Sex-specific physiology and source-sink relations in the dioecious plant Silene latifolia

Differences in reproductive demands between the sexes of dioecious plants could cause divergence in physiology between the sexes. We found that the reproductive effort of female Silene latifolia plants increased to more than twice that of male plants or female plants that were prevented from setting fruit by lack of pollination after 4 weeks of flowering. Whole-plant source/sink ratios of pollinated females were significantly lower than those of males or unpollinated females because of investment in fruit. We hypothesized that these differences in source/sink ratio between the sexes and within females, depending on pollination, would lead to differences in leaf photosynthetic rates. Within females, we found that photosynthetic capacity was consistent with measurement of whole-plant source/sink ratio. Females that were setting fruit had 30% higher light-saturated photosynthetic rates by 28 days after flowering than females that were not setting fruit. Males, however, had consistently higher photosynthetic rates than females from 10 days after flowering onwards. Males also had approximately twice the dark respiration rates of fruiting females. We found that female reproductive structures are longer-lived and contribute more carbon to their own support than male reproductive structures. Despite the higher rates of leaf dark respiration and lower calyx photosynthetic rates, males fix more carbon than do females. We conclude that females have a sink-regulated mechanism of photosynthesis that allows them to respond to variations in fruit set. This mechanism is not, however, sufficient to explain why male S. latifolia plants have higher rates of photosynthesis, higher source/sink ratios, and lower reproductive allocation, but fail to grow larger than female plants.     

Leaf area index, canopy structure and photosynthesis of red clover (Trifolium pratense L.)

Abstract. The influence of leaf age, total leaf area and its dispersion in space on canopy photosynthesis were studied using microswards of red clover ( Trifolium pratense L.) which were established in the greenhouse. Two varieties, Renova (flowering) and Molstad (non-flowering), were sown in separate plastic boxes at densities of 225, 400 and 625 plants per m².
Vertical distribution of photosynthetically active radiation (PAR), leaf area, leaf age and ¹⁴CO₂-fixation were determined periodically. Net photosynthesis and dark respiration of canopies were measured. Maximum photosynthetic capacity of individual leaves was measured on plants taken from the intact canopy or from plants where shading of the growing leaves had been prevented.
Net photosynthetic rate of canopies increased linearly with leaf area index (LAI) up to an LAI of 3.5 and then declined at higher LAI, independent of variety and sowing density. Below the optimum LAI, net photosynthesis depended mainly on interception of PAR. Decrease in canopy photosynthesis above the optimum LAI was due to a higher proportion of old leaves with decreased photosynthetic capacity, and not to an increase in respiring plant parts. It is concluded that LAI and position of leaf age categories in the canopy are more important than vertical distribution of leaf area in determining canopy photosynthesis of red clover.     

Response of Soybean Canopy Photosynthesis to CO2 Concentration, Light, and Temperature

Photosynthetic rates of outdoor-grown soybean (Glycine max L.Merr. cv. Bragg) canopies increased with increasing CO₂ concentrationduring growth, before and after canopy closure (complete lightinterception), when measured over a wide range of solar irradiancevalues. Total canopy leaf area was greater as the CO₂ concentrationduring growth was increased from 160 to 990 mm³ dm^–3.Photosynthetic rates of canopies grown at 330 and 660 mm³ CO₂dm^–3 were similar when measured at the same CO₂ concentrationsand high irradiance. There was no difference in ribulose bisphosphatecarboxylase/oxygenase (rubisco) activity or ribulose 1,5-bisphosphate(RuBP) concentration between plants grown at the two CO₂ concentrations.However, photosynthetic rates averaged 87% greater for the canopiesgrown and measured at 660 mm³ CO₂ dm^–3. A 10°C differencein air temperature during growth resulted in only a 4°Cleaf temperature difference, which was insufficient to changethe photosynthetic rate or rubisco activity in canopies grownand measured at either 330 or 660 mm³ CO₂ dm^–3. RuBP concentrationsdecreased as air temperature during growth was increased atboth CO₂ concentrations. These data indicate that the increasedphotosynthetic rates of soybean canopies at elevated CO₂ aredue to several factors, including: more rapid development ofthe leaf area index; a reduction in substrate CO₂ limitation;and no downward acclimation in photosynthetic capacity, as occurin some other species. Key words: CO₂ concentration, soybean, canopy photosynthesis     

