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Densities of Orthoptera typically vary greatly over space and time. The most important salt marsh orthopteran on the East Coast of the US is Orchelimum fidicinium, an omnivore that feeds on cordgrass (Spartina alterniflora) and arthropods. We examined spatial (34 sites) and temporal (5 sites, 17 years) variation in O. fidicinium density in coastal Georgia. Sites with considerable adjacent upland habitat had higher densities of O. fidicinium than sites with little adjacent upland. Grasshoppers fed S. alterniflora from both types of sites did not differ in growth rates, ruling out food quality as an explanation. We speculate instead that O. fidicinium require terrestrial habitat for reproduction or escape from predators during extreme high tides. At five sites where O. fidicinium was common, densities varied greatly among years. Regression models indicated that current year plant biomass (three sites) or previous year plant biomass (one site) was the best predictor of O. fidicinium density. Relationships between O. fidicinium and current year plant biomass were typically negative (more grasshoppers in years with lower plant biomass). A possible explanation for this pattern is that plant nutrients may be diluted in years with high plant biomass. We found little evidence that density of animal prey (Prokelisia spp.) or abiotic factors affected O. fidicinium densities. Our study illustrates the value of examining population densities across multiple sites and years, because results from any one site or year would likely have mischaracterized the spatial and temporal distribution of this common salt marsh consumer.

The meadow katydid Orchelimum superbum was previously known from scattered localities along the Atlantic and Gulf Coasts of North America. We found this species to be widespread and locally common on the Great Plains in a variety of habitats, including tallgrass prairie, wetlands, and roadsides. We found no evidence for cryptic species after studying the morphology of the male terminalia, comparing body size, and analyzing 14 calling song characters. Individuals from the Great Plains are consistently larger in body size than individuals from the historical range. From patterns of body size variation and abundance, we hypothesize that the eastern Great Plains is the center of distribution for O. superbum and that the coastal localities, including the type locality, are peripheral populations. We compare the songs of O. superbum and O. vulgare, showing that these two sympatric but allochronically separated species share most buzz-mode characters including statistically indistinguishable syllable re...

Top–down and bottom–up effects interact to structure communities, especially in salt marshes, which contain strong gradients in bottom–up drivers such as salinity and nutrients. How omnivorous consumers respond to variation in prey availability and plant quality is poorly understood. We used a mesocosm experiment to examine how salinity, nutrients, an omnivore (the katydid Orchelimum fidicinium) and an herbivore (the planthopper Prokelisia spp.) interacted to structure a simplified salt marsh food web based on the marsh grass Spartina alterniflora. Bottom–up effects were strong, with both salinity and nutrients decreasing leaf C/N and increasing Prokelisia abundance. Top–down effects on plants were also strong, with both the herbivore and the omnivore affecting S. alterniflora traits and growth, especially when nutrients or salt were added. In contrast, top–down control by Orchelimum of Prokelisia was independent of bottom–up conditions. Orchelimum grew best on a diet containing both Spartina and Prokelisia, and in contrast to a sympatric omnivorous crab, did not shift to an animal-based diet when prey were present, suggesting that it is constrained to consume a mixed diet. These results suggest that the trophic effects of omnivores depend on omnivore behavior, dietary constraints, and ability to suppress lower trophic levels, and that omnivorous katydids may play a previously unrecognized role in salt marsh food webs.

Although grasshoppers are common salt marsh herbivores, we know little about geographic variation in their species composition. We documented latitudinal variation in species composition of the tettigoniid grasshopper fauna of Atlantic Coast salt marshes. Tettigoniids (N = 740 adults) were collected from the Spartina alterniflora zone of 31 salt marsh sites across a latitudinal range of 13.19° (Florida to Maine), with an additional 52 individuals collected from the Juncus roemerianus zone of low-latitude marshes for comparative purposes. Eight species were collected, but some were common only at a few sites or rare throughout the entire collection range. The tettigoniid community was dominated by Orchelimum fidicinium at low latitudes and Conocephalus spartinae at high latitudes. Several factors might explain this shift, including changes in climate, plant phenology, and plant zonation patterns. O. fidicinium and C. spartinae increased in body size toward low latitudes. In laboratory feeding assays, O. fidicinium readily ate S. alterniflora and J. roemerianus leaves, Orchelimum concinnum, which is largely restricted to the J. roemerianus zone, ate only J. roemerianus leaves, and Conocephalus spp. ate neither, consistent with literature suggestions that they mainly consume seeds and flowers. Geographic variation in species composition and body size of grasshoppers may help explain documented patterns of geographic variation in plant palatability and plant–herbivore interactions in Atlantic Coast salt marshes. Because it can be difficult to identify tettigoniids to species, we present a guide to aid future workers in identifying the tettigoniid species common in these marshes.

