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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 56 (1984), S. 502-508 
    ISSN: 1432-1106
    Keywords: Visual system ; Retinopetal cells ; Lateral mesencephalic tegmentum ; Retrograde tracing ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The centrifugal innervation of the retina was reinvestigated in albino and pigmented rats with intraocular injections of horseradish peroxidase (HRP), radioactive wheat germ agglutinin (WGA) and proline. No labeled cells were found in the brains injected with HRP and proline, except some eye muscle motoneurons in one case apparently involving orbital contamination from the injection. In the cases injected with WGA and having a survival time of at least two days cells were labeled in the lateral mesencephalic tegmentum, ventral to the parabigeminal nucleus and in the periaqueductal gray. Both these findings are most likely due to transneuronal anterograde-retrograde transport of the tracer through the superior colliculus. The results yielded no compelling evidence for the existence of a direct retinopetal pathway in the rat, which is in contrast to a recently claimed retinal projection originating from the pretectum. Special attention was paid to the labeling in the lateral mesencephalic tegmentum, an area giving rise to retinal projections in various submammalian species. This finding is discussed with regard to the possibility that also in the rat the lateral tegmentum exerts an early influence on visual input, but at the “higher” collicular level and not at the “original” retinal one.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 56 (1984), S. 509-522 
    ISSN: 1432-1106
    Keywords: Tectal connectivity ; Parabigeminal nucleus ; Isthmic nuclei ; Lateral tegmentum ; Comparative anatomy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Injections of horseradish peroxidase, wheat germ agglutinin and various amino acids into the optic tectum in both the turtle and rat, and into the nucleus isthmi magnocellularis (IsM) in the turtle were used to analyse the connections of the isthmustegmentum complex. The connectivities and the selective retrograde transport properties in certain tectal pathways were taken as a basis to define more accurately isthmus-tegmentum complex subdivisions. There were several main findings. In the turtle the projection from the tectum to the IsM originated in the stratum griseum periventriculare, whereas the projection from the IsM to the tectum terminated in the superficial tectal layers (both projections homolateral). The terminations of the pathway from IsM to tectum were not uniformly distributed throughout the tectal surface; rather, alternating zones of high and low termination density along the lateral dimension were observed. The turtle nucleus isthmi parvocellularis, receiving a few tectal fibers and afferents from the ipsilateral IsM, gave rise to a bilateral tectal projection. Evidence was obtained for a crossed collicular projection to the rat parabigeminal nucleus (Pbg) in addition to the established uncrossed one. GABA was retrogradely transported from the optic tectum to the Pbg in the rat, and to the dorsolateral mesencephalic tegmentum and the IsM in the turtle. After glycine injections into the optic tectum, the dorsomedial peri-parabigeminal tegmentum was retrogradely labeled in the rat, and the IsM in the turtle. An attempt was made to outline the parallelism between the organizations of the isthmustegmentum complexes in the turtle, pigeon and rat. It was concluded that some basic features in the inter-connectivity of the isthmus-tegmentum complex and other parts of the visual system have been preserved in evolution, despite the apparent loss of the isthmoretinal projection in mammals.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: A 13C/12C mass spectrometer was interfaced with a open gas exchange system including four growth chambers to investigate CO2 exchange components of perennial ryegrass (Lolium perenne L.) stands. Chambers were fed with air containing CO2 with known δ13C (δCΟ2−2.6 or −46.8‰). The system did not fractionate C isotopes and no extraneous CO2 leaked into chambers. The on-line 13C discrimination (Δ) of ryegrass stands in light was independent of δCΟ2 when δCΟ2 was constant. The δ of CO2 exchanged by the stands in light (δNd) and darkness (δRn) differed by 0.7‰, suggesting some Δ in dark respiration at the stand-level. However, Δ decreased by ∼ 10‰ when δCΟ2 was switched from −46.8 to −2.5‰, and increased by ∼ 10‰ following a shift from −2.6 to −46.7‰ due to isotopic disequilibria between photosynthetic and respiratory fluxes. Isotopic imbalances were used to assess (non-photorespiratory) respiration in light and the replacement of the respiratory substrate pool(s) by new photosynthate. Respiration was partially inhibited by light, but increased during the light period and decreased in darkness, in association with temperature changes. The labelling kinetics of respiratory CO2 indicated the existence of two major respiratory substrate pools: a fast pool which was exchanged within hours, and a slow pool accounting for ∼ 60% of total respiration and having a mean residence time of 3.6 d.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 23 (2000), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The effect of defoliation on leaf elongation rate (LER) and on the spatial distribution of epidermal cell lengths in the leaf growth zone was studied in vegetative main tillers of perennial ryegrass (Lolium perenne L. cv Modus) grown in a controlled environment. A new material approach was used to analyse the responses of epidermal cell expansion and production during the initial, non-steady growth phase following defoliation. The analysis involved assigning an identity to individual expanding cells, assessing the displacement and estimating the expansion of cells with assigned identity during day 1 and day 2 after defoliation. LER decreased by 34% during the first 2 d after defoliation and did not recover to the pre-defoliation rate within the 14 day regrowth period. Decreased LER on day 1 and day 2 after defoliation was associated with (i) a decrease in the length of the leaf growth zone; (ii) a decrease in the length at which epidermal cells stopped expanding; (iii) a reduced expansion of cells at intermediate growth stages; and (iv) a reduction in cell production (i.e. division) and an associated decrease in the number of expanding cells in the growth zone. However, defoliation had no effect on the expansion of cells located in the proximal part of the growth zone. Reduced LER at 14 d after defoliation was associated with a reduced cell production rate (27% lower than the pre-defoliation rate) and decreased final cell size (− 28%).
