Elaeolenchus parthenonema n. g., n. sp. (Nematoda: Sphaerularioidea: Anandranematidae n. fam.) parasitic in the palm-pollinating weevil Elaeidobius kamerunicus Faust,with a phylogenetic synopsis of the Sphaerularioidea Lubbock, 1861

A new nematode, Elaeolenchus parthenonema n. g., n. sp., is described from the palm-pollinating weevil Elaeidobius kamerunicus Faust. The new genus is placed in the Anandranematidae n. fam., which, together with the genus Anandranema Poinar et al., 1993, is characterised by nematodes having only a single autotokous generation in the insect host. This is the first report of a member of this superfamily reproducing only parthenogenetically. The development of E. parthenonema and its effect on the weevil host is discussed, along with a phylogenetic synopsis of the families of the Sphaerularioidea Lubbock 1861. The Beddingiidae n. fam. is proposed for Beddingia Blinova & Korenchenko, 1986, comprising the original Deladenus parasites of Hymenoptera that possess both free-living and parasitic amphimictic generations in their life-cycles. This family is considered to have the most primitive type of development in the superfamily.     

Pennsylvanian (Late Carboniferous) calcareous microfossils from Cedro Peak (New Mexico,USA). Part 1: Algae and Microproblematica

At Cedro Peak (Manzanita Mountains, central New Mexico), the Pennsylvanian succession is divided into four formations: Sandia, Gray Mesa, Atrasado, and lower part of Bursum. The sampled limestones of the Gray Mesa and Atravasado formations yielded three age distinctive fossil assemblages: (a) latest Atokan/early Desmoinesian; (b) late early Desmoinesian, and (c) middle Virgilian. The calcareous algae, incertae sedis algae and cyanobacterial-foraminiferal consortia are described here. The following new taxa are named: Epimastoporaceae n. fam.; Anthracoporellopsis novamexicana n. sp.; Tubiphytidae n. fam.; and Latitubiphytes n. gen.     

Mesozoic chrysopid-like Planipennia: a phylogenetic approach (Insecta: Neuroptera)

The Mesozoic chrysopid-like Planipennia are revised and several new genera and species are described. The new superfamily Chrysopoidea is proposed for the extant and fossil Chrysopidae, and the fossil families Liassochrysidae n. fam., Allopteridae Zhang 1991 n. sensu, Mesochrysopidae Handlirsch, 1906 n. sensu, Tachinymphidae n. fam., and Limaiidae Martins-Neto and Vulcano 1989 n. sensu. A phylogenetic analysis of the Chrysopoidea is proposed, based on the wing venation characters. With at least the four families Allopteridae, Mesochrysopidae, Tachinymphidae, and Chrysopidae, showing different wing venation patterns, the systematic diversity and morphological disparity of the Chrysopoidea are maximal during the Late Jurassic and Early Cretaceous. The Mesozoic family Limaiidae was still present during the Paleocene/Eocene suggesting a minimal impact on the Chrysopoidea of the crisis of the diversity at the K-T boundary. Other Cenozoic Chrysopoidea can be attributed to the Chrysopidae sensu stricto.     

Pennsylvanian (Late Carboniferous) calcareous microfossils from Cedro Peak (New Mexico,USA). Part 2: Smaller foraminifers and fusulinids

The Pennsylvanian stratigraphic section of the Manzanita Mountains (central New Mexico, USA) is restudied at Cedro Peak. This Pennsylvanian succession is divided into the Sandia Formation, Gray Mesa Fm, Atrasado Fm, and lower part of Bursum Fm. The sampled limestones of the Gray Mesa and Atrasado formations yielded three age-distinctive fossil assemblages: they are of (a) latest Atokan/early Desmoinesian, (b) late early Desmoinesian, and (c) middle Virgilian. The following new taxa of foraminifers are proposed: Endoteboidea n. superfam.; Spireitlinidae n. fam.; Millerellinae n. subfam.; Pseudonovella marshalli n. sp.; Pseudonovella ohioicus nom. nov.; Pseudoacutella n. gen.; Pseudoacutella hoarei nom. nov.; Plectofusulina manzanensis n. sp. Translated or emended names are: Staffelloidea, Ozawainelloidea, Ozawainellidae, and Profusulinellidae.     

