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Bioerosion

Bioerosion is the breakdown of hard substrates, such as rocks, corals, shells, and bones, by living organisms through mechanical and chemical processes.^[1] This ecological process involves the removal or dissolution of mineral material, primarily calcium carbonate in marine settings, and occurs across diverse environments including oceans, freshwater systems, and terrestrial landscapes.^[2] It plays a pivotal role in shaping habitat structure, influencing biodiversity, and facilitating biogeochemical cycling by recycling essential nutrients like calcium and carbon.^[2]^[3] The mechanisms of bioerosion are broadly categorized into mechanical and chemical actions, often acting in concert. Mechanical bioerosion includes grazing by herbivores, such as parrotfishes and sea urchins, which scrape or bite away substrate surfaces, and boring by macroorganisms like sponges and bivalves that excavate tunnels through physical drilling or wedging.^[1] Chemical bioerosion, conversely, relies on the secretion of acids or enzymes by microborers—including algae, fungi, and bacteria—to dissolve minerals at a microscopic scale.^[1] These processes can erode substrates at rates ranging from microns per year in stable environments to over a meter per year in high-activity zones, such as those influenced by nutrient enrichment.^[1] In coral reef ecosystems, bioerosion is particularly significant, maintaining a dynamic balance with calcification to sustain reef growth and structure.^[4] Organisms like excavating sponges and lithophagine bivalves not only sculpt reef frameworks but also contribute to carbonate recycling, which supports overall ecosystem productivity in shallow, tropical waters.^[4]^[3] However, anthropogenic pressures such as ocean acidification and eutrophication are intensifying bioerosion rates, potentially shifting reefs from net producers to net losers of calcium carbonate and threatening their resilience.^[2]^[5] This interplay underscores bioerosion's dual role as both a natural shaper of ecosystems and a vulnerability amplifier under global change.^[6]

Definition and Overview

Definition

Bioerosion is defined as the removal of consolidated mineral or lithic substrates—such as rock, coral, and shells—by the direct action of living organisms.^[7] This process encompasses the breakdown of hard materials through biological means, representing a key ecological interaction between organisms and their geological environment.^[8] In distinction from abiotic erosion processes, bioerosion requires active biological agency, where organisms drive the mechanical removal or chemical dissolution of substrates, often in synergy with physical or chemical factors but fundamentally initiated by life forms.^[1] Physical erosion involves non-biological mechanical forces like wave action or wind abrasion, while chemical erosion relies on inorganic reactions such as acid dissolution; bioerosion, by contrast, integrates organismal behavior and physiology as the primary drivers.^[9] Bioerosion is most prominent in marine contexts, including coral reefs and limestone coasts, where it shapes seafloor topography and carbonate structures, though it also occurs in terrestrial environments such as soil crusts and rock surfaces affected by root penetration.^[10] The process spans scales from microscale activities, like those of phototrophic endoliths creating fine etchings, to macroscale impacts, such as large borers excavating substantial cavities in substrates.^[8]

Historical Development

Early observations of bioerosion trace back to the 19th century, when naturalists documented the erosive activity of organisms such as sponges on coral reefs, recognizing their role in breaking down hard substrates into smaller particles. These accounts laid the groundwork for understanding biological contributions to reef degradation, though systematic study remained limited until the mid-20th century. The formalization of bioerosion as a scientific concept occurred in the 1960s, with A. Conrad Neumann coining the term in 1966 to encapsulate the processes by which organisms mechanically and chemically erode indurated substrates, particularly in marine environments like coral reefs.^[1] This definition shifted focus from purely physical erosion to the integral role of living agents, enabling quantitative assessments of reef dynamics. Subsequent early works, such as those by L.R. Pomeroy on nutrient cycling and ecosystem processes at Enewetak Atoll in 1960, indirectly highlighted bioerosion's links to productivity and substrate turnover.^[11] In the 1970s, research advanced through ichnological studies that connected trace fossils to specific bioeroding organisms, exemplified by R.G. Bromley's 1970 analysis of borings as trace fossils, including the Cretaceous example Entobia cretacea, which established bioerosion traces as reliable indicators of ancient ecological interactions.^[12] This period marked a milestone in paleoecology, integrating fossil evidence with modern observations. By the late 1970s, M.J. Risk and J.K. MacGeachy quantified bioerosion rates on Caribbean reefs, demonstrating spatial variations and the dominance of internal borers.^[13] The 1980s and 1990s saw expanded focus on bioerosion within reef ecology, particularly following mass bleaching events, as explored by P.W. Glynn in studies of the eastern Pacific, where post-1982–83 El Niño bioerosion accelerated framework collapse, reducing reef accretion by over 50% in affected areas. These investigations emphasized bioerosion's role in balancing calcification and its intensification under disturbance. In the post-2000 era, attention shifted to climate interactions, with J.K.H. Fang et al. (2013) showing that ocean warming and acidification could increase sponge bioerosion rates under projected conditions, threatening net reef growth.^[14] This trend culminated in broader conceptual frameworks, such as Davidson et al. (2018), which integrate bioerosion responses to global change, predicting amplified habitat loss and altered biogeochemical cycles in warming oceans.^[2] Since 2020, research has intensified on bioerosion's responses to multiple climate stressors, with studies indicating that warming beyond 2 °C could lead to net erosional states on over 70% of tropical western Atlantic reefs by 2040, exacerbating sea-level rise vulnerabilities and highlighting the need for integrated management strategies.^[15] Recent reviews as of 2023 emphasize advances in understanding bioerosion under human-induced impacts like ocean acidification and eutrophication.^[6]

