Adjacent Sites Research Articles

Biomimetic mercury immobilization by selenium functionalized polyphenylene sulfide fabric

Highly efficient decontamination of elemental mercury (Hg0) remains an enormous challenge for public health and ecosystem protection. The artificial conversion of Hg0 into mercury chalcogenides could achieve Hg0 detoxification and close the global mercury cycle. Herein, taking inspiration from the bio-detoxification of mercury, in which selenium preferentially converts mercury from sulfoproteins to HgSe, we propose a biomimetic approach to enhance the conversion of Hg0 into mercury chalcogenides. In this proof-of-concept design, we use sulfur-rich polyphenylene sulfide (PPS) as the Hg0 transporter. The relatively stable, sulfur-linked aromatic rings result in weak adsorption of Hg0 on the PPS rather than the formation of metastable HgS. The weakly adsorbed mercury subsequently migrates to the adjacent selenium sites for permanent immobilization. The sulfur-selenium pair affords an unprecedented Hg0 adsorption capacity and uptake rate of 1621.9 mg g−1 and 1005.6 μg g−1 min−1, respectively, which are the highest recorded values among various benchmark materials. This work presents an intriguing concept for preparing Hg0 adsorbents and could pave the way for the biomimetic remediation of diverse pollutants.

Oxygen Reduction Kinetics of Fe-N-C Single Atom Catalysts Boosted by Pyridinic N Vacancy for Temperature-Adaptive Zn-Air Batteries.

The design of temperature-adaptive Zn-air batteries (ZABs) with long life spans and high energy efficiencies is challenging owing to sluggish oxygen reduction reaction (ORR) kinetics and an unstable Zn/electrolyte interface. Herein, a quasi-solid-state ZAB is designed by combining atomically dispersed Fe-N-C catalysts containing pyridinic N vacancies (FeNC-VN) with a polarized organo-hydrogel electrolyte. First-principles calculation predicts that adjacent VN sites effectively enhance the covalency of Fe-Nx moieties and moderately weaken *OH binding energies, significantly boosting the ORR kinetics and stability. In situ Raman spectra reveal the dynamic evolution of *O2- and *OOH on the FeNC-VN cathode in the aqueous ZAB, proving that the 4e- associative mechanism is dominant. Moreover, the ethylene glycol-modulated organo-hydrogel electrolyte forms a zincophilic protective layer on the Zn anode surface and tailors the [Zn(H2O)6]2+ solvation sheath, effectively guiding epitaxial deposition of Zn2+ on the Zn (002) plane and suppressing side reactions. The assembled quasi-solid-state ZAB demonstrates a long life span of over 1076 h at 2 mA cm-2 at -20 °C, outperforming most reported ZABs.

Double‐Walled Tubular Heusler‐Type Platinum–Ruthenium Phosphide as All‐pH Hydrogen Evolution Reaction Catalyst Outperforming Platinum and Ruthenium

AbstractNanostructured ionic compounds have driven major technological advancements in displays, photovoltaics, and catalysis. Current research focuses on refining the chemical composition of such compounds. In this study, a strategy for creating stoichiometrically well‐defined nanoscale multiple‐cation systems, where the atomically precise structure maximizes the synergistic cooperation between cations at the atomic scale is reported. The unprecedented construction of Heusler‐type PtRuP2 double‐walled nanotubes through sequential anion/cation exchange reactions is demonstrated. The PtRuP2 catalyst exhibits record‐high catalytic performance and durability for the hydrogen evolution reaction (HER) in alkaline electrolytes and anion‐exchange membrane water electrolyzers. The investigations highlight the crucial role of Pt/Ru dual centers, providing multiple active sites that accelerate the HER kinetics within a single phosphide material, in the sequential operation of H2O activation/dissociation at Ru and H2 production at adjacent Pt sites. These findings open new avenues for optimizing ionic compound‐based HER electrocatalysts, offering platinum‐metal alternatives in acidic and alkaline media.

Dilemma with implant placement in patients with florid cemento-osseous dysplasia: A literature review.

An electronic search was done in PUBMED, SCOPUS, and a hand search was done in radiology, periodontology, and oral surgery journals. The search yielded 428 results, from which only 6 articles were selected for this literature review. Both prospective and retrospective studies were included. Clinical studies with information on the pre-implant condition of the site, detailed implant procedure, and follow-up after implant placement of more than 6 months were only considered for this review. Limited clinical studies, shorter follow-up periods were the shortcomings of this review. However, it can be summarized that dental implants should not be placed at the site of FCOD, however can be placed at adjacent sites. Variations in implant type or the implant length had no bearing on the survival of implants at the sites of FCOD.

