不同虫态叉角厉蝽对草地贪夜蛾幼虫的室内捕食作用

为了明确叉角厉蝽 Eocanthecona furcellate (Wolff)对草地贪夜蛾 Spodoptera frugiperda (J.E.Smith)幼虫的控制作用,在实验室条件下测定了叉角厉蝽不同虫态对草地贪夜蛾不同龄期幼虫的捕食能力,研究了该蝽捕食功能反应、搜寻效应以及种内干扰作用。结果表明,叉角厉蝽3龄若虫、5龄若虫、成虫均可捕食草地贪夜蛾幼虫,总体呈现叉角厉蝽低龄若虫捕食草地贪夜蛾低龄幼虫的数量较多,高龄若虫和成虫捕食中间龄期幼虫数量较多的规律;叉角厉蝽3个虫态对草地贪夜蛾2~3龄幼虫的捕食功能反应均符合Holling II方程和HollingⅢ型功能反应新模型;5龄若虫对草地贪夜蛾2~3龄幼虫的捕食效能(a/Th)最强（214.0）、日最大捕食量(1/Th)最大（256.4头）。不同虫态叉角厉蝽的搜寻效应与草地贪夜蛾密度均呈负相关。建立了叉角厉蝽成虫密度、草地贪夜蛾4龄幼虫密度对捕食作用的干扰反应方程,干扰作用发生后该蝽的平均捕食量和捕食作用率均逐渐下降。本研究结果可为田间释放叉角厉蝽防治草地贪夜蛾提供依据。     

叉角厉蝽对草地贪夜蛾的捕食功能反应

叉角厉蝽Eocanthecona furcellate(Wolff)是一种极具应用潜力的重要捕食性天敌。为了探明叉角厉蝽3龄若虫对草地贪夜蛾Spodoptera frugiperda(J.E.Smith) 3龄幼虫的控害效果,在室内条件下,观察了叉角厉蝽对草地贪夜蛾幼虫的捕食行为,研究了叉角厉蝽对草地贪夜蛾3龄幼虫的捕食功能反应。结果表明,叉角厉蝽以口针从草地贪夜蛾腹部或者体躯末端插入取食,被取食后的草地贪夜蛾呈干瘪状死亡。叉角厉蝽3龄若虫对草地贪夜蛾3龄幼虫的捕食功能反应模型符合Holling II型方程,为:Na=0.6702 N/(1+0.0133 N),叉角厉蝽若虫对草地贪夜蛾3龄幼虫的日最大捕食量、瞬时攻击率和处理时间分别为50.25头、0.6702 d和0.0199 d。叉角厉蝽的捕食量与猎物密度正相关,寻找效应与猎物密度负相关,叉角厉蝽的捕食作用存在较强的种内干扰作用。试验证实叉角厉蝽对草地贪夜蛾具有较好的控害效果,为其田间应用释放技术提供了理论依据。     

叉角厉蝽对草地贪夜蛾幼虫的捕食功能反应

草地贪夜蛾Spodoptera frugiperda(J. E. Smith)是2019年新入侵我国的重大农业害虫,已对我国的农作物产生严重为害,筛选、利用本地天敌控制草地贪夜蛾是实现可持续控制的一个重要途径。叉角厉蝽Eocanthecona furcellate(Wolff)是一种广泛分布于热带、亚热带地区的捕食性天敌,是许多鳞翅目、鞘翅目、半翅目害虫的潜在生防因子。本文采用捕食功能反应方法评价了叉角厉蝽对草地贪夜蛾幼虫的捕食效能。研究结果表明,叉角厉蝽3龄、5龄若虫以及雌、雄成虫对草地贪夜蛾3龄及5龄幼虫的捕食功能反应均符合Holling-Ⅱ方程。在饱和猎物密度条件下,叉角厉蝽各虫态对草地贪夜蛾3龄幼虫的平均日最大捕食量依次为32.20头(5龄若虫)19.40头(雌成虫)18.20头(雄成虫)6.60头(3龄若虫),a/Th值(a为瞬时攻击率,Th为处置单头猎物时间)为82.25(5龄若虫)40.39(雌成虫)36.12(雄成虫)17.19(3龄若虫);叉角厉蝽各虫态对草地贪夜蛾5龄幼虫的平均日最大捕食量依次为7.80头(5龄若虫)6.40头(雌成虫)5.50头(雄成虫)4.60头(3龄若虫),a/Th值为11.36(5龄若虫)10.75(雌成虫)9.63(雄成虫)7.45(3龄若虫)。本研究表明叉角厉蝽对草地贪夜蛾幼虫具较强的捕食能力,尤其是5龄若虫、雌成虫和雄成虫。研究结果为利用叉角厉蝽防控草地贪夜蛾提供了理论依据,也为其田间释放应用提供技术支撑。     