Yield and composition of soybean seed as a function of potassium supply

Summary A reduction in K supply to soybean plants to deficiency levels during both vegetative and reproductive development resulted in reductions not only in yield, but also in oil and K concentrations in the seed and a concomittant increase in seed protein concentration. Correlations between mean fruit yield and oil, protein and K concentrations, over a wide range of K regimes, were 0.97, −0.94 and 0.98, respectively. When K supply was increased well above the level necessary to produce maximum yields,i.e. luxury consumption, there was no significant change in K concentration in the seed, indicating a high degree of control in the movement of K to the developing seed under high K regimes. When the K supply to the plant was limiting, the rate of accumulation of oil and carbohydrate fractions, but not of seed protein, declined during the latter part of podfilling. This resulted in a fall in the C/N ratio in the non-structural seed components during this part of seed development. Depriving plants of K only during seed development had no effect on seed composition or yield, whereas resupplying K to deficient plants after anthesis resulted in almost the same seed composition and yield as that which occurred with control plants. Possible mechanisms whereby K deficiency influences soybean seed composition and yield are discussed in terms of movement of carbohydrate and nitrogen to the seed. We suggest that potassium-deficient soils are likely to produce crops with low yields and low seed oil levels; the crop may respond to K fertilizers as late as anthesis.     

Leaflet photosynthesis rate and carbon metabolite accumulation patterns in nitrogen-limited, vegetative soybean plants

Prolonged inorganic nitrogen (NO₃ ^–+NH₄ ⁺) limitation of non-N₂-fixing soybean plants affected leaflet photosynthesis rates, photosynthate accumulation rates and levels, and anaplerotic carbon metabolite levels. Leaflets of nitrogen-limited (N-Lim), 27–31-day-old plants displayed 15 to 23% lower photosynthesis rates than leaflets of nitrogen-sufficient (N-Suff) plants. In contrast, N-Lim plant leaflets displayed higher sucrose and starch levels and rates of accumulation, as well as higher levels of carbon metabolites associated with sucrose and starch synthesis, e. g., glycerate-3-phosphate and glucose phosphates, than N-Suff plant leaflets. Concurrently, levels of soluble protein, chlorophyll, and anaplerotic metabolites, e.g., malate and phosphoenolpyruvate, were lower in leaflets of N-Lim plants than N-Suff plants, suggesting that the enzymes of the anaplerotic carbon metabolite pathway were lower in activity in N-Lim plant leaflets. Malate net accumulation rates in the earliest part of the illumination period were lower in N-Lim than in N-Suff plant leaflets; however, by the midday period, malate accumulation rate in N-Lim plant leaflets exceeded that in leaflets of N-Suff plants. Further, soluble protein accumulation rates in leaflets of N-Suff and N-Lim plants were similar, and the rate of dark respiration, measured in the early part of the dark period, was higher in N-Lim plant leaflets than in N-Suff plant leaflets. It was concluded that during prolonged N-limitation, foliar metabolite conditions favored the channelling of a large proportion of the carbon assimilate into sucrose and starch, while assimilate flow through the anaplerotic pathway was diminished. However, in some daytime periods, there was a normal level of carbon assimilate channelled through the anaplerotic pathway for ultimate use in amino acid and protein synthesis.Abbreviations ADPG-PPiase ADPglucose pyrophosphorylase - Ce CO₂ in the leaf photosynthesis measuring cuvette - Ci leaf internal CO₂ during photosynthesis measurement - Chl chlorophyll - DHAP dihydroxyacetone phosphate - GAP glyceraldehyde-3-phosphate - G_sw stomatal conductance with units as mmol H₂O m^–2 s^–1 - G1P glucose-1-phosphate - G6P glucose-6-phosphate - F6P fructose-6-phosphate - FBP fructose-1,6-bisphosphate - FBPase-pH 8.1 chloroplastic fructose-1,6-bisP (C-1) phosphatase (pH 8.1) - MAL malate - N inorganic nitrogen, i.e. NO₃ ^–+NH₄ ⁺ (at levels and molar ratios indicated) - PE post-emergence - PEP phosphoenolpyruvate - PEPCase phosphoenolpyruvate carboxylase - PGA 3-phosphoglycerate - PYR pyruvate - PYR kinase pyruvate kinase - Pn net CO₂ photoassimilation in leaves - PPFD photosynthetic photon flux density - PPRC pentose phosphate reductive cycle - RuBP ribulose-1,5-bisphosphate; rubisco-ribulose-1,5-bisphosphate carboxylase/oxygenase - SLW specific leaf mass - SPS sucrose-6-phosphate synthase - TCA cycle tricarboxylic acid cycle; triose-P-DAP+GAP     

