Reproductive biology of Mystus vittatus (Bloch) (Bagridae: Siluriformes) from Guntur,Andhra Pradesh

Maturation, minimum length at first maturity, spawning season, spawning periodicity, sex-ratio and absolute fecundity of Mystus vittatus, a common bagrid catfish, have been investigated. The observations show that spawning takes place during September and October. Each individual spawns only once in the season as evidenced by the study of the intraovarian ova. Females dominate the catches, and absolute fecundity (F) can be expressed by% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGak0dh9WrFfpC0xh9vqqj-hEeeu0xXdbba9frFj0-OqFf% ea0dXdd9vqaq-JfrVkFHe9pgea0dXdar-Jb9hs0dXdbPYxe9vr0-vr% 0-vqpWqaaeaabaGaaiaacaqabeaadaqaaqaaaOabaeqabaGaciiBai% aac+gacaGGNbGaaeiiaiaabAeacaqGGaGaaeypaiaabccacaqGTaGa% ae4maiaab6cacaqGYaGaaeyoaiaabkdacaqGGaGaae4kaiaabccaca% qG0aGaaeOlaiaabgdacaqG3aGaaeymaiaabgdacaqGGaGaaeiBaiaa% b+gacaqGNbGaaeiiaiaabYeaaeaacaqGHbGaaeOBaiaabsgacaqGGa% GaaeOraiaabccacaqG9aGaaeiiaiaab2cacaqGXaGaaeOlaiaabwda% caqG0aGaaeinaiaabwdacaqGGaGaae4kaiaabccacaqGWaGaaeOlai% aabMdacaqG0aGaae4naiaabkdacaqGGaGaae4vaaaaaa!5FCC!\[\begin{gathered} \log {\text{ F = - 3}}{\text{.292 + 4}}{\text{.1711 log L}} \hfill \\ {\text{and F = - 1}}{\text{.5445 + 0}}{\text{.9472 W}} \hfill \\ \end{gathered} \]     

Cell suspension culture from Porphyra linearis (Rhodophyta) a multicellular marine red alga

A cell-suspension culture suitable for continuous propagation was established from protoplasts of the red alga Porphyra linearis Grev., an edible, winter annual species of nori. Protoplast-derived cells that did not regenerate into thalli were used to establish a culture line of uniform-sized (average about 25 μm diam.) cells, which resembled the vegetative cells of this species in the leafy thallus phase. Cell division occurred about once per 24 to 30 h in uncrowded (1–2 cells per culture well) culture. This cell-suspension culture has now been maintained as continuously growing subcultures for more than four years without formation of organized thalli; however, the latter can be obtained at will by altering culture conditions (lowering temperature from 20° to 10 °C, lengthening photoperiod from 10: % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaca% aIXaGaaGinaaaaaaa!3777!\[\overline {14} \] or 8 : % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaca% aIXaGaaGOnaaaaaaa!3779!\[\overline {16} \] to 14: % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaca% aIXaGaaGimaaaaaaa!3773!\[\overline {10} \] or 16: % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaca% aI4aaaaaaa!36C0!\[\overline 8 \] and increasing irradiance from 10 to ≥ 30 μmol m^-2 s^-1). This appears to be the first continuous non-clonal cell-suspension culture developed for a multicellular alga. NRCC No. 30272.     

Different responses to changes in phosphorus,P, among lakes. A study of slopes in chl-a = f(P) graphs

The least squares estimator of a linear regression coefficient _L will give an overall expression for the change in with x. In fresh water ecology, however, subgroups, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaamiuaSGaci% 4Aaaaa!37BE!\[P\operatorname{k}\], of a parent population may have slopes which differ from the overall slope, _L. By constructing frequency histograms for the set of angles: Arctang % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaci4uaSGaam% yAaiaadQgaaaa!38AE!\[\operatorname{S} ij\],% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaci4uaSGaam% yAaiaadQgaaaa!38AE!\[\operatorname{S} ij\]= para sa y and x% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaaiikaiaadM% faliaadMgakiabgkHiTiaadMfaliaadQgakiaacMcacaGGVaGaaiik% aiaadIhaliaadMgakiabgkHiTiaadIhaliaadQgakiaacMcaaaa!42F0!\[(Yi - Yj)/(xi - xj)\], i < j, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaamiEaSGaam% yAaOGaeyiyIKRaamiEaSGaamOAaaaa!3BAB!\[xi \ne xj\], peaks in the distribution may be identified and related to ecological phenomenon. To identify peaks we fit Gaussian distributions to the frequency histograms. For a set consisting of 142 observations of chlorophyll-a and total phosphorus (nutrient) concentrations (TP) from 16 lakes we found four Gaussian peaks corresponding to four subgroups, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaamiuaSGaci% 4Aaaaa!37BE!\[P\operatorname{k}\]k = 1,4. One group identified a response of chl-a to changes in TP which correspond approximately to the average slope found by least square regression (the slope was 0.49). The second group consisted of steeper response than the average (1.28). A third group showed that there is an enhanced proportion of cases where chl-a does not respond to TP (zero slope, all the three deep lakes > 10 m, included in the date set contributed to this group). The size of the last group, spanning a wide range of slopes, suggested that about 30% of the inter annual changes in chl-a is unrelated to TP. The results are compared to result obtained by simple least squares regression and to the Theil non-parametric slope estimator.     

