BASF to buy seeds, herbicide businesses from Bayer for $7 billion
FRANKFURT (Reuters) – BASF BASFn.DE has agreed to buy seed and herbicide businesses from Bayer BAYGn.DE for 5.9 billion euros ($7 billion) in cash, as Bayer tries to convince competition authorities to approve its planned acquisition of Monsanto MON.N .
BASF, the world’s third-largest maker of crop chemicals, has so far avoided seed assets and instead pursued research into plant characteristics such as drought tolerance, which it sells or licenses out to seed developers.
But Bayer’s $66 billion deal to buy U.S. seeds group Monsanto, announced in September 2016, has created opportunities for rivals to snatch up assets that need to be sold to satisfy competition authorities.
Bayer said it would use the proceeds to partly refinance the Monsanto acquisition. It plans to raise $19 billion toward the deal by issuing convertible bonds and new shares, and has lined up as much as $57 billion of bridge financing from banks.
Baader Helvea analyst Markus Mayer said a higher-than-expected valuation of the assets up for sale could mean Bayer now needs to raise less than $10 billion from the sale of new shares, which would be a positive surprise.
Bayer had offered to sell assets worth around $2.5 billion. The European Commission said in August that the divestments offered by Bayer so far did not go far enough and started an in-depth investigation of the deal.
Bayer has to sell the LibertyLink-branded seeds and Liberty herbicide businesses, which generated 2016 sales of 1.3 billion euros, because they compete with Monsanto’s Roundup weed killer and Roundup Ready seeds.
LibertyLink seeds, used by soy, cotton and canola growers, are one alternative to Roundup Ready seeds for farmers suffering from weeds that have developed resistance to the Roundup herbicide, also known as glyphosate.
The spread of Roundup-resistant weeds in North America has been a major driver behind Liberty sales.
“BASF’s decision to acquire seeds assets represents something of a change to its prior view on its needs to respond to recent industry consolidation in agriculture,” Morgan Stanley analysts said.
“Nonetheless, the proposed assets for acquisition are high margin and high growth and represent a sensible bolt-on addition,” they added.
BASF Chief Executive Kurt Bock told a conference call he would look at further acquisition opportunities in the seeds sector as well but said it would take “two to tango”.
The group is also expected to look at other assets – such as vegetable seeds – that Bayer may be forced to divest, a person close to the matter said.
Shares in Bayer rose 1.2 percent to the top of Germany’s blue-chip DAX index .GDAXI by 1230 GMT, while BASF was up 0.2 percent.
The sale to BASF values Bayer’s assets at around 15 times 2016 operating profit (EBITDA) of 385 million euros, which analysts said was reasonable compared with multiples of 19.3 for ChemChina’s [CNNCC.UL] takeover of Syngenta SYNN.S and more than 20 for Dow’s DOW.N tie-up with DuPont DD.N .
BASF will finance the acquisition through a combination of cash on hand, commercial paper and bonds.
It is expected to reap sales synergies in the hundreds of millions of euros. On the cost side, however, savings will be slim at first as there is little overlap with BASF’s existing business and the group has promised to keep all permanent staff at the businesses it is buying for at least three years.
The acquisition will add to its earnings by 2020, it said.
The deal is conditional upon Bayer’s acquisition of Monsanto going through. While the European Commission could block that transaction, it has approved others, such as the Dow-DuPont deal and ChemChina’s takeover of Syngenta – although only after securing big concessions.
Bayer said it continued to work with the authorities to close the Monsanto purchase by early 2018.
As part of the asset sale to BASF, more than 1,800 staff, primarily in the United States, Germany, Brazil, Canada and Belgium, will transfer to BASF. It is also acquiring manufacturing sites for glufosinate-ammonium production and formulation, seed breeding facilities and research facilities.
Deutsche Bank advised BASF on the deal, while BofA Merrill Lynch and Credit Suisse advised Bayer.
Reporting by Maria Sheahan; Additional reporting by Arno Schuetze; Editing by Tom Pfeiffer and Keith Weir
BASF <BASFn.DE> has agreed to buy seed and herbicide businesses from Bayer <BAYGn.DE> for 5.9 billion euros ($7 billion) in cash, as Bayer tries to convince competition authorities to approve its planned acquisition of Monsanto <MON.N>.