Ulurumyiidae – a new family of calyptrate flies (Diptera)

A new monotypic and monospecific family Ulurumyiidae fam.n. , type genus Ulurumyia  gen.n. , is erected for the species Ulurumyia macalpinei  sp.n. from southeastern Australia. The family is unambiguously a member of the superfamily Oestroidea within Calyptratae, and available evidence supports noninclusion in any of the known families, but phylogenetic affinities are otherwise obscure. The species is a coprophage with obligate lecithotrophic unilarviparity, known to breed in cow dung but not known from the dung of any native Australian mammal.     

Molecular phylogeny of Sericostomatoidea (Trichoptera) with the establishment of three new families

We inferred the phylogenetic relationships among 58 genera of Sericostomatoidea, representing all previously accepted families as well as genera that were not placed in established families. The analyses were based on five fragments of the protein coding genes carbamoylphosphate synthetase (CPSase of CAD), isocitrate dehydrogenase (IDH), Elongation factor 1a (EF‐1a), RNA polymerase II (POL II) and cytochrome oxidase I (COI). The data set was analysed using Bayesian methods with a mixed model, raxml , and parsimony. The various methods generated slightly different results regarding relationships among families, but the shared results comprise support for: (i) a monophyletic Sericostomatoidea; (ii) a paraphyletic Parasericostoma due to inclusion of Myotrichia murina, leading to synonymization of Myotrichia with Parasericostoma; (iii) a polyphyletic Sericostomatidae, which is divided into two families, Sericostomatidae sensu stricto and Parasericostomatidae fam.n. ; (iv) a polyphyletic Helicophidae which is divided into Helicophidae sensu stricto and Heloccabucidae fam.n. ; (v) hypothesized phylogenetic placement of the former incerta sedis genera Ngoya, Seselpsyche and Karomana; (vi) a paraphyletic Costora (Conoesucidae) that should be divided into several genera after more careful examination of morphological data; (vii) reinstatement of Gyrocarisa as a valid genus within Petrothrincidae. A third family, Ceylanopsychidae fam.n. , is established based on morphological characters alone. A hypothesis of the relationship among 14 of the 15 families in the superfamily is presented. A key to the families is presented based on adults (males). Taxonomic history, diagnosis, habitat preference and distribution data for all sericostomatoid families are presented. This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub:CF6A6B9F‐6A72‐4265‐BD09‐3A710DFCD7B1 .     

Characterization and comparison of the mitochondrial genomes from two Alpheidae species and insights into the phylogeny of Caridea

The mitochondrial genome (mitogenome) has been widely used in phylogenetics and molecular evolution as a parameter, due to its simple genetic structure, high evolutionary rate, and compositional heterogeneity properties. Alpheidae is a large and highly diverse family of the Caridea infraorder, currently containing about 600 species dispersed all over the world. However, only a few shrimps in Alpheidae have their complete mitogenome annotated in GenBank. In our study, the entire mitogenomes of two shrimps from Alpheidae were determined, Alpheus randalli and Alpheus bellulus. The mitogenomes of both shrimps share the complete set of 37 mitochondrial genes found in other Alpheidae species. In A. randalli the AT-skew is slightly positive and GC-skew is negative, whereas in A. bellulus the AT-skew is negative and GC-skew is slightly positive. Furthermore, the secondary structures of trnS1 in the two shrimps are partially missing, and another three tRNAs formed the typical cloverleaf shaped secondary structures. Also, the trnS1 of A. randalli has an unusual anticodon stem with some unpaired nucleotides. Comparative genomic analysis suggests that the mitochondrial gene order of Alpheus genus exhibits a different gene rearrangement compared with that of Caridea. Most species in Alpheus share the same gene order, except for A. lobidens, which has an additional pseudogenomic trnQ (trnQ*). Compared with the mitochondrial gene order of Caridea the Alpheus trnE underwent both translocation and inversion, which were caused by a recombination event. Bayesian inferences (BI) and Maximum Likelihood (ML) phylogenetic analyses of 105 species amino acid datasets resulted in a well-supported topology, whereas four families in Caridea are monophyletic and can be divided into two major clades. Moreover, we demonstrated the phylogenetic relationships of six infraorders in Decapoda (Dendrobranchiata, (Caridea, (Stenopodidea, (Achelata, (Polychelida, Astacidea))))). This study used the large taxon sampling available to date for phylomitogenomic analysis. The results provide a theoretical basis for further research on the evolution of the Decapoda order, specifically Caridea infraorder.     