Comparison of gas exchange and chlorophyll fluorescence of low-potassium-tolerant and -sensitive soybean [<Emphasis Type="Italic">Glycine max</Emphasis> (L.) Merr.] cultivars under low-potassium condition

The effects of potassium (K) deficiency on chlorophyll (Chl) content, photosynthetic gas exchange, and photosystem II (PSII) photochemistry during the seedling stage were investigated in two soybean [Glycine max (L.) Merr.] cultivars, low-K sensitive Tiefeng31 and low-K tolerant Shennong6. The cultivars were grown hydroponically in K-sufficient (KS) and K-deficient (KD) solutions. Photosynthetic gas exchange and Chl content in Tiefeng31 were severely affected by the low K condition, but were almost unaffected in Shennong6. This difference is in accordance with the PSII photochemistry in the plants, indicating that the photosynthetic apparatus of Shennong6 is more tolerant to low-K stress than that of Tiefeng31.     

Photosynthetic responses of Miconia species to canopy openings in a lowland tropical rainforest

We examined the photosynthetic acclimation of three tropical species of Miconia to canopy openings in a Costa Rican rainforest. The response of photosynthesis to canopy opening was very similar in Miconia affinis, M. gracilis, and M. nervosa, despite differences in growth form (trees and shrubs) and local distributions of plants (understory and gap). Four months after the canopy was opened by a treefall, photosynthetic capacity in all three species had approximately doubled from closed canopy levels. There were no obvious signs of high light damage after treefall but acclimation to the gap environment was not immediate. Two weeks after treefall, A_max, stomatal conductance, apprarent quantum efficiency, and dark respiration rates had not changed significantly from understory values. The production of new leaves appears to be an important component of light acclimation in these species. The only variables to differ significantly among species were stomatal conductance at A_max and the light level at which assimilation was saturated. M. affinis had a higher stomatal conductance which may reduce its water use efficiency in gap environments. Photosynthesis in the more shade-tolerant M. gracilis saturated at lower light levels than in the other two species. Individual plant light environments were assessed after treefall with canopy photography but they explained only a small fraction of plant variation in most measures of photosynthesis and growth. In conclusion, we speculate that species differences in local distribution and in light requirements for reproduction may be more strongly related to species differences in carbon allocation than in carbon assimilation.     

Photosynthesis and respiration in Alocasia macrorrhiza following transfers to high and low light

Summary Photosynthetic capacities and respiration rates of Alocasia macrorrhiza leaves were measured for 4 weeks following reciprocal transfers between high (20% of full sun) and low (1% of full sun) light environments. Photosynthetic capacities and respiration rates of mature, high-light leaves were 1.7 and 4.5 times those of low-light leaves, respectively. Following transfer, respiration rates adjusted within 1 week to those characteristic of plants grown in the new environment. By contrast, photosynthetic capacities either did not adjust or changed only slowly following transfer. Most of the difference in respiration between high- and low-light leaves was related to the carbohydrate status as determined by the daily PFD and little was directly related to the maintenance costs of the photosynthetic apparatus. Leaf construction cost was directly proportional to maximum photosynthetic capacity. Consequently, although daily carbon gain per unit leaf area was the same for low-light and high to low-light transferred plants within a week after transfer, the carbon return per unit of carbon investment in the leaves remained lower in the high to low transfer plants throughout the 4 week measurement period. Conversely, in high-light, the low leaf construction cost of the low to high-light transferred plants resulted in carbon gain per unit investment just as high as that of the high-light plants.     