Some biological aspects and life history strategies of Nile tilapia Oreochromis niloticus (L.) in Lake Victoria, Kenya

The life history characteristics of introduced Nile tilapia (Oreochromis niloticus L.) in Lake Victoria, including, sex ratio, fecundity, reproduction, weight‐length relationship and body condition were studied and compared with those of other populations. Samples were collected by trawling and seining in the Kenyan sector of Lake Victoria between June 1998 and December 2000. Males predominated over females (sex ratio 1.42 : 1 : 00). O. niloticus spawned throughout the year but with a peak between December and June. Length at first maturity was (mean ± SD) 30.81 ± 0.09 for females and 34.5 ± 6 0.48 for males. There was little seasonal variation in relative condition, which ranged from 0.92 to 1.05 in males and 0.94 to 1.07 in females. Gonadosomatic index (GSI) was low during the postspawning period (July to October) and high during the protracted breeding period (December and June). Fecundity ranged from 905 to 7619 oocytes for fish of 28 to 51 cm total length (TL) respectively. The relationships between fecundity (F) and total length (L), weight (W) and ovary weight (OW) were: F = 8.159L^1.53, F = 96.269W^0.4504, F = 1806 + 39.4OW. The slope b of the weight‐length relationship was 3.08–3.32 for males and 3.07–3.22 for females. Growth was allometric in both cases and was significantly different from the expected value of 3. The life history strategy of O. niloticus is discussed in context of environmental changes occurring in the lake.     

Chemistry, ecology and seasonal succession of Charophytes in the Al-Kharj Irrigation Canal, Saudi Arabia

We surveyed (Oct. 1991–Sept. 1992) a 16.5-km-long irrigation canal in Al-Kharj City, for its water chemistry, and Charophyte periodicity and density. Marked differences occurred between the origin of a cave-lake, and the final discharge. Six species, Chara globularis, C. vulgaris f. contraria, C. vulgaris var. gymnophylla, C. vulgaris var. longibracteata, C. zeylanica, C. zeylanica var. diaphana f. oerstediana heavily encrust, as opposed to C. benthamii and C. fibrosa. The most widespread were Chara zeylanica and C. benthamii. Chara zeylanica dominated station IV for most of the study period, and ousted all its competitors, such that a 100% monospecific stand was observed here between January and February 1992. The second abundant was Chara benthamii (44%, station II). All Charophytes were seen in the month of November and December 1991, suggesting a luxuriant growth in winter.The water was calcareous, with a high amount of Mg⁺⁺ (% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmiwayaara% aaaa!36E2!\[\bar X\] = 38 mg l^–1), Ca⁺⁺ (% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmiwayaara% aaaa!36E2!\[\bar X\] = 121 mg l^–1) and reactive-Si (% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmiwayaara% aaaa!36E2!\[\bar X\] = 10.8 mg l^–1). A gradual decrease in elements/ions (Si = 12 – 8 mg l^–1, Cl^– = 357–251 mg l^–1 and CaCO₃ 390–328 mg l^–1) from source to outlet was demonstrated during June. The heavy encrustation of Charophytes is plausibly related to a high concentration of CaCO₃ (% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmiwayaara% aaaa!36E2!\[\bar X\] = 364 mg l^–1).     

Plant regeneration from explant and protoplast derived calluses of Medicago littoralis

Plant regeneration from explant and protoplast derived callus has been achieved in Medicago littoralis cv. Harbinger 1886, an annual legume resistant to the fungus Pseudopeziza medicaginis. Callus was induced from different tissue explants and the fastest growth rate was observed for hypocotyls in B5 medium with 2 mg l^–1 2,4-dichlorophenoxyacetic acid and 0.5 mg l^–1 N⁶-benzyladenine. Protoplasts were isolated from cotyledons and leaves of sterile plants and from callus; the first two kinds of protoplasts showed a plating efficiency of 5.6% and 5%, respectively, when embedded in agarose. Plant regeneration occurred on media containing % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9qq-f0-yqaqVeLsFr0-vr% 0-vr0db8meaabaqaciGacaGaaeqabaWaaeaaeaaakeaacaqGobWaaW% baaSqabeaacaqG2aaaaOGaaeOVfiaabs5adaahaaWcbeqaaiaaikda% aaGccaqG+waaaa!3F97!\[{\text{N}}^{\text{6}} {\text{\Delta }}^2 {\text{}}\]isopentenyl-adenine combined with indole-3-acetic acid or 1,2-benzisoxazole-3-acetic acid, and on media with N⁶-benzyladenine plus -naphtaleneacetic acid; a cytokinin/auxin ratio higher than 1 induced embryos while a ratio around 1 stimulated shoot formation. Embryo development and rooting of shoots were performed in RL medium without growth regulators.Abbreviations NAA -naphthaleneacetic acid - BA N⁶-benzyladenine - 2,4-D 2,4-dichlorophenoxyacetic acid - 2iP % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9qq-f0-yqaqVeLsFr0-vr% 0-vr0db8meaabaqaciGacaGaaeqabaWaaeaaeaaakeaacaqGobWaaW% baaSqabeaacaqG2aaaaOGaaeOVfiaabs5adaahaaWcbeqaaiaaikda% aaGccaqG+waaaa!3F97!\[{\text{N}}^{\text{6}} {\text{\Delta }}^2 {\text{}}\]isopentenyl-adenine - IAA indole-3-acetic acid - BOA 1,2-benzisoxazole-3-acetic acid - KIN kinetin - MS Murashige & Skoog (1962) - GRFMS growth regulator free MS medium - B5 Gamborg et al. (1968) - RL Phillips & Collins (1979) - KM8 KM8P Kao & Michayluk (1975) - CPW Frearson et al. (1973) - f. wt fresh weight - FDA fluorescoin diacetate     