Toward a natural classification: phylogeny of acontiate sea anemones (Cnidaria,Anthozoa, Actiniaria)

Acontia—nematocyst‐dense, thread‐like extensions of the mesenterial filaments―are the characteristic feature of the actiniarian group Acontiaria. Phylogenetic analyses have shown that acontiate taxa form a clade that also includes some taxa without acontia. We analyse five molecular markers from 85 actiniarians to explore the phylogenetic relationships among families in Acontiaria, including acontiate species assigned to other higher taxa and species without acontia that have been allied to Acontiaria. Based on our results, we redefine the group to accommodate those lineages that have lost acontia, and formalize it as superfamily Metridioidea. Based on stable and well supported clades, we resurrect Phelliidae and Amphianthidae, redefine Kadosactinidae and Actinoscyphiidae, and move two species to new genera: that previously termed Sagartiogeton erythraios belongs in Jasonactis gen. nov.; and that previously termed Anthosactis pearseae belongs in Ostiactis gen. nov., type genus of Ostiactinidae fam. nov. We also synonymized Halcampoididae and Halcampidae (as Halcampidae) and Andvakiidae and Isophelliidae (as Andvakiidae). The results of our phylogenetic analyses indicate that the diagnostic morphological characters used in the family‐level taxonomy of acontiate actiniarians such as the nematocysts of the acontia, the marginal sphincter muscle, and mesenteries divisible into macro‐ and micro‐cnemes, have to be revisited, as these features are highly homoplasious.     

System of Families of Enoplan Nemerteans of the Order Eumonostilifera (Nemertea: Enopla)

The paper is a review of the family-level classifications of the order Eumonostilifera. The elaboration of a phylogenetic system of Eumonostilifera is not yet possible. Some new groups, presumably monophyletic, have been distinguished, which are considered to be of a family rank (Neesiidae fam. n., Sacconemertidae stat. n., Zygonemertidae fam. n., Prostomatidae, Acteonemertidae fam. n., and Potamonemertidae fam. n.). The proposed system is a typological one; however, it can be used as a basis for further taxonomical and phylogenetic studies.     

Evolutionary Development of the Immunoglobulin Family

The origin of the ability of immunoglobulins (Ig) and T-cell receptors (TCRs) to specifically recognize antigens is related to the evolutionary development of proteins of the immunoglobulin superfamily (IgSF). The IgSF proteins are characterized by specific domain organization of molecules and statistically significant homology with known Ig. Four types of Ig domains (V1, V2, C1, and C2), differing from one another both in variations of their spatial organization and in the number of amino acid residues have been distinguished. Immunoglobulin superfamily comprises Ig; TCRs; class I and II major histocompatibility complex (MHC) molecules; one-domain proteins of thymocytes and T-cells (Thy-1); myelin protein P₀; ₂-microglobulin; two-domain proteins, such as sponge receptor tyrosine kinase (RTK), sponge adhesive protein (SAP), Drosophila tyrosine-kinase receptor (DTCR), Xenopus and human cortical-thymocyte receptors (CTX and CTH), etc.; and a large group of adhesins, coreceptors, and Ig receptors with varying number of domains. Evolutionary development of IgSF began with the evolvement of chaperones, Thy-1, and P₀ of prokaryotes and unicellular eukaryotes. Mutations, duplications, and translocations of the genes controlling both V and C domains yielded proteins with different numbers and combinations of these domains. All IgSF proteins are divided into two groups. The first group includes the proteins with nonrearranging V2 domains and homophilic mode of interaction; the second, the proteins with rearranging V1 domains and heterophilic mode of interaction (Ig, TCRs). The ability for heterophilic antigen-binding mode of interaction was apparently acquired due to the introduction of recombination-activating retroviral genes (RAG1 and RAG2) into the genome of Gnathostomata ancestors.     

Differences in Photoresponse and Phytochrome Spectrophotometry Between Etiolated and De-etiolated Pea Stem Tissue