Chapter 9 SEED TESTING (Contd.)
Combining purity and Germination Tests
Purity tests of most commercial seed lots of Eucalyptus are not made because it is difficult or impossible to separate the seed from the chaff of some species (Boland et al. 1980). Species in which seed and chaff are extremely similar in size, weight and colour include E. cloeziana, E. regnans and E. delegatensis. other small-seeded genera in which separation of pure seeds is difficult are Alnus, Betula, Populus and Salix. Even when separation is possible in these species, it is very time-consuming. In the seed laboratory in Canberra it takes only 6–7 minutes to set up a test of eucalypt seed with 4 weighed replicates, but to carry out a purity separation and set up a 4 × 100 seed test takes from 20 to 50 minutes, depending on the degree of difficulty in separating out the chaff (Turnbull 1983). The small size of seed also precludes a cutting test to determine the number of full but ungerminated seeds at the end of a test. For these reasons tests are best made on replicates by weight and results recorded as numbers of germinated seeds per unit weight of the impure mixture of seed and inert material. A squash test may also be used to give a rough estimate of viability.
Where seed is sown broadcast, the practising forester is primarily interested in the number of plants he can expect to get from a given weight of the seed lot he receives. Provided he is told that 1 kg of “impure” seed should produce 36,000 germinated seedlings, he is not worried whether this is caused by a combination of 90 % purity × 80 % pure seed germination or 80 % purity × 90 % pure seed germination. For local tests, therefore, if seed laboratory staff is insuffient, there is no objection to omitting the purity test even on species for which it would be practicable. In the case of direct sowing into individual containers, however, there are obvious advantages in having separate figures for purity and germination, since sowing is by numbers of (one to several) seeds per container rather than weight of seed per m 2 of bed or tray.
Indirect Tests of Viability
Estimating the germination potential of a seed lot by actually germinating a sample of it is often the method most relevant to practical forestry. But the tests take several weeks to complete and for some species pretreatment may take some additional weeks or months. For this reason much research has been conducted to find other methods by which seed viability can be estimated accurately but much more rapidly than by germination testing. The following account of these methods closely follows that of Turnbull (1975 d).
The objects of quick viability tests are:
- to determine quickly the viability of seeds of species which normally germinate slowly or show dormancy under the normal germination methods;
- to determine the viability of samples which at the end of the germination test reveal a high percentage of fresh ungerminated or hard seeds.
Only two methods, the topographical tetrazolium test and the embryo excision test were previously accepted by the International Seed Testing Association as official methods for some species of seeds. ISTA has recently accepted the X-ray method as a valid alternative to the cutting test for the detection of empty and insect-damaged seeds. The following tests can be applied depending on the circumstances:
The simplest viability testing method is direct eye inspection of seeds which have been cut open with a knife or scalpel. If the endosperm is of normal colour with a well developed embryo, the seed has a good chance of germinating. This test is not very reliable. Seeds with milky, unfirm, mouldy, decayed, shrivelled or rancid-smelling embryos and abortive seeds that have no embryo can be judged as non-viable without much difficulty (Bonner 1974). But it is not possible to distinguish moribund, recently dead or recently injured seeds which still appear the same as sound ones. The cutting test, as already mentioned, is used at the end of a germination test to determine the apparent viability of ungerminated seeds; it is also a useful tool in estimating the size and maturity of the seed crop before collection (Chapter 3) and the efficiency of methods used in processing.
In the philippines good correlation has been found between cutting and germination tests in fairly large-seeded species such as Leucaena, Intsia bijuga and Lagerstroemia speciosa (Seeber and Agpaoa 1976), but germination % was consistently 10–20 % less than the percentage of sound seeds on cutting test.
Topographical tetrazolium test
The tetrazolium method is only one of a number of biochemical tests which have been developed for seed testing. The various tests have been briefly reviewed by Moore (1969). The tetrazolium test was introduced in 1942 by G. Lakon in Germany.
In this method living cells are stained red by the reduction of a colourless tetrazolium salt to form a red formazan. The method emphasizes the need for a knowledge of the soundness of individual embryo parts for predicting the development of embryos into countable seedlings (Moore 1973).