人工饲料饲养的叉角厉蝽对昆虫的捕食能力评价

叉角厉蝽Eocanthecona furcellate(Wolff)是广泛分布于热带亚热带地区的一种重要捕食性天敌昆虫。为评估人工饲料饲养的叉角厉蝽的捕食能力,在实验室采用捕食功能反应的方法,以黄粉虫作为中介猎物饲养的叉角厉蝽为对照,评价了人工饲料饲养的叉角厉蝽3龄若虫、5龄若虫以及雌成虫对黄粉虫Tenebriomolitor(L.)幼虫及斜纹夜蛾Spodoptera litura(Fabricius)3龄幼虫、5龄幼虫的捕食效能。结果表明,两种饲料饲养的不同虫态叉角厉蝽的捕食量均随着猎物密度的增加而上升,当猎物密度增加到一定水平,捕食量趋于稳定,其捕食功能反应均符合HollingII模型。人工饲料组饲养的各虫态叉角厉蝽与对照组的对黄粉虫幼虫的捕食量没有明显差异;在饱和猎物密度条件下,人工饲料饲养的叉角厉蝽3龄若虫、5龄若虫以及雌成虫对斜纹夜蛾3龄幼虫的日最大捕食量分别为7.20、9.20、14.60头,对斜纹夜蛾5龄幼虫的日最大捕食量分别4.20、5.80、6.20头,均略低于对照组,但从取食猎物数量上来看,仍保持较强的捕食能力。     

环斑猛猎蝽对草地贪夜蛾低龄幼虫的捕食功能分析

为探究环斑猛猎蝽Sphedanolestes impressicollis Stal对草地贪夜蛾Spodoptera frugiperda Smith的捕食潜能,在室内条件下研究了环斑猛猎蝽4龄若虫对草地贪夜蛾1~3龄幼虫的捕食功能、搜寻效应以及环斑猛猎蝽自身密度对捕食草地贪夜蛾的干扰作用。结果表明：环斑猛猎蝽4龄若虫对草地贪夜蛾低龄幼虫的捕食功能反应符合Holling II模型。环斑猛猎蝽4龄若虫对草地贪夜蛾1龄、2龄、3龄幼虫的瞬时攻击率分别为0.900、1.229和1.259,处理时间分别为0.018 d、0.050 d和0.205 d,日最大捕食量分别为55.897头、19.853头和4.871头。环斑猛猎蝽4龄若虫的搜寻效应与草地贪夜蛾密度呈负相关。环斑猛猎蝽4龄若虫对草地贪夜蛾低龄幼虫的捕食作用率随自身密度的增加而降低。在捕食草地贪夜蛾1龄幼虫时,环斑猛猎蝽4龄若虫自身密度对其捕食能力干扰最大。研究结果表明环斑猛猎蝽4龄若虫对草地贪夜蛾低龄幼虫有一定的捕食能力,为其田间应用释放技术提供了理论依据。     

叉角厉蝽对亚洲玉米螟幼虫的捕食功能反应

叉角厉蝽Eocanthecona furcellata是一种在生物防治方面有重要作用和潜力的捕食性天敌昆虫,为探明叉角厉蝽对亚洲玉米螟Ostrinia furnacalis幼虫的控害潜力,在室内温度26℃±1℃、相对湿度65%±10%、光周期16 L∶8 D条件下,观察了叉角厉蝽4龄、5龄若虫和成虫分别对亚洲玉米螟3龄、4龄幼虫的捕食行为,测定了叉角厉蝽对不同亚洲玉米螟密度下的捕食量、搜寻效应以及自身密度和种间干扰对捕食作用的影响。结果表明,叉角厉蝽对亚洲玉米螟的捕食功能反应符合Holling-Ⅱ功能反应模型,叉角厉蝽3个虫龄对亚洲玉米螟3龄与4龄幼虫的理论最大取食量顺序均为：成虫（30.21头）>5龄若虫（24.69头）>4龄若虫（11.96头）,相同虫龄的叉角厉蝽对亚洲玉米螟3龄幼虫的最大取食量均大于对亚洲玉米螟4龄幼虫的最大取食量。在亚洲玉米螟相同虫龄内,搜寻效应与猎物密度的增加呈负相关。在生存环境和亚洲玉米螟幼虫密度固定的条件下,其平均捕食量和搜寻效应与叉角厉蝽成虫密度的增加呈负相关。叉角厉蝽成虫与亚洲玉米螟幼虫以相同比例增加时,叉角厉蝽成虫种间会产生干扰作用。结果表明了叉角厉蝽对亚洲玉米螟具有较好的控害潜力,为今后高效利用叉角厉蝽田间防治亚洲玉米螟提供了理论依据。     

