Biology subjects

Ziegler, M.

Publications and source records attributed to Ziegler, M..

At least 19 recordsLinked to original sources

bioRxiv2026

Optimization of Gadolinium-Based Contrast Agent Protocols for Reliable Ex Vivo Diffusion-Weighted Imaging in the Avian Brain

Ex vivo diffusion weighted imaging (DWI) enables high-resolution characterization of brain connectivity and is increasingly applied in comparative and evolutionary neuroscience. However, variability in tissue preparation and contrast agent exposure can substantially affect relaxation properties and compromise reproducibility, particularly in non-mammalian species. Here, we systematically assess the impact of different gadolinium-based contrast agent exposure protocols on relaxation stability and DWI compatibility in fixed pigeon brains. Brains were perfusion-fixed with 2% paraformaldehyde and assigned to four preparation protocols: (i) contrast agent exposure during perfusion, post-fixation, and rehydration; (ii) post-fixation and rehydration only; (iii) rehydration only; (iv) no contrast agent. Quantitative T1, T2, T2*, and DWI data were acquired at five time points over 70 days using a 7T MRI system. Protocols involving contrast agent during perfusion or post-fixation produced comparable relaxation trajectories, with T1, T2, and T2* stabilizing by Day 13. On day 13 the T1 values of tissue that was exposed to contrast agent, regardless of the application protocol were between 230.86 ms and 266.89 ms, while the T1 values of the control group were over 1100 ms at this point in time. T2 values of the experimental groups were between 39.97 ms and 56.17 ms while T2 values of the control group were between 58.68 ms and 77.82 ms. T2* values of the experimental groups were between 27.27 ms and 43.33 ms while T2* values of the control group were between 46.16 ms and 65.93 ms. Importantly, contrast agent exposure during rehydration alone resulted in equivalent stabilization after two weeks, reflecting gradual contrast agent diffusion into the tissue. In contrast, control samples without contrast agent exhibited significantly elevated T2 and T2* at later time points. These results demonstrate that post-fixation contrast agent exposure during rehydration is sufficient to achieve stable relaxation parameters and DWI compatibility, assessed via fractional anisotropy (FA) and mean diffusivity (MD) in ex vivo avian brain tissue. This minimal preparation protocol enhances reproducibility, reduces handling complexity, and supports standardized cross-species neuroimaging of brain connectivity.

neuroscience↗

bioRxiv2026

Diversity, host-specificity, and environmental drivers of the coral reef eukaryome

Coral reefs are among the most diverse ecosystems on Earth, yet the diversity and structure of their associated microeukaryotic communities remain poorly resolved. We characterized reef-associated eukaryomes across 113 reefs spanning the Pacific Ocean using more than 6,300 samples from corals, seawater, and sediments during the Tara Pacific expedition. We identified [~]121,000 eukaryotic ASVs, revealing one of Earths largest undocumented reservoirs of eukaryotic diversity; over 80% of the recovered diversity was previously undetected in global ocean surveys and fewer than 2% of sequences matched reference databases. Reef habitats supported highly distinct communities, with sediments and seawater harboring 20-40-fold higher richness than corals. Unexpectedly, coral-associated communities across 29 host lineages were consistently dominated by small metazoans, particularly demosponges and maxillopods, identifying these taxa as pervasive and previously unrecognized components of coral eukaryomes alongside Apicomplexa. Across the Pacific, eukaryome composition was strongly structured by environmental gradients, with thermal stress emerging as the primary driver of community turnover. Together, these results identify coral reefs as a globally important reservoir of hidden eukaryotic diversity and reveal the reef eukaryome as a sensitive indicator of ecosystem reorganization under climate change.