The testing procedure is described in detail in the ISTA Rules (ISTA 1976) which approve the test for some species of hardwoods and conifers which germinate slowly by regular germination methods. Normal practice is to soak the seeds in water for about 20 hours, then cut or puncture the seed coat to facilitate entry of the 1% aqueous solution of tetrazolium (TZ) and immerse the seeds in the dark for 48 hours (Bonner 1974). The process can be greatly speeded up by cutting through the seed at a distance of one third from the micropyle and placing it in a Vitascope vacuum machine for only half an hour. This method gives satisfactory results in Denmark but interpretation of results requires more experience in the operator than the method of seed immersion followed by excision of the stained embryo (Knudsen 1982). The test is done on 4 replicates of 100 seeds each (ISTA 1976).
Justice (1972) states that, while the tetrazolium procedure is good in principle, its practical use in routine testing is limited by many problems, including: difficulty in staining of some seeds; necessity of cutting of dissecting seeds to permit observation of stained parts; poor agreement with results of germination tests in some cases, especially for seed of low germination capacity; lack of uniform interpretation of staining and difficulty in interpreting the significance of different degrees of staining; and an increase in man-hours required to test 400 seeds compared to regular germination tests.
The necessity for an experienced analyst for the successful use of this “common sense test” is admitted by Moore (1973). There is little doubt that the test can be useful for testing the viability of certain species, providing trained staff are available to prepare the seeds and evaluate the results.
Excised embryo test
By this method, the seeds are soaked for 1 – 4 days and the embryos are then excised from the seeds and placed on moist filter paper or blotter discs in petri dishes. The tests are placed in the light at a constant temperature of 20°C. The condition of the embryos is examined daily. Depending upon the species and lot differences, the tests can be terminated after only a few days, up to a maximum of 14 days, or as soon as distinct differentiation into viable and non-viable embryos can be made.
The excised embryo test is similar to germination tests in that it measures the quality of the seed by their actual germination. In addition it allows some measure of the embryo dormancy to be made, by counting those seeds which, although not growing normally, have grown slightly, remained firm and have kept their colour for the test period. The test is not valid for previously germinated seeds and must not be applied to samples which contain any dry germinated seeds. The success of the test requires considerable skill and experience in the operator and the ISTA rules restrict it to only a few species.
In a comprehensive study, Schubert (1965) compared the excised embryo method with the tetrazolium method for determining the viability of dormant tree seeds. He concluded that the tetrazolium method should receive preference over the embryo excision method but that improvements in the tetrazolium test should be made by providing for the use of bactericides and stronger reducing solutions to resolve doubts in weakly stained tissues.
Radiography was first used to determine seed quality over 70 years ago (Lundstrom, 1903, cited by Kamra 1964). The studies of Simak and Gustafsson (1953) highlighted the X-ray technique as a diagnostic method of tree seed analysis. The X-ray contrast method which uses various contrast or radiopaque agents was developed and applied successfully to species of Pinus and Picea (Simak 1957; Kamra 1963 a, 1963 b).
The X-ray method permits the detection of empty seeds, mechanical damage and abnormally developed internal seed structures, measurement of the thickness of the seedcoat and assessment of the seed viability when combined with a contrast agent.
The X-ray contrast method is based on the principle of semipermeability. When seeds are treated with a contrast agent, for example aqueous BaCl2 or vaporous CHC13, their living tissues are able to prevent its entry due to their semi-permeability, but the dead tissues become impregnated. The impregnated tissues absorb X-radiation more intensively than the unimpregnated ones and thus appear lighter on the film than the unimpregnated ones. The contrast permits living and dead tissue to be located in the seed and an estimation of its viability (Kamra 1964). There are now possibilities of using non-toxic water, instead of toxic BaCl2 or CHC13, as a contrast agent for testing seed viability (Simak 1982).