Hard-bodied orthopteran adults, in particular Acrididae, are an important source of insect contaminants in mechanically harvested leafy greens, Brassica spp. Because contaminants are usually detected after greens are fully processed, rejection of these value-added loads can be economically severe. A survey was conducted to determine the level of orthopteran species occurring in and around leafy greens fields prior to mechanical harvesting. This survey demonstrated that the vast majority of individual Orthoptera occurred around the edges of the field prior to harvest. In the second year of the survey, growers were already applying Sevin XLR™ (Aventis CropScience, Research Trangle Park, NC) insecticide to grassy border areas in order to prevent acridid adults from moving into the field before harvest. The main taxonomic groups in Orthoptera found in this survey included Orchelimum sp. (Tettigonidae) (68.8%), Melanoplinae (Acrididae) (18.5%), other Acrididae (5.4%), Schistocerca americana (Drury) (Acrididae) (3.4%), Dissosteira Carolina (Linnaeus) (Acrididae) (2.4%), and other Tettigonidae (1.6%). Insecticide treatment of border areas prior to harvest provided a 94% reduction in Acrididae in the field prior to harvest.

Genus Orchelimum Serville, 1838 Orchelimum Serville, 1838 [1839]: 522. Type species: Orchelimum cuticulare Serville, 1838, Published as part of Yong, Sheyla & Perez-Gelabert, Daniel E., 2014, Grasshoppers, Crickets and Katydids (Insecta: Orthoptera) of Cuba: an annotated checklist, pp. 401-438 in Zootaxa 3827 (4) on page 430, DOI: 10.11646/zootaxa.3827.4.1, http://zenodo.org/record/228581

Orchelimum (Orchelimum) concinnum Scudder, 1862 Scudder, 1862: 452; Zayas, 1976: 67, fig. 61. Lectotype male, from Cape Cod, Massachusetts, Northeastern U. S. A. [ANSP]. Distribution. Caribbean and North America. Notes. Two specimens in the Zayas collection from ”Península de Zapata, Las Villas prov., V- 1960 ”., Published as part of Yong, Sheyla & Perez-Gelabert, Daniel E., 2014, Grasshoppers, Crickets and Katydids (Insecta: Orthoptera) of Cuba: an annotated checklist, pp. 401-438 in Zootaxa 3827 (4) on page 430, DOI: 10.11646/zootaxa.3827.4.1, http://zenodo.org/record/228581, {"references":["Scudder, S. H. (1862) Materials for a monograph of the North American Orthoptera, including a catalogue of the known New England species. Journal of the Boston Society of Natural History, 7, 409 - 480."]}

The katydids Orchelimum nigripes and O. pulchellum (Orthoptera: Tettigoniidae) have a largely allopatric distribution in the eastern United States, but hybridization between these species has been well documented in two contact zones. I used animals from populations just outside a narrow, recently formed upstream-downstream hybrid zone along the Potomac River near Washington, D.C., in laboratory mate-choice trials to examine the possible importance of differential patterns of mate preference in determining the structure and dynamics of this hybrid zone. Offered a choice between a male of each species, O. nigripes females showed an extreme preference for conspecific mates, but O. pulchellum females showed no clear preference. This asymmetry in mate discrimination may contribute to the apparently ongoing replacement along the Potomac of O. pulchellum by O. nigripes in the wake of a moving hybrid zone.

concinnum Scudder, 1862: 452 [Orchelimum]. One ♂ and one ♀ paralectotype. The lectotype (designated by Rehn & Hebard, 1915: 60) is in the ANSP. Orchelimum concinnum Scudder, 1862, Published as part of Hollier, John & Heads, Sam W., 2014, The type specimens of Orthoptera described by American entomologists in the collection of the Muséum d'histoire naturelle de Genève, pp. 63-76 in Revue suisse de Zoologie 121 (1) on page 72, DOI: 10.5281/zenodo.5822978, {"references":["SCUDDER, S. H. 1862. Materials for a monograph of the North American Orthoptera including a catalogue of the known New England species. Boston Journal of Natural History 7: 409 - 480.","REHN, J. A. G. & HEBARD, M. 1915. Studies in American Tettigoniidae IV, Orchelimum. Transactions of the American Entomological Society 41: 11 - 83, pl. 1 - 4."]}