叉角厉蝽对斜纹夜蛾的捕食功能反应

叉角厉蝽Cahtheconidea furcellata是一种重要的捕食性天敌昆虫,为了探明该虫的捕食潜能,在室内条件下研究了叉角厉蝽成虫对斜纹夜蛾Spodoptera litura Fab.二龄和三龄幼虫的捕食作用和种内干扰作用。结果表明,叉角厉蝽成虫的捕食量随着斜纹夜蛾幼虫的密度增加而增大,其捕食功能反应符合HollingⅡ型方程。叉角厉蝽对斜纹夜蛾2龄幼虫的捕食量符合Na=0.7364N/(1+0.0118N),对斜纹夜蛾3龄幼虫的捕食量符合Na=0.7504N/(1+0.0005N),叉角厉蝽的捕食作用有较强的种内干扰反应,捕食率与个体间相互干扰的关系符合Hassell模型。叉角厉蝽的捕食量与害虫密度正相关,寻找效应与害虫密度负相关。     

叉角厉蝽对黄野螟幼虫的捕食功能反应

为评估叉角厉蝽Eocanthecona furcellate对黄野螟Heortia vitessoides幼虫的控制作用,观察了叉角厉蝽的捕食行为,研究了不同虫态叉角厉蝽对黄野螟3龄及5龄幼虫的捕食功能反应、自身密度效应以及空间异质性对其捕食效能的影响。结果表明:叉角厉蝽对黄野螟幼虫的捕食功能反应符合HollingⅡ型方程,不同虫态叉角厉蝽对黄野螟幼虫攻击率大小顺序为:5龄若虫雌成虫3龄若虫,对3龄黄野螟幼虫理论日最大捕食量分别为21.79、15.38及12.85头。当猎物密度固定为50头/盒时,随着叉角厉蝽密度的增加,其捕食量也逐步增加,但对猎物的寻找效应则减弱,个体间存在相互干扰作用。另外,叉角厉蝽的捕食效能也因空间环境不同表现出较大的差异,空间越大,其捕食率越低。研究结果为定量评估叉角厉蝽对黄野螟的控制作用提供了基础数据,也为其田间释放应用技术提供了依据。     

叉角厉蝽对斜纹夜蛾不同龄期幼虫的选择捕食作用

应用二次回归通用旋转组合设计探讨了叉角厉蝽与斜纹夜蛾低龄幼虫,中龄幼虫和高龄幼虫共存系统中,天敌对猎物不同年龄等级的选择捕食作用,建立了3个年龄等级的幼虫被捕食量模型。根据被捕食量模型可计算出斜纹夜蛾3个年龄等级不同密度组合下,天敌对猎物的选择捕食比率,结果表明,在3个年龄等级相同密度的组合下,叉角厉蝽倾向于捕食个体大的中高龄幼虫。     