Carpels as leaves: meeting the carbon cost of reproduction in an alpine buttercup

We investigated the role of photosynthesis by reproductive organs in meeting the carbon costs of sexual reproduction in the snow-buttercup, Ranunculus adoneus. The exposed green carpels of snow-buttercup flowers have 1–2 stomata each. Net carbon assimilation rates of flowers are negative during bud expansion, but rise to zero at maturity, and become positive during early fruit growth. Experimental removal of separate whorls of flower parts demonstrated that the showy, nectary-housing petals account for most of the respiration cost of flower presentation. Conversely, photosynthesis by female organs contributes to a flower's carbon balance. Dipteran pollinators of R. adoneus are most active in sunny mid-morning to mid-afternoon intervals. At this time of day, rates of carpel photosynthesis (A_max) meet respiratory costs of pollinator attraction in fully expanded flowers. Achenes remain photosynthetically active until dispersal, and positive net carbon assimilation rates characterize infructescences throughout fruit maturation. Photosynthetic rates of achenes are positively correlated with infructescence growth rates. We tested the causal basis of this relationship by experimentally shading developing infructescences. Mature achenes from shaded infructescences were 16–18% smaller than those from unshaded controls. Leaf photosynthetic rates did not differ between plants bearing shaded and unshaded seed heads. Since female reproductive organs are only 8% more costly in terms of caloric investment than male ones and contribute to their own carbon balance, it is plausible that the energy cost of male function equals or exceeds that of female function in this hermaphroditic species.     

Effects of decreasing source/sink ratio in soybeans on photosynthesis, photorespiration, transpiration and yield

Abstract. Shading of all side leaflets of a determinate soybean cultivar during pod filling significantly increased rates of photosynthesis in the unshaded centre leaflets, compared to centre leaflets of controls. Higher rates were associated with both higher stomatal and mesophyll conductances, and were reversible within 2 days when shades were removed. These higher rates of photosynthesis were not associated with decreased percentage enhancement by low oxygen, indicating that treatment effects were probably not associated with changes in photorespiration relative to photosynthesis. Percentage enhancement did, however increase as the plants approached physiological maturity, chiefly because of a decrease in photosynthesis.
In spite of these increases in rates of photosynthesis seed weight per plant was decreased by 37% in plants with side leaflets shaded for the entire pod-filling period and by 28% in plants shaded for only the second half of the period. In plants where shades were removed during the second half of pod filling seed yield was reduced by only 19% because shade removal delayed leaf senescence. The four treatments reduced yield by different mechanisms. Plants shaded continuously during pod filling produced fewer seeds than controls, but the weight per seed was similar. When shading was applied during the second half of pod fillings seed number was unchanged but weight per seed was significantly reduced. In contrast when shades were removed for the second half of pod filling, seed number remained similar to that of continuously shaded plants, but seed weight increased.
Although all shading treatments reduced yield, the reduction was not proportional to the 63% reduction in leaf area available for photosynthesis. This was because (1) photosynthetic rates in the centre leaflet of shaded plants were higher than rates in controls, (2) stem and lower surface photosynthesis in shaded leaf-lets contributed to whole leaflet photosynthesis.     