systems biology↗

bioRxiv2026

HIDDEN APICOMPLEXAN PARASITE DIVERSITY LINKS CORAL AND PLANKTON MICROBIOMES ACROSS REEF SEASCAPES

Parasitism is one of the most widespread trophic strategies in nature, though its diversity and ecological distribution in marine ecosystems remain poorly characterized. Apicomplexa are a major clade of obligate parasites best known for medically important taxa, yet their diversity and distribution in the ocean is still largely unresolved. Here, we used metabarcoding data from the Tara expeditions to investigate the diversity, distribution, and environmental drivers of Apicomplexa across coral reef ecosystems and adjacent oceanic habitats. By integrating samples spanning planktonic communities, coral tissues, and marine sediments across multiple oceanic regions, we substantially expand the known phylogenetic breadth of marine apicomplexans. Although apicomplexans were generally low in relative abundance, they were widely distributed across marine environments. Community composition differed markedly among habitats. Corallicolid lineages were consistently associated with coral hosts, whereas planktonic samples harbored a greater diversity of apicomplexans, dominated by crustacean-associated gregarines. Sediments contained particularly high apicomplexan richness, including several poorly characterized groups. Capitalizing on the pan-Pacific transect of the expedition, we resolved biogeographic patterns in apicomplexan diversity across ocean basins: tropical regions showed the highest overall diversity, while polar environments contained distinct apicomplexan assemblages not detected in other ocean biomes. Together, these results highlight the extensive and previously underappreciated diversity of marine Apicomplexa and demonstrate that integrating multiple marine biomes is essential for resolving the phylogenetic and ecological breadth of parasitism in the ocean.

genomics↗

bioRxiv2026

Ocean-scale transcriptomic analysis of corallicolids (Apicomplexa) reveals their ubiquity and molecular interactions with Pocillopora corals.

Corals are complex holobionts, encompassing numerous prokaryotes, viruses, and protists. This associated microbial community strongly influences coral health and its resilience to global ocean warming. Corallicolid apicomplexans are widespread coral-infecting parasites, yet their impact on the coral host remains poorly understood. This knowledge gap largely stems from the low abundance of these parasites in coral tissues, which makes them difficult to isolate and access to their genetic material. Here we analyzed nearly 1,000 Pocillopora coral colonies collected from 32 islands during the Tara Pacific expedition to identify the drivers of corallicolid prevalence and abundance. Corallicolids were detected in almost all Pocillopora colonies with variable relative abundances between islands. The high abundance of specific corallicolid populations correlates with seawater temperature and levels of host protein carbonylation. We used a large collection of 297 metatranscriptomes to assemble a corallicolid transcriptome and we identified apicomplexan parasite signature genes, including the GRA9 and PV2 confirming the close phylogenetic relationship with the family of Eimeriidae. Gene expression patterns indicate that the high abundance of corallicolids correlates with a high transcription of genes encoding apical complex proteins and genes involved in the control of host immune defenses. Overall, this study provides new insights into corallicolid biology and its interaction with the coral host by combining a newly generated transcriptome with a large-scale sampling of Pocillopora corals across the Pacific Ocean.

genomics↗

bioRxiv2026

Water-mediated productivity dynamics in shifting coral reef communities

Mass mortality of reef-building stony corals has driven widespread community shifts towards reefs dominated by soft corals and macroalgae. Although physical competition for space between these organisms plays an important role, non-contact water-mediated interactions have been proposed to modulate organismal performance and community functioning, yet their independent effects remain poorly resolved. Here, we experimentally tested the hypothesis that water-mediated interactions generate non-additive effects on community productivity, altering ecosystem functioning during phase shifts. Using two controlled incubation experiments with representative stony corals, soft corals, and macroalgae, we compared monoculture baseline productivity with mixed assemblages across a gradient of biomass ratios mimicking phase shift scenarios. We found that reductions in stony coral biomass led to community-level declines in photosynthesis and calcification that exceeded expectations based on monocultures, indicating emergent negative effects of community restructuring. However, these effects were strongly species-dependent, with some assemblages showing only minor deviations from expectations, whereas others exhibited pronounced productivity losses. At the species level, both stony corals reduced photosynthetic efficiency in mixed assemblages, while soft corals maintained efficiency across treatments. Macroalgal responses diverged, with one species exhibiting reduced and another increased photosynthetic efficiency in mixed communities. These species-specific physiological responses scaled up to explain community-level deviations from expected productivity, suggesting that gains in productivity by certain taxa can partially offset, but not fully compensate for, losses in coral-driven functions such as calcification. Together, our findings indicate that sublethal, water-mediated interactions can reorganize holobiont functioning and lead to changes in ecosystem productivity, independent of direct physical competition. By altering community-wide energy acquisition and carbonate production, such interactions may reinforce feedback loops that accelerate ecosystem phase shifts. We argue that incorporating water-mediated interaction effects into ecological theory and ecosystem models is essential for predicting the stability and recovery potential of coral reefs and other transitioning ecosystems under climate change.

