Inner‐crown Microenvironments of Two Emergent Tree Species in a Lowland Wet Forest1

Vascular epiphyte communities, comprising up to 25 percent of tropical forest flora, contribute to plant diversity and thus ecosystem‐level processes; however, one of the proximal determinants of those communities, microclimate, is little studied. Here we present the first comprehensive study of microclimates in the inner crowns of two emergent tree species, Hyeronima alchorneoides and Lecythis ampla, at La Selva Biological Station, Costa Rica. We examined photon flux density, temperature, vapor pressure, and humidity in inner‐crown branches during the wet and dry seasons and during the wet‐season leafless phase of Lecythis. In both seasons, the percentage daily PFD in foliated Lecythis crowns (9%, wet season; 11%, dry season) was significantly higher than in Hyeronima crowns (5%, both seasons), with the leafless wet‐season PFD of Lecythis reaching 23 percent of full sun. Temperature and vapor pressure varied less in Hyeronima than in Lecythis crowns during the dry season. Microenvironmental conditions for epiphytes within Hyeronima crowns were more spatially and temporally homogeneous and were more buffered from ambient conditions than within Lecythis crowns. Growing conditions within the crowns of the same trees and among different trees were measurably different and are likely to affect the structure and composition of the resident epiphyte communities.     

Light adaptation and the role of autotrophic epiphytes in primary production of the temperate seagrass, Zostera marina L.

Photosynthetic features of Zostera marina L. and its autotrophic epiphyte community were investigated in a population inhabiting a shallow (1.3 m depth) water meadow in Great Harbor, Woods Hole, MA (U.S.A.). Photosynthesis versus irradiance (P-I) relationships were measured with respect to leaf age determined by the leaf position in the shoot bundle and by location of the tissue along the leaf axis. Therefore both age and light intensity gradients along the leaf axis were considered. The maximum photosynthesis (P_max) per dm² typically increased nearly two-fold along the leaf axis from leaf bases to apices. Photosynthetic rate on a chlorophyll (Chl) basis did not increase as dramatically along the leaf axis, and rates were usually lowest in tissues with the highest Chl content. The P-I relationships of leaves of different ages did not reveal photoinhibition even at light intensities > 1400 μE • m⁻² • s ⁻¹. Furthermore, no photoinhibition was observed in tissues from leaf blade bases, which never experienced high light levels (> 500 μE • m ⁻² • s⁻¹) in situ in Great Harbor. The initial slopes of the P-I curves and light compensation and saturation values varied along the leaf axis in relation to in situ light intensity gradients and in relation to leaf or tissue age. It appeared that leaf and/or tissue age was more important than light environment in determining P-I responses. The contribution of the autotrophic epiphyte community on Z. marina leaves to total photosynthesis per dm² was between 27 and 50%, and between 10 and 44% per mg chlorophyll. These levels of epiphyte photosynthesis can double the primary production of Z. marina leaves. No detrimental effects of epiphyte cover were realized in leaf maximal photosynthesis or P-I relationships. Non-epiphytized leaves and leaves from which epiphytes were removed showed essentially identical photosynthetic features. Light intensity and age gradients along the leaf axis control both the photosynthetic performance of the leaves and epiphyte biomass and photosynthesis.     

Comparative ecophysiology of CAM and C3 bromeliads. I. The ecology of the Bromeliaceae in Trinidad

Abstract This article deals with the physiological ecology of the Bromeliaceae, a large neotropical family containing both terrestrial and epiphytic forms, as well as many species with crassulacean acid metabolism (CAM). The article is in two parts. In the first, we review what is known of the occurrence of CAM and C₃ species in the Bromeliaceae. The photosynthetic pathways are discussed in the context of the major taxonomic divisions within the family and the great diversity of bromeliad life-forms. Of the three subfamilies, the Pitcairnioideae contain both C₃ and CAM species and are essentially all terrestrial. In contrast, the Tillandsioideae are entirely epiphytic or saxicolous, with CAM species being restricted to the genus Tillandsia, And in the Bromelioideae all species show CAM, but terrestrial and epiphytic forms are found in about equal numbers. The evidence suggests that both CAM and the epiphytic habit arose more than once in the family's evolutionary history. In the second part we consider the photosynthetic ecology of the various bromeliad life-forms in more detail using the specific example of Trinidad (West Indies). CAM bromeliads tend to be centred on the drier regions of the island and C₃ forms on the wetter areas. However, at any one site there is a marked vertical stratification of species within the forest profile. Based on the known habitat preferences of the bromeliads, six contrasting sites were selected for field studies in Trinidad. These ranged from arid coastal scrub to montane rain forest, the vegetational and climatic characteristics of which are described here. The constancy of δ¹³C values (carbon-isotope ratios) for individual CAM species in these markedly different habitats emphasized the need for ecophysiological studies to characterize environmental effects on CO₂ assimilation and transpiration. The following papers in this series present the results of a comparative investigation of gas exchange and leaf water relations of CAM and C₃ bromeliads in situ at the various sites.     

