SUMMARYOf various inorganic ions tested for their ability to stimulate hatching of eggs of the cyst nematodes of cereals (Heterodera avenae Woll), carrot (H. carotae Jones), cabbage (H. cruciferae Franklin), soybean (H. glycines Ichinohe), pea (H. goettingiana Liebs.), potato (H. rostochiensis Woll.), beet (H. schachtii Schm.), tobacco (H. tabacum Lownsbery & Lownsbery) and clover (H. trifolii Goffart), some were active. Zn2+ hatched many eggs of seven species and some of H. goettingiana, but inhibited hatch of H. avenae to below that in water. Zinc salts are the first recorded very active hatching stimulants for H. glycines in vitro. Many other metal ions stimulated hatching of H. schachtii eggs to varying extents; these also hatched some but not all of the other species. Vanadate ions were particularly effective for H. rostochiensis, more so than Zn2+. No ion increased the hatch of H. avenae to above that in water. The most active ions were not those most abundant in soil.The behaviour of different ions with different species did not suggest any obvious affinities between species, but the differences between the hatching of H. tabacum and H. rostochiensis add weight to the view that, despite morphological similarities and overlapping host ranges, they are distinct species rather than pathotypes of a single species.Ions and other hatching agents may be absorbed by materials within the egg or larva and alter the structure and function of these materials. The lack of correlation between the hatching of H. schachtii by ions and the known stability sequences of various biological metal‐binding systems suggests that there may be several sites of action that differ in their response.

Investigations of nematode hatching have concentrated on the parasitic forms, especially on synchronization between host and parasite life-cycles which, in some species, is so close that the parasite is dependent on the host for the hatching stimulus. Research into nematode hatching reflects the artificial separations created throughout nematology by defining research groups and their activities in terms of the host; consequently, useful comparisons between hatching of plant and animal parasitic nematodes have been few. With the increasing use by geneticists of nematodes as model animals and the interest in them by neuro-physiologists, molecular biologists and others, we hope that such distinctions will be lessened.

SUMMARYOf 444 compounds tested for their ability to stimulate eggs of Heterodera rostochiensis to hatch, forty‐five did so to varying extents. Many compounds that hatched H. schachtii Schm. eggs did not hatch H. rostochiensis eggs. The most effective compounds with H. rostochiensis were picrolonic acid, anhydro‐tetronic acid and vanadates. Tests with analogues of picrolonic and anhydro‐tetronic acids suggested some structures that may be concerned in hatching H. rostochiensis and H. schachtii. The simple analogues hatched the eggs of H. schachtii but not those of H. rostochiensis. Suitably placed polarisable atoms seemed to be an essential feature. Picrolonic acid contains pairs of polarizable atoms, about 4 and 6·7 Å apart, that may respectively be associated with the hatching of H. schachtii and H. rostochiensis. Other features of the more active hatching agents were a cis and co‐planar arrangement of the two polarizable atoms with respect to the rest of the molecule. The function of hatching agents is discussed.

1. Eggs of the potato cyst-nematode (Heterodera rostochiensis Woll.) were isolated by sieving a suspension of crushed cysts. Eggs were broken open by ultrasonic vibration and the egg shells separated from the released larvae by centrifuging in a potassium tartrate density gradient. About 1 mg. of dried egg shells was obtained from 1000 cysts. 2. The major constituent of the egg shells was protein (59%, calculated from nitrogen content). About 80% of the egg shells went into solution on acid hydrolysis. Of the 18 amino acids determined with the Technicon Auto-Analyser, proline was most abundant and, with aspartic acid, glycine and serine, made up about 64% by weight of the total amino acids. The small amounts of aromatic and sulphur-containing amino acids, and the presence of hydroxy-proline, indicate a collagen-like protein. 3. The egg shells gave a positive van Wisselingh colour test for chitin, and glucosamine was detected in their acid hydrolysate by chromatography. The glucosamine content of the egg shells, determined by the Elson-Morgan colorimetric method, was 7%, corresponding to about 9% chitin. 4. Dried egg shells contained about 7% of lipid, 6% of carbohydrate and 3% of ash. Polyphenols (3% by weight of the egg shells) were detected in the acid hydrolysates. 5. Neither the collagen nor the chitin showed evidence of crystallinity when examined by X-ray diffraction.

1. Cyst walls of the potato cyst-nematode (Heterodera rostochiensis Woll.) were isolated by sieving a suspension of crushed cysts. About 12mg. of dried cyst walls was obtained from 1000 cysts. 2. The cyst walls contained mainly protein (72%, calculated from nitrogen content). On acid hydrolysis about 77% of the cyst wall went into solution. Of 19 amino acids present, proline, glycine, and alanine were the most abundant, and made up about 50% by weight of the total amino acids. The amino acid composition suggested that collagen-like proteins predominated in the cyst wall and larval cuticle. 3. A small amount of glucosamine (1.5%) was present in the hydrolysates, but chitin was not detected in the cyst walls. 4. Other components of the cyst walls were lipid (2%), carbohydrate (0.5%) and a small amount of inorganic matter (ash, 5%). Polyphenols (2% by wt. of the cyst walls) occurred in the acid hydrolysates. The dark pigments of the cyst wall were not indole-containing melanins.