草地贪夜蛾幼虫自残捕食量分析

为了明确草地贪夜蛾Spodoptera frugiperda幼虫对同类低龄幼虫的捕食作用,在实验室条件下研究了草地贪夜蛾3~6龄幼虫对不同密度2龄幼虫和4~6龄幼虫对不同密度3龄幼虫的日捕食量,同时从捕食功能的角度解析了草地贪夜蛾高龄幼虫对低龄幼虫的捕食行为;并对不同龄期幼虫进行称重比较,用不同龄期幼虫间的重量关系来替换不同龄期幼虫间的捕食量,得到不同龄期幼虫间的捕食量方程。结果表明,草地贪夜蛾3~6龄幼虫对2龄幼虫和4~6龄幼虫对3龄幼虫的捕食功能反应均符合Holling Ⅱ型功能反应类型。草地贪夜蛾3~6龄幼虫对2龄幼虫的最大捕食量分别为76.47头、85.70头、117.92头、96.05头;4~6龄幼虫对3龄幼虫的最大捕食量分别为38.83头、59.49头、58.87头。高龄幼虫对低龄幼虫的捕食量随猎物密度的增加而增加。最大理论捕食质量方程y=47.231x^0.4591,捕食者的捕食量随着猎物虫态的增大而逐渐减小。研究结果为理解草地贪夜蛾幼虫的种间自残行为规律奠定了一定的理论基础。     

Antitumor activity of phenylene bridged binuclear bis(imino-quinolyl)palladium(II) and platinum(II) complexes

Antitumor effects of a known bis(imino-quinolyl)palladium(II) complex 1 and its newly synthesized platinum(II) analogue 2 were evaluated against human breast (MCF-7) and human colon (HT-29) cancer cell lines. The complexes gave cytotoxicity profiles that were better than the reference drug cisplatin. The highest cytotoxic activities were pronounced in complex 2 across the two examined cancer cell lines. Both compounds represent potential active drugs based on bimetallic complexes.     

Cu(II) and Zn(II) ions alter the dynamics and distribution of Mn(II) in cultured chick glial cells

Previous studies revealed that Mn(II) is accumulated in cultured glial cells to concentrations far above those present in whole brain or in culture medium. The data indicated that Mn(II) moves across the plasma membrane into the cytoplasm by facilitated diffusion or counter-ion transport with Ca(II), then into mitochondria by active transport. The fact that 1–10 M Mn(II) ions activate brain glutamine synthetase makes important the regulation of Mn(II) transport in the CNS. Since Cu(II) and Zn(II) caused significant changes in the accumulation of Mn(II) by glia, the mechanisms by which these ions alter the uptake and efflux of Mn(II) ions has been investigated systematically under chemically defined conditions. The kinetics of [⁵⁴MN]-Mn(II) uptake and efflux were determined and compared under four different sets of conditions: no adducts, Cu(II) or Zn(II) added externally, and with cells preloaded with Cu(II) or Zn(II) in the presence and absence of external added metal ions. Zn(II) ions inhibit the initial velocity of Mn(II) uptake, increase total Mn(II) accumulated, but do not alter the rate or extent Mn(II) efflux. Cu(II) ions increase both the initial velocity and the net Mn(II) accumulated by glia, with little effect on rate or extent of Mn(II) efflux. These results predict that increases in Cu(II) or Zn(II) levels may also increase the steady-state levels of Mn(II) in the cytoplasmic fraction of glial cells, which may in turn alter the activity of Mn(II)-sensitive enzymes in this cell compartment.     

真菌吸附铅锌的研究

正随着采矿业的迅速发展,越来越多的重金属通过多种途径进入土壤环境中,对生态环境造成了不可估量的破坏并严重威胁人类健康。铅锌在工业上具有非常重要的作用且其应用极为广泛,而他们具有的难去除、难迁移和生物累积等特性使得铅锌在环境中的污染尤为突出。通过微生物的生长代谢,有效降低土壤重金属毒性,是促进植物生长的重要步骤之一。同时也要求微生物自身具有抵抗重金属的功能,根际微生     

Homoleptic copper(II) and copper(I) complexes of 5,6-dihydro-5,6-epoxy-1,10-phenanthroline. Six-coordinate copper(I) in solution

