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The content of indole-3-acetic (IAA), gibberellic (GA3), abscisic acids (ABA), and cytokinins—zeatin (Z), zeatin glucoside (ZG), zeatin riboside (ZP), isopentenyladenin (iР), and isopentenyladenosine (iРА)—was determined using the method of high-performance liquid chromatography in fern Polystichum aculeatum gametophytes at different stages of morphogenesis in vitro culture. It was shown that, at the stage of spatulate prothallium development, gametophytes contained significant amounts of GA3 and IAA, while the content of ABA and cytokinins was low. The inactive ZG and active iP were dominant. At the stage of cordiform thallus formation, the level of GA3 increased by 1.6, IAA by 2.4, and ABA by 1.7 times. The content of inactive iPA increased twice, significantly increased the level of active ZR and iP. At the development stage of sporophyte on the surface of gametophyte thallus, the levels of IAA, ABA, and GA3 decreased. The accumulation of inactive ZG and decrease in the content of active zeatin and zeatin riboside were documented. At all stages of gametophytes’ morphogenesis, GA3 was dominant, and its highest content was detected during the development of archegonia and antheridia. The pattern of gibberellic acid and zeatin riboside accumulation has shown the key role of these hormones in the regulation of growth processes and the development of reproductive structures of P. aculeatum gametophytes.

The effects of exogenous phytohormones–gibberellic acid (GA3) and benzyl-aminopurine (BAP)–on the spore germination and morphogenesis of Polystichum aculeatum (L.) Roth gametophyte in vitro culture were studied. In the control, four stages of gametophyte morphogenesis were determined and their periods were established. Spore germination and protonema formation of P. aculeatum occurred according to the Vittaria-type and prothalium development according to the Aspidium-type. The spore germination percentage depended on the storage time duration. It was found that 80–95% of freshly collected spores germinated. Spore viability was within the range of 68–95% after 4–6-month storage under lab conditions and did not exceed 20% after 1.5 year of the storage period. High concentrations of exogenous GA3 (10–5 and 10–6 M) and BAP (10–5 M) significantly inhibited spore germination, whereas low concentrations (GA3 10–7–10–8 M) had an insignificant stimulating effect or did not affect germination at all (BAP 10–6, 10–7, 10–8 M). All concentrations of exogenous BAP were demonstrated to inhibit the development of P. aculeatum gametophyte at the protonema stage, which might be due to the removal of apical dominance. The inhibiting effect directly depended on BAP concentrations. The formation of abnormal thalli of the P. aculeatum gametophyte in the response to exogenous GA3 treatments occurred as a result of impairment of cell growth by elongation. A direct interrelationship between GA3 concentrations and level of morphological abnormalities and grade of thalli underdevelopment was demonstrated.