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 16 (1993), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The role of fructan metabolism in the assimilate relations of the grain of wheat (Triticum aestivum L.) was investigated by determination of the dry matter and fructan content of grain components at short intervals during grain filling. During the initial phase of rapid expansion, most of the assimilates entering the grain were partitioned to the outer pericarp. A large fraction of these assimilates were used for the synthesis of fructan. Dry matter deposition and fructan synthesis in the outer pericarp ceased at about 5d after anthesis. At the same time, the endosperm and the inner pericarp and testa started to accumulate dry matter at a fast rate. This was also associated with significant fructan synthesis in the latter tissues. The outer pericarp lost about 45% of its former maximum dry weight between 9 and 19 d after anthesis. This loss was due almost entirely to the near complete disappearance of water-soluble carbohydrates, most of which was fructan. The inner pericarp and testa accumulated dry matter until about mid-grain filling. The fructan contents of the inner pericarp and testa and the endosperm decreased slowly towards the end of grain filling. Most of the fructans in the inner pericarp and testa and the endosperm had a low molecular weight, whereas higher molecular weight fructans predominated in the outer pericarp. The embryo did not contain fructan. The presence of low molecular weight fructans in the endosperm cavity at mid-grain filling was confirmed. It is suggested that fructan synthesis is closely linked to growth-related water deposition in the different tissues of the wheat grain and serves to sequester the surplus of imported sucrose.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 24 (2001), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The effect of defoliation on the deposition of carbon (C) and nitrogen (N) and the contribution of reserves and current assimilates to the use of C and N in expanding leaf tissue of severely defoliated perennial ryegrass (Lolium perenne L.) was assessed with a new material element approach. This included 13C/12C-and 15N/14N-steady-state labelling of all post-defoliation assimilated C and N, analysis of tissue expansion and displacement in the growth zone, and investigation of the spatial and temporal changes in substrate and label incorporation in the expanding elements prior to and after defoliation. The relationship between elemental expansion and C deposition was not altered by defoliation, but total C deposition in the growth zone was decreased due to decreased expansion of tissue at advanced developmental stages and a shortening of the growth zone. The N deposition per unit expansion was increased following defoliation, suggesting that N supply did not limit expansion. Transition from reserve- to current assimilation-derived growth was rapid (〈1 d for carbohydrates and approximately 2 d for N), more rapid than suggested by label incorporation in growth zone biomass. The N deposition was highest near the leaf base, where cell division rates are greatest, whereas carbohydrate deposition was highest near the location of most active cell expansion. The contribution of reserve-derived relative to current assimilation-derived carbohydrates (or N) to deposition was very similar for elements at different stages of expansion
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: 
cv, cultivar
δ, deviation of C isotope composition from a standard
Δ, C isotope discrimination
WSC, water soluble carbohydrates

Steady-state labelling of all post-anthesis photosynthate of wheat was performed to assess the mobilization of pre-anthesis C (C fixed prior to anthesis) in vegetative plant parts during grain filling. Results were compared with estimates obtained by indirect approaches to mobilization of pre-anthesis C: ‘classical’ growth analysis and balance sheets of water soluble carbohydrates (WSC) and protein. Experiments were performed with two spring wheat cultivars grown with differential nitrogen fertilizer supply in 1991 and 1992. The fraction of pre-anthesis C mobilized in above-ground vegetative biomass ranged between 24 and 34% of total C present at anthesis. Treatment effects on mobilization of pre-anthesis C in total above-ground vegetative biomass were closely related (r2 = 0·89) to effects on mobilization of WSC-C plus protein-C (estimated as N mobilized × 3·15). On average, 81% of pre-anthesis C mobilization was attributable to the balance of pre-anthesis WSC (48%) and protein (33%) between anthesis and maturity. In roots, WSC and protein mobilization accounted for only 29% of the loss of pre-anthesis C. Notably, mobilization of pre-anthesis C was 1·4–2·6 times larger than the net loss of C from above-ground vegetative biomass between anthesis and maturity. This discrepancy was mainly due to post-anthesis C accumulation in glumes and stem. Post-anthesis C accumulation was related to continued synthesis of structural biomass after anthesis and accounted for a mean 15% of total C contained in above-ground vegetative plant parts at maturity. A close correspondence between net loss of C and mobilization of pre-anthesis C was only apparent in leaf blades and leaf sheaths. Although balance sheets of WSC and protein also underrated the mobilization of pre-anthesis C by ≈ 19%, they gave a much better estimate of pre-anthesis C mobilization than growth analysis.