Photoperiod and Temperature Interactions in Growth and Flowering of Strawberry

Growth and flowering of strawberry cultivars were studied in controlled environments. Early cultivars adapted to marginal growing areas in Scandinavia initiated flower buds in all photoperiods including continuous light at temperatures of 12 and 18°C. At 24°C they remained vegetative in photoperiods above 14 or 16 h. The later cultivars ‘Senga Sengana’ and ‘Abundance’ did not initiate flower buds in 24-h photoperiods at any of these temperatures. Their critical photoperiod changed from above 16 h at 12°C to about 14 and 13 h at 18 and 24°C, respectively. It is concluded that at high latitudes temperature is as important as photoperiod in controlling flowering in the strawberry. Stolon formation, petiole elongation, and leaf area growth were stimulated by high temperature and long days, usually with optima at 16 h and 18°C for petiole elongation and 16 h and 24°C for stolon formation. Although growth and flowering responses in general were opposite, the results indicate that they are to some extent independent. The photoperiodic growth responses were mainly of morphogenetic nature. Dry weight of stem and leaves was little influenced by photoperiod when the irradiance was kept constant.     

Direct and indirect effects of episodic frost on plant growth and reproduction in subalpine wildflowers

Frost is an important episodic event that damages plant tissues through the formation of ice crystals at or below freezing temperatures. In montane regions, where climate change is expected to cause earlier snow melt but may not change the last frost‐free day of the year, plants that bud earlier might be directly impacted by frost through damage to flower buds and reproductive structures. However, the indirect effects of frost mediated through changes in plant–pollinator interactions have rarely been explored. We examined the direct and pollinator‐mediated indirect effects of frost on three wildflower species in southwestern Colorado, USA, Delphinium barbeyi (Ranunculaceae), Erigeron speciosus (Asteraceae), and Polemonium foliosissimum (Polemoniaceae), by simulating moderate (?1 to ?5°C) frost events in early spring in plants in situ. Subsequently, we measured plant growth, and upon flowering measured flower morphology and phenology. Throughout the flowering season, we monitored pollinator visitation and collected seeds to measure plant reproduction. We found that frost had species‐specific direct and indirect effects. Frost had direct effects on two of the three species. Frost significantly reduced flower size, total flowers produced, and seed production of Erigeron. Furthermore, frost reduced aboveground plant survival and seed production for Polemonium. However, we found no direct effects of frost on Delphinium. When we considered the indirect impacts of frost mediated through changes in pollinator visitation, one species, Erigeron, incurred indirect, negative effects of frost on plant reproduction through changes in floral traits and pollinator visitation, along with direct effects. Overall, we found that flowering plants exhibited species‐specific direct and pollinator‐mediated indirect responses to frost, thus suggesting that frost may play an important role in affecting plant communities under climate change.     

Natural variation in the temperature range permissive for vernalization in accessions of Arabidopsis thaliana

Vernalization is an acceleration of flowering in response to chilling, and is normally studied in the laboratory at near‐freezing (2–4 °C) temperatures. Many vernalization‐requiring species, such as Arabidopsis thaliana, are found in a range of habitats with varying winter temperatures. Natural variation in the temperature range that elicits a vernalization response in Arabidopsis has not been fully explored. We characterized the effect of intermediate temperatures (7–19 °C) on 15 accessions and the well‐studied reference line Col‐FRI. Although progressively warmer temperatures are gradually less effective at activating expression of the vernalization‐specific gene VERNALIZATION‐INSENSITIVE 3 (VIN3) and in accelerating flowering, there is substantial natural variation in the upper threshold (T_max) of the flowering‐time response. VIN3 is required for the T_max (13 °C) response of Col‐FRI. Surprisingly, even 16 °C treatment caused induction of VIN3 in six tested lines, despite the ineffectiveness of this temperature in accelerating flowering for two of them. Finally, we present evidence that mild acceleration of flowering by 19 °C exposure may counterbalance the flowering time delay caused by non‐inductive photoperiods in at least one accession, creating an appearance of photoperiod insensitivity.     

