Effects of photoperiod on reproductive development of peanut (Arachis hypogaea L.) in a cool subtropical environment. I. Field studies

1991 ◽  
Vol 42 (7) ◽  
pp. 1133 ◽  
Author(s):  
MJ Bell ◽  
G Harch

The effects of photoperiod on reproductive development and yield of two Virginia, one Spanish and one Valencia peanut (Arachis hypogaea L.) cultivar were investigated in the field at Kingaroy, Australia. The objective was to assess the importance of photoperiod as a limitation to post-flowering reproductive development in a cool subtropical environment. A total of five experimental sowings were made between the 1986/87 and 1988/89 growing seasons. Treatments consisted of either natural photoperiods (ranging from 11 to 14 h, depending on sowing date and growth stage) or long (16 h) photoperiods during a range of phenological stages, both pre- and post-flowering. Long photoperiods were achieved by using low intensity light from incandescent bulbs with equal extension periods in both morning and evening. Different sowing dates and seasons were used to produce a range of natural photoperiods, radiation and temperature regimes, while shadecloth was used to alter incident irradiance during the 1988/89 experiments. Photoperiod responses were significant in only one experiment (S2, 1986/87), and were due to effects of treatment during the immediate post-flowering period. Numbers of flowers, pegs and pods were reduced under long photoperiods in cv. Robut 33-1, and to a lesser extent, in cv. White Spanish. The Virginia cv. Uf 781 14-5 was unaffected. The effects of long photoperiods during this 30 day post-flowering treatment were not expressed until after the treatment period. Effects were relatively small and reproductive (pod) yields at maturity were not significantly reduced. The lack of strong photoperiod responses in the reportedly sensitive Valencia cv. NC17090 and the occurrence of the strongest response in the relatively insensitive cv. Robut 33-1 were unexpected. Analysis of climatic data from these experiments, and others reported in the literature, suggested interactions between photoperiod and temperature, with photoperiod effects being only significant at higher temperatures, i.e. in our studies, when mean daily temperature during the treatment period was 26-0�C. This finding is of considerable significance in assessing the importance of photoperiod sensitivity for cultivar adaptation to long day/subtropical environments. A subsequent paper in this series examines photoperiod x temperature interactions more closely under controlled environment conditions.

1991 ◽  
Vol 18 (2) ◽  
pp. 67-71 ◽  
Author(s):  
G. Wehtje ◽  
J. W. Wilcut ◽  
J. A. McGuire ◽  
T. V. Hicks

Abstract Field studies were conducted over a three year period to examine the sensitivity of four peanut (Arachis hypogaea L.) cultivars (Florunner, Sunrunner, Southern runner, and NC 7) to foliar applications of paraquat (1, 1′-dimethyl-4, 4′-bipyridinium ion). Treatments included an untreated control and four herbicide treatments: paraquat applied alone at 0.14 and 0.28 kg/ha, or tank mixed with alachlor [2-chloro-N-(2, 6-diethylphenyl)-N-(methoxymethyl)acetamide] at 4.40 kg/ha. Weeds were hand-removed so that only herbicidal treatments were variables. Paraquat phytotoxicity did not differ between cultivars. No cultivar evaluated was abnormally sensitive nor tolerant to any paraquat-containing treatment. Laboratory studies utilizing radio labelled paraquat revealed that foliar absorption and translocation of paraquat did not vary between peanut cultivars. Yield differences were attributed to differences in yield potential between cultivars.


1991 ◽  
Vol 18 (2) ◽  
pp. 110-116 ◽  
Author(s):  
Robert E. Lynch ◽  
David M. Wilson

Abstract The relationship between injury by the lesser cornstalk borer (LCB), Elasmopalpus lignosellus (Zeller), and invasion of peanut, Arachis hypogaea L., pods and seeds by species of the Aspergillus flavus group (A. flavus Link and A. parasiticus Speare) were studied under laboratory and field conditions. In the laboratory, LCB larvae were an excellent vector of an A. parasiticus color mutant (ATCC 24690) to all developmental stages of peanut pods. Fungal invasion and aflatoxin concentration in seeds were higher in immature pods (stage 2–3) than in more mature pods (stage 4–6). Contamination of seeds with ATCC 24690 was directly related to the extent of pod injury by larvae of the LCB. In field studies, over 50% of the LCB larvae collected from peanut were naturally contaminated with species of the A. flavus group. The planting date and harvest date of peanut had little influence on the incidence of fungal contamination of pods and seeds, or on aflatoxin content in seeds. However, increased pod injury by the LCB significantly increased the percentage of seeds infected with species of the A. flavus group. Seeds in pods with only external scarification from larval feeding had a significantly higher percentage of A. flavus group infection than seeds from uninjured pods. Therefore, infection and contamination of visibly uninjured seeds with aflatoxigenic fungi were enhanced by external injury to peanut pods by the LCB.


1992 ◽  
Vol 19 (2) ◽  
pp. 111-115 ◽  
Author(s):  
W. Carroll Johnson ◽  
C. Corley Holbrook ◽  
Benjamin G. Mullinix ◽  
John Cardina

Abstract Field studies were conducted in 1988 and 1989 to compare the sensitivity of eight genetically diverse peanut (Arachis hypogaea L.) genotypes to early applications of chlorimuron. A split-plot experimental design was used to allow comparison between treated and nontreated peanut for each genotype. Chlorimuron (0.009 kg ai ha-1) was applied 30 and 37 days after emergence in 1988 and 1989, respectively, to Florunner, Tifrun, Tifton 8, GA-207–3–4, New Mexico Valencia A, New Mexico Valencia C, Tamnut 74, and Pronto peanut. Chlorimuron reduced the percentage of total sound mature kernels when averaged across all genotypes, but was not specific to genotype. Chlorimuron reduced the weight of 100 kernels of Tifrun, Tifton 8, and New Mexico Valencia C in both years. The unit values of GA-207–3–4 and New Mexico Valencia C were significantly reduced both years by early applications of chlorimuron. Yields of Tifrun, Tifton 8, and GA-207–3–4 were reduced both years. Gross returns, which reflect effects on grade, unit value, and yield, were reduced by early applications of chlorimuron for Tifton 8 and GA-207–3–4 in both years. Based on these results, Tifrun, Tifton 8, GA-207–3–4, and New Mexico Valencia C are more inherently sensitive to chlorimuron than the other genotypes.