1839 Serville, Hist. nat. Ins., Orthopt.: 522 1915a Rehn & Hebard, Trans. Amer. Ent. Soc. 41: 11-83 >>revision 1999 Naskrecki and Otte, Illustr. Cat. Orthop. I (CD ROM) >>references; types illustrated Note: The genus Orchelimum is an example of a group maintained in the taxonomic literature by tradition rather than actual diagnostic characteristics that can identify it as a natural, monophyletic assemblage. Rehn and Hebard (1915a) present a combination of characters that supposedly identify Orchelimum as a genus distinct from Conocephalus, but even they admit that none of the characters is unique to Orchelimum and all of them occur, albeit less frequently, in Conocephalus. The only relatively consistent characteristics of Orchelimum spp. are their more robust appearance and larger body form, but even these characters broadly overlap with some species of Conocephalus. There are no consistent differences between the two genera either in the male or female genitalic structures, the male stridulatory apparatus, wing venation, leg armature, or any other structures considered diagnostic for Tettigoniidae. Glenn K. Morris (personal communication) provides two behavioral characters that may indicate a degree of separateness of the two genera. The dominant spectral peak of the male���s call in Orchelimum is in the acoustic range (about 18 kHz) whereas in Conocephalus (where unfortunately only a small fraction of species have ever been recorded) the dominant spectral peak is in the ultrasonic range (30 kHz and above). Morris notes, however, that ���this song parameter is of course not unrelated to size, though it is not fair to say that frequency is simply dictated by size���. The second behavioral character apparently unique to Orchelimum is high incidence of male fighting, and many of the species known to fight do it by grappling. The latter is unknown to occur in males of Conocephalus. These observations, however, are based on a very limited number of species. Despite the lack of strong support for the separate status of the genus Orchelimum, it seems unwise to synonymize the two genera at this point as both names are well established in taxonomic literature and many species of Orchelimum are easily recognizable based on their larger size and sometimes distinct coloration. For the purpose of this review Orchelimum is treated as a separate, yet very closely related to Conocephalus genus of Conocephalinae s.l. Body slender to robust, small to medium size as for the family; macropterous or mesopterous (Figs. 3 A); tegumen smooth. Fastigium of vertex laterally compressed, rounded apically, never cone-shaped; no traces of genal carinae present; mandibles and labrum symmetrical; eyes relatively large. Pronotum short, lateral lobes approximately triangular, humeral sinus weak to well developed, posterior edge of lobe with well developed ���secondary tympanum.��� Stridulatory file with peg like teeth, strongly sinusoidal. All legs slender, fore and mid femora unarmed on lower margins. Male cercus always armed with one internal tooth; ovipositor weakly to distinctly curved, lower and upper edges of ovipositor parallel to divergent midlength. Description (male except where specified) Head.��� Fastigium of vertex 0.75 to 1.4 times as wide as scapus (Figs. 3 B-C), laterally compressed, rounded dorsally and apically, never hook- or cone-shaped, never projecting strongly in front of eyes; fastigium of vertex touching fastigium of frons. Eyes large relative to size of head, weakly protruding. Frons weakly convex, smooth; tegumen of head smooth, without traces of genal carinae; face slender to moderately wide. Mandibles and labrum symmetrical. Thorax and wings.