Thigmomorphogenic responses of epiphytic bromeliads to mechanically induced stress

Vascular epiphytes represent almost 10% of all terrestrial plant diversity. Despite the extensive research on the functional ecology and challenges of epiphytic growth, there is still very little known on how exposure to mechanically induced stress affects the growth and development of epiphytes. Therefore, this study investigated the effect of such mechanical stress on the growth and biomass allocation of epiphytic bromeliads. Juvenile plants of two species were subjected to two types of mechanical stress in the greenhouse—permanent displacement and temporary, recurring mechanical flexing. ANOVAs were used to test possible treatment effects on growth, root–shoot ratio, root diameter, and root area distribution ratio. Contrary to previous studies on herbaceous plants, these bromeliads showed little to no change in root and shoot properties in either species. The root–shoot ratio increased in disturbed Guzmania lingulata plants, but not in Vriesea sp. Treatment effects on growth were inconsistent: a stress effect on growth was significant only in the first 2 months of the experiment in G. lingulata, whilst none of the stress treatments negatively affected growth in Vriesea sp. All disturbed plants showed some degree of curvature on their stems and leaves against the area of stress to obtain an upright position. This was probably related to the maintenance of a functional tank. This study provides quantitative and qualitative data to understand thigmomorphogenic responses of bromeliads to mechanical stress. Future studies could include field surveys to quantify on-site mechanical stresses and the corresponding morphological changes in vascular epiphytes.

Nesting behavior of the Elegant Euphonia (Euphonia elegantissima, Aves: Fringillidae) in urban and suburban sites of east Mexico

Between 2005, 2014–2017, we studied six Elegant Euphonia (Euphonia elegantissima) nests from two sites (urban and suburban) in the city of Xalapa, Veracruz. They were located in a macadamia tree crown, under epiphytic bromeliads, and under hanging fern and Euphorbia pots. The two nests we extracted and measured (7.2 x 7.5 x 5.6 cm; 10.1 x 8.6 x 11 cm), were closed and globular, with a lateral entry and mainly made of plant fibers, leaves, and cobwebs. Our observations included nest construction, egg incubation and chick care (nestling phase). Nest construction took at least 10–11 days, while egg incubation took 14–18 days. Incubation was done by the female in all but one observation, and the male escorted the female to the nest on every occasion. Time of incubation sessions ranged from 36–88 min (mean = 62 min) with shorter out nest sessions (3–18 min, mean = 9 min). There were three eggs in two of the nests, and in one only two eggs hatched; four chicks were observed in another nest. The nestling phase lasted 20 days in two nests, with the male spending more time (35–300 s, mean = 109 s) than the female taking care of the chicks (25–99 s, mean = 53 s). Reciprocal escorting was observed during the nestling phase, with the male always arriving first. Breeding occurred in January, April, May (two nests), June, and July. Observing the male of the Elegant Euphonia escorting the female during the incubation period, corroborates previous observations of this behavior in genera Euphonia and Chlorophonia. Incubation and nestling time periods were similar to other species of these genera.

Go with the flow: The extent of drag reduction as epiphytic bromeliads reorient in wind

Vascular epiphytes represent almost 10% of all terrestrial plant diversity. Being structurally dependent on trees, epiphytes live at the interface of vegetation and atmosphere, making them susceptible to atmospheric changes. Despite the extensive research on vascular epiphytes, little is known about wind disturbance on these plants. Therefore, this study investigated the wind-epiphyte mechanical interactions by quantifying the drag forces on epiphytic bromeliads when subjected to increasing wind speeds (5–22 m s-1) in a wind tunnel. Drag coefficients (Cd) and Vogel exponents (B) were calculated to quantify the streamlining ability of different bromeliad species. Bromeliads’ reconfiguration occurred first via bending and aligning leaves in the flow direction. Then leaves clustered and reduced the overall plant frontal area. This reconfiguration caused drag forces to increase at a slower rate as wind velocity increased. In the extreme case, drag force was reduced by 50% in a large Guzmania monostachia individual at a wind velocity of 22 m s-1, compared to a stiff model. This species had one of the smallest Cd (0.58) at the highest wind velocity, and the largest negative mean B (-0.98), representing the largest reconfiguration capacity amongst the tested bromeliads. The streamlining ability of bromeliads was mainly restricted by the rigidity of the lower part of the plant where the leaves are already densely clustered. Wind speeds used in this study were generally low as compared to storm force winds. At these low wind speeds, reconfiguration was an effective mechanism for drag reduction in bromeliads. This mechanism is likely to lose its effectiveness at higher wind speeds when continuous vigorous fluttering results in leaf damage and aspects such as root-attachment strength and substrate stability become more relevant. This study is a first step towards an understanding of the mechanical bottleneck in the epiphyte-tree-system under wind stress.