9.15 X-ray radiograph of teak fruits showing the variation in the number of locules (two to six). (S.K. Kamra)
9.16 X-ray radiographs showing embryo and endosperm classes in coniferous seeds. (M. Simak)
|O||Neither embryo nor endosperm (= empty seed)|
|I||Endosperm, embryo cavity developed but no embryo observed.|
|IIP||Endosperm, one or more small embryos the length of which does not exceed their breadth (“point embryos”).|
|II||Endosperm, and one or several embryos, none of which is longer than half of the embryo cavity.|
|III||Endosperm, and one or more embryos, the longest of which measures between half and three quarters of the embryo cavity.|
|IV||Endosperm, with one fully developed embryo, completely or almost completely occupying the embryo cavity. Diminutive embryos rarely occur.|
|A||The endosperm almost fills the seed coat to capacity and easily absorbs the x-rays.|
|B||The endosperm fills the seed coat incompletely and is often shrunken or otherwise deformed. The x-ray absorption is inferior to that of class A.|
|Ab||Seed with abnormally developed endosperm or embryo.|
|J||Seeds damaged by insects, containing larvae (JI) or their excrement (Je).|
The development of soft X-ray equipment has greatly simplified the operation (Belcher 1973). Complicated photographic equipment is not necessary and pictures can be made with polaroid film which provides clear and detailed radiographs within 30 seconds (Edwards 1973).
X-ray radiography has been successfully applied in determining the number of seeds in fruits of teak (Tectona grandis) and for studying their degrees of development (Kamra 1973). The technique has been tried on the fruits or seeds of sixty tropical forestry species and the results show that it can be reliably applied in processing such seeds (Kamra 1974, 1976, 1980).
A technique of stereoradiography as a supplement to the X-ray contrast method for use in seed quality testing has been developed by Kamra, Meyer and Wegelius (1973). The chief advantage of stereoradiography is that it is possible for the observer to have a three-dimensional view of the object from a pair of radiographs. In this way, the exact topographical location of the contrast agent in the seed can be reliably determined. This increases the information which can be obtained from radiographs and adds to the analytical accuracy.
The X-ray method is a useful one and is likely to play an increasing role in seed testing. Earlier models of X-ray machines were expensive, but recent models, particularly from Japan are much cheaper and now cost less than a cabinet germinator. Improvements in photographic films and paper have speeded up the process and simplified the interpretation, so that technicians can be trained easily to produce consistent results. ISTA has accepted the method as a valid alternative to the cutting test for the detection of empty and insectdamaged seeds. It also shows considerable promise for distinguishing between viable and non-viable seeds among “full seeds” (Simak 1980, Simak and Sahlén 1981). For certain temperate conifers it has been possible to obtain good correlation between the Development Class (DC) of seeds, based on the development of both embryo and endosperm, and their germinability. Figure 9.16 illustrates the DCs which have been defined for conifers, and Table 9.4 illustrates the germinability corresponding to each class, for Pinus sylvestris and Picea abies (Simak 1980).
Germinability of fresh collected, undamaged seeds (in %) belonging to different DCs, selected by radiography
(Material: Widespread seed samples from the whole of Sweden. Germination test: Jacobsen’s apparatus, temperature 23°C constant, light 1000 lux 8 hours/day).
|I A||II A||III A||IV A||II P||II B||III B||IV B|
For key to Development Classes, see Fig. 9.16.
Hydrogen peroxide (H2O2) has a stimulating effect on seed germination and has been used in a rapid test for germination of several conifers in the western USA (Bonner 1974). Seeds are soaked overnight in 1% H2O2. The seedcoat is then cut open to expose the radicle tip and the seeds put back into 1% H2O2 in the dark at alternating temperatures (20° and 30°C). Counting and refreshment of H2O2 is done after 3 or 4 days and final assessment after 7 or 8 days. Radicle growth of 5 mm or more is scored “evident”, 0 – 5 mm “slight” and no growth means a nonviable or empty seed (Danielson 1972 cited by Bonner 1974). The test is quicker but less reliable than a normal germination test (usually producing a more rapid and higher final germination), slower but simpler to perform than excised embryo and easier to interpret than TZ.