��� Dorsal surface of pronotum smooth, flat or metazona slightly raised; anterior dorsal margin straight, posterior one straight or weakly convex; lateral lobes approximately triangular, with acute posterior angle; posterior edge of lateral lobe with ���secondary tympanum��� ��� a somewhat raised, narrowly elliptical area of thinner cuticle covering thoracic auditory spiracle; humeral sinus poorly to well developed (Fig. 3 A). Thoracic auditory spiracle large, elliptical, completely hidden under lateral lobe of pronotum; posterior edge of spiracle unmodified. Prosternum armed with two thin, short spines (modified basisternum); meso- and metasternum with lateral lobes of basisterna small, triangular, their inner margins touching; posterior part of metasternum strongly compressed causing hind coxa to nearly touch each other. Wings in both sexes fully developed, surpassing apices of hind femora, rarely somewhat shortened and not reaching hind knees; hind wings usually distinctly longer than tegmina. Stridulatory apparatus of male well developed; stridulatory area of left wing membranous, without a network of secondary veinlets; stridulatory file (vein AA1���new vein homology after Kukalova-Peck, personal communication; male stridulatory file used to be homologized with the vein Cu2) sinusoidal (Fig. 41 A), teeth thick, peg-like, sparsely arranged, especially on distal end of file; mirror of right wing approximately rectangular, with secondary veinlet next to AA1 always well developed, divergent from AA1. Legs.��� All legs long and slender; fore coxa with an elongate, forward projecting spine dorsally. All femora unarmed dorsally; fore and mid femora unarmed ventrally, hind femora armed ventrally with relatively few minute spines or unarmed; genicular lobes of femora usually armed with short spines. Fore and mid tibiae unarmed dorsally, both ventral margins with immovable spines as long as 1/4 to 1/2 diameter of tibia; hind tibia armed on all four dorsal and ventral margins; apex of tibia with two pairs of ventral and one pair of dorsal movable spurs. Tympanum on fore tibia bilaterally closed, tympanal slits facing forward, tympanal area weakly to distinctly swollen, with pair of small, elongated pits below tympanal slits. Abdomen.��� Dorsal surface of abdominal terga smooth, unmodified. Male 10th tergite usually strongly sclerotized, with narrow apical incision, supraanal plate small, triangular. Male cercus always with one internal spine, often accompanied by more or less developed dorsal, sinusoid groove (Fig. 41 C); female cercus, simple, slender and weakly incurved. Subgenital plate of male with a pair of styli, distinct median keel, truncated apically (Fig. 3 D) or with triangular apical emargination; female subgenital plate approximately triangular, rounded or shallowly emarginated apically. Concealed genitalia of male with paired, heavily sclerotized, hook-like titillators (Fig. 3 E). Ovipositor narrow, straight to distinctly curved; its length variable, from less than half the length to almost as long as hind femur; both dorsal and ventral margins of ovipositor smooth, parallel to divergent midlength; apex of upper valvula sharp (Fig. 3 F). Coloration.��� General coloration green to brown, almost invariably with dark, wide stripe on head and pronotum; head sometimes red dorsally (O. erythrocephalum Davis) or face with median brown stripe (O. concinnum Scudder); abdomen green or yellow; sometimes dorsal side of abdomen yellow, with dark, longitudinal stripes. Tegmina straw brown to light green; legs green to light brown. Remarks.��� The genus Orchelimum includes 23 described species, distributed from south-eastern Canada, throughout eastern United states, Mexico to northern Costa Rica. Most species occur in moist freshwater habitats among sedges or reeds, along streams or margins of ponds. Some species occur in less typical habitats such as dry weedy fields, salt marshes, and two species are arboreal. The only Costa Rican species of the genus, O. fraternum, occurs on tall grassy vegetation along edges of the dry forest of Guanacaste as well as in open, savanna-like grasslands. It is a diurnal species, with males singing all day from tall vegetation. Nothing is know of their natural diet but in captivity they accepted grass seeds and various vegetables and fruits., Published as part of Piotr Naskrecki, 2000, Katydids of Costa Rica / Vol. 1, Systematics and bioacoustics of the cone-head katydids (Orthoptera: Tettigoniidae: Conocephalinae sensu lato)., Philadelphia, PA :The Orthopterists Society at the Academy of Natural Sciences of Philadelphia, on pages 23-24, DOI: 10.5281/zenodo.270035, {"references":["Rehn, J. A. G., and Hebard, M. 1915 a. Studies in American Tettigoniidae (Orthoptera). IV. A synopsis of the species of the genus Orchelimum. Trans. Amer. Ent. Soc. 61: 11 - 83."]}