A new reproductive mode in anurans: Natural history of Bokermannohyla astartea (Anura: Hylidae) with the description of its tadpole and vocal repertoire

Anurans have the greatest diversity of reproductive modes among tetrapod vertebrates, with at least 41 being currently recognized. We describe a new reproductive mode for anurans, as exhibited by the Paranapiacaba Treefrog, Bokermannohyla astartea, an endemic and poorly known species of the Brazilian Atlantic Forest belonging to the B. circumdata group. We also describe other aspects of its reproductive biology, that are relevant to understanding the new reproductive mode, such as courtship behavior, spawning, and tadpoles. Additionally, we redescribe its advertisement call and extend its vocal repertoire by describing three additional call types: courtship, amplectant, and presumed territorial. The new reproductive mode exhibited by B. astartea consists of: (1) deposition of aquatic eggs in leaf-tanks of terrestrial or epiphytic bromeliads located on or over the banks of temporary or permanent streams; (2) exotrophic tadpoles remain in the leaf-tanks during initial stages of development (until Gosner stage 26), after which they presumably jump or are transported to streams after heavy rains that flood their bromeliad tanks; and (3) tadpole development completes in streams. The tadpoles of B. astartea are similar to those of other species of the B. circumdata group, although with differences in the spiracle, eyes, and oral disc. The vocal repertoire of B. astartea exhibits previously unreported acoustic complexity for the genus. Bokermannohyla astartea is the only bromeligenous species known to date among the 187 known species within the tribe Cophomantini. We further discuss evolutionary hypotheses for the origin of this novel reproductive mode.

Addendum: Tellez, P.H.; et al. Relationships between Foliar Fungal Endophyte Communities and Ecophysiological Traits of CAM and C3 Epiphytic Bromeliads in a Neotropical Rainforest. Diversity 2020, 12, 378

In the original article [...]

Relationships between Foliar Fungal Endophyte Communities and Ecophysiological Traits of CAM and C3 Epiphytic Bromeliads in a Neotropical Rainforest

Vascular epiphytes contribute up to 35% of the plant diversity and foliar biomass of flowering plants. The family Bromeliaceae is a monophyletic group of plants native to the Neotropics. Epiphytic bromeliads form associations with distinct groups of organisms but their relationship with foliar fungal endophytes remain underexplored. In this study we examined the relationship of foliar fungal endophytes to host photosynthetic pathways and associated ecophysiological traits. We sampled the fungal endophyte communities of 67 host individuals in six epiphytic bromeliad species differing in C3 and crassulacean acid metabolism (CAM) photosynthetic pathways. We tested whether endophyte assemblages were associated with ecophysiological leaf traits related to host photosynthetic pathways. Our results indicate that (1) C3 and CAM bromeliads host dissimilar endophyte assemblages, (2) endophyte communities in C3 bromeliads are characterized by variable relative abundances of fungal orders; conversely, CAM associated endophyte communities were characterized by consistent relative abundances of fungal orders, and (3) endophyte communities in bromeliads are distributed along a continuum of leaf toughness and leaf water content. Taken together, our study suggests that host physiology and associated ecophysiological traits of epiphytic bromeliads may represent biotic filters for communities of fungal endophytes in the tropics.