systems biology↗

bioRxiv2025

Establishment of menthol bleaching protocols for six stony coral species

The mutualistic symbiosis between stony corals and unicellular algae of the family Symbiodiniaceae forms the base of coral reef ecosystems. However, anthropogenic stressors, such as rising seawater temperatures, cause a breakdown of the coral-algal symbiosis, so-called coral bleaching, which leads to mass mortalities and a rapid loss of coral reefs. To functionally disassemble the coral-algal symbiosis, corals have been artificially rendered aposymbiotic using temperature stress, DCMU, or menthol. As menthol has proven to be an efficient and gentle bleaching agent, we tested four menthol treatments with six commonly investigated stony coral species. The overarching aim was to establish a broadly efficient bleaching protocol as a guide for future investigations. Menthol-induced bleaching was traced with chlorophyll fluorescence and tissue color analyses over time and confirmed as final symbiont cell density two weeks after the last day of menthol treatment. Here we found that the coral species varied greatly in their menthol bleaching tolerance, underlining the importance of establishing bespoke bleaching approaches. Acropora muricata and Stylophora pistillata were efficiently bleached within two days of menthol exposure with symbiont cell reductions of 94 % to 98 %. For Galaxea fascicularis, Montipora digitata and Porites cylindrica, six days of menthol exposure proved most successful in reducing symbiont density by 92 to 97 %. While these coral species suffered no mortality, fragments of Pocillopora verrucosa died or suffered severe necrosis in most of the protocols, making the tested menthol treatments unsuitable for this species. We demonstrate that repeated menthol treatment at low concentrations renders most coral species aposymbiotic within few days without visual or physiological damage. Our study, therefore, provides a guideline for efficient and customized application of menthol bleaching treatments for future coral symbiosis research.

systems biology↗

bioRxiv2025

Achieving cell-type specific transduction with adeno-associated viral vectors in pigeons

Birds are valuable models for studying learning, cognition, song, and vision, yet tools for controlling and recording brain activity with millisecond precision remain underutilized in avian research. Advances in methods such as chemogenetics, optogenetics, and in vivo imaging have transformed rodent studies but require gene delivery techniques, like adeno-associated viruses (AAVs), in non-transgenic species. This study validates AAV tools for precise gene expression in pigeons. We identified AAV8 as a highly effective vector, demonstrating strong neuronal tropism and anterograde/retrograde transgene expression, while AAVretro was ineffective. The CaMKII promoter and mDLX enhancer enabled cell-type-specific expression, targeting predominantly excitatory and inhibitory neurons, respectively. Additionally, we established proof of concept for the expression of NpHR (a chloride pump) and demonstrated the functionality of conditional gene expression systems, including Cre/loxP and Tet-On/Tet-Off. These advancements expand the genetic toolkit for pigeons, facilitating precise manipulation of neural circuits and enabling future studies on complex avian behaviors and brain functions. By bridging molecular tools and avian neuroscience, this work paves the way for comparative and translational research, offering insights into the neural basis of cognition and sensory processing in birds.