Reaction of 5,6-dihydro-5,6-epoxy-1,10-phenanthroline (L) with Cu(ClO₄)₂·6H₂O in methanol in 3:1 M ratio at room temperature yields light green [CuL₃](ClO₄)₂·H₂O (1). The X-ray crystal structure of the hemi acetonitrile solvate [CuL₃](ClO₄)₂·0.5CH₃CN has been determined which shows Jahn-Teller distortion in the CuN₆ core present in the cation [CuL₃]²⁺. Complex 1 gives an axial EPR spectrum in acetonitrile-toluene glass with g_|| = 2.262 (A_|| = 169 × 10⁻⁴ cm⁻¹) and g_⊥ = 2.069. The Cu(II/I) potential in 1 in CH₂Cl₂ at a glassy carbon electrode is 0.32 V versus NHE. This potential does not change with the addition of extra L in the medium implicating generation of a six-coordinate copper(I) species [CuL₃]⁺ in solution. B3LYP/LanL2DZ calculations show that the six Cu-N bond distances in [CuL₃]⁺ are 2.33, 2.25, 2.32, 2.25, 2.28 and 2.25 Å while the ideal Cu(I)-N bond length in a symmetric Cu(I)N₆ moiety is estimated as 2.25 Å. Reaction of L with Cu(CH₃CN)₄ClO₄ in dehydrated methanol at room temperature even in 4:1 M proportion yields [CuL₂]ClO₄ (2). Its ¹H NMR spectrum indicates that the metal in [CuL₂]⁺ is tetrahedral. The Cu(II/I) potential in 2 is found to be 0.68 V versus NHE in CH₂Cl₂ at a glassy carbon electrode. In presence of excess L, 2 yields the cyclic voltammogram of 1. From ¹H NMR titration, the free energy of binding of L to [CuL₂]⁺ to produce [CuL₃]⁺ in CD₂Cl₂ at 298 K is estimated as −11.7 (±0.2) kJ mol⁻¹.     

Synthesis and structural characterization of two new polynuclear metal thiosaccharinates: Hexakis(thiosaccharinato)hexasilver(I) and tetrakis(thiosaccharinato)tetracopper(I)

The title compounds, for short Ag₆(tsac)₆ (1) and [Cu₄(tsac)₄(MeCN)₂] · 2MeCN (2), were prepared by the reaction of thiosaccharin with Ag(I) or Cu(II) salts in different solvents. The new complexes were characterized by FT-IR, Raman, UV-Vis and NMR spectroscopy. Their crystal and molecular structures were determined by X-ray diffraction methods. The structures were solved from 1621 (1) and 7080 (2) reflections with I > 2σ(I) and refined to agreement R1-factors of 0.0261 (1) and 0.0456 (2). Ag₆(tsac)₆ molecule derives from the clustering of six Ag(tsac) moieties related to each other through the crystallographic 3-bar (S₆) symmetry operations of the space group. This results in a highly regular molecular structure where the silver atoms are at the corners of an octahedral core slightly compressed along one of its three-fold axis [inter-metallic Ag?Ag contacts of 3.1723(4) and 3.1556(4) Å]. The six thiosaccharinate ligands bridge neighboring Ag atoms along the C₃-axis through Ag-N bonds [d(Ag-N) = 2.285(2) Å] at one end and bifurcated Ag-S(thione)-Ag bonds [Ag-S distances of 2.4861(7) and 2.5014(8) Å] at the other end. In contrast, the 2 compound is arranged in the lattice as an irregular tetrameric copper complex [Cu₄(tsac)₄(MeCN)₂] where the metals show different environments. Two copper ions are four-fold coordinated to three tsac ions through the N-atom of one tsac [Cu-N distances of 2.112(3) and 2.064(3) Å] and the thione sulfur atom of the other two [Cu-S distances in the range from 2.284(1) to 2.358(1) Å] and to a MeCN solvent molecule [Cu-N distances of 1.983(4) and 2.052(3) Å]. The other two copper ions are in three-fold environment, one trans-coordinated to two tsac ions [Cu-N distances of 1.912(3) and 1.920(3) Å] and to the thione S-atom of a third ligand [d(Cu-S) = 2.531(1) Å], the other one to the thione sulfur atom of three tsac ligands [Cu-S distances in the range from 2.229(1) to 2.334(1) Å]. The clustering renders the metals to short distances from each other, the shorter Cu?Cu distance being 2.6033(7) Å, as to presume the existence of weak inter-metallic interaction within the cluster.     

Poly(etheno ADP-ribose) blocks poly(ADP-ribose) glycohydrolase activity

Poly(ADP-ribose) is a biopolymer synthesized by poly(ADP-ribose) polymerases. Recent findings suggest the possibility for modulation of cellular functions including cell death and mitosis by poly(ADP-ribose). Derivatization of poly(ADP-ribose) may be useful for investigating the effects of poly(ADP-ribose) on various cellular processes. We prepared poly(etheno ADP-ribose) (poly(epsilonADP-ribose)) by converting the adenine moiety of poly(ADP-ribose) to 1-N(6)-etheno adenine residues. Poly(epsilonADP-ribose) is shown to be highly resistant to digestion by poly(ADP-ribose) glycohydrolase (Parg). On the other hand, poly(epsilonADP-ribose) could be readily digested by phosphodiesterase. Furthermore, poly(epsilonADP-ribose) inhibited Parg activity to hydrolyse ribose-ribose bonds of poly(ADP-ribose). This study suggests the possibility that poly(epsilonADP-ribose) might be a useful tool for studying the poly(ADP-ribose) dynamics and function of Parg. This study also implies that modification of the adenine moiety of poly(ADP-ribose) abrogates the susceptibility to digestion by Parg.     