9.17 X-ray radiograph of Pinus caribaea seed. Most seeds have very poorly developed gametophyte and embryo and are dead. A few germinable are indicated by the black outlines. (M. Simak)
|9.18 Quercus seeds cut in halves for oven drying in moisture determination. (USDA Forest Service)|
|9.19 Dole electric seed moisture meter used in the USA. (USDA Forest Service)|
|9.20 Electric moisture meters used in Denmark. A: Jacoby’s infrared. B: Super-matic. C: Mettler. (DANIDA Forest Seed Centre)|
Testing Moisture Content
The importance of moisture content in affecting the longevity of seeds in storage has been stressed in Chapter 7. In order to control the operations of drying (or moistening) of seeds in preparation for storage and to check the stability of moisture content during storage, it is clearly essential to have reliable methods of measuring the amount of moisture in a given sample.
Methods of determining moisture content of seeds have been classified by Justice (1972) into (a) basic methods in which the moisture is driven out of the seeds by heat and measured by the loss of weight of the original material, or the weight or volume of the condensed moisture, and (b) practical methods designed for rapid routine work and standardized against one or more of the basic methods. Probably all the moisture cannot be driven out of seeds without driving out small amounts of other volatile constituents or causing chemical changes in the material which would result in weight changes. In applying any method, therefore, it is necessary to adhere closely to the prescribed procedure in order that the results of all tests made by that method will be comparable.
Until recently ISTA prescribed three possible procedures:
(1) Drying in an oven for 17 hours at 103°C (2) Drying in an oven for one to four hours at 130°C and (3) Toluene distillation. Method (2) is applicable only to certain agricultural seeds and method (3), previously used for Abies, Cedrus, Fagus, Picea, Pinus and Tsuga, has now been eliminated because it had ceased to be used in practice (ISTA 1981 c). This leaves only method (1) – the “Low constant temperature oven method” as applicable to forest trees.
The test should be made on two samples of about 5 g each, drawn from the working sample including impurities, not on pure seeds. Large seeds should be ground, broken or cut into small fragments to facilitate drying and a good rule of thumb is that any seeds that average over 10 mm in diameter or length should be broken (Bonner 1981). The samples should be weighed and placed in metal containers, well-spaced to facilitate air circulation, within an oven which is maintained at a temperature of 103° ± 2°C for 17 ± 1 hours. At the end of that period the seed should be placed in a desiccator to cool for 30 – 45 minutes and then reweighed. The relative humidity in the laboratory where the final weighing is done should be less than 70%, to avoid rapid re-absorption of moisture. The difference in MC of the two samples should not exceed a stated tolerance %. If it does, a further pair of samples should be tested; otherwise the mean of the two samples is the final result. The tolerance earlier prescribed by ISTA for all species was 0.2% but, as pointed out by Gordon (1979) and Bonner (1981), a single tolerance figure is not applicable to all species. At the 1983 ISTA Congress in Ottawa, the tolerances approved for moisture tests in tree seeds were agreed as follows:
|Sample Condition||Tolerance %|
|Small seeds, moisture 12%||0.5|
|Large seeds, moisture 12 to 25%||0.8|
|Large Seeds, moisture > 25%, e.g. Quercus||2.5|
For tropical tree seed laboratories wishing to conform to ISTA rules, this relaxation of tolerances will be a considerable help.
The calculation of moisture content should be made on a wet weight or fresh weight basis (see pp. 122–124) i.e.
Although wet weight basis is prescribed by ISTA and is becoming increasingly the standard form for expressing moisture content, it is not yet universal. To avoid any doubt, the method of calculating moisture content should be stated explicitly on any certificate or statement of results.
As explained by Gordon and Rowe (1982), provided that the initial fresh weight of a seed lot is measured and the initial moisture content (wet weight basis) calculated by oven-drying a sample, any new MC reached as a result of drying (or wetting) can be calculated directly from the new weight of the seed lot; there is no need for further oven-drying of samples at the new MC. The desired weight of the seed lot to be achieved through drying (or wetting) can be calculated by multiplying its initial weight by the initial dry matter percentage and dividing by the desired dry matter percentage.