Prevalence of discordance between femoral and lumbar bone mineral density among older adults in a community-based setting.

T-score measurement via dual-energy X-ray absorptiometry (DXA) is the gold standard for assessing and classifying the bone mineral density status of patients as normal, osteopenic, or osteoporotic according to the World Health Organization criteria. However, the diagnostic accuracy may be affected by the skeletal site selected for DXA. Estimate the prevalence of femoral and lumbar BMD discordance in a community-based setting in Riyadh, Saudi Arabia. Cross-sectional. Polyclinics at a tertiary care center. This study included all patients aged ≥60 years who visited the Department of Family Medicine and underwent DXA screening between 2016 and 2022. Discordance was defined as a difference in BMD status between two skeletal sites. Minor discordance occurs when adjacent sites have different diagnoses; i.e., one site exhibits osteoporosis and the other exhibits osteopenia. In contrast, major discordance occurs when one site exhibits osteoporosis and the other exhibits normal BMD. 1429 older adults. The study patients had a median age of 66 years (60-99, minimum-maximum). The prevalence of discordance was 41.6%, with major discordance present in 2.2% of patients and minor discordance in 39.4%. The distribution of discordance did not differ significantly among the sociodemographic factors. Discordance is prevalent among the Saudi geriatric population. During the analysis of DXA results, physicians should account for discordance when diagnosing and ruling out osteoporosis in high-risk patients. All factors influencing discordance were not explored thoroughly; this study mainly focused on older adults. Furthermore, diverse age groups need to be investigated for a more comprehensive understanding of the analyzed factors.

In Situ Creation of Surface Defects on Pd@NiPd with Core-shell Hierarchical Structure Toward Boosting Electrocatalytic Activity.

A deep insight into surface structural evolution of the catalyst is a challenging issue to reveal the structure-activity relationship. In this contribution, based on a surface alloying strategy, the dual-functional Pd@NiPd catalyst with a unique core-shell hierarchical structure is developed through selective crystal growth, surface cocrystallization, directional self-assembly, and reduction process. The surface defects are created in situ on the outer NiPd alloy layer in the electrochemical redox processes, which endow the Pd@NiPd catalyst with excellent electrocatalytic activity of hydrogen generation reaction (HER) and oxygen generation reaction (OER) in alkaline media. The optimal Pd@NiPd-2 catalyst requires an overpotential of only 18 mV that is far lower than Pt/C benchmark (43 mV) at the current density of 10 mA cm-2 for the HER, and 210 mV that is far lower than RuO2 benchmark (430 mV) at 50 mA cm-2 for the OER. Density functional theory (DFT) calculations reveal that the outstanding electrocatalytic activity is originated from the creation of surface defect structure that induces a significant reduction in the adsorption and dissociation energy barriers of H2O molecules in the HER and a decrease in the conversion energy from O* to OOH* that resulted from the synergy of two adjacent Pd sites by forming O-bridge. This work affords a typical paradigm for exploiting efficient catalysts and investigating the dependence of electrocatalytic activity on the surface structural evolution.

(4-Butyl-1-ethyl-1,2,4-triazol-5-yl-idene)[(1,2,5,6-η)-cyclo-octa-1,5-diene](tri-phenyl-phosphane)rhodium(I) tetra-fluorido-borate.

In the title triazole-based N-heterocyclic carbene rhodium(I) cationic complex with a tetra-fluorido-borate counter-anion, [Rh(C8H12)(C8H15N3)(C18H15P)]BF4, which crystallizes with two cations and two anions in the asymmetric unit, the Rh center has a distorted square-planar coordination geometry with expected bond distances. Several nonclassical C-H⋯F hydrogen-bonding inter-actions help to consolidate the packing. Two of the F atoms of one of the anions are disordered over adjacent sites in a 0.814 (4):0.186 (4) ratio.

