PHOTOSYNTHESIS IN PROTOPLASTS OF MACROCYSTIS PYRIFERA (PHAEOPHYTA)1

Photosynthetic rates measured in protoplasts isolated from the broivn alga Macrocystis pyrifera (L.) Ag. were compared to those for intact tissue. Both ¹⁴C incorporation and O₂ evolution gave similar rates of light-saturated protoplast photosynthesis (approximately 0.4 mmol-g chl a^?1· min^?1). Light saturated photosynthetic rates (P_max) and light harvesting efficiencies (α) of protoplasts were approximately 40% those of intact tissue. In contrast, protoplasts had a greater substrate affinity for photosynthetic HCO₃ uptake (lower K_0.5) than intact tissue (0.87 and 4.1 mMolar, respectively), presumably because of a reduction in the thickness of the unstirred boundary layer in the absence of the cell wall. Overall, the data suggest that protoplasts isolated from Macrocystis pyrifera are of valur in the study of photosynthesis. However, experiments with intact tissue are necessary as controls to aid interpretation of protoplast data.     

The response of mammals to forest fire and timber harvest in the North American boreal forest

1. This paper reviews and compares the effects of forest fire and timber harvest on mammalian abundance and diversity, throughout successional time in the boreal forest of North America. 2. Temporal trends in mammal abundance and diversity are generally similar for both harvested and burned stands, with some differences occurring in the initiation stage (0–10 years post disturbance). 3. Small mammals and ungulates are most abundant immediately post disturbance, and decrease as stands age. Lynxes and hares utilize mid-successional stands, but are rare in young and old stands. Bats, arboreal sciurids and mustelids increase in abundance with stand age, and are most abundant in old growth. 4. Substantial gaps in the data exist for carnivores; the response of these species to fire and harvest requires research, as predator–prey interactions can affect mammal community structure in both early and late successional stages. 5. The lack of explicit treatment of in-stand forest structure post disturbance, in the reviewed literature made comparisons difficult. Where forest structure was considered, the presence of downed woody material, live residual trees and standing dead wood were shown to facilitate convergence of mammal communities to a pre-disturbance state for both disturbance types. 6. Mammalian assemblages differed considerably between successional stages, emphasizing the importance of maintaining stands of each successional stage on the landscape when implementing forest management strategies.     

Energization and ultrastructural pattern of thylakoids formed under periodic illumination followed by continuous light

Bean leaves grown under periodic illumination (56 cycles of 2 min light and 98 min darkness) were subsequently exposed to continuous illumination, and in connection with granum formation and accumulation of the light-harvesting pigment-protein complex thermoluminescence and light-induced shrinkage of thylakoid membranes were studied. Juvenile chloroplasts with large double sheets of thylakoids obtained under periodic light exhibited low temperature spectra of polarized fluorescence yielding fluorescence polarization (FP) values < 1 at 695 nm, characteristic for pheophytin emission. In the course of maturation under continuous light when normal grana appeared and the chlorophyll a/b light-harvesting photosystem II complex was incorporated into the membrane, at 695 nm the relative intensity of fluorescence dropped and FP changed to a value of > 1, suggesting an overlap between the emission of pheophytin and that of the chlorophyll a/b light-harvesting photosystem II complex. Thermoluminescence glow curves recorded with juvenile thylakoids displayed a relatively high proportion of emission at low temperatures (around -10°C) while with mature chloroplasts, more thermoluminescence originated from energetically deeper traps (discharged around 28°C). This means that during thylakoid development the capacity of the membrane to stabilize the separated charges increases, which might be favourable for the ultimate conservation of energy. The more extensive energization of mature thylakoids was also indicated by a light-induced decrease in the thickness of the membranes upon illumination; a change which could not be detected in juvenile thylakoids.Abbreviations EDTA ethylenediamine tetraacetic acid - Hepes 4-(2-hydroxy ethyl)-1-piperazine ethane sulfonic acid Dedicated to Prof. L.N.M. Duysens on the occasion of his retirement.     

The detection,isolation and characterization of a light-harvesting complex which is specifically associated with Photosystem I

10% of the chlorophyll associated with a ‘native’ Photosystem (PS) I complex (110 chlorophylls/P-700) is chlorophyll (Chl) b. The Chl b is associated with a specific PS I antenna complex which we designate as LHC-I (i.e., a light-harvesting complex serving PS I). When the native PS I complex is degraded to the core complex by LHC-I extraction, there is a parallel loss of Chl b, fluorescence at 735 nm, together with 647 and 686 nm circular dichroism spectral properties, as well as a group of polypeptides of 24-19 kDa. In this paper we present a method by which the LHC-I complex can be dissociated from the native PS I. The isolated LHC-I contains significant amounts of Chl b (Chl $\text{a}\text{b ? 3.7}$). The long-wavelength fluorescence at 730 nm and circular dichroism signal at 686 nm observed in native PS I are maintained in this isolated complex. This isolated fraction also contains the low molecular weight polypeptides lost in the preparation of PS I core complex. We conclude that we have isolated the PS I antenna in an intact state and discuss its in vivo function.     