秦岭岩白菜的传粉生物学特性与繁育系统

对珍稀濒危植物秦岭岩白菜(Bergenia scopulosa T.P.Wang)的开花特性、传粉适应及繁育系统进行了分析研究。结果表明:(1)秦岭岩白菜为蝎尾状聚伞花序,具(29±10)朵单花,单花期约15d,遇低温雨雪天气花冠闭合,可延长3~5d,花序花期约30d,种群花期近4个月。(2)花粉活力在花药开裂后的12h内最高(约90%),维持单花平均花粉活力在30%以上约6d;柱头在第1~4天内保持很强的可授性,维持可授性的时间约为9d。(3)秦岭岩白菜主要有效传粉昆虫为中华蜜蜂,平均访花频率为6.5朵/min,单花停留时间为(11.0±4.8)s。(4)秦岭岩白菜的花粉胚珠比(P/O)为589.8,杂交指数(OCI)为3;人工授粉实验显示,秦岭岩白菜不存在无融合生殖,自交亲和,主动自交罕见,生殖成功主要依赖传粉者。研究认为,秦岭岩白菜是兼性异交的繁育系统,胚珠受精过程中可能存在自交衰退。     

Effect of high air and soil temperature on dry matter production,pod yield and yield components of groundnut

Groundnuts (Arachis hypogaea L.) grown in the semi-arid tropics are commonly exposed to air and soil temperatures above 35 °C during the reproductive period causing significant yield losses. The objectives of this study were to determine: (i) whether effects of high air and/or high soil temperature in two contrasting cultivars were similar; (ii) the effects of the timing of imposition of high air and soil temperature; (iii) the effects of high air, high soil and both stresses combined on yield and yield components; and (iv) whether the effects of high air and high soil temperature were additive or multiplicative. Plants were grown at optimum and ambient soil temperature from planting until start of podding at 45 d after planting (DAP) in Experiment 1, and until start of flowering at 28 DAP in Experiment 2. Thereafter, plants of each cultivar were exposed to a factorial combination of two air temperatures (optimum: 28°/22 °C and high: 38°/22 °C) and two soil temperatures (ambient: 26°/24 °C and high: 38°/30 °C) until final harvest at 90 DAP. The effects of high air and high soil temperatures imposed from start of flowering or podding were similar. Exposure to high air and/or high soil temperature significantly reduced total dry matter production, partitioning of dry matter to pods, and pod yields in both the cultivars. High air temperature had no significant effect on total flower production but significantly reduced the proportion of flowers setting pegs (fruit-set) and hence fruit numbers. In contrast, high soil temperature significantly reduced flower production, the proportion of pegs forming pods and 100 seed weight. The effects of high air and soil temperature were mostly additive and without interaction. This revised version was published online in June 2006 with corrections to the Cover Date.     

Honeybees and the nectar of Echium plantagineum L. in southeastern Australia

An account is given of the flower of Echium plantagineum in south-eastern Australia, including stages and timing of flowering, behaviour of raindrops in the flower and aspects of floral microclimate. The concentration of nectar solutes varied with time and site, with means varying from 2 to 62% (as g sucrose/100 g solution). There was a significant negative correlation between nectar solute concentration and ambient relative humidity: the drier the air, the more concentrated the nectar. Rates of nectar secretion per flower varied with the bagging method, with long-term bagging reducing net secretion rates, possibly because of re-absorption. Rates varied with time, day and site, with a temporal pattern of change suggesting a link between rates of photosynthesis and secretion. Maximum nectar secretion rates in short-term bagging experiments were ca. 300 μg sugar/flower/hr (equivalent to > 2 mglflower/24 hr). Secretion rate was correlated with flower density. As flower density increased, secretion rate per flower decreased; rate of sugar production per unit area increased relatively more slowly than flower density. E. plantagineum could produce > 500 mg sugar/m²/day. Honeybees foraged on E. plantagineum only at ambient air temperatures above ca. 17°C unless irradiance exceeded ca. 750 W m^-2. Foragers collected nectar or pollen alone, or both, with the type of visit significantly correlated with nectar solute concentration. Below 35% (as g sucrose/100 g solution) most bees took pollen only; above 40%, most took nectar. Mean standing crop of nectar was generally < 100 μg/flower when most bees were taking nectar, but could exceed 1000 μg/flower when bees were absent or foraging mainly for pollen. Honeybees did not always remove all nectar from flowers they probed. Reabsorption of residual nectar may augment the following day's secretion.     