C−C Coupling in CO2 Electroreduction on Single Cu‐Modified Covalent Triazine Frameworks: A Static and Dynamic Density Functional Theory Study

AbstractThe electrochemical reduction of CO2 into C2+ products represents a promising solution to completing the carbon cycle, thereby fostering a sustainable energy supply. Single‐atom electrocatalysts (SAECs) have garnered significant attention as efficient electrocatalysts for the CO2 reduction reaction. Herein, we carried out a first‐principles study on the mechanism of C−C bond formation on single‐Cu‐atom‐modified covalent triazine frameworks (Cu‐CTFs), which are a promising platform for SAECs. Static density functional calculations indicated that the dimerization of CO, which is the main mechanism for C−C bond formation on bulk Cu metals, was not favorable for Cu‐CTFs because of the lack of adjacent Cu sites for co‐adsorption of CO molecules. Rather than CO dimerization, the reaction between adsorbed *CHO and CO to produce *COCHO has a relatively low reaction energy barrier. Constrained ab initio molecular dynamics analyses revealed that the C−C bond‐forming reaction proceeds via insertion of CO at the *CHO intermediate, which has a modest activation energy of 0.09 eV. Specifically, when CO molecule is constrained to be brought close to *CHO, CO insertion between *CHO and Cu occurs at a C−C distance of 1.8 Å. This insertion reaction is the transition step for this C−C bond formation.

The hAT family hopper transposon exists as highly similar yet discontinuous elements in the Bactrocera tephritid fly genus.

The hAT family transposable element, hopper, was originally discovered as a defective 3120-bp full-length element in a wild-type strain of the oriental fruit fly, Bactrocera dorsalis (Hendel) (Diptera: Tephritidae), and subsequently a functional 3131-bp element, hopperBdwe, was isolated from a white eye mutant strain. The latter study showed that closely related elements exist in melonfly, Zeugodacus cucurbitae (Coquillett) (Diptera: Tephritidae), a closely related subgenus, suggesting that hopper could have a widespread presence in the Bactrocera genus. To further understand the distribution of hopper within and beyond the B. dorsalis species complex, primer pairs from hopperBdwe and its adjacent genomic insertion site were used to survey the presence and relatedness of hopper in five species within the complex and four species beyond the complex. Based on sequence identity of a 1.94 kb internal nucleotide sequence, the closest relationships were with mutated elements from B. dorsalis s.s. and species synonymized with B. dorsalis including B. papayae, B. philippinensis and B. invadens, ranging in identity between 88.4% and 99.5%. Notably, Bactrocera carambolae (Drew & Hancock) (Diptera: Tephritidae), which is most closely related to B. dorsalis beyond the synonymized species, shared hopper identities of 97.3%-99.5%. Beyond the B. dorsalis complex, Z. cucurbitae,Bactrocera tryoni (Froggatt) (Diptera: Tephritidae) and Bactrocera zonata (Saunders) (Diptera: Tephritidae) shared identities of 83.1%-97.1%, while hopper was absent from the Bactrocera oleae (Gmelin) (Diptera: Tephritidae) strain tested. While the functional autonomous hopperBdwe element was not detected in these species, another closely related hopper element isolated from a B. dorsalis genetic sexing strain has an uninterrupted transposase open reading frame. The discontinuous presence of hopper in the Bactrocera genus has implications for its use for genomic manipulation and understanding the phylogenetic relationship of these species.

Corticosteroid Injection in the Operative Hand Prior to a Trigger Finger or Carpal Tunnel Release: If It Is Not at the Surgical Site Then What Is the Big Deal?

Patients who have had a corticosteroid injection at the surgical site within 90 days of trigger finger release (TFR) or carpal tunnel release (CTR) have an elevated risk of postoperative infection. Currently, it remains unknown if a preoperative injection in proximity to the surgical site for a separate complaint alters the risk of a postoperative infection. A retrospective chart review was performed on all patients who underwent TFR or CTR between 2010 and 2022. Patients who had a corticosteroid injection at or near the surgical site within 90 days of surgery were included. Outcome measures included uncomplicated healing, superficial infection requiring antibiotics, and deep infection (DI) requiring surgical debridement. There were 564 cases in which a corticosteroid injection was performed within 90 days of TFR or CTR. Superficial infections occurred in 12 (2.1%), and DIs occurred in 6 (1.1%) cases. There was no significant difference in infection rates between the two groups relative to the location of the injection nor timing of the injection (0-30, 31-60, or 61-90 days prior to surgery). Patients who had an injection at the surgical site within 90 days of TFR or CTR had an elevated rate of postoperative infection compared with published rates in the literature. This study is unique in that preoperative injections at an adjacent site in the palm also correlated with an elevated rate of infection, similar to patients who had an injection at the surgical site. Level 4.