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 27 (2004), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Grassland plants suffer regular defoliation, causing loss of photosynthetic activity and internal resources. Consequently, re-foliation may be substrate-limited. The present study was undertaken to test the hypothesis that decreased C import in leaf growth zones is (partially) compensated by: (i) mobilization of substrate within growth zones; and (ii) increased efficiency of substrate use in leaf area expansion; but (iii) that these processes depend on the C status of growth zones at defoliation. Mixtures of a C3 (Lolium perenne L.) and a C4 grass (Paspalum dilatatum Poir.) were grown at 15 °C (C3 dominance) and 23 °C (C4 dominance). Individual plants thus grew in contrasting (light and temperature) environments before being defoliated. Defoliation caused a drastic and immediate decrease in C import, but effects on leaf area expansion were buffered by biomass mobilization in the growth zone and increases in specific leaf area of produced tissue. Thus, over the first 2 d post-defoliation, the amount of leaf area produced per unit imported C increased by 39 to 102% depending on treatment. The magnitude of these buffering responses was correlated with the concentration of water soluble carbohydrates in the growth zone at defoliation. Similar responses were observed for N, although defoliation effects were smaller and delayed relative to those on C import. This study demonstrates refoliation is sustained by short-term mobilization of reserves within the growth zone and reduced costs of produced leaf area, but that these mechanisms depend on growth zone C status at defoliation.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 28 (2005), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The CO2 respired by leaves is 13C-enriched relative to leaf biomass and putative respiratory substrates (Ghashghaie et al., Phytochemistry Reviews 2, 145–161, 2003), but how this relates to the 13C content of root, or whole plant respiratory CO2 is unknown. The C isotope composition of respiratory CO2 (δR) from shoots and roots of sunflower (Helianthus annuus L.), alfalfa (Medicago sativa L.), and perennial ryegrass (Lolium perenne L.) growing in a range of conditions was analysed. In all instances plants were grown in controlled environments with CO2 of constant concentration and δ13C. Respiration of roots and shoots of individual plants was measured with an open CO2 exchange system interfaced with a mass spectrometer. Respiratory CO2 from shoots was always 13C-enriched relative to that of roots. Conversely, shoot biomass was always 13C-depleted relative to root biomass. The δ-difference between shoot and root respiratory CO2 was variable, and negatively correlated with the δ-difference between shoot and root biomass (r2 = 0.52, P = 0.023), suggesting isotope effects during biosynthesis. 13C discrimination in respiration (R) of shoots, roots and whole plants (eShoot, eRoot, ePlant) was assessed as e = (δSubstrate − δR)/(1 + δR/1000), where root and shoot substrate is defined as imported C, and plant substrate is total photosynthate. Estimates were obtained from C isotope balances of shoots, roots and whole plants of sunflower and alfalfa using growth and respiration data collected at intervals of 1 to 2 weeks. eplant and eShoot differed significantly from zero. eplant ranged between −0.4 and −0.9‰, whereas eShoot was much greater (−0.6 to −1.9‰). eRoot was not significantly different from zero. The present results help to resolve the apparent conflict between leaf- and ecosystem-level 13C discrimination in respiration.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 22 (1999), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: 
 δ, C isotope composition relative to Pee Dee Belemnite
WSC, water-soluble carbohydrates
N, nitrogen
C, carbon
cv, cultivar
ME, efficiency of mobilized pre-anthesis C utilization in grain filling (g C g–1C)

Significant mobilization of protein and carbohydrates in vegetative plant parts of wheat regularly occurs during grain filling. While this suggests a contribution of reserves to grain filling, the actual efficiency of mobilized assimilate conversion into grain mass (ME) is unknown. In the present study the contribution of pre-anthesis C (C fixed prior to anthesis) to grain filling in main stem ears of two spring wheat (Triticum aestivum L.) cultivars was determined by 13C/12C steady-state labelling. Mobilization of pre-anthesis C in vegetative plant parts between anthesis and maturity, and the contributions of water-soluble carbohydrates (WSC) and protein to pre-anthesis C mobilization were also assessed. Experiments were performed with two levels of N fertilizer supply in each of 2 years. Pre-anthesis reserves contributed 11–29% to the total mass of C in grains at maturity. Pre-anthesis C accumulation in grains was dependent on both the mass of pre-anthesis C mobilized in above-ground vegetative plant parts (r2 = 0·87) and ME (defined as g pre-anthesis C deposited in grains per g pre-anthesis C mobilized in above-ground vegetative plant parts; r2 = 0·40). ME varied between 0·48 and 0·75. The effects of years, N fertilizer treatments and cultivars on ME were all related to differences in the fractional contribution of WSC to pre-anthesis C mobilization. Multiple regression analysis indicated that C from mobilized pre-anthesis WSC may be used more efficiently in grain filling than C present in proteins at anthesis and mobilized during grain filling. Possible causes for variability of ME are discussed.
    Type of Medium: Electronic Resource
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