Types and Mechanisms

Mechanical Processes

Mechanical processes in bioerosion refer to the physical breakdown of hard substrates, such as coral skeletons and limestone, through direct mechanical actions by organisms, distinct from chemical dissolution. These processes primarily involve surface removal or internal excavation that erodes material without altering its chemical composition, often resulting in the production of fine sediments like sand or silt. Key mechanisms include grazing, boring, and rasping, which are prevalent in marine environments, particularly on coral reefs, where they balance or exceed calcification rates under certain conditions.^[16] Grazing entails the scraping of substrate surfaces by herbivorous organisms to access attached algae and biofilms, thereby removing thin layers of calcium carbonate. Parrotfish (Scaridae) employ fused beak-like teeth and a pharyngeal mill to rasp away epilithic communities, eroding dead coral and occasionally live tissue at rates averaging 1.88 kg m⁻² yr⁻¹ on exposed fringing reefs. Sea urchins, such as Echinometra mathaei, use their Aristotle's lantern—a grinding jaw apparatus—to scrape and abrade surfaces, contributing approximately 0.52 kg m⁻² yr⁻¹ to bioerosion in similar settings. These rates, equivalent to roughly 0.2–0.7 mm yr⁻¹ assuming typical carbonate densities of ~2.7 g cm⁻³, highlight grazing as a dominant external mechanical force on reefs.^[16] Boring and rasping involve internal mechanical excavation, where organisms create tunnels or chambers by abrading the substrate with specialized appendages. Date mussels (Lithophaga lithophaga) mechanically chisel and rasp rock using foot movements and shell valves, often after minor initial weakening, at erosion rates up to 350 g CaCO₃ m⁻² yr⁻¹ in high-density populations. Sipunculan worms (e.g., Aspidosiphon spp.) similarly abrade calcareous substrates with proboscis and body undulations, forming cylindrical burrows that contribute to minor but cumulative material loss. These actions produce discrete borings that facilitate sediment ejection as fine particles.^[17] Initial mechanical borings and grazes weaken substrate integrity by increasing porosity, creating self-reinforcing cycles where fragmented pieces become more vulnerable to wave action and further biological or physical erosion. This structural compromise accelerates overall breakdown, potentially shifting reefs toward net erosion in disturbed environments.^[3]