neuroscience↗

bioRxiv2025

Coral skeletal cores as windows into past Symbiodiniaceae community dynamics

The symbiosis between the dinoflagellate Symbiodiniaceae family and reef-building corals underpins the productivity of coral reefs. This relationship facilitates the deposition of calcium- carbonate skeletons that build the reef structure thanks to the energy derived from photosynthesis. The loss of Symbiodiniaceae from coral tissues--resulting in coral bleaching--impedes coral growth and can lead to mass mortality if the symbiosis fails to recover. Given that Symbiodiniaceae communities are dynamic and can shift in response to environmental stressors in the decades- to centuries-long lifespan of coral colonies, understanding these changes is crucial. Although the reconstruction of Symbiodiniaceae communities from coral skeleton records has recently been demonstrated as feasible, no studies have yet assessed reconstructions across different species and locations. Here, we present an approach to use coral skeletons for reconstructing the Symbiodiniaceae community on decadal and centennial scales and resolving dynamics related with coral species and environmental history of sampling locations. For this, we used dated coral skeleton cores from Porites Iobata and Diploastrea heliopora, species commonly used as climate archives, sampled in Palau and Papua New Guinea. We also examined the effect of various DNA extraction protocols on community reconstruction. Here we show that the reconstructed Symbiodiniaceae communities significantly varied across all cores and DNA extraction methods, with decalcification-based protocols enhancing the retrieval of skeletal-bound DNA. Moreover, we observed distinct community dynamics related to the specific coral host and sampling location. Notably, associations of Symbiodiniaceae dynamics with past heat stress events were apparent in cores of both species from Palau. Our findings enable a deeper understanding of the temporal and spatial variability in Symbiodiniaceae communities, offering insights that may refine the use of paleobiological proxies in climate studies and reveal broader ecological trends and microbially-aided adaptation pathways in corals.

systems biology↗

bioRxiv2025

The Distribution of Nitric Oxide-Synthesizing Neurons and Soluble Guanylate Cyclase in the Pigeon Brain

Nitric oxide (NO) is a diffusible neuromodulator with roles in synaptic plasticity and memory flexibility, exerting its primary effects via the enzyme soluble guanylate cyclase (sGC). Despite its well-documented functions in mammals and insects, little is known about the neuroanatomical distribution and functional relevance of NO in birds, particularly in relation to dopaminergic systems. This study used histochemical and immunohistochemical techniques to map the distribution of NO-synthesizing neurons--identified by NADPH-diaphorase (NADPH-d) and nNOS activity--and their relation to sGC and tyrosine hydroxylase (TH)-positive dopaminergic pathways in the pigeon brain. We found extensive NADPH-d labeling throughout forebrain, midbrain, and hindbrain regions. Among TH-positive midbrain structures, the locus coeruleus exhibited high colocalization with nNOS, while moderate colocalization was seen in the ventral tegmental area substantia grisea centralis and substantia nigra. Notably, a significant proportion of sGC-positive neurons was targeted by TH and NADPH-d positive fibres in the pigeon NCL. Our findings support the potential for NO-dopamine interactions in avian species, reminiscent of memory-related mechanisms in Drosophila melanogaster, and contribute to an understanding of conserved pathways that may underlie flexible learning and memory processing during navigation or related tasks across vertebrates. This work also offers insight into comparative NADPH-d distribution among avian species, with implications for aging, spatial learning, and memory formation.

neuroscience↗

bioRxiv2025

Arrayed CRISPR/Cas9 Loss-Of-Function Screen in a Neuronal Model of Adaptor Protein Complex 4 Deficiency Identifies Modulators of ATG9A Trafficking

Biallelic loss-of-function variants in the adaptor protein complex 4 (AP-4) disrupt trafficking of transmembrane proteins at the trans-Golgi network, including the autophagy-related protein 9A (ATG9A), leading to childhood-onset hereditary spastic paraplegia (AP-4-HSP). AP-4-HSP is characterized by features of both a neurodevelopmental and degenerative neurological disease. To investigate the molecular mechanisms underlying AP-4-HSP and identify potential therapeutic targets, we conducted an arrayed CRISPR/Cas9 loss-of-function screen of 8,478 genes, targeting the druggable genome, in a human neuronal model of AP-4 deficiency. Through this phenotypic screen and subsequent experiments, key modulators of ATG9A trafficking were identified, and complementary pathway analyses provided insights into the regulatory landscape of ATG9A transport. Knockdown of ANPEP and NPM1 enhanced ATG9A availability outside the trans-Golgi network, suggesting they regulate ATG9A localization. These findings deepen our understanding of ATG9A trafficking in the context of AP-4 deficiency and offer a framework for the development of targeted interventions for AP-4-HSP.