The effect of micro-aerobic conditions on continuous ethanol production by Saccharomyces cerevisiae

Summary The effect of trace amounts of oxygen on the degree of ethanol inhibition in a continuous anaerobic culture of Saccharomyces cerevisiae was studied at the 100 gl ^–1 feed glucose concentration level. Results showed that the use of micro-aerobic conditions (0,5% of saturation) enhanced the utilisation of substrate by increasing the ethanol tolerance of the yeast without any significant decrease in the ethanol yield per unit substrate consumed. When the results were fitted to an equation of the form % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcLbyacaqG8o% GaaeypaiqabY7agaqcaiaab6cadaWcaaGcbaqcLbyacaqGdbWaaSba% aSqaaKqzagGaae4CaaWcbeaaaOqaaKqzagGaae4qamaaBaaaleaaju% gGbiaabohaaSqabaqcLbyacqGHRaWkcaqGlbWaaSbaaSqaaKqzagGa% ae4CaaWcbeaaaaqcLbyacaGGUaWaaSaaaOqaaKqzagGaae4samaaBa% aaleaajugGbiaabchaaSqabaaakeaajugGbiaabUeadaWgaaWcbaqc% LbyacaqGWbaaleqaaKqzagGaey4kaSIaaeywamaaBaaaleaajugGbi% aabchacaqGZbaaleqaaKqzagGaaiOlaiaacIcacaqGdbWaaSbaaSqa% aKqzagGaae4CaiaabAgaaSqabaqcLbyacqGHsislcaqGdbWaaSbaaS% qaaKqzagGaae4CaaWcbeaajugGbiaacMcaaaaaaa!6301!\[{\text{\mu = \hat \mu }}{\text{.}}\frac{{{\text{C}}_{\text{s}} }}{{{\text{C}}_{\text{s}} + {\text{K}}_{\text{s}} }}.\frac{{{\text{K}}_{\text{p}} }}{{{\text{K}}_{\text{p}} + {\text{Y}}_{{\text{ps}}} .({\text{C}}_{{\text{sf}}} - {\text{C}}_{\text{s}} )}}\]it was found that the values for % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabeiVdyaaja% aaaa!373F!\[{\text{\hat \mu }}\], K_s and Y_ps were the same as for the non-aerobic case while the ethanol inhibition constant, K_p , had increased from 5,2 to 14,0 gl ^–1.Notation C_sf feed substrate concentration - gl ^–1 - C_s substrate concentration gl ^–1 - C_p product concentration - gl ^–1 - C_x cell concentration - gl ^–1 - D dilution rate - h^-1 - K_s substrate saturation constant - gl ^–1 - K_p product inhibition constant - gl ^–1 - m maintenance coefficient - h^–1 - Y_ps product yield coefficient - g EtOH/g glucose - Y_xs cell yield coefficient - g cells/g glucose - specific growth rate - h^–1 - % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabeiVdyaaja% aaaa!373F!\[{\text{\hat \mu }}\] maximum specific growth rate - h^–1     

Die produktion von potamopyrgus jenkinsi (SMITH) (Gastropoda,prosobranchia) im bodensee

Two cohorts p. a. are identified. The mean annual biomass % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaci% GGcbaaaaaa!36C6!\[\overline \operatorname{B} \] is 88 mg fresh weight/ l00 cm². The ratio production/% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaci% GGcbaaaaaa!36C6!\[\overline \operatorname{B} \] is P/% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaci% GGcbaaaaaa!36C6!\[\overline \operatorname{B} \] = 2,51 for the first and P/% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaci% GGcbaaaaaa!36C6!\[\overline \operatorname{B} \] = 3,67 for the second cohort. The actual net production of the total population is 7% of potential net production.