Chemical Processes

Chemical processes in bioerosion involve the secretion of acidic substances and enzymatic activities by organisms that dissolve calcium carbonate substrates, facilitating the breakdown of marine structures such as coral reefs. These mechanisms primarily target the chemical dissolution of minerals like aragonite and calcite, often occurring within the substrate where organisms create localized low-pH microenvironments. Unlike purely mechanical actions, chemical bioerosion relies on biochemical reactions that weaken the structural integrity of the material, making it more susceptible to further degradation. Acid secretion is a key mechanism employed by macroboring organisms such as clionaid sponges (e.g., Cliona spp.) and certain polychaete worms. In sponges, specialized cells, including collencytes and vacuolated cells, produce and transport acids—potentially including carbonic and organic acids—via enzymes like carbonic anhydrase and acid phosphatase, creating pH drops to as low as 5.0 at the tissue-substrate interface to etch fine fissures in calcium carbonate. Polychaete worms, such as those in the family Spionidae, secrete acid mucopolysaccharides from ventral epithelium and mucus glands, which dissolve carbonate by lowering local pH and softening the substrate for burrow formation. These secretions enable precise chemical excavation, with dissolution rates measured through increases in seawater alkalinity during incubation experiments.^[18] Enzymatic dissolution is prominent among microbial phototrophs, particularly endolithic cyanobacteria (e.g., Mastigocoleus testarum and Ostreobium quekettii), which penetrate substrates to depths of several millimeters. These organisms utilize metabolic byproducts from photosynthesis and respiration, including ATPase-driven proton pumps, to generate undersaturated conditions that promote mineral dissolution; for instance, active transport of calcium ions away from the boring front lowers local pH and facilitates etching. This process is exclusively chemical for microborers, with rates increasing by 50-100% under elevated pCO₂ levels due to enhanced enzymatic efficiency in acidified conditions. Passive facilitation occurs as bioeroders expose fresh substrate surfaces to ambient seawater, accelerating abiotic chemical dissolution by increasing reactive surface area; microboring networks can elevate this area by 10-100 times through micropits and tunnels, thereby amplifying overall erosion without direct organismal activity. Synergistically, chemical processes often precede mechanical removal, as initial dissolution creates weakened chips or fissures that are more easily dislodged, resulting in combined bioerosion rates far exceeding either process alone—for example, in sponges where chemical etching accounts for 10-30% of total erosion but enables efficient mechanical expulsion of particles.

Organisms and Agents

Macroborers

Macroborers are larger organisms, typically exceeding 0.5 mm in size, that excavate visible borings into calcareous substrates such as coral, limestone, and mollusk shells through mechanical, chemical, or combined means. These multicellular endoliths include bivalves, sponges, and polychaetes, which create tunnels, chambers, or spirals by physical abrasion, chemical dissolution, or a combination thereof, contributing significantly to substrate breakdown.^[19] Among the key groups, bivalves of the genus Lithophaga, such as L. lithophaga, are prominent macroborers that attach to substrates using byssal threads and excavate club-shaped burrows primarily through chemical dissolution via secretions from pallial glands. These bivalves can reach lengths of up to 90 mm and produce burrows up to 5 cm long, with boring depths extending to 10 cm in limestone. Growth rates are slow, approximately 0.5-1 mm per year, allowing individuals to persist for decades while progressively deepening their excavations.^[19]^[20] Boring sponges, exemplified by Cliona celata, form extensive chambered networks within substrates by chemically etching the substrate with acids and enzymes, followed by mechanical removal of the etched chips to create interconnected galleries. These sponges create visible papillae on the surface for water flow and can bore to depths of 5-10 cm, with networks expanding over time. In some cases, C. celata accounts for up to 75% of macroborer activity on dead coral branches after several years of exposure.^[19]^[21] Polychaetes, such as species in the genus Dodecaceria (e.g., D. concharum), produce characteristic spiral or U-shaped borings by using their chaetae for mechanical scraping. These tube-dwelling worms form pouch-like tunnels typically 2-3 cm deep, often dominating early stages of bioerosion on dead corals. Their excavations are narrower than those of bivalves or sponges but proliferate rapidly in suitable substrates.^[19]^[22] Macroborers inhabit a range of environments, including tropical coral reefs and temperate rocky shores, where they preferentially colonize dead or stressed calcareous structures. On coral reefs, densities vary widely, reaching 100-500 individuals per m² on massive Porites colonies, with higher abundances in eutrophic waters near river mouths or in deeper zones (7-9 m). In temperate settings like Mediterranean rocky shores, they thrive on limestone outcrops and archaeological substrates.^[20]^[19]^[21] These organisms contribute to bioerosion by generating coarse carbonate sediments through the fragmentation of bored material, which accumulates as rubble or sand on reef flats. Their excavations also weaken structural integrity, promoting the collapse of substrates like coral branches or rock faces, with total erosion rates from macroborers reaching up to 2 kg CaCO₃ m⁻² year⁻¹ in some reef systems.^[21]^[19]