Upper thermal limits of cardiac function for Arctic cod Boreogadus saida,a key food web fish species in the Arctic Ocean

The objective of this study was to determine the upper thermal limits of Arctic cod Boreogadus saida by measuring the response of maximum heart rate (f_Hmax) to acute warming. One set of fish were tested in a field laboratory in Cambridge Bay (CB), Nunavut (north of the Arctic Circle), and a second set were tested after air transport to and 6 month temperature acclimation at the Vancouver Aquarium (VA) laboratory. In both sets of tests, with B. saida acclimated to 0° C, f_Hmax increased during acute warming up to temperatures considerably higher than the acclimation temperature and the near‐freezing Arctic temperatures in which they are routinely found. Indeed, f_Hmax increased steadily between 0·5 and 5·5° C, with no significant difference between the CB and VA tests (P > 0·05) and with an overall mean ± s.e. Q₁₀ of 2·4 ± 0·5. The first Arrhenius breakpoint temperature (T_AB) for f_Hmax was also statistically indistinguishable for the two sets of tests (mean ± s.e. 3·2 ± 0·3 and 3·6 ± 0·3° C), suggesting that the temperature optimum for B. saida could be reliably measured after live transport to a more southerly laboratory location. Continued warming above 5·5° C revealed a large variability among individuals in the upper thermal limits that triggered cardiac arrhythmia (T_arr), ranging from 10·2 to 15·2° C with mean ± s.e. 12·4 ± 0·4° C (n = 11) for the field study. A difference did exist between the CB and VA breakpoint temperatures when the Q₁₀ value decreased below 2 (the Q₁₀ breakpoint temperature; T_QB) at 8·0 and 5·5° C, respectively. These results suggest that factors, other than thermal tolerance and associated cardiac performance, may influence the realized distribution of B. saida within the Arctic Circle.     

Effects of holding temperature and handling stress on the upper thermal tolerance of threadfin shad Dorosoma petenense

The critical thermal maxima (T_MAX) of threadfin shad Dorosoma petenense exposed to standardized stress (30 s handling in a dip‐net), simulating stressors endured during fish loading before transport, were measured over a range of holding temperatures (15, 20 and 25° C). Dorosoma petenense T_MAX showed a significant thermal effect, displaying mean ±s.d . critical thermal maxima of 26·5 ± 1·6, 30·9 ± 1·2 and 33·3 ± 1·4° C, when tested at temperatures of 15, 20 and 25° C, respectively. Dorosoma petenense T_MAX levels were also affected by stress, with handled fish showing significantly lower values than control fish exposed to 15 (mean ±s.d . T_MAX = 25·6 ± 2·0° C), 20 (27·6 ± 2·8° C) and 25° C (32·0 ± 2·6° C). In addition to providing basic information on D. petenense thermal tolerance, experimental results suggest that fishery managers should consider the whole suite of potential stressors, such as air exposure during handling and fish loading, when developing management criteria.     

Time of sowing and temperature effects on the flowering of Stylosanthes guianensis

Seedlings of Stylosanthes guianensis var. guianensis cv. Cook and of two selections of S. guianensis var. pauciflora (CIAT 1280 and CIAT 1062) were grown at day/night temperatures of 20°/25°, 30°/25°, and 35°/30°C in a naturally-lit glasshouse at latitude 27°30'S. Sowings were made in decreasing daylength at 30-day intervals from 22 January to 21 May. Cv. Cook and the CIAT 1280 selection did not flower fully if sown after 22 January and the CIAT 1062 selection did not flower if sown after 22 March. This is interpreted as a long-short day flowering response. Usually, flowers were initiated earlier and at a lower node at 25?/20°C than at the warmer temperatures. At 25?/20°C the first flowers to appear were produced predominantly at the terminal apex of the main stem in cv. Cook and the CIAT 1062 selection, but not in the CIAT 1280 selection. At the two warmer temperatures first flowers were more commonly produced at the terminal apex of primary, secondary and tertiary branches. There were more inflorescences per plant on earlier than later sown plants when measured 21 days from appearance of the first flower and the most inflorescences were produced by cv. Cook at 25?/20°C, by selection CIAT 1062 at 30°/25°C, and by CIAT 1280 at 35°/30°C.     