Immobilization of Cu(II) and Cr(IV) in basidiomycete-colonized sawdust

An investigation into the feasibility of removing Cu(II) and Cr(IV) from solution with basidiomycete (Gloeophylum sepiarium, Pleurotus sp.)-colonized sawdust was undertaken. Obeche (Triplochyton scleroxylon) sawdust exposed to the basidiomycetes for 1–3 months reduced the concentration of the metals in the solution to 22.0–84.4 mg/l. The supernatant from the centrifuged mixture of a solution of 100 mg metal ions/l and aqueous extract of a 3-month basidiomycete-degraded obeche sawdust contained lower concentration of the metal ions (38.6–75.4 mg/l). Unextracted sawdust of pigmented tropical timbers, African mahogany (Khaya ivorensis), black afara (Terminalia ivorensis) and camwood (Baphia nitida) exposed to the test basidiomycetes, removed Cu and Cr significantly better than the extracted sawdust. It is hypothesised that some products of basidiomycete wood-degradative activities were ligands which immobilized the test metals.     

人血浆载脂蛋白（a）的分离及纯化

本文报道从人血浆脂蛋白Ｌｐ（ａ）中,分离纯化载脂蛋白（ａ）。收集富含Ｌｐ（ａ）的混合血浆,超离心,获密度１．０５ｇ／ｍｌ至１．０８ｇ／ｍｌ的粗制Ｌｐ（ａ）,经过Ｂｉｏ－Ｇｅｌ Ａ５ｍ层析后,证明纯化后的Ｌｐ（ａ）仅与ａｐｏ（ａ）抗血清反应,经ＤＴＴ处理过的Ｌｐ（ａ）,在琼脂糖电泳中的泳动率由胶β位移到β位,在印迹免疫反应中,对ａｐｏ（ａ）的抗血清反应依然显示在前β位,ＳＤＳ聚丙烯凝胶电脉的迁移率慢     

Poly(dG)-poly(dC) DNA appears shorter than poly(dA)-poly(dT) and possibly adopts an A-related conformation on a mica surface under ambient conditions

Three types of DNA: approximately 2700 bp polydeoxyguanylic olydeoxycytidylic acid [poly(dG)-poly(dC)], approximately 2700 bp polydeoxyadenylic polydeoxythymidylic acid [poly(dA)-poly(dT)] and 2686 bp linear plasmid pUC19 were deposited on a mica surface and imaged by atomic force microscopy. Contour length measurements show that the average length of poly(dG)-poly(dC) is approximately 30% shorter than that of poly(dA)-poly(dT) and the plasmid. This led us to suggest that individual poly(dG)-poly(dC) molecules are immobilized on mica under ambient conditions in a form which is likely related to the A-form of DNA in contrast to poly(dA)-poly(dT) and random sequence DNA which are immobilized in a form that is related to the DNA B-form.     

Bioaccumulation of copper(II), lead(II) and chromium(VI) by growing Aspergillus niger

The effect of copper(II), lead(II) and chromium(VI) ions on the growth and bioaccumulation properties of Aspergillus niger was investigated as a function of initial pH and initial metal ion concentration. The optimum pH values for growth and metal ion accumulation were determined as 5.0, 4.5 and 3.5 for copper(II), lead(II) and chromium(VI) ions, respectively. Although all metal ion concentrations caused an inhibition effect on the growth of A. niger, it was capable of removing of copper(II) and lead(II) with a maximum specific uptake capacity of 15.6 and 34.4 mg g⁻¹ at 100 mg dm⁻³ initial copper(II) and lead(II) concentration, respectively. Growth of A. niger was highly effected by chromium(VI) ions and inhibited by 75 mg dm⁻³ initial chromium(VI) concentration since some inhibition occurred at lower concentrations.