Mutual shading and the photosynthetic capacity of exposed leaves of field grown soybeans

Light-saturated photosynthetic rates at air levels of carbon dioxide were measured about weekly in upper canopy leaves of two soybean cultivars grown at stand densities of 40 and 100 plants per square meter. Early in the season, when leaf area indices differed between stand densities, plants of both cultivars grown at high stand density had photosynthetic rates which averaged 23% lower than plants at low stand density. Later in the season, when there were no differences in leaf area index between stand densities, there were no differences in photosynthetic rates in the cultivar Kent, but rate differences of about 14% persisted in the cultivar Williams. In Williams mainstem leaves emerged into full sunlight later in their development at high than at low stand density. In both cultivars the oldest fully exposed leaves were photosynthetically immature for much of the season, as higher rates could be achieved by lower leaves which were shaded in situ. The results identify shading of young developing leaves and photosynthetic immaturity of fully exposed leaves as factors limiting canopy photosynthesis in soybeans, and indicate cultivar differences in how much high stand density reduces photosynthetic capacity.     

PHYSIOLOGICAL COMPARISON OF THE ISOMORPHIC LIFE HISTORY PHASES OF THE HIGH INTERTIDAL ALGA ENDOCLADIA MURICATA (RHODOPHYTA)1

The isomorphic phases of Endocladia muricata (Post. & Rupr.) J. Ag. Were compared for photosynthetic and respiratory difference in response to a variety of environmental manipulations. Photosynthetic light response during submergence at 15° C and the pattern of respiratory recovery following prolonged emergence (3 h) at either 15° or 30° C were similar between gametophytes and tetrasporophytes. The phases showed the same ability to photosynthesize and respire during emergence at each temperature tested (15°, 25°, and 35° C, fully hydrated thalli) and at various desiccation state (measured at 25° C only). Submerged rates of photosynthesis following prolonged emergence at 15° and 30° C were, however slightly greater (17%) for tetrasporophytes as compared to gametophytes. Regardless of the life history phase, plants incubated at 15° C during emergence recovered more completely than plants incubated at 30° C. Photosynthetic recovery after 1 h in plants incubated at 15° C often “spiked” and yielded rates as great as 185% of pretreatment rates. Increased photosynthetic rates during recovery were absent for the 30° C incubations. The initial photosynthetic recovery of plants collected from the upper limits of distribution was greater than that of plants collected from the lower limits. Recovered rates of respiration were highly variable over time. Respiration often exceeded pretreatment values more then threefold, and the elevated rates were sustained for 12 h. Photosynthesis and respiration in air were comparable to rates in seawater and varied slightly with increasing temperature. Photosynthetic and respiratory rates also decreased with increasing tissue water loss. Thus, only slight differences in physiological performance were observed between phases and individuals collected from different vertical positions. Metabolic differences were transient and apparent only under experimental conditions that modeled extreme environmental conditions.     

Seasonal dynamics of photosynthesis and total carbon gain in bearing and nonbearing pistachio (<Emphasis Type="Italic">Pistacia vera</Emphasis> L.) shoots

Seasonal changes in leaf gas exchange, assimilation response to light and leaf area were monitored in bearing and nonbearing pistachio shoots. Shoot bearing status did not directly affect leaf photosynthetic rate. However, photosynthetic light-response curves strongly varied during the season demonstrating the dominant effect of the tree’s seasonal phenology on assimilation. Early in the season low photosynthetic rates were associated with high rates of dark respiration indicating limited photosynthesis in the young leaves. As leaves matured, dark respiration decreased and assimilation reached maximum values. Photosynthetic efficiency was strongly reduced late in the season due to leaf age and senescence. Fruit load precipitated an early leaf senescence and drop that resulted in a 53% decrease in leaf area in bearing vs. nonbearing shoots, strongly decreasing the seasonal photosynthetic performance of bearing shoots. Bearing shoots produced a 26% lower seasonal carbon gain compared to nonbearing shoots.     