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Die produktion von potamopyrgus jenkinsi (SMITH) (Gastropoda, prosobranchia) im bodensee

Zusammenfassung P. jenkinsi bringt jährlich zwei Generationen hervor, deren wahrscheinliche Verknüpfung untereinander in Abb. 3 dargestellt ist. Für fie Produktions berechnungen wurde eine etwas vereinfachte Vorstellung zugrundegelegt (Tab. 1), nach der die getrennten Abundanz- und Biommasse-Kurven der Abb. 4 berechnet wurden.Aus Geburtsraten und Beständen der maturen Tiere konnte die Zahl der Neonatae errechnet werden, die in jede Generation eingeht. Mit diesen Daten und mit denen der Abb. 4 wurde über Allen-Kurven die Produktion bestimmt. Die Resultate sind in Tab. 2 zusammengefaßt.

     

Population dynamics of two small cichlid fish species in a tropical man-made lake (Lake Kariba)

The population dynamics of two small cichlid fishes (Pharyngochromis darlingi andPseudocrenilabrus philander) were studied in Lake Kariba, a very large African man-made lake. They are of no economic importance but make up about 14% and 7% respectively of the inshore fish population and are the major components of the diet of fish-eating birds on the lake.P. darlingi isthe larger species (L = 156.5 mm) and is found on both shelving and steep, eroding shores. Its mortality rate differs in each habitat (Z = 0.44 and 0.72 month^–1 respectively), only 0.79% survive for 12 months and its % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaamiuaiaac+% cadaqdaaqaaiaadkeaaaaaaa!384D!\[P/\overline B \] ratio is 5.45 (on shelving shores).Ps. philander is smaller (L = 83.9 mm) and is restricted to shelving areas with abundant vegetation. Its monthly mortality rate was high (Z = 7.69), only 0.05% survive to 12 months whilst its % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaamiuaiaac+% cadaqdaaqaaiaadkeaaaaaaa!384D!\[P/\overline B \] ratio was very high (7.69). The estimates of growth obtained forP. darlingi differ considerably from those given in an earlier study in Lake Kariba and some possible reasons for this are discussed. In suitable habitats, the combined production of both species could be 40 kg ha^–1 yr^–1 which indicates their potential importance to the ecology of the lake.     

Manganese toxicity: The significance of magnesium for the sensitivity of wheat plants

The tolerance of wheat to manganese was investigated in soil and solution culture. Although no critical toxicity concentration could be identified, growth was reduced when the ratio of magnesium to manganese in the shoots (R_p) fell below 20:1 (mgg^–1/mgg^–1). In soil, plant growth relative to unstressed plants (Y) could be described by the empirical equation: % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaaeywaiabg2% da9iaaicdacaGGUaGaaGyoaiaaiwdacqGHsislcaaIWaGaaiOlaiaa% iMdacaaI1aGaaeyzaiaabIhacaqGWbGaaiikaiabgkHiTiaaicdaca% GGUaGaaGymaiaaiodacaaI5aGaaeOuamaaBaaaleaacaqGWbaabeaa% kiaacMcaaaa!4959!\[{\text{Y}} = 0.95 - 0.95{\text{exp}}( - 0.139{\text{R}}_{\text{p}} )\]In solution culture the value of R_p was related to the ratio of the two ions in the nutrient solution (R_s) according to the expression: % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaaeysaiaab6% gacaqGGaGaaeOuamaaBaaaleaacaqGWbaabeaakiabg2da9iaaicda% caGGUaGaaGinaiaaikdacqGHRaWkcaaIWaGaaiOlaiaaisdacaaI4a% GaaeiiaiaabMeacaqGUbGaaeiiaiaabkfadaWgaaWcbaGaae4Caaqa% baGccaGGPaaaaa!47B6!\[{\text{In R}}_{\text{p}} = 0.42 + 0.48{\text{ In R}}_{\text{s}}\]The magnesium concentration in the nutrient solution for optimum growth at a given concentration of manganese was given by: % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaaeysaiaab6% gacaqGGaGaae4waiaab2eacaqGNbGaaeyxaiabg2da9iaaikdacaGG% UaGaaGioaiaaiMdacqGHRaWkcaaIWaGaaiOlaiaaiwdacaaI0aGaae% iiaiaabMeacaqGUbGaaeiiaiaabUfacaqGnbGaaeOBaiaab2faaaa!4A0B!\[{\text{In [Mg]}} = 2.89 + 0.54{\text{ In [Mn]}}\]Magnesium increased the tolerance of plants to high concentrations of manganese in shoot tissue and also increased the ability of the plant to discriminate against manganese ions in translocation of nutrients from roots to shoots.     