Morphologically similar pea plants having a 4-fold difference in spectrophoto-metrically detectable phytochrome can be produced by pretreatment of etiolated plants with red light (R) or with red and far-red light combined (RF). A search for response differences which could be ascribed to differences in phytochrome content has resulted only in the establishment of differences due to de-etiolation. Segments of etiolated plants differ from those of plants de-etiolated by R and RF pretreatments in 2 ways. Segments from etiolated plants appear to respond rapidly to the far-red absorbing form of phytochrome (P_FR), while segments from de-etiolated plants do not respond rapidly to P_FR. This statement is based upon 2 observations: (i) the red light induced growth inhibition in segments from etiolated plants rapidly escapes reversibility by far-red light, while with segments from R or RF pretreated plants, the red light effect is fully reversed by subsequent far-red light for up to 2 hr; and (ii) segments from etiolated plants were inhibited to a greater degree than were segments from RF pretreated plants when various photostationary state levels of P_FR were maintained for 30 or 90 min and then removed by photoconversion to P_R. The in vivo nonphotochemical transformation curves of the phytochrome of etiolated and RF pretreated plants appear to differ in 2 related respects: (i) the amount of phytochrome destroyed in de-etiolated tissue is greater than that in etiolated tissue, perhaps as a result of the fact that (ii) the rate and extent of apparent reversion of P_FR to P_R in etiolated tissue is about twice that in de-etiolated tissue.     

The mitochondrial genome of <Emphasis Type="Italic">Euphausia superba</Emphasis> (Prydz Bay) (Crustacea: Malacostraca: Euphausiacea) reveals a novel gene arrangement and potential molecular markers

Euphausiid krill are dominant organisms in the zooplankton population and play a central role in marine ecosystems. In this paper, we described the gene organization, gene rearrangement and codon usage in the mitochondrial genome of Euphausia superba Dana 1852 (sampling from Prydz Bay, PB). The mitochondrial genome of E. superba is more than 15,498 bp in length (partial non-coding region was not determined). Translocation of four tRNAs (trnL ₁ , trnL ₂ , trnW and trnI) and duplication of one tRNA (trnN) were founded in the mitochondrial genome of E. superba when comparing its genome with the pancrustacean ground pattern. To investigate the phylogenetic relationship within Malacostraca, phylogenetic trees based on currently available malacostracan mitochondrial genomes were built with the maximum likelihood and the Bayesian models. All analyses based on nucleotide and amino acid data strongly support the monophyly of Stomatopoda, Penaeidae, Caridea, and Brachyura, which is consistent with previous research. However, the taxonomic position of Euphausiacea within Malacostraca is unstable. From comparing the mitochondrial genome between E. superba (PB) and E. superba (sampling from Weddell Sea, WS), we found that nad2 gene contains maximal variation with 61 segregating sites, following by nad5 gene which has 12 segregating sites. Thus, nad2 and nad5 genes may be used as potential molecular markers to study the inherit diversity among different E. superba groups, which would be helpful to the exploitation and management of E. superba resources.     

Phylogeny of the highly divergent zoanthid family Microzoanthidae (Anthozoa,Hexacorallia) from the Pacific

Fujii, T. & Reimer, J. D. (2011). Phylogeny of the highly divergent zoanthid family Microzoanthidae (Anthozoa, Hexacorallia) from the Pacific. —Zoologica Scripta, 40, 418–431. In this study, one new family, one new genus and two new species of zoanthids from rubble zones spanning the temperate, subtropical and tropical Pacific Ocean are described. Two new species are described, Microzoanthus occultus sp. n. and Microzoanthus kagerou sp. n., both belonging to the new genus Microzoanthus and new family Microzoanthidae, and they can be clearly distinguished both morphologically and genetically from each other and other zoanthids by their very small size, reduced or absent stolon, habitat usually on the bottom side of rubble zone rocks, and divergent and distinct DNA (cytochrome oxidase subunit I, mitochondrial 16S ribosomal DNA, internal transcribed spacer region of ribosomal DNA) sequences. The phylogenetic analyses clearly show Microzoanthidae fam. n. to be genetically far different from all other hexacorallians at the order level, but the macrocnemic arrangement of mesenteries and other morphological characters (colonial specimens with narrow stolons, two rows of tentacles sand encrustation) clearly place these specimens within the order Zoantharia. This study demonstrates how it is highly likely the existence of many marine invertebrate taxa remains overlooked, and that widely distributed groups such as Microzoanthidae fam. n. remain to be discovered.     