INORGANIC CARBON REPLETION DISRUPTS PHOTOSYNTHETIC ACCLIMATION TO LOW TEMPERATURE IN THE CYANOBACTERIUM SYNECHOCOCCUS ELONGATUS1

Acclimation of cyanobacteria to ambient fluctuations in inorganic carbon (Ci) and temperature requires reorganization of the major protein complexes involved in photosynthesis. We grew cultures of the picoplanktonic cyanobacterium Synechococcus elongatus Naegeli across most of its range of tolerable temperatures from 23 to 35°C at both low (<0.1 mM) and high Ci (approximately 4 mM). Over that range of temperatures, the chl‐based doubling time did not differ between low and high Ci grown cells but did increase with decreasing temperature. Cells grown at 23°C high Ci showed an elongated morphology, which was not present in 23°C low Ci cells nor at 35°C high and low Ci. Furthermore, 23°C high Ci cells showed premature senescence and death compared with all other treatments. Phycocyanin per cell was greater in high Ci grown cells at all temperatures but showed a characteristic decrease with decreasing temperature. Functional PSII determination showed that 23°C high Ci cells had 1.5 × 10⁵ PSII·cell^–1 compared with only 6.9 × 10⁴ PSII·cell^–1 for 23°C low Ci. The 35°C high and low Ci cells had 7.7 × 10⁴ and 6.4 × 10⁴ PSII·cell^–1, respectively. These data were supported by immunoblot determinations of PsbA content·cell^–1. As a result of their high PSII·cell^–1, 23°C high Ci cells generated more reductant from PSII than could be accommodated by downstream assimilative metabolism, resulting in early senescence and death of 23°C high Ci cells, probably as a result of the generation of reactive byproducts of electron transport.     

Plasticity of flower longevity in Corydalis ambigua

We investigated the longevity of individual flowers of Corydalis ambigua Cham. et Schlecht. during different periods of pollinator activity and at different temperatures. To measure potential (unpollinated) flower longevity of C. ambigua, this study was conducted at forest islands where pollinator visits were scarce. The longevity of individual flowers of C. ambigua indicated high plasticity. The longevity of unpollinated flowers in natural pollination ranged from 2 to 25 days and continuously decreased with the date of flower opening. The temperature increased as the flowering season progressed. Furthermore, the greenhouse transplanting experiment showed that higher temperatures shorten the life span of flowers. The longevity of pollinated flowers subjected to hand pollination of newly opened flowers was shorter than that of unpollinated flowers in natural pollination regardless of the date of flower opening. These results showed that not only high temperature but also pollination shortens flower longevity. We discuss the role of plasticity in flower longevity for C. ambigua in relation to pollination success and reduction in the maintenance cost of the flowers.     

Onion pollination by blowflies and honeybees in large cages

Three experiments to investigate the effect of pollination by blowflies (Calliphora and Lucilia spp.) and honeybees (Apis mellifera) on seed yield and crossing level were made using a mixture of plants from two open-pollinated cultivars of onions (Allium cepa) in breeders' cages. No consistent differences were found between pollinators. In two experiments, fly pollination gave significantly higher yields than bee pollination but in the third, bee pollination gave slightly more seed. Crossing between cultivars, assessed by progeny testing on one cultivar, varied between 22-7 and 55-9%. Differences in crossing level attributable to the pollinators were not consistent and were not or only just statistically significant, but there were significant and substantial differences between the experiments themselves. Where more umbels were produced by the red-bulbed cultivar than by the yellow, higher crossing levels were found in the yellow cultivar. The highest crossing levels were found in the only experiment where insects were not introduced until peak flowering time, but where seed yield was comparatively low. Crossing levels were lowest where the umbel numbers were approximately equal. Individual umbels studied showed that while seed set was usually heaviest at and just before the mid-flowering date, this period could correspond with the lowest levels of crossing during the flowering period, particularly if flowering of the two cultivars was not completely synchronous. In field plots, approximately 75% of crossed seeds sown survived to give harvestable bulbs, but fewer than 50% of selfed seeds did so. In an experiment in which crossing levels from different pollinators were similar but survival levels differed significantly, it was deduced that bees performed more crossing within a cultivar than flies.     

Influence of Temperature, Wetness Duration, and Leaf Type on the Quantification of Monocyclic Parameters of Bean Rust

Monocyclic parameters of bean rust (Uromyces phaseoli var. typical) were quantified in growth chambers, on rwo bean cultivars for three temperatures (17, 21, and 25 °C), two types of leaves (unifoliolate and trifoiiolate leaves), and nine leaf wetness periods (0, 4, 7, 10, 13, 16, 19, 22, and 25 hrs). The expression of disease was greatly influenced by past-inoculation temperatures. The incubation and latent periods were shortest at 21 °C for both cultivars and leaf types. For both cultivars, trifoiiolate leaves were more susceptible than unifoliolate leaves. A wetness period of at least four hours was required for disease to occur. The maximum disease efficiency for both cultivars occurred with 22 hrs of leaf wetness at 17 °C. The disease efficiencies for temperatures of 17–29 °C and leaf wetness periods of 0–25 hrs were adequately described by a response-surface model. Because of the great influence of temperature and leaf wetness on infection, bean rust is unlikely to occur at high temperatures (> 25°C) and short leaf wetness periods (< 7 hrs).     