Embedding electronic perpetual motion into single-atom catalysts for persistent Fenton-like reactions

In our quest to leverage the capabilities of the emerging single-atom catalysts (SACs) for wastewater purification, we confronted fundamental challenges related to electron scarcity and instability. Through meticulous theoretical calculations, we identified optimal placements for nitrogen vacancies (Nv) and iron (Fe) single-atom sites, uncovering a dual-site approach that significantly amplified visible-light absorption and charge transfer dynamics. Informed by these computational insights, we cleverly integrated Nv into the catalyst design to boost electron density around iron atoms, yielding a potent and flexible photoactivator for benign peracetic acid. This exceptional catalyst exhibited remarkable stability and effectively degraded various organic contaminants over 20 cycles with self-cleaning properties. Specifically, the Nv sites captured electrons, enabling their swift transfer to adjacent Fe sites under visible light irradiation. This mechanism accelerated the reduction of the formed "peracetic acid-catalyst" intermediate. Theoretical calculations were used to elucidate the synergistic interplay of dual mechanisms, illuminating increased adsorption and activation of reactive molecules. Furthermore, electron reduction pathways on the conduction band were elaborately explored, unveiling the production of reactive species that enhanced photocatalytic processes. A six-flux model and associated parameters were also applied to precisely optimize the photocatalytic process, providing invaluable insights for future photocatalyst design. Overall, this study offers a molecule-level insight into the rational design of robust SACs in a photo-Fenton-like system, with promising implications for wastewater treatment and other high-value applications.

Pd-Mn/NC Dual Single-Atomic Sites with Hollow Mesopores for the Highly Efficient Semihydrogenation of Phenylacetylene.

The direct pyrolysis of metal-zeolite imidazolate frameworks (M-ZIFs) has been widely recognized as the predominant approach for synthesizing atomically dispersed metal-nitrogen-carbon single-atom catalysts (M/NC-SACs), which have exhibited exceptional activity and selectivity in the semihydrogenation of acetylene. However, due to weak adsorption of reactants on the single site and restricted molecular diffusion, the semihydrogenation of large organic molecules (e.g., phenylacetylene) was greatly limited for M/NC-SACs. In this work, a dual single-atom catalyst (h-Pd-Mn/NC) with hollow mesopores was designed and prepared using a general host-guest strategy. Taking the semihydrogenation of phenylacetylene as an example, this catalyst exhibited ultrahigh activity and selectivity, which achieved a turnover frequency of 218 molC═CmolPd-1 min-1, 16-fold higher than that of the commercial Lindlar catalyst. The catalyst maintained high activity and selectivity even after 5 cycles of usage. The superior activity of h-Pd-Mn/NC was attributed to the 4.0 nm mesopore interface of the catalyst, which enhanced the diffusion of macromolecular reactants and products. Particularly, the introduction of atomically dispersed Mn with weak electronegativity in h-Pd-Mn/NC could drive the electron transfer from Mn to adjacent Pd sites and regulate the electronic structure of Pd sites. Meanwhile, the strong electronic coupling in Pd-Mn pairs enhanced the d-electron domination near the Fermi level and promoted the adsorption of phenylacetylene and H2 on Pd active sites, thereby reducing the energy barrier for the semihydrogenation of phenylacetylene.

Understanding the Distance Effect of the Single-Atom Active Sites in Fenton-Like Reactions for Efficient Water Remediation.

Emerging single-atom catalysts (SACs) are promising in water remediation through Fenton-like reactions. Despite the notable enhancement of catalytic activity through increasing the density of single-atom active sites, the performance improvement is not solely attributed to the increase in the number of active sites. The variation of catalytic behaviors stemming from the increased atomic density is particularly elusive and deserves an in-depth study. Herein, single-atom Fe catalysts (FeSA-CN) with different distances (dsite) between the adjacent single-atom Fe sites are constructed by controlling Fe loading. With the decrease in dsite value, remarkably enhanced catalytic activity of FeSA-CN is realized via the electron transfer regime with peroxymonosulfate (PMS) activation. The decrease in dsite value promotes electronic communication and further alters the electronic structure in favor of PMS activation. Moreover, the two adjacent single-atom Fe sites collectively adsorb PMS and achieve single-site desorption of the PMS decomposition products, maintaining continuous PMS activation and contaminant removal. Moreover, the FeSA-CN/PMS system exhibits excellent anti-interference performance for various aquatic systems and good durability in continuous-flow experiments, indicating its great potential for water treatment applications. This study provides an in-depth understanding of the distance effect of single-atom active sites on water remediation by designing densely populated SACs.