Sequences of colonization,diversity, biomass,and productivity of macroinvertebrates on artificial substrates in a freshwater canal

The sequence of colonization, species diversity (% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaca% qGKbaaaaaa!36E5!\[\overline {\text{d}} \]), biomass, and productivity of macroinvertebrates on artificial substrates was determined in a relatively constant environment freshwater canal. Three substrates were removed weekly during a 16 week test period. Community structure of benthic macroinvertebrates was determined at the onset and end of the test period and compared with substrate community structure. Calopsectra sp. was the dominant early colonizing organism; Dicrotendipes sp. and Dicrotendipes modestus were also abundant. In late collections other chironomids, ephemeropterans, gastropods, oligochaetes, amphipods, and trichopterans occurred. Trichopterans were generally dominant in numbers and biomass in later collections. A total of 104 were collected on the substrates.Collection diversity (% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaca% qGKbaaaaaa!36E5!\[\overline {\text{d}} \]) began at 3.42 (week 1), decreased to 2.72 in the third week, and then continually increased for the remainder of the test period to 4.43. Cumulative diversity had a similar trend, decreasing from 3.42 (week 1) to 3.06 in the fourth week, and then increasing to 4.05. Neither collection % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaca% qGKbaaaaaa!36E5!\[\overline {\text{d}} \] or cumulative % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaca% qGKbaaaaaa!36E5!\[\overline {\text{d}} \] reached an asymptote in the 16 week period.Collection biomass began at 0.0867 g/0.26 m² for week one and was 1.0575 g/0.26 m² at the end of the test period. Biomass increased linearly for seven weeks, fluctuated widely until week 14, then increased sharply for the remainder of the test period. Productivity ranged from –3.42 g/m²/wk in the eighth week to 5.10 g/m²/wk in the last collection. Biomass and productivity were greatly affected by the presences or absences of a relatively few large organisms.One hundred two taxa were collected from the benthic samples, 34 not being present on the substrates. Limodrilus hoffmeisteri was the dominant benthic organism, while Calopsectra sp. and Polypedilum sp. were also abundant. The February benthic diversity % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaca% qGKbaaaaaa!36E5!\[\overline {\text{d}} \] was 4.54 and the June % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaa0aaaeaaca% qGKbaaaaaa!36E5!\[\overline {\text{d}} \] was 4.05.     

Measurement of amount of nitrogen fixed by a legume crop

Summary The amount of nitrogen fixed by a legume crop can be calculated from the relationship % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGceaqabeaacaqGbb% GaaeyBaiaab+gacaqG1bGaaeOBaiaabshacaqGGaGaae4BaiaabAga% caqGGaGaaeOzaiaabMgacaqG4bGaaeyzaiaabsgacaqGGaGaaeOtai% aabccacaqG9aaabaGaaeypaiaabccadaqadaqaaiaaigdacqGHsisl% daWcaaqaaiGacggacaGG0bGaai4Baiaac2gacaGGGaGaaiyjaiaacc% cacaGGobGaaiylaiaacgdacaGG1aGaaiiiaiaacwgacaGG4bGaai4y% aiaacwgacaGGZbGaai4CaiaacccacaGGPbGaaiOBaiaacccacaGGSb% GaaiyzaiaacEgacaGG1bGaaiyBaiaacwgacaGGGaGaai4yaiaackha% caGGVbGaaiiCaaqaaiGacggacaGG0bGaai4Baiaac2gacaGGGaGaai% yjaiaacccacaGGobGaaiylaiaacgdacaGG1aGaaiiiaiaacwgacaGG% 4bGaai4yaiaacwgacaGGZbGaai4CaiaacccacaGGPbGaaiOBaiaacc% cacaqGYbGaaeyzaiaabAgacaqGLbGaaeOCaiaabwgacaqGUbGaae4y% aiaabwgacaGGGaGaai4yaiaackhacaGGVbGaaiiCaaaaaiaawIcaca% GLPaaacaqI4bGaaKiiaiaabshacaqGVbGaaeiDaiaabggacaqGSbGa% aeiiaiaab6eacaqGGaGaaeyAaiaab6gacaqGGaGaaeiBaiaabwgaca% qGNbGaaeyDaiaab2gacaqGLbGaaeiiaiaabogacaqGYbGaae4Baiaa% bchaaaaa!9A78!\[\begin{gathered} {\text{Amount of fixed N = }} \hfill \\ {\text{ = }}\left( {1 - \frac{{\operatorname{atom} \% N - 15 excess in legume crop}}{{\operatorname{atom} \% N - 15 excess in {\text{reference}} crop}}} \right)\user1{x }{\text{total N in legume crop}} \hfill \\ \end{gathered} \]when a suitable reference crop is chosen. The implications and interpretation of this method of measurement are described.     

Limnology and plankton periodicity of Jos Plateau water reservoir,Nigeria, West Africa

Limnological data (Dec. 1980–Jan. 1982) on the plankton and water chemistry of Lamingo Dam, located within the Jos biotite granite area of the Plateau State (Nigeria) are presented. The water-body falls in Beadle's (1981) category I of African lakes (conductivity < 40 µS cm^–1). Alkalinity (% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGak0Jf9crFfpeea0xh9v8qiW7rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmiEayaara% aaaa!3914!\[\bar x\] = 0.3 meq l^–1), principally composed of bicarbonates, dominated the anions % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGak0Jf9crFfpeea0xh9v8qiW7rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaaK4waiaajI% eacaqIdbGaaK4tamaaxababaGaeyOeI0caleaacaaIZaaabeaakiaa% b6dacaqIdbGaaKiBaiaaj2cacaqG+aGaaK4uaiaaj+eadaqhaaWcba% GaaKinaaqaaiaajkdacaqITaaaaOGaaKyxaaaa!4657!\[\user1{[HCO}\mathop -\limits_3 {\text{ > }}\user1{Cl - }{\text{ > }}\user1{SO}_\user1{4}^{\user1{2 - }} \user1{]}\]The plankton were characterized by a moderate standing crop of phytoplankton, and zooplankton were, generally, very limited in species and abundance. The order of dominance for the categories of phyto and zooplankton was: [Bacillariophyceae > Chlorophyceae > Dinophyceae] and [Rotifera > Crustacea] respectively. A diel cycle was characterized by nocturnal upward migration of the zooplankton, and the reverse behaviour in the phytoplankton.Interrelations between the biotic assemblages of plankters and various physical and chemical variables are discussed.     