Microborers and Other Agents

Microborers are microscopic organisms, typically smaller than 0.5 mm, that penetrate carbonate substrates such as coral skeletons and mollusc shells through chemical and enzymatic mechanisms, forming intricate tunnel networks.^[23] Among these, endolithic fungi, such as dikaryomycotan anamorphs, play a key role by releasing proteolytic enzymes that break down organic matrices within the substrate, facilitating dissolution of calcium carbonate.^[24] Bacteria, including cyanobacteria, contribute similarly by producing organic acids that etch surfaces, often colonizing upper photic zones where light supports their activity.^[24] The green alga Ostreobium quekettii exemplifies algal microborers, forming dense filamentous networks that penetrate substrates via chemical dissolution at the hyphal tips, achieving colonization rates up to 100% within 1–3 months in coral skeletons.^[23] Grazers, including echinoids and certain fish, act as surface-dwelling agents by mechanically removing thin layers of carbonate material during feeding, distinct from internal boring but contributing significantly to overall erosion. Sea urchins like Diadema setosum scrape algal-covered surfaces, with individual daily bioerosion rates ranging from 0.20 g to 1.57 g of CaCO₃, varying by size and location.^[25] Parrotfish (Scaridae), such as Sparisoma viride, graze on epilithic algae while ingesting substrate, with large individuals eroding up to 534 g of CaCO₃ per day through repeated bites that abrade skeletal material.^[26] These activities expose fresh surfaces for further colonization by microborers. Other agents include encrusting organisms that promote erosion through attachment and physical wedging. Barnacles (Cirripedia) attach firmly to substrates via adhesive cements, exerting mechanical stress that can wedge and fracture carbonates, while some species actively bore shallow chambers.^[27] Bryozoans, particularly endolithic forms, dissolve carbonate during settlement and colony growth, contributing to bioerosion by creating dissolution traces in reef frameworks.^[28] In terrestrial settings, endolithic lichens produce chemical corrosion via oxalic acid excretion, forming linear grooves and pits on exposed calcareous substrates like fossil bones.^[29] Microbes among these agents often rely on chemical dissolution, such as acid production, to initiate penetration.^[3] These microborers and agents are ubiquitous in photic zones, where light enables photosynthetic forms like Ostreobium, with higher densities in warm, tropical waters due to enhanced metabolic rates.^[23] In carbonates, microborer networks can reach densities of up to 10⁶ tunnels per cm², creating extensive porosity that amplifies erosion over time.^[30]

Ecological and Environmental Impacts

Effects on Marine Ecosystems

Bioerosion significantly alters habitats in marine ecosystems, particularly coral reefs, by eroding calcium carbonate structures and reducing overall structural complexity. This process weakens reef frameworks, increasing their porosity and susceptibility to physical breakage, which can lead to the collapse of branching corals and a flattening of reef profiles. While moderate bioerosion creates cavities and microhabitats that shelter smaller fish, invertebrates, and algae, excessive rates diminish the three-dimensional architecture essential for diverse assemblages, as observed in post-disturbance scenarios where erosion rates reach 10-40 kg CaCO₃ m⁻² yr⁻¹.^[31] In terms of biodiversity, bioerosion maintains ecological balance by counteracting calcification, preventing overgrowth while generating fine sediments that support additional habitats such as seagrass beds and beaches. On coral reefs, this sediment production, driven by macroborers like parrotfish and excavating sponges, averages 1-5 kg CaCO₃ m⁻² yr⁻¹ in many systems, with peaks up to 9.1 kg CaCO₃ m⁻² yr⁻¹ from large parrotfish species, thereby promoting nutrient-rich substrates for benthic organisms and facilitating larval settlement. These dynamics enhance species diversity under equilibrium conditions, though imbalances can reduce habitat availability for reef-associated biota.^[31]^[32] Geomorphically, bioerosion regulates net reef accretion by removing carbonate material at rates that, in healthy reefs, align with construction to sustain framework growth at 3-5 kg CaCO₃ m⁻² yr⁻¹. However, in overfished areas, the removal of predators allows herbivorous urchin populations to surge, accelerating erosion to levels that exceed production—such as 2 G (g cm⁻² yr⁻¹) or more—resulting in framework degradation and a transition from net accretion to net erosion, which compromises long-term reef stability.^[31]^[32] Bioerosion also influences trophic interactions by connecting herbivores to primary producers, as grazing activities recycle essential nutrients back into the system. For instance, parrotfish bioerosion through substrate scraping not only controls algal overgrowth but releases nutrients via fecal pellets, boosting primary productivity and supporting the broader food web in coral reef ecosystems.^[33]