cell biology↗

bioRxiv2025

Polycomb group proteins protect latent Kaposi sarcoma-associated herpesvirus from episome clearance and HUSH-dependent chromatin silencing

Kaposi sarcoma-associated herpesvirus (KSHV) is the causative agent of a number of human neoplasms. KSHV causes lifelong chronic infections by establishing persistent reservoirs of latently infected cells in which the viral double-stranded DNA genome is present in the form of an extrachromosomal episome. Polycomb group protein (PcG) mediated gene repression is detected early after entry of the CpG-rich and epigenetically naive viral DNA into the host nucleus. Here we show that the establishment and maintenance of KSHV latency is strongly influenced by Polycomb Repressive Complexes 1 and 2 (PRC1, and PRC2, respectively). Using a series of genetic deletion models, we dissect the functional interdependence of PRC1 and PRC2 on KSHV and identify KSHV episomes as a prime target for independent as well as collaborative de novo PRC recruitment. Loss of PRC function leads to a severely altered chromatin state on KSHV and we show that PRC mediated gene repression is not only preventing transcription of viral genomes but also protects KSHV episomes from detection by the human silencing hub (HUSH). Furthermore, we demonstrate that PRC complexes play an important role in ensuring episomal maintenance in dividing cells. Taken together, our results show that absence of PRC complexes creates a metastable state of KSHV latency and suggest early chromatinization as an integral step for KSHV latency establishment.

microbiology↗

bioRxiv2025

Spatiotemporal analysis of de novo KSHV infection using Crispr/Cas9-based 3D live cell imaging at single episome resolution

Kaposi Sarcoma-associated herpesvirus (KSHV) persists as a latent episome in infected cells. While the virus efficiently infects established cell lines and primary cells in vitro, the early events guiding establishment of latent infection and the dynamic interplay between viral episomes and host factors remain incompletely understood. Here, we describe the development and application of a CRISPR/Cas9-based 3D live cell imaging system capable of tracking single KSHV episomes in real-time. Our approach exploits the SunTag technology, wherein deactivated Cas9 (dCas9) molecules are fused to repetitive epitope arrays recognized by superfolder GFP-fused single-chain antibodies. By targeting these complexes to terminal repeat units of KSHV, we achieve high level signal amplification, allowing us not only to detect newly incoming viral genomes within the first hours of de novo infection, but also to follow their spatiotemporal trajectories through different stages of the viral lifecycle. Furthermore, to facilitate efficient generation of stable reporter cell lines, we adapted the transposon-based piggyBac system to combine all SunTag components into a single-vector targeting system (SunSeT). Using these systems, we demonstrate the ability to observe both transient and stable interactions between KSHV episomes and key cellular regulators, including the variant polycomb-repressive complex 1 (vPRC) component KDM2B and the innate immune sensor IFI16. Furthermore, our platform allows detailed visualization of episodic changes in episome localization, abundance and distribution during de novo and long-term infection, providing critical insights into how viral genome positioning and dynamics correlate with host subnuclear environments. Overall, our study introduces a robust and adaptable imaging platform to dissect the earliest events of KSHV infection. The ability to track viral episomes in living cells offers a powerful tool to advance our understanding of the spatial and temporal regulation of individual KSHV genomes, shedding light on fundamental mechanisms of herpesvirus latency and persistence.

microbiology↗

bioRxiv2024

RGB color indices as proxy for symbiont cell density and chlorophyll content during coral bleaching