Promotion effect of epoxy group neighboring single-atom Cu site on acetylene hydrochlorination

Carbon materials have been used as the support for catalysts in the field of acetylene hydrochlorination, the influence of inevitable oxygen-containing moieties on the reaction is often ignored and the mechanism of the oxygen-doping structure remains ambiguous. Herein, we explored the effect of the oxygen-containing group (COC) in the support on the activity of single-atom dispersed Cu catalysts. By immersing the Cu single-atom catalyst in an alkaline solution, the epoxy species on the carbon support was cleaved to obtain a pure ether species while the Cu site was modified to a more electron-deficient state. The turnover frequency value of Cu/O-FLP catalyst with epoxy groups was 1.6-fold higher than that of alkaline treated catalyst. Our result indicated that the epoxy groups could assist adjacent single-atom Cu sites to synergistically promote the adsorption and cleavage of the reactant hydrogen chloride toward form COH and CuCl bonds, and reduce the reaction energy barrier. The presence of electron deficient Cu sites and ether species could induce competitive adsorption of the acetylene and hydrogen chloride, thereby reducing the activity of the catalyst. This study highlights the influence of surface oxygen species and the tunability of the support, providing the foundation for the fabrication of higher-activity Cu catalysts for acetylene hydrochlorination.

Revealing Distance-Dependent Synergy between MnCo2O4 and Co-N-C in Boosting the Oxygen Reduction Reaction.

Synergistic effects have been applied to a variety of hybrid electrocatalysts to improve their activity and selectivity. Understanding the synergistic mechanism is crucial for the rational design of these types of catalysts. Here, we synthesize a MnCo2O4/Co-N-C hybrid electrocatalyst for the oxygen reduction reaction (ORR) and systematically investigate the synergy between MnCo2O4 nanoparticles and Co-N-C support. Theoretical simulations reveal that the synergy is closely related to the distance between active sites. For a pair of remote active sites, the ORR proceeds through the known 2e- + 2e- relay catalysis while the direct 4e- ORR occurs on a pair of adjacent active sites. Therefore, the formation of the undesired byproduct (H2O2) is inhibited at the interface region between MnCo2O4 and Co-N-C. This synergistic effect is further verified on an anion-exchange membrane fuel cell. The findings deepen the understanding of synergistic catalysis and will provide guidance for the rational design of hybrid electrocatalysts.

Large electronegativity differences between adjacent atomic sites activate and stabilize ZnIn2S4 for efficient photocatalytic overall water splitting

Photocatalytic overall water splitting into hydrogen and oxygen is desirable for long-term renewable, sustainable and clean fuel production on earth. Metal sulfides are considered as ideal hydrogen-evolved photocatalysts, but their component homogeneity and typical sulfur instability cause an inert oxygen production, which remains a huge obstacle to overall water-splitting. Here, a distortion-evoked cation-site oxygen doping of ZnIn2S4 (D-O-ZIS) creates significant electronegativity differences between adjacent atomic sites, with S1 sites being electron-rich and S2 sites being electron-deficient in the local structure of S1–S2–O sites. The strong charge redistribution character activates stable oxygen reactions at S2 sites and avoids the common issue of sulfur instability in metal sulfide photocatalysis, while S1 sites favor the adsorption/desorption of hydrogen. Consequently, an overall water-splitting reaction has been realized in D-O-ZIS with a remarkable solar-to-hydrogen conversion efficiency of 0.57%, accompanying a ~ 91% retention rate after 120 h photocatalytic test. In this work, we inspire an universal design from electronegativity differences perspective to activate and stabilize metal sulfide photocatalysts for efficient overall water-splitting.

Predation and Biophysical Context Control Long-Term Carcass Nutrient Inputs in an Andean Ecosystem

Animal carcass decomposition is an often-overlooked component of nutrient cycles. The importance of carcass decomposition for increasing nutrient availability has been demonstrated in several ecosystems, but impacts in arid lands are poorly understood. In a protected high desert landscape in Argentina, puma predation of vicuñas is a main driver of carcass distribution. Here, we sampled puma kill sites across three habitats (plains, canyons, and meadows) to evaluate the impacts of vicuña carcass and stomach decomposition on soil and plant nutrients up to 5 years after carcass deposition. Soil beneath both carcasses and stomachs had significantly higher soil nutrient content than adjacent reference sites in arid, nutrient-poor plains and canyons, but not in moist, nutrient-rich meadows. Stomachs had greater effects on soil nutrients than carcasses. However, we did not detect higher plant N concentrations at kill sites. The biogeochemical effects of puma kills persisted for several years and increased over time, indicating that kills do not create ephemeral nutrient pulses, but can have lasting effects on the distribution of soil nutrients. Comparison to broader spatial patterns of predation risk reveals that puma predation of vicuñas is more likely in nutrient-rich sites, but carcasses have the greatest effects on soil nutrients in nutrient-poor environments, such that carcasses increase localized heterogeneity by generating nutrient hotspots in less productive environments. Predation and carcass decomposition may thus be important overlooked factors influencing ecosystem functioning in arid environments.