Root biomass fraction as a function of growth degree days in wheat

Root, underground and above-ground biomass were measured on various wheat cultivars from 1986 to 1988 in the south-east of France. The results are expressed as root: total (f _r) or underground: total (f _u) biomass fractions. Observed f _r and f _u values are in good agreement with previous results. f _r and f _u decrease steadily from emergence to maturity, with an exponential tendency. When using cumulative growth degree days since emergence relative to cumulative growth degree days until ear emergence () as time scale, f _r and f _u can be expressed as simple functions of % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGceaqabeaacaWGMb% addaWgaaqaaiaadkhaaeqaamaabmaabaGccqaH4oqCdaahaaWcbeqa% aiaacQcaaaaamiaawIcacaGLPaaakiabg2da9iaaicdacaGGUaGaaG% imaiaaiwdacqGHRaWkcaaIWaGaaiOlaiaaiwdacaaI4aGaamyzamaa% CaaaleqabaGaeyOeI0IaaGymaiaac6cacaaI0aGaaGioaiabeI7aXn% aaCaaameqabaGaaiOkaaaaaaaakeaacaWGMbaddaWgaaqaaiaadwha% aeqaamaabmaabaGccqaH4oqCdaahaaWcbeqaaiaacQcaaaaamiaawI% cacaGLPaaakiabg2da9iaaicdacaGGUaGaaGymaiaaikdacqGHRaWk% caaIWaGaaiOlaiaaiIdacaaI4aGaamyzamaaCaaaleqabaGaeyOeI0% IaaGOmaiaac6cacaaIYaGaaGioaiabeI7aXnaaCaaameqabaGaaiOk% aaaaaaaaaaa!610D!\[\begin{gathered} f_r \left( {\theta ^* } \right) = 0.05 + 0.58e^{ - 1.48\theta ^* } \hfill \\ f_u \left( {\theta ^* } \right) = 0.12 + 0.88e^{ - 2.28\theta ^* } \hfill \\ \end{gathered} \]The incremental root biomass partitioning coefficient, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaeqySde2aaS% baaSqaaiaadkhaaeqaaOGaeyypa0JaaiikaiaadsgacaWGxbWaaSba% aSqaaiaadkhaaeqaaOGaai4laiaadsgacaWG0bGaaiykaiaac+caca% GGOaGaamizaiaadEfadaWgaaWcbaGaamiDaaqabaGccaGGVaGaamiz% aiaadshacaGGPaaaaa!4834!\[\alpha _r = (dW_r /dt)/(dW_t /dt)\], which describes the net increase in root biomass dW _r over time dt relative to the increase in total biomass (dW _r) over the same time period, has been derived from f and the relative growth rate. Its time course is accurately represented by% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaeqySdegdda% WgaaqaaiaadkhaaeqaamaabmaabaGccqaH4oqCdaahaaWcbeqaaiaa% cQcaaaaamiaawIcacaGLPaaakiabg2da9iabgkHiTiaaicdacaGGUa% GaaGymaiaaiwdacqGHRaWkcaaIWaGaaiOlaiaaiAdacaaIZaGaamyz% amaaCaaaleqabaGaeyOeI0IaaGimaiaac6cacaaI5aGaaGioaiabeI% 7aXnaaCaaameqabaGaaiOkaaaaaaaaaa!4D15!\[\alpha _r \left( {\theta ^* } \right) = - 0.15 + 0.63e^{ - 0.98\theta ^* } \]Under our experimental conditions, with no severe water stresses or nutrient deficiencies, and for our sampling frequency, around 2 weeks, the development scale , is the main factor governing the time courses of f _r, f _u and _r.     

Super-unstable mutations associated with P-M hybrid dysgenesis in Drosophila melanogaster

Super-unstable mutations occasionally appear either in natural populations of Drosophila melanogaster or in P-M hybrid dysgenesis. We found that they may be reproducibly obtained with a high frequency from crosses between males from the % MathType!MTEF!2!1!+-% feaafeart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaaubiaeqale% qabaWaaubiaeqameqaleaacaGGQaaaoeaacaWGHbGaam4raaaaa0qa% aiaadEhaaaaaaa!3A01!\[\mathop w\nolimits^{\mathop {aG}\nolimits^* } \] strain and females from the w ^aG* strain or its derivatives. Super-unstable mutations in the ocelliless, singed, white, yellow and other loci have been obtained. Each super-unstable mutation gives rise to a large family of new super-unstable mutations with a wide range of phenotypic expression. Mutations with the same phenotype often differ in the specificity of their potential for further mutation. As a rule, a super-unstable mutation is associated with a specific reversible mutation and paired alleles are formed in this way. Other mutations are usually irreversible, but new mutations of these may also form paired alleles. Active transposase encoded by transposable P elements is necessary to maintain super-instability. Finally, some preliminary molecular data are discussed which suggest that this type of super-instability is a result of interaction between P elements and a novel mobile element, designated as X.     