A revision of the Neotropical species of Bolitogyrus Chevrolat,a geographically disjunct lineage of Staphylinini (Coleoptera,Staphylinidae)

The Neotropical species of the rarely collected genus Bolitogyrus (Coleoptera: Staphylinidae: Staphylininae: Staphylinini) are revised. The genus exhibits an uncommon, disjunct distribution between the Neotropical and Oriental Regions and is of unknown phylogenetic position within Staphylinini. Morphological evolution remarkable for Staphylinini was discovered within Bolitogyrus, including sexually dimorphic modifications of the pronotum that may be involved in male competition for females. rSEM interactive animations were used to establish morphological species boundaries between two highly variable species and are provided to illustrate diagnostic characters of the genitalia in unconventional views. The genus is redescribed based on the world fauna and twenty-eight Neotropical species are considered valid. Of these, nineteen are described as new to science: Bolitogyrus ashei sp. n.; B. apicofasciatus sp. n.; B. brevistellus sp. n.; B. bufo sp. n.; B. cheungi sp. n.; B. cornutus sp. n.; B. divisus sp. n.; B. falini sp. n.; B. gracilis sp. n.; B. inexspectatus sp. n.; B. longistellus sp. n.; B. marquezi sp. n.; B. newtoni sp. n.; B. pseudotortifolius sp. n.; B. pulchrus sp. n.; B. silex sp. n.; B. thomasi sp. n.; B. tortifolius sp. n.; and B. viridescens sp. n. Bolitogyrus sallei (Kraatz), stat. r. is removed from synonymy with B. buphthalmus (Erichson) and the following new synonyms are proposed: Cyrtothorax cyanescens Sharp, 1884, syn. n. = Quedius buphthalmus Erichson, 1840; C. nevermanni Scheerpeltz, 1974, syn. n. = C. costaricensis Wendeler, 1927. A summary of all available bionomic and distributional data, as well as an illustrated identification key to and diagnoses of all Neotropical species are provided.     

Molecular systematics of caridean shrimps based on five nuclear genes: Implications for superfamily classification

Caridean shrimps are the second most diverse group of Decapoda. Over the years, several different systematic classifications, exclusively based on morphology, have been proposed, but the classification of the infraorder Caridea remains unresolved. In this study, five nuclear genes, 18S rRNA, enolase, histone 3, phosphoenolpyruvate carboxykinase and sodium–potassium ATPase α-subunit, were used to examine the systematic status of caridean families and superfamilies. We constructed gene trees based on a combined dataset of 3819 bp, containing 35 caridean species from 19 families in 11 superfamilies. At the family level, and based on our restricted representation, our molecular data support monophyly of the families Glyphocrangonidae, Crangonidae, Pandalidae, Alpheidae, Rhynchocinetidae, Nematocarcinidae, Pasiphaeidae, Atyidae and Stylodactylidae. In contrast, both the Hippolytidae and Palaemonidae are polyphyletic in our analysis. Two major clades are revealed. The Alpheidae, Hippolytidae, Crangonidae, Glyphocrangonidae, Barbouriidae, Pandalidae, Hymenoceridae, Gnathophyllidae and Palaemonidae make up the first clade, while the second clade comprises the Rhynchocinetidae, Oplophoridae, Nematocarcinidae, Alvinocarididae, Campylonotidae, Pasiphaeidae and Eugonatonotidae. Two families, Bathypalaemonellidae and Stylodactylidae, are shown to be basal groups in our tree. At the superfamily level, our results do not support the currently accepted superfamily classification, although there is support for a superfamily Palaemonoidea, though only three out of its eight families are included. The results suggest that the currently accepted superfamily classification of the Caridea does not reflect their evolutionary relationships. A major revision of the higher systematics of Caridea appears thus to be vital, ideally incorporating both molecular and morphological evidence.     

A new concept of the generic composition of the geometrid moth tribe Ennomini (Lepidoptera, Geometridae) based on functional morphology of the male genitalia

Two unique apomorphies in the skeleto-muscular apparatus of the male genitalia in a series of genera of the subfamily Ennominae have been discovered: (1) a more or less broad membranous area on the ventral side of the vinculum, partly or completely dividing this sclerite along the sagittal plane, and (2) the paired muscle m ₃ attached distally to the medial invagination of the basal portion of the juxta. Such a structure provides resilient flexion of the ventral portion of the vinculum in the sagittal plane as the valvae are abducted by contraction of muscle m ₃. Based on these apomorphies and taking into account the general morphological pattern in the Ennominae, a new generic composition of the tribe Ennomini including 148 valid genera is proposed. A new diagnosis for Ennomini as a monophyletic group is given, with the following synonymy of the family group names established: Ennomini sensu novo = Urapteridae, syn. n.; = Odopteridi; = Emplocidae, syn. n.; = Oxydiidae, syn. n.; = Pantheridae, syn. n.; = Nephodiinae, syn. n.; = Leuculinae, syn. n.; = Cingiliini, syn. n. The musculature of the male genitalia in Ennomos infidelis and Ourapteryx koreana is described for the first time and that of Tristrophis veneris is revised. The American origin of the tribe Ennomini is hypothesized. The mainly Palaearctic tribe Prosopolophini is regarded as a probable sister group of Ennomini sensu novo.     