Influences from Climate Change

Ocean acidification, driven by increasing atmospheric CO₂ levels, lowers aragonite saturation states in seawater, which enhances chemical bioerosion processes by making calcium carbonate structures more susceptible to dissolution.^[34] Studies on the bioeroding sponge Cliona orientalis in the Great Barrier Reef demonstrate that bioerosion rates can increase by 17% under moderately elevated pCO₂ levels (571 µatm) and up to 61% under strongly elevated conditions (1410 µatm), relative to present-day levels.^[34] Similarly, microbioerosion by endolithic communities on coral skeletons such as Porites cylindrica and Isopora cuneata rises by 46–89% under combined acidification and warming scenarios projecting pCO₂ increases of 610 µatm and temperature rises of 4°C.^[35] Ocean warming exacerbates mechanical bioerosion by altering grazer populations and behaviors, often leading to outbreaks following coral bleaching events.^[36] In Hawaiʻi, post-bleaching coral mortality and overfishing have triggered urchin (Tripneustes gratilla) population surges, suppressing net reef growth through intensified bioerosion rates exceeding 1 kg CaCO₃ m⁻² yr⁻¹ in shallow areas.^[37] Warmer conditions disrupt the balance between herbivore densities and benthic cover, promoting higher grazer abundances that accelerate skeleton breakdown.^[36] These climate stressors interact synergistically, with acidification weakening coral skeletons and thereby amplifying the impacts of borers and grazers.^[5] Nutrient enrichment from land-based pollution further magnifies this effect, as seen in studies where eutrophication combined with lowered pH boosts micro- and macro-bioerosion, potentially shifting reefs from net accretion to net erosion.^[5] Projections under a low-emission scenario (RCP2.6) indicate that global coral reef net carbonate production could decline by 71% by 2050, primarily due to reduced coral cover from bleaching, with minor contributions from changes in bioerosion and calcification.^[38] In vulnerable regions, this could result in 70–90% loss of live coral cover by mid-century without stringent mitigation.^[39] Studies on the Great Barrier Reef, including experiments with Cliona orientalis, indicate that bioerosion rates are projected to increase under future ocean acidification and warming conditions.^[34] The 2024 mass bleaching event on the Great Barrier Reef, the most severe on record and the fourth in eight years, resulted in 14-30% coral cover losses regionally (up to 70% on some individual reefs), increasing vulnerability to bioerosion by exposing dead skeletons to borers and grazers, and further threatening reef frameworks as of 2025.^[40]

Measurement and Research

Methods of Assessment

Field methods for quantifying bioerosion primarily rely on gravimetric analysis, which measures the weight loss of carbonate substrate blocks deployed in situ over extended periods to capture cumulative erosion effects. Limestone tiles or coral cores, typically standardized in size and composition, are placed on reef substrates or racks at various depths and retrieved after 1–2 years to assess mass reduction attributable to boring organisms, with controls accounting for physical dissolution or encrustation. This approach isolates biological contributions by comparing initial and final dry weights after cleaning and drying, providing a direct proxy for total bioerosion volume loss.^[41]^[42] Imaging and microscopy techniques enable detailed visualization and measurement of internal boring structures, particularly through computed tomography (CT) scans and scanning electron microscopy (SEM). Micro-CT (μCT) scans, with resolutions down to 50 μm voxels, allow non-destructive 3D reconstruction of tunnels and cavities by segmenting high-porosity regions within substrates, quantifying boring volumes and distinguishing active from legacy erosion via pre- and post-deployment comparisons. SEM complements this by revealing fine-scale surface features and microborer traces at magnifications up to 10,000×, facilitating identification of agent-specific patterns. Ichnological tracing extends these methods to fossil borings, where trace fossils (ichnofossils) like Oichnus or Scolecia are cataloged morphologically to infer past bioerosion intensity and diversity without direct organismal evidence.^[43]^[44]^[45] Experimental approaches in controlled settings help disentangle bioerosion from abiotic factors, such as deploying caged versus uncaged substrates to exclude macro-grazers like fish or urchins while permitting micro- and endolithic activity. Caged blocks, often mesh-enclosed, are compared to open exposures over months to years, revealing bioerosion dominance in protected setups (e.g., higher internal boring in cages) versus combined physical-biological loss in uncaged ones, with differences analyzed via weight or volume metrics. Dye staining techniques, using DNA-specific fluorophores like DAPI, target active borers by highlighting nuclei in trace-making organisms within fresh substrates, enabling differentiation of live versus inactive erosion paths under fluorescence microscopy.^[46]^[47] Quantitative metrics standardize these assessments, expressing erosion rates as linear penetration (mm/year) for surface or tunnel depth, percentage volume loss (% of substrate), or mass flux (kg m⁻² year⁻¹) derived from gravimetric or volumetric data, with skeletal density (e.g., 1.57 g cm⁻³) applied for conversions. For instance, μCT-derived volume loss is normalized by surface area and deployment time to yield rates like 0.5–1 mm/year on limestone surfaces. These metrics integrate with calcification models in reef budget frameworks, subtracting bioerosion from production rates (e.g., coral growth in mm/year) to estimate net accretion, often revealing balances where erosion offsets up to 50% of framework building in vulnerable systems.^[44]^[1]^[48]

