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Naglis, A.

Publications and source records attributed to Naglis, A..

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Species richness and trait diversity show parallel island-biogeographic patterns across Australian islands

Island biogeography is the theoretical and empirically validated expectation that an islands biodiversity is ultimately limited by its size and isolation, with larger and less isolated (from mainland communities) islands supporting greater diversity. Island biogeography is generally applied to simple metrics of diversity such as species richness (number of different species); however, fewer studies have used traits to measure biodiversity. An organisms traits -- e.g., body mass, age at sexual maturity, trophic level -- can be used to measure biodiversity and understand how ecological communities function. We quantified species richness for birds, mammals, reptiles, and amphibians, and functional diversity for birds and mammals (for which sufficient trait data were available), and tested whether this diversity can be predicted using the theory of island biogeography. We identified 9,103 Australian islands, of which 1,661 had at least one (native and/or non-native) non-marine species present according to the Atlas of Living Australia. As expected, tetrapod species richness (S) increased with island area (A) (z = 0.299 {+/-} 0.012) following a typical power-law relationship (i.e., S = cAz, where z = 0.2-0.4), but was not predicted by distance from mainland -- consistent with the pattern observed on other recently (< 10,000 years) isolated continental islands. We found that trait richness increased at the same rate with island area as species richness for mammals, but for birds, trait richness increased more slowly than species richness. Trait turnover increased modestly with inter-island distance, whereas trait nestedness was unrelated to distance. Trait richness increased strongly with species richness in both birds and mammals, and island area and isolation explained no additional variation in functional richness after accounting for species richness. These results indicate that island geography influences functional diversity primarily through species accumulation, rather than through direct effects on occupied trait space. Overall, the trait space of smaller islands tended to be nested within that of larger, nearby islands; the main differences among similar-sized islands are due to turnover (change in species/trait combinations among assemblages), and the effects are more pronounced in mammals compared to birds. We also found evidence for an asymptotic relationship between trait and species turnover in both birds and mammals, suggesting close coupling between taxonomic and functional turnover, with some saturation of trait turnover at high species turnover. Large islands that are simultaneously more isolated might offer conservation advantages by reducing the influence of threatening processes on the mainland if distance limits access of people and invasive species.

ecology↗

Retinal electrical synapse plasticity is required for optimal visual performance

Most electrical synapses in the mammalian central nervous system are composed of Connexin 36 (Cx36). Electrical synapses are functionally plastic, changing their degree of coupling based on the activity of the cell or connected cells, or based on activation of neurotransmitter or neurohormone receptors. Plasticity can reach an extreme in which electrical synapses become functionally silent, which is a normal operational condition for some circuits. Cx36 coupling is regulated by phosphorylation, which opens the channels. In retinal circuits, Cx36 is often maintained in a poorly phosphorylated, poorly coupled state. We reasoned that phosphomimetic mutants of Cx36 could remain constitutively open and maintain circuits in a well-coupled state that will interrogate the need for plasticity. We developed a constitutively open Cx36 mutant by systematically replacing phosphorylatable residues that regulate coupling with acidic residues. Single mutants of serine 315 significantly modified functional regulation of coupling in HeLa cells, but mutation of four residues was required to produce a mutant that was constitutively open. This mutant, Cx36-S110D, T111E, S293D, S315D, called Cx36-DEDD, displayed high coupling in control conditions and only modest changes under phosphorylating and dephosphorylating conditions. We developed a conditional knockin mouse that expresses Cx36-DEDD and cytoplasmic tdTomato in cells that expressed Cre recombinase. When crossed with Six3-Cre mice, Cx36-DEDD expressed widely in the retina including in photoreceptors, bipolar, amacrine and ganglion cells. Rod-cone electrical coupling displayed the maximum of its physiological dynamic range, and photopic visual acuity and contrast sensitivity were significantly reduced in Cx36-DEDD homozygous animals. We conclude that reduction of coupling in some retinal circuits is required for optimal daylight vision. Significance StatementTwo types of synapses, chemical and electrical, work together throughout the central nervous system to perform neurological functions. While it is widely understood for chemical synapses that plasticity, changing the strength of synaptic connections, plays critical roles in many processes, this is far less understood for electrical synapses. By developing an electrical synapse protein mutant that locks channels in an open state, we have investigated retinal circuits that retain functional electrical synapses but lack their latitude for plasticity. This perturbation significantly compromises visual acuity and contrast sensitivity in the daylight, revealing that electrical synapse plasticity is necessary to tune retinal functions for optimal performance. Thus, electrical synapse plasticity along with chemical synapse plasticity is required for neural function.

neuroscience↗