Orchelimum fraternum Rehn and Hebard, 1915 Figs. 3 A-F, 41A-C, 51E-F, Map 3 1915a Rehn & Hebard, Trans. Amer. Ent. Soc. 41: 22, 79 >> O. (Metarhoptrum); type locality: Mexico: Jalisco, Guadalajara; type depository: Academy of Natural Sciences, Philadelphia, PA, USA >> holotype male 1932 Hebard, Trans. Amer. Ent. Soc. 58: 334 Diagnostic description.��� General characteristics as described above; mesopterous, with tegmina surpassing apex of abdomen but not reaching apices of hind femora (Fig. 3 A). Stridulatory file of male 1.62 mm long, with 68 primary teeth (see Fig. 41 A-B), maximum width of file 72.9 ��m; teeth of file thick, peg-like, more densely arranged at ends of file than in its middle portion. Left (upper) mirror of stridulatory apparatus as in Fig. 3 C, about as long as eye diameter. Fastigium of 1.2 times wider than scapus. Ventral edges of hind femur unarmed. Male cercus as in Fig. 41 C; ovipositor distinctly shorter than hind femur (ratio ovipositor/hind femur 0.6-0.7), weakly upcurved (Fig. 3 F). Coloration.��� Coloration light green; dorsum of head and pronotum with wide, dark band border with thin, yellow stripes (Fig. 3 C). Abdomen yellow dorsally, male cerci dark yellow, with reddish tips. Measurements (mm).��� Measurements (4 males, 5 females). ��� body with wings: male 22.6-24.4, female 23- 23.1; pronotum: male 4.9-5.1, female 5-5.4; tegmen: male 16.5-17.3, female 15-16; hind femur: male 18.7-19, female 18.7-18.7; ovipositor: female 11.1-12.4. Bioacoustics.��� The call of O. fraternum consists of regular series of short buzzes, each lasting 0.49- 0.77 s (at 28��C) and separated by 0.6- 0.77 s of silence (Fig. 51 E-F). Each buzz has two pulse train groups. The first group consists of 6-7 pulse trains produced at a slow rate (24.5-28.5/s), with trains separated by 7-14 ms (avrg. 11.26��2.4, n=19) of silence. The second, faster (47-48.2/s) and longer group consists of 11-25 train groups separated by only 1-3 ms (avrg. 1.8��0.5, n=18) of silence. Individual train groups are of similar length in both the slow and fast pulse train groups, and last 19-26 ms (avrg. 21��2.3, n=17). The call is low Q, with most energy apparently allocated between 9 and 16 kHz. Material examined.��� COSTA RICA: Guanacaste Prov., Area de Conservacion Guanacaste, Santa Rosa National Park, 21 - 24 August 1999 (coll. P. Naskrecki, D. Otte, G. Morris) - 4 males, 5 females (GKM, PN collection); Mexico: Jalisco, Guadalajara, (coll. Crawford) - 1 male (holotype) (Philadelphia)., Published as part of Piotr Naskrecki, 2000, Katydids of Costa Rica / Vol. 1, Systematics and bioacoustics of the cone-head katydids (Orthoptera: Tettigoniidae: Conocephalinae sensu lato)., Philadelphia, PA :The Orthopterists Society at the Academy of Natural Sciences of Philadelphia, on pages 24-26, DOI: 10.5281/zenodo.270035, {"references":["Rehn, J. A. G., and Hebard, M. 1915 a. Studies in American Tettigoniidae (Orthoptera). IV. A synopsis of the species of the genus Orchelimum. Trans. Amer. Ent. Soc. 61: 11 - 83."]}