|e.g.||(1)||If initial wet weight of a seed lot = 50 kg and the MC (wet weight basis), determined by oven-drying a sample, is 25%, the oven-dry weight = 75% of wet weight = 37.5 kg.|
|(2)||If a period of drying reduces the wet weight to 46.5 kg, the new MC|
|(3)||If it is desired to reduce the MC (wet weight basis) to 10%, then desired oven-dry weight will be 90% of new wet weight and the seed lot must be further dried until its wet weight|
Electric moisture meters give rapid estimates of seed moisture but they are not considered accurate enough for official seed testing. Their rapid operation does make them very useful in certain situations, for example they should be accurate enough to check tree seed moisture as a guide to drying seeds for storage (Bonner 1974, 1981). Meter readings are converted to seed moisture content by means of charts supplied by the manufacturer or developed from calibration curves in the laboratory for the species in question. Most meters will not measure moisture above 15 – 20 % and require a minimum of 90 – 100 g of seeds for a test (Bonner 1981). A locally made, cheap and portable electric moisture meter has been used successfully in Thailand for several years to measure the MC of rice grains (Kosol 1984) and could be used for tree seed of similar size. It measures electric capacitance and uses a 9-volt battery as the source of power.
Electric moisture meters are well suited to small seeds, but cannot be used for large seeds such as Juglans or Quercus; winged seeds such as Fraxinus are also difficult to measure (Bonner 1978). Large or winged seeds can be rapidly dried in a microwave oven. If the oven is preheated, drying can be completed in 5 minutes and weighing in 6 minutes immediately afterwards if in an electronic balance, or after 30 – 45 minutes’ cooling in a desiccator if weighing is done in an ordinary balance (Bonner and Turner 1980). Results can be expected to be within 7 % at a probability of 0.05 in the case of large seeds of high MC such as Quercus, and within 2 % in Fraxinus and Carya, as compared with the more accurate results of the slower conventional methods.
A simple and cheap method of drying seeds quickly is to use an infra-red lamp (Gordon and Rowe 1982). A weighed sample is subjected to heat from an infra-red lamp with such an intensity that it loses all its moisture, without being burnt, in about 20 minutes. When the loss of weight ceases, the new weight is measured and the percentage loss calculated.
An up-to-date account of the measurement of tree seed moisture content has been published recently (Bonner 1981).
Other qualitative tests or observations may be made as the need arises, but do not call for detailed prescriptions. In many cases they can be combined with the purity test. They include:
There are several methods of determining whether the seeds are of the species stated. They are:
Positive identification of the parent trees and their certification preferably on the basis of herbarium samples.
Identification of the seeds by use of an analytical key or by comparison with a reference collection.
Identification of the seedling. This may be the only way of determining if the seedlot is contaminated by hybrids or a mixture of two or more species with similar seed characteristics. A key and reference collection of seedlings will assist in identification (Turnbull 1975 d).
Authenticating seeds as to provenance is not possible for most species, but some progress has been made in this field for Pseudotsuga and Abies (Bonner 1974) and the use of isoenzyme techniques may open new possibilities (Burley 1976).
During the purity test, the operator should be alert to the incidence of mechanical damage and pathogenic infestation, which may indicate the need to improve the methods of transport or processing in use.
Calculation of Results
The following examples indicate the type of calculations required in the various stages of seed testing.
|Weight of full working sample||62.52 g|
|Weight of pure seed||56.89 g|
The weight of 1000 seeds may be calculated as follows:
(a) Seed weight determination carried out on 8 × 100 seeds from the pure seed component of the purity test.
Since this is considerably less than the maximum of 4.0 prescribed by ISTA, the sample is judged to be homogeneous and no further sampling is needed.
Weight of 1000 seeds = 3.76 × 10 = 37.6 g
(b) Seed weight determination carried out on 1000 seeds from the pure seed component of the purity test, without replication.
Weight of 1000 seeds = 37.6 g
The number of seeds per unit weight may be derived as follows:
Test made on 4 × 100 seed replicates from the pure seed component of the purity test.
|No. germinated on completion of test||79||85||76||88||328||82|
|Sound seeds on cutting test||4||3||6||3||16||4|
The range in number of germinated seeds from the largest to smallest of the replicates is 88 – 76 = 12. Reference to Table 9.3 on p. 220 shows that the maximum tolerated range for a mean germination of 82% is 15. Since the actual range is less, the sample is accepted as homogeneous.
