograph from the side of a culture vessel for in vitro culturing Sphagnum of Figure 1, after 16 weeks of growth.

Figure 4 shows a table of measured wet weights of samples of Sphagnum after 10 weeks of 30 growth.

Figure 5 shows a graph of measured wet weights of the results in the table of Figure 4.

Examples

Example 1

Materials and Methods A trial was conducted involving taking a fragment from a capitulum of in vivo Sphagnum. The fragment was surface cleaned with 70 % abv propanol for 30 seconds. The fragment was then washed in sterile water for 1 minute and placed to dry on sterile absorbing paper. The fragment was then dissected by hand using a scalpel under sterile conditions to provide a piece of Sphagnum. The piece had a length less than 1 mm and was placed into a culture medium for initiation. The initiated Sphagnum on the culture medium is shown in the photograph of Figure 1.

Referring to Figure 1, a photograph of an apparatus 100 for culturing Sphagnum is shown as used for the present trial. The apparatus 100 comprises a culture vessel 102 in the form of a glass jar of a volume of around 300 ml. The culture vessel 102 contains a culture medium 104. 15 A piece of Sphagnum 106 is shown arranged on the culture medium 104.

The culture medium 104 contained nutrients comprising 48.23 mg per L of nitrogen, 9.67 mg per L of phosphorus, 123.46 mg per L of potassium, 32.63 mg per L of calcium, 9.12 mg per L of magnesium, 1.32 mg per L of sodium, 5.49 mg per L of manganese, 0.02 mg per L of copper, 1.96 mg per L of zinc, 62.55 mg per L of sulfur, 1.08 mg per L of boron, 1.40 mg per L of iron, 0.10 mg per L of molybdenum, 11.69 mg per L of chlorine, 0.006 mg per L of cobalt, and 0.63 mg per L of iodine. The culture medium 104 was a solid culture medium solidified with agar. There was no sugar in the culture medium 104.

The Sphagnum was then cultured for 16 weeks Results Figure 2 shows an apparatus 200 which corresponds to the apparatus 100 of Figure 1 after a period of 6 weeks. During this time, the Sphagnum 106 has been cultured, and as shown in Figure 2 the resultant Sphagnum 206 has grown in size.

Figure 3 shows an apparatus 300 which corresponds to the apparatus 200 of Figure 2 after a further period of 10 weeks (being 16 weeks after the apparatus 100 of Figure 1). The Sphagnum 306 in Figure 3 has significantly grown in size between Figure 1 and Figure 2.

This shows that the in vitro culturing techniques of surface cleaning with alcohol have been successful and contamination has been avoided.

Example 2

Materials and Methods A trial was conducted involving taking initial samples of Sphagnum originally initiated following surface cleaning with alcohol and subsequently grown under in vitro conditions, in accordance

with the present disclosure, such as in Example 1.

12 samples of Sphagnum palustre were taken with a wet weight of 13 g ± 1 g. The samples were then placed into a culture medium containing nutrients. The culture medium contained nutrients comprising 48.23 mg per L of nitrogen, 9.67 mg per L of phosphorus, 123.46 mg per L of potassium, 32.63 mg per L of calcium, 9.12 mg per L of magnesium, 1.32 mg per L of sodium, 5.49 mg per L of manganese, 0.02 mg per L of copper, 1.96 mg per L of zinc, 62.55 mg per L of sulfur, 1.08 mg per L of boron, 1.40 mg per L of iron, 0.10 mg per L of molybdenum, 11.69 mg per L of chlorine, 0.006 mg per L of cobalt, and 0.63 mg per L of iodine. The culture medium was a solid culture medium solidified with agar. There was no sugar in the culture medium.

The Sphagnum was then cultured for 10 weeks. After 10 weeks, the wet weights of the samples were measured.

Results Figure 4 shows a table of the final wet weights of the samples.

The mean weight of the 12 samples was 60.4 mg, with a standard deviation of 20.7 mg. This provided a percentage increase in weight of 365% as a result of 10 weeks of growth.

Sample 2 was identified as an anomaly as it did not grow well during the trial and showed poor growth compared to the other samples and was deemed non-viable.

Removing sample 2 from the results, the mean weight of the 11 remaining samples was 64.5 mg, with a standard deviation of 15.7 mg. This provided a percentage increase in weight of 396% as a result of 10 weeks of growth.

Figure 5 shows a graph of the final wet weights of the samples, with sample 2 omitted from the calculation of the average.

The disclosure of this application also contains the following numbered clauses: 1. A method for in vitro culturing Sphagnum, comprising: providing a vegetative fragment of Sphagnum; surface cleaning the fragment with alcohol; dissecting the fragment to provide a piece of Sphagnum; and initiating the piece of Sphagnum in a culture medium.

2. The method according to clause 1, wherein the fragment has a length of less than 10 mm.

3. The method according to clause 1 or 2, wherein the fragment is from a capitulum of Sphagnum.

4. The method according to any preceding clause, wherein the piece of Sphagnum has a length of less than 1 mm.

5. The method according to any preceding clause, wherein the surface cleaning the fragment with alcohol is performed for less than 30 seconds.