Effect of Diurnally Fluctuating vs. Constant Temperatures on Flower Induction and Sex Expression in the Olive (Olea europaea)

Olive trees must be exposed to a period of winter chilling temperatures in order to form inflorescences the following spring. The effects of diurnally fluctuating and constant temperatures on flower induction and sex expression in the olive were compared under controlled environment conditions. The effect on flowering of diurnally fluctuating temperatures depends upon the length of time at the higher temperatures. While daily exposure to the high temperatures (21° to 26°C) for a short period (four hours) intensified the effectiveness of the low temperatures (7° to 12.5°C), when the high temperature duration was 12 hours it counteracted the low temperature action. Possibly, daily low temperatures act to stimulate reactions leading to floral hormone synthesis, while daily short exposures to high temperatures act to maintain metabolic activity, promote energy-yielding reactions, and possibly stimulate cell-division activity. In the olive, an intermediate constant temperature (12.5°C) favors both types of reactions and induces flowering; however, in this case, the pistils fail to develop. The olive has very specific temperature requirements for flowering and neither the mean temperature nor the accumulated number of hours below a given value, e.g. 7°C, adequately characterizes these requirements.     

The influence of irradiance,photoperiod and temperature on the growth kinetics of three planktonic diatoms

The influence of irradiance, photoperiod and temperature was determined for the growth kinetics of the diatoms Aulacoseira subarctica, Stephanodiscus astraea and Stephanodiscus hantzschii and the results compared with those of cyanobacteria. Irradiance and photoperiod relationships were qualitatively similar to those for cyanobacteria in that: (1) growth rate (K) was proportionally greater under short photoperiods, with ratios of K under continuous light to K under 3:21 light:dark (LD) cycles of 1·50, 1·80 and 2·96 for A. subarctica, S. astraea and S. hantzschii respectively; (2) at subsaturating irradiances, K was proportional to irradiance and independent of temperature with a negligible predicted maintenance growth rate requirement. Apparent growth efficiencies (GE) at subsaturating irradiances were 0·26±0·03, 0·42±0·03 and 0·50±0·03 divisions mol^-1m² for A. subarctica, S. astraea and S. hantzschii with the values for Stephanodiscus species comparable to values for Oscillatoria species. Under a 3:21 LD cycle at 4 °C, light-saturated growth rates were 0·066±0·004, 0·197±0·033 and 0·285±0·018 divisions day^-1 for A. subarctica, S. astraea and S. hantzschii. S. hantzschii growth rate at 4 °C exceeded maximum Oscillatoria growth rates at 23 °C and the S. astraea growth rate at 4 °C was equivalent to O. agardhii growth rate at 20 °C. Temperature increases above 4 °C gave Q₁₀ values between 4 °C and 12 °C of 3·68, 2·39 and 1·92 for A. subarctica, S. astraea and S. hantzschii, but higher temperatures resulted in minor increases in K. S. astraea growth rate peaked at 16 °C, declining sharply at higher temperatures. February to March in situ growth rates in Lough Neagh, mean temperature 4·3 °C, showed that the A. subarctica in situ K of 0·058 divisions day^-1 was close to the laboratory K at 4 °C, but that S. astraea in situ K of 0·101 divisions day^-1 was lower than the laboratory K at 4 °C.     

Heart rate as an indicator of metabolic rate and activity in adult Atlantic salmon, Salmo salar