|Viability %||=||82 + 4 = 86%|
Viable seeds per unit weight. A combination of the Viability % and weight of pure seed will give a figure for the number of viable seeds expected per unit weight of pure seed, while use of the germination % will indicate the number of germinable seeds. Incorporation of a factor for purity % will express the numbers in terms of the number of viable or germinable seeds per unit weight of “impure” seed.
|per g||per kg|
|No. of viable seeds||26.6 × 86 ÷ 100 = 22.9||22,900|
|No. of germinable seeds||26.6 × 82 ÷ 100 = 21.8||21,800|
|per g||per kg|
|No. of viable seeds||22.9 × 91 ÷ 100 = 20.8||20,800|
|No. of germinable seeds||21.8 × 91 ÷ 100 = 19.8||19,800|
In the case of very small-seeded species for which the purity test is impracticable, the number of germinated seeds per unit weight of impure seed is determined directly by test. Figures for numbers of pure seeds per unit weight are not obtainable for this type of seed. Although usually expressed as “viable seeds per g”, it should be noted that a cutting test is also impracticable for these small seeds, so strictly speaking the figures refer to germinable seeds. As an example:
Weight of replicate of impure seed (E. grandis) 0.10 g
|No. germinated on completion of test||65||73||63||71||272||68|
No. of germinable (“viable”) seeds per g = 680
No. of germinable (“viable”) seeds per kg = 680,000
Germination energy. Calculation of germination energy and energy period depends on the criterion used to define this. Table 9.5 gives an actual example extracted from paul (1972). As mentioned above, the energy period may be arbitrarily defined in advance but is normally much less than the full period of the test. A single assessment is sufficient in this case. If, in the present example, the energy period had been defined as 12 days, then
Energy period = 12 days
If, on the other hand, the energy period is taken as that up to the day of peak germination, then daily assessment is necessary as shown in the table and
Energy period = 10 days
Germination Test Sheet (extracted from Paul 1972)
|Species: Pinus caribaea var. hondurensis||Test No. 26/72|
|Seed Lot No. 85/71|
|Date sown: 2/11/72||Place: Mantin Nursery|
|Date completed: 30/11/72||Germination Percent: 64%|
|Days after Sowing||Sub-Samples (4 × 100 seeds)||Daily Total||CumulativeTotal||Cumulative Total as % of total seeds.||Mean daily germination %.||Daily Total as % of germinable seeds.||Cumulative total as % of germinable seeds|
Inspection of the pattern of germination suggests that rejection of all seeds germinating after peak germination would result in the rejection of an excessive proportion (60 %) of the potentially germinable seeds, while acceptance of all germinable seeds would unduly prolong the period of test and probably result in the inclusion of some seedlings of very poor vigour. A sensible rule of thumb applicable to the type of germination pattern in this example would be to define the energy period as lasting until daily germination falls to less than 25 % of peak. With this definition
Energy period = 16 days
Percentage of total germinable seeds which germinate within the energy period = 84 %.
Another commonsense measure of germination energy, used in Zimbabwe (Seward 1980), is the percentage of germination when mean daily germination (cumulative germination divided by time elapsed since sowing date) reaches its peak. In the present example (Table 9.5) the peak of mean daily germination percent is 3.48 %, the energy period 13 days and the germination % is
Percentage of total germinable seeds which germinate within the energy period measured in this way
Germination Value. Calculation of germination value, by the methods of Czabator (1962) and Djavanshir and Pourbeik (1976), is shown in Table 9.6, using the data from Table 9.5.
Calculation of Germination Value
(Methods of (1) Czabator and (2) Djavanshir and Pourbeik)
|Days since sowing||Daily Germination Percent||Cumulative Germination Percent||Daily Germination Speed (or Mean Germination) (Col. 3 ÷ Col. 1)||∑ DGS||Number of counts||∑ DGS/N (Col.5 ÷ Col.6)|
Germination value = Final DSG × Peak Value DGS = 2.29 × 3.48 = 7.97.
Germination value = (Final ∑ DGS (N) × (Final Cumulative Germination %/10) = 2.78 × 6.4 = 17.79.
Indirect tests of viability
Similar methods should be used as for germination tests i.e. 4 replicates should be used, the results tested for homogeneity and the mean number of apparently sound full seeds (cutting test) or stained embryos (tetrazolium test) expressed as a percentage of the total pure seeds tested.