Diversity among nemertean egg predators of decapod crustaceans

The chemistry of water in fields at two Bangladesh deepwater rice locations is compared. Although Manikganj lies in the Jamuna (-Brahmaputra) floodplain and Sonargaon in the old Meghna floodplain, their chemistries during the flood season are similar, apart from higher Mg % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGadiiEayaara% aaaa!3703!\[\bar x\]: 3.57 v.1.8 mg 1^–1), Ca (% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGadiiEayaara% aaaa!3703!\[\bar x\]: 13.1 v.4.5 mg l^–1 ), pH and total alkalinity at the former.Diel changes in oxygen and sometimes also pH were evident 10 cm below the surface in deepwater rice fields, but such changes were typically much greater in fallow fields. Measurements made between 1400 and 1600 h in a range of habitats showed a trend for high pH values to be associated with high O₂ values. Water in Eichhornia beds had the lowest values, deepwater rice fields were intermediate and fallow fields and other open areas typically had the highest values. O₂ concentrations in excess of 15 mg l^–1 and pH values of about 10.0 sometimes occurred in fallow fields with dense masses of submerged plants and loosely associated algal flocs.There was an increasing tendency for the water to become anoxic towards the end of the season and water 10 cm above the bottom was almost or entirely anoxic in deepwater rice fields at both locations over the whole 24-h period of 4/5 October, at a time when the depth of the water was starting to drop. Nitrite increased and sulphate decreased at both locations towards the end of the season.     

Culture and mental disorder: The case of bebainan in Bali

This is an investigation of bebainan, a disorder which Balinese believe to be caused by sorcery. Most attacks are brief, lasting % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaWaaSGaaeaaca% aIXaaabaGaaGinaaaaaaa!3778!\[{\raise0.7ex\hbox{$1$} \!\mathord{\left/ {\vphantom {1 4}}\right.\kern-\nulldelimiterspace}\!\lower0.7ex\hbox{$4$}}\]–1 hour. The most common symptoms are sudden feelings of confusion, crying, screaming and shouting, followed by inability of the sufferer to control his or her actions. Most sufferers are aware of their behavior during an attack, and remember the occurrence afterwards.The investigator interviewed all the members (296 persons) in the compound of the descendants of the former royal family of Klungkung, among whom 27 people had suffered bebainan attacks. The victims, mostly females, offspring of endogamous marriges, experienced their first attack between the ages of 16 and 30. Analysis of the psychological and social pressures acting on these women suggests that bebainan attacks provide sufferers with an opportunity to release feelings of frustration and anger without risk of widespread disapprobation or stigmatization. However, bebainan is not instrumental in altering access to resources within the restricted environment of the royal compound, nor does it empower the victim within this environment in any but the most transitory ways. Bebainan cannot be regarded as a form of psychosis, even of the reactive or atypical type, it is neither an organic mental disorder, nor a form of neurosis. Instead bebainan can be considered a form of dissociation which is only understandable in the local context of Balinese culture.     

Management of the Nile perch, Lates niloticus fishery in Lake Victoria in light of the changes in its life history characteristics

Nile perch was introduced into lakes Victoria and Kyoga in the 1950s and 1960s from Lake Albert. The changes in prey eaten and the life history characteristics of Nile perch in lakes Victoria and Kyoga from the 1960s to 1990s were examined and compared with Lake Albert. The dominant prey eaten changed from haplochromines, Caridina nilotica, Rastrineobola argentea, and Nile perch juveniles. The condition factor deteriorated from 1.4 in 1960s to 1.2 in 1990s, compared with 1.3 in Lake Albert suggesting a reduction in food supply. Therefore, exploitation of Nile perch prey should be controlled. The size at first maturity increased from 30–40 to 40–50 cm and 50–59 to 80–100 cm for males and females, which is similar to Lake Albert. Sex ratios decreased from 85–100 to 20–65 females for every 100 males suggesting that Nile perch had less capacity to replenish its stocks such that breeding females should be protected. As males mature at 50–55 cm and females at 80–100 cm, immature males of <50 cm and breeding females of >100 cm could be protected through size selective exploitation of fish of 50–100 cm using gillnets of 127–254 mm.     