2001 ◽  
Vol 28 (1) ◽  
pp. 13-19 ◽  
Author(s):  
T. L. Grey ◽  
D. C. Bridges ◽  
E. F. Eastin

Abstract Field studies were conducted from 1996 to 1998 in Georgia to determine peanut (Arachis hypogaea L.) and weed response to ethalfluralin (0.8 kg ai/ha) plus diclosulam applied preplant incorporated (PPI) at 9, 18, 26, 35 and 52 g ai/ha. Other treatments included ethalfluralin PPI followed by paraquat plus bentazon (140 and 280 g ai/ha, respectively) early postemergence (EPOST) applied alone or following ethalfluralin plus diclosulam (18 and 26 g ai/ha) PPI, ethalfluralin PPI followed by imazapic (71 g ai/ha) postemergence (POST), and ethalfluralin PPI. Ethalfluralin was applied PPI in all herbicide programs. Diclosulam controlled Florida beggarweed [Desmodium tortuosum (Sweet) D.C.], sicklepod [Senna obtusifolia (L.) Irwin and Barneby], and yellow nutsedge (Cyperus esculentus L.) inconsistently, and POST application of paraquat plus bentazon was needed for acceptable control. However, diclosulam controlled common ragweed (Ambrosia artemisiifolia L.), tropic croton (Croton glandulosus Muell-Arg.), wild poinsettia (Euphorbia heterophylla L.), and prickly sida (Sida spinosa L.) without the need for POST herbicides. Higher yields were recorded with diclosulam PPI followed by a sequential application of paraquat plus bentazon than herbicide programs not containing diclosulam or diclosulam alone. Diclosulam PPI followed by sequential applications of paraquat plus bentazon provided greater control of sicklepod and prickly sida that resulted in greater yields. Yields from dicosulam PPI followed by paraquat plus bentazon EPOST were equivalent to yields with paraquat plus bentazon EPOST followed by imazapic POST or imazapic EPOST.


2002 ◽  
Vol 29 (1) ◽  
pp. 24-29 ◽  
Author(s):  
T. L. Grey ◽  
D. C. Bridges ◽  
E. F. Eastin ◽  
G. E. MacDonald

Abstract Field studies were conducted during 1997 and 1998 at three different locations in Georgia to determine peanut and weed response to pendimethalin at 1.1 kg ai/ha applied preplantincorporated (PPI) followed by flumioxazin at 71, 87, and 105 g ai/ha applied preemergence (PRE). Other residual treatments combinations with pendimethalin PPI included flumioxazin mixed with metolachlor or dimethenamid PRE, diclosulam PRE, norflurazon PRE, and imazapic applied postemergence (POST). Herbicide combinations that included flumioxazin controlled Florida beggarweed, tropic croton, and small flower morningglory at least 78% or greater. Late season Florida beggarweed control was 90% or greater with pendimethalin PPI plus flumioxazin at 87 to 105 g/ha applied PRE. Pendimethalin plus flumioxazin did not control sicklepod or yellow nutsedge. Smallflower morningglory control with all herbicide treatments was 90% or greater. Entireleaf morningglory control (when used in combination with pendimethalin PPI) increased from 80% with flumioxazin at 105 g/ha to 90% for flumioxazin in combination with metolachlor. Yields were similar for flumioxazin, norflurazon, imazapic, and diclosulam treated peanut.


1991 ◽  
Vol 42 (7) ◽  
pp. 1151 ◽  
Author(s):  
MJ Bell ◽  
DJ Bagnall ◽  
G Harch

The effects of temperature on the response to photoperiod by peanut (Arachis hypogaea L.) cultivars were examined under glasshouse and phytotron conditions at two locations (Kingaroy and Canberra). Two Virginia cultivars (Early Bunch and Robut 33-l), two Spanish cultivars (White Spanish and TMV-2) and a single Valencia (NC 17090) cultivar were grown in the experiments. White Spanish was common to both studies. Strong photoperiodxtemperature interactions were shown for all cultivars in both experiments, with the sensitivity of peg number to photoperiod increasing at higher temperatures. Photoperiod responses were all indicative of short-day (SD) response types, and were always expressed in post-flowering reproductive development. No effects of photoperiod on time to first flower were evident, but numbers of pegs and pods and total pod weight per plant were reduced in long (16 or 17 h) photoperiods. Data from field experiments at Kingaroy were pooled with those from the glasshouse and controlled environment studies to estimate the critical temperatures above which photoperiod sensitivity became significant. Hourly temperature readings were used to calculate a daily heat sum (�C h) above a base temperature of 10�C for each experiment. This index of the temperature condition proved satisfactory as a possible discriminatory method to describe environments based on likely photoperiod response. Environments where daily heat unit accumulations greater than 340-350�C h were recorded during the treatment period showed significant photoperiod responses. The possibility of minimum temperature being the predominant component of the temperaturexphotoperiod interaction is also discussed. This proved less effective in discriminating between environments for photoperiod response, but data were insufficient to discount this possibility and further studies are needed. Results question the relevance of photoperiod as a factor limiting reproductive development of peanuts in cooler, subtropical environments.


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