Coral bleaching, the breakdown of the symbiosis between the coral host and endosymbiotic microalgae, is the main cause of widespread coral reef degradation. Current methods for assessing coral health based on visual appearance, such as the use of color reference cards, are limited by subjective human color perception and low resolution. Digital photography with RGB (Red, Green, Blue) color channel analyses offers a fast, non-invasive, and standardized alternative to estimate physiological parameters. However, the link between coral color and physiological parameters during bleaching may vary depending on the type of stressor. While such approaches are extensively used in plant studies, their application in estimating Symbiodiniaceae cell density and chlorophyll content in corals requires further attention. In this study, we analyzed the correlation between Symbiodiniaceae cell density and chlorophyll content across three coral species (Acropora muricata, Pocillopora verrucosa, and Stylophora pistillata) with 19 color indices derived from the RGB channels currently established as predictors of chlorophyll content in plants. Corals were exposed to three bleaching conditions (acute short-term and chronic long-term heat stress and menthol bleaching) to identify the best color indices for assessing coral health through image analysis. We found that the Red index had the strongest linear correlation with symbiont cell density and chlorophyll content across species (R2 up to 0.97), so that relative changes in this color index can be directly interpreted as corresponding changes in tissue parameters. To train a model that predicts symbiont densities of a distinct sample set using the Red index, we found 10 to 12 samples to be sufficient to achieve an accuracy of > 95 % of the models trained on the full datasets. This research contributes to improved image analysis as a reliable and non-invasive tool for monitoring, by providing guidelines for a systematic use of RGB data to interpret coral health.

ecology↗

bioRxiv2024

Unveiling novel conserved HIV-1 open reading frames encoding T cell antigens using ribosome profiling.

The development of ribosomal profiling (Riboseq) revealed the immense coding capacity of human and viral genomes. Here, we used Riboseq to delineate the first translatome of HIV-1 in infected CD4+ T cells. In addition to canonical viral protein coding sequences (CDSs), we identify 98 alternative open reading frames (ARFs), corresponding to small Open Reading Frames (sORFs) that are distributed across the HIV genome including the UTR regions. Using a database of HIV genomes, we observed that most ARF amino-acid sequences are likely conserved among clade B and C of HIV-1, with 8 ARF-encoded amino-acid sequences being more conserved than the overlapping CDSs. Using T cell-based assays and mass spectrometry-based immunopeptidomics, we demonstrate that ARFs encode viral polypeptides. In the blood of HIV-infected individuals, ARF-derived peptides elicit potent poly-functional T cell responses mediated by both CD4+ and CD8+ T cells. Our discovery expands the list of conserved viral polypeptides that are targets for vaccination strategies and might reveal the existence of viral microproteins or pseudogenes.

immunology↗

bioRxiv2024

Resolving Symbiodiniaceae diversity across coral microhabitats and reef niches

Dinoflagellates of the family Symbiodiniaceae are main symbionts of diverse marine animals. A large diversity of Symbiodiniaceae also occur beyond the bounds of their multicellular hosts, occupying environmental niches on coral reefs. The link between spatial diversity at ecosystem scale to microhabitats of Symbiodiniaceae within the coral holobiont are largely unknown. Using ITS2 amplicon sequencing, we compared Symbiodiniaceae communities across four environments (seawater, near-reef and distant sediments, and turf algae mats) and two coral microhabitats (tissue and mucus) on a coral reef in the Red Sea. Analysis of ITS2 sequences revealed that coral and environmental habitats were both dominated by the genera Symbiodinium, Cladocopium, and Durusdinium, but environmental habitats additionally harbored Fugacium, Gerakladium, and Halluxium. Each environmental habitat harbored a distinct Symbiodiniaceae community, with 14-27 % exclusive ITS2 sequences. Nonetheless, 17 ITS2 sequences were shared among all habitat types and were variants defining nearly half of the ITS2 type profiles used to further resolve Symbiodiniaceae identity of coral-based communities. Tissues and surface mucus layers of 49 coral colonies from 17 genera had largely identical Symbiodiniaceae communities. Together with the large difference between environmental Symbiodiniaceae communities and those in the mucus, our results indicate a clear barrier between host-associated and environmental Symbiodiniaceae communities marked by only few shared complete type profiles under normal conditions. It remains to be determined how Symbiodiniaceae community dynamics between coral microhabitats and environmental reservoirs change during coral bleaching events. Monitoring coral colonies after mucus sampling confirmed its suitability for repeated long-term monitoring of coral-associated Symbiodiniaceae communities.

systems biology↗

bioRxiv2024

Genome-resolved diversity and biosynthetic potential of the coral reef microbiome