6. The method according to any preceding clause, wherein the alcohol comprises between % and 80 % alcohol by volume.

7. The method according to any preceding clause, wherein the alcohol comprises propanol.

8. The method according to any preceding clause, further comprising surface cleaning the fragment with sterile water before the surface cleaning with alcohol.

9. The method according to any preceding clause, further comprising surface cleaning the fragment with sterile water after the surface cleaning with alcohol.

10. The method according to any preceding clause, further comprising placing the piece of Sphagnum onto a sterile absorption surface before initiating.

11. The method according to any preceding clause, wherein the surface cleaning does not comprise using a chlorine-based sterilant.

12. The method according to any preceding clause, wherein the surface cleaning does not comprise using a detergent.

13. The method according to any preceding clause, wherein the culture medium does not comprise sugar.

14. The method according to any preceding clause, wherein the culture medium comprises nutrients comprising nitrogen, phosphorus, potassium, calcium, magnesium, sodium, manganese, copper, zinc, sulfur, boron, iron, molybdenum, chlorine, cobalt, and iodine.

15. The method according to any preceding clause, wherein the culture medium is a solid culture medium.

16. The method according to any preceding clause, further comprising culturing the piece of Sphagnum in the culture medium.

17. The method according to clause 16, wherein the culturing is performed for at least 8 weeks.

18. The method according to clause 16 or 17, wherein the culturing is performed to form a gametophore.

19. The method according to any of clauses 16 to 18, further comprising, after the culturing, transferring the Sphagnum to a second culture medium.

20. The method according to clause 19, wherein the second culture medium does not comprise sugar.

21. The method according to any of clauses 19 or 20, wherein the second culture medium comprises a liquid culture medium.

22. The method according to any of clauses 19 to 21, wherein the second culture medium comprises nutrients comprising nitrogen, phosphorus, potassium, calcium, magnesium, sodium, manganese, copper, zinc, sulfur, boron, iron, molybdenum, chlorine, cobalt, and iodine.

23. The method according to any of clauses 19 to 22, further comprising culturing the Sphagnum in the second culture medium.

24. The method according to clause 23, wherein the culturing the Sphagnum in the second culture medium comprises supplying carbon dioxide.

25. Sphagnum obtainable by the method according to any preceding clause.

Claims

CLAIMS: 1. A method for in vitro culturing Sphagnum, comprising: providing a vegetative fragment of Sphagnum; surface cleaning the fragment with alcohol; initiating the fragment of Sphagnum in a culture medium; and culturing the fragment of Sphagnum in vitro for at least 8 weeks without pulverising the Sphagnum.
2. The method according to claim 1, wherein the fragment has a length of less than 10 MM.
3. The method according to claim 1 or 2, wherein the fragment is from a capitulum of Sphagnum.
The method according to any preceding claim, wherein the surface cleaning the fragment with alcohol is performed for less than 30 seconds.
5. The method according to any preceding claim, wherein the alcohol comprises between 50 % and 80 % alcohol by volume.
The method according to any preceding claim, wherein the alcohol comprises propanol.
7. The method according to any preceding claim, further comprising surface cleaning the fragment with sterile water before the surface cleaning with alcohol.
The method according to any preceding claim, further comprising surface cleaning the fragment with sterile water after the surface cleaning with alcohol.
9. The method according to any preceding claim, further comprising placing the fragment of Sphagnum onto a sterile absorption surface before initiating.
10. The method according to any preceding claim, wherein the surface cleaning does not comprise using a chlorine-based sterilant.
11. The method according to any preceding claim, wherein the surface cleaning does not comprise using a detergent.
12. The method according to any preceding claim, wherein the culture medium does not comprise sugar.
13. The method according to any preceding claim, wherein the culture medium comprises nutrients comprising nitrogen, phosphorus, potassium, calcium, magnesium, sodium, manganese, copper, zinc, sulfur, boron, iron, molybdenum, chlorine, cobalt, and iodine.
14. The method according to any preceding claim, wherein the culture medium is a solid culture medium.
15. The method according to any preceding claim, wherein the culturing is performed to form a gametophore.
16. The method according to any preceding claim, further comprising, after the culturing, transferring the Sphagnum to a second culture medium.
17. The method according to claim 16, wherein the second culture medium does not comprise sugar.
18. The method according to claim 16 or 17, wherein the second culture medium comprises a liquid culture medium.
19. The method according to any of claims 16 to 18, wherein the second culture medium comprises nutrients comprising nitrogen, phosphorus, potassium, calcium, magnesium, sodium, manganese, copper, zinc, sulfur, boron, iron, molybdenum, chlorine, cobalt, and iodine.
20. The method according to any of claims 16 to 19, further comprising culturing the Sphagnum in the second culture medium.
21. The method according to claim 20, wherein the culturing the Sphagnum in the second culture medium comprises supplying carbon dioxide.