Key Studies and Findings

Pivotal studies on Indo-Pacific coral reefs have established that bioerosion rates typically range from 0.5 to 2 mm per year, often balancing calcification rates of 1 to 3 mm per year under natural conditions, thereby maintaining net reef accretion. These findings, initially detailed in seminal work on biological destruction processes, have been corroborated and refined through ongoing research up to the late 2010s, emphasizing the role of macro- and microborers in sculpting reef frameworks.^[3] Global patterns reveal significantly higher bioerosion rates in tropical regions compared to temperate zones, with tropical rates up to five times greater due to elevated biodiversity and metabolic activity of eroders. For instance, in the Caribbean, post-hurricane studies following events like Hurricane Allen in 1980 documented surges in boring sponge populations colonizing freshly dead coral skeletons, accelerating structural degradation by up to several-fold within years.^[3]^[49] Recent advances include frameworks integrating bioerosion dynamics with climate models, projecting enhanced erosion under ocean acidification scenarios, as outlined in analyses of environmental drivers on reef budgets. Complementary mesocosm experiments have demonstrated microborer dominance in acidified conditions, with bioerosion rates increasing by 50-100% at elevated pCO₂ levels (>750 ppm), primarily driven by euendolithic algae and fungi. Post-2020 developments, such as 2023-2025 studies using airborne imaging spectroscopy and advanced μCT for large-scale assessments, have further quantified erosion in dynamic environments, highlighting sea urchin contributions and net erosional shifts in warming reefs.^[3]^[35]^[6]^[50]^[16]^[15] Despite these insights, notable knowledge gaps persist, particularly in terrestrial bioerosion processes on carbonate landscapes, which remain understudied relative to marine systems. Additionally, there is a critical need for expanded long-term monitoring networks to track bioerosion responses in rapidly changing ocean environments influenced by multiple stressors.^[51]^[3]

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[42]
Quantifying attributes of boring bivalve populations in corals using ...
Sep 23, 2024 · Bioerosion plays a crucial factor in shaping the structure and function of coral reef ecosystems, with bioeroders actively altering both the ...
[43]
A Novel μCT Analysis Reveals Different Responses of Bioerosion ...
Apr 13, 2016 · Using before and after scans allows for the removal of any pre-existing boring scars ... While before and after μCT scans do cost more than single ...
[44]
Ichnotaxobases for bioerosion trace fossils in bones
Jul 14, 2015 · Bioerosion trace fossils in bones are defined as biogenic structures that cut or destroy hard bone tissue as the result of mechanical and/or ...
[45]
Cross-shelf differences in the pattern and pace of bioerosion of ...
Aug 10, 2025 · The averaged tunnel ingress had statistically significant differences between uncaged and caged carcasses overall (p-value=0.02). Results of ...
[46]
Bioerosion along a bathymetric gradient in a cold-temperate setting ...
Aug 7, 2025 · Among the tested methods, specific staining with dyes against the DNA (nuclei) of the trace making organisms turned out to be a useful and ...
[47]
Improving estimates of coral reef construction and erosion with in ...
Apr 25, 2019 · The decline in living coral since the 1970s has conspicuously slowed reef construction on a global scale, but the related process of reef ...
[48]
Growth Rate of Jamaican Coral Reef Sponges After Hurricane Allen
These were determined from the size of individual sponges growing on the coral rubble that was deposited when Hurricane Allen struck the north coast of Jamaica ...Missing: bioerosion | Show results with:bioerosion
[49]
Reconceptualising the role of organisms in the erosion of rock coasts
Firstly, we reconceptualise the biological contributions to erosion of rock coasts into direct and facilitative types, and secondly we discuss the need for more ...