Coral reefs are marine biodiversity hotspots that provide a wide range of ecosystem services. They are also reservoirs of bioactive compounds, many of which are produced by microbial symbionts associated with reef invertebrate hosts. However, for the keystone species of coral reefs--the reef-building corals themselves--we still lack a systematic assessment of their microbially encoded biosynthetic potential, and thus the molecular resources that may be at stake due to the alarming decline in reef biodiversity and cover. Here, we analysed microbial genomes reconstructed from 820 reef-building coral samples of three representative coral genera collected at 99 reefs across 32 islands during a two-year expedition throughout the Pacific Ocean (Tara Pacific). By contextualising our analyses with the microbiomes of other reef species, we found that genomic information was previously available for only 10% of the 4,224 microbial species overall and for less than 1% of the 645 species exclusively identified in Tara Pacific samples. We found reef-building coral microbiomes to be host-specific and their biosynthetic potential to rival or even surpass that found in traditional targets for natural product discovery, such as sponges and soft corals. Fire corals were not only particularly diverse in microbially encoded biosynthetic gene clusters (BGCs), but also in BGC-rich bacteria, including Acidobacteriota spp., which have been recently highlighted for their promising natural product repertoire. Together, this study unveils new candidate sources for bioactive compound discovery, prioritises targets for microbial isolation, and underscores the importance of conservation efforts by linking macro-organismal biodiversity loss to host-specific microbiomes and their biotechnological potential.

microbiology↗

bioRxiv2024

Thermal preconditioning modulates coral physiology and heat tolerance: A multi-species perspective

Global warming threatens reef-building corals by challenging their natural adaptive capacity. Therefore, interventions such as stress hardening by thermal preconditioning could become crucial for their survival. Stress-hardening approaches recognize that organisms living in thermally variable environments are better able to withstand marine heat waves. However, a systematic assessment of preconditioning effects on the baseline physiology and thermal tolerance across coral species is lacking. We assessed the changes of thermal tolerance in six stony coral species (Galaxea fascicularis, Porites rus, Acropora muricata, Montipora digitata, and Stylophora pistillata) in three thermal preconditioning treatments of stable-high 29 {degrees}C and variable-high 29 {degrees}C with a daily oscillation of {+/-} 1.5 {degrees}C, compared to corals in stable-ambient 26 {degrees}C. We quantified changes in photosynthetic efficiency and coral bleaching intensity before and after a short-term heat stress assay and up to 30 days later. Stress-hardening success after preconditioning was observed in nearly all preconditioned corals, but the increases in thermal tolerance were species-specific. The greatest increase was recorded in G. fascicularis and A. muricata, with stress responses reduced by over 80 %. In contrast, preconditioning regimes had minor effects on stress tolerance of S. pistillata, making it least receptive to this intervention. After 30 days, most stress-hardened species demonstrated higher survival and recovery rates than their conspecifics from the stable-ambient regime. Notably, both preconditioning regimes affected baseline physiology, especially in the branching species, as indicated by minor tissue paling and decreased photosynthetic efficiency. We conclude that implementing thermal stress hardening protocols will require careful consideration of the species-specific receptiveness and evaluation of the potential trade-offs that can be inflicted with the post-conditioning shifts in physiological baselines.

ecology↗

bioRxiv2024

Species identity and composition shape productivity of stony corals

Coral biodiversity has an enhancing but saturating effect on community productivity, however, the direct effects of neighbouring coral colonies on productivity remain poorly understood due to the complex interplay of biotic and abiotic factors. We set up a fully controlled aquarium experiment, in which we quantified the effects of species identity and composition on the productivity of nine stony coral species from three families. Baseline productivity and the response to neighbouring organisms strongly differed between species. Regardless of whether species increased or decreased productivity, the responses were consistently more pronounced and positive towards conspecific than heterospecific neighbours, indicating kin selection effects between closely related species. Species productivity in monoculture and productivity in polyculture were inversely correlated, with inherently less productive species overperforming in polyculture and vice versa. Our results highlight that contact-free interactions in marine animals shape biodiversity-productivity effects otherwise known from plant communities.

ecology↗