Moisture content (example of small seeds 2
Desired final stocking of seedlings = 2400/m 2 Number of seeds/kg of pure seed = 26,600 Purity percent = 91% or 0.91 Germination percent = 82% or 0.82 Expected seedbed recovery rate (Seedlings which survive until transplanting as a proportion of germinated seeds reported by test) =0.65
then the required sowing rate
In the case of nursery 2 above, the number of seedbeds needed
The concept of “effective kilogram” of seed, which is in use now in several countries, has been found useful in planning sowing programmes and in calculating seed prices (Aldhous 1972). The “effective kilogram” is defined as the weight of seed of any particular seed lot which can be expected to produce the same number of viable seeds (as used in UK) or of plantable plants (as used in Zimbabwe) as would be produced by one kilogram of standard seed; this number is determined for each species from the average of previous experience. In Zimbabwe separate standard seedling recoveries have been established for (a) Orchard seed (b) Select and ordinary seed e.g. for Pinus elliottii the standard seedling recovery (= plantable plants per kg of seeds) is 15,500 for orchard seed and 14,500 for select or ordinary seed (Seward 1980).
The Kilogram Effective Factor (KEF) is the ratio of standard seedling recovery to actual seedling recovery of a given seed lot. It can be calculated from the equation:
Using the previous example (26,600 pure seeds/kg, purity factor 91 % or 0.91, germination factor 82 % or 0.82 and nursery recovery factor 65 % or 0.65) and assuming a standard seedling recovery of 15,000/kg,
The KEF can then be used, in conjunction with standard seedling recovery, to calculate the weight of seed required to raise any given number of plants. The equation is:
For example, to raise 1.5 million plants from the above seed lot
The 116 kg actual seed weight is equivalent to 100 effective kilograms or 100 kg of standard seed. Only when KEF = 1.0 are actual and effective seed weights identical.
In the case of eucalypts and other small-seeded species in which purity analysis is not done, the KEF equation is modified as follows:
For E. grandis, the KEF of a particular seed lot might be
and the quantity of seed needed to raise 1.5 million seedlings would be:
The main testing of a seed lot is done after processing and before storage or immediate despatch to nurseries. If a seed lot remains in storage for any length of time, it is essential to retest the germination or viability before use in case there has been any deterioration with time. Many seed centres retest annually, setting aside a representative sample of the whole seed lot in a small container in advance, so as to avoid recurrent opening of the bulk seed containers. Purity % does not need retesting and moisture content should be retested only if there is reason to believe that leaks have developed in sealed containers.
Special measures have been suggested for recurrent testing of agricultural seed in storage for long-term genetic conservation (Ellis et al. 1980). The authors suggest that, in view of the high value of the stored germ plasm and the need to avoid unnecessary wastage of it in testing, a sequential sampling system may be more economic of material than the standard ISTA method of 4 × 100 replicates. The objective is to detect loss of viability in the early stages of ageing, i.e. as soon as it falls to below 80–90% of the initial rate and to initiate rejuvenation by growing out the seed to produce a new generation. The proposed method would be equally suitable for conservation of forest genetic resources although, because of the much longer generation cycle in trees, conservation as growing plants will be more important than in agricultural crops, as compared with conservation as seed.
Special Considerations for Recalcitrant Seeds of Tropical Rainforests
Many of the tests prescribed in this chapter depend for their usefulness on the ability to keep the bulk of the seed alive during the period while the sample is being tested. Seeds of most species in tropical rainforests are recalcitrant and lose viability at such a rapid rate that any certificate of quality is already obsolete at the time it is issued. In normal practice all recalcitrant seeds are sown in a nursery as soon as possible after collection (Ng 1983).
For purposes of documentation, a germination record is usually maintained, based on a random sample of the seeds being sown. This sample (conveniently 50–100 seeds) is sown separately from the rest, in an enclosure protected by wire mesh, to keep out birds, rats and other pests. The medium (usually soil) should be the same as that used in germinating the bulk of the seeds.
Chapter 9 SEED TESTING (Contd.) Combining purity and Germination Tests Purity tests of most commercial seed lots of Eucalyptus are not made because it is difficult or impossible to