Telemetered heart rate (f_H) was examined as an indicator of activity and oxygen consumption rate (VO₂) in adult, cultivated, Atlantic salmon, Salmo salar L. Heart rate was measured during sustained swimming in a flume for six fish at 10° C [mean weight, 1114 g; mean fork length (f. l.), 50·6 cm] and seven fish at 15° C (mean weight, 1119 g; mean f. l., 50·7 cm) at speeds of up to 2·2 body lengths/s. Semi–logarithmic relationships between heart rate and swimming speed were obtained at both temperatures. Spontaneously swimming fish in still water exhibited characteristic heart rate increases associated with activity. Heart rate and Vo₂ were monitored simultaneously in a 575–1 circular respirometer for six fish (three male, three female) at 4° C (mean weight, 1804 g; mean F. L., 62· cm) and six fish (three male, three female) at 10° C (mean weight, 2045 g; mean f. l., 63·2 cm) during spontaneous but unquantified activity. Linear regressions were obtained by transforming data for both f_H and Vo₂ to log values. At each temperature, slopes of the regressions between f_H and Vo₂ for individual fishes were not significantly different, but in some cases elevations were. All differences in elevation were between male and female fish. There were no significant differences in regression slope or elevation for fish of the same sex at the two temperatures and so regressions were calculated for the sexes, pooling data from 4 and 10° C. There was no significant difference in the mean ± S. D. Vo₂ between the sexes at 4° C (male, 66·0 ± 59·6 mgO₂ kg^?1 h^?1; female, 88·0 ± 60·1 mgO₂ kg^?1 h^?1) or 10° C (male, 166·2 ± 115·4 mgO₂ kg^?1 h^?1; female, 169·2 ± 111–1 mgO₂ kg^?1h^?1). Resting Vo₂ (x?± s. d.) at 4°C was 36·7 ± 8.4 mgO₂ kg^?1 h^?1, and 10° C was 72·8 ± 11·9 mgO₂ kg^?1 h^?1. Maximum Vo₂ (x?± S. D.) at 4° C was 250·6 ± 40·2 mgO₂ kg^?1 h^?1, and at 10° C was 423·6 ± 25·2 mgO₂ kg^?1 h^?1. Heart rate appears to be a useful indicator of metabolic rate over the temperature range examined, for the cultivated fish studied, but it is possible that the relationship for wild fish may differ.     

Upper thermal tolerance of closely related Danio species

The main finding of this study was that measuring maximum heart rate during incremental warming was an effective tool to estimate upper thermal limits in three small cyprinid Danio species, which differed significantly. Arrhenius breakpoint temperature for maximum heart rate, purportedly an index of optimum temperature, was 21·2 ± 0·4, 20·1 ± 0·4 and 18·9 ± 0·8° C (mean ± s.e .) for zebrafish Danio rerio, pearl danio Danio albolineatus and glowlight danio Danio choprae, respectively. The temperature where cardiac arrhythmias were first induced during warming (T_arr) was 36·6 ± 0·7, 36·9 ± 0·8 and 33·2 ± 0·8° C (mean ± s.e .) and critical thermal maximum (T_Cm) was 39·9 ± 0·1, 38·9 ± 0·1 and 37·2 ± 0·1° C (mean ± s.e .) for D. rerio, D. albolineatus and D. choprae, respectively. The finding that T_arr was consistently 3–4° C lower than T_Cm suggests that collapse of the cardiac life support system may be a critical trigger for upper temperature tolerance. The upper thermal limits established here, which correlate well with a broad natural environmental temperature range for D. rerio and a narrow one for D. choprae, suggest that upper thermal tolerance may be a genetic trait even among closely related species acclimated to common temperatures.     

Studies on the synthesis,characterization, human serum albumin binding and biological activity of single chain surfactant–cobalt(III) complexes

The interaction of surfactant–cobalt(III) complexes [Co(bpy)(dien)TA](ClO₄)₃ · 3H₂O (1) and [Co(dien)(phen)TA](ClO₄)₃ · 4H₂O (2), where bpy = 2,2′‐bipyridine, dien = diethylenetriamine, phen = 1,10‐phenanthroline and TA = tetradecylamine with human serum albumin (HSA) under physiological conditions was analyzed using steady state, synchronous, 3D fluorescence, UV/visabsorption and circular dichroism spectroscopic techniques. The results show that these complexes cause the fluorescence quenching of HSA through a static mechanism. The binding constant (K_b) and number of binding‐sites (n) were obtained at different temperatures. The corresponding thermodynamic parameters (?G°, ?H° and ?S°) and E_a were also obtained. According to Förster's non‐radiation energy transfer theory, the binding distance (r) between the complexes and HSA were calculated. The results of synchronous and 3D fluorescence spectroscopy indicate that the binding process has changed considerably the polarity around the fluorophores, along with changes in the conformation of the protein. The antimicrobial and anticancer activities of the complexes were tested and the results show that the complexes have good activities against pathogenic microorganisms and cancer cells. Copyright © 2015 John Wiley & Sons, Ltd.