Crassulacean acid metabolism,CO2-recycling,and tissue desiccation in the Mexican epiphyte Tillandsia schiedeana Steud (Bromeliaceae)

After 23 days without water in a greenhouse, rates of nocturnal CO₂ uptake in Tillandsia schiedeana decreased substantially and maximum rates occurred later in the dark period eventually coinciding with the onset of illumination. Nocturnal CO₂ uptake accounted for less than half the total nighttime increase in acidity measured in well-watered plants. With increased tissue desiccation, only 11–12% of measured acid accumulation was attributable to atmospheric CO₂ uptake. Plants desiccated for 30 days regained initial levels of nocturnal acid accumulation and CO₂ uptake after rehydration for 10h. These results stress the importance of CO₂ recycling via CAM in this epiphytic bromeliad, especially during droughts.Partially supported by Biomedical Sciences Support Grant RR07037.     

Cultivation of Gracilaria in outdoor tanks and ponds

This review deals with the major problems of unattached Gracilaria intensive cultivation in outdoor tanks and ponds. These problems are presented through the main variables affecting the Gracilaria annual yield and the updated solutions evolved. The physical variables include tank and pond structure, seawater characteristics such as velocity, agitation practice, exchange rate, and salinity, light characteristics such as quantity and quality, and temperature modelling. The chemical variables include nutrient composition and regime of application, and inorganic carbon supply with the pH changes involved. The biological variables include seaweed density, epiphyte competition, grazer damage, bacterial disintegration, integrated mariculture and strain selection. The experience gained in the Israeli research on Gracilaria cultivation is discussed in view of other Gracilaria and seaweed intensive cultivation research.     

Gas Exchange and Water Vapor Uptake in the Atmospheric CAM Bromeliad Tillandsia recurvata L.: The Influence of Trichomes

Tillandsia recurvata is an epiphytic atmospheric CAM bromeliad without functional roots. As an adaptation to very exposed and often dry habitats T. recurvata takes up liquid water via trichomes, which cover the plant. Gas exchange measurements also show an absorption of water vapor at the trichomes simultaneously with an increase in relative humidity at the beginning of the dark period. A similar amount of water is lost again when the relative humidity is decreased. Experiments with heat-killed plants show that this was due exclusively to physical equilibration of the hygroscopic walls of the dead trichome cells. This effect would have prevented an accurate calculation of transpiration and conductance, but can be accounted for by substracting water vapor exchange of heat-killed plants from that of the living tissue which yields the true water vapor conductance of the tissue. This is found to be rather low (3.37 mmol H₂O kg^?1 s^?1) in comparison to other plants, and the proportion of total conductance due to trichomes is relatively high (0.53 mmol H₂O kg^?1 s^?1). This explains the slow rates of photosynthesis and growth found in this plant.     

ARE “GREEN TIDES” HARMFUL ALGAL BLOOMS? TOXIC PROPERTIES OF WATER‐SOLUBLE EXTRACTS FROM TWO BLOOM‐FORMING MACROALGAE,ULVA FENESTRATA AND ULVARIA OBSCURA (ULVOPHYCEAE)

Toxic properties are more often associated with microalgal blooms than with macroalgal blooms, although herbivore deterrents are well known in macroalgae, and inhibition of invertebrate larval development by extracts from Ulva spp. has been suggested. This study was prompted from our observation that substantial discoloration of seawater occurred in small bays after mass desiccation-induced mortality of Ulvaria obscura (Kützing) Gayral. We examined the effects of extracts from Ulva fenestrata Postels et Ruprecht and Ulvaria obscura on Fucus gardneri Silva zygote development, growth of Ulva and Ulvaria , epiphytic algal accumulation, and oyster larval development. Fucus zygote development was inhibited by extracts from both species, although the effects of Ulvaria extracts were significantly greater. Epiphytic algal accumulation and the growth of Ulva and Ulvaria were inhibited by extracts from both species. Oyster larval development was arrested by the presence of extracts from each species. We conclude that extracts from both Ulva fenestrata and Ulvaria obscura have allelopathic properties. The effects are more widespread and occur at lower concentrations for extracts from Ulvaria than Ulva. These properties could alter competitive interactions by inhibiting germination or development of algae and invertebrates.     

Association between rainfall seasonality and the flowering of epiphytic plants in a Neotropical montane forest

The association between the reproductive phenology of epiphytic communities with environmental and ecological factors remains largely unexplored. Because epiphytes depend on environmental moisture, seasonal changes in moisture conditions likely act as the primary determinants of their reproductive timing. We examined whether water limitation or pollinator competition structures the flowering phenologies of an epiphytic community in a seasonal mountain forest in Costa Rica. Additionally, we addressed the environmental factors that might trigger floral induction. Using a 24‐month dataset of bimonthly flowering records from 104 species, we found high seasonality of flowering at the species level but somewhat lower seasonality at the community level. The flowering mid‐dates of most epiphytes, particularly from monocotyledonous species, occurred during the wettest months, as predicted if water limitation structures flowering. The increased moisture and nutrient availability during the rainy season give epiphytes the resources needed to complete floral development and anthesis, and later fruit and seed maturation. The observed flowering pattern of epiphytes coincides with reproductive patterns of terrestrial herbs and shrubs from seasonal tropical ecosystems, and suggests shared constraints to sexual reproduction in both ecological guilds under similar climatic conditions. In contrast, flowering patterns of congeneric epiphytes in the same pollination guild mostly did not follow the expectations of a pollinator competition scenario. Finally, we discuss the possible combined effect of precipitation, temperature, and daily insolation on floral induction of epiphytic plants.