Relationship between photosynthetic and respiratory carbon metabolism in freshwater phytoplankton

Measurements of algal carbon metabolism in the light and the dark were conducted in (1) short-term (3-h) light and dark incubations, (2) a diel (24-h) experiment, and (3) a longer-term (4-d) carbon accumulation experiment to examine the relationship between photosynthetic rates, photosynthetic carbon metabolism in the light, and respiration and carbon metabolism in the ensuing dark period in natural assemblages of freshwater phytoplankton. High rates of photosynthesis and polysaccharide synthesis in the light were followed by high rates of respiration and polysaccharide utilization in the dark. Polysaccharide was the major respiratory substrate in the dark, and small molecular weight metabolites, lipids, and protein were less important sources of metabolic energy. The protein pool accumulated carbon during dark incubations, but more slowly than during active photosynthesis in the light. Because the intracellular macromolecular pools turn over at very different rates (polysaccharide > protein and lipid), patterns of short-term photosynthetic carbon metabolism are not necessarily indicative of the biochemical composition of the phytoplankton.     

Differential responses to K deficiency among soybean cultivars

The seed yield per unit of potassium applied differed for five soybean cultivars which were grown to maturity under different K regimes in a glasshouse. Whereas Dodds was the most responsive cultivar to moderate increases in K supply, the cultivar Bragg was the most efficient in its ability to produce seed with low levels of available K; Lee and Forest were the least efficient cultivars while Bossier and Dodds were of intermediate efficiency. The basis for the efficiency of cv. Bragg was that the growth of its tops, as indicated by mature stem weights and its roots, were less affected by reduced K supply than those of other cultivars. This enabled it to produce more pods under K-deficient regimes, resulting in a greater seed yield per plant. The percentage reduction in oil/protein ratios in the seed of the five cultivars under moderate K deficiency correlated closely with reductions in seed yield. However, changes in this ratio were poorly related to the K percentages in the seed. All cultivars experienced an impairment of plant senescence under K deficiency as evidenced by a reduction in leaf abcission and a delay in pod maturity. The existence of genetic diversity in K-use efficiency means that breeding programmes could utilize K-efficient germplasm in developing new cultivars for soils not naturally high in potassium.     

Stomatal and photosynthetic responses to shade in sorghum, soybean and eastern gamagrass

We studied photosynthetic and stomatal responses of grain sorghum ( Sorghum bicolor [L.] Moench cv. Pioneer 8500), soybean ( Glycine max L. cv. Flyer) and eastern gamagrass ( Tripsacum dactyloides L.) during experimental sun and shade periods simulating summer cloud cover. Leaf gas exchange measurements of field plants showed that short-term (5 min) shading of leaves to 300–400 μmol m⁻² s⁻¹ photosynthetic photon flux density reduced photosynthesis, leaf temperature, stomatal conductance, transpiration and water use efficiency and increased intercellular CO₂ partial pressure. In all species, photosynthetic recovery was delayed when leaves were reilluminated, apparently by stomatal closure. The strongest stomatal response was in soybean. Photosynthetic recovery was studied further with soybeans grown indoors (maximum photosynthetic photon flux density 1 200 μmol m⁻² s⁻¹). Plants grown indoors had responses to shade similar to those of field plants, except for brief nonstomatal limitation immediately after reillumination. These responses indicated the importance of the light environment during leaf development on assimilation responses to variable light, and suggested different limitations on carbon assimilation in different parts of the soybean canopy. Photosynthetic oxygen evolution recovered immediately upon reillumination, indicating that the light reactions did not limit soybean photosynthetic recovery. While shade periods caused stomatal closure and reduced carbon gain and water loss in all species, the consequences for carbon gain/water loss were greatest in soybean. The occurrence of stomatal closure in all three species may arise from their shared phenologies and herbaceous growth forms.     

Microclimate, Canopy Structure and Photosynthesis in Canopies of Three Contrasting Temperate Forage Grasses: III. Canopy Photosynthesis, Individual Leaf Photosynthesis and the Distribution of Current Assimilate

The rates of canopy and individual leaf photosynthesis and ¹⁴Cdistribution for three temperate forage grasses Lolium perennecv. S24, L. perenne cv. Reveille and Festuc'a arundinacea cv.SI70 were determined in the field during a summer growth period.Canopy photosynthesis declined as the growth period progressed,reflecting a decline in the photosynthetic capacity of successiveyoungest fully expanded leaves. The decline in the maximum photosyntheticcapacity of the canopies was correlated with a decline in theirquantum efficiencies at low irradiance. Changes in canopy structureresulted in changes in canopy net photosynthesis and dark respiration.No clear relationships between changes in the environment andchanges in canopy net photosynthesis and dark respiration wereestablished. The relative distributions of ¹⁴C in the shootsof the varieties gave a good indication of the amount of drymatter per ground area in the varieties.     