A terminology useful in describing conocephaline amplitude modulation patterns is presented in this first part of a three-part study of calling songs inOrchelimummeadow katydids. Geographical distributions are mapped for the 18 species which occur in North America north of Mexico and several substantial range extensions reported, Comparison of stridulatory files indicates two types within the genus, one characterized by more widely spaced teeth near the basal end of the file. Teeth are asymmetrical in accordance with the generation of the loudest song components on wing closure.

1. Male calling songs of 10 species ofOrchelimum were tape-recorded 9 to 52 times over ranges of ambient temperatures as great as 20 °C. 2. For each species the relation between wingstroke rate and temperature was approximately linear. Calculated regression lines had coefficients of determination (r2) between 0.76 and 0.99 (aver.r2=0.93). The slopes of the regression lines varied from 0.9 to 5.1, but when extrapolated downward toŷ=0, the lines tended to converge at 11 °C (x±SD=10.9±1.9). 3. These results are similar to those published for 27 species of crickets and known for 20 additional species of katydids. 4. In previous studies, by others, the effects of temperature on rates within poikilotherm nervous systems have generally been reported asQ10 values. Such values are appropriate if rates approximate an exponential function of temperature. However, reanalysis of 15 published data sets that were adequate to justify a comparison showed that 13 fit a linear model more closely than an exponential one. Furthermore, if one half a data set was used to predict the other half, the linear model was superior to the exponential model 26 of 30 times. The temperature ranges of the 15 data sets were as small as 12 and great as 26 Celsius degrees. 5. For those 13 data sets with anr2>0.90, the regression lines tended to converge like those of katydids and crickets. For seven species of electric fish the values ofx whenŷ (discharge rate)=0 clustered about 4 °C (x±SD=4.0±1.8 C). 6. Empirically the linear model is superior to the exponential one in (1) goodness of fit, (2) prediction of effects beyond the temperature range studied, and (3) prediction of data sets from a single or no datum. 7. The origin and slope of the linear regression are generally more useful thanQ10 values as short-hand expressions of temperature effects on rates in poikilotherm nervous systems. 8. Rates in poikilotherm nervous systems are more complex in their determinants than are rates ofin vitro chemical reactions. It is therefore not surprising that the former rates fail to show the simple exponential relations to temperature that the latter show. On the other hand, that poikilotherm nervous systems should generally have approximately linear relations to temperature and that the extrapolations of linear regression lines should tend to converge at zero rate are unexpected and reveal a need for more study of underlying causes.

Discovery of the "lost types" of Xiphidium glaberrimum Burmeister, 1838, has made possible the clarification of use of several names which have been used for two species of Orchelimum. O. glaberrimum is shown to be the senior synonym for the species known as O. vulgare Harris, 1841. To preserve stability, an application has been made to the International Commission on Zoological Nomenclature to suppress both glaberrimum Burmeister and cuticulare Audinet-Serville, 1838. O. erythrocephalum Davis, 1905, is removed from synonymy with O. glaberrimum, and is the valid name for that species. Characters for distinguishing vulgare and erythrocephalum are discussed and illustrated. Type specimens are designated for glaberrimum, cuticulare, and vulgare.

Orchelimum Vulgare Harris, not hitherto reported as destructive to raspberry, did much damage by ovipositing in canes of Illinois plantations adjoining crops of clover, cowpeas and alfalfa in 1928 and 1929. Egg-laying scars, oviposition, hatching, and molting are described. Cultural and mechanical control measures are suggested. An egg parasite is recorded.

During the past four years the writer has been getting together a collection of Locustidæ from various parts of the State of Indiana, with a view a preparing a general descriptive paper of the species of that family found in the State. In working over the material thus gathered thirty-seven species are found to be represented, four of which are evidently new to science. Of the four, three belong to the genus Orchelimum and one to the genus Conocephalus. The former genus is represented in the collection by ten specis and the latter by four. Below is given a descritption of each of the four species believed to be new, together with such notes concerning the distribution of each as I find in my field note-book.

It seems quite certain in considering Redtenbacher' description of Xiphidium agile, DeGeer, which he considers the same as Orchelimum vulgare, Harris, that he took for his type of the species what is generally identified as O. vulgare. His figure (80) is also a typical vulgare. He says the elytra not at all or scarcely exceeding the hind femora, very little shorter than or equalling the wings. All the femora unarmed. These are charactes of O. vulgare, Harris.

The following table made as simple as possible, and based almost exclusively upon the female sex, will serve to distinguish the species of Xiphidium hitherto described or recorded from the United States and Canada. It included only the species of Xiphidium proper; i. e., those of slender form with straight or nearly straight ovipositor, excluding the stouter species with distinctly arcuate ovipositor, commonly referred to Orchelimum, though both are classed together by Redtenbacher.

Orchelimum carinatum, known from western Tennessee and western Florida, is easily distinguished from other Orchelimum by morphology and by calling song. O. pulchellum Davis, O. nigripes Scudder, O. bullatum Rehn and Hebard, and O. carinatum constitute the nigripes group of Orchelimum.

Those who visit the pine-barrens of New Jersey know what a pleasure it is to ramble along the narrow wooded-ppaths among the pine trees ; old paths that after once being made continue for many years, and may seldom entertain a pedestrian. Along these paths and by the side of the sandy roads, any time during late summer arrd until frost, one may hear a faint, lisping little song from a grasshopper corning from the pines, often from their topmost branches. It is an easy matter to climb the pitch-pine, which is usually arranged admirably for the purpose, and the grasshopper is also friendly to investigation, and commonly continues to stridulate.