Predominance of picoplankton and nanoplankton in eutrophic Calder Lake

A study was conducted to examine factors regulating the biomass of algal picoplankton in Calder Lake, a small eutrophic lake in southern New York state. A particular focus was a current paradigm which suggests that larger cells may dominate in nutrient-rich waters, while smaller cells may predominate only in oligotrophic waters. Over two years, phytoplankton biomass consisted predominantly (74% on average) of very small organisms; nanoplankton (<20 to 2 µm: 39%) and picoplankton (<2 µm to 0.2 µm: 35%), despite the presence of surface blooms of colonial cyanobacteria (Microcystis aeruginosa, Anabaena limnetica), and dense metalimnetic populations of the dinoflagellate Ceratium hirundinella. This dimictic system is characterized by relatively high levels of total P (max = 85, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmiEayaara% aaaa!3702!\[\bar x\] = 9.7 µg P/L), inorganic P (max = 26, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmiEayaara% aaaa!3702!\[\bar x\] = 4.5 µg P/L), and total inorganic N (max = 285, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmiEayaara% aaaa!3702!\[\bar x\] = 85 µg P/L), but larger forms were rarely the most abundant. Unlike some marine systems, greater abundance of algal picoplankton was not associated with deeper strata (low light), or warmer temperatures. Data suggest that midsummer nutrient limitation, especially P-limitation, favors the development of pico- and nanoplankton in the limnetic zone of eutrophic lakes.     

Response by macrozoobenthos biomass to water level regulation in some Finnish lake littoral zones

The relationship of the macrozoobenthos biomass in the littoral area to the yearly fluctuation in water level and the characteristics of the area or lake are studied using data collected from sheltered bays in regulated and natural waters. Most of the lakes were clear and oligotrophic. The benthos biomass at all depths in the littoral decreased with increased water level fluctuation, provided that the transparency of the water was uniform.The macrozoobenthos biomass in the 0–3 m depth zone could be predicted fromlog macrozoobenthos biomass (mg ODW) m^-2=4.25-1.33 (log Biomass Index) in which the Biomass Index is calculated as% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaaeOqaiaabM% gacaqGVbGaaeyBaiaabggacaqGZbGaae4CaiaabccacaqGjbGaaeOB% aiaabsgacaqGLbGaaeiEaiaab2dacaqGGaGaaeiiaiaabccacaqGGa% GaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabcca% caqGGaGaaeiiaiaabccacaqGGaGaaeiiaiaabccacaqGGaGaaeiiai% aabccadaWcaaabaeqabaGaae4DaiaabggacaqG0bGaaeyzaiaabkha% caqGGaGaaeiBaiaabwgacaqG2bGaaeyzaiaabYgacaqGGaGaaeOzai% aabYgacaqG1bGaae4yaiaabshacaqG1bGaaeyyaiaabshacaqGPbGa% ae4Baiaab6gacaqGGaGaaeyAaiaab6gacaqGGaGaaeiDaiaabIgaca% qGLbGaaeiiaiaabchacaqGYbGaaeyzaiaabAhacaqGPbGaae4Baiaa% bwhacaqGZbGaaeiiaiaabMhacaqGLbGaaeyyaiaabkhaaeaacaqGOa% GaaeyBaiaabUdacaqGGaGaae4yaiaabggacaqGSbGaae4yaiaabwha% caqGSbGaaeyyaiaabshacaqGLbGaaeizaiaabccacaqGMbGaaeOCai% aab+gacaqGTbGaaeiiaiaab2gacaqGVbGaaeOBaiaabshacaqGObGa% aeiBaiaabMhacaqGGaGaaeyBaiaabwgacaqGHbGaaeOBaiaabccaca% qG2bGaaeyyaiaabYgacaqG1bGaaeyzaiaabohacaqGPaaaaeaacaqG% tbGaaeyzaiaabogacaqGJbGaaeiAaiaabMgacaqGGaGaaeizaiaabM% gacaqGZbGaae4AaiaabccacaqG2bGaaeyyaiaabYgacaqG1bGaaeyz% aiaabccacaqGPbGaaeOBaiaabccacaqG0bGaaeiAaiaabwgacaqGGa% Gaae4CaiaabggacaqGTbGaaeyzaiaabccacaqGVbGaaeiCaiaabwga% caqGUbGaaeiiaiaabEhacaqGHbGaaeiDaiaabwgacaqGYbGaaeiiai% aabohacaqGLbGaaeyyaiaabohacaqGVbGaaeOBaiaabccacaqGOaGa% aeyBaiaabMcaaaaccaGae8hiaaIaaKiEaiab-bcaGiaaigdacaaIWa% GaaGimaiaac6caaaa!CBD8!\[{\text{Biomass Index = }}\frac{\begin{gathered} {\text{water level fluctuation in the previous year}} \hfill \\ {\text{(m; calculated from monthly mean values)}} \hfill \\ \end{gathered} }{{{\text{Secchi disk value in the same open water season (m)}}}} \user1{x} 100.\]The whole illuminated littoral shifts due to water level fluctuation, which disturbs the zonation of the benthos. Such an increase or decrease in benthic biomass has been observed after one year of disturbance due to water level fluctuation. It need, however, a study based on the carefully planned and collected data, in which it can be taken account by a multivariate statistical analysis also the interactions between the important factors affected the littoral benthos.