Ecophysiological traits may explain the abundance of climbing plant species across the light gradient in a temperate rainforest

Climbing plants are a key component of rainforests, but mechanistic approaches to their distribution and abundance are scarce. In a southern temperate rainforest, we addressed whether the dominance of climbing plants across light environments is associated with the expression of ecophysiological traits. In mature forest and canopy gaps, we measured leaf size, specific leaf area, photosynthetic rate, and dark respiration in six of the most abundant woody vines. Mean values of traits and their phenotypic change (%) between mature forest and canopy gaps were predictor variables. Leaf size and specific leaf area were not significantly associated with climbing plant dominance. Variation in gas-exchange traits between mature forest and canopy gaps explained, at least partly, the dominance of climbers in this forest. A greater increase in photosynthetic rate and a lower increase in dark respiration rate when canopy openings occur were related to the success of climbing plant species. Dominant climbers showed a strategy of maximizing exploitation of resource availability but minimizing metabolic costs. Results may reflect phenotypic plasticity or genetic differentiation in ecophysiological traits between light environments. It is suggested that the dominant climbers in this temperate rainforest would be able to cope with forest clearings due to human activities.     

Effects of leaf and sap feeding insects on photosynthetic rates of goldenrod

Summary Herbivory can alter the balance between sources and sinks within a plant, and changes in the source-sink ratio often lead to changes in plant photosynthetic rates. We investigated how feeding by three insect herbivores affected photosynthetic rates and growth of goldenrod (Solidago altissima). One, a phloem-sap feeding aphid (Uroleucon caligatum), creates an additional sink, and the other two, a leaf-chewing beetle (Trirhabda sp.) and a xylem-sap feeding spittlebug (Philaenus spumarius) both reduce source supply by decreasing leaf area. Plants were grown outside in large pots and insects were placed on them at predetermined densities, with undamaged plants included as controls. All insects were removed after a 12-day feeding period. We measured photosynthetic rates both of damaged leaves and of undamaged leaves that were produced after insect removal. Photosynthetic rates per unit area of damaged leaves were reduced by spittlebug feeding, but not by beetle or aphid feeding. Conductance of spittlebugdamaged leaves did not differ from controls, but internal carbon dioxide concentrations were increased. These results indicate that spittlebug feeding does not cause stomatal closure, but impairs fixation within the leaf. Effects of spittlebug feeding on photosynthetic rates persisted after the insects were removed from the plants. Photosynthetic rates per unit area of leaves produced after insect removal on spittlegug-damaged plants were lower than control levels, even though the measurements were taken 12 days after insect removal. The measurement leaf on spittlebugdamaged plants was reduced in area by 27% relative to the controls, but specific leaf area (leaf area/leaf weight) was increased by 18%. Because of the shift in specific leaf area, photosynthetic rates were also examined per unit leaf weight, and when this was done there were no significant differences between control and spittlebug-damaged plants. Beetle and aphid feeding had no effects on the photosynthetic rate of the leaves produced after insect removal. Plant relative growth rates (in terms of height) were reduced by spittlebugs during the period that the insects were feeding on the plants. Relative growth rates of spittlebug-damaged plants were increased above control levels after insect removal, but these plants were still shorter than controls 17 days after insect removal. Beetles and aphids did not affect plant relative growth rates or plant height. Feeding by both spittlebugs and beetles reduced leaf area, and the effect of the spittlebug was more severe than that of the beetle. These results show that effects of herbivory on photosynthetic rates cannot be predicted simply by considering changes in the source-sink ratio, and that spittlebug feeding is more damaging to the host plant than beetle or aphid feeding.