New taxa refresh the phylogeny and classification of pleurostomatid ciliates (Ciliophora,Litostomatea)

A high diversity of pleurostomatid ciliates has been discovered in the last decade, and their systematics needs to be improved in the light of new findings concerning their morphology and molecular phylogeny. In this work, a new genus, Protolitonotus gen. n., and two new species, Protolitonotus magnus sp. n. and Protolitonotus longus sp. n., were studied. Furthermore, 19 novel nucleotide sequences of SSU rDNA, LSU rDNA and ITS1‐5.8S‐ITS2 were collected to determine the phylogenetic relationships and systematic positions of the pleurostomatid ciliates in this study. Based on both molecular and morphological data, the results demonstrated that: (i) as disclosed by the sequence analysis of SSU rDNA, LSU rDNA and ITS1‐5.8S‐ITS2, Protolitonotus gen. n. is sister to all other pleurostomatids and thus represents an independent lineage and a separate family, Protolitonotidae fam. n., which is defined by the presence of a semi‐suture formed by the right somatic kineties near the dorsal margin of the body; (ii) the families Litonotidae and Kentrophyllidae are both monophyletic based on both SSU rDNA and LSU rDNA sequences, whereas Amphileptidae are non‐monophyletic in trees inferred from SSU rDNA sequences; and (iii) the genera Loxophyllum and Kentrophyllum are both monophyletic, whereas Litonotus is non‐monophyletic based on SSU rDNA analyses. ITS1‐5.8S‐ITS2 sequence data were used for the phylogenetic analyses of pleurostomatids for the first time; however, species relationships were less well resolved than in the SSU rDNA and LSU rDNA trees. In addition, a major revision to the classification of the order Pleurostomatida is suggested and a key to its families and genera is provided.     

不同的麻醉方案对脑幕上肿瘤手术患者麻醉苏醒期血流动力学的影响

摘要 目的：对比不同麻醉方案对脑幕上肿瘤手术患者麻醉苏醒期血流动力学的影响。方法：选取2017年10月至2019年10月于我院择期行脑幕上肿瘤手术患者为本次研究对象,将其随机分为研究组(n=40)和对照组(n=40)。对照组术中接受右美托咪定麻醉,研究组术中接受异氟醚麻醉,观察并对比研究组和对照组在麻醉诱导前(T₀)、麻醉后30 min(T₁)、麻醉后1 h(T₂)以及手术结束时(T3)血流动力学指标[心率(Heart rate,HR),平均动脉压(Mean arterial pressure,MAP)]、脑氧代谢情况[颈内静脉球部血氧饱和度(Oxygen saturation of the bulb of internal jugular vein,SjvO₂), 动脉血氧含量(Arterial oxygen content,CaO₂),脑静脉氧含量(Cerebral jugular venous oxygen content,CjvO₂),脑氧摄取率(Cerebralextractionofoxygen,CERO₂)],并分析研究组和对照组麻醉效果(优、良、差)和手术相关指标(手术时间、麻醉时间、苏醒时间、输液量)情况。结果：与T₀时相比,研究组和对照组在T₁~T₂时MAP和HR均降低,且对照组明显低于研究组(P<0.05);与T₀时相比,T₃时研究组MAP和HR均增加(P＜0.05);与T₀、T₁、T₃时相比,研究组和对照组T₂时MAP和HR均较低,对照组低于研究组(P<0.05);与T₀时相比,研究组和对照组在T₁~T₃时CjvO₂明显增高,CERO₂明显降低,研究组在T₁~T₃时CjvO₂高于对照组,研究组在T₁~T₃时CERO₂低于对照组(P<0.05),在T₀~T₃时研究组和对照组SjvO₂、CaO₂差异不明显(P＞0.05);与对照组相比,研究组患者麻醉效果优良率较高(P<0.05),苏醒时间明显缩短(P<0.05),研究组和对照组手术时间、麻醉时间、输液量差异不明显(P＞0.05)。结论：：右美托咪定用于脑幕上肿瘤手术患者麻醉效果较好,可以有效稳定血流动力学,降低脑氧代谢,缩短苏醒时间。