Connectivity of Greenland halibut in the northwestern Atlantic Ocean inferred from otolith chemistry

Greenland Halibut (Reinhardtius hippoglossoides) is a deepwater flatfish having a circumpolar distribution. Understanding the spatial connectivity and migratory patterns of this commercially valuable species is essential for ensuring a sustainable fishery; nonetheless, this information remains relatively scarce for many Greenland Halibut populations. Here we evaluate the connectivity and the population structure of halibut along coastal Greenland and Canada to better characterize the contribution of each production zone to the various stocks found in the northwestern Atlantic Ocean. In 2014 and 2016, we sampled 411 large Greenland Halibut from coastal Nunavut, Labrador, and Greenland. We used the elemental fingerprint (magnesium, strontium, and barium) from the otolith core and margin of the sampled fish to determine spatial differentiation of the source areas of the collected halibut. From the 17 sample sites, margin elemental fingerprint delineated four “elemental sectors”, representing pooled adjacent sites having similar chemistry. Overall, 62% of Greenland Halibut were correctly assigned to their sampled coast. Elemental fingerprint of the otolith cores indicated three chemically distinct natal sources for the captured halibut. The chemical record in the otolith cores suggested a high connectivity of Greenland Halibut in the northwestern Atlantic and a main natal source located potentially along the west coast of Greenland. Given that our results suggest the presence of a large nursery around Disko Bay–Hellefiske Bank, protection measures should be considered for this area.

Influence of wastewater discharge from dredging mariculture pond sediments on the food sources of two intertidal crab species

The present study δ13C, δ15N and fatty acid compositions of two dominant mangrove crabs, Tubuca arcuata and Parasesarma plicatum were compared between a mangrove site frequently receiving dredged wastewater from mariculture ponds and an adjacent reference site, to investigate the impact of wastewater discharge on their diets. A laboratory experiment was also conducted to further test how their diets changed with the wastewater input. The result showed no significant change in the δ13C while clear 15N enrichment of crabs in association with the wastewater discharge. Changes in 15N signature and fatty acid composition of the crabs due to the wastewater discharge indicated that the impact of wastewater discharge was related to crab species, being more apparent on the deposit feeder (T. arcuata) than the herbivorous P. plicatum. The results suggested that the discharge of dredged wastewater into mangroves resulted in the uptake of wastewater-derived materials and nutrients by mangrove crabs.

ОСОБЕННОСТИ СИНХРОНИЗАЦИИ ДИНАМИКИ ЧИСЛЕННОСТИ В СИСТЕМЕ ТРЕХ МИГРАЦИОННО СВЯЗАННЫХ ПОПУЛЯЦИЙ

The article is devoted to the study of oscillations (cycles) synchronization in a system of three populations coupled by migration in a circle. We consider a discrete time model of population dynamics, which is a system of three identical dissipatively connected logistic maps. One-dimensional bifurcation diagrams (trees) were constructed, supplemented with the capture index of the population numbers cycles phases at adjacent sites. We conducted numerical experiments that show phase multistability – the cycles coexistence with different phases. Using qualitative methods for studying dynamic systems, a complete phase portrait of the model is constructed, showing that in the phase space there are several periodic points corresponding to elements of synchronous (in-phase) and asynchronous (out-of-phase) cycles. The 2- and 3-cycle stability conditions are investigated. It is shown that these two cycles are represented by three options: 1) a fully synchronous regime, when the abundances in the three populations coincide at any point in time; 2) a partially synchronous regime, when abundances coincide only for two populations, 3) a non-synchronous (out-of-phase) regime, when all three numbers have different values. For a 2-cycle, the third regime is unstable, possible as part of a long transition process. We found that for the 3-cycle, besides to the synchronous and partially synchronous regime, it is possible a stable out-of-phase behavior of three populations. It is shown that stable and unstable periodic points lie on certain surfaces (invariant manifolds), which separate the areas of attraction for regimes with different degrees of phase synchronization.