Analysis of the complicated dynamics of some harvesting models

In this paper we will study in a qualitative way discrete single species population models including harvesting. The class of models under consideration is quite general. In fact, we will study models with fixed parameter values. However, the obtained results do have implications for the models if one varies the parameters slightly. The models with so-called Allee-effect, i.e. the population will die out whenever the size of the population is below some threshold, are included in the class of models we studied.Research supported in part by the Netherlands organization for the advancement of pure research (Z.W.O.), a Fulbright grant, and a NSF grant. A part of this paper has been written while H.E.N. was visiting the Institute for Physical Science and Technology, University of Maryland, College Park, USA     

A model for growth of Artemia franciscana cultures based on food ration-dependent gross growth efficiencies

Laboratory cultures of Artemia franciscana grown under batch regimes at constant temperatures (28 °C) and salinity (35 g l^–1), three initial food concentrations (0.1, 0.4 and 1 M cells ml^–1), various daily food rations (0.1–9M Dunaliella tertiolecta cells Artemia ^–1), and different population densities (1–16 ind ml^–1) were used to develop a model of population growth. Growth rates and gross growth efficiencies (K ₁) were largely independent of population densities and initial food concentrations but determined by age and daily amount of food ingested. While maximum growth rates were found with the highest rations, K _{1 max} peaked at rations of 0.5 million cells d^–1 and decreased at feeding levels above this. A contour plot showing the trend relating K ₁ to Artemia size and ingestion rate in combination and was used to model growth in analogous controlled feeding conditions. Computer simulations using this model paralleled published results of final 15-day average individual sizes of Artemia. Optimal results for near constant food utilization are predicted for high initial population densities (100 Artemia nauplii ml ^–1) and daily culls of enough animals to equilibrate food demand with food availability. This strategy could permit a range of Artemia sizes harvested, maximize final individual sizes and retain high total yields (> 1.2 kg dry wt 1^–1). Effects of different culture strategies are discussed.     

Complex formation in plant thylakoid membranes. Competition studies on membrane protein interactions using synthetic peptide fragments

Thylakoid membranes of pea were used to study competition between extra-membrane fragments and their parental membrane-bound proteins. Phosphorylated and unphosphorylated fragments of light harvesting complex II (LHC II) from higher plants were used to compete with LHC II for interactions with itself and with other thylakoid protein complexes. Effects of these peptide fragments of LHC II and of control peptides were followed by 80 K chlorophyll fluorescence spectroscopy of isolated thylakoids. The phosphorylated LHC II fragment competes with membrane-bound phosphoproteins in the phosphatase reaction. The same fragment accelerates the process of dark-to-light adaptation and decreases the rate of the light-to-dark adaptation when these are followed by fluorescence spectroscopy. In contrast, the non-phosphorylated LHC II peptide does not affect the rate of adaptation but produces results consistent with inhibition of formation of a quenching complex. In this quenching complex we propose that LHC II remains inaccessible to the LHC II kinase, explaining an observed decrease in LHC II phosphorylation in the later stages of the time-course of phosphorylation. The most conspicuous protein which is steadily phosphorylated during the time-course of phosphorylation is the 9 kDa (psbH) protein. The participation of the phosphorylated form of psbH in the quenching complex, where it is inaccessible to the phosphatase, may explain its anomalously slow dephosphorylation. The significance of the proposed complex of LHC II with phospho-psbH is discussed.Abbreviations LHC II light harvesting complex II - PS II Photosystem II - PS I Photosystem I     

Diurnal Lhc gene expression is present in many but not all species of the plant kingdom

The diurnal and circadian expression of light-harvesting genes (Lhc) is well documented for many plant species of the Angiospermae division. Here we present the diurnal mRNA levels of species of the Gymnospermae, Pteridophyta, Bryophyta and Phycophyta divisions. Except for four Coniferophytina species, diurnal Lhc mRNA accumulation is detected in fern, moss and algae, supporting the idea that the concept of circadian clock-controlled gene expression is an ancient process. Possible reasons why plants need the circadian clock control mechanism are discussed.Dedicated to Dr H. W. Heldt on the occasion of his 60th birthday.     

Implication of D1 degradation in phosphorylation-induced state transitions

State transitions and lateral migration of phosphorylated mobile-LHC II upon thylakoid unstacking have been reported as being interdependent. However, now the thyakoid unstacking event can be separated from the thyakoid phosphorylation and the associated F730/F685 enhancement by using the serine-type-protease inhibitor benzamidine. Thus, lateral migration appears not be necessary, and it can be shown that LHC II-rich fragments, originating in peripheral granal membranes, can be released by digitonin although in reduced amounts. On the other hand, phosphorylation of thylakoid proteins greatly stimulates the light-induced D1 degradation, which is observed in chloroplasts phosphorylated even at very low light (15 µmol m^–2s^–1). Thylakoid pretreatment with FSBA (the PS II protein-kinase inhibitor) blocks the light-induced and ATP-stimulated D1 degradation, and the F730/F685 ratio increase; this suggests that the dissociation of the PS II unit, resulting from the introduction of repulsive negative charges ( ATP groups) into LHC II and PS II core proteins, leads to D1 degradation. In chloroplast samples transferred to darkness following short-time phosphorylation, the D1 level is recovered. The results suggest that disassembly of PS II and D1 degradation occur parallel to State transitions. The removal of outer phospho-LHC II from PS II and its association with PS I at the periphery of grana may allow D1 degradation and increased light utilization by PS I, while net de novo synthesis of D1, stimulated by ATP, may lead to the assembly of new PS II units which could bind dephosphorylated LHC II in the dark, resulting in increased light utilization by PS II.